ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
EIPGFFGA_00001 | 2.5e-21 | fnt | P | Formate nitrite transporter | ||
EIPGFFGA_00002 | 9.3e-231 | XK27_09615 | C | reductase | ||
EIPGFFGA_00003 | 6.3e-108 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
EIPGFFGA_00004 | 1.4e-62 | clpE | O | Belongs to the ClpA ClpB family | ||
EIPGFFGA_00005 | 1.7e-287 | clpE | O | Belongs to the ClpA ClpB family | ||
EIPGFFGA_00006 | 4.3e-177 | yubA | S | permease | ||
EIPGFFGA_00007 | 9.3e-73 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
EIPGFFGA_00008 | 5.6e-92 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
EIPGFFGA_00009 | 5.3e-98 | XK27_07830 | 2.3.1.128 | J | Acetyltransferase GNAT Family | |
EIPGFFGA_00010 | 1.7e-114 | yxeN | P | ABC transporter (Permease | ||
EIPGFFGA_00011 | 1.4e-130 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
EIPGFFGA_00012 | 5e-10 | S | Protein of unknown function (DUF4059) | |||
EIPGFFGA_00013 | 1.8e-245 | 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 | ||
EIPGFFGA_00014 | 8.9e-170 | 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 | |
EIPGFFGA_00015 | 3.8e-78 | asp3 | S | Accessory Sec system protein Asp3 | ||
EIPGFFGA_00016 | 6.3e-90 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
EIPGFFGA_00017 | 3.2e-20 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
EIPGFFGA_00018 | 8.2e-160 | miaA | 2.5.1.75 | J | 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) | |
EIPGFFGA_00019 | 2.3e-87 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
EIPGFFGA_00020 | 8.9e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
EIPGFFGA_00021 | 8.6e-145 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
EIPGFFGA_00022 | 1.8e-113 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
EIPGFFGA_00023 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
EIPGFFGA_00024 | 2.1e-227 | noxE | P | NADH oxidase | ||
EIPGFFGA_00025 | 9.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
EIPGFFGA_00026 | 5.7e-10 | O | ADP-ribosylglycohydrolase | |||
EIPGFFGA_00027 | 1.9e-62 | paaI | Q | protein possibly involved in aromatic compounds catabolism | ||
EIPGFFGA_00028 | 3e-60 | ycaO | O | OsmC-like protein | ||
EIPGFFGA_00029 | 2e-155 | pstA | P | phosphate transport system permease | ||
EIPGFFGA_00030 | 8e-112 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
EIPGFFGA_00031 | 7.9e-88 | 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) | |
EIPGFFGA_00032 | 6.9e-33 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
EIPGFFGA_00033 | 3e-104 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
EIPGFFGA_00034 | 9.4e-147 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
EIPGFFGA_00035 | 7e-72 | argR | K | Regulates arginine biosynthesis genes | ||
EIPGFFGA_00036 | 5e-121 | M | domain protein | |||
EIPGFFGA_00037 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
EIPGFFGA_00038 | 3.9e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
EIPGFFGA_00039 | 2.1e-146 | XK27_08360 | S | EDD domain protein, DegV family | ||
EIPGFFGA_00040 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
EIPGFFGA_00041 | 8e-99 | metI | P | ABC transporter (Permease | ||
EIPGFFGA_00042 | 3.9e-148 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
EIPGFFGA_00043 | 3.3e-256 | glnP | P | ABC transporter | ||
EIPGFFGA_00044 | 2.2e-123 | glnQ | E | abc transporter atp-binding protein | ||
EIPGFFGA_00045 | 1.7e-105 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
EIPGFFGA_00046 | 6.1e-106 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
EIPGFFGA_00047 | 2.3e-286 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
EIPGFFGA_00048 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
EIPGFFGA_00049 | 2.3e-111 | lytC | 3.4.17.14, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
EIPGFFGA_00050 | 3e-106 | 3.5.1.28 | M | N-Acetylmuramoyl-L-alanine amidase | ||
EIPGFFGA_00051 | 3.8e-235 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
EIPGFFGA_00053 | 3e-60 | divIC | D | Septum formation initiator | ||
