CRISPRimmunity

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Overview of predicted results

Overview of the results

Contig_ID	Contig_def	CRISPR array number	Contig Signature genes	Self targeting spacer number	Target MGE spacer number	Prophage number	Anti-CRISPR protein number
NZ_HG917869	Clostridium bornimense strain M2/40 chromosome M2/40_rep2	1 crisprs	DEDDh,WYL,csa3	0	2	0	0
NZ_HG917868	Clostridium bornimense strain M2/40 chromosome M2/40_rep1	4 crisprs	cas14j,WYL,cas6,cas8b2,cas7,cas5,cas3,cas4,cas1,cas2,csa3,DinG,DEDDh	0	3	6	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_HG917869_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_HG917869_1

90443-91519

Orphan

III-B

Consensus_repeat	Method
GTTGAACAATAACATGTGATGTTTTTAAAT	PILER-CR
GTTGAACAATAACATGTGATGTTTTTAAAT	CRISPRCasFinder
GTTGAACAATAACATGTGATGTTTTTAAAT	CRT

16 spacers

The CRISPR arrays of NZ_HG917869_1

>merge|NZ_HG917869|1|90443-91519|PILER-CR,CRISPRCasFinder,CRT
GTTGAACAATAACATGTGATGTTTTTAAATGCAACTTTATAATTTTCATATTCTTTAGTATTTTGCGTTGAACAATAACATGTGATGTTTTTAAATTTTGTAAATTTTAATGTGCCTAATAATTCAATAGTGTTGAACAATAACATGTGATGTTTTTAAATTTGTTGTCCCTAATTCTTCGAATAAATAGCCATGCCGTTGAACAATAACATGTGATGTTTTTAAATCCTCACTTTTTGCATAAAAAAAGAACTAGTAAAAACGTTGAACAATAACATGTGATGTTTTTAAATGTAGAATTAGATAAGTTCTAACTCTACTGAATAATAGTTGAACAATAACATGTGATGTTTTTAAATATGGTAAGGATATAAACTTCTTAATCGTAGCTAGGTTGAACAATAACATGTGATGTTTTTAAATTCTTGATGATAAGTGGCAAGAGGTTGAACCTCCTACGTTGAACAATAACATGTGATGTTTTTAAATTTTAATGATGGAGTTAAGTAGTGGAGCGACTATTGTTGAACAATAACATGTGATGTTTTTAAATACTACAGGATGTTCAAGTTGTAGTAGGATGGCTACGTTGAACAATAACATGTGATGTTTTTAAATTTACACCAGAAGCAGTGGCACAATATAGCGGTTCTGGTTGAACAATAACATGTGATGTTTTTAAATTAAAGTGGATTATGTGGTAAATTATATTTTTTATGGTTGAACAATAACATGTGATGTTTTTAAATAAACTATAATAACTATTATCTCCTTGCCAACTCTCGTTGAACAATAACATGTGATGTTTTTAAATTAATCACTTAATTTATCTTTTGCAGTTGCTACAGTTGTTGAACAATAACATGTGATGTTTTTAAATTTAACAAGGTTTTTCATTTCCTCATATTGGAAAAGGGTTGAACAATAACATGTGATGTTTTTAAATTATTGGAAAAGGTAATCCATGTTTAGTTTATCACTGTTGAACAATAACATGTGATGTTTTTAAATCATCTACTTTTACTAAAATATCTAACAGTAGTTTTAGTTGAACAATAACATAAGATGTTTTAATGT

>NZ_HG917869|1|1|90443-91453|PILER-CR
GTTGAACAATAACATGTGATGTTTTTAAAT	GCAACTTTATAATTTTCATATTCTTTAGTATTTTGC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTTGTAAATTTTAATGTGCCTAATAATTCAATAGT
GTTGAACAATAACATGTGATGTTTTTAAAT	TTGTTGTCCCTAATTCTTCGAATAAATAGCCATGCC
GTTGAACAATAACATGTGATGTTTTTAAAT	CCTCACTTTTTGCATAAAAAAAGAACTAGTAAAAAC
GTTGAACAATAACATGTGATGTTTTTAAAT	GTAGAATTAGATAAGTTCTAACTCTACTGAATAATA
GTTGAACAATAACATGTGATGTTTTTAAAT	ATGGTAAGGATATAAACTTCTTAATCGTAGCTAG
GTTGAACAATAACATGTGATGTTTTTAAAT	TCTTGATGATAAGTGGCAAGAGGTTGAACCTCCTAC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTTAATGATGGAGTTAAGTAGTGGAGCGACTATT
GTTGAACAATAACATGTGATGTTTTTAAAT	ACTACAGGATGTTCAAGTTGTAGTAGGATGGCTAC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTACACCAGAAGCAGTGGCACAATATAGCGGTTCTG
GTTGAACAATAACATGTGATGTTTTTAAAT	TAAAGTGGATTATGTGGTAAATTATATTTTTTATG
GTTGAACAATAACATGTGATGTTTTTAAAT	AAACTATAATAACTATTATCTCCTTGCCAACTCTC
GTTGAACAATAACATGTGATGTTTTTAAAT	TAATCACTTAATTTATCTTTTGCAGTTGCTACAGTT
GTTGAACAATAACATGTGATGTTTTTAAAT	TTAACAAGGTTTTTCATTTCCTCATATTGGAAAAGG
GTTGAACAATAACATGTGATGTTTTTAAAT	TATTGGAAAAGGTAATCCATGTTTAGTTTATCACT
GTTGAACAATAACATGTGATGTTTTTAAAT

>NZ_HG917869|1|1|90443-91519|CRISPRCasFinder
GTTGAACAATAACATGTGATGTTTTTAAAT	GCAACTTTATAATTTTCATATTCTTTAGTATTTTGC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTTGTAAATTTTAATGTGCCTAATAATTCAATAGT
GTTGAACAATAACATGTGATGTTTTTAAAT	TTGTTGTCCCTAATTCTTCGAATAAATAGCCATGCC
GTTGAACAATAACATGTGATGTTTTTAAAT	CCTCACTTTTTGCATAAAAAAAGAACTAGTAAAAAC
GTTGAACAATAACATGTGATGTTTTTAAAT	GTAGAATTAGATAAGTTCTAACTCTACTGAATAATA
GTTGAACAATAACATGTGATGTTTTTAAAT	ATGGTAAGGATATAAACTTCTTAATCGTAGCTAG
GTTGAACAATAACATGTGATGTTTTTAAAT	TCTTGATGATAAGTGGCAAGAGGTTGAACCTCCTAC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTTAATGATGGAGTTAAGTAGTGGAGCGACTATT
GTTGAACAATAACATGTGATGTTTTTAAAT	ACTACAGGATGTTCAAGTTGTAGTAGGATGGCTAC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTACACCAGAAGCAGTGGCACAATATAGCGGTTCTG
GTTGAACAATAACATGTGATGTTTTTAAAT	TAAAGTGGATTATGTGGTAAATTATATTTTTTATG
GTTGAACAATAACATGTGATGTTTTTAAAT	AAACTATAATAACTATTATCTCCTTGCCAACTCTC
GTTGAACAATAACATGTGATGTTTTTAAAT	TAATCACTTAATTTATCTTTTGCAGTTGCTACAGTT
GTTGAACAATAACATGTGATGTTTTTAAAT	TTAACAAGGTTTTTCATTTCCTCATATTGGAAAAGG
GTTGAACAATAACATGTGATGTTTTTAAAT	TATTGGAAAAGGTAATCCATGTTTAGTTTATCACT
GTTGAACAATAACATGTGATGTTTTTAAAT	CATCTACTTTTACTAAAATATCTAACAGTAGTTTTA
GTTGAACAATAACATAAGATGTTTTAATGT

>NZ_HG917869|1|1|90443-91519|CRT
GTTGAACAATAACATGTGATGTTTTTAAAT	GCAACTTTATAATTTTCATATTCTTTAGTATTTTGC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTTGTAAATTTTAATGTGCCTAATAATTCAATAGT
GTTGAACAATAACATGTGATGTTTTTAAAT	TTGTTGTCCCTAATTCTTCGAATAAATAGCCATGCC
GTTGAACAATAACATGTGATGTTTTTAAAT	CCTCACTTTTTGCATAAAAAAAGAACTAGTAAAAAC
GTTGAACAATAACATGTGATGTTTTTAAAT	GTAGAATTAGATAAGTTCTAACTCTACTGAATAATA
GTTGAACAATAACATGTGATGTTTTTAAAT	ATGGTAAGGATATAAACTTCTTAATCGTAGCTAG
GTTGAACAATAACATGTGATGTTTTTAAAT	TCTTGATGATAAGTGGCAAGAGGTTGAACCTCCTAC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTTAATGATGGAGTTAAGTAGTGGAGCGACTATT
GTTGAACAATAACATGTGATGTTTTTAAAT	ACTACAGGATGTTCAAGTTGTAGTAGGATGGCTAC
GTTGAACAATAACATGTGATGTTTTTAAAT	TTACACCAGAAGCAGTGGCACAATATAGCGGTTCTG
GTTGAACAATAACATGTGATGTTTTTAAAT	TAAAGTGGATTATGTGGTAAATTATATTTTTTATG
GTTGAACAATAACATGTGATGTTTTTAAAT	AAACTATAATAACTATTATCTCCTTGCCAACTCTC
GTTGAACAATAACATGTGATGTTTTTAAAT	TAATCACTTAATTTATCTTTTGCAGTTGCTACAGTT
GTTGAACAATAACATGTGATGTTTTTAAAT	TTAACAAGGTTTTTCATTTCCTCATATTGGAAAAGG
GTTGAACAATAACATGTGATGTTTTTAAAT	TATTGGAAAAGGTAATCCATGTTTAGTTTATCACT
GTTGAACAATAACATGTGATGTTTTTAAAT	CATCTACTTTTACTAAAATATCTAACAGTAGTTTTA
GTTGAACAATAACATAAGATGTTTTAATGT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_HG917869.1\|WP_044040093.1\|95924_96755_+\|sulfate-ABC-transporter-permease-subunit-CysT	unknown	unknown	gnl\|CDD\|131194
NZ_HG917869.1\|WP_044040094.1\|96765_97587_+\|sulfate-ABC-transporter-permease-subunit-CysW	unknown	unknown	gnl\|CDD\|226665
NZ_HG917869.1\|WP_044040082.1\|81946_83344_+\|MBOAT-family-protein	unknown	unknown	gnl\|CDD\|224610
NZ_HG917869.1\|WP_044040085.1\|85135_86005_+\|carbon-nitrogen-hydrolase-family-protein	unknown	unknown	gnl\|CDD\|143587
NZ_HG917869.1\|WP_051483868.1\|88216_90202_+\|sensor-histidine-kinase	unknown	unknown	gnl\|CDD\|223715
NZ_HG917869.1\|WP_044040083.1\|83679_84129_+\|hypothetical-protein	unknown	unknown	unknown
NZ_HG917869.1\|WP_044040096.1\|98674_100366_+\|adenylyl-sulfate-reductase-subunit-alpha	unknown	unknown	gnl\|CDD\|235879
NZ_HG917869.1\|WP_044040084.1\|84144_84915_+\|trypsin-like-peptidase-domain-containing-protein	unknown	unknown	gnl\|CDD\|379142
NZ_HG917869.1\|WP_044040092.1\|94877_95912_+\|sulfate-ABC-transporter-substrate-binding-protein	unknown	unknown	gnl\|CDD\|224529
NZ_HG917869.1\|WP_044040097.1\|100349_100664_+\|4Fe-4S-binding-protein	unknown	unknown	gnl\|CDD\|131115
NZ_HG917869.1\|WP_044040098.1\|100681_101581_+\|sulfate-adenylyltransferase-subunit-CysD	unknown	unknown	gnl\|CDD\|235375
NZ_HG917869.1\|WP_044040088.1\|87346_87787_+\|bacitracin-resistance-protein-BacA	unknown	unknown	gnl\|CDD\|237337
NZ_HG917869.1\|WP_044040087.1\|86671_87067_-\|Rrf2-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224870
NZ_HG917869.1\|WP_044040090.1\|92892_93651_+\|pilus-assembly-protein	unknown	unknown	gnl\|CDD\|368639
NZ_HG917869.1\|WP_044040091.1\|93690_94470_+\|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl\|CDD\|376667
NZ_HG917869.1\|WP_051483867.1\|81173_81764_-\|DUF4358-domain-containing-protein	unknown	unknown	gnl\|CDD\|379531
NZ_HG917869.1\|WP_044040086.1\|86182_86350_-\|hypothetical-protein	unknown	unknown	unknown
NZ_HG917869.1\|WP_044040095.1\|97603_98665_+\|sulfate-ABC-transporter-ATP-binding-protein	unknown	unknown	gnl\|CDD\|226361
NZ_HG917869.1\|WP_044040081.1\|79935_81060_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|379541
NZ_HG917869.1\|WP_044040089.1\|92210_92861_+\|helix-turn-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|238045

Protein	Function_ID	Function_description	E-value
NZ_HG917869.1\|WP_044040094.1\|96765_97587_+\|sulfate-ABC-transporter-permease-subunit-CysW	gnl\|CDD\|226665	COG4208, CysW, ABC-type sulfate transport system, permease component [Inorganic ion transport and metabolism].	2.02411e-118
NZ_HG917869.1\|WP_044040082.1\|81946_83344_+\|MBOAT-family-protein	gnl\|CDD\|224610	COG1696, DltB, Predicted membrane protein involved in D-alanine export [Cell envelope biogenesis, outer membrane].	6.66638e-75
NZ_HG917869.1\|WP_044040085.1\|85135_86005_+\|carbon-nitrogen-hydrolase-family-protein	gnl\|CDD\|143587	cd07197, nitrilase, Nitrilase superfamily, including nitrile- or amide-hydrolyzing enzymes and amide-condensing enzymes. This superfamily (also known as the C-N hydrolase superfamily) contains hydrolases that break carbon-nitrogen bonds; it includes nitrilases, cyanide dihydratases, aliphatic amidases, N-terminal amidases, beta-ureidopropionases, biotinidases, pantotheinase, N-carbamyl-D-amino acid amidohydrolases, the glutaminase domain of glutamine-dependent NAD+ synthetase, apolipoprotein N-acyltransferases, and N-carbamoylputrescine amidohydrolases, among others. These enzymes depend on a Glu-Lys-Cys catalytic triad, and work through a thiol acylenzyme intermediate. Members of this superfamily generally form homomeric complexes, the basic building block of which is a homodimer. These oligomers include dimers, tetramers, hexamers, octamers, tetradecamers, octadecamers, as well as variable length helical arrangements and homo-oligomeric spirals. These proteins have roles in vitamin and co-enzyme metabolism, in detoxifying small molecules, in the synthesis of signaling molecules, and in the post-translational modification of proteins. They are used industrially, as biocatalysts in the fine chemical and pharmaceutical industry, in cyanide remediation, and in the treatment of toxic effluent. This superfamily has been classified previously in the literature, based on global and structure-based sequence analysis, into thirteen different enzyme classes (referred to as 1-13). This hierarchy includes those thirteen classes and a few additional subfamilies. A putative distant relative, the plasmid-borne TraB family, has not been included in the hierarchy.	2.13904e-28
NZ_HG917869.1\|WP_044040098.1\|100681_101581_+\|sulfate-adenylyltransferase-subunit-CysD	gnl\|CDD\|235375	PRK05253, PRK05253, sulfate adenylyltransferase subunit CysD.	0
NZ_HG917869.1\|WP_051483868.1\|88216_90202_+\|sensor-histidine-kinase	gnl\|CDD\|223715	COG0642, BaeS, Signal transduction histidine kinase [Signal transduction mechanisms].	1.38527e-43
NZ_HG917869.1\|WP_044040096.1\|98674_100366_+\|adenylyl-sulfate-reductase-subunit-alpha	gnl\|CDD\|235879	PRK06854, PRK06854, adenylyl-sulfate reductase subunit alpha.	0
NZ_HG917869.1\|WP_044040091.1\|93690_94470_+\|sulfite-exporter-TauE/SafE-family-protein	gnl\|CDD\|376667	pfam01925, TauE, Sulfite exporter TauE/SafE. This is a family of integral membrane proteins where the alignment appears to contain two duplicated modules of three transmembrane helices. The proteins are involved in the transport of anions across the cytoplasmic membrane during taurine metabolism as an exporter of sulfoacetate. This family used to be known as DUF81.	2.56826e-18
NZ_HG917869.1\|WP_044040092.1\|94877_95912_+\|sulfate-ABC-transporter-substrate-binding-protein	gnl\|CDD\|224529	COG1613, Sbp, ABC-type sulfate transport system, periplasmic component [Inorganic ion transport and metabolism].	0
NZ_HG917869.1\|WP_044040097.1\|100349_100664_+\|4Fe-4S-binding-protein	gnl\|CDD\|131115	TIGR02060, adenylylsulfate_reductase_beta_subunit, adenosine phosphosulphate reductase, beta subunit. During dissimilatory sulfate reduction and sulfur oxidation, adenylylsulfate (APS) reductase catalyzes reversibly the two-electron reduction of APS to sulfite and AMP. Found in several bacterial lineages and in Archaeoglobales, APS reductase is a heterodimer composed of an alpha subunit containing a noncovalently bound FAD, and a beta subunit containing two [4Fe-4S] clusters. Described by this model is the beta subunit of APS reductase, sharing common evolutionary origin with other iron-sulfur cluster-binding proteins. [Central intermediary metabolism, Sulfur metabolism].	3.4525e-11
NZ_HG917869.1\|WP_044040088.1\|87346_87787_+\|bacitracin-resistance-protein-BacA	gnl\|CDD\|237337	PRK13289, PRK13289, NO-inducible flavohemoprotein.	1.34689e-86
NZ_HG917869.1\|WP_044040087.1\|86671_87067_-\|Rrf2-family-transcriptional-regulator	gnl\|CDD\|224870	COG1959, COG1959, Predicted transcriptional regulator [Transcription].	5.06822e-34
NZ_HG917869.1\|WP_044040090.1\|92892_93651_+\|pilus-assembly-protein	gnl\|CDD\|368639	pfam05857, TraX, TraX protein. This family consists of several bacterial TraX proteins. TraX is responsible for the amino-terminal acetylation of F-pilin subunits.	2.5954e-41
NZ_HG917869.1\|WP_044040084.1\|84144_84915_+\|trypsin-like-peptidase-domain-containing-protein	gnl\|CDD\|379142	pfam13365, Trypsin_2, Trypsin-like peptidase domain. This family includes trypsin-like peptidase domains.	2.14833e-07
NZ_HG917869.1\|WP_051483867.1\|81173_81764_-\|DUF4358-domain-containing-protein	gnl\|CDD\|379531	pfam14270, DUF4358, Domain of unknown function (DUF4358). This domain family is found in bacteria, and is approximately 110 amino acids in length.	1.51997e-15
NZ_HG917869.1\|WP_044040093.1\|95924_96755_+\|sulfate-ABC-transporter-permease-subunit-CysT	gnl\|CDD\|131194	TIGR02139, permease_CysT, sulfate ABC transporter, permease protein CysT. This model represents CysT, one of two homologous, tandem permeases in the sulfate ABC transporter system; the other is CysW (TIGR02140). The sulfate transporter has been described in E. coli as transporting sulfate, thiosulfate, selenate, and selenite. Sulfate transporters may also transport molybdate ion if a specific molybdate transporter is not present. [Transport and binding proteins, Anions].	9.20201e-133
NZ_HG917869.1\|WP_044040095.1\|97603_98665_+\|sulfate-ABC-transporter-ATP-binding-protein	gnl\|CDD\|226361	COG3842, PotA, ABC-type spermidine/putrescine transport systems, ATPase components [Amino acid transport and metabolism].	1.65261e-132
NZ_HG917869.1\|WP_044040081.1\|79935_81060_+\|hypothetical-protein	gnl\|CDD\|379541	pfam14286, DHHW, DHHW protein. This family of proteins is found in bacteria. Proteins in this family are typically between 366 and 404 amino acids in length. There is a conserved DHHW motif. There is some distant homology to the Lipase_GDSL_2 family.	2.29583e-23
NZ_HG917869.1\|WP_044040089.1\|92210_92861_+\|helix-turn-helix-domain-containing-protein	gnl\|CDD\|238045	cd00093, HTH_XRE, Helix-turn-helix XRE-family like proteins. Prokaryotic DNA binding proteins belonging to the xenobiotic response element family of transcriptional regulators.	4.63912e-16

>NZ_HG917869.1|WP_051483868.1|88216_90202_+|sensor-histidine-kinase
MRYKYRAIISVCVTLYMFLFICDIDDVFGDIDNNDDEINVLVISSYYGYSKWEKGVLEGFTDSDELGVNLINVSLYFDGIEGIAEKTYVDSVNKMIQEKYGEKYIDCIVTLDDESFMFARANLFNENSVMYKKPIVFLGVNFDMNLSEDEKQYISGIIDDTDEVGAINLILDSDKHIENIYLVAGESKYAEAMASKMPFFRKFANRDYEFEIIQDSRLGNVEERLKDISDEDSAILLVGKFVDDVGVIMESKSVISSIQSKSDVPIYSTAQAYIEGGAIGGVVGNPYKSGKVLAEMVDSVLSHGDIHVSVNPDNKLSVPIVNFRALREYGINPLLLPKDSVVMNKRSYELMVPLYIQNILWISAALIIMVLFYMIYRHIRDMRYAKYIIDEAMYREKVRSDFIVAISHEFRTPINVISSCLKLLEVTVDRGNYEKEYILEKFSLMKKNSNRLLKQVNNLIDTSELNNGYLNLSLNNYNIVEVVEDSVGTIINFAKNKGIEVVFDSEEEEIILAIDKNKIERVILNLLSNSVKYIGDGSNILVMVSISNVTEDERYVSVSVKDDGIGISKDIVDLVFQQFKRGDVDNGLIRECEGSGLGLYIVRRIVELHNGEINIISEVGKGTEVIFKLPLYTIEGDSSGVLATDMSSVDYKADIEFSDLN
>NZ_HG917869.1|WP_044040088.1|87346_87787_+|bacitracin-resistance-protein-BacA
MLDQKTIEIVKSTVPALKEHGVEITKTFYKNMFENNPEVKRLFNMDRQASGEQPKALAMTILAAAQNIDNLEVLLPAVKKIGERHCDVQIKEEHYPIVGANLLVAIKEVLGDAATDEVIDAWGKAYEVIAKIFIDVEKEIYESRNK
>NZ_HG917869.1|WP_044040087.1|86671_87067_-|Rrf2-family-transcriptional-regulator
MQISKFTDYAFRSLIYLARNRDETTTVDKLAKYLEVSEHHMKKVIHKLAKTGYIISTKGRNGGLKLGLEPSEINLGKVLVATEENLNLVECMANPKLCPLMTSDCNLKRILSKSLQAFINELSKYTLEDIL
>NZ_HG917869.1|WP_044040086.1|86182_86350_-|hypothetical-protein
MDMLELIIKSFATIYIIRLVLKHNLFISKLIIKIKFLGIHIELNGKEKKHPSDQE
>NZ_HG917869.1|WP_044040085.1|85135_86005_+|carbon-nitrogen-hydrolase-family-protein
MRIFALELNNDIKGIQNRKQYIESLIAKLPSPDLVVLPELAICSYMASQDIWQYADDCGKDTAVWATEISRKYNTYIGVGYLDKENGDYYNRYMIAGQKGVCGTVTKSEGEAAVFKRGWFENTISTPFGNVGIAICYDSKRKHFYESVKTKELSLIIFPHGCPADPKKSKEEIENNDFFCTTYMKAFDIPVVYVNSKGKLEYMPGIMGRMMAEAGFMMNGKSKIYAPSGKSIEVDVAEVIAMDISLSSKKIKNNIHFYGDDLVKGNWLFRQFVLKPDTKAGIKEYYTNR
>NZ_HG917869.1|WP_044040084.1|84144_84915_+|trypsin-like-peptidase-domain-containing-protein
MNINDLSTQLLYTTVPIFGIKSDGSQVSGTGFIFSIFDKDDTSKSIPLLITNYHVMEDVINGFIEFSLAENNMPIKGKSIRINFDGDVLKNKLGSLDLIAIPLADALNNLNKNNINVFYRTISKEMIPTTSQVEELSALEQITFIGYPSGLYDNYNKTSLIRQGITATPIWNDFKGEPIFLIDAGVFPGSSGSPVFIYNQGSYPTKDGISIGSRLLFVGIISETILRQGTTYLDLGRVINSRAMYNELENIMRPYI
>NZ_HG917869.1|WP_044040083.1|83679_84129_+|hypothetical-protein
MDNTFEPIDTTTNCTVADVSINDTNIGSATTTLTYPIRQPEEYVNDFMVSLRASEIRKVRKYCEDAKKSEFPWSEILLAISTTCIGCFLGALTSNVELNSLKGIIMYVVSLVIASGTFVAYLFIRRGSISDVNDLADKVKEYIVDPDNI
>NZ_HG917869.1|WP_044040082.1|81946_83344_+|MBOAT-family-protein
MVFSSLTFMFAFLPMVLLAYFIMPKAVRNLTLFLFSLLFYAWGEPIYILIMIFSTIVDYFHGMLIYKYKQCDNNKKSRLILISSIFINLSLLVFFKYSDFFISSVNTIFGSNLKLLNLSLPIGISFYTFQTMSYSIDIYRGTVTPQRNIIDFGTYVALFPQLIAGPIVQYKTIAHQLRNRKESLDQFTYGIIRFVSGLGKKVLIANNVGLIWEEIISSDLSTISVLSSWIGIIMFALQIYFDFSGYSDMAIGLGNMFGFKFKENFNYPYESKSITEFWRRWHISLGSWFKEYVYIPLGGNRRYQVRNICIVWLLTGLWHGASWNFVIWGIYFGSTLLLEKFILKKFFNINSRIYALLLILIGWVIFAFDNLQHGLIYIKSMFSISSNVFIDSNALYILTSNITIIVIGIIASTSIPKKITRYFLKGKENSWTFSIVTSVYILGILILSTASLVNSSYNPFLYFRF
>NZ_HG917869.1|WP_051483867.1|81173_81764_-|DUF4358-domain-containing-protein
MKKKILVLFLAATLGVTSLVGCAKSDVTLNNQQSTGIENSENNDGVVAEKSVEAIRKAVVDAYGDKYLATMSLSKEEINERFGLTDDMYKDAVADIPAMSTHVDTFVAVEAKEGKVNEVFDALTEYRDMLINDTMMYPMNELKTQSSEVYKYDDYVFFIMLGGYDDSLEEDSELLAYYEDQNDIAKNIIDDMLNTK
>NZ_HG917869.1|WP_044040081.1|79935_81060_+|hypothetical-protein
MKNKNFIVAGVFVVFIFIVSLLNIISPTKIYSEKEKRKLAQSPELNKETIFSGKFTREYEEYFNDQFVFRDNWISLNTKYKILSLNKDINDVYLGKDNYLFEDTSSYDTKKLYKNMDHLKNLIIKYKDSIGENNINIMLIPNGSEILSDKLPKYATVLDQQRILKDAEVMYKDNFINTYDILKRNKSKYIYYKTDHHWTTLGAYYAYNAWADKTNHEIETFSSDNTKIVSTNFLGTIYSKINYAKEPDIITIYNPEEKYSVNYDSNTSSSTSLYNLEYLEKKDQYSVFLDGNHGLVTITSSNTNGKNLLIIKDSYANCFIPFIADEYEKIHVIDLRYYNSSLESYIEDNDISELLVLYNINSIAKDTNLYKVTR
>NZ_HG917869.1|WP_044040089.1|92210_92861_+|helix-turn-helix-domain-containing-protein
MSIGEKINDLRKKNNLSQDQFAELFNVTRQTVSNWENGKSYPDLEMTLKISNKFRISVDELLQNNETIVRKINSEKKEKSNLLILLGILFFAVIVFVFCFYIKYEEKNEISFEMNKSKTYHTQETNRSFLDAGVGYFTLIKDGKVDIKAIGDTDDGELHIVITDDKNKKIYYQIDGEEIEDSQSVYFNSGSYMIQVTADDYTEDIVSLTYHVKVNN
>NZ_HG917869.1|WP_044040090.1|92892_93651_+|pilus-assembly-protein
MNKKILSGSTIKIIAVITMCIDHFGQVVLKNGVVMNAPYKFFSDAQFSALLSIVDLCHMLGRVAFPLFCYLLVEGFIHTHNLRRYILNLGLFAIVSEPIYDLTFYGSVFSSEGQNVLFTLLIGILTLTCIKKLNDNIWVAIFFNFISGSVAYILNLDGWYYGAIMITVMYMFRRHKFMKYLLTAVVMYLCELDYSLKGLLDPYFWMALLSLFIMVLYNGQRGMKIKYFFYIFYPGHLLFLYVLTTFIIVPQL
>NZ_HG917869.1|WP_044040091.1|93690_94470_+|sulfite-exporter-TauE/SafE-family-protein
MMLYVIYILAGIGAGIVTGLAGLSAAVVITTLLVSICGWKSYDAVTVALAADVLASLLTAYTYYKNKNIDLKNGMLVTITAFIGTIIGSYSGFLFSQSQPDGLGYISMLTTIFLGIKFLVKPIEEGYDADSGSEQISKKKIILAMFFGCGIGWICGFTGSGGGILMLTVFTLLLGYNLKVAVGTSTMIMTLVALTGTISHFYMGATIQLIPMLLVIIFCVSAAYFSAKFANKCEIKKLNKVVGTCLGILGVITILIKLI
>NZ_HG917869.1|WP_044040092.1|94877_95912_+|sulfate-ABC-transporter-substrate-binding-protein
MKIKKVVSLLLVAIIGGTLLTSCSDENKNKDTVEITNVSYDPTRELYEAYNKEFQKYYKDKTNKDVVITQSHGGSGKQARAVIEGNEADVVTLALGYDISAIEKAGLIESGWQSKFDKNSSPYTSTIVFLVRKGNPKNINDWDDLVREDVGIITPNPKTSGGARWNYLAAWAYSYKKNNGDEEKVKKYMKDLFGNVLVLDSGARGATTTFVENGQGDVLLAWENEAYLSLKEHPDEFEIVTPSISMLAEPPVAVVDEVVDKKGTREVATEYLEYLYSDIGQRIAGENYYRPTNEEIAKEFSDVFNLDMELINIDDKIFGGWDKAQKEHFDDGGIFDEIYDGEQG
>NZ_HG917869.1|WP_044040093.1|95924_96755_+|sulfate-ABC-transporter-permease-subunit-CysT
MGKSKKRAVIPGYKVSMGVTITFLSLIVLIPLASLAINASGMGFNKFISTVTNPRVIAAYKVSFLCAFIATIVNSFFGVIIAWTLVRYDFKGKRIIDGLIELPFALPTAVAGIALTTLYSDKGMIGKYFDAIGIKISYTRVGIIAAMIFIGIPFVVRSIQPVLEGIDKQYEEAATMLGASRVRIFFKVIFPEILPALLTGFGLAFARAVGEYGSVVFISGNMPFKTEIAPLLIMSKLEQYDYTGANAIALVMLVISFLILFLINSIQVYTNKFVKE
>NZ_HG917869.1|WP_044040094.1|96765_97587_+|sulfate-ABC-transporter-permease-subunit-CysW
MEKSKFVKWLLISVTVIFLFLMLIMPLVVVIIEALKKGLISYKDAITDEYTIQALILTLEATIAAVVINTVFGLFAAWTITKFHFRGKKLLTTLIDIPFAISPVIAGLIFILTFGRIGWAYDFLQAANIKIVFAVPGIILATIFVTFPFVAREIIPVLNAQGKDEEEAAALMGAKGFKIFTKITLPHIKWALLYGIILCTARAMGEFGAVSVLSGHLKGKTNTLPLHIECLYNEFNSNAAFAVSSILVILAIIILILRNIAEHKSKKYSKVSK
>NZ_HG917869.1|WP_044040095.1|97603_98665_+|sulfate-ABC-transporter-ATP-binding-protein
MYVELKNINKGFENYKASDNVNFQIEKGKLIALLGPSGSGKTTILRMIAGLETPDSGDIIIDGVRVNDVEASKRGIGFVFQNYALFRYMTVFDNIAFGLEVQKKDKKFINERVKELISLIGLEGLEKRYPHQLSGGQRQRVAFARALAPNPQLLLLDEPFAAIDAKVRHELRTWLREMIDKVGVTSIFVTHDQDEAIEVADEIIVTNKGRVEQKGTPLEIYNKPATPFVAKFIGQSIVINDFGKLRGFDEYSHYSKAVIRPEFIKVLKKGAINQHISATEEGVVEAVAYRGSYLEVKVRIGDISVTTTVQLSEELVEVGEKVQVLIYKLYAFNNEEVILIKNRKMENNNSVYI
>NZ_HG917869.1|WP_044040096.1|98674_100366_+|adenylyl-sulfate-reductase-subunit-alpha
MKEVRIEKITTDVLIIGGGTAGCYSAITLGEESNLNVLVVEKANIKRSGCLAAGVNAINAYIVKGKTAEDYVDYAKKDADGIVREDLLLTMSEGLNKVTKKLEDLGLVILKDENGEYVARGTRNIKINGENIKPILAEATKAQKNVSILNKVNITDFIVKDNRIYGAIGVAVDDNILYEISAKAVICATGGAAGLYRPNNPGFSRHKMWYPPFNTGAGYAMGIRAGAEMTTFEMRFIALRCKDTIAPTGTIAQGVGAKQVNSKGEVYENKYGLTTSERVYGTVKENQEGRGPCYLRTEGIDNSKNDDLKKAYLNMAPSQTLKWVESGKNPSEANVEIEGTEPYIVGGHTASGYWVDSNRRTTIKGLYAAGDVAGGCPQKYVTGALVEGEIAAKAVIKDLENYTATVVDEIDNFVAEKKKEVESFLNNEEGLFSIEAIEEAMQKVMDSYAGGISTNYQYNEKQLKVAEEKINQIEKLTDSLKANDFHELMFIYEIKERLVICKSVIAHLNARKETRWHSFAENLDYPNKDDKWLKYVNSKVVDGKIEIILRDLVGRGEVYEHSN
>NZ_HG917869.1|WP_044040097.1|100349_100664_+|4Fe-4S-binding-protein
MSIAINKEKCVGCKGCTKVCPGSLLEIDENNKAYIKYPKDCWGCCSCIKECKFSAISLYLGADIGGRGSKLSVNIEGDIAHWKIEEGNGNIEEININRKDSNKY
>NZ_HG917869.1|WP_044040098.1|100681_101581_+|sulfate-adenylyltransferase-subunit-CysD
MRELSHLDQLEAEAIYIIREVAAECEKPVMLYSIGKDSSVMLHLAMKAFYPEKPPFPFMHIDTTWKFKEMIEFRDKTAKELGIDMIVYSNEEGVKNGINPFEHGSAYTDIMKTQALKQGLKKYGFTAAFGGGRRDEEKSRAKERVFSFRNEAQAWDPKNQRPEMWKLYNTKINKGESIRVFPLSNWTEKDIWQYIKREKIDIVPLYFAKERPVVYRDGNIIMVDDDRFKFLPGEKVEYKKVRFRTLGCYPLTGGCESEADTLDEIIEETLGAVSSERTTRVIDNEAAGSMERRKREGYF

