ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AJOHDNBE_00001 | 3.1e-55 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
AJOHDNBE_00002 | 1.5e-76 | yxaM | EGP | Major facilitator Superfamily | ||
AJOHDNBE_00003 | 2.2e-85 | yxaM | EGP | Major facilitator Superfamily | ||
AJOHDNBE_00004 | 2.4e-136 | S | Alpha/beta hydrolase family | |||
AJOHDNBE_00005 | 6.7e-90 | rimL | J | Acetyltransferase (GNAT) domain | ||
AJOHDNBE_00006 | 5.1e-230 | |||||
AJOHDNBE_00007 | 1.3e-107 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
AJOHDNBE_00008 | 7.5e-116 | S | Fic/DOC family | |||
AJOHDNBE_00009 | 2.1e-23 | S | Protein of unknown function (DUF3923) | |||
AJOHDNBE_00010 | 1.2e-58 | |||||
AJOHDNBE_00011 | 6.9e-47 | S | MazG-like family | |||
AJOHDNBE_00012 | 2e-149 | S | Protein of unknown function (DUF2785) | |||
AJOHDNBE_00013 | 1.4e-78 | |||||
AJOHDNBE_00014 | 1.2e-102 | speG | J | Acetyltransferase (GNAT) domain | ||
AJOHDNBE_00015 | 4.8e-49 | |||||
AJOHDNBE_00016 | 1.5e-281 | V | ABC transporter transmembrane region | |||
AJOHDNBE_00017 | 5.8e-288 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
AJOHDNBE_00018 | 1e-229 | S | Tetratricopeptide repeat protein | |||
AJOHDNBE_00019 | 2.3e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
AJOHDNBE_00020 | 1.9e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
AJOHDNBE_00021 | 5.5e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
AJOHDNBE_00022 | 2.2e-114 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
AJOHDNBE_00023 | 2.7e-18 | M | Lysin motif | |||
AJOHDNBE_00024 | 8.7e-114 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
AJOHDNBE_00025 | 3.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
AJOHDNBE_00026 | 4.1e-104 | scpB | D | 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 | ||
AJOHDNBE_00027 | 2.9e-131 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
AJOHDNBE_00028 | 2.6e-61 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
AJOHDNBE_00029 | 7.6e-166 | xerD | D | recombinase XerD | ||
AJOHDNBE_00030 | 6.8e-167 | cvfB | S | S1 domain | ||
AJOHDNBE_00031 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
AJOHDNBE_00032 | 3.3e-183 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
AJOHDNBE_00033 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
AJOHDNBE_00034 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
AJOHDNBE_00035 | 7.3e-310 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
AJOHDNBE_00036 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
AJOHDNBE_00037 | 2.5e-34 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
AJOHDNBE_00038 | 1.6e-143 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AJOHDNBE_00039 | 1.3e-176 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
AJOHDNBE_00040 | 3.7e-295 | I | Acyltransferase | |||
AJOHDNBE_00041 | 1.7e-243 | obg | S | 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 | ||
AJOHDNBE_00042 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
AJOHDNBE_00043 | 1.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
AJOHDNBE_00044 | 4.8e-244 | yfnA | E | Amino Acid | ||
AJOHDNBE_00045 | 3.6e-182 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
AJOHDNBE_00046 | 5.2e-150 | yxeH | S | hydrolase | ||
AJOHDNBE_00047 | 2.9e-156 | S | reductase | |||
AJOHDNBE_00048 | 2e-214 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
AJOHDNBE_00049 | 2.4e-220 | patA | 2.6.1.1 | E | Aminotransferase | |
AJOHDNBE_00050 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
AJOHDNBE_00051 | 6.8e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
AJOHDNBE_00052 | 6e-76 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
AJOHDNBE_00053 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
AJOHDNBE_00054 | 2.9e-60 | |||||
AJOHDNBE_00055 | 9.3e-175 | prmA | J | Ribosomal protein L11 methyltransferase | ||
AJOHDNBE_00056 | 8.2e-85 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AJOHDNBE_00057 | 2.8e-249 | yjjP | S | Putative threonine/serine exporter | ||
AJOHDNBE_00058 | 2.6e-177 | citR | K | Putative sugar-binding domain | ||
AJOHDNBE_00059 | 1.3e-51 | |||||
AJOHDNBE_00060 | 5.5e-09 | |||||
AJOHDNBE_00061 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
AJOHDNBE_00062 | 7.4e-95 | S | UPF0397 protein | |||
AJOHDNBE_00063 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
AJOHDNBE_00064 | 3.6e-146 | cbiQ | P | cobalt transport | ||
AJOHDNBE_00065 | 1.8e-22 | |||||
AJOHDNBE_00066 | 9.3e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
AJOHDNBE_00067 | 4.9e-290 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
AJOHDNBE_00068 | 8.2e-168 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
AJOHDNBE_00069 | 1.2e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
AJOHDNBE_00070 | 2.2e-196 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
AJOHDNBE_00071 | 4.5e-154 | ydjP | I | Alpha/beta hydrolase family | ||
AJOHDNBE_00072 | 4.7e-274 | P | Sodium:sulfate symporter transmembrane region | |||
AJOHDNBE_00073 | 1.3e-133 | hxlA | 6.2.1.3 | H | Aldolase/RraA | |
AJOHDNBE_00074 | 6.6e-65 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
AJOHDNBE_00075 | 1.2e-32 | skfE | V | ATPases associated with a variety of cellular activities | ||
AJOHDNBE_00076 | 1.1e-142 | |||||
AJOHDNBE_00077 | 1.7e-137 | |||||
AJOHDNBE_00078 | 6.7e-145 | |||||
AJOHDNBE_00079 | 3.8e-27 | |||||
AJOHDNBE_00080 | 3.9e-104 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
AJOHDNBE_00081 | 1.8e-144 | |||||
AJOHDNBE_00082 | 4.3e-169 | |||||
AJOHDNBE_00083 | 2.4e-264 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
AJOHDNBE_00084 | 1.3e-116 | 3.1.3.102, 3.1.3.104, 3.1.3.23 | G | Sucrose-6F-phosphate phosphohydrolase | ||
AJOHDNBE_00085 | 8.2e-185 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
AJOHDNBE_00086 | 2.1e-202 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
AJOHDNBE_00087 | 3.7e-179 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
AJOHDNBE_00088 | 6.3e-136 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | GHMP kinases N terminal domain | |
AJOHDNBE_00089 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
AJOHDNBE_00090 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
AJOHDNBE_00091 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
AJOHDNBE_00092 | 8.3e-90 | ypmB | S | Protein conserved in bacteria | ||