EIPGFFGA_00054 | 9.2e-15 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
EIPGFFGA_00055 | 2.4e-276 | nptA | P | COG1283 Na phosphate symporter | ||
EIPGFFGA_00056 | 4.2e-308 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
EIPGFFGA_00057 | 1.5e-81 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
EIPGFFGA_00058 | 2.4e-121 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
EIPGFFGA_00059 | 1.8e-223 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
EIPGFFGA_00060 | 1.9e-181 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
EIPGFFGA_00061 | 1.6e-102 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
EIPGFFGA_00062 | 6.6e-114 | papP | P | ABC transporter (Permease | ||
EIPGFFGA_00063 | 4.6e-107 | P | ABC transporter (Permease | |||
EIPGFFGA_00064 | 1.9e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
EIPGFFGA_00065 | 2.1e-88 | 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 | ||
EIPGFFGA_00066 | 6.1e-123 | 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 | |
EIPGFFGA_00067 | 3.9e-99 | thiT | S | Thiamine transporter | ||
EIPGFFGA_00068 | 3.3e-62 | yjqA | S | Bacterial PH domain | ||
EIPGFFGA_00069 | 1.3e-152 | corA | P | CorA-like protein | ||
EIPGFFGA_00070 | 1.3e-79 | hmpT | S | cog cog4720 | ||
EIPGFFGA_00071 | 1.5e-135 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
EIPGFFGA_00072 | 3.8e-139 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
EIPGFFGA_00073 | 3.7e-48 | 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 | |
EIPGFFGA_00074 | 1e-85 | 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 | ||
EIPGFFGA_00075 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
EIPGFFGA_00076 | 1.5e-56 | 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 | ||
EIPGFFGA_00077 | 9.3e-225 | XK27_05680 | 6.3.2.2, 6.3.2.4 | M | carbamoylphosphate synthase large subunit | |
EIPGFFGA_00078 | 2.7e-153 | XK27_05675 | S | Esterase | ||
EIPGFFGA_00079 | 3.1e-29 | XK27_05670 | S | Putative esterase | ||
EIPGFFGA_00080 | 3.4e-149 | 2.4.1.83 | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
EIPGFFGA_00082 | 1.4e-212 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
EIPGFFGA_00083 | 9.5e-29 | nrdD_1 | 1.1.98.6, 1.17.4.1 | F | Ribonucleoside-triphosphate reductase | |
EIPGFFGA_00084 | 4.3e-31 | S | Beta-lactamase superfamily domain | |||
EIPGFFGA_00085 | 1.6e-133 | glpQ1_1 | 3.1.4.46 | C | Psort location Cytoplasmic, score 8.96 | |
EIPGFFGA_00086 | 5.7e-105 | 3.1.4.46 | C | Psort location Cytoplasmic, score 8.96 | ||
EIPGFFGA_00087 | 1.5e-32 | 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) | |
EIPGFFGA_00088 | 9.6e-217 | 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 | |
EIPGFFGA_00089 | 1.1e-86 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
EIPGFFGA_00090 | 3e-104 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
EIPGFFGA_00091 | 4.3e-178 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
EIPGFFGA_00092 | 3.1e-300 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
EIPGFFGA_00093 | 0.0 | scrA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
EIPGFFGA_00094 | 3.9e-53 | amt | P | Ammonium Transporter | ||
EIPGFFGA_00095 | 1.8e-99 | amt | P | Ammonium Transporter | ||
EIPGFFGA_00096 | 1.9e-53 | glnB | K | Belongs to the P(II) protein family | ||
EIPGFFGA_00097 | 3.5e-104 | mur1 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | |
EIPGFFGA_00098 | 1.9e-101 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
EIPGFFGA_00099 | 8.6e-104 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
EIPGFFGA_00100 | 1.5e-222 | ytfP | S | Flavoprotein | ||
EIPGFFGA_00101 | 6.3e-97 | radC | E | Belongs to the UPF0758 family | ||
EIPGFFGA_00102 | 1.7e-128 | puuD | T | peptidase C26 | ||
EIPGFFGA_00103 | 2.1e-117 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
EIPGFFGA_00104 | 4.5e-222 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
EIPGFFGA_00106 | 3e-84 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
EIPGFFGA_00107 | 1.1e-166 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