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Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_HG917869_1	1.1\|90473\|36\|NZ_HG917869\|PILER-CR,CRISPRCasFinder,CRT	90473-90508	36	MN694404	Marine virus AFVG_250M623, complete genome	26531-26566	9	0.75
NZ_HG917869_1	1.11\|91127\|35\|NZ_HG917869\|PILER-CR,CRISPRCasFinder,CRT	91127-91161	35	MF360958	Salicola phage SCTP-2, complete genome	229619-229653	9	0.743

1. spacer 1.1|90473|36|NZ_HG917869|PILER-CR,CRISPRCasFinder,CRT matches to MN694404 (Marine virus AFVG_250M623, complete genome) position: , mismatch: 9, identity: 0.75

gcaactttataattttcatattctttagtattttgc	CRISPR spacer
tctaatttataattttcatattctttactatcagat	Protospacer
 * * ********************** ***.  ..

2. spacer 1.11|91127|35|NZ_HG917869|PILER-CR,CRISPRCasFinder,CRT matches to MF360958 (Salicola phage SCTP-2, complete genome) position: , mismatch: 9, identity: 0.743

taaagtggattatgtggtaaattatattttttatg	CRISPR spacer
aatacttcattaggtgttaaattatattttttaac	Protospacer
 * * *  **** *** ****************

Prophage detection

Region	Region Position	Protein_number	Hit_taxonomy	Key_proteins	Att_site	Prophage annotation

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

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CRISPR-Cas detection and classification

Crispr_ID: NZ_HG917868_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_HG917868_1

217843-223120

TypeV

I-A

Consensus_repeat	Method
CTTTTATCTTAACTATGAGGAATGTAAAT	PILER-CR
CTTTTATCTTAACTATGAGGAATGTAAAT	CRISPRCasFinder
CTTTTATCTTAACTATGAGGAATGTAAAT	CRT

80 spacers

cas2,cas1,cas4,cas3,cas5,cas7,cas8b2,cas6,WYL

The CRISPR arrays of NZ_HG917868_1

>merge|NZ_HG917868|1|217843-223120|PILER-CR,CRISPRCasFinder,CRT
CTTTTATCTTAACTATGAGGAATGTAAATATTAAAGAAAATAAATTTATAAGTCGTAAGATAAGACTTTTATCTTAACTATGAGGAATGTAAATATATTAGTTCAAAATGCGTAGATATTTATTTTTATTCTTTTATCTTAACTATGAGGAATGTAAATCGTTTAGGTGCTAATGAGATTAGAAGAAGTTATACAACTTTTATCTTAACTATGAGGAATGTAAATTTTATTTACCTTTTAGGCTTGTATATGATTATTCTATGCTTTTATCTTAACTATGAGGAATGTAAATATAGATAAATGAGATTTCCCTGCTCCAGGATTACCTCTTTTATCTTAACTATGAGGAATGTAAATTTAGATAAATATAAAGATGATGTACCAGAAGAGATTCTTTTATCTTAACTATGAGGAATGTAAATATTGTATACAAATACAATATACAAACTATACAAACACTTTTATCTTAACTATGAGGAATGTAAATATTACTGTGTTTCTATCATTCTTTGTAAAATTAATCGCCTTTTATCTTAACTATGAGGAATGTAAATACAAATTGGAGGGTATGAATATGAGATCAATATTACCTTTTATCTTAACTATGAGGAATGTAAATCTTAATTTGAAACCACACTATTCTATTGAAACTTTAACTTTTATCTTAACTATGAGGAATGTAAATTGTAAGTATGCCTTGTTGTTCATAATTAATTACTGCCTTTTATCTTAACTATGAGGAATGTAAATGAGGATATACAATCTCAAATAGATAATAATGCTACGGCTTTTATCTTAACTATGAGGAATGTAAATTCTAGTAGCATTGTTACTATAGTTCTTATTGTCTTTCTTTTATCTTAACTATGAGGAATGTAAATGTGGCATCAATATATCCTGTTTTTATTGTATCTTTACTTTTATCTTAACTATGAGGAATGTAAATTACAATCTTTTTTATATATTCCGTAATATATTCCATTCTTTTATCTTAACTATGAGGAATGTAAATTTGGGAAATGCTTATGGAACTTTGGTATGTTTAGGTCTTTTATCTTAACTATGAGGAATGTAAATTCTATAGTAAAACCATATTGATATTCTCCATAATATCCTTTTATCTTAACTATGAGGAATGTAAATTATAGTGCTGATGTAATAGGCAATATAGACAACAGTCTTTTATCTTAACTATGAGGAATGTAAATATATGAAGCAATTCAAGGTACTGAAGACAACTCATTCTTTTATCTTAACTATGAGGAATGTAAATTTCTACAAGAGATACTTATAAATTTTATGGTGTGGCTACTTTTATCTTAACTATGAGGAATGTAAATATTAACACTTATATAATATCATACATTGTAATACTTTCTTTTATCTTAACTATGAGGAATGTAAATAGAGAAACACCAAGCGCAACTTTAACTATTGAATCACTTTTATCTTAACTATGAGGAATGTAAATAAGTACGAAAAAGACACAGAATAATCAAACGAACCACTTTTATCTTAACTATGAGGAATGTAAATTTGATTTTTAACCCCTCGTGTTTCACGACCCCTTTACCTTTTATCTTAACTATGAGGAATGTAAATTTTTCAGTAAGTACTTTTGTATATTTACTTGTCATACTTTTATCTTAACTATGAGGAATGTAAATTAAATAGAATTAATATTCCTAAGGCTGTATCCCATGCTTTTATCTTAACTATGAGGAATGTAAATTCTAAAATGGTTTTATATGCATTAGTAAAATCGTTTGCTTTTATCTTAACTATGAGGAATGTAAATAAAAATGGTTGTTCTTCTATTAGACAAACTTTTAATCCTTTTATCTTAACTATGAGGAATGTAAATTCACCAACACTTTTGCTATATACAGATTCAAAATACCTTTTATCTTAACTATGAGGAATGTAAATTTTAAAACACTCCTAACTTAAAAACCTTCTTAACTTCTTTTATCTTAACTATGAGGAATGTAAATTTATCTGTTTCTATACTTATTATTTTATTGTTCTTATCTTTTATCTTAACTATGAGGAATGTAAATTTTTACATCTCACCTTTCTCTATTTTGTATTTATTACTTTTATCTTAACTATGAGGAATGTAAATGTTATAAGCATATCTATAAATAATTTACTAGATAGACTTTTATCTTAACTATGAGGAATGTAAATTGATTTACTAGGGTTTAGAAGGCTATATAGATTATCCTTTTATCTTAACTATGAGGAATGTAAATCCAACTAGTTTGATTGGATTATAACAAGTGTTTCCAGCTTTTATCTTAACTATGAGGAATGTAAATTTGTAAACAGGTATTTGTAACCGTTTATCAAAAATACTTTTATCTTAACTATGAGGAATGTAAATCTAGAGCTGTATTGATGTCCTGCGTAGTTATTACCCTTTTATCTTAACTATGAGGAATGTAAATTTGTAAGTTTCAGTGGAATCTATTGATAAAGTGTGAGCTTTTATCTTAACTATGAGGAATGTAAATTCTATTAATTCGGCATCTCCTGTAGTCGAACCACTACTTTTATCTTAACTATGAGGAATGTAAATATGGTTTCGTTTGTAGCAATGATTGTTTTTTCTACTATTCTTTTATCTTAACTATGAGGAATGTAAATATCAAATTACCCAAACACCCATTATGTCGTTGTACTCTTTTATCTTAACTATGAGGAATGTAAATAAGTTGTTAACTGGTTTAATCAACTTTCACCGGCAGCTTTTATCTTAACTATGAGGAATGTAAATTTAAAAGCACTCGGCATCAATATGTCAGTTGCTAATCTTTTATCTTAACTATGAGGAATGTAAATTAAGAACGGAAAAGACGTACAGGGTGCTATTTTGAAACTTTTATCTTAACTATGAGGAATGTAAATTGTGTTAATATTCATGAGTTAATTATAAAATAAAAAACTTTTATCTTAACTATGAGGAATGTAAATCCAGGTATTGGAAATGGTGTAAAGGCGGCTATGCCAACTTTTATCTTAACTATGAGGAATGTAAATTCATAAGTTTGCATAGAATAACTATAAGTGCCATCACCTTTTATCTTAACTATGAGGAATGTAAATTTCCACTTGTTCTTCTTGCTTTGGAACGTTGTTCTTCCTTTTATCTTAACTATGAGGAATGTAAATCTCTCTATCACTTGGCAATTCATGCATAAGATTTTTTCTTTTATCTTAACTATGAGGAATGTAAATTAGTCTAATTTAACTTTTATTATAGATTTTTCCATAACTTTTATCTTAACTATGAGGAATGTAAATACGAGATTATAACACGTTTTAATTTTTAATGTCAAGGCTTTTATCTTAACTATGAGGAATGTAAATGGTAAATAAAAGAAATTACTTATAGTATCCAATTGACTTTTATCTTAACTATGAGGAATGTAAATAATACTAAAGTGTTTTCTAGTATACTAAAAAAACTTGCTTTTATCTTAACTATGAGGAATGTAAATAAGTATTCTAAAAACTTCTCTTCATCTGTTTCTGTTTCTTTTATCTTAACTATGAGGAATGTAAATGCGGGTAAATCTGTATCAGTAGGAAGATACATTTTACTTTTATCTTAACTATGAGGAATGTAAATATAAATGATGTAGAAAAAGTTGAATATGAAGGTCTTGTCTTTTATCTTAACTATGAGGAATGTAAATCTCTTTTTTTTTATGTTGTGGGGTGGGGGGTCCCCACGCTTTTATCTTAACTATGAGGAATGTAAATTTGATTTAACATCTATTGAAGATAAAAAAGAGCGTCTTTTATCTTAACTATGAGGAATGTAAATACTATAATACAGCGAGAAACTTATCTAAAAGTCATTCTTTTATCTTAACTATGAGGAATGTAAATAGAAAAAAGAGCCAGTTGTTAGGAATAATTGTATTATGCTTTTATCTTAACTATGAGGAATGTAAATTGGTTGGCATACTGTTCTTTAAGGTCTGATATTATTCCTTTTATCTTAACTATGAGGAATGTAAATGCCAATAAATTTGTTTCTTTACCTATCTCTCGATAAGCTTTTATCTTAACTATGAGGAATGTAAATAAAACAGCTATAACAAACTTTATCATAACTGTTAACCTTTTATCTTAACTATGAGGAATGTAAATTAAGAATAACTACAAATGGGTTGATAAGACAGAACAACTTTTATCTTAACTATGAGGAATGTAAATAAACATAAACATGTAAAAGTAGCTGTGCCATCATCATCTTTTATCTTAACTATGAGGAATGTAAATTAGTTGCATATGCAACATCAGAACCTAAAGAAGTTTTCTTTTATCTTAACTATGAGGAATGTAAATTCATCATAATTATTGTTGTTAGGTGTTGTATTACTCTCTTTTATCTTAACTATGAGGAATGTAAATTACACATAAGAAGAATAAAAATAGCCGCCACCAGTTACTTTTATCTTAACTATGAGGAATGTAAATATTACTATAAACTTAGTATCTATACCCTGTTTTTTGCCTTTTATCTTAACTATGAGGAATGTAAATAAATCCATACTCTTTTGAGTTGGCTTGTTGTAACTACTTTTATCTTAACTATGAGGAATGTAAATTCACCTAACACATCATAAGCTTGTGATCTAGTTAAGCCTTTTATCTTAACTATGAGGAATGTAAATAGATCATCGAGAATTATTAAATCTGCTTTAGTAATGCTTTTATCTTAACTATGAGGAATGTAAATTAGATGAAGATGTATATAAGAAACTTTGTGAACTTGCCTTTTATCTTAACTATGAGGAATGTAAATGGTTTGTAATTCTATGTAATTAAATTCTTTATCTATCCTTTTATCTTAACTATGAGGAATGTAAATCTAAAAATCAATATCTTCAAATCCTACATTGTACTTCTTTTATCTTAACTATGAGGAATGTAAATTAGTGTTTTTTGTAATATTCTCTAATGCAATCTTCTACTTTTATCTTAACTATGAGGAATGTAAATGATACAGAGGTTAATGTATCTTATAAAGAAGATTGGTCTTTTATCTTAACTATGAGGAATGTAAATCTAGTATCAGAGGCCGGGAAGAATATTAAATTATAAACTTTTATCTTAACTATGAGGAATGTAAATTTTACTATGTTAATACCAATCTTACTCCAATCCACCTTTTATCTTAACTATGAGGAATGTAAATTTAGATTCTAAATATCCTTCTTTAAAAGGTGTTTTTGCTTTTATCTTAACTATGAGGAATGTAATA

>NZ_HG917868|1|1|217843-223120|PILER-CR
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTAAAGAAAATAAATTTATAAGTCGTAAGATAAGA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATATTAGTTCAAAATGCGTAGATATTTATTTTTATT
CTTTTATCTTAACTATGAGGAATGTAAAT	CGTTTAGGTGCTAATGAGATTAGAAGAAGTTATACAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTATTTACCTTTTAGGCTTGTATATGATTATTCTATG
CTTTTATCTTAACTATGAGGAATGTAAAT	ATAGATAAATGAGATTTCCCTGCTCCAGGATTACCT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAGATAAATATAAAGATGATGTACCAGAAGAGATT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTGTATACAAATACAATATACAAACTATACAAACA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTACTGTGTTTCTATCATTCTTTGTAAAATTAATCGC
CTTTTATCTTAACTATGAGGAATGTAAAT	ACAAATTGGAGGGTATGAATATGAGATCAATATTAC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTTAATTTGAAACCACACTATTCTATTGAAACTTTAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGTAAGTATGCCTTGTTGTTCATAATTAATTACTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	GAGGATATACAATCTCAAATAGATAATAATGCTACGG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTAGTAGCATTGTTACTATAGTTCTTATTGTCTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	GTGGCATCAATATATCCTGTTTTTATTGTATCTTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	TACAATCTTTTTTATATATTCCGTAATATATTCCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGGGAAATGCTTATGGAACTTTGGTATGTTTAGGT
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTATAGTAAAACCATATTGATATTCTCCATAATATC
CTTTTATCTTAACTATGAGGAATGTAAAT	TATAGTGCTGATGTAATAGGCAATATAGACAACAGT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATATGAAGCAATTCAAGGTACTGAAGACAACTCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTCTACAAGAGATACTTATAAATTTTATGGTGTGGCTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTAACACTTATATAATATCATACATTGTAATACTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	AGAGAAACACCAAGCGCAACTTTAACTATTGAATCA
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTACGAAAAAGACACAGAATAATCAAACGAACCA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGATTTTTAACCCCTCGTGTTTCACGACCCCTTTAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTTCAGTAAGTACTTTTGTATATTTACTTGTCATA
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAATAGAATTAATATTCCTAAGGCTGTATCCCATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTAAAATGGTTTTATATGCATTAGTAAAATCGTTTG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAAAATGGTTGTTCTTCTATTAGACAAACTTTTAATC
CTTTTATCTTAACTATGAGGAATGTAAAT	TCACCAACACTTTTGCTATATACAGATTCAAAATAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTAAAACACTCCTAACTTAAAAACCTTCTTAACTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTATCTGTTTCTATACTTATTATTTTATTGTTCTTAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTTACATCTCACCTTTCTCTATTTTGTATTTATTA
CTTTTATCTTAACTATGAGGAATGTAAAT	GTTATAAGCATATCTATAAATAATTTACTAGATAGA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGATTTACTAGGGTTTAGAAGGCTATATAGATTATC
CTTTTATCTTAACTATGAGGAATGTAAAT	CCAACTAGTTTGATTGGATTATAACAAGTGTTTCCAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGTAAACAGGTATTTGTAACCGTTTATCAAAAATA
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAGAGCTGTATTGATGTCCTGCGTAGTTATTACC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGTAAGTTTCAGTGGAATCTATTGATAAAGTGTGAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTATTAATTCGGCATCTCCTGTAGTCGAACCACTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATGGTTTCGTTTGTAGCAATGATTGTTTTTTCTACTATT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATCAAATTACCCAAACACCCATTATGTCGTTGTACT
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTTGTTAACTGGTTTAATCAACTTTCACCGGCAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAAAAGCACTCGGCATCAATATGTCAGTTGCTAAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAGAACGGAAAAGACGTACAGGGTGCTATTTTGAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGTGTTAATATTCATGAGTTAATTATAAAATAAAAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	CCAGGTATTGGAAATGGTGTAAAGGCGGCTATGCCAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TCATAAGTTTGCATAGAATAACTATAAGTGCCATCAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTCCACTTGTTCTTCTTGCTTTGGAACGTTGTTCTTC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTCTCTATCACTTGGCAATTCATGCATAAGATTTTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTCTAATTTAACTTTTATTATAGATTTTTCCATAA
CTTTTATCTTAACTATGAGGAATGTAAAT	ACGAGATTATAACACGTTTTAATTTTTAATGTCAAGG
CTTTTATCTTAACTATGAGGAATGTAAAT	GGTAAATAAAAGAAATTACTTATAGTATCCAATTGA
CTTTTATCTTAACTATGAGGAATGTAAAT	AATACTAAAGTGTTTTCTAGTATACTAAAAAAACTTG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTATTCTAAAAACTTCTCTTCATCTGTTTCTGTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	GCGGGTAAATCTGTATCAGTAGGAAGATACATTTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATAAATGATGTAGAAAAAGTTGAATATGAAGGTCTTGT
CTTTTATCTTAACTATGAGGAATGTAAAT	CTCTTTTTTTTTATGTTGTGGGGTGGGGGGTCCCCACG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGATTTAACATCTATTGAAGATAAAAAAGAGCGT
CTTTTATCTTAACTATGAGGAATGTAAAT	ACTATAATACAGCGAGAAACTTATCTAAAAGTCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	AGAAAAAAGAGCCAGTTGTTAGGAATAATTGTATTATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TGGTTGGCATACTGTTCTTTAAGGTCTGATATTATTC
CTTTTATCTTAACTATGAGGAATGTAAAT	GCCAATAAATTTGTTTCTTTACCTATCTCTCGATAAG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAAACAGCTATAACAAACTTTATCATAACTGTTAAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAGAATAACTACAAATGGGTTGATAAGACAGAACAA
CTTTTATCTTAACTATGAGGAATGTAAAT	AAACATAAACATGTAAAAGTAGCTGTGCCATCATCAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTTGCATATGCAACATCAGAACCTAAAGAAGTTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TCATCATAATTATTGTTGTTAGGTGTTGTATTACTCT
CTTTTATCTTAACTATGAGGAATGTAAAT	TACACATAAGAAGAATAAAAATAGCCGCCACCAGTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTACTATAAACTTAGTATCTATACCCTGTTTTTTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	AAATCCATACTCTTTTGAGTTGGCTTGTTGTAACTA
CTTTTATCTTAACTATGAGGAATGTAAAT	TCACCTAACACATCATAAGCTTGTGATCTAGTTAAGC
CTTTTATCTTAACTATGAGGAATGTAAAT	AGATCATCGAGAATTATTAAATCTGCTTTAGTAATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGATGAAGATGTATATAAGAAACTTTGTGAACTTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	GGTTTGTAATTCTATGTAATTAAATTCTTTATCTATC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAAAAATCAATATCTTCAAATCCTACATTGTACTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTGTTTTTTGTAATATTCTCTAATGCAATCTTCTA
CTTTTATCTTAACTATGAGGAATGTAAAT	GATACAGAGGTTAATGTATCTTATAAAGAAGATTGGT
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAGTATCAGAGGCCGGGAAGAATATTAAATTATAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTACTATGTTAATACCAATCTTACTCCAATCCAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAGATTCTAAATATCCTTCTTTAAAAGGTGTTTTTG
CTTTTATCTTAACTATGAGGAATGTAATA

