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_CP011306	Stenotrophomonas maltophilia strain ISMMS2R chromosome, complete genome	2 crisprs	csa3,DEDDh,cas3,WYL,Cas9_archaeal,DinG,PD-DExK	0	0	3	0

Results visualization

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CRISPR-Cas detection and classification

Crispr_ID: NZ_CP011306_1

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP011306_1

412596-412687

Orphan

Consensus_repeat	Method
CCCCGGCTGCCGATGCCGCCGCC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP011306_1

>merge|NZ_CP011306|1|412596-412687|CRISPRCasFinder
CCAAGCCGGCCGACACCGCTGCCCCGGCTGCCGATGCCGCCGCCCCGGCCACCACCGAGCAGGCCGCCACCCCGGCTGCCGATGCCGCCGCC

>NZ_CP011306|1|1|412596-412687|CRISPRCasFinder
CCAAGCCGGCCGACACCGCTGCC	CCGGCTGCCGATGCCGCCGCCCCGGCCACCACCGAGCAGGCCGCCA
CCCCGGCTGCCGATGCCGCCGCC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011306.1\|WP_049428616.1\|424748_425954_+\|nucleoside-2-deoxyribosyltransferase	unknown	unknown	gnl\|CDD\|226140
NZ_CP011306.1\|WP_019660853.1\|416099_418787_+\|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	unknown	unknown	gnl\|CDD\|236500
NZ_CP011306.1\|WP_053442438.1\|414136_414934_-\|siderophore-interacting-protein	unknown	unknown	gnl\|CDD\|99790
NZ_CP011306.1\|WP_049428619.1\|425950_426556_+\|7-cyano-7-deazaguanine-synthase	unknown	unknown	gnl\|CDD\|223676
NZ_CP011306.1\|WP_049454461.1\|419767_420532_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_053442430.1\|401374_402736_+\|VOC-family-protein	unknown	unknown	gnl\|CDD\|319958
NZ_CP011306.1\|WP_049454459.1\|422367_423651_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_010484198.1\|407787_408348_-\|queuosine-precursor-transporter	unknown	unknown	gnl\|CDD\|224652
NZ_CP011306.1\|WP_053442437.1\|413503_413905_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_053442439.1\|414993_415554_-\|helix-turn-helix-transcriptional-regulator	unknown	unknown	gnl\|CDD\|224609
NZ_CP011306.1\|WP_053442433.1\|408423_408939_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_053442434.1\|409512_410364_-\|DUF2145-domain-containing-protein	unknown	unknown	gnl\|CDD\|227071
NZ_CP011306.1\|WP_053442436.1\|411857_412448_+\|malonic-semialdehyde-reductase	unknown	unknown	gnl\|CDD\|180040
NZ_CP011306.1\|WP_053442432.1\|404709_407505_+\|bifunctional-[glutamate--ammonia-ligase]-adenylyl-L-tyrosine-phosphorylase/[glutamate--ammonia-ligase]-adenylyltransferase	unknown	unknown	gnl\|CDD\|236836
NZ_CP011306.1\|WP_053442435.1\|410771_411731_-\|mitochondrial-fission-ELM1-family-protein	unknown	unknown	gnl\|CDD\|377637
NZ_CP011306.1\|WP_065428068.1\|424398_424719_+\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_053442431.1\|402831_404346_-\|acetyl-CoA-hydrolase/transferase-family-protein	unknown	unknown	gnl\|CDD\|274588
NZ_CP011306.1\|WP_053443782.1\|408971_409493_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_148563069.1\|421574_422075_-\|hypothetical-protein	unknown	unknown	unknown
NZ_CP011306.1\|WP_049443513.1\|410412_410643_-\|hypothetical-protein	unknown	unknown	unknown

Protein	Function_ID	Function_description	E-value
NZ_CP011306.1\|WP_049428616.1\|424748_425954_+\|nucleoside-2-deoxyribosyltransferase	gnl\|CDD\|226140	COG3613, COG3613, Nucleoside 2-deoxyribosyltransferase [Nucleotide transport and metabolism].	8.22481e-18
NZ_CP011306.1\|WP_053442438.1\|414136_414934_-\|siderophore-interacting-protein	gnl\|CDD\|99790	cd06193, siderophore_interacting, Siderophore interacting proteins share the domain structure of the ferredoxin reductase like family. Siderophores are produced in various bacteria (and some plants) to extract iron from hosts. Binding constants are high, so iron can be pilfered from transferrin and lactoferrin for bacterial uptake, contributing to pathogen virulence. Ferredoxin reductase (FNR), an FAD and NAD(P) binding protein, was intially identified as a chloroplast reductase activity, catalyzing the electron transfer from reduced iron-sulfur protein ferredoxin to NADP+ as the final step in the electron transport mechanism of photosystem I. FNR transfers electrons from reduced ferredoxin to FAD (forming FADH2 via a semiquinone intermediate) and then transfers a hydride ion to convert NADP+ to NADPH. FNR has since been shown to utilize a variety of electron acceptors and donors and has a variety of physiological functions including nitrogen assimilation, dinitrogen fixation, steroid hydroxylation, fatty acid metabolism, oxygenase activity, and methane assimilation in a variety of organisms. FNR has an NAD(P)-binding sub-domain of the alpha/beta class and a discrete (usually N-terminal) flavin sub-domain which vary in orientation with respect to the NAD(P) binding domain. The N-terminal moeity may contain a flavin prosthetic group (as in flavoenzymes) or use flavin as a substrate. Because flavins such as FAD can exist in oxidized, semiquinone (one-electron reduced), or fully reduced hydroquinone forms, FNR can interact with one and two electron carriers. FNR has a strong preference for NADP(H) vs NAD(H).	1.20402e-88
NZ_CP011306.1\|WP_053442430.1\|401374_402736_+\|VOC-family-protein	gnl\|CDD\|319958	cd16348, VOC_YdcJ_like, uncharacterized metal-dependent enzyme similar to Shigella flexneri YdcJ. The vicinal oxygen chelate (VOC) superfamily is composed of structurally related proteins with paired beta.alpha.beta.beta.beta motifs that provide a metal coordination environment with two or three open or readily accessible coordination sites to promote direct electrophilic participation of the metal ion in catalysis. VOC domain is found in a variety of structurally related metalloproteins, including the bleomycin resistance protein, glyoxalase I, and type I ring-cleaving dioxygenases. A bound metal ion is required for protein activities for the members of this superfamily. A variety of metal ions have been found in the catalytic centers of these proteins including Fe(II), Mn(II), Zn(II), Ni(II) and Mg(II). The protein superfamily contains members with or without domain swapping. The proteins of this family share three conserved metal binding amino acids with the type I extradiol dioxygenases, which shows no domain swapping.	0
NZ_CP011306.1\|WP_010484198.1\|407787_408348_-\|queuosine-precursor-transporter	gnl\|CDD\|224652	COG1738, yhhQ, Uncharacterized member of the PurR regulon [General function prediction only].	9.75536e-33
NZ_CP011306.1\|WP_049428619.1\|425950_426556_+\|7-cyano-7-deazaguanine-synthase	gnl\|CDD\|223676	COG0603, COG0603, Predicted PP-loop superfamily ATPase [General function prediction only].	9.42639e-38
NZ_CP011306.1\|WP_019660853.1\|416099_418787_+\|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type	gnl\|CDD\|236500	PRK09405, aceE, pyruvate dehydrogenase subunit E1; Reviewed.	0
NZ_CP011306.1\|WP_053442434.1\|409512_410364_-\|DUF2145-domain-containing-protein	gnl\|CDD\|227071	COG4727, COG4727, Uncharacterized protein conserved in bacteria [Function unknown].	3.13716e-86
NZ_CP011306.1\|WP_053442436.1\|411857_412448_+\|malonic-semialdehyde-reductase	gnl\|CDD\|180040	PRK05365, PRK05365, malonic semialdehyde reductase; Provisional.	2.64484e-126
NZ_CP011306.1\|WP_053442432.1\|404709_407505_+\|bifunctional-[glutamate--ammonia-ligase]-adenylyl-L-tyrosine-phosphorylase/[glutamate--ammonia-ligase]-adenylyltransferase	gnl\|CDD\|236836	PRK11072, PRK11072, bifunctional [glutamate--ammonia ligase]-adenylyl-L-tyrosine phosphorylase/[glutamate--ammonia-ligase] adenylyltransferase.	0
NZ_CP011306.1\|WP_053442435.1\|410771_411731_-\|mitochondrial-fission-ELM1-family-protein	gnl\|CDD\|377637	pfam06258, Mito_fiss_Elm1, Mitochondrial fission ELM1. In plants, this family is involved in mitochondrial fission. It binds to dynamin-related proteins and plays a role in their relocation from the cytosol to mitochondrial fission sites. Its function in bacteria is unknown.	5.54154e-92
NZ_CP011306.1\|WP_053442431.1\|402831_404346_-\|acetyl-CoA-hydrolase/transferase-family-protein	gnl\|CDD\|274588	TIGR03458, Propionyl-CoA:succinate_CoA_transferase, succinate CoA transferase. This family of CoA transferases includes enzymes catalyzing at least two related but distinct activities. The E. coli YgfH protein has been characterized as a propionyl-CoA:succinate CoA transferase where it appears to be involved in a pathway for the decarboxylation of succinate to propionate. The Clostridium kluyveri CAT1 protein has been characterized as a acetyl-CoA:succinate CoA transferase and is believed to be involved in anaerobic succinate degradation. The propionate:succinate transferase activity has been reported in the propionic acid fermentation of propionibacterium species, where it is distinct from the coupled activities of distinct nucleotide-triphosphate dependent succinate and propionate/acetate CoA transferases (as inferred from activity in the absence of NTPs). The family represented by this model includes a member from Propionibacterium acnes KPA171202 which is likely to be responsible for this activity. A closely related clade not included in this family are the Ach1p proteins of fungi which are acetyl-CoA hydrolases. This name has been applied to many of the proteins represented by this model, possibly erroneously.	0
NZ_CP011306.1\|WP_053442439.1\|414993_415554_-\|helix-turn-helix-transcriptional-regulator	gnl\|CDD\|224609	COG1695, COG1695, Predicted transcriptional regulators [Transcription].	1.14062e-17

