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| | gene:10742103 | NifU_N domain-containing protein. (148 aa) |
| | BAC18491.1 | Conserved hypothetical protein; CE1681, similar to AE007020-14|AAK45777.1| percent identity: 66 in 115 aa. (136 aa) |
| | gene:10742080 | NLPC_P60 domain-containing protein. (691 aa) |
| | bacA | Putative membrane protein BacA; Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin; Belongs to the UppP family. (327 aa) |
| | BAC18396.1 | Putative ATP-dependent RNA helicase; CE1586, similar to AL646059-158|CAD14067.1| percent identity: 37 in 457 aa. (460 aa) |
| | argR | Arginine repressor; Regulates arginine biosynthesis genes. (190 aa) |
| | rplT | 50S ribosomal protein L20; 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. (128 aa) |
| | BAC18312.1 | Conserved hypothetical protein; CE1502, similar to AL138978-15|CAB72415.1| percent identity: 43 in 748 aa. (781 aa) |
| | BAC18298.1 | Putative PS1 protein; CE1488, similar to AB055224-1|BAB62413.1| percent identity: 31 in 287 aa. (390 aa) |
| | BAC18261.1 | Conserved hypothetical protein; CE1451, similar to AE001701-10|AAD35257.1| percent identity: 26 in 286 aa. (350 aa) |
| | BAC17122.1 | Putative cytochrome c-type biogenesis protein; CE0312, similar to AL596162-29|CAC44608.1| percent identity: 39 in 263 aa. (293 aa) |
| | topA | DNA topoisomerase 1; 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 [...] (999 aa) |
| | gene:10740702 | Uncharacterized protein. (898 aa) |
| | gene:10740670 | Uncharacterized protein. (784 aa) |
| | gene:10740613 | Uncharacterized protein. (1421 aa) |
| | BAC17025.1 | Hypothetical protein; CE0215. (1207 aa) |
| | BAC17023.1 | Conserved hypothetical protein; CE0213, similar to AL023596-16|CAA19164.1| percent identity: 56 in 408 aa. (423 aa) |
| | gene:10740608 | Putative cobyric acid synthase. (250 aa) |
| | gene:10740595 | Putative membrane protein. (899 aa) |
| | BAC16985.1 | Putative glycosyl transferase; CE0175, similar to Z80343-15|CAB02461.1| percent identity: 60 in 297 aa. (310 aa) |
| | gene:10740554 | Putative oxidoreductase. (488 aa) |
| | BAC16973.1 | Putative oxidoreductase; CE0163, similar to AX064581-1|CAC25530.1| percent identity: 88 in 253 aa. (253 aa) |
| | gene:10740552 | Putative membrane protein. (703 aa) |
| | BAC16971.1 | Putative arabinosyltransferase; CE0161, similar to AX065349-1|CAC25914.1| percent identity: 76 in 1148 aa. (1157 aa) |
| | gyrA | Putative DNA gyrase subunit A; 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. (863 aa) |
| | gyrB | DNA gyrase subunit B; 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. (687 aa) |
| | gene:10742107 | Uncharacterized protein. (481 aa) |
| | gene:10741852 | Putative ATP-dependent DNA helicase recG. (707 aa) |
| | ddl | Putative D-alanine--D-alanine ligase; Cell wall formation. (361 aa) |
| | BAC18140.1 | Putative cysteine desulfurase; CE1330, similar to AL583923-39|CAC30661.1| percent identity: 48 in 369 aa. (373 aa) |
| | BAC18117.1 | Conserved hypothetical protein; CE1307, similar to AL583920-196|CAC31518.1| percent identity: 54 in 371 aa. (388 aa) |
| | prfA | Peptide chain release factor 1; Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA. (358 aa) |
| | gene:10741703 | Putative respiratory nitrate reductase delta chain. (246 aa) |
| | gene:10741671 | Putative chromodomain helicase. (1034 aa) |
| | gene:10741669 | HNHc domain-containing protein. (183 aa) |
| | deaD | ATP-dependent RNA helicase DeaD; DEAD-box RNA helicase involved in various cellular processes at low temperature, including ribosome biogenesis, mRNA degradation and translation initiation. (736 aa) |
| | gene:10741629 | Uncharacterized protein. (456 aa) |
| | gene:10741589 | Iron-sulfur cluster carrier protein; Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP; Belongs to the Mrp/NBP35 ATP-binding proteins family. (375 aa) |
| | BAC17966.1 | Putative GTP-binding protein; CE1156, similar to AL596043-7|CAC44318.1| percent identity: 60 in 632 aa. (640 aa) |