>NZ_HG917868|1|1|217843-223120|CRISPRCasFinder
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTAAAGAAAATAAATTTATAAGTCGTAAGATAAGA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATATTAGTTCAAAATGCGTAGATATTTATTTTTATT
CTTTTATCTTAACTATGAGGAATGTAAAT	CGTTTAGGTGCTAATGAGATTAGAAGAAGTTATACAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTATTTACCTTTTAGGCTTGTATATGATTATTCTATG
CTTTTATCTTAACTATGAGGAATGTAAAT	ATAGATAAATGAGATTTCCCTGCTCCAGGATTACCT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAGATAAATATAAAGATGATGTACCAGAAGAGATT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTGTATACAAATACAATATACAAACTATACAAACA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTACTGTGTTTCTATCATTCTTTGTAAAATTAATCGC
CTTTTATCTTAACTATGAGGAATGTAAAT	ACAAATTGGAGGGTATGAATATGAGATCAATATTAC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTTAATTTGAAACCACACTATTCTATTGAAACTTTAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGTAAGTATGCCTTGTTGTTCATAATTAATTACTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	GAGGATATACAATCTCAAATAGATAATAATGCTACGG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTAGTAGCATTGTTACTATAGTTCTTATTGTCTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	GTGGCATCAATATATCCTGTTTTTATTGTATCTTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	TACAATCTTTTTTATATATTCCGTAATATATTCCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGGGAAATGCTTATGGAACTTTGGTATGTTTAGGT
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTATAGTAAAACCATATTGATATTCTCCATAATATC
CTTTTATCTTAACTATGAGGAATGTAAAT	TATAGTGCTGATGTAATAGGCAATATAGACAACAGT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATATGAAGCAATTCAAGGTACTGAAGACAACTCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTCTACAAGAGATACTTATAAATTTTATGGTGTGGCTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTAACACTTATATAATATCATACATTGTAATACTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	AGAGAAACACCAAGCGCAACTTTAACTATTGAATCA
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTACGAAAAAGACACAGAATAATCAAACGAACCA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGATTTTTAACCCCTCGTGTTTCACGACCCCTTTAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTTCAGTAAGTACTTTTGTATATTTACTTGTCATA
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAATAGAATTAATATTCCTAAGGCTGTATCCCATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTAAAATGGTTTTATATGCATTAGTAAAATCGTTTG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAAAATGGTTGTTCTTCTATTAGACAAACTTTTAATC
CTTTTATCTTAACTATGAGGAATGTAAAT	TCACCAACACTTTTGCTATATACAGATTCAAAATAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTAAAACACTCCTAACTTAAAAACCTTCTTAACTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTATCTGTTTCTATACTTATTATTTTATTGTTCTTAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTTACATCTCACCTTTCTCTATTTTGTATTTATTA
CTTTTATCTTAACTATGAGGAATGTAAAT	GTTATAAGCATATCTATAAATAATTTACTAGATAGA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGATTTACTAGGGTTTAGAAGGCTATATAGATTATC
CTTTTATCTTAACTATGAGGAATGTAAAT	CCAACTAGTTTGATTGGATTATAACAAGTGTTTCCAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGTAAACAGGTATTTGTAACCGTTTATCAAAAATA
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAGAGCTGTATTGATGTCCTGCGTAGTTATTACC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGTAAGTTTCAGTGGAATCTATTGATAAAGTGTGAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTATTAATTCGGCATCTCCTGTAGTCGAACCACTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATGGTTTCGTTTGTAGCAATGATTGTTTTTTCTACTATT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATCAAATTACCCAAACACCCATTATGTCGTTGTACT
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTTGTTAACTGGTTTAATCAACTTTCACCGGCAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAAAAGCACTCGGCATCAATATGTCAGTTGCTAAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAGAACGGAAAAGACGTACAGGGTGCTATTTTGAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGTGTTAATATTCATGAGTTAATTATAAAATAAAAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	CCAGGTATTGGAAATGGTGTAAAGGCGGCTATGCCAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TCATAAGTTTGCATAGAATAACTATAAGTGCCATCAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTCCACTTGTTCTTCTTGCTTTGGAACGTTGTTCTTC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTCTCTATCACTTGGCAATTCATGCATAAGATTTTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTCTAATTTAACTTTTATTATAGATTTTTCCATAA
CTTTTATCTTAACTATGAGGAATGTAAAT	ACGAGATTATAACACGTTTTAATTTTTAATGTCAAGG
CTTTTATCTTAACTATGAGGAATGTAAAT	GGTAAATAAAAGAAATTACTTATAGTATCCAATTGA
CTTTTATCTTAACTATGAGGAATGTAAAT	AATACTAAAGTGTTTTCTAGTATACTAAAAAAACTTG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTATTCTAAAAACTTCTCTTCATCTGTTTCTGTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	GCGGGTAAATCTGTATCAGTAGGAAGATACATTTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATAAATGATGTAGAAAAAGTTGAATATGAAGGTCTTGT
CTTTTATCTTAACTATGAGGAATGTAAAT	CTCTTTTTTTTTATGTTGTGGGGTGGGGGGTCCCCACG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGATTTAACATCTATTGAAGATAAAAAAGAGCGT
CTTTTATCTTAACTATGAGGAATGTAAAT	ACTATAATACAGCGAGAAACTTATCTAAAAGTCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	AGAAAAAAGAGCCAGTTGTTAGGAATAATTGTATTATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TGGTTGGCATACTGTTCTTTAAGGTCTGATATTATTC
CTTTTATCTTAACTATGAGGAATGTAAAT	GCCAATAAATTTGTTTCTTTACCTATCTCTCGATAAG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAAACAGCTATAACAAACTTTATCATAACTGTTAAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAGAATAACTACAAATGGGTTGATAAGACAGAACAA
CTTTTATCTTAACTATGAGGAATGTAAAT	AAACATAAACATGTAAAAGTAGCTGTGCCATCATCAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTTGCATATGCAACATCAGAACCTAAAGAAGTTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TCATCATAATTATTGTTGTTAGGTGTTGTATTACTCT
CTTTTATCTTAACTATGAGGAATGTAAAT	TACACATAAGAAGAATAAAAATAGCCGCCACCAGTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTACTATAAACTTAGTATCTATACCCTGTTTTTTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	AAATCCATACTCTTTTGAGTTGGCTTGTTGTAACTA
CTTTTATCTTAACTATGAGGAATGTAAAT	TCACCTAACACATCATAAGCTTGTGATCTAGTTAAGC
CTTTTATCTTAACTATGAGGAATGTAAAT	AGATCATCGAGAATTATTAAATCTGCTTTAGTAATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGATGAAGATGTATATAAGAAACTTTGTGAACTTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	GGTTTGTAATTCTATGTAATTAAATTCTTTATCTATC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAAAAATCAATATCTTCAAATCCTACATTGTACTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTGTTTTTTGTAATATTCTCTAATGCAATCTTCTA
CTTTTATCTTAACTATGAGGAATGTAAAT	GATACAGAGGTTAATGTATCTTATAAAGAAGATTGGT
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAGTATCAGAGGCCGGGAAGAATATTAAATTATAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTACTATGTTAATACCAATCTTACTCCAATCCAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAGATTCTAAATATCCTTCTTTAAAAGGTGTTTTTG
CTTTTATCTTAACTATGAGGAATGTAATA

>NZ_HG917868|1|1|217843-223120|CRT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTAAAGAAAATAAATTTATAAGTCGTAAGATAAGA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATATTAGTTCAAAATGCGTAGATATTTATTTTTATT
CTTTTATCTTAACTATGAGGAATGTAAAT	CGTTTAGGTGCTAATGAGATTAGAAGAAGTTATACAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTATTTACCTTTTAGGCTTGTATATGATTATTCTATG
CTTTTATCTTAACTATGAGGAATGTAAAT	ATAGATAAATGAGATTTCCCTGCTCCAGGATTACCT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAGATAAATATAAAGATGATGTACCAGAAGAGATT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTGTATACAAATACAATATACAAACTATACAAACA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTACTGTGTTTCTATCATTCTTTGTAAAATTAATCGC
CTTTTATCTTAACTATGAGGAATGTAAAT	ACAAATTGGAGGGTATGAATATGAGATCAATATTAC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTTAATTTGAAACCACACTATTCTATTGAAACTTTAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGTAAGTATGCCTTGTTGTTCATAATTAATTACTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	GAGGATATACAATCTCAAATAGATAATAATGCTACGG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTAGTAGCATTGTTACTATAGTTCTTATTGTCTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	GTGGCATCAATATATCCTGTTTTTATTGTATCTTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	TACAATCTTTTTTATATATTCCGTAATATATTCCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGGGAAATGCTTATGGAACTTTGGTATGTTTAGGT
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTATAGTAAAACCATATTGATATTCTCCATAATATC
CTTTTATCTTAACTATGAGGAATGTAAAT	TATAGTGCTGATGTAATAGGCAATATAGACAACAGT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATATGAAGCAATTCAAGGTACTGAAGACAACTCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTCTACAAGAGATACTTATAAATTTTATGGTGTGGCTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTAACACTTATATAATATCATACATTGTAATACTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	AGAGAAACACCAAGCGCAACTTTAACTATTGAATCA
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTACGAAAAAGACACAGAATAATCAAACGAACCA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGATTTTTAACCCCTCGTGTTTCACGACCCCTTTAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTTCAGTAAGTACTTTTGTATATTTACTTGTCATA
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAATAGAATTAATATTCCTAAGGCTGTATCCCATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTAAAATGGTTTTATATGCATTAGTAAAATCGTTTG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAAAATGGTTGTTCTTCTATTAGACAAACTTTTAATC
CTTTTATCTTAACTATGAGGAATGTAAAT	TCACCAACACTTTTGCTATATACAGATTCAAAATAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTAAAACACTCCTAACTTAAAAACCTTCTTAACTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTATCTGTTTCTATACTTATTATTTTATTGTTCTTAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTTACATCTCACCTTTCTCTATTTTGTATTTATTA
CTTTTATCTTAACTATGAGGAATGTAAAT	GTTATAAGCATATCTATAAATAATTTACTAGATAGA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGATTTACTAGGGTTTAGAAGGCTATATAGATTATC
CTTTTATCTTAACTATGAGGAATGTAAAT	CCAACTAGTTTGATTGGATTATAACAAGTGTTTCCAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGTAAACAGGTATTTGTAACCGTTTATCAAAAATA
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAGAGCTGTATTGATGTCCTGCGTAGTTATTACC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGTAAGTTTCAGTGGAATCTATTGATAAAGTGTGAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TCTATTAATTCGGCATCTCCTGTAGTCGAACCACTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATGGTTTCGTTTGTAGCAATGATTGTTTTTTCTACTATT
CTTTTATCTTAACTATGAGGAATGTAAAT	ATCAAATTACCCAAACACCCATTATGTCGTTGTACT
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTTGTTAACTGGTTTAATCAACTTTCACCGGCAG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAAAAGCACTCGGCATCAATATGTCAGTTGCTAAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAGAACGGAAAAGACGTACAGGGTGCTATTTTGAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TGTGTTAATATTCATGAGTTAATTATAAAATAAAAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	CCAGGTATTGGAAATGGTGTAAAGGCGGCTATGCCAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TCATAAGTTTGCATAGAATAACTATAAGTGCCATCAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTCCACTTGTTCTTCTTGCTTTGGAACGTTGTTCTTC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTCTCTATCACTTGGCAATTCATGCATAAGATTTTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTCTAATTTAACTTTTATTATAGATTTTTCCATAA
CTTTTATCTTAACTATGAGGAATGTAAAT	ACGAGATTATAACACGTTTTAATTTTTAATGTCAAGG
CTTTTATCTTAACTATGAGGAATGTAAAT	GGTAAATAAAAGAAATTACTTATAGTATCCAATTGA
CTTTTATCTTAACTATGAGGAATGTAAAT	AATACTAAAGTGTTTTCTAGTATACTAAAAAAACTTG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAGTATTCTAAAAACTTCTCTTCATCTGTTTCTGTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	GCGGGTAAATCTGTATCAGTAGGAAGATACATTTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATAAATGATGTAGAAAAAGTTGAATATGAAGGTCTTGT
CTTTTATCTTAACTATGAGGAATGTAAAT	CTCTTTTTTTTTATGTTGTGGGGTGGGGGGTCCCCACG
CTTTTATCTTAACTATGAGGAATGTAAAT	TTGATTTAACATCTATTGAAGATAAAAAAGAGCGT
CTTTTATCTTAACTATGAGGAATGTAAAT	ACTATAATACAGCGAGAAACTTATCTAAAAGTCATT
CTTTTATCTTAACTATGAGGAATGTAAAT	AGAAAAAAGAGCCAGTTGTTAGGAATAATTGTATTATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TGGTTGGCATACTGTTCTTTAAGGTCTGATATTATTC
CTTTTATCTTAACTATGAGGAATGTAAAT	GCCAATAAATTTGTTTCTTTACCTATCTCTCGATAAG
CTTTTATCTTAACTATGAGGAATGTAAAT	AAAACAGCTATAACAAACTTTATCATAACTGTTAAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TAAGAATAACTACAAATGGGTTGATAAGACAGAACAA
CTTTTATCTTAACTATGAGGAATGTAAAT	AAACATAAACATGTAAAAGTAGCTGTGCCATCATCAT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTTGCATATGCAACATCAGAACCTAAAGAAGTTTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TCATCATAATTATTGTTGTTAGGTGTTGTATTACTCT
CTTTTATCTTAACTATGAGGAATGTAAAT	TACACATAAGAAGAATAAAAATAGCCGCCACCAGTTA
CTTTTATCTTAACTATGAGGAATGTAAAT	ATTACTATAAACTTAGTATCTATACCCTGTTTTTTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	AAATCCATACTCTTTTGAGTTGGCTTGTTGTAACTA
CTTTTATCTTAACTATGAGGAATGTAAAT	TCACCTAACACATCATAAGCTTGTGATCTAGTTAAGC
CTTTTATCTTAACTATGAGGAATGTAAAT	AGATCATCGAGAATTATTAAATCTGCTTTAGTAATG
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGATGAAGATGTATATAAGAAACTTTGTGAACTTGC
CTTTTATCTTAACTATGAGGAATGTAAAT	GGTTTGTAATTCTATGTAATTAAATTCTTTATCTATC
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAAAAATCAATATCTTCAAATCCTACATTGTACTT
CTTTTATCTTAACTATGAGGAATGTAAAT	TAGTGTTTTTTGTAATATTCTCTAATGCAATCTTCTA
CTTTTATCTTAACTATGAGGAATGTAAAT	GATACAGAGGTTAATGTATCTTATAAAGAAGATTGGT
CTTTTATCTTAACTATGAGGAATGTAAAT	CTAGTATCAGAGGCCGGGAAGAATATTAAATTATAAA
CTTTTATCTTAACTATGAGGAATGTAAAT	TTTACTATGTTAATACCAATCTTACTCCAATCCAC
CTTTTATCTTAACTATGAGGAATGTAAAT	TTAGATTCTAAATATCCTTCTTTAAAAGGTGTTTTTG
CTTTTATCTTAACTATGAGGAATGTAATA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_HG917868.1\|WP_162148679.1\|237366_240999_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|376628
NZ_HG917868.1\|WP_044035849.1\|223309_223522_-\|DUF2922-domain-containing-protein	unknown	unknown	gnl\|CDD\|378571
NZ_HG917868.1\|WP_051483618.1\|223991_224822_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|368199
NZ_HG917868.1\|WP_044035842.1\|210262_212062_+\|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1	cas8b2	cd09665_cas8b2_CAS-I-B	gnl\|CDD\|187796
NZ_HG917868.1\|WP_051483620.1\|226355_226784_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	unknown	unknown	gnl\|CDD\|227305
NZ_HG917868.1\|WP_044035840.1\|208475_209417_+\|WYL-domain-containing-protein	WYL	COG2378_WYL_CAS-I:CAS-III	gnl\|CDD\|379100
NZ_HG917868.1\|WP_044035843.1\|212062_212968_+\|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	cas7	cd09687_cas7_CAS-I-B	gnl\|CDD\|187818
NZ_HG917868.1\|WP_044035852.1\|226972_228085_+\|ATP-binding-protein	unknown	unknown	gnl\|CDD\|99707
NZ_HG917868.1\|WP_044035845.1\|213684_215877_+\|CRISPR-associated-helicase/endonuclease-Cas3	cas3	COG1203_cas3_CAS-I	gnl\|CDD\|273707
NZ_HG917868.1\|WP_044035853.1\|228244_231100_+\|SNF2-helicase-associated-domain-containing-protein	unknown	unknown	gnl\|CDD\|223627
NZ_HG917868.1\|WP_044035850.1\|223539_223755_-\|DUF1659-domain-containing-protein	unknown	unknown	unknown
NZ_HG917868.1\|WP_044035846.1\|215889_216408_+\|CRISPR-associated-protein-Cas4	cas4	pfam01930_cas4_CAS-I	gnl\|CDD\|366863
NZ_HG917868.1\|WP_044035841.1\|209512_210250_+\|CRISPR-associated-endoribonuclease-Cas6	cas6	cd09652_cas6_CAS-I:CAS-III	gnl\|CDD\|187783
NZ_HG917868.1\|WP_044035848.1\|217393_217657_+\|CRISPR-associated-endonuclease-Cas2	cas2	cd09725_cas2_CAS-I:CAS-II:CAS-III:CAS-V	gnl\|CDD\|187856
NZ_HG917868.1\|WP_051483619.1\|224901_225618_-\|C39-family-peptidase	unknown	unknown	gnl\|CDD\|379241
NZ_HG917868.1\|WP_044035851.1\|225806_226355_+\|metal-dependent-hydrolase	unknown	unknown	unknown
NZ_HG917868.1\|WP_044035854.1\|231277_237295_+\|hypothetical-protein	unknown	unknown	gnl\|CDD\|173886
NZ_HG917868.1\|WP_044035844.1\|212972_213635_+\|type-I-B-CRISPR-associated-protein-Cas5	cas5	cd09658_cas5_CAS-I-B	gnl\|CDD\|187789
NZ_HG917868.1\|WP_044035839.1\|207881_208310_+\|hypothetical-protein	unknown	unknown	unknown
NZ_HG917868.1\|WP_044035847.1\|216407_217391_+\|type-I-B-CRISPR-associated-endonuclease-Cas1	cas1	cd09722_cas1_CAS-I-B	gnl\|CDD\|274695

Protein	Function_ID	Function_description	E-value
NZ_HG917868.1\|WP_162148679.1\|237366_240999_+\|hypothetical-protein	gnl\|CDD\|376628	pfam01841, Transglut_core, Transglutaminase-like superfamily. This family includes animal transglutaminases and other bacterial proteins of unknown function. Sequence conservation in this superfamily primarily involves three motifs that centre around conserved cysteine, histidine, and aspartate residues that form the catalytic triad in the structurally characterized transglutaminase, the human blood clotting factor XIIIa'. On the basis of the experimentally demonstrated activity of the Methanobacterium phage pseudomurein endoisopeptidase, it is proposed that many, if not all, microbial homologs of the transglutaminases are proteases and that the eukaryotic transglutaminases have evolved from an ancestral protease.	1.64115e-12
NZ_HG917868.1\|WP_044035849.1\|223309_223522_-\|DUF2922-domain-containing-protein	gnl\|CDD\|378571	pfam11148, DUF2922, Protein of unknown function (DUF2922). This bacterial family of proteins has no known function.	1.35246e-17
NZ_HG917868.1\|WP_051483618.1\|223991_224822_+\|hypothetical-protein	gnl\|CDD\|368199	pfam04931, DNA_pol_phi, DNA polymerase phi. This family includes the fifth essential DNA polymerase in yeast EC:2.7.7.7. Pol5p is localized exclusively to the nucleolus and binds near or at the enhancer region of rRNA-encoding DNA repeating units.	1.88536e-05
NZ_HG917868.1\|WP_044035842.1\|210262_212062_+\|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1	gnl\|CDD\|187796	cd09665, Cas8a1_I-A, CRISPR/Cas system-associated protein Cas8a1. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Large proteins, some contain Zn-finger domain; signature gene for I-A subtype; also known as CXXC_CXXC family.	1.491e-18
NZ_HG917868.1\|WP_051483620.1\|226355_226784_-\|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein	gnl\|CDD\|227305	COG4970, FimT, Tfp pilus assembly protein FimT [Cell motility and secretion / Intracellular trafficking and secretion].	1.7391e-08
NZ_HG917868.1\|WP_044035840.1\|208475_209417_+\|WYL-domain-containing-protein	gnl\|CDD\|379100	pfam13280, WYL, WYL domain. WYL is a Sm-like SH3 beta-barrel fold containing domain. It is a member of the WYL-like superfamily, named for three conserved amino acids found in a subset of the superfamily. However, these residues are not strongly conserved throughout the family. Rather, the conservation pattern includes four basic residues and a position often occupied by a cysteine, which are predicted to line a ligand-binding groove typical of the Sm-like SH3 beta-barrels. A WYL domain protein (sll7009) is a negative regulator of the I-D CRISPR-Cas system in Synechocystis sp. It is predicted to be a ligand-sensing domain that could bind negatively charged ligands, such as nucleotides or nucleic acid fragments, to regulate CRISPR-Cas and other defense systems such as the abortive infection AbiG system.	2.22086e-38
NZ_HG917868.1\|WP_044035843.1\|212062_212968_+\|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR	gnl\|CDD\|187818	cd09687, Cas7_I-C, CRISPR/Cas system-associated RAMP superfamily protein Cas7. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas7 is a RAMP superfamily protein; Subunit of the Cascade complex; also known as Cst2/DevR family.	4.60389e-54
NZ_HG917868.1\|WP_044035852.1\|226972_228085_+\|ATP-binding-protein	gnl\|CDD\|99707	cd00009, AAA, The AAA+ (ATPases Associated with a wide variety of cellular Activities) superfamily represents an ancient group of ATPases belonging to the ASCE (for additional strand, catalytic E) division of the P-loop NTPase fold. The ASCE division also includes ABC, RecA-like, VirD4-like, PilT-like, and SF1/2 helicases. Members of the AAA+ ATPases function as molecular chaperons, ATPase subunits of proteases, helicases, or nucleic-acid stimulated ATPases. The AAA+ proteins contain several distinct features in addition to the conserved alpha-beta-alpha core domain structure and the Walker A and B motifs of the P-loop NTPases.	0.00176926
NZ_HG917868.1\|WP_044035845.1\|213684_215877_+\|CRISPR-associated-helicase/endonuclease-Cas3	gnl\|CDD\|273707	TIGR01587, CRISPR-associated_endonuclease/helicase_Cas3, CRISPR-associated helicase Cas3. This model represents the highly conserved core region of an alignment of Cas3, a protein found in association with CRISPR repeat elements in a broad range of bacteria and archaea. Cas3 appears to be a helicase, with regions found by pfam00270 (DEAD/DEAH box helicase) and pfam00271 (Helicase conserved C-terminal domain). Some but not all members have an N-terminal HD domain region (pfam01966) that is not included within this model.	2.64014e-65
NZ_HG917868.1\|WP_044035853.1\|228244_231100_+\|SNF2-helicase-associated-domain-containing-protein	gnl\|CDD\|223627	COG0553, HepA, Superfamily II DNA/RNA helicases, SNF2 family [Transcription / DNA replication, recombination, and repair].	6.10338e-105
NZ_HG917868.1\|WP_044035846.1\|215889_216408_+\|CRISPR-associated-protein-Cas4	gnl\|CDD\|366863	pfam01930, Cas_Cas4, Domain of unknown function DUF83. This domain has no known function. The domain contains three conserved cysteines at its C-terminus.	7.40941e-55
NZ_HG917868.1\|WP_044035841.1\|209512_210250_+\|CRISPR-associated-endoribonuclease-Cas6	gnl\|CDD\|187783	cd09652, Cas6-I-III, CRISPR/Cas system-associated RAMP superfamily protein Cas6. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas6 is an endoribonuclease that generates crRNAs, predicted subunit of Cascade complex; RAMP superfamily protein; Possesses double RRM/ferredoxin fold.	6.21815e-19
NZ_HG917868.1\|WP_044035848.1\|217393_217657_+\|CRISPR-associated-endonuclease-Cas2	gnl\|CDD\|187856	cd09725, Cas2_I_II_III, CRISPR/Cas system-associated protein Cas2. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas2 is present in majority of CRISPR/Cas systems along with Cas1; RNAse specific to U-rich regions; Possesses an RRM/ferredoxin fold.	8.63564e-28
NZ_HG917868.1\|WP_051483619.1\|224901_225618_-\|C39-family-peptidase	gnl\|CDD\|379241	pfam13529, Peptidase_C39_2, Peptidase_C39 like family.	3.80359e-30
NZ_HG917868.1\|WP_044035854.1\|231277_237295_+\|hypothetical-protein	gnl\|CDD\|173886	cd01951, lectin_L-type, legume lectins. The L-type (legume-type) lectins are a highly diverse family of carbohydrate binding proteins that generally display no enzymatic activity toward the sugars they bind. This family includes arcelin, concanavalinA, the lectin-like receptor kinases, the ERGIC-53/VIP36/EMP46 type1 transmembrane proteins, and an alpha-amylase inhibitor. L-type lectins have a dome-shaped beta-barrel carbohydrate recognition domain with a curved seven-stranded beta-sheet referred to as the "front face" and a flat six-stranded beta-sheet referred to as the "back face". This domain homodimerizes so that adjacent back sheets form a contiguous 12-stranded sheet and homotetramers occur by a back-to-back association of these homodimers. Though L-type lectins exhibit both sequence and structural similarity to one another, their carbohydrate binding specificities differ widely.	5.03795e-18
NZ_HG917868.1\|WP_044035844.1\|212972_213635_+\|type-I-B-CRISPR-associated-protein-Cas5	gnl\|CDD\|187789	cd09658, Cas5_I-B, CRISPR/Cas system-associated RAMP superfamily protein Cas5. CRISPR (Clustered Regularly Interspaced Short Palindromic Repeats) and associated Cas proteins comprise a system for heritable host defense by prokaryotic cells against phage and other foreign DNA; Cas5 is a RAMP superfamily protein; Subunit of the Cascade complex.	1.82648e-38
NZ_HG917868.1\|WP_044035847.1\|216407_217391_+\|type-I-B-CRISPR-associated-endonuclease-Cas1	gnl\|CDD\|274695	TIGR03641, cas1_HMARI, CRISPR-associated endonuclease Cas1, subtype I-B/HMARI/TNEAP. The CRISPR-associated protein Cas1 is virtually universal to CRISPR systems. CRISPR, an acronym for Clustered Regularly Interspaced Short Palindromic Repeats, is prokaryotic immunity system for foreign DNA, mostly from phage. CRISPR systems belong to different subtypes, distinguished by both nature of the repeats, the makeup of the cohort of associated Cas proteins, and by molecular phylogeny within the more universal Cas proteins such as this one. This model is of type EXCEPTION and provides more specific information than the EQUIVALOG model TIGR00287. It describes Cas1 subgroup that includes Cas1 proteins of the related HMARI and TNEAP subtypes of CRISPR/Cas system.	2.64281e-152