>NZ_CP011306.1|WP_053442436.1|411857_412448_+|malonic-semialdehyde-reductase
MSHALDAAALDQLFRTARTQNAFLDKPVPESLLKELYDLVKWGPTAANTTPARFVFVTSKDAKDKLAPALSEGNLAKTMAAPVTVIIGFDLDFHEKLPYLFPHTDAKAWFDGPQEGRHEAAVRNGSLQGAYLILAARALGLDAGPMSGFDPAKVDEAFFAGTSIKSNFLVNLGYGDSAGLFPRLPRLSFDEAARIA
>NZ_CP011306.1|WP_053442435.1|410771_411731_-|mitochondrial-fission-ELM1-family-protein
MVKRSSAPWTVTDGRAGNVRQAVALASALRQGTHRPLVLQPRAPWRWLSPRRLPGDVNGYGEAFATLAADAPALAIGCGRQAAGALRVLRARGSQVVQILDPRIGARHWDVVVVPEHDALRGSNVLTLLGSLNPVDDDWLAWGRAAFAGFSTLPGPRTALLVGGPTPLAPWDETSMVGVFRALADQIHSEGGSLLATTSRRTPPALAEILRATFADLPHVIWGDGGDGTNPYGGLLGWANRVVVSPDSVNLLSEACATRMPVMVALADTAQGRLARFQQQLRERGRLQTHWLDWQCDRIEPLRETARVAAEVKQRLALG
>NZ_CP011306.1|WP_049443513.1|410412_410643_-|hypothetical-protein
MRTLLLLPLALLAACSTAPTELDPISYQCQQQLDAYREQPALRDPKTGERPPLPIAPISDACDRELKRKGVDRPLR
>NZ_CP011306.1|WP_053442434.1|409512_410364_-|DUF2145-domain-containing-protein
MDRFSRLPRAALLIASLLATAPAWANSTECRERYPSVASQAAMLDVAWTTAERLDALPDVDVVVAARGGQDLSRYGLRHSHLAFLLREDDGRWRAMHLLNRCKTDSSQLYHEGLGNFVGESGGHTDLRIGVPAAPLRAALKAMLVSPSIQPKALHETRYNAVAYPFATDYQNSNQWVLEVLAAAMAQAEGAPAIVKREQAQQWLRQQKYQPSVLHIGLGKRVGARLFVANATTTDHPAGERISGNYSVVTVESVFDFLHQRSQLQQELVIPHVPVAGAAAATP
>NZ_CP011306.1|WP_053443782.1|408971_409493_-|hypothetical-protein
MRTLPAFLMPMLMLMLMLIVASLAWSTAAHAERRIVIIHDPGPQGPSLEMSSQMVNSARAAAAKEAQDAADAGQPLARPQQIKLPQMQVSAIATTVDGRREVLLRDANDPQNTASMQYPRGIGDPAVQFTVGQTVNFEPTGNDQGWQLKDNQGRPLEYLPEATGPRDIFDTRR
>NZ_CP011306.1|WP_053442433.1|408423_408939_-|hypothetical-protein
MFRCLRVPATALLLSALVVPTVHAGAAPQLNSGQTSVLVTSLIVLSIPLATSMGLAELSKAPFKASERNGKVAARTPAVPLPPMEVKQVATTPAGDRQVHLQVPGKADQTATLQWPAAAGDDPVAGFVVGQQVHFDPTEAGAGWTVKSAQGQALAYVPTAYAAGDVMSEVL
>NZ_CP011306.1|WP_010484198.1|407787_408348_-|queuosine-precursor-transporter
MSVRPAPVFAPLTPRALVLAVLAMGAVVLLSNVLVQYPINDWLTWGAFSYPVAFLVSNLINRRFGPGPARRVAWIGFAVAVLLSIWVATPRIAIASCSAFIVAQLLDITVFDRLRRGSWWRAPMVATTCSATVDTTIFWSIAFAGSALPWVSWAAGDLAVKLAIGVCLLAPFRALLWKMAPLRATS
>NZ_CP011306.1|WP_053442432.1|404709_407505_+|bifunctional-[glutamate--ammonia-ligase]-adenylyl-L-tyrosine-phosphorylase/[glutamate--ammonia-ligase]-adenylyltransferase
MTLAPADLPASLQPLVDRALARLAQVLPEPVPADLLPLLTRLAVTSDFALDTLVRQPALVAQLAAPGCPPIPAPVLDPLQPSDWPAQLRRWRTAMSTRLIWRDLAGLDDVAQTLAGATTLAEDCLRLALDALQQEFAQRHGVVRDGEGAPQQLVVFGLGKLGGGELNFSSDIDLVYAYPHGGESDGPRALAAEEYFARLGQRLAKLLDETTVDGFSHRVDLRLRPFGSAGRVALSFAAMDQYFQREGRDWERYAWLKARAVAGDIEAGEAWLQTLRPFVYRRYLDFTALDGLREMKAAITAEVARRELHEDIKRGAGGIREIEFLCQALQLIRGGREPALRERRLLVALDTLVAAGQIAPEDGSALREAYLFLRRLENRLQMLRDAQTHVLPSDALDRERIAVGLGYPDWDVLRAALAEQQQRVSTEFAALLAPRKGQAAPDALANYWRSLPEGSNAPLLAEAGFLDANGADQSLRDFAQGTGVKSLSDAARARLDRVLPALLHAATRSPQPDAALKRVLGLLQAVLRRTSYLALLDEQPSALARLVDVLARSALLAERLAAYPLLLDELLDVRVSGPMPDAAGMLAECQQVLAVEDPESALRWLNETRLALSFRMAMATLDGRQGAVDSTRQLAELAQAVVVTVLAMAEADMRAAHGEIPGGRFAIIGYGSLGGLELGFGSDLDLVFLHDNPAGVDASDGARPLEPGRWYARLAQKVMALLGAVTAAGRLYDIDVRLRPDGGKGSLVSSLASYTEYQRERAWTWEHQALVRARGVAGDASLLADFEQVRAQTLGRERDPATLYADVLKMRGRMRTELDRSDAARLDLKQGAGGVVDLEFLLQTGVLARSAQHAALLQPRDTPSLIDALAVAGFLPEDTAQALHGAHATLLEVGLVCTLDRRPRLAPTTPAIEEACAAITAACRAAALPFA
>NZ_CP011306.1|WP_053442431.1|402831_404346_-|acetyl-CoA-hydrolase/transferase-family-protein
MSVDRIANARLRDRVVSAEAAAALIQPGETVAMSGFTGSGYPKAVPVELARRIESVHAQGQPFQISLMTGASTAPELDGALAKADGIAMRMPFQSDPDARNRINEGRLDYIDIHLSHVAQHVWFGFYGEIDTAVIEVSAIHEDGSLVPSTSVGNNKTWLDLAKKVIVEVNEWQPAGVDGMHDIYYGTALPPHRKPIPLVNANDRIGDTALRCDPDKIVAVVRTNGPDRNSPFSPIDATSEQIASHLIEFLQHEVKKGRLPPNLLPLQSGVGNIPNAVLAGLAKSGFRDLAAFTEVIQDGMLDLLRDGVLSYASCTGFALSPQANETFKENIDFYRERIIMRTQEISNHPELVRRLGCIGMNGMIEVDIYGNVNSTHVMGTRIMNGIGGSGDFARNGFLSAFLSPSTAKNGTISAIVPMASHVDHTEHDVSVIVTEQGLADLRGLTPRKRAQVLIDNCAHPDFRPQLQDYFDRASRESYGKHTPHLLPEALSWHQRWLDTGTMKG
>NZ_CP011306.1|WP_053442430.1|401374_402736_+|VOC-family-protein
MSASFVSPDVIRRLFAQAMSRMYRTEVPLYGTLVELVERINAQVLAQDPALAAQLQRNDERARLDEERHGAIRVGTVQELATLRRLFAVMGMYPVGYYDLSVAGVPVHSTAFRPLTGAALAQNPFRVFTSLLRLELIEDEALRAESAKILARRRIFTEGALALIDQAERDGGLAQADAERFVEQALETFRWHGDATVDLPTYHALHNAHRLVADVVSFRGPHINHLTPRTLDIDAAQAAMIEHGMAAKAVIEGPPRRACPILLRQTSFKALEEAVHFPDAEGGDAGTHTARFGEIEQRGLALTPKGRALYDQLLSQARDAGGEGSTGGDYGQRLQAVFASFPDDHDTLRQEGLGYYRYQLTDAGRAAPERVADLPAEVLVAAGLATADPIVYEDFLPVSAAGIFQSNLGGEEQRAYAAHANREAFEQALGVAVNDEFEIYERLQAESLAALRA
