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arsA | Putative Arsenical pump-driving ATPase; Anion-transporting ATPase; Belongs to the arsA ATPase family. (579 aa) | ||||
hmrR | Heavy metal-dependent transcriptional regulator, MerR family; Function of strongly homologous gene; regulator. (519 aa) | ||||
XM1_0028 | Homologs of previously reported genes of unknown function. (310 aa) | ||||
XM1_0043 | Bacteriophage tail assembly protein; No homology to any previously reported sequences. (664 aa) | ||||
XM1_0089 | Homologs of previously reported genes of unknown function. (428 aa) | ||||
XM1_0168 | Conserved protein of unknown function (Sec-C motif 144-165); Homologs of previously reported genes of unknown function; Belongs to the Nudix hydrolase family. (327 aa) | ||||
flhF | Protein of unknown function (Methyl-accepting chemotaxis protein (MCP) signaling domain 365-548); Function of homologous gene experimentally demonstrated in an other organism; enzyme. (333 aa) | ||||
XM1_0252 | Putative ATPase, AAA family; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (281 aa) | ||||
ffh | Signal Recognition Particle (SRP) component with 4.5S RNA (ffs); Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY. Interaction with FtsY leads to the transfer of the RNC complex to the Sec translocase for insertion into the membrane, the hydrolysis of GTP by both Ffh and FtsY, and the dissociation of the SRP-FtsY complex [...] (454 aa) | ||||
infB | Translation initiation factor IF-2; One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex; Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase family. IF-2 subfamily. (872 aa) | ||||
obgE | GTPase involved in cell partioning and DNA repair; An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control. Belongs to the TRAFAC class OBG-HflX-like GTPase superfamily. OBG GTPase family. (417 aa) | ||||
XM1_0328 | Putative argK, membrane ATPase/protein kinase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (329 aa) | ||||
XM1_0398 | Protein of unknown function; No homology to any previously reported sequences. (413 aa) | ||||
XM1_0432 | Putative ATPase (MoxR-like); Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (330 aa) | ||||
XM1_0434 | Conserved protein of unknown function, putative NUDIX hydrolase domain; Homologs of previously reported genes of unknown function. (231 aa) | ||||
fixI | Nitrogen fixation protein FixI; Function of strongly homologous gene; enzyme. (781 aa) | ||||
mutL | DNA mismatch repair protein MutL; This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a 'molecular matchmaker', a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex. (602 aa) | ||||
htpG | Molecular chaperone HSP90 family; Molecular chaperone. Has ATPase activity. (623 aa) | ||||
bipA | GTP-binding protein; Function of homologous gene experimentally demonstrated in an other organism; factor. (606 aa) | ||||
XM1_0629 | Homologs of previously reported genes of unknown function. (207 aa) | ||||
ychF | Putative GTP-binding protein; ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner. (367 aa) | ||||
ppa | Inorganic pyrophosphatase; Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions. (181 aa) | ||||
yggV | dITP/XTP pyrophosphatase; Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA/RNA and avoiding chromosomal lesions. Belongs to the HAM1 NTPase family. (206 aa) | ||||
hisE | Phosphoribosyl-ATP pyrophosphatase; Function of strongly homologous gene; enzyme. (109 aa) | ||||
hslU | Molecular chaperone and ATPase component of HslUV protease; ATPase subunit of a proteasome-like degradation complex; this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis. (442 aa) | ||||
XM1_0832 | Conserved protein of unknown function (maf-like protein) Nucleoside triphosphate pyrophosphatase. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. (196 aa) | ||||
mnmE | tRNA modification GTPase MnmE; Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34; Belongs to the TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily. TrmE GTPase family. (441 aa) | ||||
XM1_0908 | Putative adenylyl-sulfate kinase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (174 aa) | ||||
prfC | Peptide chain release factor RF-3; 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) | ||||
acyP | Acylphosphatase; Function of strongly homologous gene; enzyme. (94 aa) | ||||
ftsY | Signal recognition particle receptor FtsY; Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC). Interaction with SRP-RNC leads to the transfer of the RNC complex to the Sec translocase for insertion into the membrane, the hydrolysis of GTP by both Ffh and FtsY, and the dissociation of the SRP-FtsY complex into the individual components. (334 aa) | ||||
dut | Deoxyuridinetriphosphatase; This enzyme is involved in nucleotide metabolism: it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA; Belongs to the dUTPase family. (151 aa) | ||||