>NZ_HG917868.1|WP_044035848.1|217393_217657_+|CRISPR-associated-endonuclease-Cas2
MFVILTYDVGEKRVNRVRKTLKKYLTWTQNSVFEGQITEAKLHKCLAEVNKSLDKNDDSLYVYMVGNIHNINKQVVGKEKNYDELFL
>NZ_HG917868.1|WP_044035847.1|216407_217391_+|type-I-B-CRISPR-associated-endonuclease-Cas1
MARDYYIFSNGRLKRKDNTIYFLDVEGNKKAIPIEDIERLHLFGEVDFNTKFLNYISRYSILISIYNYYGFYSGSYYSKKKNVSGMLIVDQVRAYDKDEYRLYFAKSFIDSAIHHMLRNIRRHRYKTEEYIKSIEAERVLMLEAKTIQEVMGAEGRARKNYYESFNKFIKEEFYFEKREKRPPKDPINALISFGNSLMYTTVLGEIYKTPLDPTISYLHEPSTKRFSLSLDIAEIFKPLIIDSIIFSLINKKIIKKTDFVYEGDICYLNEMGKKKFIKEYENKLSTTIKHRTLNRKVSYKSLIRLECYKIIKMLIGDDIYKPLKAWW
>NZ_HG917868.1|WP_044035846.1|215889_216408_+|CRISPR-associated-protein-Cas4
MKINFDDFKVQGIKFNYYFICKRKLWLFDKGICMEENSDRVLHGKIVHENSYNKFPSKEKLIDDMIKIDVLEDDNIKEVKISSKMKKSDRMQLLYYLYYLKQLGINKSGTLNYVKEKKVEKVYLTKNDEIEIEKILLEIKRLLLEKKPPKIVKLPYCKKCAYYEFCYIKEEE
>NZ_HG917868.1|WP_044035845.1|213684_215877_+|CRISPR-associated-helicase/endonuclease-Cas3
MKFLAKTIPEVETLREHTDRLLEEFSRLKNIYEDNINDIIRKYIDPSDFWCILNMCCEYHDYGKANKQFQNKLLRILNKEQIENNLEEIPHNFLSPGYLPISFLEYVKERYPDDILYIIIQAIAYHHERNKEPEYTNIKRCIEEDLKKSLLELSESMNKSIKDISSWYVKYISYNERIKASNQYYELYIILKGLLHKIDHAASAHCKIEEVADRGVGEYIEDYMKKNKWIFREPQIFAKENQDENLVIVASTGIGKTETALLWINDSKAFFTLPLRVSINALYSRVKDDIGYDYVGLIHSSALEYLEDNRYENADLLYEESKLLSKKLSFSTIDQIFKYPFKYIGYEKVLATLSYSKVVIDEIQGYSPSIVAVILYAIKQLSEVGGKFLIMTATLPRIYKDKLYEFGIEFKERSFISKIRRHRVSLRNDEIVSAIDEIEEKGKMSKVLVIVNTVDKAIEVYNKLKNKSNVKVLHSLFINEDRSRLEREIKQFTEKENSDNGIWITTQIVEASLDVDFDYLYTEMSTLDSQFQRYGRCYRKRSLDKNQSNIFIYIKNISGAGSIYDKDILEKSINALYEYDDKVIEEDVKVKMVDKIYSKEMLMGTDYYKEFINACRYLENVIPYETTSKEAQKILRDITSIKVIPEDIYNENIELIENFKNSYGDKRRELSNKIGKISVSIPLYKINKFKGINSEIKIIEIEGLSNYSTINVKYSHEVGILLDELNDNIF
>NZ_HG917868.1|WP_044035844.1|212972_213635_+|type-I-B-CRISPR-associated-protein-Cas5
MKSLKIKIYQETVCYKKPFAFKVTETYPLPPYSTIIGMLHNVMGVRSGEYIPMDISVQGSYEEIFNTYNTTMFYKKKNVTSMPMNVHLLLGVNLIIHVLAEENILLQIIDGFKDSKESFTLGRREDLARLDSIKLVNLEKRYISKFSGEEYRLKNNAYIPQKYNYRVNGITYMLNKKYTTLNELRNWEKVEAIYVEKGELIDQEYLIDDDIIEQDIVFLG
>NZ_HG917868.1|WP_044035843.1|212062_212968_+|type-I-B-CRISPR-associated-protein-Cas7/Cst2/DevR
MSKSISCSVIFQAQSLNYGESIGNISELKKLTRGDGNFYSIATRQAIGYDIRRIGKEIFGWNLYTVDKSKGTIQFKNEYTIKDSIEMDLFGYMKTEKKGKNGDGGSTIRTAVARLSNAISLEPYKSDMDFLSNKGLADRIGEHPNLANIEQHLSFYTYTITVDLDRVGEDGEISLLSKEKANRVNQLLDILKILNRNIRGRQENLSPLFIIGGIYSIANPFFLGRIKLKTNEGKYNIDTKLLKDTLDMTILDCNVRKNTSIGIISDIFGNEEEIKNIVDTSLGIEDFFEGLKEKVNQYYEV
>NZ_HG917868.1|WP_044035842.1|210262_212062_+|type-I-B-CRISPR-associated-protein-Cas8b1/Cst1
MRINNSDNWFYKAGIVGFDRIIRYNEDFCNLDSGLYNYVVHDNYIEFDEKLLENFHKYYFNYFFGRYNSAKDQEEKIRFYIRRCEKEDKFKDNLGKIRELVKNNNKKIKKFEVKEVNRCLEIQKELGMVKKYSEKNKVEELLNEYIDILKDNYINTQITLNKFKSILSKSFFGQVSFLNVCNNSKTLAQQEDILFKDYIDPILVMCKLNEILKKNDEEMLREFIEECLLKNKRNGEIEKVLKDFKKGLFGKIRKEKDAMSIFMQYNSCSMCGNEVSIGSNYYEGNFVPLAISNENAENMYWNFNTKHPICSLCKLILLCTSAGMTDIYKGYLDDKYDYNNKLYYGFISIDGDLRDVIKQNNNLANKKDKDSKLQAYILDSIAEKEQISKWQLDNILYIEFNTDYSSKNTKMNYLNIPRYLAEFLKSKSELLYKIKDKKVRVEIFDAILKQVDLKHLIDKFLRSTLQENEQYVVNVFPIIKVRVYLKLYKGECDMVDKLYDKKLNYVYMQGREVGGILKSNSQENKILGLSYRLLNATKATNKKEFMDTVIRIFMSVEKEVPMIFLDVIKEGSLEFEDISYSFISGLTSQDSKIKEGGEK
>NZ_HG917868.1|WP_044035841.1|209512_210250_+|CRISPR-associated-endoribonuclease-Cas6
MRIRIVGRVKDGIIPIGYRMMIVSLLKKAIEKGDKEYFNKLYYYNEKKNKKIKSFCFGTYLQNFMFEEEGIKVDGKINITISTPDYMLGVSMYNGLLKLSTYKYKDKYEFIKEKVILEKEKIISDEHVVLKTLSPIVMKDSEGKKVDIDSENYEKELNYISNIILESYRGYGLKRKLVFIPVNMKKSVVKEEIAGFTKEINKRYIYINGYSGIFTMEGDVEDLNLLLQLGIGFRRSEGFGLISLV
>NZ_HG917868.1|WP_044035840.1|208475_209417_+|WYL-domain-containing-protein
MLGNLLKMWFMLLDGRVRQIKDIARELEVSERQVKRYKEELAVYVDIESITGKYGGYRLRETYIPFKGLLTEEETELLRYYIDSLDSFPLEEKDKINKIIGKINYSILNKNDNVSNFNEIIPYSTVRMMDENRKNLISDIYKAIVENREVDITYKNNNGKCTKRKVQPYKYITYKGEKYLVAYCLMREDIRYFKMIRIQCYKLLDSIFNRTIDIDNVINQEIHNSVGIFGGKEYKLVLEVSPPMANTISERIWVEDQCVEELEQGEIRFTATMKGGPEIISWILSMGDTVKVIEPLELKDEIGEKLKKMIRNL
>NZ_HG917868.1|WP_044035839.1|207881_208310_+|hypothetical-protein
MLCKNAELFLEEAKRRGIEGIEVKEEEHNLQRAMFYQDLDNGIEMRNMVIFDSNNDVVVVSGMDFVTGVNMEKRYIIYDVLSQLNRVIDNFTYILKKGQIVIDSTYLVGGGDNFDAAILFDILIKMKAIVNRDAIHLIKLAH
>NZ_HG917868.1|WP_044035849.1|223309_223522_-|DUF2922-domain-containing-protein
MKSLVMKFITETGSKVSINVPKVKENLDETKVKEVMNLIKEKAVFTFKGGDIIALDSAQITETNTTEITL
>NZ_HG917868.1|WP_044035850.1|223539_223755_-|DUF1659-domain-containing-protein
MATTVQTNKNIQLSFLTTDENGKESTTKVTLPNLKVDANLDDVAAVVDSYAELKEGSLSKAAIIDESLLVK
>NZ_HG917868.1|WP_051483618.1|223991_224822_+|hypothetical-protein
MNDRKGLVVIKIISIISIVITIVYTLTGFVSGNCEDLLISKIQSIVKAEDDAADEELDKEVKNVTLADEEEDTEYQDEEDIEHVEEDVEDDVDIEEEEECTNTEEDEEITEEPVNNNEDTEDIEENTVEVSNVTVDNENKNTIVDSKVENPTEVNVEQVTYPRIVKNSDGTIALLRSQQEQPIAIVLDEYVNGFLEFNYNYCVITAPEVEYSIEFECNGNVEVAVGTGSTNVYRRYVNRKVKNNDKLNIKLTAKINGTEESTSFQRTINRGIFGFR
>NZ_HG917868.1|WP_051483619.1|224901_225618_-|C39-family-peptidase
MRKIKIISILISIIMVLIGVISLIYNDSNSETSNKNIFSAMPSGEYKIEGIDTLNQFPEMPTGCEITSTTMLLNWYGVNVDKEELGESIEKADVPSYVDGTLQGASPNEYFIGDPFSSDGYGVYHKPIANLIDQYTDGKSKDITGCSFNKLLRTVANGYPVVTWVTINMKESSVGSYWTNGDETIEWIIPEHAVLLVGFNENEVIINDPYTGTEYTVDKDIFENRWISLGRQAVTISD
>NZ_HG917868.1|WP_044035851.1|225806_226355_+|metal-dependent-hydrolase
MKGRQHVLIGTTATVATGIGLICSGSSVTNFIPIVIGGIIGSYIPDIDSHKSKAAQIFNKLFVILIVVLAILYCLGITLDLERFIGGLDANDPKTLAVLIFAVVTILGKLSPHRMFTHKWFGTMLFCYSVYLMGNMYFTIGFTTGYILHIVADTMTKNGKYLKFFQFKLPCRNSKNKFDISW
>NZ_HG917868.1|WP_051483620.1|226355_226784_-|prepilin-type-N-terminal-cleavage/methylation-domain-containing-protein
MLKNNKKKSGYTLMELIIVLSIIALLAAIAIPKYSKMTMEAKKSTDKMNAKLIHNNVSILLADSTSGFSEAISYNTYIKITDSGHSIAEQKIASTFQNVPKAKAIPGDFFAYIKTDESVEIYVEKNTGNYIAVYPKGEDLYN
>NZ_HG917868.1|WP_044035852.1|226972_228085_+|ATP-binding-protein
MGEVSAENVFKPGCFSRYTYVCRHAPCIEETYEDKLEQDLKVSGCLISIVGPSKSGKTLLCEKVVENNRLIEISGIDFDEDNNLWKVILKKLNFTLEEWNKDKIINYFNKNNLVLLLDDFHYASKATQLNIAKQLKYALNKELKVIVISLPLLTDEAIRKNVDLIGRLILINVEPWKEKELQWIAINGYKKLDMNISRKNISNMATESLTSPQLMQSICLNLYFLIANSNIKNEDIGDKLLEKAYKITTLNFDYKDVIKALREGIRSRLNTRETYMVSGGKYLNSNELVINAIALNPPKMIMTVDELFLRVDSIIIDDKKTIKSEIEATLAKIVEMLKVEDPLYQVISYDGINLEILDPLFLFYLRWSGM
>NZ_HG917868.1|WP_044035853.1|228244_231100_+|SNF2-helicase-associated-domain-containing-protein
MRIEDFEDIIIKKVSPIVRSGGKELYKKGLVKSIKGKRFETFYALYGVVESENRIKEFNTYMKINLVNGNIDKASCGCDNFKRLSRGNNFFICSHLVATTEKFLVAMKKKTGVNPSKKVNKDNTILRILRKVSNDKILYEIRTYLGKDKIVIKDKNLRDFLEVNIDKKIKFTYEYLEINTKIINKPLPLSFTIKDDEKNLIVTTHKKMPISLTEKNDVYFFNNEIYLPPKDQIDNYIDTYNDEKIYPKTIKSYNEILDNLSKISSNIIIKESVREFASEYYKPEFFLYKEENKIYCTVNIYYGNKRINILVDSNDVIREKKKEETLLIKICGIGFVRKGERLEFIGDDEVLFDILSSKNEGIHKLGKVILGKAFKENGVYNYCNINGEIVKDDDKYIFYYSIDGMNNDEIFSAYEAYKEGKEFYKSNNGGFINFRDKGVKDFFNLLGGLGISVGSNEIIVDEDKEIYISEAVTNLPMIKGKENLHRAEEILSEEIEVPQGFKGNLRNYQVEGFRWFKGLSKLGLGGILSDEMGLGKTIQTIAFILSEKGEKFIIVAPTSLIYNWKSELEKFAEGLKVAVVHGAKRKEIIKNIQEYDALLTSYGTLKRDIELYKDIEFGYCILDEGQNIKNPDAESTKIVKAINSKNRFVLTGTPIENNLMELWSIFDFIMPGYLFSKEVFKKKFIFNNDVETLKLLINPFILRRTKKDVITELPDKIEKKVFVDMTAKQSKVYKDYMKDVLSTLQNYGDNKIEIFSYLTKLRQICLDPSIIIEDYEGGSGKVKAALKLIKERDGKILLFSQFTSILDKLKEELEGANIKYLHLDGSVAAKQRIKRVEEFNNEESIKVFLISLKAGGTGLNLTSASTVIHFDPWWNPAVEDQATDRAHRIGQRNVVEVIKLIAKDTIEEKIIQLQENKRLLIENVISGELGEGDLLKKLSVEDIKEIFRENK
>NZ_HG917868.1|WP_044035854.1|231277_237295_+|hypothetical-protein
MKKNKSKKIAIKTKQMIAKVLIIICLITNINTNYIVLAQDENTNTEIESAIEWLETNQNEDGTWGDSIQQITTYQVLDVLQSELDSEKSYKEGLKWAKEQEESTVDYQARRLMIKELVTKDNIEDLIKNQNEDGGFGLTDLYGSDVVDANLVLTVLLDQNEQEVDVENRLVNYILNHQNEDGSFSYFEDTTESVKLTAEVIIALNKFSNICENNSYNVQQSIRKAGDYLLSKQNDNKLWGDSLEDIRASLKAFSAVLNTEGIQESSYIEKVVSGLQLENGSVMNDAYATALYIELMKKISEIPKAEIDSINIYKKDNADKTLCKSYKAYEDMTIEVAANYDEEKAEVNVFILDEHGGVVFQDNKLKTDWEVKNQSPGQYRVVVQIIDSKSRYIISSAEENFTIEESVQVDNFETLIDCDSTMVGEPITINTKVAFDNLSNVDVNLILRTQILKGDVVVKEDSKIQELSKSKESYDVELMTFEPEVTEPATYTFKVEAIQNDNLVGSNEKEFIVYERLSNTGVYITQDKDKEKLYPGKDNLKLNFHLKGLKENDEKVMSYRSFSVLAALADESTSSFAYSGNIMSNEYIEFYLNGRGYTLGTKEGNPEYISDNNKNLLYGHPGSGTSYTTVNIDDNKYIYSPNVQGVTPDLSEGSVTSVEKIGNVKIKQKFAIVNNSNTGRNDMVEIRYIVKNEDTVSHSAGLRIMLDTMLGYNDAAPFRVPGIGALSYEKELVGDKIPQYWQAFDNLSNPSVVAQGTFYKEGMIKPDLVQFMNWSRVNSYSWYLTPTGSSTGDSAVTVFWNPTELLPGEEREYVTYYGIGELNSDISGSLVASITGASKLEATEEGYDPNPFLVTAYAYNMGLEEIGNVKARVVLPTGLKLAEEEKETHLFGNMGVGEEKQTSWNVVAEDSLVDKTLTYSVVYSVNGVDIKTINRNVFVPKQINNIAGRDVVLETVIPSSEFKINPEKVTPAPSEIIEKEDGNQLLRWNFDKIDIDEVIDLQVELNGESLISEAKYVVTKDTTLSYTNRENERETRKLKNMSVEVNKYELESEITTDKKEYTANENVIITNKTKNLHDYSMNLTGKVTIYDSNNEVVEVLDNNIESIWQGNEEKEDNYTFNTKELLMGTYKIEVQWFEGSKIIQTTDAYFNINKDGSIKHNVFVDKQQYNANDVVTYTNKISNTSINCIEKGLTLETVITNEQNEVVKNELVSLEDILSSTQVTKNGTFKLNDNKAGQYKVTATIYLDDKKISEETTLFEVISTQENLFGVKGNLKVLNSIITPAEEVSFESLIENTGNENIHNMPQIIRIIQVGTEKEMKKYQWESNVEVGNSDNKTFTWGDKSIEAGDYIIQYEAIKPNGETKLIASNNFTVKYIEDDFEKENDLWNYMGTAHRSDGGYAVLTENKNHENGAMWLKQGISLPFVTTFKYKAGGGTGADGFTFMFAKKANELGNEGREMGFNTGNGYAIEFDSFYNKFHGEQTSVNRAHIALGKDLLSTGNKGEIIDSLAMNVTEEVASKLSDDNWHDVEVRVTEDGVQLYLDGERVLVYKGKLDTTYDGFGFSSATGTENNHHYIDNVIIRENTEIALEDIKDDFTETNSKWDYLGSAYRSDEGYAVLTENKTWQTGAMWLNDVVSAPFTSKFKYKAGEGNGADGFVFMFGKESNKIGASGGTLGFSEGNGYGLEFDSFYNGSSENINNNNRHIALFKDKLTSTLKVNATDAIAAKVSDNKWHDVEVKVKTDGIEVFIDGESVMTWYGKIDKTYNGFGFAAATGDYTNSHFIDDVEIKEDVEEITENIKDDFSADTGLWNYMGTAARLEDGFARITPNENWKNGAMWLKKETTNKFTTKFKYKAGESSCGTNSDGFTYMFYKNPNQLGNTGETLGVQADSGYFIEFDSFYNGSNSEKIGKNSAHIALMKNSTSGEVLQFNNDDSITSKIADGQWHDVEVSVTSESVQVYVDSLLVIDYKGTLDTTYTGTGFSGATGGYNQNTFIDDFEIDITR
>NZ_HG917868.1|WP_162148679.1|237366_240999_+|hypothetical-protein
MKDKWKVTFKSIALTLIVIMTINCSSPGEVWREIKSNANKLWGDKETLTTVDRTKLGSLQETVSANKEKSKEAIENDNLDESKKLLEETLEAIESNEDKINKEFKNIEKYLDKNNLDVAKSRLTEVKNQFKDLVNSKDKIEEAINSDDKDKILAVLDDESIFGKDENTYKSLGDDALPHNNEEAVYVTEEATAISNDAIEYSLDKDTDDNEEYLKETLDTKITEVIKKKSDELSDNPLDIYKFVRNNVDFEAYAGSRKGAAGALEQLAGNDYDQSSLLIALLRSKNIPARYVTGTVDVSVENAMVWTGAETPKVAADMLASMGNKTTAITSGGEIVTIRIEHVWVEAYCSLCEYRGQGEVTDEKEWIPFDPSFKTYKKVEGTINSVEKDIETSDIADDFYYGGVKTEDNFGVKNIYNDDLKYAADDIKSQLEKYINEETLEGKRLIDVVGGLEIIPEEIDLLPFSIPNTLVSIDSRSSEIDNNKREKVSIEVSDTYGIGGELSLNKTAVELYGKKLTLSWIPATDSDEEIISNYGSVFDTPAYLVEVKPVIKADGEVIAEGSAIGLGQVENFSIVLDRVGLSSQSVTAVLTAGGYYALGLDYGAISENEITNIQSRMKEAEENAAEKDYYSDEVAGEILNGIIKSYFGELDSMNKISAEMSGVKDTRCLSFGISGFKPTVKYLYGTPVDLKLGSVYVDIGGDAHSVVSRDGDKEKEKSYMIKTGMIASAMESSIIEQMCGLPAVSTVSILNKATEQGETLYSVTKENVNEVLPLLNVGDYVKNEIVNVVNSGKEVTIPKNEINYYDWTGSVYIVMDNDTGAAGYMIAGGYAGGEGANDLSSVNVWEVFEHFIDGFTEGIKGAIPFIIIGTIVAIIAPEIVAVVATILCYAFIISSIVSFTELTILYAKGEYTTQEYLNFVAEIEGMLCSGLAMEKVMKSSLYKSIQEKFTNTFIKTYNVSKETVSKVWDRYGKNKADSLLGKIKSAKEAGATETELIKVTEVLTADQYSKYLEVMEKVYSKGEIEAKNIDKAKDSALRDVKNEKLSVDEIYENAVKSSISSVTDIIKAVENGDIVLSNNLQKGNYGEMKMDVYFESQGYDRISIDKVTDLNEPTHHGIDGVYYKADGEPKYIIGEAKYGSSTLGNTKDGKQMSSNWIDKRLVDAVGETNADKIIMEKMLNADNIKSQLVHISDKGEITISILDDEANIVK

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Crispr_ID: NZ_HG917868_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_HG917868_2

379114-379206

Orphan

Consensus_repeat	Method
TTATTCTACAGATGACATAGTTAATCCACA	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_HG917868_2

>merge|NZ_HG917868|2|379114-379206|CRISPRCasFinder
TTATTCTACAGATGACATAGTTAATCCACAAAATGATATACAGGCACTTAAGAAGGAGGAACCTTATTCTACAGATGACATAATTAATCCACA

>NZ_HG917868|2|2|379114-379206|CRISPRCasFinder
TTATTCTACAGATGACATAGTTAATCCACA	AAATGATATACAGGCACTTAAGAAGGAGGAACC
TTATTCTACAGATGACATAATTAATCCACA

Protein	Signature genes	Signature genes Name	Protein_function
NZ_HG917868.1\|WP_044035958.1\|380999_381818_+\|hypothetical-protein	unknown	unknown	unknown
NZ_HG917868.1\|WP_044035959.1\|381951_382806_+\|Mrp/NBP35-family-ATP-binding-protein	unknown	unknown	gnl\|CDD\|378455
NZ_HG917868.1\|WP_051483629.1\|374360_374654_+\|DUF1292-domain-containing-protein	unknown	unknown	gnl\|CDD\|377740
NZ_HG917868.1\|WP_044035951.1\|370398_370701_+\|hypothetical-protein	unknown	unknown	unknown
NZ_HG917868.1\|WP_044035953.1\|374711_375482_+\|TatD-family-hydrolase	unknown	unknown	gnl\|CDD\|223162
NZ_HG917868.1\|WP_044035952.1\|371088_373017_+\|methionine--tRNA-ligase	unknown	unknown	gnl\|CDD\|237028
NZ_HG917868.1\|WP_044035963.1\|386602_387796_-\|alanyl-tRNA-editing-protein-AlaX-L	unknown	unknown	gnl\|CDD\|237551
NZ_HG917868.1\|WP_044035950.1\|369271_370201_-\|tetratricopeptide-repeat-protein	unknown	unknown	gnl\|CDD\|273380
NZ_HG917868.1\|WP_051483627.1\|368571_369147_+\|GNAT-family-N-acetyltransferase	unknown	unknown	gnl\|CDD\|173926
NZ_HG917868.1\|WP_051483630.1\|375644_376691_+\|DUF348-domain-containing-protein	unknown	unknown	gnl\|CDD\|270620
NZ_HG917868.1\|WP_044039648.1\|382822_383272_-\|PadR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_HG917868.1\|WP_051483840.1\|384380_385229_+\|YitT-family-protein	unknown	unknown	gnl\|CDD\|224203
NZ_HG917868.1\|WP_051483631.1\|387893_389006_+\|FAD-dependent-oxidoreductase	unknown	unknown	gnl\|CDD\|224171
NZ_HG917868.1\|WP_084485342.1\|389075_389813_+\|tRNA-pseudouridine(38-40)-synthase-TruA	unknown	unknown	gnl\|CDD\|171495
NZ_HG917868.1\|WP_044035957.1\|380207_380999_+\|prolipoprotein-diacylglyceryl-transferase	unknown	unknown	gnl\|CDD\|376615
NZ_HG917868.1\|WP_044035954.1\|376893_377442_+\|ribonuclease-M5	unknown	unknown	gnl\|CDD\|273019
NZ_HG917868.1\|WP_044035962.1\|385406_385967_+\|50S-ribosomal-protein-L25	unknown	unknown	gnl\|CDD\|235534
NZ_HG917868.1\|WP_044035955.1\|377468_378323_+\|16S-rRNA-(adenine(1518)-N(6)/adenine(1519)-N(6))--dimethyltransferase-RsmA	unknown	unknown	gnl\|CDD\|234708
NZ_HG917868.1\|WP_044035960.1\|383273_384128_-\|DegV-family-protein	unknown	unknown	gnl\|CDD\|273257
NZ_HG917868.1\|WP_051483628.1\|373545_374310_+\|DUF3298-and-DUF4163-domain-containing-protein	unknown	unknown	gnl\|CDD\|378702

Protein	Function_ID	Function_description	E-value
NZ_HG917868.1\|WP_044035959.1\|381951_382806_+\|Mrp/NBP35-family-ATP-binding-protein	gnl\|CDD\|378455	pfam10609, ParA, NUBPL iron-transfer P-loop NTPase. This family contains ATPases involved in plasmid partitioning. It also contains the cytosolic Fe-S cluster assembling factor NBP35 which is required for biogenesis and export of both ribosomal subunits.	1.98188e-107
NZ_HG917868.1\|WP_051483629.1\|374360_374654_+\|DUF1292-domain-containing-protein	gnl\|CDD\|377740	pfam06949, DUF1292, Protein of unknown function (DUF1292). This family consists of several hypothetical bacterial proteins of around 90 residues in length. The function of this family is unknown.	2.31612e-08
NZ_HG917868.1\|WP_044035953.1\|374711_375482_+\|TatD-family-hydrolase	gnl\|CDD\|223162	COG0084, TatD, Mg-dependent DNase [DNA replication, recombination, and repair].	5.43296e-114
NZ_HG917868.1\|WP_044035952.1\|371088_373017_+\|methionine--tRNA-ligase	gnl\|CDD\|237028	PRK12267, PRK12267, methionyl-tRNA synthetase; Reviewed.	0
NZ_HG917868.1\|WP_044035963.1\|386602_387796_-\|alanyl-tRNA-editing-protein-AlaX-L	gnl\|CDD\|237551	PRK13902, alaS, alanyl-tRNA synthetase; Provisional.	1.65439e-67
NZ_HG917868.1\|WP_044035950.1\|369271_370201_-\|tetratricopeptide-repeat-protein	gnl\|CDD\|273380	TIGR00990, Mitochondrial_import_receptor_subunit_TOM70, mitochondrial precursor proteins import receptor (72 kDa mitochondrial outermembrane protein) (mitochondrial import receptor for the ADP/ATP carrier) (translocase of outermembrane tom70). [Transport and binding proteins, Amino acids, peptides and amines].	3.44923e-19
NZ_HG917868.1\|WP_051483627.1\|368571_369147_+\|GNAT-family-N-acetyltransferase	gnl\|CDD\|173926	cd04301, NAT_SF, N-Acyltransferase superfamily: Various enzymes that characteristically catalyze the transfer of an acyl group to a substrate. NAT (N-Acyltransferase) is a large superfamily of enzymes that mostly catalyze the transfer of an acyl group to a substrate and are implicated in a variety of functions, ranging from bacterial antibiotic resistance to circadian rhythms in mammals. Members include GCN5-related N-Acetyltransferases (GNAT) such as Aminoglycoside N-acetyltransferases, Histone N-acetyltransferase (HAT) enzymes, and Serotonin N-acetyltransferase, which catalyze the transfer of an acetyl group to a substrate. The kinetic mechanism of most GNATs involves the ordered formation of a ternary complex: the reaction begins with Acetyl Coenzyme A (AcCoA) binding, followed by binding of substrate, then direct transfer of the acetyl group from AcCoA to the substrate, followed by product and subsequent CoA release. Other family members include Arginine/ornithine N-succinyltransferase, Myristoyl-CoA: protein N-myristoyltransferase, and Acyl-homoserinelactone synthase which have a similar catalytic mechanism but differ in types of acyl groups transferred. Leucyl/phenylalanyl-tRNA-protein transferase and FemXAB nonribosomal peptidyltransferases which catalyze similar peptidyltransferase reactions are also included.	3.21557e-09
NZ_HG917868.1\|WP_051483630.1\|375644_376691_+\|DUF348-domain-containing-protein	gnl\|CDD\|270620	cd14667, 3D_containing_proteins, Non-mltA associated 3D domain containing proteins, named for 3 conserved aspartate residues. This family contains the 3D domain, named for its 3 conserved aspartates, including similar uncharacterized proteins. These proteins contain the critical active site aspartate of mltA-like lytic transglycosylases where the 3D domain forms a larger domain with the N-terminal region. This domain is also found in conjunction with numerous other domains such as the Escherichia coli MltA, a membrane-bound lytic transglycosylase comprised of 2 domains separated by a large groove, where the peptidoglycan strand binds. Domain A is made up of an N-terminal and a C-terminal portion, corresponding to the 3D domain and Domain B is inserted within the linear sequence of domain A. MltA is distinct from other bacterial LTs, which are similar to each other. Escherichia coli peptidoglycan lytic transglycosylase (LT) initiates cell wall recycling in response to damage, during bacterial fission, and cleaves peptidoglycan (PG) to create functional spaces in its wall. PG chains (also known as murein), the major components of the bacterial cell wall, are comprised of alternating beta-1-4-linked N-acetylmuramic acid (MurNAc) and N-acetyl-D-glucosamine (GlcNAc), and lytic transglycosylases cleave this beta-1-4 bond.	4.78136e-35
NZ_HG917868.1\|WP_044039648.1\|382822_383272_-\|PadR-family-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	3.93152e-19
NZ_HG917868.1\|WP_051483840.1\|384380_385229_+\|YitT-family-protein	gnl\|CDD\|224203	COG1284, COG1284, Uncharacterized conserved protein [Function unknown].	7.70403e-62
NZ_HG917868.1\|WP_051483631.1\|387893_389006_+\|FAD-dependent-oxidoreductase	gnl\|CDD\|224171	COG1251, NirB, NAD(P)H-nitrite reductase [Energy production and conversion].	4.3046e-89
NZ_HG917868.1\|WP_084485342.1\|389075_389813_+\|tRNA-pseudouridine(38-40)-synthase-TruA	gnl\|CDD\|171495	PRK12434, PRK12434, tRNA pseudouridine(38-40) synthase TruA.	4.73981e-133
NZ_HG917868.1\|WP_044035957.1\|380207_380999_+\|prolipoprotein-diacylglyceryl-transferase	gnl\|CDD\|376615	pfam01790, LGT, Prolipoprotein diacylglyceryl transferase.	4.42576e-62
NZ_HG917868.1\|WP_044035954.1\|376893_377442_+\|ribonuclease-M5	gnl\|CDD\|273019	TIGR00334, Ribonuclease_M5, ribonuclease M5. This family of orthologous proteins shows a weak but significant similarity to the central region of the DnaG-type DNA primase. The region of similarity is termed the Toprim (topoisomerase-primase) domain and is also shared by RecR, OLD family nucleases, and type IA and II topoisomerases. [Transcription, RNA processing].	4.55826e-43
NZ_HG917868.1\|WP_044035962.1\|385406_385967_+\|50S-ribosomal-protein-L25	gnl\|CDD\|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	5.88378e-37
NZ_HG917868.1\|WP_044035955.1\|377468_378323_+\|16S-rRNA-(adenine(1518)-N(6)/adenine(1519)-N(6))--dimethyltransferase-RsmA	gnl\|CDD\|234708	PRK00274, ksgA, 16S rRNA (adenine(1518)-N(6)/adenine(1519)-N(6))-dimethyltransferase RsmA.	4.67542e-144
NZ_HG917868.1\|WP_044035960.1\|383273_384128_-\|DegV-family-protein	gnl\|CDD\|273257	TIGR00762, DegV, EDD domain protein, DegV family. This family of proteins is related to DegV of Bacillus subtilis and includes paralogous sets in several species (B. subtilis, Deinococcus radiodurans, Mycoplasma pneumoniae) that are closer in percent identity to each than to most homologs from other species. This suggests both recent paralogy and diversity of function. DegV itself is encoded immediately downstream of DegU, a transcriptional regulator of degradation, but is itself uncharacterized. Crystallography suggested a lipid-binding site, while comparison of the crystal structure to dihydroxyacetone kinase and to a mannose transporter EIIA domain suggests a conserved domain, EDD, with phosphotransferase activity. [Unknown function, General].	1.52724e-103
NZ_HG917868.1\|WP_051483628.1\|373545_374310_+\|DUF3298-and-DUF4163-domain-containing-protein	gnl\|CDD\|378702	pfam11738, DUF3298, Protein of unknown function (DUF3298). This family of bacterial protein C-terminal regions is highly conserved but the function is not known. Several members are annotated as being endo-1,4-beta-xylanase-like, but this could not be confirmed, and the structure can be defined as a heat-shock cognate 70kd protein 44kd ATPase.	8.48966e-16

