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| | mpl | Unannotated protein; Reutilizes the intact tripeptide L-alanyl-gamma-D-glutamyl- meso-diaminopimelate by linking it to UDP-N-acetylmuramate. Belongs to the MurCDEF family. Mpl subfamily. (454 aa) |
| | cvrA | Unannotated protein; K(+)/H(+) antiporter that extrudes potassium in exchange for external protons and maintains the internal concentration of potassium under toxic levels; Belongs to the monovalent cation:proton antiporter 1 (CPA1) transporter (TC 2.A.36) family. NhaP2 subfamily. (575 aa) |
| | yifE | Unannotated protein. (136 aa) |
| | GCA_000819825_00210 | Unannotated protein. (185 aa) |
| | GCA_000819825_00211 | Unannotated protein. (455 aa) |
| | murI | Unannotated protein; Provides the (R)-glutamate required for cell wall biosynthesis. (262 aa) |
| | ypdA | Unannotated protein. (557 aa) |
| | gyrB | Unannotated protein; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. (804 aa) |
| | glmU_2 | Unannotated protein; Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP-GlcNAc). The C- terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N- acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5-monophosphate (from uridine 5- triphosphate), a reaction catalyzed by the N-terminal domain. (453 aa) |
| | GCA_000819825_00348 | Unannotated protein. (253 aa) |
| | GCA_000819825_00413 | Unannotated protein. (110 aa) |
| | GCA_000819825_00456 | Unannotated protein. (254 aa) |
| | prfB | Unannotated protein; Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA. (284 aa) |
| | prfC | Unannotated protein; Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF-1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP. Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. PrfC subfamily. (528 aa) |
| | glmU_1 | Unannotated protein. (153 aa) |
| | slt_1 | Unannotated protein; Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella. In the N-terminal section; belongs to the bacterial solute- binding protein 3 family. (474 aa) |
| | mshI1 | Unannotated protein. (197 aa) |
| | mshP | Unannotated protein. (154 aa) |
| | GCA_000819825_00702 | Unannotated protein. (591 aa) |
| | cyaY | Unannotated protein; Involved in iron-sulfur (Fe-S) cluster assembly. May act as a regulator of Fe-S biogenesis. (104 aa) |
| | cpdA | Unannotated protein; Hydrolyzes cAMP to 5'-AMP. Plays an important regulatory role in modulating the intracellular concentration of cAMP, thereby influencing cAMP-dependent processes. (260 aa) |
| | parE | Unannotated protein; Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule; Belongs to the type II topoisomerase family. ParE type 1 subfamily. (631 aa) |
| | parC | Unannotated protein; Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule; Belongs to the type II topoisomerase GyrA/ParC subunit family. ParC type 1 subfamily. (764 aa) |
| | GCA_000819825_00827 | Unannotated protein. (137 aa) |
| | dsbD_1 | Unannotated protein. (687 aa) |
| | pbpG_1 | Unannotated protein; Belongs to the peptidase S11 family. (275 aa) |
| | hupA | Unannotated protein; Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions. (90 aa) |
| | pilT_1 | Unannotated protein. (344 aa) |
| | yaeJ | Unannotated protein. (138 aa) |
| | argR_2 | Unannotated protein; Regulates arginine biosynthesis genes. (156 aa) |
| | ypjD | Unannotated protein. (263 aa) |
| | mviN | Unannotated protein; Involved in peptidoglycan biosynthesis. Transports lipid- linked peptidoglycan precursors from the inner to the outer leaflet of the cytoplasmic membrane. (522 aa) |
| | pilV | Unannotated protein. (139 aa) |
| | GCA_000819825_00969 | Unannotated protein. (360 aa) |
| | GCA_000819825_00970 | Unannotated protein. (155 aa) |
| | pilE1 | Unannotated protein. (135 aa) |
| | fimA | Unannotated protein. (125 aa) |
| | GCA_000819825_00976 | Unannotated protein. (375 aa) |
| | GCA_000819825_00977 | Unannotated protein. (700 aa) |
| | rapA | Unannotated protein; Transcription regulator that activates transcription by stimulating RNA polymerase (RNAP) recycling in case of stress conditions such as supercoiled DNA or high salt concentrations. Probably acts by releasing the RNAP, when it is trapped or immobilized on tightly supercoiled DNA. Does not activate transcription on linear DNA. Probably not involved in DNA repair; Belongs to the SNF2/RAD54 helicase family. RapA subfamily. (956 aa) |