EIPGFFGA_00108 | 2.9e-17 | yjdB | S | Domain of unknown function (DUF4767) | ||
EIPGFFGA_00109 | 2.3e-198 | yyaQ | S | YjbR | ||
EIPGFFGA_00110 | 2.6e-109 | ccpA | K | Catabolite control protein A | ||
EIPGFFGA_00111 | 1.3e-222 | fasC | 2.7.13.3 | T | protein histidine kinase activity | |
EIPGFFGA_00112 | 1.1e-306 | 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 | |
EIPGFFGA_00113 | 4.2e-167 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
EIPGFFGA_00114 | 7e-141 | cppA | E | CppA N-terminal | ||
EIPGFFGA_00115 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
EIPGFFGA_00117 | 6.7e-93 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
EIPGFFGA_00118 | 3e-221 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
EIPGFFGA_00119 | 1.8e-71 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
EIPGFFGA_00120 | 1.6e-144 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
EIPGFFGA_00121 | 2.6e-28 | MA20_06245 | S | yiaA/B two helix domain | ||
EIPGFFGA_00122 | 2e-210 | uup | S | abc transporter atp-binding protein | ||
EIPGFFGA_00123 | 6e-303 | dnaK | O | Heat shock 70 kDa protein | ||
EIPGFFGA_00124 | 8.4e-34 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
EIPGFFGA_00125 | 0.0 | 3.2.1.26, 3.2.1.65 | GH32 | G | Belongs to the glycosyl hydrolase 32 family | |
EIPGFFGA_00126 | 1.2e-82 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
EIPGFFGA_00127 | 1.3e-156 | yvgN | C | reductase | ||
EIPGFFGA_00128 | 1.8e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
EIPGFFGA_00129 | 3.7e-230 | 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 | |
EIPGFFGA_00130 | 3.8e-113 | 3.5.1.28 | M | domain protein | ||
EIPGFFGA_00131 | 8.6e-113 | 3.5.1.28 | M | domain protein | ||
EIPGFFGA_00132 | 1.6e-11 | ycdA | S | Domain of unknown function (DUF4352) | ||
EIPGFFGA_00133 | 3.2e-47 | ybhL | S | Belongs to the BI1 family | ||
EIPGFFGA_00134 | 1.6e-36 | yneF | S | UPF0154 protein | ||
EIPGFFGA_00135 | 1.6e-116 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
EIPGFFGA_00136 | 1.6e-247 | pbuO | S | permease | ||
EIPGFFGA_00137 | 3.2e-98 | treB | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
EIPGFFGA_00139 | 9.2e-21 | S | Domain of unknown function (DUF4767) | |||
EIPGFFGA_00140 | 2.9e-81 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
EIPGFFGA_00141 | 5.3e-186 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
EIPGFFGA_00143 | 1.1e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
EIPGFFGA_00144 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
EIPGFFGA_00145 | 2.4e-184 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
EIPGFFGA_00146 | 2.8e-123 | XK27_09800 | I | Acyltransferase | ||
EIPGFFGA_00147 | 1.6e-81 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
EIPGFFGA_00148 | 4.5e-61 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
EIPGFFGA_00149 | 4.1e-81 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
EIPGFFGA_00150 | 2.2e-69 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
EIPGFFGA_00151 | 4.3e-97 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
EIPGFFGA_00152 | 2e-120 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
EIPGFFGA_00153 | 1.9e-88 | L | COG1943 Transposase and inactivated derivatives | |||
EIPGFFGA_00154 | 1.3e-114 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
EIPGFFGA_00155 | 2e-71 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
EIPGFFGA_00156 | 5.4e-61 | |||||
EIPGFFGA_00157 | 1e-198 | L | Replication initiation factor | |||
EIPGFFGA_00158 | 1.7e-43 | yegQ | O | Peptidase U32 | ||
EIPGFFGA_00159 | 4.1e-223 | yegQ | O | Peptidase U32 | ||
EIPGFFGA_00160 | 0.0 | fruA | 2.7.1.202 | G | phosphotransferase system | |
EIPGFFGA_00161 | 8.7e-164 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
EIPGFFGA_00162 | 2.3e-150 | cobQ | S | glutamine amidotransferase | ||
EIPGFFGA_00163 | 7.3e-239 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
EIPGFFGA_00165 | 2.6e-147 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