>NZ_HG917868.1|WP_044035955.1|377468_378323_+|16S-rRNA-(adenine(1518)-N(6)/adenine(1519)-N(6))--dimethyltransferase-RsmA
MNQRKDVIDTADVVKKYGFKFTKSLGQNFLIDHNVIDQIVEGAGVSSEDTVIEIGPGVGTLTKELLKRAKKVIAIEIDSDLIPILSEELKEHNNFQLIHQDAMKVDFNKIIEENENVKVVANLPYYVTTPIITNLLNAKYKFKSITVMIQKEVAERMNSEPNCKDYGSLSLLVQYYCDTKIIMKVPPMCFIPRPKVDSIVIRLDRLEETRVTVDDEKLFFRVIRDSFNMRRKTLWNGMKNIGLDKEKLEEAFKDSGIDQKRRGETLTIQEFADLANAINKKINN
>NZ_HG917868.1|WP_044035954.1|376893_377442_+|ribonuclease-M5
MIKEIIVVEGRDDVTAVKAAVDAEVIAVSGFGINKNTIDKIKEAQKRKGVIILTDPDFAGEKIRRIISKRVDGVKHAYISREEGTKDGDIGVENASPESIREALSKAKAVIEEKREVFTANHLVYYKLVGDTKSKERRQLLGKILGIGYCNGSQMVKRLNNFNIKEEEFVKAMDKIEKQLSK
>NZ_HG917868.1|WP_051483630.1|375644_376691_+|DUF348-domain-containing-protein
MKIDFKGFFKKPMAVISIVLSVGLVFTGISFKKTVYIDVDGTTTKVTTYKGKVEDVISDIDLKLETEDSVKPKLTSEIKNGQTIKIKRAVSLDLIVDGKTVVIKSAADSVKDLIESKSMSKKLQSEKISPIREQDKIEPTLDTKITSNMKVIIKRIEKKNEVTQAEIPYSTEKVVDDSMYKDDKEKVVVAGKPGIKEVTTEVTTEDGNVVATSVIGERVIEEPTNEKIAYGTKEKVVPTVNVPSRGGNIPYKSKLTMKSTAYSSSDKGVTGITASGMKATRDPNGTSTVAVDPRVIPLGTKLYIEGYGYAIACDTGSAIKGNKVDVYFNSVSECYSWGSRNVDVYILE
>NZ_HG917868.1|WP_044035953.1|374711_375482_+|TatD-family-hydrolase
MKIFDTHSHYDDEAFDGDREELIKIIIENDVVGIINCAADMKSVKSTIELTKKYPMFYGAIGVHPCSADEINEETIEELRMAAKNEKIVAIGEIGLDYYYEDNPSREIQKNAFRAQMQLAKELSKPVIIHIRDAHEDALKILEEFEEVRGIIHCFSGSVEIARKCVKIGYMLGIGGVVTFKNARKLVEVVKEIPMENLLLETDCPYMAPVPHRGERNNSMYISEVIKKIAEIKSISEEEVADIALRNSHNFTKNIW
>NZ_HG917868.1|WP_051483629.1|374360_374654_+|DUF1292-domain-containing-protein
MDKEVIQADHCECEEEHNEKSNIVSFMTEDGEKVDLELIETVVVKGKKYILLAPVGNEDDAYVYKVVTNADGKDELIAIEDDKELSLVMKEYEKTFA
>NZ_HG917868.1|WP_051483628.1|373545_374310_+|DUF3298-and-DUF4163-domain-containing-protein
MKRAATMVLGIFMALTSIISFCRYGNGMIFLSEECANASQNITINEEKPIVIKDIVKEENKPEYKFRIHIPKITGLKDIKKQNSINDTISEEILRFKDYFIENTKSGNNSEAEVHYTVTNNKKIFSLLIYYYEYYGGAHGLTTKRSINIYVPNSGGIKENENFLLLEDFFLDKVDYKTMINNYIINEIKKEPEKYFEDTLQKYSGFNENNFYFNDKGLVVYFQSYEIAPYASGSPEFNIPYSFLKNYIKKDFIP
>NZ_HG917868.1|WP_044035952.1|371088_373017_+|methionine--tRNA-ligase
MCKKNFYITTPIYYPSDKLHIGNTYTTVAADALARYKRLTGYDVMFLTGTDEHGQKIQQRAEAKDMQPKAFVDEIVAGIKDLWNMMDISYDKFIRTTDDYHVKTVQKIFKKLYDQGDIYKGSYEGWYCTPCESFFTDTQLVNGNCPDCGRPVEKTKEESYFFKMSKYADRLIEYIETHPEFIQPESRKNEMLNNFLRPGLQDLCISRTSFSWGIPVEFDPGHVVYVWIDALSNYISALGYGSDNDELYKKFWPADVHLIGKDILRFHTIYWPIILMALGEPLPKQVFGHGWLLVDGGKMSKSKGNVVDPVLLVNEFGCDAVRYYLLHEIPFGSDGLYNSEIFMNKFNSDLANDLGNLVSRTSAMIIKYFGGEVLAPSSEEDNFDKELKAVTLSMPEKVEAAMNAFKIPEALDEIWTVVRRANKYIDETTPWILGKDESKKDRLATVLYNLLEALRFVTVELEAFLPNTASKIKEQLKFENVSYESLKSFDGVKVGTKLEKGEVIFPRIDVEKKLEELAAMKEAQAPKREIKPIKEEITIEDFEKIDLRVVKVLACEPIKGAKKLLKLKVDLGGEERQVVSGISQYYKPEELVGKNVVLVANLKPVKLRGELSQGMILAASSDDDKELFVVDPGKLETGSVVR
>NZ_HG917868.1|WP_044035951.1|370398_370701_+|hypothetical-protein
MDKTDERKEIGKAINDMGDRLHILKIYIAKMERMSSLYRDLITDLNNNKVQNFTDRMKKIKNVENEDNIEVVFSNLWVIVKDFEKDYRTLKNNEEKDKYK
>NZ_HG917868.1|WP_044035950.1|369271_370201_-|tetratricopeptide-repeat-protein
MSNRRHKRKHNNKPFIVTSIIFLIFIVLMISILITYLTSSKKTRNDMIQAAKIENYEEVLKDSNKLISKGDYLDLAYEYKGYSLMHLNKSDEALDTYLKLVKKGTKNALIYNQIGIIYNDKLHNHEEALNYFNKAIDLDDSNANFYTNRGITYQWLNNNSEAINNFDKSIELDSKNSYNYYYKGVSLLNENDLDNSIENLEKAIKLNNNDATFYVSLGNAYIKKSSFDKALDSFNEAIKLDKKSINAFIGKGSSLYEEKQYDEALEAFDTALELDKNNKYALIGKGNVLSAKGDTTTAEEYYNKADAIK
>NZ_HG917868.1|WP_051483627.1|368571_369147_+|GNAT-family-N-acetyltransferase
MRNIEITNGCSEDAPSIAALIYETEEYPEHEWGPYPKEKIIKKLEQLVQVKGNRYSYDRTKVIKIDNKVVGVLLTLRGNEIRKLTYNTYFKFIDFDRSFKNVICNVRNILSYIFFKECNINEYYIANLAVDKEYREFGIGKTLLEEAEDLAKEKGYNKISLLAKDRGIVRYYKKFKYNLENMNHLKMVKFI
>NZ_HG917868.1|WP_044035957.1|380207_380999_+|prolipoprotein-diacylglyceryl-transferase
MKPFLLEIGKLKIAGYGTMILIGVIVAYCLFTYRGKKRGYNVDNLFDITVFSLIGGFLCSKLLYIVIENPKLLLNPVEIVKTFSQGFVVYGGIIGGFIVFILMCKRYKYSPLKVGDLAVASLAIGQGFGRIGCLLAGCCYGRTTDSVIGITFHNSFIAPNEVALVPTQIISSIFDFILAGVLIWYLSFLEKKNIGHNPGKVTGAYLILYSIGRFIIEFFRGDLERGFIGTLSTSQFISIGIIVFGLIVFNLDKIKRLKYKEGI
>NZ_HG917868.1|WP_044035958.1|380999_381818_+|hypothetical-protein
MKKVISVILIFMTIFLNSCAMTDKIGWTNSDFEYIKDGMVTEIKIQNTRDKGYTFVISDPVKLQGFYKILSSAKSVKSKSEYVPDYSIEIEKVDGSVENFNYVIGNPNDGGNFYSEDKYYNVSSRLDSEVFNYFEDIRKPKDFDEVYYYGVIRGSLNKFREDTKTNDTVTLNLNDDVTIQKYITSIELEGYKKKMKDLEIVETSKNEGKITMSVKTTGFRTTTSSGKYVSIYKAIITFHNRGTNEEKVYYSVSNNSGGKWVTDITDTKPEDF
>NZ_HG917868.1|WP_044035959.1|381951_382806_+|Mrp/NBP35-family-ATP-binding-protein
MVGCESCNECEKKTKKDICNLKFGTIKNVIAVISGKGGVGKSTVSGLLATELRKSGYEVGILDADITGPSIPRFFGVNEKRSLINPEPYTGDAMFEPVITTLGLKIMSLNLLVDKEDDPVIWTSSVAHKVLKQMYTDTKWGDLDYLIIDMPPGTGGIAITIMNTFPIDGLLVVGTPQDMVSVIVKKVINMAEKLSIPMIGLVENMAYITCGCCGQEIKLFSNKTTEQYENYFGIPLIAELPMDLKLLESLDEGNAEEYVFKVNKYKDLFEKFMDRYKEMKTEAK
>NZ_HG917868.1|WP_044039648.1|382822_383272_-|PadR-family-transcriptional-regulator
MMSPEDIKKEEKRLYEEYKAKLSELKKVKKEREAVGSIFTKGLLPIYVLYILSLQPTNGNDISNKIGERTNGLWTPSTGGIYPLLKKLEKEGLIEGKWDNPKKKVQKIYELTSLGKEEFNHRKELLKDKMLESLQVFNMVYEDLYNDIK
>NZ_HG917868.1|WP_044035960.1|383273_384128_-|DegV-family-protein
MEKIALITDSICDLSKEIIKKYDIKVLPLKIIYKNREYIDGVDISAEDVYAKLKIEIPTTSMPSVGEVEALYEKLVAEGYTHVIGTCISSGLSGTFNNFNLVAEDFSDRIKSYIIDSLSISKAEGELMVVAGEMIEQGKSFDEIIKVLPKCRDNIKCFFTFSTLEYLKKGGRIGKISGTIGELLNLKPIVSIDSKDGKYYTYDKVRGDKNAFNKLVSIATDLINEGPCKVKVLHGDALPKAERLYEILKQLPNVKSIELGVLSAVAGVHSGPGFLAFGVIKDFE
>NZ_HG917868.1|WP_051483840.1|384380_385229_+|YitT-family-protein
MIVIGTAILALGVNWFLEPVGLVTGGLSGFSIVVKTVSENIIGYGIPLSVTTFVLNIPLFIIIFMQRGFNFMKKTLYGVVSLSLALWYTEYIPNIFNVNDDLFLCSIFGGAFVGAGLGIVLKVSATTGGTDTLASIIKFKFPYFPIQQLMLIIDGIIILSGFFIFGPKNGMYAILAVLVTSKVISVILEGMHYAKAAFIMTDKTEEVAKEVMEKIPRGATGLKARGMYSKNDKEMLFVVVSQKQITQLRDLVKSIDEKAFITIADVREVLGEGFIENYGESL
>NZ_HG917868.1|WP_044035962.1|385406_385967_+|50S-ribosomal-protein-L25
MTNVAFNISERNESGKVVRRRGEIPCVLYGEHLEKPISAKITRGEVDKLLTCAKSSILSLNLNGTTENCVVKELQKDNYGKVIHIDFQYVNKDENIKLGIPVIYTGQGLLESKRLFLETFLSEVELYGEADKFPENIEFDVSTFNYGDTVLAGDLKLEEGMKLVTNSDVVLAKVDGNNAVEEDTEE
>NZ_HG917868.1|WP_044035963.1|386602_387796_-|alanyl-tRNA-editing-protein-AlaX-L
MKKLFYTDPYIKEFTAEILEIKEIDSKFHVTLDQTAFFPGGGGQCGDLGFIENHKVVDVYESEDTIYHVVEKKPIKIHKVKCSIDWNRRFDGMQQHLGQHVLSGCFYKLFGANTFAIHLGSEISTVDIEGTLTEEQVREAERYANEVISEGLTVDFLIPTKKELKSLTLRRALPNTKEDISIVKIDDLDINACCGVHPRNTRDLRMIKIKKYEKHKQGTRIEFLSGDRAISDSLKKDNFANMICKYLNCNEEEVINGIKNLNASLKDTLDENKKIKNQLATYEIKELINEAETIGDMKVLKKIYTAETVKYVNTVISKIVENDNMVTLMAVVSEDKVNLIFACSKNLKDVKVNEILKDTITLIDGRGGGSPFLAQGGGKNNGNLENALNYAFNKLKN
>NZ_HG917868.1|WP_051483631.1|387893_389006_+|FAD-dependent-oxidoreductase
MKKFICTICGYIHEGNTPPEVCPLCGAGPELFKEVKEESNDRFTKNTEEKFVILGNGAAGFYAAKAIRERNKTAEITMVTNEGDLSYYRPALSDLINDEVNEEFYLADYKWYNGKNIKNIVNTNIVKIDEENKTLISDDGENIKYDKLILANGSSNFIPPFKGKDLDGVYTLRNIKDLEKIKKALKEAKKVVVIGGGALGLEAAYEIYLQKKGLTVIEAAPVLLGRQLKPEQSEELLKTIRNTGTEVIVSGAVEEIVGETKVTGVKLQDGTIIEADMVLTSIGVRSNIALCQNTSIDSNRGVLVNEFMETTLENVYACGDVAEFEGLVIGLWPIAVEQGKVAGANAAGEKIEFKYDKYPLILDVFGMKFQ
>NZ_HG917868.1|WP_084485342.1|389075_389813_+|tRNA-pseudouridine(38-40)-synthase-TruA
MRNLKMTIQYDGGRYKGWQKQKEGESTIQWKIENVLKRMTGEEIQVIGCGRTDAGVHAENYIANFHTNSELSVETMMDYLYEFLPEDIVVKSIKDTTERFHARYNAKGKTYVYRINNGEVRNVFNRKYTYHTSVKLNLDAMREGAKYLVGTHDFQSFTSQKPKTKSTERHIKYININKTGDMIEIEVDGNGFLWNMVRIIVGTLLEVGMGHMKPSDVGRILEEKKRSESGPIAQAKGLCLKEVHY

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Crispr_ID: NZ_HG917868_3

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_HG917868_3

1653092-1653183

Orphan

Consensus_repeat	Method
TTCCACCATTACCACCATCGCCT	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_HG917868_3

>merge|NZ_HG917868|3|1653092-1653183|CRISPRCasFinder
TTCCACCATTACCACCATCGCCTCCATCTGGCCCTCCAAGTGGAACATACTTTTCTCTTCTGAAAGAAATTGCACCATTACCACCATCGCCT

>NZ_HG917868|3|3|1653092-1653183|CRISPRCasFinder
TTCCACCATTACCACCATCGCCT	CCATCTGGCCCTCCAAGTGGAACATACTTTTCTCTTCTGAAAGAAA
TTGCACCATTACCACCATCGCCT

Protein	Signature genes	Signature genes Name	Protein_function
NZ_HG917868.1\|WP_044037897.1\|1650418_1651594_-\|nicotinate-nucleotide-adenylyltransferase	unknown	unknown	gnl\|CDD\|235947
NZ_HG917868.1\|WP_044037919.1\|1661387_1662182_-\|septum-site-determining-protein-MinD	unknown	unknown	gnl\|CDD\|131023
NZ_HG917868.1\|WP_044037906.1\|1653338_1653641_-\|50S-ribosomal-protein-L27	unknown	unknown	gnl\|CDD\|235464
NZ_HG917868.1\|WP_044037908.1\|1653645_1653972_-\|ribosomal-processing-cysteine-protease-Prp	unknown	unknown	gnl\|CDD\|377307
NZ_HG917868.1\|WP_044037912.1\|1654398_1655838_-\|ribonuclease-E/G	unknown	unknown	gnl\|CDD\|378414
NZ_HG917868.1\|WP_044037885.1\|1641749_1642766_-\|DNA-polymerase-III-subunit-delta	unknown	unknown	gnl\|CDD\|235511
NZ_HG917868.1\|WP_044037900.1\|1651629_1651920_-\|ribosome-assembly-RNA-binding-protein-YhbY	unknown	unknown	gnl\|CDD\|376702
NZ_HG917868.1\|WP_044037889.1\|1644439_1646815_-\|cation-transporting-P-type-ATPase	unknown	unknown	gnl\|CDD\|223550
NZ_HG917868.1\|WP_044037914.1\|1656692_1658552_-\|TIGR03960-family-B12-binding-radical-SAM-protein	unknown	unknown	gnl\|CDD\|188475
NZ_HG917868.1\|WP_044037916.1\|1658620_1659442_-\|M50-family-metallopeptidase	unknown	unknown	gnl\|CDD\|100082
NZ_HG917868.1\|WP_044039815.1\|1659841_1660975_-\|rod-shape-determining-protein-RodA	unknown	unknown	gnl\|CDD\|274033
NZ_HG917868.1\|WP_044037891.1\|1646845_1647472_-\|helix-hairpin-helix-domain-containing-protein	unknown	unknown	gnl\|CDD\|213597
NZ_HG917868.1\|WP_044037895.1\|1648487_1648874_-\|RidA-family-protein	unknown	unknown	gnl\|CDD\|129116
NZ_HG917868.1\|WP_051483748.1\|1649042_1650407_-\|LCP-family-protein	unknown	unknown	gnl\|CDD\|224235
NZ_HG917868.1\|WP_044037893.1\|1647528_1648422_-\|RluA-family-pseudouridine-synthase	unknown	unknown	gnl\|CDD\|223638
NZ_HG917868.1\|WP_156930525.1\|1656004_1656715_-\|DUF2344-domain-containing-protein	unknown	unknown	gnl\|CDD\|378393
NZ_HG917868.1\|WP_044037883.1\|1641456_1641717_+\|30S-ribosomal-protein-S20	unknown	unknown	gnl\|CDD\|376586
NZ_HG917868.1\|WP_044037918.1\|1661106_1661370_-\|cell-division-topological-specificity-factor-MinE	unknown	unknown	gnl\|CDD\|237579
NZ_HG917868.1\|WP_044037887.1\|1642768_1644388_-\|ComEC/Rec2-family-competence-protein	unknown	unknown	gnl\|CDD\|377126
NZ_HG917868.1\|WP_044037910.1\|1653974_1654286_-\|50S-ribosomal-protein-L21	unknown	unknown	gnl\|CDD\|235510

Protein	Function_ID	Function_description	E-value
NZ_HG917868.1\|WP_044037897.1\|1650418_1651594_-\|nicotinate-nucleotide-adenylyltransferase	gnl\|CDD\|235947	PRK07152, nadD, nicotinate-nucleotide adenylyltransferase.	4.79594e-89
NZ_HG917868.1\|WP_044037919.1\|1661387_1662182_-\|septum-site-determining-protein-MinD	gnl\|CDD\|131023	TIGR01968, Septum_site-determining_protein_MinD, septum site-determining protein MinD. This model describes the bacterial and chloroplast form of MinD, a multifunctional cell division protein that guides correct placement of the septum. The homologous archaeal MinD proteins, with many archaeal genomes having two or more forms, are described by a separate model. [Cellular processes, Cell division].	9.90076e-145
NZ_HG917868.1\|WP_044037906.1\|1653338_1653641_-\|50S-ribosomal-protein-L27	gnl\|CDD\|235464	PRK05435, rpmA, 50S ribosomal protein L27; Validated.	2.53654e-53
NZ_HG917868.1\|WP_044037908.1\|1653645_1653972_-\|ribosomal-processing-cysteine-protease-Prp	gnl\|CDD\|377307	pfam04327, Peptidase_Prp, Cysteine protease Prp. This is a family of cysteine protease that are found to cleave the N-terminus extension of ribosomal subunit L27 in eubacteria. Proteins in this family are distinguished by a pair of invariant histidine and cysteine residues with conserved spacing that form the classic catalytic dyad of a cysteine protease.	2.83176e-38
NZ_HG917868.1\|WP_044037912.1\|1654398_1655838_-\|ribonuclease-E/G	gnl\|CDD\|378414	pfam10150, RNase_E_G, Ribonuclease E/G family. Ribonuclease E and Ribonuclease G are related enzymes that cleave a wide variety of RNAs.	2.37357e-89
NZ_HG917868.1\|WP_044037885.1\|1641749_1642766_-\|DNA-polymerase-III-subunit-delta	gnl\|CDD\|235511	PRK05574, holA, DNA polymerase III subunit delta; Reviewed.	9.43679e-80
NZ_HG917868.1\|WP_044037900.1\|1651629_1651920_-\|ribosome-assembly-RNA-binding-protein-YhbY	gnl\|CDD\|376702	pfam01985, CRS1_YhbY, CRS1 / YhbY (CRM) domain. Escherichia coli YhbY is associated with pre-50S ribosomal subunits, which implies a function in ribosome assembly. GFP fused to a single-domain CRM protein from maize localizes to the nucleolus, suggesting that an analogous activity may have been retained in plants. A CRM domain containing protein in plant chloroplasts has been shown to function in group I and II intron splicing. In vitro experiments with an isolated maize CRM domain have shown it to have RNA binding activity. These and other results suggest that the CRM domain evolved in the context of ribosome function prior to the divergence of Archaea and Bacteria, that this function has been maintained in extant prokaryotes, and that the domain was recruited to serve as an RNA binding module during the evolution of plant genomes. YhbY has a fold similar to that of the C-terminal domain of translation initiation factor 3 (IF3C), which binds to 16S rRNA in the 30S ribosome.	1.80878e-34
NZ_HG917868.1\|WP_044037889.1\|1644439_1646815_-\|cation-transporting-P-type-ATPase	gnl\|CDD\|223550	COG0474, MgtA, Cation transport ATPase [Inorganic ion transport and metabolism].	4.93229e-59
NZ_HG917868.1\|WP_044037914.1\|1656692_1658552_-\|TIGR03960-family-B12-binding-radical-SAM-protein	gnl\|CDD\|188475	TIGR03960, radical_SAM_domain_protein, radical SAM family uncharacterized protein. This model describes a radical SAM protein, or protein region, regularly found paired with or fused to a region described by TIGR03936. PSI-BLAST analysis of TIGR03936 suggests a relationship to the tRNA pseudouridine synthase TruA, suggesting that this system may act in RNA modification. [Unknown function, Enzymes of unknown specificity].	0
NZ_HG917868.1\|WP_044037916.1\|1658620_1659442_-\|M50-family-metallopeptidase	gnl\|CDD\|100082	cd06161, S2P-M50_SpoIVFB, SpoIVFB Site-2 protease (S2P), a zinc metalloprotease (MEROPS family M50B), regulates intramembrane proteolysis (RIP), and is involved in the pro-sigmaK pathway of bacterial spore formation. SpoIVFB (sporulation protein, stage IV cell wall formation, F locus, promoter-distal B) is one of 4 proteins involved in endospore formation; the others are SpoIVFA (sporulation protein, stage IV cell wall formation, F locus, promoter-proximal A), BofA (bypass-of-forespore A), and SpoIVB (sporulation protein, stage IV cell wall formation, B locus). SpoIVFB is negatively regulated by SpoIVFA and BofA and activated by SpoIVB. It is thought that SpoIVFB, SpoIVFA, and BofA are located in the mother-cell membrane that surrounds the forespore and that SpoIVB is secreted from the forespore into the space between the two where it activates SpoIVFB.	1.29444e-37
NZ_HG917868.1\|WP_044039815.1\|1659841_1660975_-\|rod-shape-determining-protein-RodA	gnl\|CDD\|274033	TIGR02210, Rod_shape-determining_protein_RodA, rod shape-determining protein RodA. This protein is a member of the FtsW/RodA/SpoVE family (pfam01098). It is found only in species with rod (or spiral) shapes. In many species, mutation of rodA has been shown to correlate with loss of the normal rod shape. Note that RodA homologs are found, scoring below the cutoffs for this model, in a number of both rod-shaped and coccoid bacteria, including four proteins in Bacillus anthracis, for example. [Cell envelope, Biosynthesis and degradation of murein sacculus and peptidoglycan, Cellular processes, Cell division].	2.21831e-130
NZ_HG917868.1\|WP_044037891.1\|1646845_1647472_-\|helix-hairpin-helix-domain-containing-protein	gnl\|CDD\|213597	TIGR01259, ComE_operon_protein_1, comEA protein. This model describes the ComEA protein in bacteria. The com E locus is obligatory for bacterial cell competence - the process of internalizing the exogenous added DNA. Lesions in the loci has been variously described for the appearance of competence-related pheonotypes and impairment of competence, suggesting their intimate functional role in bacterial transformation. [Cellular processes, DNA transformation].	2.78109e-28
NZ_HG917868.1\|WP_044037895.1\|1648487_1648874_-\|RidA-family-protein	gnl\|CDD\|129116	TIGR00004, RutC_family_protein, reactive intermediate/imine deaminase. This protein was described initially as an inhibitor of protein synthesis intiation, then as an endoribonuclease active on single-stranded mRNA, endoribonuclease L-PSP. Members of this family, conserved in all domains of life and often with several members per bacterial genome, appear to catalyze a reaction that minimizes toxic by-products from reactions catalyzed by pyridoxal phosphate-dependent enzymes. [Cellular processes, Other].	1.25073e-62
NZ_HG917868.1\|WP_051483748.1\|1649042_1650407_-\|LCP-family-protein	gnl\|CDD\|224235	COG1316, LytR, Transcriptional regulator [Transcription].	2.11411e-50
NZ_HG917868.1\|WP_044037893.1\|1647528_1648422_-\|RluA-family-pseudouridine-synthase	gnl\|CDD\|223638	COG0564, RluA, Pseudouridylate synthases, 23S RNA-specific [Translation, ribosomal structure and biogenesis].	6.63271e-100
NZ_HG917868.1\|WP_156930525.1\|1656004_1656715_-\|DUF2344-domain-containing-protein	gnl\|CDD\|378393	pfam10105, DUF2344, Uncharacterized protein conserved in bacteria (DUF2344). This domain, found in various hypothetical bacterial proteins and Radical Sam domain proteins, has no known function. This domain is distantly related to tRNA pseudouridine synthases, suggesting this family may carry out a function related to RNA modification. But this family appears to lack the catalytic aspartate found in pseudouridine synthases.	7.40703e-73
NZ_HG917868.1\|WP_044037883.1\|1641456_1641717_+\|30S-ribosomal-protein-S20	gnl\|CDD\|376586	pfam01649, Ribosomal_S20p, Ribosomal protein S20. Bacterial ribosomal protein S20 interacts with 16S rRNA.	4.906e-26
NZ_HG917868.1\|WP_044037918.1\|1661106_1661370_-\|cell-division-topological-specificity-factor-MinE	gnl\|CDD\|237579	PRK13987, PRK13987, cell division topological specificity factor MinE; Provisional.	4.21531e-37
NZ_HG917868.1\|WP_044037887.1\|1642768_1644388_-\|ComEC/Rec2-family-competence-protein	gnl\|CDD\|377126	pfam03772, Competence, Competence protein. Members of this family are integral membrane proteins with 6 predicted transmembrane helices. Some members of this family have been shown to be essential for bacterial competence in uptake of extracellular DNA. These proteins may transport DNA across the cell membrane. These proteins contain a highly conserved motif in the amino terminal transmembrane region that has two histidines that may form a metal binding site.	6.7081e-42
NZ_HG917868.1\|WP_044037910.1\|1653974_1654286_-\|50S-ribosomal-protein-L21	gnl\|CDD\|235510	PRK05573, rplU, 50S ribosomal protein L21; Validated.	6.06476e-50