| | BAC17924.1 | Putative cysteine desulfurase NifS; CE1114, similar to AE000705-9|AAC06912.1| percent identity: 42 in 360 aa. (362 aa) |
| | murD | UDP-N-acetylmuramoylalanine--D-glutamate ligase; Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA). Belongs to the MurCDEF family. (475 aa) |
| | murG | Peptidoglycan biosynthesis protein MurG; 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. (360 aa) |
| | murC | UDP-N-acetylmuramate--alanine ligase; Cell wall formation; Belongs to the MurCDEF family. (489 aa) |
| | ftsZ | Cell division protein FtsZ; 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. (430 aa) |
| | BAC19711.1 | Putative ATP-dependent helicase; CE2901, similar to AE005149-5|AAG20812.1| percent identity: 22 in 861 aa. (941 aa) |
| | BAC19705.1 | Conserved hypothetical protein; CE2895, similar to AE005661-3|AAG59487.1| percent identity: 27 in 2062 aa. (2100 aa) |
| | gene:10743344 | DNA helicase. (777 aa) |
| | gene:10743266 | Replicative DNA helicase; Participates in initiation and elongation during chromosome replication; it exhibits DNA-dependent ATPase activity. Belongs to the helicase family. DnaB subfamily. (527 aa) |
| | gene:10743220 | RNase_H_2 domain-containing protein. (506 aa) |
| | gene:10743211 | Uncharacterized protein. (183 aa) |
| | BAC19556.1 | Conserved hypothetical protein; CE2746, similar to AL596138-2|CAC44512.1| percent identity: 32 in 382 aa. (417 aa) |
| | BAC19529.1 | Putative UDP-galactopyranose mutase; CE2719, similar to AX065129-1|CAC25804.1| percent identity: 85 in 401 aa. (460 aa) |
| | gene:10743162 | Glft2_N domain-containing protein. (698 aa) |
| | BAC19523.1 | Conserved hypothetical protein; CE2713, similar to AL360055-27|CAB96032.1| percent identity: 32 in 172 aa. (307 aa) |
| | gene:10743160 | Putative membrane protein; Belongs to the UbiA prenyltransferase family. (341 aa) |
| | BAC19521.1 | Conserved hypothetical protein; CE2711, similar to AE007185-3|AAK48278.1| percent identity: 41 in 576 aa. (676 aa) |
| | gene:10743146 | Putative membrane protein. (774 aa) |
| | gene:10743121 | Putative membrane protein. (1003 aa) |
| | murA | UDP-N-acetylglucosamine 1-carboxyvinyltransferase; Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine; Belongs to the EPSP synthase family. MurA subfamily. (421 aa) |
| | murI | Glutamate racemase; Provides the (R)-glutamate required for cell wall biosynthesis. (316 aa) |
| | rsfS | Ribosomal silencing factor RsfS; 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. (157 aa) |
| | gene:10742630 | CHY-type domain-containing protein. (105 aa) |
| | gene:10742517 | Fe-S_biosyn domain-containing protein; Belongs to the HesB/IscA family. (154 aa) |
| | murE | UDP-N-acetylmuramoylalanyl-D-glutamate--2, 6-diaminopimelate ligase; 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. (526 aa) |
| | murF | UDP-N-acetylmuramoylalanyl-D-glutamyl-2, 6-diaminopimelate--D-alanyl-D-alanyl ligase; 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. (528 aa) |
| | BAC18495.1 | Conserved hypothetical protein; CE1685, similar to Z99125-22|CAB16170.1| percent identity: 54 in 391 aa. (394 aa) |
| | mraY | Putative phospho-N-acetylmuramoyl-pentapeptidetransferase; First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan; Belongs to the glycosyltransferase 4 family. MraY subfamily. (366 aa) |
| | BAC17847.1 | Conserved hypothetical protein; CE1037, similar to AL442120-9|CAC09541.1| percent identity: 32 in 202 aa. (203 aa) |
| | mfd | Transcription-repair-coupling factor; 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. (1218 aa) |
| | gene:10741434 | SWIM-type domain-containing protein. (612 aa) |
| | glmU | Glucosamine-1-phosphate N-acetyltransferase; 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. In the C-terminal section; belongs to the transferase hexapeptide repeat family. (501 aa) |