EIPGFFGA_00166 | 7.8e-152 | XK27_08835 | S | ABC transporter substrate binding protein | ||
EIPGFFGA_00167 | 4.1e-142 | peb1A | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
EIPGFFGA_00168 | 8.8e-43 | gltJ | P | ABC transporter (Permease | ||
EIPGFFGA_00169 | 1.4e-40 | gltJ | P | ABC transporter (Permease | ||
EIPGFFGA_00170 | 2.4e-29 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
EIPGFFGA_00171 | 6e-183 | 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 | |
EIPGFFGA_00172 | 2.1e-55 | cylA | V | abc transporter atp-binding protein | ||
EIPGFFGA_00173 | 3.1e-129 | cylB | V | ABC-2 type transporter | ||
EIPGFFGA_00174 | 9e-75 | K | COG3279 Response regulator of the LytR AlgR family | |||
EIPGFFGA_00175 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
EIPGFFGA_00176 | 2.2e-21 | I | mechanosensitive ion channel activity | |||
EIPGFFGA_00178 | 6.8e-72 | copY | K | negative regulation of transcription, DNA-templated | ||
EIPGFFGA_00179 | 1.4e-41 | ylxQ | J | ribosomal protein | ||
EIPGFFGA_00180 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
EIPGFFGA_00181 | 4.2e-22 | nusA | K | Participates in both transcription termination and antitermination | ||
EIPGFFGA_00182 | 4.3e-36 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
EIPGFFGA_00183 | 4.2e-59 | fruR | K | transcriptional | ||
EIPGFFGA_00184 | 2.4e-95 | S | Carbohydrate-binding domain-containing protein Cthe_2159 | |||
EIPGFFGA_00186 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
EIPGFFGA_00187 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
EIPGFFGA_00188 | 4.2e-303 | yloV | S | kinase related to dihydroxyacetone kinase | ||
EIPGFFGA_00189 | 1.4e-57 | asp | S | cog cog1302 | ||
EIPGFFGA_00190 | 1.5e-223 | norN | V | Mate efflux family protein | ||
EIPGFFGA_00191 | 4.3e-275 | thrC | 4.2.3.1 | E | Threonine synthase | |
EIPGFFGA_00194 | 1.6e-203 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
EIPGFFGA_00195 | 4.3e-40 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
EIPGFFGA_00196 | 1.5e-86 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
EIPGFFGA_00197 | 1.1e-49 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
EIPGFFGA_00199 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
EIPGFFGA_00200 | 2.2e-162 | rsgA | 3.1.3.100 | G | 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 | |
EIPGFFGA_00202 | 6e-112 | ksgA | 2.1.1.182 | J | Specifically dimethylates two adjacent adenosines (A1518 and A1519) in the loop of a conserved hairpin near the 3'-end of 16S rRNA in the 30S particle. May play a critical role in biogenesis of 30S subunits | |
EIPGFFGA_00203 | 2.9e-252 | gatA | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
EIPGFFGA_00204 | 1.6e-94 | 2.3.1.128 | K | acetyltransferase | ||
EIPGFFGA_00205 | 4.4e-230 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
EIPGFFGA_00206 | 7.5e-104 | thiJ-2 | 3.5.1.124 | S | DJ-1/PfpI family | |
EIPGFFGA_00207 | 2.5e-124 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
EIPGFFGA_00208 | 2.9e-161 | acoA | C | Dehydrogenase E1 component | ||
EIPGFFGA_00209 | 3.9e-12 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
EIPGFFGA_00210 | 1.6e-46 | K | DNA-binding transcription factor activity | |||
EIPGFFGA_00211 | 1.1e-21 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
EIPGFFGA_00212 | 1.4e-98 | yqeG | S | hydrolase of the HAD superfamily | ||
EIPGFFGA_00213 | 7.7e-180 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dihydroxyacetone kinase | |
EIPGFFGA_00214 | 1.5e-95 | dhaL | 2.7.1.121 | S | Dihydroxyacetone kinase | |
EIPGFFGA_00215 | 4.8e-72 | GM | domain, Protein | |||
EIPGFFGA_00216 | 2.7e-85 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
EIPGFFGA_00217 | 3e-114 | azlC | E | AzlC protein | ||
EIPGFFGA_00218 | 3.7e-46 | azlD | S | branched-chain amino acid | ||
EIPGFFGA_00219 | 1.2e-172 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
EIPGFFGA_00220 | 3.3e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