| | rplT | Unannotated protein; Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit. (118 aa) |
| | gyrA | Unannotated protein; A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner. (927 aa) |
| | mltA | Unannotated protein; Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and/or cell division. (383 aa) |
| | rlpA | Unannotated protein; Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides. (129 aa) |
| | mukB | Unannotated protein. (1480 aa) |
| | mukE | Unannotated protein. (245 aa) |
| | mukF | Unannotated protein; Involved in chromosome condensation, segregation and cell cycle progression. May participate in facilitating chromosome segregation by condensation DNA from both sides of a centrally located replisome during cell division. Not required for mini-F plasmid partitioning. Probably acts via its interaction with MukB and MukE. Overexpression results in anucleate cells. It has a calcium binding activity. (439 aa) |
| | ddl | Unannotated protein; Cell wall formation; Belongs to the D-alanine--D-alanine ligase family. (329 aa) |
| | GCA_000819825_01091 | Unannotated protein. (183 aa) |
| | GCA_000819825_01112 | Unannotated protein. (162 aa) |
| | recQ_2 | Unannotated protein. (640 aa) |
| | mltF_1 | Unannotated protein; Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella. In the N-terminal section; belongs to the bacterial solute- binding protein 3 family. (510 aa) |
| | nrfE | Unannotated protein. (657 aa) |
| | dsbE_2 | Unannotated protein. (188 aa) |
| | nrfG | Unannotated protein; Possible subunit of a heme lyase. (394 aa) |
| | pbpG_2 | Unannotated protein; Belongs to the peptidase S11 family. (306 aa) |
| | GCA_000819825_01165 | Unannotated protein. (193 aa) |
| | GCA_000819825_01201 | Unannotated protein. (196 aa) |
| | mltF_2 | Unannotated protein; Murein-degrading enzyme that degrades murein glycan strands and insoluble, high-molecular weight murein sacculi, with the concomitant formation of a 1,6-anhydromuramoyl product. Lytic transglycosylases (LTs) play an integral role in the metabolism of the peptidoglycan (PG) sacculus. Their lytic action creates space within the PG sacculus to allow for its expansion as well as for the insertion of various structures such as secretion systems and flagella. (486 aa) |
| | yfgL | Unannotated protein; Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane. (394 aa) |
| | hscA | Unannotated protein; Chaperone involved in the maturation of iron-sulfur cluster- containing proteins. Has a low intrinsic ATPase activity which is markedly stimulated by HscB. (615 aa) |
| | hscB | Unannotated protein; Co-chaperone involved in the maturation of iron-sulfur cluster-containing proteins. Seems to help targeting proteins to be folded toward HscA; Belongs to the HscB family. (172 aa) |
| | iscA | Unannotated protein; Is able to transfer iron-sulfur clusters to apo-ferredoxin. Multiple cycles of [2Fe2S] cluster formation and transfer are observed, suggesting that IscA acts catalytically. Recruits intracellular free iron so as to provide iron for the assembly of transient iron-sulfur cluster in IscU in the presence of IscS, L-cysteine and the thioredoxin reductase system; Belongs to the HesB/IscA family. (107 aa) |
| | iscU | Unannotated protein; A scaffold on which IscS assembles Fe-S clusters. It is likely that Fe-S cluster coordination is flexible as the role of this complex is to build and then hand off Fe-S clusters. (127 aa) |
| | iscS | Unannotated protein; Master enzyme that delivers sulfur to a number of partners involved in Fe-S cluster assembly, tRNA modification or cofactor biosynthesis. Catalyzes the removal of elemental sulfur atoms from cysteine to produce alanine. Functions as a sulfur delivery protein for Fe-S cluster synthesis onto IscU, an Fe-S scaffold assembly protein, as well as other S acceptor proteins. (404 aa) |
| | zapA | Unannotated protein; Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division. (110 aa) |
| | smpA | Unannotated protein; Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane. (112 aa) |
| | GCA_000819825_01369 | Unannotated protein. (488 aa) |
| | mlaA | Unannotated protein. (269 aa) |
| | nrfG2 | Unannotated protein. (426 aa) |
| | ccmH | Unannotated protein; Possible subunit of a heme lyase. (159 aa) |