AJOHDNBE_00093 | 5.8e-260 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
AJOHDNBE_00094 | 1.3e-114 | dnaD | L | DnaD domain protein | ||
AJOHDNBE_00095 | 6.1e-114 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
AJOHDNBE_00096 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
AJOHDNBE_00097 | 4.5e-117 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
AJOHDNBE_00098 | 1e-107 | ypsA | S | Belongs to the UPF0398 family | ||
AJOHDNBE_00099 | 1.1e-68 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
AJOHDNBE_00100 | 1.6e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
AJOHDNBE_00101 | 8.8e-242 | cpdA | S | Calcineurin-like phosphoesterase | ||
AJOHDNBE_00102 | 3.4e-79 | |||||
AJOHDNBE_00103 | 1.9e-115 | rdgB | 3.6.1.66, 5.1.1.3 | F | Ham1 family | |
AJOHDNBE_00104 | 3.4e-33 | |||||
AJOHDNBE_00105 | 3.6e-63 | |||||
AJOHDNBE_00108 | 1.3e-118 | |||||
AJOHDNBE_00109 | 1e-104 | pncA | Q | Isochorismatase family | ||
AJOHDNBE_00111 | 1.4e-36 | |||||
AJOHDNBE_00113 | 5.7e-115 | snf | 2.7.11.1 | KL | domain protein | |
AJOHDNBE_00114 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
AJOHDNBE_00115 | 3.5e-109 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
AJOHDNBE_00116 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AJOHDNBE_00117 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
AJOHDNBE_00118 | 1.9e-183 | K | Transcriptional regulator | |||
AJOHDNBE_00119 | 7.3e-172 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
AJOHDNBE_00120 | 1.1e-112 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
AJOHDNBE_00121 | 4e-57 | K | Helix-turn-helix domain | |||
AJOHDNBE_00122 | 2.7e-123 | yoaK | S | Protein of unknown function (DUF1275) | ||
AJOHDNBE_00123 | 2e-39 | S | Transglycosylase associated protein | |||
AJOHDNBE_00124 | 1.5e-211 | M | Glycosyl hydrolases family 25 | |||
AJOHDNBE_00125 | 8e-111 | XK27_00160 | S | Domain of unknown function (DUF5052) | ||
AJOHDNBE_00126 | 4.1e-67 | |||||
AJOHDNBE_00127 | 1.8e-66 | M | LysM domain protein | |||
AJOHDNBE_00128 | 1.1e-152 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
AJOHDNBE_00129 | 7.9e-67 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AJOHDNBE_00130 | 9.2e-65 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
AJOHDNBE_00131 | 3.3e-11 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AJOHDNBE_00132 | 3.8e-127 | mmuP | E | amino acid | ||
AJOHDNBE_00133 | 7.6e-274 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
AJOHDNBE_00134 | 1.6e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
AJOHDNBE_00135 | 1.7e-284 | E | Amino acid permease | |||
AJOHDNBE_00136 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
AJOHDNBE_00137 | 9.3e-247 | ynbB | 4.4.1.1 | P | aluminum resistance | |
AJOHDNBE_00138 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
AJOHDNBE_00139 | 3.4e-82 | C | Flavodoxin | |||
AJOHDNBE_00140 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
AJOHDNBE_00141 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
AJOHDNBE_00142 | 4.4e-112 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AJOHDNBE_00143 | 1.9e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
AJOHDNBE_00144 | 4.1e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
AJOHDNBE_00145 | 2.7e-203 | pbpX1 | V | Beta-lactamase | ||
AJOHDNBE_00146 | 1.7e-100 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
AJOHDNBE_00147 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
AJOHDNBE_00148 | 2e-230 | S | Putative peptidoglycan binding domain | |||
AJOHDNBE_00149 | 2.8e-84 | K | Acetyltransferase (GNAT) domain | |||
AJOHDNBE_00150 | 4.9e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AJOHDNBE_00151 | 4.7e-190 | yrvN | L | AAA C-terminal domain | ||
AJOHDNBE_00152 | 2.8e-64 | spxA_2 | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
AJOHDNBE_00153 | 2.9e-270 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
AJOHDNBE_00154 | 1.3e-17 | |||||
AJOHDNBE_00155 | 9.5e-239 | G | Bacterial extracellular solute-binding protein | |||
AJOHDNBE_00156 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
AJOHDNBE_00157 | 5.9e-238 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
AJOHDNBE_00160 | 6.7e-12 | S | CAAX amino terminal protease | |||
AJOHDNBE_00161 | 2.4e-311 | 1.3.5.4 | C | FMN_bind | ||
AJOHDNBE_00162 | 0.0 | L | Type III restriction enzyme, res subunit | |||
AJOHDNBE_00163 | 4.6e-17 | |||||
AJOHDNBE_00164 | 1.8e-90 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
AJOHDNBE_00165 | 9.2e-111 | |||||
AJOHDNBE_00166 | 1.3e-160 | 3.6.4.12 | KL | ATP-dependent helicase | ||
AJOHDNBE_00167 | 2.9e-47 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
AJOHDNBE_00168 | 2.4e-112 | S | SLAP domain | |||
AJOHDNBE_00169 | 1.9e-88 | |||||
AJOHDNBE_00170 | 3e-09 | isdH | M | Iron Transport-associated domain | ||
AJOHDNBE_00171 | 5.7e-124 | M | Iron Transport-associated domain | |||
AJOHDNBE_00172 | 1.5e-158 | isdE | P | Periplasmic binding protein | ||
AJOHDNBE_00173 | 5.1e-149 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
AJOHDNBE_00174 | 2e-138 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
AJOHDNBE_00175 | 6.7e-44 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
AJOHDNBE_00176 | 1.2e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
AJOHDNBE_00177 | 1.3e-38 | S | RelB antitoxin | |||
AJOHDNBE_00178 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
AJOHDNBE_00179 | 0.0 | S | membrane | |||
AJOHDNBE_00180 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
AJOHDNBE_00181 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
AJOHDNBE_00182 | 2.1e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
AJOHDNBE_00183 | 1.1e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
AJOHDNBE_00184 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
AJOHDNBE_00185 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
AJOHDNBE_00186 | 9.2e-170 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
AJOHDNBE_00187 | 2e-225 | ynbB | 4.4.1.1 | P | aluminum resistance | |
AJOHDNBE_00188 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
AJOHDNBE_00189 | 1e-170 | |||||
AJOHDNBE_00190 | 3.1e-144 | |||||
AJOHDNBE_00191 | 1.8e-13 | hicA | S | HicA toxin of bacterial toxin-antitoxin, | ||
AJOHDNBE_00192 | 7e-32 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