EIPGFFGA_00221 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
EIPGFFGA_00222 | 9.5e-272 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
EIPGFFGA_00223 | 1.2e-74 | yjbK | S | Adenylate cyclase | ||
EIPGFFGA_00224 | 1.4e-122 | 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 | ||
EIPGFFGA_00225 | 6.5e-134 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
EIPGFFGA_00226 | 2.8e-31 | ykuL | S | CBS domain | ||
EIPGFFGA_00228 | 2.3e-96 | typA | T | GTP-binding protein TypA | ||
EIPGFFGA_00229 | 5.6e-247 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
EIPGFFGA_00230 | 2.2e-262 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
EIPGFFGA_00231 | 6.8e-122 | clcA | P | Chloride transporter, ClC family | ||
EIPGFFGA_00233 | 9.5e-102 | clcA_2 | P | Chloride transporter, ClC family | ||
EIPGFFGA_00234 | 2.3e-133 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
EIPGFFGA_00235 | 7.1e-153 | higA | K | Pfam:DUF955 | ||
EIPGFFGA_00236 | 4.8e-15 | higA | K | Pfam:DUF955 | ||
EIPGFFGA_00237 | 7.1e-275 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
EIPGFFGA_00238 | 9.3e-139 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
EIPGFFGA_00239 | 4e-138 | pts33BCA | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
EIPGFFGA_00240 | 1.2e-277 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
EIPGFFGA_00241 | 5e-102 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
EIPGFFGA_00242 | 1.1e-93 | sepF | D | cell septum assembly | ||
EIPGFFGA_00243 | 3.8e-30 | yggT | D | integral membrane protein | ||
EIPGFFGA_00244 | 2.6e-145 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
EIPGFFGA_00245 | 4e-46 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
EIPGFFGA_00246 | 1.5e-157 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
EIPGFFGA_00247 | 3.9e-08 | MU | outer membrane autotransporter barrel domain protein | |||
EIPGFFGA_00248 | 1.3e-168 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
EIPGFFGA_00250 | 9e-101 | srtB | 3.4.22.70 | S | Sortase family | |
EIPGFFGA_00251 | 1.3e-190 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
EIPGFFGA_00252 | 3.3e-95 | XK27_09825 | V | abc transporter atp-binding protein | ||
EIPGFFGA_00253 | 5.7e-119 | yvfS | V | Transporter | ||
EIPGFFGA_00255 | 6.7e-248 | 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 | ||
EIPGFFGA_00256 | 6.4e-91 | 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 | ||
EIPGFFGA_00257 | 1.7e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
EIPGFFGA_00258 | 5.6e-200 | 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) |
EIPGFFGA_00259 | 4.3e-95 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
EIPGFFGA_00260 | 7.2e-134 | ecfA1 | P | ATP-binding (A) component of a common 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 | ||
EIPGFFGA_00261 | 1.1e-147 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common 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 | |
EIPGFFGA_00262 | 1.7e-180 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
EIPGFFGA_00263 | 9.7e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
EIPGFFGA_00264 | 2.4e-45 | ftsL | D | cell division protein FtsL | ||
EIPGFFGA_00265 | 1.9e-53 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
EIPGFFGA_00267 | 2.6e-121 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
EIPGFFGA_00268 | 3e-84 | 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 | ||
EIPGFFGA_00269 | 4.3e-139 | 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 | ||
EIPGFFGA_00270 | 5.1e-201 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
EIPGFFGA_00271 | 1.2e-80 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
EIPGFFGA_00272 | 5.4e-156 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
EIPGFFGA_00273 | 5.1e-284 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
EIPGFFGA_00274 | 6.2e-202 | mloB | K | Transcriptional regulator | ||
EIPGFFGA_00275 | 5.7e-173 | ctpE | P | E1-E2 ATPase | ||
EIPGFFGA_00276 | 3e-78 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