| | dsbE_1 | Unannotated protein. (176 aa) |
| | ccmF-1 | Unannotated protein. (651 aa) |
| | ccmE | Unannotated protein; Heme chaperone required for the biogenesis of c-type cytochromes. Transiently binds heme delivered by CcmC and transfers the heme to apo-cytochromes in a process facilitated by CcmF and CcmH. Belongs to the CcmE/CycJ family. (163 aa) |
| | ccmD | Unannotated protein; Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes; Belongs to the CcmD/CycX/HelD family. (68 aa) |
| | ccmC | Unannotated protein; Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes; Belongs to the CcmC/CycZ/HelC family. (246 aa) |
| | ccmB | Unannotated protein; Required for the export of heme to the periplasm for the biogenesis of c-type cytochromes; Belongs to the CcmB/CycW/HelB family. (222 aa) |
| | ccmA | Unannotated protein; Part of the ABC transporter complex CcmAB involved in the biogenesis of c-type cytochromes; once thought to export heme, this seems not to be the case, but its exact role is uncertain. Responsible for energy coupling to the transport system; Belongs to the ABC transporter superfamily. CcmA exporter (TC 3.A.1.107) family. (211 aa) |
| | flhF | Unannotated protein. (471 aa) |
| | flhA | Unannotated protein; Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin; Belongs to the FHIPEP (flagella/HR/invasion proteins export pore) family. (700 aa) |
| | fliR | Unannotated protein; Role in flagellar biosynthesis. Belongs to the FliR/MopE/SpaR family. (265 aa) |
| | fliQ | Unannotated protein; Role in flagellar biosynthesis. Belongs to the FliQ/MopD/SpaQ family. (89 aa) |
| | fliP_1 | Unannotated protein; Plays a role in the flagellum-specific transport system. Belongs to the FliP/MopC/SpaP family. (251 aa) |
| | fliO | Unannotated protein. (124 aa) |
| | fliK | Unannotated protein. (672 aa) |
| | GCA_000819825_01448 | Unannotated protein. (146 aa) |
| | fliH | Unannotated protein. (265 aa) |
| | topA_1 | Unannotated protein; Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA- (5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supe [...] (873 aa) |
| | prfA | Unannotated protein; Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA. (362 aa) |
| | GCA_000819825_01554 | Unannotated protein. (177 aa) |
| | GCA_000819825_01555 | Unannotated protein. (199 aa) |
| | pilN | Unannotated protein. (189 aa) |
| | tapM | Unannotated protein. (353 aa) |
| | fimD_2 | Unannotated protein. (241 aa) |
| | fimC | Unannotated protein. (862 aa) |
| | fimD_1 | Unannotated protein. (251 aa) |
| | frdC | Unannotated protein; Seems to be involved in the anchoring of the catalytic components of the fumarate reductase complex to the cytoplasmic membrane; Belongs to the FrdC family. (132 aa) |
| | rlpB | Unannotated protein; Together with LptD, is involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane. Required for the proper assembly of LptD. Binds LPS and may serve as the LPS recognition site at the outer membrane. (160 aa) |
| | ybeB | Unannotated protein; Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation. (112 aa) |
| | penA | Unannotated protein; Catalyzes cross-linking of the peptidoglycan cell wall. Belongs to the transpeptidase family. MrdA subfamily. (641 aa) |
| | mrdB_2 | Unannotated protein; Peptidoglycan polymerase that is essential for cell wall elongation; Belongs to the SEDS family. MrdB/RodA subfamily. (367 aa) |
| | mrdB_1 | Unannotated protein. (45 aa) |
| | rlpA-2 | Unannotated protein; Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides. (311 aa) |
| | dacC | Unannotated protein; Belongs to the peptidase S11 family. (415 aa) |
| | GCA_000819825_01663 | Unannotated protein. (98 aa) |
| | torD | Unannotated protein; Involved in the biogenesis of TorA. Acts on TorA before the insertion of the molybdenum cofactor and, as a result, probably favors a conformation of the apoenzyme that is competent for acquiring the cofactor; Belongs to the TorD/DmsD family. TorD subfamily. (222 aa) |
| | GCA_000819825_01707 | Unannotated protein. (96 aa) |
| | gntY | Unannotated protein; Involved in iron-sulfur cluster biogenesis. Binds a 4Fe-4S cluster, can transfer this cluster to apoproteins, and thereby intervenes in the maturation of Fe/S proteins. Could also act as a scaffold/chaperone for damaged Fe/S proteins. (192 aa) |