>NZ_CP011306.1|WP_053442437.1|413503_413905_-|hypothetical-protein
MAKLTLASVDALRTRFTDDAACDAALAAFADTVALRTPLRELVEAQHRYLQAEFEVAQVADVLRRDQKYAPVGRPSVHIVQLRKQQAATKQAALIARQVVAQAAQTFVRVSGMTVKAKQSPSETCVAWLGALR
>NZ_CP011306.1|WP_053442438.1|414136_414934_-|siderophore-interacting-protein
MTEHNNTRLRLDVRFRELTVLRTEEVTPHMRRIVLGGDALAGFDSPGADDHIKLFFPNAAGEMVLPVLTAEGRSYPDGKEPSPARDYTPRWWDHETGELAIDFVLHHQGIAGPWAERAQPGDVLVIGGPRGSFVVADTYDAYVLIGDETALPAIARWLDVLPEDAEVQAFIEVSDEAERQDLPQYENVRIHWLERNGFPAATSTLLEDMLTDFEAPEGDVFYWIATESRRARMMRKFIEGHLGVPRDWIRSTGYWKAHPDETDGD
>NZ_CP011306.1|WP_053442439.1|414993_415554_-|helix-turn-helix-transcriptional-regulator
MSRSPSPRARSIDSAVPRRNGQPRVLSRGDLRLLVLALIGEQPRHGYELMQLISNQFMQAYTPSAGTMYPLLASFEQAGWIEAEEVDGKRIFRITAAGEFELKVQRTQVRLAQRRAFDRAREITKASLPAPLACALREFKRALVHHHGRWAEGEADEVAALLTRASALLNGTAGSEQPPLSTTQPD
>NZ_CP011306.1|WP_019660853.1|416099_418787_+|pyruvate-dehydrogenase-(acetyl-transferring),-homodimeric-type
MNWLNEVLNNDPNPVETQEWIESLKAVIDVEGSERAHQLLEGMVELTRRSGAYLPFSPTTEYVNTIEPQLEAKSPGNAELEWRIRSIIRWNAMATVVRANRKPGDLGGHIASFASGATLYDVGFNHFWRAPSENHPGDLLFIQGHSAPGIYARSFLEGRISEEQLDKFRMEVDGGGLSSYPHPWLMPDYWQTPTVSMGLGPLAAIYQAQFMRYLENRGLIEKSDRKVWCFIGDGESDEPETLGAIALAGREGLDNLIFVVNCNLQRLDGPVRGNGKIIQELEGVFRGGGWNVIKLLWGGYWDALLAKDTNGVLKKLMMETVDGEYQNCKAFGGAYTREHFFGKYPETAAMVAGLSDDDIWRLNRGGHDPHKVYAAYHQAVNTKGMPTVILAKTVKGYGMGSAGEALNPTHQTKKLDDEAVRHFRDRFNIPVTDAQLADGQVPFYHPGPDSPEVQYLQERRAALGGYLPQRRRKADKTFVAPKLEAYERLLKSSGERSYSTTMAFVQSLNITLRDKELGPHIVPIVADEARTFGMEGLFRQIGIYAPFGQKYKPVDADQLMFYREDQSGQVLQQGISEPGAISSWMAAGTSYSVSNVPMLPFYIYYSMFGFQRVGDIAWQAADMRTRGFLLGGTAGRTTLNGEGLQHEDGFSHLVAGGIPNVRSYDPTFGFEVTVILQHGTKRMMEDQVDEYYYVTLMNENYTHPEMPEGAAEGIVKGMYLLTDAGKPKKGELRVQLLGSGTILREAIAAAELLDKDFGVTADIWSCPSFNELRRDGFDVERANRLHPEGEQRKAYVTELLEGRQGPAIAATDYVRAYADQIRAFVPMSYTVLGTDGFGRSDTRANLRRFFEVDRYYIAHAAIAALAKEGKMTAKDVARAIKQYKIDPEKANPVGV
>NZ_CP011306.1|WP_049454461.1|419767_420532_-|hypothetical-protein
MPDDALQIVYIVRGFHRLLYVPPPQWPGCHFEQGENLDVTLRIAQTEVAPGTDLDTLIALTDARMQQLVLAWELSLGQRLQLRRLHVSLPRLPVMKGGATSQDGVSFSDRCEATIIHAAAPVQMPQIPLAAERWVRTLAEAGDFGGYVEEQLRRHFLIIEELWETYASRFDNADQAKCKEIRCVRNFVSHYDCTREPVLGFIIINLPSAEVQRSSHRAVRFDRTSQEHRTFVARFAVDSERIARRLVELAIVDL
>NZ_CP011306.1|WP_148563069.1|421574_422075_-|hypothetical-protein
MKASLGPGVAALGVAVAAAQWHTNRVKLRLDSYDRRLVVYKATVALLNAMQEEISTRRGPSARLKNGQPSKAYLLLPREVVSNFESGLLEAPFLFDKDVAIFLHYIDRHRTMIHMYANHCSKIDPEAHETHRADFERLKDSEEGVDRARSMVQQRFAPYLRLSRRL
>NZ_CP011306.1|WP_049454459.1|422367_423651_-|hypothetical-protein
MFNTHEDEIEMDLNWLKKQDSCPLAVELTAKIEAIDLEKLELPRRRLLVGFVHVLADEVKAMLDLGAKDYDSNEVARMTDVIGGTTLARACQAPITKRQPGEDLRDKIAEETNKVTLASEQTGAGHTARLMAKWAKSAASDISKNESFGSWHLLLLCYAHFLICMESRCSRKSSSPPTADLRARLNACLDLMRQLHRKSDAIEADEASIEAELAYENQMLGGFIFQLGYASGAAGTPVPVNMFQQTPNDGCFGDLVAGNARCLAIEFKREAKSIQTEAEKWTSEALASLINETNLVSQSLKCHLLCYGNADGQTMSFSSMLYATAIGASEEVVEMSGDEIIACILGKAVNGELLKNSTMGLPPRQLERYLRSLAHIRDSSKGGGKATWLALAIDEKGFHFRIAATLSALIEPTTAPGVKVSAGMTRG
>NZ_CP011306.1|WP_065428068.1|424398_424719_+|hypothetical-protein
MSGSGGGSFGGGGVQEIACDRLSFETQLSSPKPSVVAGINVGDVLFVAIEQQLAAQVVVIKHGNQVAGGITSPKMSRLLECMRQGTQYQATVLSKAGGQVTIRISP
>NZ_CP011306.1|WP_049428616.1|424748_425954_+|nucleoside-2-deoxyribosyltransferase
MLTIVGGIYREVCLRPQWDEVYGSAGRAASAVSRLGGQVTLHGYLDAGLQPILECRAADEGFGLSIAPLPRSASFHYSHGLSVPWIQQPERQSPLSVKADHVLRFGMLESTAIVDAEYAVFDPQNVTGTEAFGANGSKAQHLALVLNLTEARSLLQRFDLTSEQMAAELASQHGAEVVVLKMGPKGALVHHEGGTECVPAYATSRVWKIGSGDQFAANFAYAWMEERRSPFEAADRASRSAAFYAQHRRYPDVGELDAFAPAPLRLSDTYLQGRAPTVYLAGPFFTLGQLWVVEQARNCLLDMGLDVFSPYHDVGPGPAEMVVGKDIEGIHRSQVMLAIADGLDSGTVFEVGYARSRGIPVVMYAENVSPEDLKMMEGTDCFLRDDFVSAIYQTAWNGVCV
>NZ_CP011306.1|WP_049428619.1|425950_426556_+|7-cyano-7-deazaguanine-synthase
MKSALLLSGGMDSIALAWWKRPDMAFTVDYGQLAAAAEVVAARAVSERLQVPHYIIRFDGRELGSGDMAGSTPDVHAPASDWWPYRNQLLLTLAGMKAISLGAQRLWVGTVASDGSHQDGTPRFVDLISKLMQSQEGGMVVEAPAIQLQTSDLVRTSGIPRDLLSWAHSCHKASVACGNCRGCNKYFQVWHELEGYVGDAG