EIPGFFGA_00277 | 1.7e-117 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
EIPGFFGA_00278 | 1.4e-107 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
EIPGFFGA_00279 | 1.4e-141 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
EIPGFFGA_00280 | 5.4e-11 | 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 | |
EIPGFFGA_00281 | 4.6e-98 | |||||
EIPGFFGA_00282 | 3.6e-192 | sbcC | L | ATPase involved in DNA repair | ||
EIPGFFGA_00283 | 1.5e-197 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
EIPGFFGA_00284 | 1.2e-36 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
EIPGFFGA_00285 | 8.2e-134 | prs | 2.7.6.1 | F | Involved in the biosynthesis of the central metabolite phospho-alpha-D-ribosyl-1-pyrophosphate (PRPP) via the transfer of pyrophosphoryl group from ATP to 1-hydroxyl of ribose-5-phosphate (Rib-5-P) | |
EIPGFFGA_00286 | 6e-47 | feoA | P | FeoA domain protein | ||
EIPGFFGA_00287 | 9.3e-112 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
EIPGFFGA_00288 | 2.4e-130 | comEC | S | Competence protein ComEC | ||
EIPGFFGA_00289 | 9.3e-156 | XK27_03015 | S | permease | ||
EIPGFFGA_00290 | 2.5e-258 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EIPGFFGA_00291 | 2.1e-111 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
EIPGFFGA_00292 | 4.5e-45 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
EIPGFFGA_00293 | 5.7e-62 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
EIPGFFGA_00294 | 4.1e-283 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
EIPGFFGA_00295 | 2.2e-63 | S | SseB protein N-terminal domain | |||
EIPGFFGA_00296 | 3.3e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
EIPGFFGA_00297 | 2.8e-73 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
EIPGFFGA_00298 | 1e-248 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
EIPGFFGA_00299 | 1.8e-192 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
EIPGFFGA_00300 | 2.6e-46 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
EIPGFFGA_00301 | 2.4e-166 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon | |
EIPGFFGA_00302 | 5.3e-256 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
EIPGFFGA_00303 | 6e-32 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
EIPGFFGA_00304 | 2.3e-64 | gtrA | S | GtrA-like protein | ||
EIPGFFGA_00305 | 4e-119 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
EIPGFFGA_00306 | 5.7e-163 | ET | ABC transporter substrate-binding protein | |||
EIPGFFGA_00307 | 6.5e-104 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
EIPGFFGA_00308 | 2.7e-25 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
EIPGFFGA_00309 | 1.3e-125 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
EIPGFFGA_00310 | 4.7e-126 | XK27_08875 | O | Zinc-dependent metalloprotease | ||
EIPGFFGA_00311 | 4.8e-122 | estA | CE1 | S | Esterase | |
EIPGFFGA_00312 | 5.8e-200 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
EIPGFFGA_00314 | 2.2e-96 | ytqB | J | (SAM)-dependent | ||
EIPGFFGA_00315 | 5.2e-104 | yhcC | S | radical SAM protein | ||
EIPGFFGA_00316 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
EIPGFFGA_00317 | 1.3e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
EIPGFFGA_00318 | 1.9e-23 | rpmD | J | ribosomal protein l30 | ||
EIPGFFGA_00319 | 3e-221 | norM | V | Multidrug efflux pump | ||
EIPGFFGA_00320 | 6.8e-133 | ecsA_2 | V | abc transporter atp-binding protein | ||
EIPGFFGA_00321 | 3.8e-163 | rmuC | S | RmuC domain protein | ||
EIPGFFGA_00322 | 1.6e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
EIPGFFGA_00323 | 8e-230 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
EIPGFFGA_00324 | 3.8e-32 | V | permease protein | |||
EIPGFFGA_00325 | 3.9e-58 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
EIPGFFGA_00326 | 7.9e-45 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
EIPGFFGA_00327 | 4.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
EIPGFFGA_00328 | 7.2e-80 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
EIPGFFGA_00329 | 6.7e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