>NZ_HG917868.1|WP_044037900.1|1651629_1651920_-|ribosome-assembly-RNA-binding-protein-YhbY
MITSKQRSYLRSLSNNITPIFQIGKGGIDDNMLKAIESALEARELIKISILNNSDYGAREASDEICKKLKCDGVQAIGKKIVLYKKSSKKPVIELP
>NZ_HG917868.1|WP_044037897.1|1650418_1651594_-|nicotinate-nucleotide-adenylyltransferase
MKKAIFGGTFDPLHIGHLNIAFEALYLLDLDEVIFVPTGNPPHKKNITSNYHRVNMIKGTIDKYDKLSLSTYEIEKEDKSYTFETLEYFRNIEKNTEWYFIVGEDCLLNIEKWKNPDKVLNYATLVVFKRTDNNVNRLKEYKDVIEKKYNTDIILLDNKVIDISSTFIRKSIYQNREVSFLLPSYVRKYIKKFRLYEKGDTLILKEKIKNALKDTLNSDRYDHTIRVVDEAKKLALLYGIDEEKAEIAALAHDCAKNISYDELKEICEKGNMIFTEDDLNSKPIWHAYAAAIIAKEEFNINDEDILNAIKYHTTGRRNMTALEKIIYLADYIEPGRTFEKIQEVRVLAYDKNIDEALIKAINNTIEFLISKGSIIHKSTIEARNYLIMNTK
>NZ_HG917868.1|WP_051483748.1|1649042_1650407_-|LCP-family-protein
MNNKWGRILRNILVMMMVITGSIGSAVTYLYSGFIFKSDVYGSSETKKEEEIPKITDPVNILITGVDIGTPGEESGSASNPQRTDTIMVAHYEPSLDQMTVISIPRDTKVYSKRQNCYIKITEVHAYGDLHNSGIQDLEETVEELLGININYYMKIDYSGFHEMIDAIGGVTVTIPQTMIYDDPVQDLHINFTKGDVVTLDGQKAEEFFRWRKNNEGIANEKDGGDLGRIDNQVVFIKAFIEKVASPSIVTKIPVLLQSLSNVLYTNMDGDYILKYALNFAKLGVDKVEFATLRGDTPPWEPGEASYFIYYPEWNRDILQALNGKQFFSRYDKNVKIINKSSDSGIGDKLKTILVNDYSYNKYNVNIENNSEEVVENTSLDVYGIDEKYDNVIKDDFLTNVINHNEKSEDTKYDIVVTLGNNSIDIINNYTLKEKVIDTSSNSSTSTNSSNSSY
>NZ_HG917868.1|WP_044037895.1|1648487_1648874_-|RidA-family-protein
MEKEIISTINAPAAIGPYSQAIRVGNLVFTSGQLPLIPSTGELVKYDIKKATVQCLENIKAILDEAGTSFDKVVKTMVFLRDMEDFEDMNEIYSKYFAVKQPARSCVQVAKLPKNAPIEIEVIALVTE
>NZ_HG917868.1|WP_044037893.1|1647528_1648422_-|RluA-family-pseudouridine-synthase
MSNFISYIVDEVDNGEKIRNYLKYKCNLSSRFCRSAALNKNILVNGEIVKLSYILKAGDKIEINLKKEENQDIEAEKMDLDIIYEDSDIIIINKPPNLVVHPTKSHQSGTLANGVLYHFRENGDSSIVRLVSRLDMNTSGLIIIAKNQFSHMALQRDMTEGHVDKIYRAICHNKMKYSEGTINLPIYASEESKPRRIIDDRGQRSITHYKVIEELNDATYIELKLETGRTHQIRVHLAYYEYPIFGDNLYGKEEKEFIDRQSLHAYKLRFNHPKTGERMEFIAPIPDDMNNLLNKLK
>NZ_HG917868.1|WP_044037891.1|1646845_1647472_-|helix-hairpin-helix-domain-containing-protein
MKEFFNKYKILIIVVICLLGFLLIFSNFNSSINDEEDAFKKYSKETEIKEDSEDSYTEKNKEEEIFVYIGGAVVKPNVYKLMEGSRIKDLVQVAGGFLDNAESKDINLAQKLNDEDYIYVYSVGESEVDATIDSVVNSSIRKDGCININKATVEELKSIDGIGEVRASKIVEYREENGPYKNIDELKTIGARIGEKTFETIKDKVYVP
>NZ_HG917868.1|WP_044037889.1|1644439_1646815_-|cation-transporting-P-type-ATPase
MHSLRWDEVLRNLDTTISTGLSSDEIDARRSKYGDNVIKEYRNKIFNNLKNFIMSKFFLIATVYSVFTWFYSQYKIVCYISLLFVLLIAFIIIRKVNNPISFDRVNNKEVRVKRDGLIKYIKSAELVVGDIVFIEEDDISPADIRIIQGNNITVKEIFINGEDVPVNKFSLEIDESSDFKERSNILYKGSKIVSGHGIGVVIAVGYNTKLGEKLLDHVIENNRLKLLKYIDNMISPIYVLSMIISIFELILMKNSYSKSLAITLPLIPVYILLFIKCIKNEFRKDEIEVSGILDLEKLNNTDYIVIEDKDSFYDDDIDIIEIIIDEKRYSTLSLAPDEYMITRAFEILHICSLDVPEGFDNKISKKIIDFLDDMKFNYNESKSKIKSIFTLPYNIENDVVTKVIAVENGYRAYSLGNINTIINSSTFRISNELEVKLEEDYIEKIKELDIEMSKKGFKTVAFSYRAFNYKPSEYENIESNMVFVGVLVYKSRVNCNYETNIQLIRDMNIKVLTYTNDNKLVAFNKGKLLGNIYKESDIISGVELKNIDKDEMNRNIEGYKVLSKVTKDQIEDIVKELRIKKYNILYSGDSIGDLGILKESSVSIYKGNNNNSLCKEVCDFTIKNNHLTKILKGMELSKQIIKRFNYIQGFFISFFGTVLLSNIIIMKLCERSLYNYIELFILNVVCISIYIGYLMLNLESEKVTYYKKYKFNNSLACIKLNIKDIVISTLIILIPFIIPFLQFSVKKYLSLIIFILIYTIKALLNGYRESKVQDIILILPSIIILLYIFLM
>NZ_HG917868.1|WP_044037887.1|1642768_1644388_-|ComEC/Rec2-family-competence-protein
MKNILSFIKIFCEEKLQGKYIGGFPLLAIILSINYWFNDCKIITTIMLFIVTIFIFSYYKVRYTIIFIVAFFSTSFLCINYLSYSDVNKLCIVENNGINSIGESGNHLILVNNSDLKVGYEYLLEGKFTKALDLNKGYYGIYDVENIKECKKTYRYFIIRLRGIIKDKYSEKLDKKAAMKIDSLLLGDTSTLPSIEKEKMKSLGIYHIISISGFHLSLLFKLLDKFTSKTLSIVFILSYIIFLGAPVPVLRAFIMILINIFSYKLYRNYDGVNALIISAIIILILNPIKLYSLGFLLSYAGVFGIYFFNDFFKKKLIFLPETIGESIAVSISATVATAPFIFATIKGISVNCIIANLFLAPIFSLIIALIFISLFSIFFNPVLDFLCYVINIVSRIIDYMIDKLYYNTLDEIFFSSEVAILLIAYIFIAFLYKSNIEVKRIILGTTILFYIFILNPIHRVELIKYKDSYGIVEREAKNSTFYYYGKIKSMKEEEFLKKYLLVNEIYSNANKKFDIINCRENYYYQSSPVVIDTYILEGE
>NZ_HG917868.1|WP_044037885.1|1641749_1642766_-|DNA-polymerase-III-subunit-delta
MIDYFKLKDDIKNNKFKNNYILMGVNEHLIKECVEDIVKKNVKEEFLDLNYIKFDGFKLDFQEVINACETLPFFDEKKVVVIYRGDFLRNSKDKEHKKNFKEYKEYIKNIPSTTILITYCVFDNKREKIPSEVKPLSKNSELVEFKQLKGEALNKVLRSLFKEKEKEIGRAELSYLSSILDGNIDVINNEIEKLINYCKDRPITKEDIIKLMPPLNENDIFNLVDSISKRKIKDALDILSELINRGEKEPMILFMILRQYRLLYKIKSFSEQGYDSKSISKELKINEFVCNNLYILSKKYSFITLEKSIEKILETEKAIKSTSSEDNLELLLISLGAL
>NZ_HG917868.1|WP_044037883.1|1641456_1641717_+|30S-ribosomal-protein-S20
MANIKSAKKRIKVTEKKTLRNKMIKSALKTTIKKFEVAVAAGNTEEATVAFGAAVKALDMAASKGIIHKNKAARGKSRLNAKLVAM
>NZ_HG917868.1|WP_044037906.1|1653338_1653641_-|50S-ribosomal-protein-L27
MFIIDLQLFAHKKGVGSSKNGRDSESKRLGTKCADGEFVLAGNILVRQRGTKIHPGTNVGKGGDDTLFAKVDGIVRYERMGRDKKKASVYPIAVEEAINE
>NZ_HG917868.1|WP_044037908.1|1653645_1653972_-|ribosomal-processing-cysteine-protease-Prp
MIKIDFQKHCDKLISFNISGHAGFDESGRDIVCSAVSVLSGAVINGVTEILKIDAPYDFSDGHMSISLSSLSDEEIEKCQVLMETMLVSLKSLEVNYKDYVNVHIKEV
>NZ_HG917868.1|WP_044037910.1|1653974_1654286_-|50S-ribosomal-protein-L21
MYAVVVTGGKQYKVEEGNTIFVEKLEAEVGSTVELDKVLAVSKDGEIKVGKPVVEGAKVVAKVVAQDKAKKIIVFKYKPKKDYRKKQGHRQPYTKLVIEKIEA
>NZ_HG917868.1|WP_044037912.1|1654398_1655838_-|ribonuclease-E/G
MKELFIDRDKDILRIAIKNKGKLEKLYIEEEEKEPIQGEIYKGIVKKVIPNLRSAFIDIGFKKNAYMYIDDKFNNNEIKNGDEVIVEILKEGTRDKGPKVTNMLSIQGKYIVLDSSSDKLRFSSKIDNEENKVNIVQGILKPKDIGVIIRTKAIGVSVSDINEEIGLLYDTYLNILKKGQFSLKPSKIYDGGGTIGKVLRNIVEDDIKITLNNINDYNRIIEMKFLQMNKKYDINYYEENIPIFEKYGIENEILKLRNKKVKLPCGGDIVIDRTEAMTVIDVNTGKNIKGKNAEKTIFDTNVEAAKEIVRQILLRNISGIIAIDFINMNSKTYKKNIIDILKKYLHEDDNKFSIVNFNELNIVHISRMKKGKSILEYIDERCTICHGKGTILKFSYLKMLMRNEIVRQMKEYTVRKFHIAINKAYKDVIENKKQLLIDEYREIECDIYITYTNEIDTYKVEPIIFENMRKKLEEFKITK
>NZ_HG917868.1|WP_156930525.1|1656004_1656715_-|DUF2344-domain-containing-protein
MKVRYLIKFTKESNIKFISHLDLMRTIHRTVRRSGIKAKYSKGFNPHMIMSIAQPLSVGVYSDSEYLDIELEEIISEKTVIDKLNMAAPSGIKFLDAKMIVEKENTKKPPTAMAAVEGAKYIIKIKYNDDILLKDELQDLYLKENWQTIKKSKKGEKLVDIKPMIKEFEYTIENNLLTIETIVACGSRENLSADLLGNFIKENTSNAVSDAFIEIRRLELYGMKNKKLVPLNKAIV
>NZ_HG917868.1|WP_044037914.1|1656692_1658552_-|TIGR03960-family-B12-binding-radical-SAM-protein
MNRINDDILYRVEKPARYIGGEYNSFNKDLNNVDIRFAFCFPDVYEVGMSHLGMKILYHTLNQREDTFCERVFAPWDDMEKLLREKEIKLFTLETKDSIDNFDFVAFTLQYEMSYTNILNMLNLGGITIRASERGEDEPIVLMGGPCSTNPETLYDIADIFSLGEGEDHLNEIIDCYKKCKAKGMSKKEFLREASHIESTYIPSLYDVTYNEDNTIKEFKPKYEDVPKTVKRRVINNYNDVEYPDKLVVPYTEIVHDRIMLETMRGCTRGCRFCQAGMIYRPVREKKTETLMKQADKLLKATGYEEISLTSLSICDYSDVKNLVLSMVERYKDDKIGVSLPSLRIDSFSVDLINEIQKVRKTGLTFAPEAGSQRMRDVINKGVNEEDLLTSVSDAFKNGWSTIKLYFMVGLPYETVEDVKGIAHLGEKVVDEYYKIPKNERNRGLKVTISTSIFVPKPFTPFQWAPMDNLENVREKIAALRGEIKSRAISYNWHETLVSYMEAVIARGDRRICDVIIKAYEKGARLDGWSEFFNYDIWMEAFKECNVDPEFYVHRERDYEEILPWDFIEIGVTKNYLKKENEKAKKAALTQDCRLGCTGCGVNRNAFAKGECFEGALFN
>NZ_HG917868.1|WP_044037916.1|1658620_1659442_-|M50-family-metallopeptidase
MIKINKRFFIYVIIIVIATRSLSILYSFLFIIIHEIAHLLVAICFKYKGYTIEIDILGARLHYKDIEDMSIKEDIIISLAGPIINIIMGLIFCLLSLYEEMIINYILGFFNLIPVIPLDGGRILKNLLTKRYLYKKANVITIYISMVIGVFFLVTAIILGIEFKFNISLLLISILIIYCSYREKRRIVYVVMGDLMKKREKFFKKGYIESIVVSISYNKSLLSVLTLIDKGKYTLFYILDDSMNVIKVISEEEVLKGVKEYGDITIKEYINLP
>NZ_HG917868.1|WP_044039815.1|1659841_1660975_-|rod-shape-determining-protein-RodA
MLSNLKINKKLLGEIDFTILMIAIVIVIFGVLNIYSATYNKTLDGVPIGFEYAKLQLMWLGVGLIAIYFILTIDYSFFRNYAYVFYGASIILLLINKVAGTVSKGANSWIQIGSRAIQPSEFAKLAIIIIVAKKIEDMDGKIDSFKKLFIIFIYAIIPTSLVIIQPDMGMTMVIFFTVLGMVVVGKLDWKIIGGGFLALFIAIAVVWNSGLIEDYQKNRIITVFNPARDPLGDGYHVIQAKIAIGSGGLTGSGYMNGSQTKGGFIPEAWTDFIFSVVGEEWGLLGSVGLLALYGIMIFRMINIARESKDVFGSILVAGVTGSMLFSILENAGMNVGLMPITGITLPFMSYGGSSMLVYFMSLALVLNVGMRRKKINF
>NZ_HG917868.1|WP_044037918.1|1661106_1661370_-|cell-division-topological-specificity-factor-MinE
MDFFKFFTEKQAPKDVAKERLKLILIHDRQDLSPTILEKMKNEILEVISKYVEIDNADVDVKLTTDNNMDGCGPALIANIPIKKLKE
>NZ_HG917868.1|WP_044037919.1|1661387_1662182_-|septum-site-determining-protein-MinD
MGEAIVITSGKGGVGKTTTTANIGTALASLGKSVVVVDGDTGLRNLDVLMGLENRIVYTLLDVIEEKCRLKQALIKDKRFENLALLPTAQTRNKEDINMEQMVSLVGELKKMYDYVLIDCPAGIEQGFENSIAAADRALIVVNPEVTSVRDADRVIGKLDAKGIEDHKLIINRMNPAMAASGDMLNVNDIVEILAVKLIGVVPDDKGITVSTNKGEPIVLEDSAISGRAFKNIARRILGEEVPFLQLKAEEKGFLASIKKIFSK

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Crispr_ID: NZ_HG917868_4

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_HG917868_4

2299388-2299478

Orphan

Consensus_repeat	Method
TAGTTAAGTAGTGGTGACAAGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_HG917868_4

>merge|NZ_HG917868|4|2299388-2299478|CRISPRCasFinder
TAGTTAAGTAGTGGTGACAAGCCTCCACTGCATCTATATATGTCTAATTGTCATATTAACACCTGTTCTAGTTAAGTAGTGGCGACAAGCC

>NZ_HG917868|4|4|2299388-2299478|CRISPRCasFinder
TAGTTAAGTAGTGGTGACAAGCC	TCCACTGCATCTATATATGTCTAATTGTCATATTAACACCTGTTC
TAGTTAAGTAGTGGCGACAAGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_HG917868.1\|WP_044038968.1\|2290364_2291834_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	unknown	unknown	gnl\|CDD\|224893
NZ_HG917868.1\|WP_044038966.1\|2287205_2287865_-\|sugar-transferase	unknown	unknown	gnl\|CDD\|376775
NZ_HG917868.1\|WP_084485416.1\|2289646_2290210_-\|50S-ribosomal-protein-L25	unknown	unknown	gnl\|CDD\|235534
NZ_HG917868.1\|WP_044038980.1\|2311299_2311656_-\|50S-ribosomal-protein-L20	unknown	unknown	gnl\|CDD\|179959
NZ_HG917868.1\|WP_044038971.1\|2296881_2299221_-\|endonuclease-MutS2	unknown	unknown	gnl\|CDD\|234750
NZ_HG917868.1\|WP_044038979.1\|2309796_2311164_-\|ATP-synthase-subunit-J	unknown	unknown	gnl\|CDD\|273349
NZ_HG917868.1\|WP_051483801.1\|2287894_2289277_-\|polysaccharide-biosynthesis-tyrosine-autokinase	unknown	unknown	gnl\|CDD\|349772
NZ_HG917868.1\|WP_044038970.1\|2296442_2296877_-\|DUF523-domain-containing-protein	unknown	unknown	gnl\|CDD\|377367
NZ_HG917868.1\|WP_051483803.1\|2293154_2296064_-\|insulinase-family-protein	unknown	unknown	gnl\|CDD\|223957
NZ_HG917868.1\|WP_044038973.1\|2303211_2303607_-\|DUF1284-domain-containing-protein	unknown	unknown	gnl\|CDD\|377735
NZ_HG917868.1\|WP_044038975.1\|2304514_2306887_-\|phenylalanine--tRNA-ligase-subunit-beta	unknown	unknown	gnl\|CDD\|234804
NZ_HG917868.1\|WP_051483802.1\|2291990_2292866_-\|hypothetical-protein	unknown	unknown	gnl\|CDD\|226202
NZ_HG917868.1\|WP_044038974.1\|2303593_2304136_-\|biotin-transporter-BioY	unknown	unknown	gnl\|CDD\|224187
NZ_HG917868.1\|WP_044038978.1\|2309107_2309788_-\|TrkA-family-potassium-uptake-protein	unknown	unknown	gnl\|CDD\|223643
NZ_HG917868.1\|WP_044038965.1\|2285846_2287193_-\|UDP-glucose/GDP-mannose-dehydrogenase-family-protein	unknown	unknown	gnl\|CDD\|223936
NZ_HG917868.1\|WP_044038977.1\|2308311_2309106_-\|RNA-methyltransferase	unknown	unknown	gnl\|CDD\|223640
NZ_HG917868.1\|WP_051483804.1\|2301897_2303031_-\|cell-division-protein-ZapA	unknown	unknown	gnl\|CDD\|377476
NZ_HG917868.1\|WP_084485414.1\|2284265_2285594_-\|polysaccharide-biosynthesis-tyrosine-autokinase	unknown	unknown	gnl\|CDD\|349772
NZ_HG917868.1\|WP_044038972.1\|2299508_2301845_-\|U32-family-peptidase	unknown	unknown	gnl\|CDD\|223896
NZ_HG917868.1\|WP_044038976.1\|2306906_2307929_-\|phenylalanine--tRNA-ligase-subunit-alpha	unknown	unknown	gnl\|CDD\|234780

Protein	Function_ID	Function_description	E-value
NZ_HG917868.1\|WP_044038968.1\|2290364_2291834_+\|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme	gnl\|CDD\|224893	COG1982, LdcC, Arginine/lysine/ornithine decarboxylases [Amino acid transport and metabolism].	0
NZ_HG917868.1\|WP_044038966.1\|2287205_2287865_-\|sugar-transferase	gnl\|CDD\|376775	pfam02397, Bac_transf, Bacterial sugar transferase. This Pfam family represents a conserved region from a number of different bacterial sugar transferases, involved in diverse biosynthesis pathways.	7.38757e-96
NZ_HG917868.1\|WP_084485416.1\|2289646_2290210_-\|50S-ribosomal-protein-L25	gnl\|CDD\|235534	PRK05618, PRK05618, 50S ribosomal protein L25/general stress protein Ctc; Reviewed.	3.34838e-42
NZ_HG917868.1\|WP_044038980.1\|2311299_2311656_-\|50S-ribosomal-protein-L20	gnl\|CDD\|179959	PRK05185, rplT, 50S ribosomal protein L20; Provisional.	3.62849e-65
NZ_HG917868.1\|WP_044038971.1\|2296881_2299221_-\|endonuclease-MutS2	gnl\|CDD\|234750	PRK00409, PRK00409, recombination and DNA strand exchange inhibitor protein; Reviewed.	0
NZ_HG917868.1\|WP_044038979.1\|2309796_2311164_-\|ATP-synthase-subunit-J	gnl\|CDD\|273349	TIGR00933, Trk_system_potassium_uptake_protein_trkH., potassium uptake protein, TrkH family. The proteins of the Trk family are derived from Gram-negative and Gram-positive bacteria, yeast and wheat. The proteins of E. coli K12 TrkH and TrkG as well as several yeast proteins have been functionally characterized.The E. coli TrkH and TrkG proteins are complexed to two peripheral membrane proteins, TrkA, an NAD-binding protein, and TrkE, an ATP-binding protein. This complex forms the potassium uptake system. [Transport and binding proteins, Cations and iron carrying compounds].	1.17863e-98
NZ_HG917868.1\|WP_051483801.1\|2287894_2289277_-\|polysaccharide-biosynthesis-tyrosine-autokinase	gnl\|CDD\|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	9.38292e-71
NZ_HG917868.1\|WP_044038970.1\|2296442_2296877_-\|DUF523-domain-containing-protein	gnl\|CDD\|377367	pfam04463, DUF523, Protein of unknown function (DUF523). Family of uncharacterized bacterial proteins.	3.1925e-62
NZ_HG917868.1\|WP_051483803.1\|2293154_2296064_-\|insulinase-family-protein	gnl\|CDD\|223957	COG1026, COG1026, Predicted Zn-dependent peptidases, insulinase-like [General function prediction only].	0
NZ_HG917868.1\|WP_044038973.1\|2303211_2303607_-\|DUF1284-domain-containing-protein	gnl\|CDD\|377735	pfam06935, DUF1284, Protein of unknown function (DUF1284). This family consists of several hypothetical bacterial and archaeal proteins of around 130 residues in length. The function of this family is unknown, although it is thought that they may be iron-sulphur binding proteins.	5.75552e-29
NZ_HG917868.1\|WP_044038975.1\|2304514_2306887_-\|phenylalanine--tRNA-ligase-subunit-beta	gnl\|CDD\|234804	PRK00629, pheT, phenylalanyl-tRNA synthetase subunit beta; Reviewed.	0
NZ_HG917868.1\|WP_051483802.1\|2291990_2292866_-\|hypothetical-protein	gnl\|CDD\|226202	COG3677, COG3677, Transposase and inactivated derivatives [DNA replication, recombination, and repair].	3.99832e-06
NZ_HG917868.1\|WP_044038974.1\|2303593_2304136_-\|biotin-transporter-BioY	gnl\|CDD\|224187	COG1268, BioY, Uncharacterized conserved protein [General function prediction only].	2.2811e-33
NZ_HG917868.1\|WP_044038978.1\|2309107_2309788_-\|TrkA-family-potassium-uptake-protein	gnl\|CDD\|223643	COG0569, TrkA, K+ transport systems, NAD-binding component [Inorganic ion transport and metabolism].	3.56747e-57
NZ_HG917868.1\|WP_044038965.1\|2285846_2287193_-\|UDP-glucose/GDP-mannose-dehydrogenase-family-protein	gnl\|CDD\|223936	COG1004, Ugd, Predicted UDP-glucose 6-dehydrogenase [Cell envelope biogenesis, outer membrane].	0
NZ_HG917868.1\|WP_044038977.1\|2308311_2309106_-\|RNA-methyltransferase	gnl\|CDD\|223640	COG0566, SpoU, rRNA methylases [Translation, ribosomal structure and biogenesis].	1.35828e-81
NZ_HG917868.1\|WP_051483804.1\|2301897_2303031_-\|cell-division-protein-ZapA	gnl\|CDD\|377476	pfam05164, ZapA, Cell division protein ZapA. ZapA is a cell division protein which interacts with FtsZ. FtsZ is part of a mid-cell cytokinetic structure termed the Z-ring that recruits a hierarchy of fission related proteins early in the bacterial cell cycle. The interaction of FtsZ with ZapA drives its polymerization and promotes FtsZ filament bundling thereby contributing to the spatio-temporal tuning of the Z-ring.	2.24446e-12
NZ_HG917868.1\|WP_084485414.1\|2284265_2285594_-\|polysaccharide-biosynthesis-tyrosine-autokinase	gnl\|CDD\|349772	cd05387, BY-kinase, bacterial tyrosine-kinase. Bacterial tyrosine (BY)-kinases catalyze the autophosphorylation on a C-terminal tyrosine cluster and also phosphorylate endogenous protein substrates by using ATP as phosphoryl donor. Besides their capacity to function as tyrosine kinase, most of these proteins are also involved in the production and transport of exopolysaccharides. BY-kinases are involved in a number of physiological processes ranging from stress resistance to pathogenicity.	3.92157e-69
NZ_HG917868.1\|WP_044038972.1\|2299508_2301845_-\|U32-family-peptidase	gnl\|CDD\|223896	COG0826, COG0826, Collagenase and related proteases [Posttranslational modification, protein turnover, chaperones].	3.13447e-113
NZ_HG917868.1\|WP_044038976.1\|2306906_2307929_-\|phenylalanine--tRNA-ligase-subunit-alpha	gnl\|CDD\|234780	PRK00488, pheS, phenylalanyl-tRNA synthetase subunit alpha; Validated.	0