| | secB | Unannotated protein; One of the proteins required for the normal export of preproteins out of the cell cytoplasm. It is a molecular chaperone that binds to a subset of precursor proteins, maintaining them in a translocation-competent state. It also specifically binds to its receptor SecA. (156 aa) |
| | recG | Unannotated protein; Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y- DNA); Belongs to the helicase family. RecG subfamily. (689 aa) |
| | typA | Unannotated protein. (603 aa) |
| | engB | Unannotated protein; Necessary for normal cell division and for the maintenance of normal septation; Belongs to the TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily. EngB GTPase family. (205 aa) |
| | topA_2 | Unannotated protein. (185 aa) |
| | uvrD | Unannotated protein. (723 aa) |
| | erpA | Unannotated protein; Required for insertion of 4Fe-4S clusters for at least IspG. (116 aa) |
| | yeiU | Unannotated protein. (234 aa) |
| | mrcB | Unannotated protein; Cell wall formation. Synthesis of cross-linked peptidoglycan from the lipid intermediates. The enzyme has a penicillin-insensitive transglycosylase N-terminal domain (formation of linear glycan strands) and a penicillin-sensitive transpeptidase C-terminal domain (cross- linking of the peptide subunits). (773 aa) |
| | dsbD_2 | Unannotated protein; Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps. Belongs to the thioredoxin family. DsbD subfamily. (593 aa) |
| | emtA | Unannotated protein; Murein-degrading enzyme. May play a role in recycling of muropeptides during cell elongation and/or cell division. (366 aa) |
| | GCA_000819825_02047 | Unannotated protein. (548 aa) |
| | GCA_000819825_02069 | Unannotated protein. (162 aa) |
| | ctaG | Unannotated protein. (184 aa) |
| | zapD | Unannotated protein; Cell division factor that enhances FtsZ-ring assembly. Directly interacts with FtsZ and promotes bundling of FtsZ protofilaments, with a reduction in FtsZ GTPase activity. (240 aa) |
| | ftsZ | Unannotated protein; Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity. (383 aa) |
| | ftsQ | Unannotated protein; Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic. May control correct divisome assembly. (250 aa) |
| | murC | Unannotated protein; Cell wall formation; Belongs to the MurCDEF family. (484 aa) |
| | murG | Unannotated protein; Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II); Belongs to the glycosyltransferase 28 family. MurG subfamily. (355 aa) |
| | ftsW | Unannotated protein; Peptidoglycan polymerase that is essential for cell division. Belongs to the SEDS family. FtsW subfamily. (394 aa) |
| | murD | Unannotated protein; Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA). Belongs to the MurCDEF family. (427 aa) |
| | mraY | Unannotated protein; First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan; Belongs to the glycosyltransferase 4 family. MraY subfamily. (360 aa) |
| | murF | Unannotated protein; Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein; Belongs to the MurCDEF family. MurF subfamily. (451 aa) |
| | murE | Unannotated protein; Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan. Belongs to the MurCDEF family. MurE subfamily. (494 aa) |
| | ftsI | Unannotated protein; Catalyzes cross-linking of the peptidoglycan cell wall at the division septum; Belongs to the transpeptidase family. FtsI subfamily. (584 aa) |
| | lafE | Unannotated protein. (362 aa) |
| | lafC | Unannotated protein. (130 aa) |
| | lfgK | Unannotated protein. (439 aa) |
| | flgJ_2 | Unannotated protein. (132 aa) |
| | flgD_2 | Unannotated protein; Required for flagellar hook formation. May act as a scaffolding protein. (227 aa) |
| | lfgA | Unannotated protein. (263 aa) |
| | lfgM | Unannotated protein. (91 aa) |
| | lfgN | Unannotated protein. (147 aa) |
| | lfiH | Unannotated protein. (230 aa) |
| | lfhA | Unannotated protein; Required for formation of the rod structure of the flagellar apparatus. Together with FliI and FliH, may constitute the export apparatus of flagellin; Belongs to the FHIPEP (flagella/HR/invasion proteins export pore) family. (691 aa) |
| | lfiR | Unannotated protein; Role in flagellar biosynthesis. Belongs to the FliR/MopE/SpaR family. (260 aa) |
| | lfiQ | Unannotated protein; Role in flagellar biosynthesis. Belongs to the FliQ/MopD/SpaQ family. (89 aa) |