AJOHDNBE_00194 | 3e-33 | |||||
AJOHDNBE_00195 | 4.9e-99 | L | An automated process has identified a potential problem with this gene model | |||
AJOHDNBE_00196 | 6.5e-252 | E | Amino acid permease | |||
AJOHDNBE_00197 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
AJOHDNBE_00198 | 1.4e-62 | |||||
AJOHDNBE_00199 | 1.3e-259 | uvrX | 2.7.7.7 | L | Belongs to the DNA polymerase type-Y family | |
AJOHDNBE_00200 | 0.0 | O | Belongs to the peptidase S8 family | |||
AJOHDNBE_00201 | 1.3e-174 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
AJOHDNBE_00202 | 1.9e-93 | dhaL | 2.7.1.121 | S | Dak2 | |
AJOHDNBE_00203 | 1.3e-55 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
AJOHDNBE_00204 | 2e-121 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AJOHDNBE_00205 | 3.2e-104 | S | Domain of unknown function DUF1829 | |||
AJOHDNBE_00206 | 8e-82 | |||||
AJOHDNBE_00207 | 3.8e-78 | O | OsmC-like protein | |||
AJOHDNBE_00208 | 3.9e-187 | lplA2 | 6.3.1.20 | H | Bacterial lipoate protein ligase C-terminus | |
AJOHDNBE_00209 | 3.7e-134 | V | Abi-like protein | |||
AJOHDNBE_00210 | 3.8e-27 | |||||
AJOHDNBE_00211 | 0.0 | snf | 2.7.11.1 | KL | domain protein | |
AJOHDNBE_00212 | 6.6e-31 | |||||
AJOHDNBE_00213 | 4.6e-33 | |||||
AJOHDNBE_00214 | 8.5e-23 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
AJOHDNBE_00215 | 1.6e-23 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
AJOHDNBE_00216 | 3.3e-12 | T | SpoVT / AbrB like domain | |||
AJOHDNBE_00217 | 8.8e-109 | V | Abi-like protein | |||
AJOHDNBE_00219 | 4.3e-189 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
AJOHDNBE_00220 | 6.9e-104 | rfbC | 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
AJOHDNBE_00221 | 1.1e-156 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
AJOHDNBE_00223 | 8.1e-09 | tuaH_2 | 5.4.99.9 | M | Glycosyltransferase like family 2 | |
AJOHDNBE_00224 | 4.8e-133 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
AJOHDNBE_00225 | 3.3e-100 | epsI | GM | polysaccharide biosynthetic process | ||
AJOHDNBE_00226 | 8.7e-79 | M | Glycosyl transferases group 1 | |||
AJOHDNBE_00227 | 2.1e-122 | cps1B | GT2,GT4 | M | Glycosyl transferases group 1 | |
AJOHDNBE_00228 | 1.2e-88 | S | EpsG family | |||
AJOHDNBE_00229 | 2.1e-94 | GT8 | S | Protein conserved in bacteria | ||
AJOHDNBE_00230 | 3.1e-95 | pglI | 2.4.1.293 | GT2 | M | Glycosyl transferase family 2 |
AJOHDNBE_00231 | 1.7e-65 | cps4G | M | Glycosyl transferases group 1 | ||
AJOHDNBE_00232 | 6.8e-68 | cps4F | 2.4.1.306 | GT4 | M | Glycosyl transferases group 1 |
AJOHDNBE_00233 | 1.9e-94 | tuaA | M | Bacterial sugar transferase | ||
AJOHDNBE_00234 | 3.3e-164 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
AJOHDNBE_00235 | 1.7e-137 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
AJOHDNBE_00236 | 2.4e-120 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
AJOHDNBE_00237 | 3.1e-140 | epsB | M | biosynthesis protein | ||
AJOHDNBE_00238 | 2e-151 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
AJOHDNBE_00239 | 2.3e-69 | K | Transcriptional regulator, HxlR family | |||
AJOHDNBE_00240 | 6.3e-139 | |||||
AJOHDNBE_00241 | 1.1e-106 | K | DNA-templated transcription, initiation | |||
AJOHDNBE_00242 | 9.5e-39 | |||||
AJOHDNBE_00243 | 3.7e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
AJOHDNBE_00244 | 7.7e-233 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
AJOHDNBE_00245 | 4e-216 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
AJOHDNBE_00246 | 3.3e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
AJOHDNBE_00247 | 8.3e-151 | |||||
AJOHDNBE_00248 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AJOHDNBE_00249 | 1.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
AJOHDNBE_00250 | 6.7e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
AJOHDNBE_00251 | 2.6e-175 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
AJOHDNBE_00252 | 0.0 | comEC | S | Competence protein ComEC | ||
AJOHDNBE_00253 | 5.7e-81 | comEA | L | Competence protein ComEA | ||
AJOHDNBE_00254 | 3.3e-189 | ylbL | T | Belongs to the peptidase S16 family | ||
AJOHDNBE_00255 | 3.6e-82 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
AJOHDNBE_00256 | 4.5e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
AJOHDNBE_00257 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
AJOHDNBE_00258 | 2.7e-211 | ftsW | D | Belongs to the SEDS family | ||
AJOHDNBE_00259 | 0.0 | typA | T | GTP-binding protein TypA | ||
AJOHDNBE_00260 | 4e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
AJOHDNBE_00261 | 4.6e-32 | ykzG | S | Belongs to the UPF0356 family | ||
AJOHDNBE_00262 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
AJOHDNBE_00263 | 6.7e-181 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
AJOHDNBE_00264 | 1e-293 | L | Nuclease-related domain | |||
AJOHDNBE_00265 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
AJOHDNBE_00266 | 8.3e-106 | S | Repeat protein | |||
AJOHDNBE_00267 | 1.5e-126 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
AJOHDNBE_00268 | 4.6e-221 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
AJOHDNBE_00269 | 2.2e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
AJOHDNBE_00270 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
AJOHDNBE_00271 | 3.5e-126 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
AJOHDNBE_00272 | 9.1e-34 | |||||
AJOHDNBE_00273 | 9.8e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
AJOHDNBE_00274 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
AJOHDNBE_00275 | 8.3e-168 | V | ABC transporter | |||
AJOHDNBE_00276 | 3e-123 | S | domain protein | |||
AJOHDNBE_00277 | 3.5e-105 | yyaR | K | Acetyltransferase (GNAT) domain | ||
AJOHDNBE_00278 | 2.2e-73 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
AJOHDNBE_00279 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
AJOHDNBE_00280 | 3e-57 | rplT | J | 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 | ||
AJOHDNBE_00281 | 5.6e-154 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
AJOHDNBE_00282 | 9.2e-201 | tnpB | L | Putative transposase DNA-binding domain | ||
AJOHDNBE_00283 | 4.2e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
AJOHDNBE_00284 | 1.4e-201 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
AJOHDNBE_00285 | 2e-120 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