>NZ_HG917868.1|WP_044038971.1|2296881_2299221_-|endonuclease-MutS2
MEERTFKILEVQKVLDKLVSYSNTEKGKEMSATLMPFNNEYEVNRALKETKEAYTYVIKKGRAPIYSDKGLKEVLSRAEKGGELNAKEILIVGRSLRTAREITVYLDSDDIDENSLRDSAVNITTIKWLEDKIEQCIIDEDEISDNASRALGAIRRNLREKGIEIKERVGSMVRNYSKYLMENIYTVRGDRYVLPVKVEYKSTVKGLVHDVSSTGSTVFIEPMELVTLNNEIKELKLKEMAEIERILNEISRDINKNVKALKMNREIISDLDFIFAKGAYGLEIEGIVPEINSNGIYNIVQGRHPLIPSDKVVPLDINSGEDFTTIVITGPNTGGKTVTLKTVGLLHVMALSGMMIPAYQGSVINVFEGIYADIGDEQSIEQSLSTFSSHMTNIISILGKAKSNSLVLFDELGSGTDPTEGSALAISILEELRSRGCSIISTTHYSELKRYGLNTAGVENASVEFDVATLRPTYRLLMGIPGKSNAFEISRKLGLSDDIIKFARENIAKDTLEFEDLIRSLSEKTMEAEKLSRENETLRNEAKDLYEKYKTKLDRIDEVREKSVEAGKEKAKKIIEEAKEEADKILKEMREMERHGITSNMRHEMEKKRKALKDKAEKMESAKKAQGGGLTKVSEGQEVKIISLNAKGVVLSFDDKKQEAVVQAGIMKITSKYSDLQGATVTKSEKKATKREVKLNLKSVSTSLDIRGLDGEEGKYRTDIYLDEAFVAGLEEVTIIHGKGTGALKTAILSMLRNHPHVKKFRDGEYSEGGNGVTVVTLK
>NZ_HG917868.1|WP_044038970.1|2296442_2296877_-|DUF523-domain-containing-protein
MKLVSMCLCGVNCKYSGGNNFDEGVLEIINCGEAIPVCPEVMGGLGTPRIPHEIVGGDGFDVLEGRARVISKDGEDNTAAFIAGAEKVLEIAKKLDIKEVILKSKSPSCGNGKIYDGSFSGILIDGVGVTTALLIKNGISVSSI
>NZ_HG917868.1|WP_051483803.1|2293154_2296064_-|insulinase-family-protein
MMVNNLNPNYTIVEETKVEEINSEAYSLEHNGTGAKILILKNEDDNKTFSITFRTTPENSTGVAHILEHSVLCGSEKYPVKEPFVEMAKGSLNTFLNAMTYPDKTMYPIASRNNKDFKNLMSVYLDAVFFPNIYKDETILMQEGWHYELENPEDELKYKGVVYNEMKGVYSSPDSMVYRKIYRGLLPDTTYGVDSGGNPKDIPNLTQEEFINFHKKYYHPSNAYIVLYGDIDVNERLEFLHNEYLSKFSKEKIDSKIKLQKPFKETKEIQEYYSISKDDDDKNKSFFTYNFAVSSTSDVTKNLAYEVLEYVLIDAQGAPLKKALLEKGLCEDVYGSFDKGIAQPVFSIIAKNVDENKKDEIKNVIMDVLKNVIDEGVDKKFLEAALNKKEFYLREGDFDRYPKGVIYSMVVNDSWIYDGDPLRYLVYEDDLKELREKINTNYYEELVKEAFIDNKFATLMMVSPKKGLEEEETKALHDKLQKIKASMDKDTIDTIVKNTELLKKKQETPDSPEALKVIPTLELSDIDKEAEKLPLTVGKYNNNTYLYSNIFTNKILYPTFLFNTKSVAEEDISYIPILARLLTRVNTKNYTYEELAKEIDFYTGGIDCGSSAFFYNDTDTDFFPYMSVKGKTTEANTKKLLELMDEVILNSSFEDKNRVKEIIFELKSRIESSLNSRSHVIAATRALSYVNKNHRYLERNSGYSFYLFLCKLCEDIDNDFDGFKNKMEQLRSEIFNKDNLYILLTCGEEEEKIFKNEIDIFYNSLGDKKFEPKDYKLELEADNEGFTTSGTVQYVAKAGKIDNYNGSAAVLKSILSLDYLWNKVRVMGGAYGCFASIGRSGNLFFTSYRDPNLNNTIDVYNNAYEYIKNFDATKDEMKKYIIGTIAEIDAPLTPAAMGEKAQANYLKRLTYEEVQKEREEILSTTVEDIRAHSEDIKKVMEDNNLCVIGNEKKIKENCDEFHSIEPLVK
>NZ_HG917868.1|WP_051483802.1|2291990_2292866_-|hypothetical-protein
MHRKSIFLTEKSKYYTILKCINDMNRDITINRACPHCCGDNIIKYGKVKSNKAQIFYCKTCERRVVETIGTPFYRSRKNNEIWDKYFENMWNGYNIRECAKKIDISQNTSFSWRHKILSYYLKFFKRKPLNDEVDVMVRTYVQNSKKEKESAIENVEKEALTLKLGEKCYFFFTKNNDGTIEFLPFDKYPLARLSLKRKLDIIFSNVKKVGIYGNNVIKSYAKKCVKEVTKVMVDSELFLYERDMRSWISGFWGVSFRYISNYFNWFRIYYINNKRYKETRQYIYGAEKII
>NZ_HG917868.1|WP_044038968.1|2290364_2291834_+|aminotransferase-class-I/II-fold-pyridoxal-phosphate-dependent-enzyme
MYKLEQNKTPLFDALISYVNNETIPFHVPGHKKGLGVDEDFKNFIGENPFKIDVTVFKSVDSLHHPKGAIKEAQILAADAYGADATFFSVHGTSGAIQAMIMSVVSDGDKIIIPRNVHKSITTGIILAGAIPVYMTPEFDKNLGIAHGVTKATVEEALKNNPDAKAVLIINPTYYGVATEIKAIANLVHSYNIPLIVDEAHGPHLAFSEKLPISALEAGADICAQSTHKIIGAMTQVSLLHVKSKLVDTNKVKQMLSLLQTTSPSYILMASLDTSRRQIALHGKELLKDTIELYTYAREEINKIPGFYSFGNEILGKPGVFALDPTKLTISCRELGITGDELEKILATKYHIQMELSDFYNVLAVGSFGDTKENIDLLISALKKISEEFYGKKTPLQDFLDIPDIPESKLTPRQAFYSSKVSVRLEDSIGKISGEFLMAYPPGIPILCPGEIITSKIISYVNQLKSAGLYVQGTEDPEVEFIKIVTDSL
>NZ_HG917868.1|WP_084485416.1|2289646_2290210_-|50S-ribosomal-protein-L25
MMKNLNINNREGSNNSLRRKGLLPGVLYGEKIKNTLFEISEMELASELAREGSSGMCNVHYGNEDFTAIVREVQKDPVTRKIIHIDLEKISASDKVTSEVPLNFIGEGAVESIGGVVIKEKEKLKVKGPASEIPSSINIDVSKLKYGETITGSDVEFGSEISLAEDGNSVLAVVLSKGNQVEEENVE
>NZ_HG917868.1|WP_051483801.1|2287894_2289277_-|polysaccharide-biosynthesis-tyrosine-autokinase
MEEVKVVEEFSNEISFSQIIFALKKRWKIIFATTIFFTALVALITFFFIDPVYEVHTKVFIGKDAEVNYDNNDVQMYQKLLLTYAQILKTEDLIGTALNNVDSDMTMEEVMKDITVEPITDTQILQIKLTGKNKDDLAVVLESITEEFIKESKEIVPNGNVKIIRHVKEAEAPISPNKKMNIILGFLIGLVSGMAIVFLIEYMNNTYKSKEEVERNLKLPVLGVIPKFGRKREKLVMEEEPRSLEAECYRTMVTNIQYSSIDSRCKTIVVTSSQKGEGKTTISGNLALSLAGWGNRVVLIDCDIRRAALHKAFNISNSKGLTDVLVNQASLKDVAVGIKETLLLIPAGRVSPNPTELLNSKAMELLLEELKETCDYVILDTAPVEAVADAQILSAKADGTLVVIKSGDTRINVIQDALNLLNKVRGKILGVVLNATEDGRLSKMYQYYGEEHKKKGDKVS
>NZ_HG917868.1|WP_044038966.1|2287205_2287865_-|sugar-transferase
MERLVLENVESDAIEVKTSKIYLFIKRIIDIMGALIGLILLSPLLVIVGVLIKIESKGPIIFSQDRIGKNGKIFRMYKLRSMVANAEELKEKLIKENEMSGPMFKIKDDPRVTKIGRFIRKTSIDELPQLLNVLKGNMSLVGPRPSLPNEVLEFEPWMNKRLMVKPGLTCYWQVMGRNNIDFEQWMLLDIKYVETRSIIVDIKLIIKTFFVLFGDKNAS
>NZ_HG917868.1|WP_044038965.1|2285846_2287193_-|UDP-glucose/GDP-mannose-dehydrogenase-family-protein
MEIVVAGTGYVGLVTGACLAEVGHKVTCVDIDEKKIEIMKKGISPIYEPGLDEILDKNYKKGKLDFTTDYKEAYRKADVVFIGVGTPERVDGSANLDYVFSVCRQIAKNVTKDCLVVVKSTVPIGTNDKVEEFLRENVENNIHIEVASNPEFLAQGTAVRDTLFASRIVIGVESEKARDILMNIYERFNQPIVVTNRRSAEMIKYASNDFLALKISFINEMANVCEIVGADIEDVAKGMSYDSRIGNKFLSAGIGYGGSCFPKDTKALHWLANDHGYEVKTIKATIEVNENQKYKLFRKAKEVFGSLKNKRVAILGLTFKPGTDDLREAPSIENVRRLLDEGAKVIAYDPVGENNFKKIYPTEIIYAESMEEAINDSDMAFIFTEWDEIKSIGIDVFIEKMKTPIIFDGRNCFNLDNIYEKEVYYYSIGRKTIKNFSKKKLNEKIFLK
>NZ_HG917868.1|WP_084485414.1|2284265_2285594_-|polysaccharide-biosynthesis-tyrosine-autokinase
MSEALVEKPVNIIRLVRIIRTRWKIVIFVTSFLTLLTIILNLFVLQPVYQCNVKMFIGKSIDEDGNYSNNDIVMYQSLMKTYVEIIKTEDLVERSLSKIDSKIEPAEVLSNLSVDAINDTQILQVTLEGEDKREIYEILASITEEFVATAKTVVPNGNVQVIRNAKEPQNQISPNIEINIVIGILSGVLLSGIIVFIKEFKGSCIETKEEVEGKLGIPVLGMIPKNYKDTDIFEVDKNPKSVISEEYRRLRTNLKYTSFEKYHRVFQVTSAVSGEGKSTVSINLALALAEEAKVVLIDCDMRKPSIHKKLNISRKGGLSDILIGKCDIMDVAYRYNKNLLIITSGNSIENPSEMLSSRAMERMVRRLKDVVDYVIIDSPPVQAVTDAQILSTRCDGTILVVKSGETKAKEVLNTIDLLNKVKGNILGIVLKYVEVNNKKYVQ
>NZ_HG917868.1|WP_044038972.1|2299508_2301845_-|U32-family-peptidase
MEKIELLAPAGSLESLYAAVNSGCDAVYLGGSKFSARAYASNFGEEEMKEAVLYCHLNSVKIYVTINTLIKDKEVREAIEYVNFLQSIGVDGVIVQDLGLAYLIRKNFKDIELHGSTQISIHNGEGAKALNDLGFKRIVLARECTLKEIEYISKDLGIETEIFVHGALCVSYSGQCLMSSMIGGRSGNRGKCAQSCRQNYKLINEKTGEETEGYLLSPKDLAFIENIGEIIESGTASLKIEGRMKRPEYVAGVVSMYRKAIDAYYAGEPFDYDTAMKNLAKLFNREGFSKGYLFKNTGSDMMSFKFPRNTGVVIGEAVSSNEVLLKENIVIGDGIRFGEEGFTISSISVKGKSVEEAYMGDVAKLKEGKFKEGEKIYKTSDVKLLKSYENTFKTQYLKKNPLDIEVYFKIGDKMKLTTSFKGKVFEVYGEEVQTPLKRPLFKENIEENLKKTGNTPFEVNSITFSEYEEGFMAISALNNLRRTLIEKIINWVKIDRGLVEKLDLNRETKNIKELPSLLVIVQNLKQLKGAYEGGARDIAINPFMRGTNIDFSQIPEDLNLYLRLPTIIKEEYRMVSAYIEQNIDKIKGLITSNFGITSEFHNRTSIIFDYKGNLFNKYSIDFLESMVDGVTLSLELNKSELKDVSKGTPLTPYVYIYGKVESMISEYCPIGATFGGKCEVKGCNIACEKGDFVLRDRLKEDFRVKTDKFCRSHIYNSHPLNLIDNIKELKGINISNFRVDFVDEDEDRVHHIVEAILSGDNIEGEGKFTKGQYKRGVE
>NZ_HG917868.1|WP_051483804.1|2301897_2303031_-|cell-division-protein-ZapA
MNKVVVKVNGVEYTLKGEEKEEYLQSVAAYVDKKVQMILDKNSKLSSTDASVLASMNIADELFKWDKYIAELEDKNSILKSSQKSYNDKINELQSKINELEENAKKAASEDTEEIKKELDDLRNNYIELDKKYATLKEKYNGVKNYNNKVKEEKTNVIKEKEAKIKELEVANKEIVELKKVNTELESSQKDFEKIRNRSSEIENELKTCMGQLEDTKSKLEETTRQLEAADRKVQYSNQTVEDTSKNLRECNKKLNETKEKLREAEVKIENDTKMINNLNMKISRMEKDSKQEPSDQANALREAVEKEAANVKAQFEILEEESKKLKGENEKLLSRNKELKFSLQSAKYKVMDLEKKFLDSQITIATLKKNSNKMFK
>NZ_HG917868.1|WP_044038973.1|2303211_2303607_-|DUF1284-domain-containing-protein
MKEIKLRYHHIMCIHTYSGHGYDEKFAENIEKIIKIFKEEPNINIRFIDNCDDVCKSCPNRNGEYCLGEDSIREKDNRVKKYFELDRKSIDTYKDLVGEIKPTFSELQDISEVCGRCDFKKLCNKVLPKNI
>NZ_HG917868.1|WP_044038974.1|2303593_2304136_-|biotin-transporter-BioY
MKIKDITLIALFTALISVCAQITIPIQPVPITGAIIGIFITGAVLEKKQGLIVGIVYLLLGAVGIPVFTGFGAGISSIIGPTGGYLITYPIMIYLIAWCIEKFKKENIVFLSIYMIFSLVPCYLVGTIWLAISCKLGIYEAILSGVAPFVIFDVMKGILGAVVAVAINRALVKGHIYERN
>NZ_HG917868.1|WP_044038975.1|2304514_2306887_-|phenylalanine--tRNA-ligase-subunit-beta
MLVPIDWLKDYVEIKEDAKDLGDALTLSGSKVEKVEVYGEEIQNVVTGKIVKITKHPEADKLSICQVDIGAEEPIQIVTAATNMKEQDVVPVALHGSTLHGGLKIKKGKLRGEVSNGMFCSLEELGLAEEGTCHGLHIMDTNTPLGVDIKEAVDFGGGVIEFEITSNRQDCFSVYGIAREVAATYGRELKGLNTSYKTSGGNVNDIVKAEIKDSLCRRYMARAIKNVKIGPSPSWMQNRLNEAGIRPINNIVDITNYVMVELGQPMHAYDRRDIAEGTIIVERAKDNEKFTTLDEVERTLTSEMLTIRDGKGTIGLAGIMGGLNSEVKEDTTEIIFEAANFEGVNIRLTSKELNLRTDASGKFEKDLDPNLPALALDRACALVEELGCGEIVNGTIDIYNEKKEEGHLTVSISWINKFLGTEIHGIEMKRILESLGMATEINGDNLEITTPTFRSDMNIREDVAEEVVRIYGYNKVEATMPSIHATKSGKSEKMQLNDELAKVLIGSGLYESIAYSFVSPKVFDKILLPADSELRNVVEIKNPLGEDYSIMRTTTIPSMMESLARNYSRNNKECRLFENGKIYIKEEGKELPNEINILTIGLYGGVDYLNLKGVVENILDHFKVKSAKFERESENPSFHPGKTAKVVIGREVIATVGEVHPDVAENYGIDERAFIAVINLDKLYSFIKKNNKYTPLPKFPSVTRDLAVLIDDEVLVADIEEVIKKQGGNLVEEYSLFDVYKGAQVPEGKKSVAYSIVYRDPNKTLKDSDVNKVHDKIVRTLEHKLGATLR
>NZ_HG917868.1|WP_044038976.1|2306906_2307929_-|phenylalanine--tRNA-ligase-subunit-alpha
MQEKLKLIETTAIDELNKAVTKEDIEAVRVKYLGKKGEVTLILRGMGGLSPEERPIVGKLVNDVRGNLEGRIENALTDIKKKEKEERLKNEVIDISMPGDKSPLGGKNPLTITMEEIQDIFLSMGFSIEEGPEVELDYYNFEALNIPKNHPARGEQDTFYINDNVVLRTQTSPVQIRVMENQKPPIKMISPGKVYRSDAVDATHSPIFYQVEGLVIDKGITFADLKGMLETFVKKMFGDKMVTKFRPHHFPFTEPSAEMDATCFVCGGEGCKVCKGEGFIEILGCGMVHPKVLENCGIDPNEYSGFAFGFGLDRMVMQKFGIDDIRLLYEADMRFLKQFK
>NZ_HG917868.1|WP_044038977.1|2308311_2309106_-|RNA-methyltransferase
MNVITSKDNNIIKEIKKLKDRKTRSAKGEFLVEGFRFVEEALKSDFEIKTLIIEESVEDKLSNYNIDKYLDKVETIYVTKSIMKILASTETPQGILAVVKNKDIKLKDNEGFYIFCDKVQDPGNLGTIIRTAHASGALGVILRKGTVDLYNDKTLRSTMGSVFNVPVVYDNDDLDIIMSLKNKGFKVVSSSLDTDYNFYDIDLTGKCIIVVGNEGNGISSEIFAISDEKFKIPMPGGAESLNVGIATSVIAFEAVRQRNFKIKC
>NZ_HG917868.1|WP_044038978.1|2309107_2309788_-|TrkA-family-potassium-uptake-protein
MRKKVKEKQYIVIGMGRFGTSVALTLAELGREVLAIDKDVDRIQDISDKVTHAVTLDSTDENDLKAVGIGNFDVAIVAIGKDIQASIMTTLLLKELGVKYIAVKANNDLQEKVLIKIGADKVISPEKEMGIRVANNLVSSNILDYIEVSPDYSLTEFLVPKSWVNKTIKELNLRVEYGINVMAIKRDGVIEVSPSPDLALLSGDIIVAIGSNDIEELRDFVATEEE
>NZ_HG917868.1|WP_044038979.1|2309796_2311164_-|ATP-synthase-subunit-J
MSKHILGRIKIKPVQVLALGFMAVLLIGAGILMLPISTATGEKTSFIDALFTSTSAVCVTGLVTVDTASHWSYFGKTVIIFLIQIGGLGFMSFATLFALILGKRVSLKERLILQEAVNATYISGIVKLVKYILSFTFAIEGIGAAILATQFIPEHGLLKGIYFSIFHAISAFCNAGFDLIGDSLFPYQNNAVVILTISALIIIGGIGFAVLLDLFNASQSTRLYTHTKFVLVLTAILLVTGTVFIFIMEYNNPETIGNMGFGGKLLNSFFASVSSRTAGFYSIPLEYLTTGSIFLYFILMFIGGSPGSTAGGVKTTTIGLICLTVVSGLRGKEDTELFKRRISKDVIYKAFSILFLSLMIVVAITMLLSNTEADTLVNGELVPLEGIIFEAISAFGTVGVTLGITPYLSFVGKLLIILTMYIGRVGPITLVMAITRQKKKNAGNIKYPEAKILIG
>NZ_HG917868.1|WP_044038980.1|2311299_2311656_-|50S-ribosomal-protein-L20
MARVKRAMNARKKHKKVLKLAKGYYGGKSKLYRTANETVIRALRNAYVGRKLKKRDFRKLWIARINAAARMNDMSYSKFMNGLKKAGIEINRKMLSEIAIHDPKAFAELVETAKKSLA

You can click texts colored in the table to view more detailed information

Click the colored protein region to show detailed information

Self-targeting detection

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_ID	Protospacer_location	Mismatch	Identity

MGE targeting detection<

CRISPR_ID	Spacer_Info	Spacer_region	Spacer_length	Hit_phage_ID	Hit_phage_def	Protospacer_location	Mismatch	Identity
NZ_HG917868_1	1.66\|222136\|37\|NZ_HG917868\|PILER-CR,CRISPRCasFinder,CRT	222136-222172	37	JN800508	Clostridium phage phi24R, complete genome	6315-6351	10	0.73
NZ_HG917868_1	1.79\|222991\|35\|NZ_HG917868\|PILER-CR,CRISPRCasFinder,CRT	222991-223025	35	MN693045	Marine virus AFVG_25M135, complete genome	19787-19821	10	0.714
NZ_HG917868_1	1.80\|223055\|37\|NZ_HG917868\|PILER-CR,CRISPRCasFinder,CRT	223055-223091	37	LR721753	Aliivibrio wodanis 06/09/160 plasmid 2 complete sequence	73973-74009	10	0.73
NZ_HG917868_1	1.80\|223055\|37\|NZ_HG917868\|PILER-CR,CRISPRCasFinder,CRT	223055-223091	37	NZ_AP019717	Clostridium butyricum strain NBRC 13949 plasmid pCBU1, complete sequence	404352-404388	10	0.73

1. spacer 1.66|222136|37|NZ_HG917868|PILER-CR,CRISPRCasFinder,CRT matches to JN800508 (Clostridium phage phi24R, complete genome) position: , mismatch: 10, identity: 0.73

tagttgcatatgcaacatcagaacctaaagaagtttt	CRISPR spacer
ttttagagggagcaacatcagaaactaaaaaagtttt	Protospacer
*  * * . . ************ *****.*******

2. spacer 1.79|222991|35|NZ_HG917868|PILER-CR,CRISPRCasFinder,CRT matches to MN693045 (Marine virus AFVG_25M135, complete genome) position: , mismatch: 10, identity: 0.714

tttactatgttaataccaatcttactccaatccac	CRISPR spacer
ttacaaatgttaatagtaatcttactccaataaca	Protospacer
**    ********* .**************

3. spacer 1.80|223055|37|NZ_HG917868|PILER-CR,CRISPRCasFinder,CRT matches to LR721753 (Aliivibrio wodanis 06/09/160 plasmid 2 complete sequence) position: , mismatch: 10, identity: 0.73

ttagattctaaatatccttctttaaaaggtgtttttg	CRISPR spacer
tttcattttaaatatccttctttaaaaggttccacaa	Protospacer
**  ***.********************** .. . .

4. spacer 1.80|223055|37|NZ_HG917868|PILER-CR,CRISPRCasFinder,CRT matches to NZ_AP019717 (Clostridium butyricum strain NBRC 13949 plasmid pCBU1, complete sequence) position: , mismatch: 10, identity: 0.73

ttagattctaaatatccttctttaaaaggtgtttttg	CRISPR spacer
atttatgaaaaatatgcttatttaaaaggtgttttca	Protospacer
 *  **   ****** *** ***************..

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

166022 : 175966

Clostridium_phage(50.0%)

The bacterium proteins that are colored denote the protein is present at specific phage-related keywords (such as 'capsid', 'head', 'integrase', 'plate', 'tail', 'fiber', 'coat', 'transposase', 'portal', 'terminase', 'protease' or 'lysin' and 'tRNA')

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_051483611.1\|166022_167102_+	C40 family peptidase	A0A0A8WF62	Clostridium_phage	1.1e-26	51.6
WP_051483612.1\|167311_168382_+	C40 family peptidase	A0A0A8WF62	Clostridium_phage	4.5e-25	49.6
WP_051483613.1\|168941_170057_+	C40 family peptidase	A0A0A8WF62	Clostridium_phage	4.3e-26	49.2
WP_044035809.1\|170401_171460_+	C40 family peptidase	A0A0A8WF62	Clostridium_phage	4.8e-27	51.5
WP_044035810.1\|171527_171770_-	AbrB/MazE/SpoVT family DNA-binding domain-containing protein	A0A2I7SC16	Paenibacillus_phage	2.2e-20	58.8
WP_044035811.1\|172072_172735_+	response regulator transcription factor	W8CYM9	Bacillus_phage	2.5e-37	38.1
WP_044035812.1\|172712_174176_+	HAMP domain-containing sensor histidine kinase	W8CYF6	Bacillus_phage	7.9e-28	30.8
WP_051483614.1\|174664_175966_-	trypsin-like peptidase domain-containing protein	A0A1B1IT49	uncultured_Mediterranean_phage	1.8e-15	29.9