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Crispr_ID: NZ_CP011306_2

CRISPR_ID

CRISPR_location

CRISPR_type

Repeat_type

Spacer_info

Cas_protein_info

CRISPR-Cas_info

NZ_CP011306_2

907926-908014

Orphan

Consensus_repeat	Method
TGGTAGGTGTCGACCTTGGTCGACAC	CRISPRCasFinder

1 spacers

The CRISPR arrays of NZ_CP011306_2

>merge|NZ_CP011306|2|907926-908014|CRISPRCasFinder
TGGTAGGTGTCGACCTTGGTCGACACTGATCCAATCCCGATCAGAATCGGTGCCTGCCGCTCCTGGTAGGTGTCGACCTTGGTCGACAC

>NZ_CP011306|2|2|907926-908014|CRISPRCasFinder
TGGTAGGTGTCGACCTTGGTCGACAC	TGATCCAATCCCGATCAGAATCGGTGCCTGCCGCTCC
TGGTAGGTGTCGACCTTGGTCGACAC

Protein	Signature genes	Signature genes Name	Protein_function
NZ_CP011306.1\|WP_010483920.1\|906127_907654_-\|exopolyphosphatase	unknown	unknown	gnl\|CDD\|223326
NZ_CP011306.1\|WP_019337026.1\|908020_910108_-\|polyphosphate-kinase-1	unknown	unknown	gnl\|CDD\|235469
NZ_CP011306.1\|WP_004154542.1\|914432_914825_+\|carboxymuconolactone-decarboxylase-family-protein	unknown	unknown	gnl\|CDD\|223672
NZ_CP011306.1\|WP_053442568.1\|899589_902514_-\|TonB-dependent-receptor	unknown	unknown	gnl\|CDD\|238657
NZ_CP011306.1\|WP_173581532.1\|912356_914057_-\|M48-family-metalloprotease	unknown	unknown	gnl\|CDD\|227122
NZ_CP011306.1\|WP_010483932.1\|895627_896881_+\|zinc-dependent-metalloprotease	unknown	unknown	gnl\|CDD\|372673
NZ_CP011306.1\|WP_053442566.1\|893944_895402_-\|DUF2235-domain-containing-protein	unknown	unknown	gnl\|CDD\|370774
NZ_CP011306.1\|WP_049412624.1\|893050_893875_+\|ferritin-like-domain-containing-protein	unknown	unknown	gnl\|CDD\|377292
NZ_CP011306.1\|WP_053442567.1\|898300_899446_-\|glycosyltransferase-family-1-protein	unknown	unknown	gnl\|CDD\|340842
NZ_CP011306.1\|WP_019336562.1\|916348_917092_+\|cysteine-hydrolase	unknown	unknown	gnl\|CDD\|238245
NZ_CP011306.1\|WP_005415460.1\|910112_911444_-\|phosphate-regulon-sensor-histidine-kinase-PhoR	unknown	unknown	gnl\|CDD\|274368
NZ_CP011306.1\|WP_053442570.1\|917145_918054_+\|LysR-family-transcriptional-regulator	unknown	unknown	gnl\|CDD\|176114
NZ_CP011306.1\|WP_053442569.1\|902851_905821_-\|TonB-dependent-receptor	unknown	unknown	gnl\|CDD\|369481
NZ_CP011306.1\|WP_053442565.1\|891574_893041_+\|amidophosphoribosyltransferase	unknown	unknown	gnl\|CDD\|236427
NZ_CP011306.1\|WP_053442571.1\|918079_918829_+\|sulfite-exporter-TauE/SafE-family-protein	unknown	unknown	gnl\|CDD\|376667
NZ_CP011306.1\|WP_019336563.1\|915143_916148_+\|isocitrate-dehydrogenase	unknown	unknown	gnl\|CDD\|181606
NZ_CP011306.1\|WP_010483930.1\|896968_897715_-\|UDP-2,3-diacylglucosamine-diphosphatase	unknown	unknown	gnl\|CDD\|235420
NZ_CP011306.1\|WP_010483913.1\|914145_914436_+\|glutaredoxin-3	unknown	unknown	gnl\|CDD\|274017
NZ_CP011306.1\|WP_010483928.1\|897780_898320_-\|phosphatase-PAP2-family-protein	unknown	unknown	gnl\|CDD\|239486
NZ_CP011306.1\|WP_005408258.1\|911550_912240_-\|phosphate-regulon-transcriptional-regulator-PhoB	unknown	unknown	gnl\|CDD\|131209

Protein	Function_ID	Function_description	E-value
NZ_CP011306.1\|WP_010483920.1\|906127_907654_-\|exopolyphosphatase	gnl\|CDD\|223326	COG0248, GppA, Exopolyphosphatase [Nucleotide transport and metabolism / Inorganic ion transport and metabolism].	3.76616e-153
NZ_CP011306.1\|WP_019337026.1\|908020_910108_-\|polyphosphate-kinase-1	gnl\|CDD\|235469	PRK05443, PRK05443, polyphosphate kinase; Provisional.	0
NZ_CP011306.1\|WP_004154542.1\|914432_914825_+\|carboxymuconolactone-decarboxylase-family-protein	gnl\|CDD\|223672	COG0599, COG0599, Uncharacterized homolog of gamma-carboxymuconolactone decarboxylase subunit [Function unknown].	1.37132e-17
NZ_CP011306.1\|WP_053442568.1\|899589_902514_-\|TonB-dependent-receptor	gnl\|CDD\|238657	cd01347, ligand_gated_channel, TonB dependent/Ligand-Gated channels are created by a monomeric 22 strand (22,24) anti-parallel beta-barrel. Ligands apparently bind to the large extracellular loops. The N-terminal 150-200 residues form a plug from the periplasmic end of barrel. Energy (proton-motive force) and TonB-dependent conformational alteration of channel (parts of plug, and loops 7 and 8) allow passage of ligand. FepA residues 12-18 form the TonB box, which mediates the interaction with the TonB-containing inner membrane complex. TonB preferentially interacts with ligand-bound receptors. Transport thru the channel may resemble passage thru an air lock. In this model, ligand binding leads to closure of the extracellular end of pore, then a TonB-mediated signal facillitates opening of the interior side of pore, deforming the N-terminal plug and allowing passage of the ligand to the periplasm. Such a mechanism would prevent the free diffusion of small molecules thru the pore.	1.57294e-29
NZ_CP011306.1\|WP_173581532.1\|912356_914057_-\|M48-family-metalloprotease	gnl\|CDD\|227122	COG4783, COG4783, Putative Zn-dependent protease, contains TPR repeats [General function prediction only].	1.25816e-121
NZ_CP011306.1\|WP_010483932.1\|895627_896881_+\|zinc-dependent-metalloprotease	gnl\|CDD\|372673	pfam13688, Reprolysin_5, Metallo-peptidase family M12.	2.86409e-26
NZ_CP011306.1\|WP_053442566.1\|893944_895402_-\|DUF2235-domain-containing-protein	gnl\|CDD\|370774	pfam09994, DUF2235, Uncharacterized alpha/beta hydrolase domain (DUF2235). This domain, found in various hypothetical bacterial proteins, has no known function.	6.70459e-11
NZ_CP011306.1\|WP_049412624.1\|893050_893875_+\|ferritin-like-domain-containing-protein	gnl\|CDD\|377292	pfam04305, DUF455, Protein of unknown function (DUF455).	4.4544e-130
NZ_CP011306.1\|WP_053442567.1\|898300_899446_-\|glycosyltransferase-family-1-protein	gnl\|CDD\|340842	cd03814, GT4-like, glycosyltransferase family 4 proteins. This family is most closely related to the GT4 family of glycosyltransferases and includes a sequence annotated as alpha-D-mannose-alpha(1-6)phosphatidyl myo-inositol monomannoside transferase from Bacillus halodurans. Glycosyltransferases catalyze the transfer of sugar moieties from activated donor molecules to specific acceptor molecules, forming glycosidic bonds. The acceptor molecule can be a lipid, a protein, a heterocyclic compound, or another carbohydrate residue. This group of glycosyltransferases is most closely related to the previously defined glycosyltransferase family 1 (GT1). The members of this family may transfer UDP, ADP, GDP, or CMP linked sugars. The diverse enzymatic activities among members of this family reflect a wide range of biological functions. The protein structure available for this family has the GTB topology, one of the two protein topologies observed for nucleotide-sugar-dependent glycosyltransferases. GTB proteins have distinct N- and C- terminal domains each containing a typical Rossmann fold. The two domains have high structural homology despite minimal sequence homology. The large cleft that separates the two domains includes the catalytic center and permits a high degree of flexibility. The members of this family are found mainly in bacteria and eukaryotes.	2.36442e-134
NZ_CP011306.1\|WP_019336562.1\|916348_917092_+\|cysteine-hydrolase	gnl\|CDD\|238245	cd00431, cysteine_hydrolases, Cysteine hydrolases; This family contains amidohydrolases, like CSHase (N-carbamoylsarcosine amidohydrolase), involved in creatine metabolism and nicotinamidase, converting nicotinamide to nicotinic acid and ammonia in the pyridine nucleotide cycle. It also contains isochorismatase, an enzyme that catalyzes the conversion of isochorismate to 2,3-dihydroxybenzoate and pyruvate, via the hydrolysis of the vinyl ether bond, and other related enzymes with unknown function.	5.72134e-32
NZ_CP011306.1\|WP_005415460.1\|910112_911444_-\|phosphate-regulon-sensor-histidine-kinase-PhoR	gnl\|CDD\|274368	TIGR02966, Phosphate_regulon_sensor_protein_PhoR, phosphate regulon sensor kinase PhoR. Members of this protein family are the regulatory histidine kinase PhoR associated with the phosphate ABC transporter in most Proteobacteria. Related proteins from Gram-positive organisms are not included in this model. The phoR gene usually is adjacent to the response regulator phoB gene (TIGR02154). [Signal transduction, Two-component systems].	2.1228e-161
NZ_CP011306.1\|WP_053442570.1\|917145_918054_+\|LysR-family-transcriptional-regulator	gnl\|CDD\|176114	cd08422, PBP2_CrgA_like, The C-terminal substrate binding domain of LysR-type transcriptional regulator CrgA and its related homologs, contains the type 2 periplasmic binding domain. This CD includes the substrate binding domain of LysR-type transcriptional regulator (LTTR) CrgA and its related homologs. The LTTRs are acting as both auto-repressors and activators of target promoters, controlling operons involved in a wide variety of cellular processes such as amino acid biosynthesis, CO2 fixation, antibiotic resistance, degradation of aromatic compounds, nodule formation of nitrogen-fixing bacteria, and synthesis of virulence factors, to name a few. In contrast to the tetrameric form of other LTTRs, CrgA from Neisseria meningitides assembles into an octameric ring, which can bind up to four 63-bp DNA oligonucleotides. Phylogenetic cluster analysis further showed that the CrgA-like regulators form a subclass of the LTTRs that function as octamers. The CrgA is an auto-repressor of its own gene and activates the expression of the mdaB gene which coding for an NADPH-quinone reductase and that its action is increased by MBL (alpha-methylene-gamma-butyrolactone), an inducer of NADPH-quinone oxidoreductase. The structural topology of this substrate-binding domain is most similar to that of the type 2 periplasmic binding proteins (PBP2), which are responsible for the uptake of a variety of substrates such as phosphate, sulfate, polysaccharides, lysine/arginine/ornithine, and histidine. The PBP2 bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.	5.45118e-68
NZ_CP011306.1\|WP_053442569.1\|902851_905821_-\|TonB-dependent-receptor	gnl\|CDD\|369481	pfam07715, Plug, TonB-dependent Receptor Plug Domain. The Plug domain has been shown to be an independently folding subunit of the TonB-dependent receptors. It acts as the channel gate, blocking the pore until the channel is bound by ligand. At this point it under goes conformational changes opens the channel.	3.17698e-24
NZ_CP011306.1\|WP_053442565.1\|891574_893041_+\|amidophosphoribosyltransferase	gnl\|CDD\|236427	PRK09246, PRK09246, amidophosphoribosyltransferase; Provisional.	0
NZ_CP011306.1\|WP_053442571.1\|918079_918829_+\|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.	2.66182e-16
NZ_CP011306.1\|WP_019336563.1\|915143_916148_+\|isocitrate-dehydrogenase	gnl\|CDD\|181606	PRK08997, PRK08997, isocitrate dehydrogenase; Provisional.	0
NZ_CP011306.1\|WP_010483930.1\|896968_897715_-\|UDP-2,3-diacylglucosamine-diphosphatase	gnl\|CDD\|235420	PRK05340, PRK05340, UDP-2,3-diacylglucosamine hydrolase; Provisional.	1.70431e-143
NZ_CP011306.1\|WP_010483913.1\|914145_914436_+\|glutaredoxin-3	gnl\|CDD\|274017	TIGR02181, GRX_bact, Glutaredoxin, GrxC family. Glutaredoxins are thioltransferases (disulfide reductases) which utilize glutathione and NADPH as cofactors. Oxidized glutathione is regenerated by glutathione reductase. Together these components compose the glutathione system. Glutaredoxins utilize the CXXC motif common to thioredoxins and are involved in multiple cellular processes including protection from redox stress, reduction of critical enzymes such as ribonucleotide reductase and the generation of reduced sulfur for iron sulfur cluster formation. Glutaredoxins are capable of reduction of mixed disulfides of glutathione as well as the formation of glutathione mixed disulfides. This family of glutaredoxins includes the E. coli protein GrxC (Grx3) which appears to have a secondary role in reducing ribonucleotide reductase (in the absence of GrxA) possibly indicating a role in the reduction of other protein disulfides. [Energy metabolism, Electron transport].	2.44078e-45
NZ_CP011306.1\|WP_010483928.1\|897780_898320_-\|phosphatase-PAP2-family-protein	gnl\|CDD\|239486	cd03392, PAP2_like_2, PAP2_like_2 proteins. PAP2 is a super-family of phosphatases and haloperoxidases. This subgroup, which is specific to bacteria, lacks functional characterization and may act as a membrane-associated lipid phosphatase.	2.86854e-16
NZ_CP011306.1\|WP_005408258.1\|911550_912240_-\|phosphate-regulon-transcriptional-regulator-PhoB	gnl\|CDD\|131209	TIGR02154, PhoB, phosphate regulon transcriptional regulatory protein PhoB. PhoB is a DNA-binding response regulator protein acting with PhoR in a 2-component system responding to phosphate ion. PhoB acts as a positive regulator of gene expression for phosphate-related genes such as phoA, phoS, phoE and ugpAB as well as itself. It is often found proximal to genes for the high-affinity phosphate ABC transporter (pstSCAB; GenProp0190) and presumably regulates these as well. [Regulatory functions, DNA interactions, Signal transduction, Two-component systems].	2.84143e-138

>NZ_CP011306.1|WP_010483920.1|906127_907654_-|exopolyphosphatase
MPHTTTTPPALQDGDLLAAIDLGSNSFHMVIARYTLGQLRVIDRLRETVRMADGLDGKGGLSSAARQRALECLARFGQRIRNVPPHRVRALATNTVRQLRSPQSFLVPAETALGHAIEVVSGREEARLIYLGVAHAQPPKPGQRRLVIDIGGGSTEFIIGMGMQTLERESLQAGCIASTRRFFPGGKLSKKRWKDALAEIGREFQPFASKYRALGWQEALGSSGTHKAISEICATMKLSKGAITAEALPQLRDELLKAKKIDDIQLPGLSSDRRPIIAGGILVLEAAFQALGLQKLLVSKAAMREGILYDIVGRAGENDLRDESVSALSQRYGIDTVQADRVQDTALSLLEQVQERWRLDADDARMLGWAARLHELGLMIAHSGYHVHGSYVLEHSDIAGFSRQEQQMLAALVRSHRRSVTKTAFDALPERLLLTARRLAALLRLAVLLNRAHEDDPLPALELTADDNRLSLIVPQAFIDARPLLRADLIGETDGIAGLGIQFRPFVA
>NZ_CP011306.1|WP_053442569.1|902851_905821_-|TonB-dependent-receptor
MTSRTTPLGQAIRYALATTATLAALPAFAQSGSTAAPTTLDRIEITGSRIRQVDVETAQPVLALSRLDIERQGFSSVADILQNVTAMGSPAISRANALSSGENTGGTYIDMRNLGAQRTLVLVNGKRLGISTSGLQDVSSLPVSAVERIEVLKDGASAIYGSDAMAGVINIITRSNVNGVTANVYHGQYSEGDGARDRFDVVGGWSNDRVSLTLALEHSEEKSVWAKDRWFSKYGVSDRHPNDASNWTTLSQWGQVTGLKGGPGCTNTSQGCGYSLNRGADPTNPANYHLTDATPFTGDVSNANEQMHVMYPLKRDSVYFDGRFKITDQVNLRTEFGYNKRSAERQIAGYPLQSSSVSISGDPTATGLMSKDSYFNPFGNQHGYAKPTDVAWNRRTWEIPRVSTSELKTYRAVVSLDGSFEIGQRYFDWDVGYQYNRNELTATATGNLHKKRVRDAVGPSFLDPATGKVMCGRPGAVISGCTPWNPLVPYGKNDPNGLTGNEELMAWLFPAEHTTGRTTTKNAFANLSGSIMTLPAGDLGFAFGVESRKEDGRYTPDALAQTGATTNLAAGPTGGSYNVKEAYLELSVPVLADLPGARELSFSAATRYSKYNTFGNTLNSKFGFKWKPIDQLLVRGTWAEGFRAPTINDLYGGGSETFAQFSDPCDTVFGSAKGSAEVRSRCARDIADAANFRQLKQGNTPVTTAQDATPTPFVSGSNPLLVPETSTSKTLGLVWSPTFVSNLNVALDWWKIRIDNTIVGDSPNQILKDCYEQGIESRCSRFTRDPSNGIVTGLKFGNRNAGFAETEGYDLDVSYRVDTSYGKLSAGWTSTYVSKNVYRSTNDVRDAITPINGVANTIGTATSLAFRVRSNLVLGWDVGDFGVSWTARYYSGVKERCLNASRYPDECSDPTFLAPWLKSPTAYNERGAVTFHDVQFRYNLPWDATVSVGANNVFGKEAPVMYSKPNSSFSYYGGYDIGRFMYMKYQQRF
>NZ_CP011306.1|WP_053442568.1|899589_902514_-|TonB-dependent-receptor
MTIRIPELGLAIRRALTMTATTALAAPAFAQHAPEATTLDRIEITGSRIRQVDLETAQPVLTISRADIERQGFNSVADILQNLTATGSPALSRASPLSSGEASGGSYVDMRGLGAQRTLVLVNGKRLGMTTSGYQDISSIPAAAVERMEVLKDGASAIYGSDAMAGVVNIITRRNVQGVTANVYHGQFSEGDGARTQYDVVAGWSNDRASISVAAEHVEEKGVWAKDRGFSAYTYTDRHPDDGWTTVGQWGRIVGFKGPGCSSARGCSYSLDRGSQPGGPDSFHLSDNTPFTGDVSNSNEQMHVQTPIKRDSLFVDARMDLNDQIRFNTQLAYNRRTTTRQVAGYPFQSGAAGITPMSADSWFNPFGSHHGYERPSDVHWNRRSWEIPRVSISELTTWQGVAAFEGSFQFVGREFDWEAGYQYNRSELEQRATGNLHKQRVADSTGPSFYNPATGKVECGTPDAPIAGCKPWNPLVPYGQDDPYGLTGNSELQDWLFPEELTRGRNTTRNLFASLSGGLATLPAGELGFALGVESRREEGRFIPDALAQTGATTNLAAGPTGGGYRVDEAYLELSVPLLHDLPGARQLTLDTATRYSDYTTFGGTLNSKFGVSWKPIDQLLVRGTWAQGFRAPTISNLYGGGSQTFTTGFRDPCDTVHGAAASSPEVRARCAADIANADSYRQLGQGNEPITGSSGQTPLPFTNGSNPDLKPETSTSRTLGLVWSPTFAEGLNIALDWWKVRIDNTIVADHPNDILRDCYELGIAERCGSFTRDPELGIVNTLSYGSRNSGFRQAEGYDLEIGHKFETSWGTLSADWKTTYVVAAEERTTNEVDVPPIPSNGIATNGGIGFRVRSNASLGWERGNLGLGWGLRYFSAVKERCLDAATYPGECSHPGQRAPWFSGSRDYNRRGSVTFHDVQARYNLPWDATVSIGANNVFGRQGPIMYSQPSANFSYYGGFDIGRFIYMKYQQRF
>NZ_CP011306.1|WP_053442567.1|898300_899446_-|glycosyltransferase-family-1-protein
MRYAIVTETYPPEVNGVALTVQGLEQGLRTSGHDIDLIRPRQTSEALDSAPGTLLVPGAALPRYPGLRFGLPAPIRLNRHWQQQRPDAVYIATEGPLGWSALRTARRLGIPVASGFHTRFDEYLPDYGVAWLQAAAMRWMRRFHNQADATLVPTRELQQFLGEQGFERVRLLARAVDSQQFDPGRRDPGLREEWGVDGNGLVAIHVGRIAAEKNLGLAVKAFRRLQQIRPKARFVWVGDGPAREKLAHENPDFIFCGIQRGEALARHFASGDLFLFPSRSETFGNVTLESMASGLATVAFDYGAAREYLRDGENGAAVENDEQFIEAAVQLAADDARRREFGSSAARAMKRLHPQQVVAEFDALLSELAQSRRSGHAHHAA
>NZ_CP011306.1|WP_010483928.1|897780_898320_-|phosphatase-PAP2-family-protein
MRTTPLELLAGREARLCRRANHYCRRRRVRRLFSVISRLGDGVFWYVLMGALVLLDGFDGLRASVHMAATGLAALLLYKGLKRWTRRPRPYAADLRIRAWVAPLDEFSFPSGHTLHAVSFTIVALAYYPWLAPLLVPFTFGVALSRVVLGLHYPSDVLAATGIAILLASASLAWLPLPV
>NZ_CP011306.1|WP_010483930.1|896968_897715_-|UDP-2,3-diacylglucosamine-diphosphatase
MTTLFISDLHLDPSRPEITDLFLRFLREQAPGADALYILGDLFEAWIGDDTPSPAADAVADALKVLSDSGVPVYFIRGNRDFLLGEDYARRAGLRILPDPCVIELYGRPVLLQHGDLLCTDDIPYQQFRAQTRDPAFQAQFLSQPLAARIAFAQKARDASQARQSEMKQGDRAQFETVTDVAPAEVDATFVRHGVDTMIHGHTHRPAVHTLQAGGRTCNRIVLGDWYEQGSVLRVDAGGWSLDTLARE
>NZ_CP011306.1|WP_010483932.1|895627_896881_+|zinc-dependent-metalloprotease
MLSRSIGKAAGGLVLGLSVAAAAHAAPLFEPVTVISRASANSEPALGKLLATPSTATVQEVRVDAAATAQPQLEFELLGQRVQAVRSKVEALPDGGSIWYGQLRSPSDRLTAATSNGQDDPGNSVILVRSGNTLTGSIRKDGKLYRLRPLGNRHVLVEVDESRMPADHPADYNQLPKIPMGNNDRIGIAQASSGTPATIRVLVVATNAAVTAYGGNMQSLVQLAVAESNQGYVNSNVGITLQLAGYETTNYTESGNFTTDLTRFRNTSDGYMDSIHTSRNNTAADVGVLLINNTSYCGLASGIGSTASTAFAAVYWDCATGYYSFAHEIGHLQSARHDIASDPSTSPYAYGHGYRYEPSSGSRWRTIMAYDCSAGCPRLNYWSNPNISYNGIPMGNASTADNQRVLVNTKATIAAFR
>NZ_CP011306.1|WP_053442566.1|893944_895402_-|DUF2235-domain-containing-protein
MAPSQDTDEDVGMLRIGLFFDGTRNNAHNLARGRPQVPQPRPAQLRADDDSTYQSRLTSSYDNGLTNIARLQQLYPDSRRNAMGAPSLSIYLEGVGTRDDADDDLIGLAFGIGASGVRAKVQRALQVLLPAALAELSARWQRPLRGVQLDLFGYSRGAAAARDIANQLQGWDSARWRQLLQGAGLSCTADFAPATPVLRFIGLFDTVVAVNGGRADEQPQLALHSGIAGRVVQLTARDEHRQHYPLTSVAPPFAEIVLPGVHANIGGGYNQLEEGPKLLSRPRRQQLRRPAVADYQVPPLALLQATTAYAETQADAERWRQQLGVGEKEIWVDVWHQWQQQRRAGSRSVLLSPVLYVTAAVVLRRRIDWRYQLIALQVMQQQAIDAGVQWTANAAGVPGWELPSALQPIARRLLAGQPLTQTQEALLRRRYLMQSAHWNFDALGDTALTYAADAGVSELPYRPGPGLFYINRPTVDGKRVVLPNA
>NZ_CP011306.1|WP_049412624.1|893050_893875_+|ferritin-like-domain-containing-protein
MVDVPDVGGDLLRAAQQCLAEADPLRKVALTQAYAAAFRAGRLRVAADAPPPEPIRMPGRPAQLVLVHPREVPRRGLGGVEGRAAFIHAIAHIELNAIDLAWDAVYRFRGLPPAFHADWVSCADDESRHFMLLRERLQVHGHDYADFPAHNGLWEMCEKTAHDGLARMALVPRVLEARGLDVTPGMIEKLRNVGDGETADVLEVILREEVAHVAAGSRWYRWYCDRADVEPRARFKELLVEYAGGYLHGPFNIEARLLAGFDADELANLVEQAG
>NZ_CP011306.1|WP_053442565.1|891574_893041_+|amidophosphoribosyltransferase
MCGIVGIVGNQNVAGQLYDGLTVLQHRGQDAAGIATVNGSRLRVQKATGLVRDVFDARTMSTLEGSVGIAHVRYPTAGSEGMDEAQPFYVNSPYGIALAHNGNLINTEALRQQVFEQDRRNVNTDSDSEVLLNVFAYELEQQRQLSPEAAIRAVAGVHRRCKGGYAVVSVVLGLGLVAFRDPHGIRPLVLGKRSHAEGDEYIVASESAALDVLGFQRVRDVQPGEALVITARGELFSEICAEPAEHTPCIFEYVYFARPDSMIDNVSVHKARMRMGIKLGEKILRLRPDHDIDTIIPIPDTSRDAALEISNVLGVKYREGFIKNRYIGRTFIMPGQGERVKSVRRKLNPIHLEFRNRVVLLVDDSIVRGTTSQQIVQMARDAGARKVYLASAAPPVRYPNIYGIDMPAAEELVAHNRSVEEIEAHLGCDWLIYQDLEDMEAAVSEGNPALRNFDSSCFNGHYPTGIEPGYFERIQQLRSDDAKHRRRA
>NZ_CP011306.1|WP_019337026.1|908020_910108_-|polyphosphate-kinase-1
MSSLGSLPLPVSPDNDPLRDPALYINRELSQLDFNFRVLAQAMDPQVPLLERLRFMCISCTNLDEFFEIRAAAVRHAQEFGLPPAPDGMSPQAILNAIHDRAAELVDQQYRCWNETLRPALMEAGIGVLGRHSWTDRQKRWLRAYFRNEIMPVLSPLGLDPVHPFPKILNKSLNIVVVLKGTDAFGRAGHLAIVRAPRSLPRIIQLPEKLGGSQNFVFLSSVLSTFVDELFPGMEVQGAYQFRVTRNSELVVDEEEVENLALALRDELVDRGYRPAVRLEIAQDMPRDIVRTLLQNFGLTENAVYRIDGPVNLNRIIQLYDLIAQPDLKYPPMTPRTLRDSDGIFETAARQDLLLHHPFDAFTAVLDLIRQAAIDPNVLAIKQTLYRTGKDSLIVDALIQAARNGKDVTVVVELRARFDEEANLGLADRLQEAGVQVVYGVVGYKTHAKMLLIVRREGRKLRRYVHLGTGNYHSGTARAYTDISLITADADIGNDVHLLFQQLSGLASKMKLKRLLQSPFTLHTGILGRIERETRIAAAGRPARIIAKMNALNEPQVVRALYAASQAGVQIDLIIRGACTLRPGVPGISDNIRVRSIVGRFLEHSRVYWFGNDGAPEMYCASADWLERNLLRRVETCFPILDPELAKRVYREVLQNYLDDNLNAWELDADGIYHKRAPAHDEAPHSAQMALMQGL
>NZ_CP011306.1|WP_005415460.1|910112_911444_-|phosphate-regulon-sensor-histidine-kinase-PhoR
MPRHIRSAWLKTLATVAAVLLFAGLVGWFTGHLWLCIALGALATLAWHYWRLRSVLRRLTARQRWDTAEEGTGVWNELDRLLYRNQVEMRVRKRRLLDMLRSYRAAAAALPDAVVVLDRNSQRVQWFNEAATALLGLHHPGDLGEALVERLQPMPLAHWLAGGRNAEPILDVPSPVDPAIRLNLRLIPYSSDYWLLIARDVSKLLRLEQVRRDFVANVSHELRTPLTVVHGYLDMMDPEDFPGTGPMLEEMRKQSQRMAQLVEDLLTLSRLESQEHSEEETVAMQPMLATLRREAEAHSQGRHQISIDDLAGVDLQGSTKELHSAFSNLVTNAVRYTPAGGRIAVEFRREGDGAVLAVRDSGYGIPATHLPRLTERFYRVSSSRSRESGGTGLGLSIVKHILGLHHARLEIESEVGKGSVFSCHFDADHVRPRESAPLTSIEE
>NZ_CP011306.1|WP_005408258.1|911550_912240_-|phosphate-regulon-transcriptional-regulator-PhoB
MQKRILIVDDEPAIREMVAFALRKGDYEPVHAGDAREAQTAIADRVPDLILLDWMLPGTSGLDLARRWRKETLTREVPIIMLTARGEENDRVGGLEAGVDDYVVKPFSARELLARIRAVMRRAREDDEDGSVAVGPIRIDGAAHRVFANDQPVPIGPTEYRLLHFFMTHPERVYTRAQLLDHVWGGSVYVEERTIDVHIRRLRKTLEPFNAENMVQTVRGAGYRFSTAT
>NZ_CP011306.1|WP_173581532.1|912356_914057_-|M48-family-metalloprotease
MVAPCPATLGAPRPRTSCLRALLLTTAVTLALATPLAQAQEKLPDIGSSAGELLTPARQAEYGAMMLRELRNYGYLLDDPLVNDWLQTMGTRLGSNSDQPRQPYTFFVMKDRQINAFATLGGYIGVNAGLVLTAEREDEVAAVLSHEIAHVTQQHVLRGVERAQRDQIPILLGMLAAVVAAQASNSTSSGNATMAAISSGMGLMQQRQINYTRSNESEADRLGIRTLSRSGYDVDAMAGFFERMASAMRGNEGGYSVPEFLRTHPVNITRISEAKARAEQMKKDTVLLTTTTPSGERRERVDPTDPSLAEPLLRGNNPLLPSSVLRIPMGQLSRGASGDFDWARERLRVLSADSTPELEREYADLAKRQKDGLNDAQRYGQALAVMRSGRAGAAQARQTLAGLLQTRPDNLWLALGLGEAESRAGQTAQANSRFEQLLRQHPNSRPVALTYAEILNEQGSREAGQRAQAMLRPLLSQSGNDPVFQQRYARASELAGDSVRASEAYAEAAFLSGRPEQSLMQLQALKRNPALDYVGRARVDARIEAITPTVLELRRQGVQDPDLDRR
>NZ_CP011306.1|WP_010483913.1|914145_914436_+|glutaredoxin-3
MTAQTAGGAPAITIYSTAVCPYCVAAKNFLKSKGQQWTEVRIDLDPVEREKMMAKTRRTSVPQIFVGDVHVGGYDDMMALHREGKLEPLLAGQGQA
>NZ_CP011306.1|WP_004154542.1|914432_914825_+|carboxymuconolactone-decarboxylase-family-protein
MSAADDGSKDRIAEFTEFRKRMNERILGEPNQVVRRFFALDTQTYQAGALDVKTKELLGLVASMVLRCDDCISYHVAQCKDAGVTREEFFETFSVGLVVGGSIVIPHLRRAVDFLDQLEGGAAAPAAHEH
>NZ_CP011306.1|WP_019336563.1|915143_916148_+|isocitrate-dehydrogenase
MTQKITVIRGDGIGPEIMDATLFVLDQLKTGLEYEDADAGLVALEKHGDLMPAVTLESIARNKVALKSPLTTPVGGGFTSINVSLRRHFDLYANVRPAHTFPNTKSRFDNVDLITVRENTEGAYLAEGQEVSADGETAFSGTRITRKGSERIVRYAFELAKSTGRKKVTAVHKANIIKSTSGLFLNVAREVAAQYPDIEFQEMIVDNCCMQLVMRPEQFDVIVTTNLFGDIISDLCAGLVGGLGLAPGANIGKDAAIFEAVHGTAPDIAGQGKANPCALLLAAAQMLDHIGQPENAARLRKAIVATMEAKDSLTGDLGGTGTTMSFAKAIASRL
>NZ_CP011306.1|WP_019336562.1|916348_917092_+|cysteine-hydrolase
MNLTAFGLASLIGMAATAPVAAAEPSHPTIRHMAGAPVAASLDAAKTAVLVIDFQNEYFDASAAPGFAGGRMVIPDGVAALRQARRVVEFADTHGIRVIHVQHVLPAGAPLFAQGSVNAAFHHDLKPRKGETVVQKDNVSVFAGNSAAVLDTVLKDAGIDTLIVTGLQTHACVAGAARDAAAAPRGYRVIVSSDASASRDLDLASGQRIDHRALHDASLAQIEDAFGDVMNTDAILALPVRKAGDGA
>NZ_CP011306.1|WP_053442570.1|917145_918054_+|LysR-family-transcriptional-regulator
MDHFAALRALRAIVDAGSFTAAAERLGTTHSAMSRQLRQLEEHLQVRLLDRNSRRLSLTEAGRDYYREAAALLDRLQEADDRVRAGQAQPGGIVRISVPQVVASQELPHWLPSFLQRYPQVALDLSADDQLVDVVGGGFDLALRIAASLPDSQLVARELASCPRILVAAPAYLARRGLPRQAADLEQHTLLGFSPTPSMPPWQLQGPRGASVSIEAGQRLRVDATPALYAAALAGMGISLFTALTVQEDLRAGRLIRVLPAWHAGQRRYFALYPHARALAPKVRALVEHLAAHYAAQVGAAG
>NZ_CP011306.1|WP_053442571.1|918079_918829_+|sulfite-exporter-TauE/SafE-family-protein
MESVYLLVALGAIVAGFVQGLSGFAFGMVAMSFWAWGLEPRLAATLSVFGALVGQLVAVFTVRRGFNLRLLLPFVLGGLAGIPLGVMVLPRLDMDWFKALLGGFLALWCPVMLMARSLPPVRVGGRIGDAIAGMAGGVLSGIGGFAGPVPTLWSTLRGFGKDEQRAVIQNFNLAMLAVTMATYVGSGLVSRQMLPYFAIVAPAMLVPTLLGARVYIGISEARFRQLVLGLLTASGIALLASSLPVLLAR

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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

Prophage detection

Region

Region Position

Protein_number

Hit_taxonomy

Key_proteins

Att_site

Prophage annotation

DBSCAN-SWA_1

566431 : 575428

Enterobacteria_phage(42.86%)

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_010480669.1\|566431_567487_+	dTDP-glucose 4,6-dehydratase	I7HTA3	Enterobacteria_phage	4.1e-79	46.5
WP_053442487.1\|567501_568389_+	glucose-1-phosphate thymidylyltransferase RfbA	I7I009	Enterobacteria_phage	1.6e-95	57.7
WP_010480673.1\|568385_568943_+	dTDP-4-dehydrorhamnose 3,5-epimerase	I7HJC4	Enterobacteria_phage	6.0e-45	50.0
WP_049480751.1\|568939_569833_+	dTDP-4-dehydrorhamnose reductase	A0A291LA50	Escherichia_phage	1.8e-27	37.5
WP_053442488.1\|569937_571341_-	mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase	A0A1V0SH58	Hokovirus	1.1e-47	28.9
WP_010480679.1\|571353_572700_-	phosphomannomutase/phosphoglucomutase	A0A127AWJ1	Bacillus_phage	2.0e-30	26.8
WP_053442489.1\|572797_575428_-	DEAD/DEAH box helicase	Q9YNZ9	Choristoneura_fumiferana_nuclear_polyhedrosis_virus	8.5e-49	30.5

DBSCAN-SWA_2

926336 : 999583

Enterobacter_phage(16.0%)

protease,tail,plate

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_010483890.1\|926336_927626_+\|protease	ATP-dependent Clp protease ATP-binding subunit ClpX	G3M9Z9	Bacillus_virus	1.7e-135	58.0
WP_053442573.1\|927768_930222_+	endopeptidase La	A0A0R6PGP8	Moraxella_phage	1.9e-220	51.9
WP_004146343.1\|930439_930712_+	HU family DNA-binding protein	A7KV42	Bacillus_phage	7.7e-22	61.8
WP_019336553.1\|931589_933545_+	peptidylprolyl isomerase	NA	NA	NA	NA
WP_010483881.1\|933742_934942_-	lytic transglycosylase domain-containing protein	NA	NA	NA	NA
WP_053442574.1\|934938_935703_-	hydroxyacylglutathione hydrolase	NA	NA	NA	NA
WP_010483877.1\|935714_936359_+	methyltransferase domain-containing protein	NA	NA	NA	NA
WP_010483875.1\|936372_936825_+	ribonuclease HI	J9Q745	Salmonella_phage	3.8e-42	52.7
WP_019336550.1\|936829_937561_+	DNA polymerase III subunit epsilon	A2I2Z6	Vibrio_virus	1.3e-07	28.9
WP_010483871.1\|937623_938328_-	serine/threonine-protein phosphatase	NA	NA	NA	NA
WP_010483869.1\|938866_939271_+	hypothetical protein	A0A1C9C5K8	Heterosigma_akashiwo_virus	7.7e-18	35.3
WP_010483867.1\|939289_940336_-	glycosyltransferase family 9 protein	NA	NA	NA	NA
WP_010483865.1\|940356_941106_+	3-deoxy-D-manno-octulosonic acid kinase	NA	NA	NA	NA
WP_010483863.1\|941105_941873_+	MBL fold metallo-hydrolase	NA	NA	NA	NA
WP_010483861.1\|941869_942259_+	nuclear transport factor 2 family protein	NA	NA	NA	NA
WP_010483859.1\|942733_943051_+	quaternary ammonium compound efflux SMR transporter SugE	NA	NA	NA	NA
WP_053442575.1\|943408_954313_+	autotransporter-associated beta strand repeat-containing protein	NA	NA	NA	NA
WP_049453599.1\|954370_954814_-	GNAT family N-acetyltransferase	NA	NA	NA	NA
WP_053442576.1\|954889_955999_-	DUF3667 domain-containing protein	NA	NA	NA	NA
WP_053443790.1\|956760_958824_+	DNA polymerase III subunit gamma/tau	A0A1U9WR94	Streptococcus_virus	2.1e-47	41.4
WP_010483846.1\|958830_959151_+	YbaB/EbfC family nucleoid-associated protein	NA	NA	NA	NA
WP_053442577.1\|959233_959833_+	recombination protein RecR	NA	NA	NA	NA
WP_053442578.1\|959899_960259_+	histidine triad nucleotide-binding protein	NA	NA	NA	NA
WP_005408301.1\|960338_960866_-	Slp family lipoprotein	NA	NA	NA	NA
WP_053442579.1\|960862_962812_-	DUF3488 domain-containing transglutaminase family protein	NA	NA	NA	NA
WP_032952475.1\|962804_963728_-	DUF58 domain-containing protein	NA	NA	NA	NA
WP_053442580.1\|963751_964705_-	AAA family ATPase	NA	NA	NA	NA
WP_043398217.1\|964747_966583_+	glycosyltransferase family 39 protein	NA	NA	NA	NA
WP_053442581.1\|966690_967260_-	septum formation inhibitor Maf	NA	NA	NA	NA
WP_019659501.1\|967373_967883_+	DUF177 domain-containing protein	NA	NA	NA	NA
WP_005408308.1\|967990_968185_+	50S ribosomal protein L32	NA	NA	NA	NA
WP_014036188.1\|968276_969254_+	ketoacyl-ACP synthase III	NA	NA	NA	NA
WP_010483824.1\|969331_970114_+	hypothetical protein	NA	NA	NA	NA
WP_053442582.1\|970282_971227_+	ACP S-malonyltransferase	NA	NA	NA	NA
WP_005408312.1\|971309_972053_+	3-oxoacyl-ACP reductase FabG	Q06VL0	Trichoplusia_ni_ascovirus	4.7e-13	32.3
WP_005415509.1\|972205_972445_+	acyl carrier protein	B2ZXV3	Ralstonia_phage	5.9e-10	44.6
WP_019338749.1\|972588_973851_+	beta-ketoacyl-ACP synthase II	NA	NA	NA	NA
WP_010483816.1\|973943_975308_+	aminodeoxychorismate synthase component I	NA	NA	NA	NA
WP_053442583.1\|975429_976491_+	endolytic transglycosylase MltG	NA	NA	NA	NA
WP_053442584.1\|976487_977153_+	dTMP kinase	W8D0J5	Erwinia_phage	7.2e-21	34.9
WP_053442585.1\|977149_978106_+	DNA polymerase III subunit delta'	NA	NA	NA	NA
WP_005412452.1\|978102_978456_+	PilZ domain-containing protein	NA	NA	NA	NA
WP_049453542.1\|978749_979313_-	hypothetical protein	NA	NA	NA	NA
WP_053442586.1\|979365_979773_-	hypothetical protein	NA	NA	NA	NA
WP_005408320.1\|980338_980719_+	tautomerase family protein	NA	NA	NA	NA
WP_053442587.1\|980750_981824_-\|tail	phage tail protein	D5LGY1	Escherichia_phage	3.0e-93	51.0
WP_010483798.1\|981814_982030_-\|tail	tail protein X	A0A219Y9W1	Aeromonas_phage	2.2e-08	47.0
WP_049410185.1\|982013_982481_-\|tail	phage tail protein	A4PE53	Ralstonia_virus	1.3e-08	30.4
WP_053442588.1\|982483_984955_-\|tail	phage tail tape measure protein	K4ICR4	Acidithiobacillus_phage	2.9e-22	26.6
WP_019336908.1\|985075_985366_-\|tail	phage tail assembly protein	A0A193GYZ8	Enterobacter_phage	4.2e-18	58.5
WP_010483789.1\|985443_985947_-\|tail	phage major tail tube protein	A0A193GYM4	Enterobacter_phage	3.1e-40	50.6
WP_010483787.1\|985949_987149_-\|tail	phage tail sheath subtilisin-like domain-containing protein	D5LGY7	Escherichia_phage	1.1e-125	53.8
WP_019336909.1\|987256_987847_-	hypothetical protein	NA	NA	NA	NA
WP_010483783.1\|987851_989369_-\|tail	tail fiber protein	V9IQX0	Stenotrophomonas_phage	2.7e-71	56.8
WP_019336910.1\|989376_990678_-\|tail	phage tail protein I	V9IQK7	Stenotrophomonas_phage	7.4e-46	52.0
WP_010483779.1\|990670_991567_-\|plate	baseplate J/gp47 family protein	V5YTH6	Pseudomonas_phage	1.8e-83	58.1
WP_010483777.1\|991569_991908_-	GPW/gp25 family protein	A0A193GYY8	Enterobacter_phage	1.0e-31	61.3
WP_053442589.1\|991960_992551_-\|plate	phage baseplate assembly protein V	A0A193GYL5	Enterobacter_phage	2.8e-24	37.7
WP_053442590.1\|992547_993102_-	hypothetical protein	NA	NA	NA	NA
WP_158003730.1\|993212_993518_-	hypothetical protein	NA	NA	NA	NA
WP_053442591.1\|993459_993837_-	hypothetical protein	NA	NA	NA	NA
WP_049410196.1\|993833_994319_-	glycoside hydrolase family 104 protein	D5LH07	Escherichia_phage	1.0e-40	53.8
WP_053442592.1\|994315_994666_-	hypothetical protein	NA	NA	NA	NA
WP_029550699.1\|994662_995112_-	helix-turn-helix domain-containing protein	NA	NA	NA	NA
WP_019336915.1\|995451_995835_-	hypothetical protein	NA	NA	NA	NA
WP_019336916.1\|995988_996627_-	hypothetical protein	A0A1V0DYI4	Shewanella_phage	2.0e-20	41.8
WP_010483758.1\|996668_996896_-	hypothetical protein	NA	NA	NA	NA
WP_049410201.1\|996971_997247_-	hypothetical protein	NA	NA	NA	NA
WP_049410203.1\|997246_999583_-	toprim domain-containing protein	V5YUR8	Pseudomonas_phage	1.4e-135	42.1

DBSCAN-SWA_3

2215206 : 2222823

Stenotrophomonas_phage(57.14%)

Protein_ID	Protein_Def	Hit_ID	Hit_Def	E-value	Identity
WP_100050554.1\|2215206_2215851_-	hypothetical protein	S0F2J2	Stenotrophomonas_phage	2.8e-30	57.5
WP_187296455.1\|2215983_2216148_+	hypothetical protein	NA	NA	NA	NA
WP_187296456.1\|2216144_2216306_+	hypothetical protein	NA	NA	NA	NA
WP_187296460.1\|2216681_2217560_+	replication initiation protein	A0A077JDC0	Xanthomonas_phage	2.9e-126	74.7
WP_053443007.1\|2217556_2217847_+	DNA-binding protein	O80282	Xanthomonas_phage	3.2e-26	63.6
WP_053443008.1\|2217850_2218072_+	hypothetical protein	NA	NA	NA	NA
WP_053443009.1\|2218089_2218332_+	hypothetical protein	NA	NA	NA	NA
WP_148563089.1\|2218595_2219840_+	hypothetical protein	S0F309	Stenotrophomonas_phage	7.1e-46	41.4
WP_053443011.1\|2219839_2220160_+	DUF2523 domain-containing protein	NA	NA	NA	NA
WP_053443012.1\|2220156_2221347_+	zonular occludens toxin family protein	S0F3F8	Stenotrophomonas_phage	6.5e-57	37.3
WP_053443013.1\|2221343_2221970_+	conjugal transfer protein	A0A1W6DY89	Xanthomonas_phage	2.5e-55	57.2
WP_053443014.1\|2221966_2222299_-	hypothetical protein	NA	NA	NA	NA
WP_100050555.1\|2222484_2222823_-	hypothetical protein	S0F2N2	Stenotrophomonas_phage	2.2e-50	88.4

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_CP011306

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CRISPR-Cas detection and classification

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Self-targeting detection

MGE targeting detection<

Prophage detection

Anti-CRISPR protein detection