AJOHDNBE_00286 | 6.6e-110 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
AJOHDNBE_00287 | 5.3e-59 | rsfS | J | 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 | ||
AJOHDNBE_00288 | 1.2e-216 | ylbM | S | Belongs to the UPF0348 family | ||
AJOHDNBE_00289 | 5.5e-98 | yceD | S | Uncharacterized ACR, COG1399 | ||
AJOHDNBE_00290 | 1.2e-126 | K | response regulator | |||
AJOHDNBE_00291 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
AJOHDNBE_00292 | 2.9e-131 | S | CAAX protease self-immunity | |||
AJOHDNBE_00293 | 1.4e-223 | S | SLAP domain | |||
AJOHDNBE_00294 | 1.2e-54 | S | Abi-like protein | |||
AJOHDNBE_00295 | 1.5e-72 | S | Aminoacyl-tRNA editing domain | |||
AJOHDNBE_00296 | 1.7e-160 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
AJOHDNBE_00297 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
AJOHDNBE_00298 | 9.7e-138 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
AJOHDNBE_00299 | 3.6e-63 | yodB | K | Transcriptional regulator, HxlR family | ||
AJOHDNBE_00301 | 5.1e-111 | papP | P | ABC transporter, permease protein | ||
AJOHDNBE_00302 | 2.8e-117 | P | ABC transporter permease | |||
AJOHDNBE_00303 | 2.8e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
AJOHDNBE_00304 | 2.9e-162 | cjaA | ET | ABC transporter substrate-binding protein | ||
AJOHDNBE_00305 | 3.2e-200 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
AJOHDNBE_00306 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AJOHDNBE_00307 | 4.9e-63 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
AJOHDNBE_00308 | 4.3e-169 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
AJOHDNBE_00309 | 1.9e-158 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
AJOHDNBE_00310 | 5.7e-25 | |||||
AJOHDNBE_00311 | 7.5e-38 | mco | Q | Multicopper oxidase | ||
AJOHDNBE_00312 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
AJOHDNBE_00313 | 1.1e-103 | srtA | 3.4.22.70 | M | sortase family | |
AJOHDNBE_00314 | 0.0 | lepA | M | 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 | ||
AJOHDNBE_00315 | 8.3e-202 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
AJOHDNBE_00316 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
AJOHDNBE_00317 | 2.3e-67 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
AJOHDNBE_00318 | 4.5e-194 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
AJOHDNBE_00319 | 7.5e-177 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
AJOHDNBE_00320 | 3.4e-158 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
AJOHDNBE_00321 | 3e-60 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
AJOHDNBE_00322 | 0.0 | infB | J | 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 | ||
AJOHDNBE_00323 | 3.2e-47 | rplGA | J | ribosomal protein | ||
AJOHDNBE_00324 | 8.8e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
AJOHDNBE_00325 | 2.6e-198 | nusA | K | Participates in both transcription termination and antitermination | ||
AJOHDNBE_00326 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
AJOHDNBE_00327 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
AJOHDNBE_00328 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
AJOHDNBE_00329 | 1.7e-195 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
AJOHDNBE_00330 | 9.6e-136 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
AJOHDNBE_00331 | 1.6e-137 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
AJOHDNBE_00332 | 5.3e-93 | frr | J | 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 | ||
AJOHDNBE_00333 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
AJOHDNBE_00334 | 8.3e-185 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
AJOHDNBE_00335 | 8.2e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
AJOHDNBE_00336 | 2.1e-102 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
AJOHDNBE_00337 | 3.7e-199 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
AJOHDNBE_00338 | 7.4e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
AJOHDNBE_00339 | 1.2e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
AJOHDNBE_00340 | 7.9e-111 | G | Phosphoglycerate mutase family | |||
AJOHDNBE_00341 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
AJOHDNBE_00342 | 6.5e-151 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AJOHDNBE_00343 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
AJOHDNBE_00344 | 7.2e-56 | yheA | S | Belongs to the UPF0342 family | ||
AJOHDNBE_00345 | 5.7e-225 | yhaO | L | Ser Thr phosphatase family protein | ||
AJOHDNBE_00346 | 0.0 | L | AAA domain | |||
AJOHDNBE_00347 | 2.8e-182 | cbf | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
AJOHDNBE_00348 | 3.8e-15 | |||||
AJOHDNBE_00349 | 2e-26 | K | Helix-turn-helix XRE-family like proteins | |||
AJOHDNBE_00350 | 9.6e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
AJOHDNBE_00351 | 3.9e-25 | |||||
AJOHDNBE_00352 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
AJOHDNBE_00353 | 2e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
AJOHDNBE_00354 | 2.2e-221 | ecsB | U | ABC transporter | ||
AJOHDNBE_00355 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
AJOHDNBE_00356 | 3.8e-13 | S | Protein of unknown function (DUF805) | |||
AJOHDNBE_00357 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
AJOHDNBE_00358 | 1.7e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
AJOHDNBE_00359 | 1.4e-248 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
AJOHDNBE_00360 | 5.9e-129 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
AJOHDNBE_00361 | 2.4e-184 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AJOHDNBE_00362 | 8.3e-41 | M | Peptidase family M1 domain | |||
AJOHDNBE_00363 | 1.7e-162 | M | Peptidase family M1 domain | |||
AJOHDNBE_00364 | 7.8e-51 | S | Alpha beta hydrolase | |||
AJOHDNBE_00367 | 2e-255 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
AJOHDNBE_00368 | 1.4e-150 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
AJOHDNBE_00369 | 1.7e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
AJOHDNBE_00370 | 7.8e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
AJOHDNBE_00371 | 3e-196 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
AJOHDNBE_00372 | 4.9e-102 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
AJOHDNBE_00373 | 3.4e-71 | yqhY | S | Asp23 family, cell envelope-related function | ||
AJOHDNBE_00374 | 2.1e-64 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
AJOHDNBE_00375 | 3.4e-144 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
AJOHDNBE_00376 | 3.8e-185 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
AJOHDNBE_00377 | 1.1e-34 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
AJOHDNBE_00378 | 2.4e-153 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
AJOHDNBE_00379 | 1.2e-151 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
AJOHDNBE_00380 | 4.8e-307 | recN | L | May be involved in recombinational repair of damaged DNA | ||
AJOHDNBE_00381 | 1.1e-77 | 6.3.3.2 | S | ASCH | ||
AJOHDNBE_00382 | 2.1e-111 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
AJOHDNBE_00383 | 1.1e-33 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
AJOHDNBE_00384 | 0.0 | priA | L | 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 | ||
AJOHDNBE_00385 | 7.4e-172 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
AJOHDNBE_00386 | 5.7e-242 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
AJOHDNBE_00387 | 1.3e-139 | stp | 3.1.3.16 | T | phosphatase | |
AJOHDNBE_00388 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
AJOHDNBE_00389 | 3.3e-166 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
AJOHDNBE_00390 | 1.7e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
AJOHDNBE_00391 | 1.4e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
AJOHDNBE_00392 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
AJOHDNBE_00393 | 4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
AJOHDNBE_00394 | 2e-305 | yloV | S | DAK2 domain fusion protein YloV | ||
AJOHDNBE_00395 | 5.3e-172 | fpaP | 3.4.11.5 | I | Releases the N-terminal proline from various substrates | |
AJOHDNBE_00396 | 5.3e-50 | S | PFAM Neutral alkaline nonlysosomal ceramidase | |||
AJOHDNBE_00397 | 3.1e-123 | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |||
AJOHDNBE_00398 | 3.4e-42 | K | Helix-turn-helix domain, rpiR family | |||
AJOHDNBE_00399 | 1.9e-80 | L | helicase | |||
AJOHDNBE_00400 | 9.5e-255 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
AJOHDNBE_00401 | 6.8e-72 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
AJOHDNBE_00402 | 3.2e-159 | L | Belongs to the 'phage' integrase family | |||
AJOHDNBE_00403 | 7.4e-62 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AJOHDNBE_00404 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
AJOHDNBE_00406 | 1.9e-298 | yfjM | S | Protein of unknown function DUF262 | ||
AJOHDNBE_00407 | 2.1e-219 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AJOHDNBE_00408 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AJOHDNBE_00409 | 3e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
AJOHDNBE_00410 | 3e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
AJOHDNBE_00411 | 1.9e-98 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
AJOHDNBE_00412 | 9.3e-81 | S | AAA domain | |||
AJOHDNBE_00413 | 6.9e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
AJOHDNBE_00414 | 3.1e-144 | 2.4.2.3 | F | Phosphorylase superfamily | ||
AJOHDNBE_00415 | 2.2e-149 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
AJOHDNBE_00416 | 7.6e-100 | yagE | E | Amino acid permease | ||
AJOHDNBE_00417 | 1.3e-38 | yagE | E | amino acid | ||
AJOHDNBE_00418 | 4.3e-86 | 3.4.21.96 | S | SLAP domain | ||
AJOHDNBE_00419 | 4.6e-160 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
AJOHDNBE_00420 | 1.1e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
AJOHDNBE_00421 | 1.2e-107 | hlyIII | S | protein, hemolysin III | ||
AJOHDNBE_00422 | 2.8e-146 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
AJOHDNBE_00423 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
AJOHDNBE_00424 | 3.6e-40 | yjcE | P | NhaP-type Na H and K H | ||
AJOHDNBE_00425 | 2.9e-185 | yjcE | P | Sodium proton antiporter | ||
AJOHDNBE_00426 | 7.3e-155 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
AJOHDNBE_00427 | 4.6e-132 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
AJOHDNBE_00428 | 3.1e-153 | dprA | LU | DNA protecting protein DprA | ||
AJOHDNBE_00429 | 0.0 | topA | 5.99.1.2 | L | 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 supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
AJOHDNBE_00430 | 2.7e-249 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
AJOHDNBE_00431 | 2.2e-141 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
AJOHDNBE_00432 | 1.9e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
AJOHDNBE_00433 | 8.2e-236 | hslU | O | 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 | ||
AJOHDNBE_00434 | 8.7e-60 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
AJOHDNBE_00435 | 1.6e-55 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
AJOHDNBE_00436 | 3.7e-128 | K | UTRA domain | |||
AJOHDNBE_00437 | 8.9e-294 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
AJOHDNBE_00438 | 2.2e-90 | alkD | L | DNA alkylation repair enzyme | ||
AJOHDNBE_00439 | 2.8e-176 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
AJOHDNBE_00440 | 2.3e-82 | |||||
AJOHDNBE_00441 | 3.6e-39 | C | FMN_bind | |||
AJOHDNBE_00442 | 1.8e-298 | I | Protein of unknown function (DUF2974) | |||
AJOHDNBE_00443 | 5.6e-195 | pbpX1 | V | Beta-lactamase | ||
AJOHDNBE_00444 | 1.6e-199 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
AJOHDNBE_00445 | 3.2e-217 | aspC | 2.6.1.1 | E | Aminotransferase | |
AJOHDNBE_00446 | 7e-144 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
AJOHDNBE_00447 | 4.4e-177 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
AJOHDNBE_00448 | 1.4e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
AJOHDNBE_00449 | 2.8e-75 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
AJOHDNBE_00450 | 1.1e-247 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
AJOHDNBE_00451 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AJOHDNBE_00452 | 8.9e-192 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
AJOHDNBE_00453 | 2.1e-97 | yjeM | E | Amino acid permease | ||
AJOHDNBE_00454 | 3.4e-46 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
AJOHDNBE_00455 | 2e-92 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
AJOHDNBE_00456 | 2.5e-283 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
AJOHDNBE_00457 | 8.9e-173 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
AJOHDNBE_00458 | 1.8e-238 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
AJOHDNBE_00459 | 9e-72 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
AJOHDNBE_00460 | 4.1e-31 | ywzB | S | Protein of unknown function (DUF1146) | ||
AJOHDNBE_00461 | 2.5e-178 | mbl | D | Cell shape determining protein MreB Mrl | ||
AJOHDNBE_00462 | 2e-51 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
AJOHDNBE_00463 | 1.5e-33 | S | Protein of unknown function (DUF2969) | |||
AJOHDNBE_00464 | 1.2e-216 | rodA | D | Belongs to the SEDS family | ||
AJOHDNBE_00465 | 6.8e-78 | usp6 | T | universal stress protein | ||
AJOHDNBE_00466 | 8.4e-39 | |||||
AJOHDNBE_00467 | 1.1e-237 | rarA | L | recombination factor protein RarA | ||
AJOHDNBE_00468 | 2.9e-84 | yueI | S | Protein of unknown function (DUF1694) | ||
AJOHDNBE_00469 | 2.6e-109 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
AJOHDNBE_00470 | 2.1e-294 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
AJOHDNBE_00471 | 1.8e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
AJOHDNBE_00472 | 5.1e-226 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
AJOHDNBE_00474 | 3.5e-82 | K | Helix-turn-helix XRE-family like proteins | |||
AJOHDNBE_00475 | 1.7e-61 | |||||
AJOHDNBE_00476 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
AJOHDNBE_00477 | 6.7e-150 | ylmH | S | S4 domain protein | ||
AJOHDNBE_00478 | 1.7e-45 | yggT | S | YGGT family | ||
AJOHDNBE_00479 | 7.3e-74 | sepF | D | 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 | ||
AJOHDNBE_00480 | 1.3e-214 | ftsZ | D | 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 | ||
AJOHDNBE_00481 | 2.6e-247 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
AJOHDNBE_00482 | 4.1e-153 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AJOHDNBE_00483 | 4.4e-208 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | 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) |
AJOHDNBE_00484 | 7.3e-261 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AJOHDNBE_00485 | 1.1e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
AJOHDNBE_00486 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
AJOHDNBE_00487 | 4.1e-54 | ftsL | D | Cell division protein FtsL | ||
AJOHDNBE_00488 | 1.3e-176 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
AJOHDNBE_00489 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
AJOHDNBE_00490 | 2.5e-239 | L | transposase, IS605 OrfB family | |||
AJOHDNBE_00491 | 1.1e-136 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
AJOHDNBE_00492 | 4.6e-179 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
AJOHDNBE_00493 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
AJOHDNBE_00494 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
AJOHDNBE_00495 | 9.9e-200 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
AJOHDNBE_00496 | 2.3e-127 | S | Peptidase family M23 | |||
AJOHDNBE_00497 | 4.8e-81 | mutT | 3.6.1.55 | F | NUDIX domain | |
AJOHDNBE_00498 | 1.2e-123 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
AJOHDNBE_00499 | 2.9e-153 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
AJOHDNBE_00500 | 7.5e-241 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
AJOHDNBE_00501 | 1.6e-61 | yvoA_1 | K | Transcriptional regulator, GntR family | ||
AJOHDNBE_00502 | 1.8e-282 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
AJOHDNBE_00503 | 8e-79 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
AJOHDNBE_00504 | 5.6e-169 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
AJOHDNBE_00505 | 4.6e-199 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AJOHDNBE_00506 | 0.0 | carB1 | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AJOHDNBE_00507 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
AJOHDNBE_00508 | 1.1e-66 | |||||
AJOHDNBE_00509 | 3.5e-160 | degV | S | EDD domain protein, DegV family | ||
AJOHDNBE_00510 | 1.3e-305 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
AJOHDNBE_00511 | 1.8e-203 | xerS | L | Belongs to the 'phage' integrase family | ||
AJOHDNBE_00512 | 9.7e-126 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
AJOHDNBE_00513 | 4e-245 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
AJOHDNBE_00514 | 6.4e-212 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
AJOHDNBE_00515 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
AJOHDNBE_00516 | 9.9e-251 | lctP | C | L-lactate permease | ||
AJOHDNBE_00517 | 6.1e-149 | glcU | U | sugar transport | ||
AJOHDNBE_00518 | 4.9e-47 | |||||
AJOHDNBE_00519 | 2.8e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
AJOHDNBE_00520 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
AJOHDNBE_00521 | 2.6e-42 | S | Alpha beta hydrolase | |||
AJOHDNBE_00522 | 1.9e-37 | |||||
AJOHDNBE_00523 | 2.6e-52 | |||||
AJOHDNBE_00524 | 3.3e-53 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
AJOHDNBE_00525 | 4.9e-260 | yfnA | E | amino acid | ||
AJOHDNBE_00526 | 5.2e-301 | V | FtsX-like permease family | |||
AJOHDNBE_00527 | 2.4e-133 | cysA | V | ABC transporter, ATP-binding protein | ||
AJOHDNBE_00529 | 1.5e-288 | pipD | E | Dipeptidase | ||
AJOHDNBE_00530 | 1.1e-162 | ftsY | U | 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) | ||
AJOHDNBE_00531 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
AJOHDNBE_00532 | 4.2e-124 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
AJOHDNBE_00533 | 1.7e-111 | oppA | E | ABC transporter substrate-binding protein | ||
AJOHDNBE_00534 | 2.1e-222 | sptS | 2.7.13.3 | T | Histidine kinase | |
AJOHDNBE_00535 | 1.1e-209 | EGP | Major facilitator Superfamily | |||
AJOHDNBE_00536 | 2.3e-69 | O | OsmC-like protein | |||
AJOHDNBE_00537 | 1.2e-94 | S | Protein of unknown function (DUF805) | |||
AJOHDNBE_00538 | 2.2e-78 | |||||
AJOHDNBE_00539 | 1.8e-286 | |||||
AJOHDNBE_00540 | 1.2e-137 | S | Fic/DOC family | |||
AJOHDNBE_00541 | 6.6e-304 | S | SLAP domain | |||
AJOHDNBE_00542 | 1.7e-279 | yjeM | E | Amino Acid | ||
AJOHDNBE_00543 | 4.4e-222 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
AJOHDNBE_00544 | 4.4e-244 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
AJOHDNBE_00546 | 1.8e-21 | rpiB | 5.3.1.6 | G | Ribose/Galactose Isomerase | |
AJOHDNBE_00547 | 7.1e-74 | |||||
AJOHDNBE_00548 | 4.1e-284 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AJOHDNBE_00549 | 2.1e-280 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AJOHDNBE_00550 | 2.1e-95 | |||||
AJOHDNBE_00551 | 1.8e-116 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
AJOHDNBE_00552 | 9e-98 | |||||
AJOHDNBE_00553 | 2e-109 | K | LysR substrate binding domain | |||
AJOHDNBE_00554 | 1e-20 | |||||
AJOHDNBE_00555 | 2.1e-213 | S | Sterol carrier protein domain | |||
AJOHDNBE_00556 | 2e-97 | citX | 2.4.2.52, 2.7.7.61 | HI | Apo-citrate lyase phosphoribosyl-dephospho-CoA transferase | |
AJOHDNBE_00557 | 3e-108 | argF | 2.1.3.3, 2.7.2.2 | E | Belongs to the carbamate kinase family | |
AJOHDNBE_00558 | 3.1e-33 | L | PFAM Integrase catalytic region | |||
AJOHDNBE_00559 | 3e-29 | |||||
AJOHDNBE_00560 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
AJOHDNBE_00562 | 4.3e-87 | yxiO | S | Vacuole effluxer Atg22 like | ||
AJOHDNBE_00563 | 2e-93 | yxiO | S | Vacuole effluxer Atg22 like | ||
AJOHDNBE_00564 | 5.5e-214 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AJOHDNBE_00565 | 7.9e-32 | npp | S | type I phosphodiesterase nucleotide pyrophosphatase | ||
AJOHDNBE_00566 | 2.3e-238 | E | amino acid | |||
AJOHDNBE_00567 | 6.7e-181 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
AJOHDNBE_00569 | 3.3e-219 | yxjG_1 | E | methionine synthase, vitamin-B12 independent | ||
AJOHDNBE_00574 | 1.3e-40 | |||||
AJOHDNBE_00575 | 8.1e-60 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
AJOHDNBE_00576 | 3.4e-91 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
AJOHDNBE_00579 | 4.2e-160 | repB | EP | Plasmid replication protein | ||
AJOHDNBE_00580 | 9.7e-18 | |||||
AJOHDNBE_00581 | 1.5e-161 | L | Belongs to the 'phage' integrase family | |||
AJOHDNBE_00582 | 6e-54 | L | An automated process has identified a potential problem with this gene model | |||
AJOHDNBE_00583 | 2.6e-48 | S | Bacteriocin helveticin-J | |||
AJOHDNBE_00584 | 8e-51 | L | RelB antitoxin | |||
AJOHDNBE_00585 | 2.7e-136 | qmcA | O | prohibitin homologues | ||
AJOHDNBE_00586 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
AJOHDNBE_00587 | 9.4e-155 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
AJOHDNBE_00588 | 1.3e-105 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
AJOHDNBE_00589 | 6e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
AJOHDNBE_00590 | 6.6e-251 | dnaB | L | Replication initiation and membrane attachment | ||
AJOHDNBE_00591 | 6.2e-168 | dnaI | L | Primosomal protein DnaI | ||
AJOHDNBE_00592 | 2.4e-251 | yifK | E | Amino acid permease | ||
AJOHDNBE_00593 | 2.3e-282 | V | ABC-type multidrug transport system, ATPase and permease components | |||
AJOHDNBE_00594 | 3.8e-182 | P | ABC transporter | |||
AJOHDNBE_00595 | 5.3e-85 | P | ABC transporter | |||
AJOHDNBE_00596 | 5.1e-37 | |||||
AJOHDNBE_00598 | 8.9e-124 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
AJOHDNBE_00599 | 2.5e-86 | K | GNAT family | |||
AJOHDNBE_00600 | 1.9e-203 | XK27_00915 | C | Luciferase-like monooxygenase | ||
AJOHDNBE_00601 | 4.6e-118 | rbtT | P | Major Facilitator Superfamily | ||
AJOHDNBE_00602 | 1.9e-80 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
AJOHDNBE_00603 | 6.9e-228 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
AJOHDNBE_00604 | 4e-107 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
AJOHDNBE_00605 | 4.2e-203 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
AJOHDNBE_00606 | 1.9e-141 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
AJOHDNBE_00607 | 4.5e-65 | S | Protein of unknown function (DUF3021) | |||
AJOHDNBE_00608 | 3e-75 | K | LytTr DNA-binding domain | |||
AJOHDNBE_00609 | 5.5e-158 | K | Transcriptional regulator | |||
AJOHDNBE_00610 | 2.1e-105 | S | Alpha beta hydrolase | |||
AJOHDNBE_00611 | 9.7e-283 | lsa | S | ABC transporter | ||
AJOHDNBE_00612 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
AJOHDNBE_00613 | 6.6e-262 | frdC | 1.3.5.4 | C | FAD binding domain | |
AJOHDNBE_00614 | 9e-267 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
AJOHDNBE_00615 | 2e-73 | metI | P | ABC transporter permease | ||
AJOHDNBE_00616 | 1e-190 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
AJOHDNBE_00617 | 2.9e-159 | metQ2 | P | Belongs to the nlpA lipoprotein family | ||
AJOHDNBE_00618 | 3.3e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
AJOHDNBE_00619 | 1.4e-38 | ynzC | S | UPF0291 protein | ||
AJOHDNBE_00620 | 2e-112 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
AJOHDNBE_00621 | 1.1e-144 | E | GDSL-like Lipase/Acylhydrolase family | |||
AJOHDNBE_00622 | 1.7e-122 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
AJOHDNBE_00623 | 2.1e-213 | S | SLAP domain | |||
AJOHDNBE_00624 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
AJOHDNBE_00625 | 5e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
AJOHDNBE_00626 | 5.8e-94 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
AJOHDNBE_00627 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
AJOHDNBE_00628 | 7.2e-115 | ffh | 3.6.5.4 | U | 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 | |
AJOHDNBE_00629 | 8.9e-248 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
AJOHDNBE_00630 | 1.8e-210 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
AJOHDNBE_00631 | 4.7e-131 | M | Glycosyl hydrolases family 25 | |||
AJOHDNBE_00632 | 6.3e-230 | potE | E | amino acid | ||
AJOHDNBE_00633 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
AJOHDNBE_00634 | 5e-221 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
AJOHDNBE_00635 | 1.1e-281 | thrC | 4.2.3.1 | E | Threonine synthase | |
AJOHDNBE_00636 | 2.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
AJOHDNBE_00637 | 9.6e-103 | pgm3 | 5.4.2.11 | G | Histidine phosphatase superfamily (branch 1) | |
AJOHDNBE_00638 | 0.0 | L | PLD-like domain | |||
AJOHDNBE_00639 | 4.5e-42 | recG | 3.6.4.12 | L | 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) | |
AJOHDNBE_00640 | 4.9e-182 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
AJOHDNBE_00641 | 9.8e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
AJOHDNBE_00642 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
AJOHDNBE_00643 | 8.8e-168 | oppF | P | Belongs to the ABC transporter superfamily | ||
AJOHDNBE_00644 | 5.7e-172 | oppB | P | ABC transporter permease | ||
AJOHDNBE_00645 | 6.9e-130 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
AJOHDNBE_00646 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
AJOHDNBE_00647 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
AJOHDNBE_00648 | 2.7e-241 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
AJOHDNBE_00649 | 2e-126 | S | Haloacid dehalogenase-like hydrolase | |||
AJOHDNBE_00650 | 2.3e-108 | radC | L | DNA repair protein | ||
AJOHDNBE_00651 | 1.8e-176 | mreB | D | cell shape determining protein MreB | ||
AJOHDNBE_00652 | 6.7e-148 | mreC | M | Involved in formation and maintenance of cell shape | ||
AJOHDNBE_00655 | 7.3e-08 | S | HEPN domain | |||
AJOHDNBE_00656 | 2.4e-66 | S | Bacteriophage holin family | |||
AJOHDNBE_00657 | 1.2e-34 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
AJOHDNBE_00658 | 2e-200 | 3.5.1.104 | M | hydrolase, family 25 | ||
AJOHDNBE_00659 | 2.4e-152 | |||||
AJOHDNBE_00660 | 1.3e-72 | |||||
AJOHDNBE_00661 | 3.6e-108 | xtp | 2.5.1.15, 3.6.1.66 | F | Ham1 family | |
AJOHDNBE_00662 | 1.1e-51 | |||||
AJOHDNBE_00663 | 2.7e-33 | |||||
AJOHDNBE_00665 | 1.5e-86 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
AJOHDNBE_00666 | 0.0 | L | Plasmid pRiA4b ORF-3-like protein | |||
AJOHDNBE_00667 | 1.1e-245 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
AJOHDNBE_00668 | 8.2e-119 | 3.6.1.55 | F | NUDIX domain | ||
AJOHDNBE_00669 | 5.7e-77 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
AJOHDNBE_00670 | 9.6e-113 | S | Protein of unknown function (DUF1211) | |||
AJOHDNBE_00671 | 1.5e-178 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
AJOHDNBE_00673 | 1.5e-191 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
AJOHDNBE_00674 | 2.2e-102 | 3.6.1.27 | I | Acid phosphatase homologues | ||
AJOHDNBE_00675 | 1.3e-148 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
AJOHDNBE_00676 | 1.5e-244 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
AJOHDNBE_00677 | 2e-88 | S | Domain of unknown function (DUF4767) | |||
AJOHDNBE_00678 | 1.2e-38 | C | nitroreductase | |||
AJOHDNBE_00679 | 9.4e-237 | mepA | V | MATE efflux family protein | ||
AJOHDNBE_00680 | 1.7e-78 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
AJOHDNBE_00681 | 7.1e-69 | S | Putative adhesin | |||
AJOHDNBE_00682 | 5.6e-101 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
AJOHDNBE_00684 | 8.3e-14 | 1.3.5.4 | C | succinate dehydrogenase | ||
AJOHDNBE_00685 | 1.1e-14 | K | Acetyltransferase (GNAT) domain | |||
AJOHDNBE_00686 | 7.2e-39 | argF | 2.1.3.3, 2.7.2.2 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
AJOHDNBE_00687 | 1.5e-236 | arcA | 3.5.3.6 | E | Arginine | |
AJOHDNBE_00688 | 3.4e-136 | lysR5 | K | LysR substrate binding domain | ||
AJOHDNBE_00689 | 0.0 | mgtA | 3.6.3.2, 3.6.3.6 | P | Cation transporter/ATPase, N-terminus | |
AJOHDNBE_00690 | 2.1e-49 | S | Metal binding domain of Ada | |||
AJOHDNBE_00691 | 4.8e-154 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
AJOHDNBE_00692 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
AJOHDNBE_00693 | 1.4e-112 | tdk | 2.7.1.21 | F | thymidine kinase | |
AJOHDNBE_00694 | 1.7e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
AJOHDNBE_00695 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
AJOHDNBE_00696 | 0.0 | mdlB | V | ABC transporter | ||
AJOHDNBE_00697 | 5.4e-99 | mdlA | V | ABC transporter | ||
AJOHDNBE_00698 | 1.5e-94 | S | Protein of unknown function (DUF3990) | |||
AJOHDNBE_00699 | 2.9e-44 | |||||
AJOHDNBE_00701 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
AJOHDNBE_00702 | 2e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
AJOHDNBE_00703 | 1.6e-71 | yqeY | S | YqeY-like protein | ||
AJOHDNBE_00704 | 1.1e-175 | phoH | T | phosphate starvation-inducible protein PhoH | ||
AJOHDNBE_00705 | 2.2e-93 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
AJOHDNBE_00706 | 2.1e-168 | era | S | 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 | ||
AJOHDNBE_00707 | 1.6e-117 | fhuC | P | ABC transporter | ||
AJOHDNBE_00708 | 5e-129 | znuB | U | ABC 3 transport family | ||
AJOHDNBE_00709 | 4.1e-265 | lctP | C | L-lactate permease | ||
AJOHDNBE_00710 | 6.1e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
AJOHDNBE_00711 | 3.9e-57 | F | DNA/RNA non-specific endonuclease | |||
AJOHDNBE_00712 | 0.0 | aha1 | P | E1-E2 ATPase | ||
AJOHDNBE_00713 | 1.5e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
AJOHDNBE_00714 | 5.2e-83 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
AJOHDNBE_00715 | 2.1e-221 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
AJOHDNBE_00716 | 9.7e-288 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
AJOHDNBE_00717 | 5e-195 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
AJOHDNBE_00719 | 1.1e-211 | S | Bacterial protein of unknown function (DUF871) | |||
AJOHDNBE_00720 | 3.3e-202 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
AJOHDNBE_00721 | 6.2e-34 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
AJOHDNBE_00722 | 4.2e-150 | |||||
AJOHDNBE_00724 | 6.3e-246 | ydaM | M | Glycosyl transferase | ||
AJOHDNBE_00725 | 2.6e-205 | G | Glycosyl hydrolases family 8 | |||
AJOHDNBE_00726 | 5.3e-192 | V | Beta-lactamase | |||
AJOHDNBE_00727 | 1.7e-93 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
AJOHDNBE_00728 | 1.8e-98 | yhiD | S | MgtC family | ||
AJOHDNBE_00729 | 3.1e-42 | S | GyrI-like small molecule binding domain | |||
AJOHDNBE_00730 | 6.8e-53 | S | GyrI-like small molecule binding domain | |||
AJOHDNBE_00731 | 6.9e-121 | S | Alpha beta hydrolase | |||
AJOHDNBE_00732 | 5.7e-217 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
AJOHDNBE_00733 | 1.7e-97 | |||||
AJOHDNBE_00734 | 9.6e-67 | yciB | M | ErfK YbiS YcfS YnhG | ||
AJOHDNBE_00735 | 7.7e-135 | K | Helix-turn-helix domain, rpiR family | |||
AJOHDNBE_00737 | 1.4e-94 | |||||
AJOHDNBE_00739 | 6.3e-111 | |||||
AJOHDNBE_00740 | 9.6e-41 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
AJOHDNBE_00741 | 1.5e-12 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
AJOHDNBE_00742 | 5.5e-51 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
AJOHDNBE_00743 | 7.7e-39 | S | Aldo keto reductase | |||
AJOHDNBE_00744 | 1.2e-38 | hxlR | K | HxlR-like helix-turn-helix | ||
AJOHDNBE_00745 | 5e-75 | K | LytTr DNA-binding domain | |||
AJOHDNBE_00746 | 2.3e-182 | |||||
AJOHDNBE_00747 | 9.2e-30 | |||||
AJOHDNBE_00748 | 8.5e-78 | S | HIRAN | |||
AJOHDNBE_00749 | 2.8e-41 | S | Sel1-like repeats. | |||
AJOHDNBE_00750 | 1.1e-158 | ypbG | 2.7.1.2 | GK | ROK family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)