DBSCAN-SWA_2

664953 : 766170

105

Erysipelothrix_phage(78.02%)

tail,head,protease,portal,terminase,capsid,holin

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_051483656.1\|664953_665904_+	AAA family ATPase	Q6DMW9	Streptococcus_phage	1.9e-38	34.0
WP_044036300.1\|665935_667192_+	LlaJI family restriction endonuclease	NA	NA	NA	NA
WP_044036302.1\|667215_669084_+	helix-turn-helix transcriptional regulator	E4ZFJ9	Streptococcus_phage	1.3e-75	29.6
WP_051483657.1\|669413_670088_+	sigma-70 family RNA polymerase sigma factor	A0A2K5B267	Erysipelothrix_phage	2.5e-13	33.0
WP_044036305.1\|670133_670352_+	hypothetical protein	A0A2I4R673	Erysipelothrix_phage	7.5e-20	62.5
WP_044036307.1\|670326_670650_+	hypothetical protein	A0A2K5B2A7	Erysipelothrix_phage	5.4e-22	60.7
WP_044036309.1\|670642_671791_+	DUF2800 domain-containing protein	A0A2K5B2A8	Erysipelothrix_phage	3.1e-181	79.9
WP_044036310.1\|671783_672332_+	DUF2815 family protein	A0A2K5B2A9	Erysipelothrix_phage	1.2e-90	89.5
WP_044036312.1\|672410_674345_+	DNA polymerase	A0A2K5B2B0	Erysipelothrix_phage	6.0e-294	74.3
WP_044036314.1\|674438_675191_+	phage antirepressor KilAC domain-containing protein	A0A2H4IZX7	uncultured_Caudovirales_phage	3.6e-61	49.8
WP_044036316.1\|675190_675625_+	hypothetical protein	A0A2K5B270	Erysipelothrix_phage	6.9e-57	70.1
WP_044036317.1\|675621_677988_+	phage-like protein	A0A1W6JQ82	Corynebacterium_phage	2.0e-243	52.2
WP_044036319.1\|678207_678489_+	VRR-NUC domain-containing protein	A0A2K5B272	Erysipelothrix_phage	4.4e-28	68.9
WP_084485357.1\|678442_679831_+	DEAD/DEAH box helicase	A0A2K5B273	Erysipelothrix_phage	2.1e-187	79.9
WP_171011288.1\|679827_680049_+	hypothetical protein	A0A2K5B274	Erysipelothrix_phage	4.6e-17	60.6
WP_035150326.1\|680045_680456_+	DUF1492 domain-containing protein	A0A2K5B275	Erysipelothrix_phage	8.9e-14	32.4
WP_044036327.1\|680610_680970_+	HNH endonuclease	A0A2K5B276	Erysipelothrix_phage	6.8e-42	65.3
WP_044036329.1\|681084_681633_+	hypothetical protein	A0A2K5B277	Erysipelothrix_phage	1.1e-51	56.6
WP_044036331.1\|681635_682418_+	S-adenosylmethionine synthetase	NA	NA	NA	NA
WP_044036333.1\|682429_683695_+	site-specific DNA-methyltransferase	A0A2I4R670	Erysipelothrix_phage	1.8e-113	50.6
WP_044036335.1\|683687_685505_+	DNA cytosine methyltransferase	A0A2K9V3X0	Faecalibacterium_phage	1.9e-31	59.6
WP_044036337.1\|685606_686326_+	hypothetical protein	A0A2K5B280	Erysipelothrix_phage	2.4e-54	48.8
WP_044036339.1\|686309_686696_+	DUF4314 domain-containing protein	A0A2K5B281	Erysipelothrix_phage	1.3e-19	63.8
WP_044036341.1\|686688_686868_+	DUF5049 domain-containing protein	NA	NA	NA	NA
WP_044036342.1\|686870_687110_+	hypothetical protein	A0A2K5B284	Erysipelothrix_phage	1.1e-16	48.1
WP_044036343.1\|687222_688827_+\|terminase	terminase large subunit	A0A2K5B285	Erysipelothrix_phage	1.6e-247	77.3
WP_044036344.1\|688845_690210_+\|portal	phage portal protein	A0A2K5B287	Erysipelothrix_phage	2.2e-186	74.9
WP_084485358.1\|690106_690835_+\|protease	Clp protease ClpP	Q6DMU1	Streptococcus_phage	8.6e-68	62.7
WP_044036347.1\|690841_692044_+\|capsid	phage major capsid protein	A0A2I4R671	Erysipelothrix_phage	2.8e-108	51.9
WP_044036349.1\|692061_692373_+\|head,tail	phage gp6-like head-tail connector protein	A0A2K5B290	Erysipelothrix_phage	7.9e-39	78.0
WP_044036350.1\|692374_692710_+\|head,tail	head-tail adaptor protein	A0A2K5B291	Erysipelothrix_phage	1.5e-38	69.4
WP_044036352.1\|692702_693134_+	HK97 gp10 family phage protein	A0A2K5B292	Erysipelothrix_phage	7.6e-56	72.0
WP_044036353.1\|693130_693472_+	hypothetical protein	A0A2K5B293	Erysipelothrix_phage	6.9e-36	64.0
WP_044036354.1\|693475_694072_+\|tail	phage tail protein	A0A2K5B294	Erysipelothrix_phage	2.4e-84	79.7
WP_044036356.1\|694086_694470_+	hypothetical protein	A0A2K5B295	Erysipelothrix_phage	8.3e-46	75.6
WP_044036358.1\|694676_697232_+\|tail	phage tail protein	A0A2K5B297	Erysipelothrix_phage	2.4e-104	74.4
WP_044036360.1\|697248_698025_+\|tail	phage tail family protein	A0A2I4R672	Erysipelothrix_phage	1.9e-105	69.0
WP_044036362.1\|698029_700555_+\|tail	phage tail protein	A0A2K5B298	Erysipelothrix_phage	0.0e+00	74.8
WP_044036364.1\|700566_700764_+	hypothetical protein	A0A2K5B299	Erysipelothrix_phage	4.4e-27	84.6
WP_044036366.1\|700756_701320_+	hypothetical protein	A0A2K5B2A0	Erysipelothrix_phage	2.2e-71	68.6
WP_044039686.1\|701346_703785_+	glycosyl hydrolase	A0A2K5B2A1	Erysipelothrix_phage	0.0e+00	80.4
WP_044039687.1\|703860_704283_+\|holin	phage holin family protein	A0A2K5B2A2	Erysipelothrix_phage	1.7e-52	70.6
WP_044036368.1\|704284_705229_+	N-acetylmuramoyl-L-alanine amidase	H7BVK7	unidentified_phage	5.2e-49	48.8
WP_051483658.1\|705358_705574_+	hypothetical protein	A0A2K5B2B1	Erysipelothrix_phage	5.0e-08	50.9
WP_044036370.1\|705634_707197_+	recombinase family protein	A0A2K5B2B2	Erysipelothrix_phage	1.2e-143	51.0
WP_044036372.1\|707196_707622_+	recombinase	A0A2K5B2B3	Erysipelothrix_phage	8.6e-28	51.8
WP_044036373.1\|707614_709180_+	recombinase family protein	A0A2K5B2B4	Erysipelothrix_phage	6.4e-177	61.6
WP_044036375.1\|709345_709570_+	hypothetical protein	NA	NA	NA	NA
WP_044036377.1\|711159_712854_+	methyl-accepting chemotaxis protein	A0A2H4J162	uncultured_Caudovirales_phage	1.1e-09	52.1
WP_044036378.1\|712887_713916_+	hypothetical protein	NA	NA	NA	NA
WP_044036380.1\|713951_714446_+	hypothetical protein	NA	NA	NA	NA
WP_044036382.1\|714432_715314_+	hypothetical protein	NA	NA	NA	NA
WP_044036383.1\|715314_716373_+	hypothetical protein	NA	NA	NA	NA
WP_044036384.1\|716838_717054_+	helix-turn-helix transcriptional regulator	A0A2K5B263	Erysipelothrix_phage	3.3e-12	53.8
WP_044036386.1\|717056_717332_+	hypothetical protein	NA	NA	NA	NA
WP_044036388.1\|717353_718577_+	DNA cytosine methyltransferase	A0A191SB20	Nostoc_phage	2.6e-32	28.4
WP_044036390.1\|718576_719614_+	DNA (cytosine-5-)-methyltransferase	A7XXH6	Thermus_virus	5.9e-30	30.7
WP_051483659.1\|719606_721223_+	AAA family ATPase	Q6DMW9	Streptococcus_phage	4.1e-38	33.3
WP_044036392.1\|721225_722533_+	LlaJI family restriction endonuclease	NA	NA	NA	NA
WP_044036394.1\|722558_724427_+	helix-turn-helix transcriptional regulator	E4ZFJ9	Streptococcus_phage	3.1e-77	29.6
WP_084485464.1\|724848_725394_+	sigma-70 family RNA polymerase sigma factor	NA	NA	NA	NA
WP_041160340.1\|725505_725715_+	hypothetical protein	NA	NA	NA	NA
WP_044036397.1\|725707_726025_+	rRNA biogenesis protein rrp5	A0A2K5B2A7	Erysipelothrix_phage	7.1e-19	53.8
WP_044036399.1\|726021_727149_+	DUF2800 domain-containing protein	A0A2K5B2A8	Erysipelothrix_phage	1.3e-152	69.3
WP_021400962.1\|727154_727715_+	DUF2815 family protein	A0A2K5B2A9	Erysipelothrix_phage	4.1e-70	73.8
WP_044036407.1\|727711_729646_+	DNA polymerase	A0A2K5B2B0	Erysipelothrix_phage	2.4e-250	65.4
WP_044036408.1\|729732_730524_+	phage antirepressor KilAC domain-containing protein	A0A0B5A507	Paenibacillus_phage	2.5e-68	49.1
WP_009052904.1\|730527_730947_+	hypothetical protein	A0A2K5B270	Erysipelothrix_phage	8.2e-39	50.0
WP_044036411.1\|730943_733289_+	phage-like protein	A0A1W6JQ82	Corynebacterium_phage	7.0e-212	46.5
WP_044036413.1\|733546_733828_+	VRR-NUC domain-containing protein	A0A2K5B272	Erysipelothrix_phage	8.8e-29	67.8
WP_044036414.1\|733808_735158_+	DEAD/DEAH box helicase	A0A2K5B273	Erysipelothrix_phage	5.7e-166	72.3
WP_044036416.1\|735162_735621_+	phage-associated protein	NA	NA	NA	NA
WP_009052900.1\|735740_736100_+	HNH endonuclease	A0A2K5B276	Erysipelothrix_phage	9.8e-41	64.4
WP_044039691.1\|736211_736763_+\|terminase	terminase	A0A2K5B277	Erysipelothrix_phage	7.4e-80	76.5
WP_156930503.1\|736780_737962_+	methionine adenosyltransferase	A0A2K5B278	Erysipelothrix_phage	3.7e-177	77.6
WP_044036420.1\|737936_739178_+	DNA modification methylase	A0A2I4R670	Erysipelothrix_phage	9.8e-189	76.0
WP_044036422.1\|739170_741321_+	DNA cytosine methyltransferase	A0A2K9V3X0	Faecalibacterium_phage	1.1e-33	61.5
WP_044036430.1\|741421_742210_+	hypothetical protein	A0A2K5B280	Erysipelothrix_phage	2.8e-48	45.7
WP_019155121.1\|742209_742437_+	DUF4314 domain-containing protein	E4ZFL7	Streptococcus_phage	1.1e-08	41.2
WP_044036445.1\|742572_743472_+	amidoligase family protein	A0A2K9V489	Faecalibacterium_phage	3.3e-53	42.3
WP_044036447.1\|743509_743959_+	gamma-glutamylcyclotransferase	G3MAQ5	Bacillus_virus	3.5e-19	36.9
WP_044036449.1\|743955_744141_+	DUF5049 domain-containing protein	NA	NA	NA	NA
WP_051483841.1\|744220_745819_+\|terminase	terminase large subunit	A0A2K5B285	Erysipelothrix_phage	3.0e-254	80.0
WP_084485359.1\|745837_747094_+\|portal	phage portal protein	A0A2K5B287	Erysipelothrix_phage	1.1e-198	80.9
WP_044036453.1\|747090_747771_+\|protease	Clp protease ClpP	A0A2K5B288	Erysipelothrix_phage	6.5e-78	65.1
WP_044036455.1\|747782_748982_+\|capsid	phage major capsid protein	A0A2I4R671	Erysipelothrix_phage	1.1e-171	74.4
WP_012268679.1\|748997_749216_+	hypothetical protein	A0A2K5B289	Erysipelothrix_phage	1.1e-15	62.2
WP_009052885.1\|749235_749544_+\|head,tail	phage gp6-like head-tail connector protein	A0A2K5B290	Erysipelothrix_phage	2.4e-43	82.4
WP_044036458.1\|749547_749883_+\|head,tail	head-tail adaptor protein	A0A2K5B291	Erysipelothrix_phage	2.3e-31	60.4
WP_009052883.1\|749875_750307_+	HK97 gp10 family phage protein	A0A2K5B292	Erysipelothrix_phage	1.8e-44	61.5
WP_044036460.1\|750303_750657_+	hypothetical protein	A0A2K5B293	Erysipelothrix_phage	5.0e-29	54.5
WP_044036462.1\|750660_751263_+\|tail	phage tail protein	A0A2K5B294	Erysipelothrix_phage	1.2e-80	76.0
WP_044036464.1\|751275_751659_+	hypothetical protein	A0A2K5B295	Erysipelothrix_phage	1.8e-40	67.5
WP_044036465.1\|751873_754432_+	tape measure protein	A0A2K9V3J7	Faecalibacterium_phage	2.0e-39	39.0
WP_044036467.1\|754445_755219_+\|tail	phage tail family protein	A0A2I4R672	Erysipelothrix_phage	1.2e-75	53.5
WP_044036469.1\|755223_757746_+\|tail	phage tail protein	A0A2K5B298	Erysipelothrix_phage	0.0e+00	63.4
WP_009052876.1\|757761_757956_+	hypothetical protein	A0A2K5B299	Erysipelothrix_phage	1.0e-15	58.5
WP_044036472.1\|757965_758547_+	hypothetical protein	A0A2K5B2A0	Erysipelothrix_phage	3.8e-50	54.0
WP_044036474.1\|758543_761015_+	glycosyl hydrolase	A0A2K5B2A1	Erysipelothrix_phage	0.0e+00	69.9
WP_044036476.1\|761097_761508_+\|holin	phage holin family protein	A0A2K5B2A2	Erysipelothrix_phage	5.0e-49	66.2
WP_044036478.1\|761504_762206_+	N-acetylmuramoyl-L-alanine amidase	H7BVK7	unidentified_phage	4.0e-46	42.4
WP_044036480.1\|762338_762569_+	hypothetical protein	A0A2K5B2B1	Erysipelothrix_phage	2.5e-05	42.4
WP_044036482.1\|762621_764181_+	recombinase family protein	A0A2K5B2B2	Erysipelothrix_phage	1.6e-156	53.8
WP_084485360.1\|764150_764615_+	recombinase	A0A2K5B2B3	Erysipelothrix_phage	3.8e-29	48.9
WP_044036485.1\|764604_766170_+	recombinase family protein	A0A2K5B2B4	Erysipelothrix_phage	3.1e-171	60.3

DBSCAN-SWA_3

1234376 : 1242295

Clostridium_phage(16.67%)

protease

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_051483714.1\|1234376_1235627_+	M23 family metallopeptidase	I2E8W3	Clostridium_phage	2.1e-21	56.8
WP_044037199.1\|1235654_1236335_+	cell division ATP-binding protein FtsE	G9BWD6	Planktothrix_phage	1.9e-29	37.9
WP_044037200.1\|1236331_1237252_+	ABC transporter permease	NA	NA	NA	NA
WP_044037201.1\|1237363_1237663_+\|protease	ATP-dependent Clp protease adaptor ClpS	A0A1B1IT64	uncultured_Mediterranean_phage	8.5e-14	46.3
WP_044037203.1\|1237666_1239895_+\|protease	ATP-dependent Clp protease ATP-binding subunit ClpA	A0A223W0B1	Agrobacterium_phage	2.6e-139	38.7
WP_044037204.1\|1239944_1240970_+	glycoside hydrolase family 18 protein	T1QZM9	Chrysodeixis_chalcites_nucleopolyhedrovirus	4.6e-35	32.7
WP_044037206.1\|1241005_1242295_-	glutamate-5-semialdehyde dehydrogenase	A0A1X9I5D4	Streptococcus_phage	7.5e-75	39.4

DBSCAN-SWA_4

1508377 : 1597285

Erysipelothrix_phage(56.45%)

tail,head,integrase,protease,tRNA,portal,terminase,capsid,holin

attL 1500781:1500798|attR 1602167:1602184

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
1500781:1500798	attL	NA	NA	NA	NA
WP_044037611.1\|1508377_1509526_-\|tRNA	tRNA 4-thiouridine(8) synthase ThiI	NA	NA	NA	NA
WP_044037614.1\|1509522_1510665_-	cysteine desulfurase	A0A1X7C038	Faustovirus	3.5e-31	29.0
WP_044037616.1\|1510831_1511692_+	YitT family protein	NA	NA	NA	NA
WP_044037618.1\|1511734_1512118_-	hypothetical protein	NA	NA	NA	NA
WP_044037620.1\|1512279_1512609_-	single-stranded DNA-binding protein	A0A2H4J202	uncultured_Caudovirales_phage	8.5e-15	45.0
WP_044037622.1\|1512749_1513676_+	cysteine synthase A	A0A1X9I5K7	Streptococcus_phage	5.2e-78	51.8
WP_044037623.1\|1513857_1514688_-\|tRNA	tRNA 2-thiocytidine biosynthesis protein TtcA	A0A0U2S5Z2	Escherichia_phage	1.8e-29	33.2
WP_044037625.1\|1514696_1515821_-	cysteine desulfurase	NA	NA	NA	NA
WP_044037627.1\|1515849_1517745_-	ABC-F family ATP-binding cassette domain-containing protein	A0A2K9L0W2	Tupanvirus	2.1e-49	29.1
WP_044037629.1\|1517756_1519592_-	hypothetical protein	B5WZL2	Staphylococcus_phage	3.0e-16	31.3
WP_156930521.1\|1519654_1520749_-	glycosyl hydrolase family 8	NA	NA	NA	NA
WP_051483739.1\|1521378_1522236_-	hypothetical protein	NA	NA	NA	NA
WP_044037631.1\|1522430_1523168_+	hypothetical protein	NA	NA	NA	NA
WP_044037633.1\|1523573_1524809_-	DUF1015 domain-containing protein	NA	NA	NA	NA
WP_044037635.1\|1524786_1525725_-	D-2-hydroxyacid dehydrogenase	A0A1B1IVB5	uncultured_Mediterranean_phage	4.3e-27	31.1
WP_044037636.1\|1525748_1526822_-	alanine--glyoxylate aminotransferase family protein	NA	NA	NA	NA
WP_044037638.1\|1527749_1528649_-	Mph(B) family macrolide 2'-phosphotransferase	NA	NA	NA	NA
WP_044039803.1\|1528677_1529529_-	alpha/beta hydrolase	A0A1J0GNR5	Mycobacterium_phage	4.3e-10	28.7
WP_044037640.1\|1530293_1531865_-	recombinase family protein	A0A2K5B2B4	Erysipelothrix_phage	1.3e-174	61.1
WP_044037642.1\|1531868_1532282_-	recombinase	NA	NA	NA	NA
WP_044037644.1\|1532282_1533845_-	recombinase family protein	A0A2K5B2B2	Erysipelothrix_phage	1.5e-157	54.2
WP_046128486.1\|1533906_1534113_-	hypothetical protein	A0A2K5B2B1	Erysipelothrix_phage	2.0e-06	50.0
WP_044037646.1\|1534343_1535045_-	N-acetylmuramoyl-L-alanine amidase	H7BVK7	unidentified_phage	7.8e-50	43.9
WP_044037648.1\|1535041_1535458_-\|holin	phage holin family protein	A0A2K5B2A2	Erysipelothrix_phage	4.9e-52	69.9
WP_044037650.1\|1535542_1538011_-	glycosyl hydrolase	A0A2K5B2A1	Erysipelothrix_phage	0.0e+00	66.7
WP_044037652.1\|1538007_1538577_-	hypothetical protein	A0A2K5B2A0	Erysipelothrix_phage	2.5e-46	50.8
WP_044037656.1\|1538799_1541319_-\|tail	phage tail protein	A0A2K5B298	Erysipelothrix_phage	2.0e-305	60.4
WP_044037658.1\|1541324_1542098_-\|tail	phage tail family protein	A0A2I4R672	Erysipelothrix_phage	1.3e-74	52.7
WP_044037660.1\|1542113_1544570_-\|tail	phage tail protein	A0A2K5B297	Erysipelothrix_phage	1.7e-27	49.1
WP_044037662.1\|1544778_1545162_-	hypothetical protein	A0A2K5B295	Erysipelothrix_phage	5.0e-43	69.0
WP_044037664.1\|1545164_1545764_-\|tail	phage tail protein	A0A2K5B294	Erysipelothrix_phage	5.6e-81	75.3
WP_044037666.1\|1545766_1546111_-	hypothetical protein	A0A2K5B293	Erysipelothrix_phage	8.2e-29	53.2
WP_044037668.1\|1546107_1546539_-	HK97 gp10 family phage protein	A0A2K5B292	Erysipelothrix_phage	1.8e-44	60.8
WP_044037671.1\|1546531_1546867_-\|head,tail	head-tail adaptor protein	A0A2K5B291	Erysipelothrix_phage	5.0e-31	61.3
WP_044037674.1\|1546870_1547179_-\|head,tail	phage gp6-like head-tail connector protein	A0A2K5B290	Erysipelothrix_phage	1.2e-42	81.4
WP_044037676.1\|1547197_1547416_-	Head fiber protein	A0A2K5B289	Erysipelothrix_phage	1.2e-17	64.9
WP_044037678.1\|1547428_1548622_-\|capsid	phage major capsid protein	A0A2I4R671	Erysipelothrix_phage	5.4e-184	80.6
WP_044037680.1\|1548641_1549331_-\|protease	Clp protease ClpP	Q6DMU1	Streptococcus_phage	1.1e-72	63.2
WP_044037682.1\|1549331_1550576_-\|portal	phage portal protein	A0A2K5B287	Erysipelothrix_phage	1.1e-179	72.1
WP_044037684.1\|1550619_1552224_-\|terminase	terminase large subunit	A0A2K5B285	Erysipelothrix_phage	1.2e-266	83.3
WP_044037686.1\|1552312_1552501_-	DUF5049 domain-containing protein	NA	NA	NA	NA
WP_044037687.1\|1552493_1552952_-	gamma-glutamylcyclotransferase	G3MAQ5	Bacillus_virus	8.2e-16	34.3
WP_044037689.1\|1552990_1553890_-	amidoligase family protein	A0A2K9V489	Faecalibacterium_phage	3.3e-53	42.2
WP_044037691.1\|1554024_1554252_-	DUF4314 domain-containing protein	E4ZFL7	Streptococcus_phage	3.1e-08	39.7
WP_044037693.1\|1554248_1554941_-	hypothetical protein	A0A2K5B280	Erysipelothrix_phage	2.4e-51	51.5
WP_044037695.1\|1555037_1557200_-	DNA cytosine methyltransferase	A0A2K9V3X0	Faecalibacterium_phage	2.4e-33	60.6
WP_044037697.1\|1557192_1558434_-	DNA modification methylase	A0A2I4R670	Erysipelothrix_phage	1.4e-190	77.3
WP_156930522.1\|1558423_1559590_-	methionine adenosyltransferase	A0A2K5B278	Erysipelothrix_phage	4.3e-178	78.2
WP_042357509.1\|1559610_1560162_-\|terminase	terminase	A0A2K5B277	Erysipelothrix_phage	1.3e-79	77.6
WP_044037701.1\|1560273_1560633_-	HNH endonuclease	A0A2K5B276	Erysipelothrix_phage	2.3e-42	66.1
WP_042357512.1\|1560788_1561202_-	DUF1492 domain-containing protein	A0A2K5B275	Erysipelothrix_phage	5.1e-25	43.4
WP_044039804.1\|1561198_1561417_-	hypothetical protein	A0A2K5B274	Erysipelothrix_phage	1.1e-13	55.7
WP_044037703.1\|1561416_1562778_-	DEAD/DEAH box helicase	A0A2K5B273	Erysipelothrix_phage	8.5e-186	78.3
WP_044037705.1\|1562758_1563040_-	VRR-NUC domain-containing protein	A0A2K5B272	Erysipelothrix_phage	3.1e-26	67.8
WP_044037707.1\|1563258_1565625_-	phage-like protein	A0A1W6JQ82	Corynebacterium_phage	2.8e-245	51.8
WP_044037717.1\|1565621_1566056_-	hypothetical protein	A0A2K5B270	Erysipelothrix_phage	1.6e-58	72.9
WP_044037719.1\|1566055_1566808_-	phage antirepressor KilAC domain-containing protein	A0A2H4IZX7	uncultured_Caudovirales_phage	4.6e-64	51.4
WP_039236448.1\|1567195_1567414_-	hypothetical protein	NA	NA	NA	NA
WP_044037723.1\|1567439_1568153_-	GAP family protein	NA	NA	NA	NA
WP_001124455.1\|1568256_1568856_+	TetR/AcrR family transcriptional regulator	NA	NA	NA	NA
WP_044037726.1\|1569145_1571080_-	DNA polymerase	A0A2K5B2B0	Erysipelothrix_phage	3.3e-292	74.5
WP_044037728.1\|1571152_1571701_-	DUF2815 family protein	A0A2K5B2A9	Erysipelothrix_phage	3.2e-91	89.5
WP_044037730.1\|1571693_1572842_-	DUF2800 domain-containing protein	A0A2K5B2A8	Erysipelothrix_phage	2.4e-181	80.2
WP_044037732.1\|1572834_1573158_-	hypothetical protein	A0A2K5B2A7	Erysipelothrix_phage	1.1e-22	60.6
WP_000682242.1\|1573132_1573351_-	hypothetical protein	A0A2I4R673	Erysipelothrix_phage	2.2e-19	61.1
WP_044037736.1\|1573398_1574064_-	sigma-70 family RNA polymerase sigma factor	A0A2K5B267	Erysipelothrix_phage	4.5e-15	31.9
WP_044037738.1\|1574404_1576273_-	helix-turn-helix transcriptional regulator	E4ZFJ9	Streptococcus_phage	3.1e-77	30.1
WP_044037740.1\|1576710_1577859_+	NgoFVII family restriction endonuclease	NA	NA	NA	NA
WP_044037742.1\|1577870_1579730_+	restriction endonuclease CglIIR	NA	NA	NA	NA
WP_051483740.1\|1579744_1580701_+	NgoFVII family restriction endonuclease	NA	NA	NA	NA
WP_044037744.1\|1580743_1581796_-	DNA cytosine methyltransferase	Q6DMX0	Streptococcus_phage	1.5e-20	28.2
WP_039236610.1\|1581800_1582154_-	helix-turn-helix transcriptional regulator	NA	NA	NA	NA
WP_044037746.1\|1582476_1583844_-	23S rRNA (uracil(1939)-C(5))-methyltransferase RlmD	F5CA72	Streptococcus_phi-m46.1-like_phage	5.2e-50	29.7
WP_044037748.1\|1583853_1584114_-	hypothetical protein	NA	NA	NA	NA
WP_044037750.1\|1584296_1584830_+	hypothetical protein	NA	NA	NA	NA
WP_044037752.1\|1584838_1585336_+	hypothetical protein	NA	NA	NA	NA
WP_051483741.1\|1585368_1587030_-	glucosaminidase domain-containing protein	F8WPZ6	Bacillus_phage	5.2e-20	42.8
WP_044037754.1\|1587800_1588406_-	SMI1/KNR4 family protein	NA	NA	NA	NA
WP_044039807.1\|1588560_1588953_+	hypothetical protein	A0A1X9I733	Streptococcus_phage	2.0e-07	31.9
WP_044037756.1\|1589123_1590425_-	pyrimidine-nucleoside phosphorylase	A0A0H3UZD4	Geobacillus_virus	1.8e-129	57.5
WP_044037758.1\|1590430_1591249_-	purine-nucleoside phosphorylase	Q5YBA4	Grouper_iridovirus	1.1e-55	43.4
WP_044037760.1\|1591257_1592073_-	purine-nucleoside phosphorylase	Q5YBA4	Grouper_iridovirus	9.3e-55	38.5
WP_156930523.1\|1592084_1593257_-	phosphopentomutase	NA	NA	NA	NA
WP_044037764.1\|1593325_1594201_-\|integrase	tyrosine-type recombinase/integrase	A0A142F1N9	Bacillus_phage	1.1e-24	27.7
WP_044037766.1\|1594210_1594828_-	stage II sporulation protein M	NA	NA	NA	NA
WP_044037768.1\|1594889_1595408_-	NUDIX hydrolase	A0A2K9VDH1	Lactobacillus_phage	9.6e-13	27.8
WP_044037770.1\|1595614_1597285_-	biosynthetic-type acetolactate synthase large subunit	A0A0P0CDR3	Ostreococcus_lucimarinus_virus	9.2e-57	29.0
1602167:1602184	attR	NA	NA	NA	NA

DBSCAN-SWA_5

2359618 : 2370101

Prochlorococcus_phage(28.57%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_044039013.1\|2359618_2361112_-	bifunctional phosphoribosylaminoimidazolecarboxamide formyltransferase/IMP cyclohydrolase	E3SNU8	Prochlorococcus_phage	3.1e-32	43.2
WP_084485417.1\|2361200_2361449_-	four helix bundle protein	NA	NA	NA	NA
WP_044039014.1\|2361438_2362056_-	phosphoribosylglycinamide formyltransferase	M4QRX9	Synechococcus_phage	5.5e-23	35.4
WP_044039015.1\|2362043_2363048_-	phosphoribosylformylglycinamidine cyclo-ligase	Q58MH8	Prochlorococcus_phage	3.1e-68	46.9
WP_044039016.1\|2363072_2364479_-	amidophosphoribosyltransferase	A0A1B1ISH6	uncultured_Mediterranean_phage	1.8e-58	34.7
WP_044039017.1\|2364480_2365194_-	phosphoribosylaminoimidazolesuccinocarboxamide synthase	A0A0E3FUQ7	Synechococcus_phage	1.5e-45	43.0
WP_044039018.1\|2365193_2365673_-	5-(carboxyamino)imidazole ribonucleotide mutase	A0A2P0VNU7	Tetraselmis_virus	2.1e-30	46.2
WP_044039019.1\|2365726_2366095_-	four helix bundle protein	NA	NA	NA	NA
WP_044039020.1\|2366339_2370101_-	phosphoribosylformylglycinamidine synthase	A6N228	Microbacterium_phage	5.9e-27	24.4

DBSCAN-SWA_6

2619281 : 2627221

Enterobacteria_phage(33.33%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_156930578.1\|2619281_2621237_-	glycosyltransferase	R9S8I6	Prochlorococcus_phage	2.3e-06	23.1
WP_044039334.1\|2621618_2622359_-	ABC transporter ATP-binding protein	A0A2H4PQG7	Staphylococcus_phage	8.9e-12	28.6
WP_044039335.1\|2622377_2623154_-	ABC transporter permease	NA	NA	NA	NA
WP_044039336.1\|2623251_2623809_-	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	9.9e-48	51.4
WP_044039337.1\|2623827_2624883_-	dTDP-glucose 4,6-dehydratase	K7QJG5	Escherichia_phage	1.1e-76	45.0
WP_044039338.1\|2624900_2625767_-	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	2.0e-103	63.9
WP_044039339.1\|2625871_2627221_-	phosphoglucosamine mutase	A0A127AWJ1	Bacillus_phage	3.6e-27	26.4

Anti-CRISPR protein detection

Acr ID	Acr position	Acr size	Homology with known anti	Neighbor HTH/AcRanker	Neighbor Aca	In prophage	Protospacer in prophage

Overview of predicted results

Overview of the results

Cas Category Instructions

Results visualization

1. NZ_HG917869

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection

2. NZ_HG917868

Click the left colored region to show detailed information

CRISPR-Cas detection and classification

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Click the colored protein region to show detailed information

Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection