ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
AGCNGIMD_00001 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
AGCNGIMD_00002 | 7.9e-136 | divIVA | D | Cell division protein DivIVA | ||
AGCNGIMD_00003 | 1.2e-143 | ylmH | T | S4 RNA-binding domain | ||
AGCNGIMD_00004 | 1.2e-34 | yggT | D | integral membrane protein | ||
AGCNGIMD_00005 | 2e-95 | 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 | ||
AGCNGIMD_00006 | 2.7e-123 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
AGCNGIMD_00007 | 4.6e-236 | 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 | ||
AGCNGIMD_00008 | 8e-252 | 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 | ||
AGCNGIMD_00009 | 2.6e-176 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
AGCNGIMD_00010 | 2.9e-201 | murG | 2.4.1.227 | 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) |
AGCNGIMD_00011 | 1.6e-252 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
AGCNGIMD_00012 | 2.2e-07 | S | Protein of unknown function (DUF3165) | |||
AGCNGIMD_00013 | 0.0 | typA | T | GTP-binding protein TypA | ||
AGCNGIMD_00014 | 2.9e-179 | glk | 2.7.1.2 | G | Glucokinase | |
AGCNGIMD_00015 | 8.4e-28 | yqgQ | S | protein conserved in bacteria | ||
AGCNGIMD_00016 | 8.9e-80 | perR | P | Belongs to the Fur family | ||
AGCNGIMD_00017 | 1.6e-91 | dps | P | Belongs to the Dps family | ||
AGCNGIMD_00018 | 7.4e-115 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
AGCNGIMD_00019 | 9.1e-195 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
AGCNGIMD_00020 | 8.5e-113 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
AGCNGIMD_00021 | 2.4e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
AGCNGIMD_00022 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
AGCNGIMD_00023 | 2e-54 | S | Domain of unknown function (DUF4430) | |||
AGCNGIMD_00024 | 4.2e-75 | S | Psort location CytoplasmicMembrane, score | |||
AGCNGIMD_00025 | 2.9e-141 | htpX | O | Belongs to the peptidase M48B family | ||
AGCNGIMD_00026 | 1.5e-92 | lemA | S | LemA family | ||
AGCNGIMD_00027 | 6.4e-174 | spd | F | DNA RNA non-specific endonuclease | ||
AGCNGIMD_00028 | 1.7e-107 | |||||
AGCNGIMD_00030 | 1.1e-138 | hsdS | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | |
AGCNGIMD_00031 | 4.1e-271 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
AGCNGIMD_00032 | 0.0 | hsdR | 3.1.21.3 | V | Type I restriction enzyme R protein N terminus (HSDR_N) | |
AGCNGIMD_00033 | 1.1e-66 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AGCNGIMD_00034 | 2e-13 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AGCNGIMD_00035 | 6.5e-17 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
AGCNGIMD_00036 | 2.1e-23 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
AGCNGIMD_00037 | 1.4e-23 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
AGCNGIMD_00038 | 2.3e-113 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
AGCNGIMD_00039 | 1.2e-27 | P | Hemerythrin HHE cation binding domain protein | |||
AGCNGIMD_00040 | 1.6e-145 | XK27_00880 | 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
AGCNGIMD_00041 | 7.9e-82 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
AGCNGIMD_00042 | 5.1e-116 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase | |
AGCNGIMD_00043 | 1.2e-174 | S | hydrolase | |||
AGCNGIMD_00044 | 7.6e-16 | |||||
AGCNGIMD_00045 | 6.1e-62 | M | LysM domain | |||
AGCNGIMD_00046 | 2.1e-08 | M | LysM domain | |||
AGCNGIMD_00047 | 2.2e-287 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
AGCNGIMD_00048 | 9.4e-117 | |||||
AGCNGIMD_00049 | 7.7e-238 | dcm | 2.1.1.37 | L | Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family | |
AGCNGIMD_00050 | 3.4e-09 | |||||
AGCNGIMD_00051 | 4.6e-236 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
AGCNGIMD_00052 | 1.1e-33 | XK27_12190 | S | protein conserved in bacteria | ||
AGCNGIMD_00054 | 2.7e-86 | bioY | S | biotin synthase | ||
AGCNGIMD_00055 | 3.4e-252 | yegQ | O | Peptidase U32 | ||
AGCNGIMD_00056 | 3e-178 | yegQ | O | Peptidase U32 | ||
AGCNGIMD_00058 | 5.5e-69 | ytxH | S | General stress protein | ||
AGCNGIMD_00060 | 4e-147 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
AGCNGIMD_00061 | 6.8e-170 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
AGCNGIMD_00062 | 4.9e-41 | pspC | KT | PspC domain | ||
AGCNGIMD_00063 | 4.9e-86 | ydcK | S | Belongs to the SprT family | ||
AGCNGIMD_00064 | 0.0 | yhgF | K | Transcriptional accessory protein | ||
AGCNGIMD_00066 | 3.2e-156 | XK27_03015 | S | permease | ||
AGCNGIMD_00067 | 4.2e-147 | ycgQ | S | TIGR03943 family | ||
AGCNGIMD_00068 | 1.3e-188 | S | CRISPR-associated protein Csn2 subfamily St | |||
AGCNGIMD_00069 | 3.1e-53 | cas2 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
AGCNGIMD_00070 | 3.2e-172 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
AGCNGIMD_00071 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
AGCNGIMD_00072 | 1.5e-96 | |||||
AGCNGIMD_00073 | 2.6e-34 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
AGCNGIMD_00074 | 3.9e-49 | dam | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
AGCNGIMD_00075 | 1.5e-18 | K | Cro/C1-type HTH DNA-binding domain | |||
AGCNGIMD_00076 | 1.2e-106 | |||||
AGCNGIMD_00077 | 3.5e-255 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
AGCNGIMD_00078 | 8.5e-96 | mip | S | hydroperoxide reductase activity | ||
AGCNGIMD_00079 | 4.5e-202 | I | acyl-CoA dehydrogenase | |||
AGCNGIMD_00080 | 1e-58 | ydiA | P | C4-dicarboxylate transporter malic acid transport | ||
AGCNGIMD_00081 | 3.6e-247 | msrR | K | Transcriptional regulator | ||
AGCNGIMD_00082 | 2.3e-153 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
AGCNGIMD_00083 | 1.7e-87 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
AGCNGIMD_00084 | 1.7e-235 | aroA | 1.3.1.12, 1.3.1.43, 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
AGCNGIMD_00085 | 5.1e-173 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
AGCNGIMD_00086 | 3.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
AGCNGIMD_00087 | 5.9e-205 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
AGCNGIMD_00088 | 4.5e-219 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
AGCNGIMD_00089 | 2.3e-201 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
AGCNGIMD_00090 | 1.7e-162 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
AGCNGIMD_00091 | 1.6e-120 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
AGCNGIMD_00092 | 6.9e-220 | ywbD | 2.1.1.191 | J | Methyltransferase | |
AGCNGIMD_00093 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
AGCNGIMD_00095 | 8.2e-246 | 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 | |
AGCNGIMD_00096 | 1.4e-75 | yueI | S | Protein of unknown function (DUF1694) | ||
AGCNGIMD_00097 | 5.4e-206 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
AGCNGIMD_00098 | 1.3e-142 | yyaQ | S | YjbR | ||
AGCNGIMD_00099 | 8e-28 | yyaQ | S | YjbR | ||
AGCNGIMD_00100 | 4.9e-182 | ccpA | K | Catabolite control protein A | ||
AGCNGIMD_00101 | 4.2e-211 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
AGCNGIMD_00102 | 1.7e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
AGCNGIMD_00103 | 4.1e-275 | 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 | |
AGCNGIMD_00104 | 1.1e-80 | smpB | O | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
AGCNGIMD_00105 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
AGCNGIMD_00106 | 2e-33 | secG | U | Preprotein translocase subunit SecG |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)