| | fliP_2 | Unannotated protein; Plays a role in the flagellum-specific transport system. Belongs to the FliP/MopC/SpaP family. (244 aa) |
| | lptA | Unannotated protein; Involved in the assembly of lipopolysaccharide (LPS). Required for the translocation of LPS from the inner membrane to the outer membrane. May form a bridge between the inner membrane and the outer membrane, via interactions with LptC and LptD, thereby facilitating LPS transfer across the periplasm. (177 aa) |
| | lptC | Unannotated protein; Involved in the assembly of lipopolysaccharide (LPS). Required for the translocation of LPS from the inner membrane to the outer membrane. Facilitates the transfer of LPS from the inner membrane to the periplasmic protein LptA. Could be a docking site for LptA. Belongs to the LptC family. (186 aa) |
| | mlaF | Unannotated protein. (266 aa) |
| | ttg2D | Unannotated protein. (211 aa) |
| | GCA_000819825_02225 | Unannotated protein. (90 aa) |
| | yrbA | Unannotated protein; Belongs to the BolA/IbaG family. (85 aa) |
| | murA | Unannotated protein; Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine; Belongs to the EPSP synthase family. MurA subfamily. (418 aa) |
| | ruvA | Unannotated protein; The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB. (204 aa) |
| | ruvB | Unannotated protein; The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. (336 aa) |
| | ybgF | Unannotated protein; Mediates coordination of peptidoglycan synthesis and outer membrane constriction during cell division; Belongs to the CpoB family. (266 aa) |
| | GCA_000819825_02296 | Unannotated protein. (271 aa) |
| | recD | Unannotated protein; A helicase/nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme [...] (699 aa) |
| | recB | Unannotated protein; A helicase/nuclease that prepares dsDNA breaks (DSB) for recombinational DNA repair. Binds to DSBs and unwinds DNA via a highly rapid and processive ATP-dependent bidirectional helicase activity. Unwinds dsDNA until it encounters a Chi (crossover hotspot instigator) sequence from the 3' direction. Cuts ssDNA a few nucleotides 3' to the Chi site. The properties and activities of the enzyme are changed at Chi. The Chi-altered holoenzyme produces a long 3'-ssDNA overhang and facilitates RecA-binding to the ssDNA for homologous DNA recombination and repair. Holoenzyme [...] (1206 aa) |
| | mccF | Unannotated protein. (336 aa) |
| | GCA_000819825_02459 | Unannotated protein. (137 aa) |
| | mfd | Unannotated protein; Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site; In the C-terminal section; belongs to the helicase family. RecG subfamily. (1147 aa) |
| | GCA_000819825_02670 | Unannotated protein. (455 aa) |
| | azr | Unannotated protein. (190 aa) |
| | zapC | Unannotated protein; Contributes to the efficiency of the cell division process by stabilizing the polymeric form of the cell division protein FtsZ. Acts by promoting interactions between FtsZ protofilaments and suppressing the GTPase activity of FtsZ. (178 aa) |
| | cutC | Unannotated protein; Participates in the control of copper homeostasis. Belongs to the CutC family. (240 aa) |
| | zipA | Unannotated protein; Essential cell division protein that stabilizes the FtsZ protofilaments by cross-linking them and that serves as a cytoplasmic membrane anchor for the Z ring. Also required for the recruitment to the septal ring of downstream cell division proteins. (370 aa) |
| | smc | Unannotated protein; Required for chromosome condensation and partitioning. Belongs to the SMC family. (1124 aa) |
| | skp | Unannotated protein; Belongs to the skp family. (156 aa) |
| | yaeT | Unannotated protein; Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane. (807 aa) |
| | uppS | Unannotated protein; Catalyzes the sequential condensation of isopentenyl diphosphate (IPP) with (2E,6E)-farnesyl diphosphate (E,E-FPP) to yield (2Z,6Z,10Z,14Z,18Z,22Z,26Z,30Z,34E,38E)-undecaprenyl diphosphate (di- trans,octa-cis-UPP). UPP is the precursor of glycosyl carrier lipid in the biosynthesis of bacterial cell wall polysaccharide components such as peptidoglycan and lipopolysaccharide. (258 aa) |
| | frr | Unannotated protein; Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another; Belongs to the RRF family. (185 aa) |
| | GCA_000819825_03090 | Unannotated protein. (212 aa) |