rppH | RNA pyrophosphohydrolase; Accelerates the degradation of transcripts by removing pyrophosphate from the 5'-end of triphosphorylated RNA, leading to a more labile monophosphorylated state that can stimulate subsequent ribonuclease cleavage; Belongs to the Nudix hydrolase family. RppH subfamily. (170 aa) | ||||
XM1_1275 | Conserved protein of unknown function(NERD,16-109) Homologs of previously reported genes of unknown function. (385 aa) | ||||
uppP1 | Undecaprenyl-diphosphatase 1(Bacitracin resistance protein BacA,6-257); Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin; Belongs to the UppP family. (265 aa) | ||||
smc | Chromosome partition protein Smc(Structural maintenance of chromosomes protein, prokaryotic,3-1142); Required for chromosome condensation and partitioning. Belongs to the SMC family. (1155 aa) | ||||
clpA | ATP-dependent Clp protease ATP-binding subunit ClpA; Function of homologous gene experimentally demonstrated in an other organism; enzyme; Belongs to the ClpA/ClpB family. (764 aa) | ||||
cpaE | Flp pilus assembly protein, ATPase CpaE; Function of strongly homologous gene; transporter. (396 aa) | ||||
XM1_1398 | AFG1-like ATPase; Function of strongly homologous gene; enzyme. (387 aa) | ||||
cobS-2 | Aerobic cobaltochelatase subunit CobS; Function of homologous gene experimentally demonstrated in an other organism; enzyme. (333 aa) | ||||
XM1_1469 | P-type Ca2+ transporter type 2C; Function of strongly homologous gene; transporter. (874 aa) | ||||
lepA | GTP-binding membrane protein(Elongation factor, Elongation factor 4,6-597); Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back-translocation proceeds from a post-translocation (POST) complex to a pre- translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP- dependent manner. (600 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. (538 aa) | ||||
uvrB | UvrABC system protein B; The UvrABC repair system catalyzes the recognition and processing of DNA lesions. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. Upon binding of the UvrA(2)B(2) complex to a putative damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and [...] (703 aa) | ||||
XM1_1582 | Putative exopolyphosphatase(Ppx/GppA phosphatase,29-324) Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (333 aa) | ||||
XM1_1671 | Putative Rad3-related DNA helicase(ATP-dependent helicase, C-terminal,743-881); Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (918 aa) | ||||
XM1_1734 | Conserved protein of unknown function(AAA+ ATPase domain,194-344); Homologs of previously reported genes of unknown function. (412 aa) | ||||
XM1_1893 | Protein of unknown function(Domain of unknown function DUF59,4-78); No homology to any previously reported sequences. (101 aa) | ||||
nudF | ADP-ribose pyrophosphatase(NUDIX hydrolase domain,3-197); Function of homologous gene experimentally demonstrated in an other organism; enzyme. (202 aa) | ||||
XM1_2009 | Homologs of previously reported genes of unknown function. (193 aa) | ||||
XM1_2049 | Superfamily I DNA/RNA helicase; Function of strongly homologous gene; enzyme. (637 aa) | ||||
tufB | Protein chain elongation factor EF-Tu, possible GTP-binding factor (duplicate of tufA); This protein promotes the GTP-dependent binding of aminoacyl- tRNA to the A-site of ribosomes during protein biosynthesis. (396 aa) | ||||
fusA | Protein chain elongation factor EF-G, GTP-binding; Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post-translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome; Belongs to the TRAFAC class translation factor GTPase superfamily. Classic translation factor GTPase f [...] (694 aa) | ||||
tufB-2 | Protein chain elongation factor EF-Tu, possible GTP-binding factor (duplicate of tufA); Function of homologous gene experimentally demonstrated in an other organism; factor. (396 aa) | ||||
XM1_2305 | Putative ATP-dependent Zn protease (fragment); Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme; Belongs to the AAA ATPase family. (298 aa) | ||||
mamK | Magnetosome cytoskeleton protein MamK; Function of strongly homologous gene; putative enzyme. (347 aa) | ||||
XM1_2406 | Heavy metal-(Cd/Co/Hg/Pb/Zn)-translocating P-type ATPase:Heavy metal translocating P-type ATPase; Function of strongly homologous gene; transporter. (757 aa) | ||||
ftsZ-2 | 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. (311 aa) | ||||
XM1_2567 | Putative HAD superfamily P-type ATPase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (883 aa) | ||||
XM1_2614 | Putative Prophage LambdaW4, terminase large subunit; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (662 aa) | ||||
XM1_2620 | Putative Replicative DNA helicase; 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. (488 aa) | ||||
XM1_2681 | Putative adenylate cyclase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (511 aa) | ||||
XM1_2809 | Putative Helicase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (954 aa) | ||||
dnaB-2 | Replicative DNA helicase dnaB; 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. (505 aa) | ||||
cysC | Adenylylsulphate kinase; Catalyzes the synthesis of activated sulfate. (641 aa) | ||||
