NZ_CP024964.1|WP_028124224.1|361014_361797_+|Nif3-like-dinuclear-metal-center-hexameric-protein |
gnl|CDD|376614 |
pfam01784, NIF3, NIF3 (NGG1p interacting factor 3). This family contains several NIF3 (NGG1p interacting factor 3) protein homologs. NIF3 interacts with the yeast transcriptional coactivator NGG1p which is part of the ADA complex, the exact function of this interaction is unknown.
|
5.64636e-51 |
NZ_CP024964.1|WP_051584603.1|373434_373995_+|dephospho-CoA-kinase |
gnl|CDD|238980 |
cd02022, DPCK, Dephospho-coenzyme A kinase (DPCK, EC 2.7.1.24) catalyzes the phosphorylation of dephosphocoenzyme A (dCoA) to yield CoA, which is the final step in CoA biosynthesis.
|
2.01612e-30 |
NZ_CP024964.1|WP_084485296.1|370140_372438_+|bifunctional-(p)ppGpp-synthetase/guanosine-3',5'-bis(diphosphate)-3'-pyrophosphohydrolase |
gnl|CDD|223394 |
COG0317, SpoT, Guanosine polyphosphate pyrophosphohydrolases/synthetases [Signal transduction mechanisms / Transcription].
|
0 |
NZ_CP024964.1|WP_028124213.1|376389_376656_+|30S-ribosomal-protein-S15 |
gnl|CDD|180170 |
PRK05626, rpsO, 30S ribosomal protein S15; Reviewed.
|
2.64723e-44 |
NZ_CP024964.1|WP_028124214.1|375732_376278_+|hypothetical-protein |
gnl|CDD|185679 |
cd02064, FAD_synthetase_N, FAD synthetase, N-terminal domain of the bifunctional enzyme. FAD synthetase_N. N-terminal domain of the bifunctional riboflavin biosynthesis protein riboflavin kinase/FAD synthetase. These enzymes have both ATP:riboflavin 5'-phosphotransferase and ATP:FMN-adenylyltransferase activities. The N-terminal domain is believed to play a role in the adenylylation reaction of FAD synthetases. The C-terminal domain is thought to have kinase activity. FAD synthetase is present among all kingdoms of life. However, the bifunctional enzyme is not found in mammals, which use separate enzymes for FMN and FAD formation.
|
1.15948e-25 |
NZ_CP024964.1|WP_028124215.1|374872_375733_+|tRNA-pseudouridine(55)-synthase-TruB |
gnl|CDD|211339 |
cd02573, PseudoU_synth_EcTruB, Pseudouridine synthase, Escherichia coli TruB like. This group consists of bacterial pseudouridine synthases similar to E. coli TruB and Mycobacterium tuberculosis TruB. Pseudouridine synthases catalyze the isomerization of specific uridines in an RNA molecule to pseudouridines (5-ribosyluracil, psi). E. coli TruB and M. tuberculosis TruB make psi55 in the T loop of tRNAs. Psi55 is nearly universally conserved. E. coli TruB is not inhibited by RNA containing 5-fluorouridine.
|
7.23302e-105 |
NZ_CP024964.1|WP_028124225.1|360347_361028_+|SAM-dependent-methyltransferase |
gnl|CDD|378972 |
pfam12847, Methyltransf_18, Methyltransferase domain. Protein in this family function as methyltransferases.
|
3.30447e-55 |
NZ_CP024964.1|WP_028124226.1|358924_360346_+|sigma-70-family-RNA-polymerase-sigma-factor |
gnl|CDD|235640 |
PRK05901, PRK05901, RNA polymerase sigma factor; Provisional.
|
4.99855e-128 |
NZ_CP024964.1|WP_028124212.1|376876_377617_+|hypothetical-protein |
gnl|CDD|237177 |
PRK12704, PRK12704, phosphodiesterase; Provisional.
|
2.46789e-05 |
NZ_CP024964.1|WP_028124223.1|361786_363169_+|DEAD/DEAH-box-helicase |
gnl|CDD|223587 |
COG0513, SrmB, Superfamily II DNA and RNA helicases [DNA replication, recombination, and repair / Transcription / Translation, ribosomal structure and biogenesis].
|
6.8844e-107 |
NZ_CP024964.1|WP_028124230.1|353345_353861_+|rRNA-maturation-RNase-YbeY |
gnl|CDD|376735 |
pfam02130, UPF0054, Uncharacterized protein family UPF0054.
|
1.99781e-39 |
NZ_CP024964.1|WP_100608973.1|357021_358908_+|DNA-primase |
gnl|CDD|235551 |
PRK05667, dnaG, DNA primase; Validated.
|
2.36303e-137 |
NZ_CP024964.1|WP_034971172.1|363261_364803_+|YitT-family-protein |
gnl|CDD|224203 |
COG1284, COG1284, Uncharacterized conserved protein [Function unknown].
|
1.44185e-22 |
NZ_CP024964.1|WP_028124229.1|353847_354753_+|GTPase-Era |
gnl|CDD|234624 |
PRK00089, era, GTPase Era; Reviewed.
|
7.59357e-140 |
NZ_CP024964.1|WP_051584604.1|354752_355562_+|DNA-repair-protein-RecO |
gnl|CDD|273175 |
TIGR00613, DNA_repair_protein_RecO, DNA repair protein RecO. All proteins in this family for which functions are known are DNA binding proteins that are involved in the initiation of recombination or recombinational repair. [DNA metabolism, DNA replication, recombination, and repair].
|
7.5292e-26 |
NZ_CP024964.1|WP_028124228.1|355644_357000_+|glycine--tRNA-ligase |
gnl|CDD|235240 |
PRK04173, PRK04173, glycyl-tRNA synthetase; Provisional.
|
0 |
NZ_CP024964.1|WP_028124220.1|368927_369440_+|adenine-phosphoribosyltransferase |
gnl|CDD|235028 |
PRK02304, PRK02304, adenine phosphoribosyltransferase; Provisional.
|
1.02087e-81 |
NZ_CP024964.1|WP_028124211.1|377690_378746_+|phosphatidate-cytidylyltransferase |
gnl|CDD|366491 |
pfam01148, CTP_transf_1, Cytidylyltransferase family. The members of this family are integral membrane protein cytidylyltransferases. The family includes phosphatidate cytidylyltransferase EC:2.7.7.41 as well as Sec59 from yeast. Sec59 is a dolichol kinase EC:2.7.1.108.
|
2.08077e-31 |
NZ_CP024964.1|WP_028124210.1|378759_380031_+|RIP-metalloprotease-RseP |
gnl|CDD|100084 |
cd06163, S2P-M50_PDZ_RseP-like, RseP-like Site-2 proteases (S2P), zinc metalloproteases (MEROPS family M50A), cleave transmembrane domains of substrate proteins, regulating intramembrane proteolysis (RIP) of diverse signal transduction mechanisms. In Escherichia coli, the S2P homolog RseP is involved in the sigmaE pathway of extracytoplasmic stress responses. Also included in this group are such homologs as Bacillus subtilis YluC, Mycobacterium tuberculosis Rv2869c S2P, and Bordetella bronchiseptica HurP. Rv2869c S2P appears to have a role in the regulation of prokaryotic lipid biosynthesis and membrane composition and YluC of Bacillus has a role in transducing membrane stress. This group includes bacterial and eukaryotic S2P/M50s homologs with either one or two PDZ domains present. PDZ domains are believed to have a regulatory role. The RseP PDZ domain is required for the inhibitory reaction that prevents cleavage of its substrate, RseA.
|
7.98765e-35 |