| | GCA_000819825_03135 | Unannotated protein; Belongs to the Dps family. (155 aa) |
| | dnaB | Unannotated protein; Participates in initiation and elongation during chromosome replication; it exhibits DNA-dependent ATPase activity and contains distinct active sites for ATP binding, DNA binding, and interaction with DnaC protein, primase, and other prepriming proteins. Belongs to the helicase family. DnaB subfamily. (466 aa) |
| | GCA_000819825_03261 | Unannotated protein. (342 aa) |
| | lptD | Unannotated protein; Together with LptE, is involved in the assembly of lipopolysaccharide (LPS) at the surface of the outer membrane. (803 aa) |
| | surA | Unannotated protein; Chaperone involved in the correct folding and assembly of outer membrane proteins. Recognizes specific patterns of aromatic residues and the orientation of their side chains, which are found more frequently in integral outer membrane proteins. May act in both early periplasmic and late outer membrane-associated steps of protein maturation. (430 aa) |
| | nlpB | Unannotated protein; Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane. (342 aa) |
| | murB | Unannotated protein; Cell wall formation. (345 aa) |
| | topB | Unannotated protein; Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA- (5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supe [...] (652 aa) |
| | yfiO | Unannotated protein; Part of the outer membrane protein assembly complex, which is involved in assembly and insertion of beta-barrel proteins into the outer membrane. (251 aa) |
| | GCA_000819825_03378 | Unannotated protein. (172 aa) |
| | argR_1 | Unannotated protein; Regulates arginine biosynthesis genes. (163 aa) |
| | uppP | Unannotated protein; Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin; Belongs to the UppP family. (271 aa) |
| | recQ_1 | Unannotated protein. (611 aa) |
| | priA | Unannotated protein; Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA; Belongs to the helicase family. PriA subfamily. (735 aa) |
| | comM | Unannotated protein. (504 aa) |
| | fliS | Unannotated protein. (140 aa) |
| | yehU | Unannotated protein. (563 aa) |
| | GCA_000819825_03611 | Unannotated protein. (510 aa) |
| | GCA_000819825_03681 | Unannotated protein. (161 aa) |
| | GCA_000819825_03770 | Unannotated protein. (285 aa) |
| | yceG | Unannotated protein; Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation. (333 aa) |
| | minD_2 | Unannotated protein; Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP; Belongs to the Mrp/NBP35 ATP-binding proteins family. (359 aa) |
| | minC | Unannotated protein; Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization; Belongs to the MinC family. (238 aa) |
| | minD_1 | Unannotated protein. (270 aa) |
| | mtgA | Unannotated protein; Peptidoglycan polymerase that catalyzes glycan chain elongation from lipid-linked precursors; Belongs to the glycosyltransferase 51 family. (235 aa) |
| | GCA_000819825_03934 | Unannotated protein. (281 aa) |
| | flgK | Unannotated protein. (666 aa) |
| | flgJ_1 | Unannotated protein. (358 aa) |
| | flgD_1 | Unannotated protein; Required for flagellar hook formation. May act as a scaffolding protein. (245 aa) |
| | flgA | Unannotated protein; Involved in the assembly process of the P-ring formation. It may associate with FlgF on the rod constituting a structure essential for the P-ring assembly or may act as a modulator protein for the P- ring assembly; Belongs to the FlgA family. (227 aa) |
| | flgM | Unannotated protein. (105 aa) |
| | flgN | Unannotated protein. (137 aa) |
| | GCA_000819825_03979 | Unannotated protein. (1280 aa) |
| | acrH | Unannotated protein. (165 aa) |
| | sufE | Unannotated protein. (145 aa) |
| | rep | Unannotated protein; Rep helicase is a single-stranded DNA-dependent ATPase involved in DNA replication; it can initiate unwinding at a nick in the DNA. It binds to the single-stranded DNA and acts in a progressive fashion along the DNA in the 3' to 5' direction. (670 aa) |
| | zapB | Unannotated protein; Non-essential, abundant cell division factor that is required for proper Z-ring formation. It is recruited early to the divisome by direct interaction with FtsZ, stimulating Z-ring assembly and thereby promoting cell division earlier in the cell cycle. Its recruitment to the Z-ring requires functional FtsA or ZipA. (69 aa) |