| | ureE | Urease accessory protein UreE; Involved in urease metallocenter assembly. Binds nickel. Probably functions as a nickel donor during metallocenter assembly. Belongs to the UreE family. (149 aa) |
| | prfC | Putative peptide chain release factor; 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. (546 aa) |
| | BAC17796.1 | Conserved hypothetical protein; CE0986, similar to AB001488-124|BAA19377.1| percent identity: 34 in 794 aa. (797 aa) |
| | BAC17740.1 | Putative ATP-dependent DNA helicase; CE0930, similar to Y15254-6|CAA75552.1| percent identity: 43 in 785 aa. (825 aa) |
| | BAC17701.1 | Putative DNA helicase; CE0891, similar to AL583924-93|CAC31112.1| percent identity: 75 in 547 aa. (557 aa) |
| | BAC17690.1 | Conserved hypothetical protein; CE0880, similar to AL023635-5|CAA19188.1| percent identity: 39 in 200 aa. (203 aa) |
| | prfB | Peptide chain release factor 2; Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA. (389 aa) |
| | gene:10741196 | DNA helicase. (694 aa) |
| | BAC17601.1 | Putative ATP-dependent DNA helicase; CE0791, similar to AL021646-46|CAA16666.1| percent identity: 43 in 1075 aa; Belongs to the helicase family. UvrD subfamily. (1175 aa) |
| | gene:10741192 | Putative helicase; Belongs to the helicase family. UvrD subfamily. (1024 aa) |
| | gene:10741188 | Putative ATP-dependent RNA helicase; Belongs to the DEAD box helicase family. (369 aa) |
| | BAC17595.1 | Conserved hypothetical protein; CE0785, similar to Z95120-10|CAB08304.1| percent identity: 28 in 397 aa. (401 aa) |
| | BAC17564.1 | Conserved hypothetical protein; CE0754, similar to U15187-21|AAA63142.1| percent identity: 35 in 508 aa. (524 aa) |
| | gene:10741101 | Putative penicillin-binding protein; Belongs to the peptidase S11 family. (447 aa) |
| | gene:10741072 | Putative phenylacetic acid degradation protein. (180 aa) |
| | BAC17275.1 | Putative cytochrome c biogenesis protein; CE0465, similar to U00018-1|AAA17249.1| percent identity: 43 in 354 aa. (357 aa) |
| | gene:10740862 | ResB domain-containing protein. (544 aa) |
| | BAC17273.1 | Putative cytochrome C-type biogenesis protein CcsA; CE0463, similar to U00018-4|AAA17226.1| percent identity: 53 in 248 aa. (283 aa) |
| | murB | Putative UDP-N-acetylenolpyruvoylglucosamine reductase; Cell wall formation. (563 aa) |
| | BAC17171.1 | Putative undecaprenyl phosphate alpha-n-acetylglucosaminyltransferase; CE0361, similar to AF236052-10|AAF72959.1| percent identity: 27 in 325 aa. (336 aa) |
| | BAC17124.1 | Hypothetical protein; CE0314. (181 aa) |
| | sepF | Conserved hypothetical protein; Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA. (155 aa) |
| | gene:10742459 | Uncharacterized protein. (205 aa) |
| | smc | Putative chromosome segregation SMC protein; Required for chromosome condensation and partitioning. Belongs to the SMC family. (1169 aa) |
| | gene:10742347 | Putative magnesium chelatase. (507 aa) |
| | frr | Putative ribosome recycling factor; 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) |
| | BAC18650.1 | Conserved hypothetical protein; CE1840, similar to Z98209-10|CAB10907.1| percent identity: 51 in 447 aa. (454 aa) |
| | BAC18600.1 | Conserved hypothetical protein; CE1790, similar to AL583922-58|CAC30455.1| percent identity: 22 in 390 aa. (470 aa) |
| | gene:10742201 | Uncharacterized protein. (155 aa) |
| | rubA | Holliday junction DNA-helicase RuvA; 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) |
| | rubB | Holliday junction DNA-helicase RuvB; 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. (360 aa) |
| | BAC18564.1 | Conserved hypothetical protein; CE1754, similar to AB056583-2|BAB64333.1| percent identity: 34 in 708 aa. (886 aa) |
| | mltG | Conserved hypothetical protein; Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation. Belongs to the transglycosylase MltG family. (396 aa) |
| | priA | Conserved hypothetical 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. (685 aa) |
| | gene:10742109 | Uncharacterized protein. (590 aa) |