era | GTPase Era; An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism. (303 aa) | ||||
XM1_3097 | Protein of unknown function; No homology to any previously reported sequences. (194 aa) | ||||
hppA | K(+)-insensitive pyrophosphate-energized proton pump; Proton pump that utilizes the energy of pyrophosphate hydrolysis as the driving force for proton movement across the membrane. Generates a proton motive force. (693 aa) | ||||
hflX | Putative GTPase; GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis. Belongs to the TRAFAC class OBG-HflX-like GTPase superfamily. HflX GTPase family. (435 aa) | ||||
uvrA | ATPase and DNA damage recognition protein of nucleotide excision repair excinuclease UvrABC; The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate. (947 aa) | ||||
mazG | Nucleoside triphosphate pyrophosphohydrolase; Function of homologous gene experimentally demonstrated in an other organism; enzyme. (278 aa) | ||||
XM1_3222 | Protein of unknown function; No homology to any previously reported sequences. (272 aa) | ||||
XM1_3288 | Putative segregation and condensation protein B homolog; Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves. (216 aa) | ||||
XM1_3510 | Putative NADH pyrophosphatase; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (306 aa) | ||||
copA | Copper transporter ATPase; Function of homologous gene experimentally demonstrated in an other organism; transporter. (724 aa) | ||||
lon | DNA-binding ATP-dependent protease La; ATP-dependent serine protease that mediates the selective degradation of mutant and abnormal proteins as well as certain short- lived regulatory proteins. Required for cellular homeostasis and for survival from DNA damage and developmental changes induced by stress. Degrades polypeptides processively to yield small peptide fragments that are 5 to 10 amino acids long. Binds to DNA in a double-stranded, site-specific manner. (803 aa) | ||||
clpX | ATPase and specificity subunit of ClpX-ClpP ATP-dependent serine protease; ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP. (421 aa) | ||||
XM1_3789 | Putative ATPase domain (N-terminal fragment); Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme; Belongs to the AAA ATPase family. (675 aa) | ||||
hypB | GTP hydrolase involved in nickel liganding into hydrogenases; Function of homologous gene experimentally demonstrated in an other organism; enzyme. (315 aa) | ||||
hypF | Hydrogenase maturation factor; Function of homologous gene experimentally demonstrated in an other organism; enzyme. (358 aa) | ||||
clpB | Protein disaggregation chaperone; Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE; Belongs to the ClpA/ClpB family. (863 aa) | ||||
bacA | Undecaprenyl pyrophosphate phosphatase; Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin; Belongs to the UppP family. (264 aa) | ||||
XM1_3973 | Putative periplasmic protein kinase ArgK; Function proposed based on presence of conserved amino acid motif, structural feature or limited homology; putative enzyme. (314 aa) | ||||
copA-2 | Copper transporter ATPase; Function of strongly homologous gene; enzyme. (802 aa) | ||||
norQ | NorQ protein required for nitric oxide reductase (Nor) activity; Function of homologous gene experimentally demonstrated in an other organism; enzyme. (260 aa) | ||||
XM1_4094 | Protein of unknown function (putative phage tail fiber protein); No homology to any previously reported sequences. (168 aa) | ||||
ftsH | Protease, ATP-dependent zinc-metallo (Cell division protein FtsH) Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins; Belongs to the AAA ATPase family. In the central section; belongs to the AAA ATPase family. (638 aa) | ||||
ruvB | ATP-dependent DNA helicase, component of RuvABC resolvasome; 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. (347 aa) | ||||
ruvA | Holliday junction ATP-dependent 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. (210 aa) | ||||
XM1_4218 | Putative septum formation protein (Maf-like protein); Nucleoside triphosphate pyrophosphatase that hydrolyzes dTTP and UTP. May have a dual role in cell division arrest and in preventing the incorporation of modified nucleotides into cellular nucleic acids. (190 aa) | ||||
rarA | Replication-associated recombination protein A; Function of homologous gene experimentally demonstrated in an other organism; enzyme. (429 aa) | ||||
XM1_4363 | Putative iron-sulfur protein NUBPL (Protein mrp homolog); Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP; Belongs to the Mrp/NBP35 ATP-binding proteins family. (372 aa) | ||||
XM1_4608 | Protein of unknown function; No homology to any previously reported sequences. (501 aa) | ||||
guaA | GMP synthetase (glutamine aminotransferase); Catalyzes the synthesis of GMP from XMP. (518 aa) | ||||
uvrD | DNA-dependent ATPase I and helicase II; Function of strongly homologous gene; enzyme. (760 aa) | ||||
fusA-2 | Elongation factor G-like protein; Function of strongly homologous gene; factor. (675 aa) | ||||
fliI | Flagellum-specific ATP synthase; Function of strongly homologous gene; structure. (450 aa) |