EIPGFFGA_00330 | 1.6e-73 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
EIPGFFGA_00331 | 1.7e-72 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
EIPGFFGA_00332 | 6.8e-116 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
EIPGFFGA_00333 | 1.7e-73 | ecfT | P | Transmembrane (T) component of an 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 | ||
EIPGFFGA_00334 | 2.7e-71 | lytE | M | LysM domain protein | ||
EIPGFFGA_00335 | 8e-120 | ecsA | V | abc transporter atp-binding protein | ||
EIPGFFGA_00336 | 1.6e-202 | 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 | |
EIPGFFGA_00337 | 1.1e-121 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
EIPGFFGA_00339 | 5.4e-193 | L | Transposase IS116 IS110 IS902 | |||
EIPGFFGA_00340 | 1.2e-71 | marR | K | Transcriptional regulator, MarR family | ||
EIPGFFGA_00341 | 7.3e-25 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
EIPGFFGA_00342 | 6e-74 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
EIPGFFGA_00343 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
EIPGFFGA_00344 | 5.2e-170 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
EIPGFFGA_00345 | 5.2e-125 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
EIPGFFGA_00346 | 7e-110 | drgA | C | nitroreductase | ||
EIPGFFGA_00347 | 1.5e-158 | argC | 1.2.1.38 | E | Catalyzes the NADPH-dependent reduction of N-acetyl-5- glutamyl phosphate to yield N-acetyl-L-glutamate 5-semialdehyde | |
EIPGFFGA_00348 | 1.9e-164 | 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 | |
EIPGFFGA_00349 | 1.2e-109 | S | dextransucrase activity | |||
EIPGFFGA_00350 | 2.7e-147 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
EIPGFFGA_00352 | 1.8e-237 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
EIPGFFGA_00353 | 1e-72 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
EIPGFFGA_00355 | 2.4e-71 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
EIPGFFGA_00356 | 1.8e-135 | S | dextransucrase activity | |||
EIPGFFGA_00358 | 6.5e-129 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
EIPGFFGA_00359 | 1.1e-167 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
EIPGFFGA_00360 | 5.2e-78 | glcR | K | transcriptional regulator (DeoR family) | ||
EIPGFFGA_00361 | 2.7e-146 | cof | S | Sucrose-6F-phosphate phosphohydrolase | ||
EIPGFFGA_00362 | 2e-83 | XK27_07020 | S | Belongs to the UPF0371 family | ||
EIPGFFGA_00363 | 3.9e-159 | cobW | S | CobW P47K family protein | ||
EIPGFFGA_00364 | 1.5e-150 | yitS | S | EDD domain protein, DegV family | ||
EIPGFFGA_00366 | 2.4e-87 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
EIPGFFGA_00367 | 9.4e-37 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
EIPGFFGA_00368 | 1e-79 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
EIPGFFGA_00369 | 1e-75 | fld | C | Flavodoxin | ||
EIPGFFGA_00370 | 1.6e-123 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
EIPGFFGA_00371 | 1.6e-260 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
EIPGFFGA_00372 | 5.4e-98 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
EIPGFFGA_00373 | 5.9e-17 | glk | 2.7.1.2 | G | Glucokinase | |
EIPGFFGA_00374 | 6.2e-148 | S | Protein of unknown function (DUF3114) | |||
EIPGFFGA_00376 | 1.2e-129 | rnjA | S | 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 | ||
EIPGFFGA_00377 | 9.1e-86 | pscB | M | CHAP domain protein | ||
EIPGFFGA_00378 | 2.1e-38 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
EIPGFFGA_00379 | 9.2e-102 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
EIPGFFGA_00380 | 8.7e-133 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
EIPGFFGA_00381 | 2e-82 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
EIPGFFGA_00382 | 2.2e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
EIPGFFGA_00383 | 2.4e-16 | atpE | 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 | ||
EIPGFFGA_00384 | 3.4e-121 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
EIPGFFGA_00385 | 9.5e-236 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
EIPGFFGA_00386 | 1.6e-70 | argJ | 2.3.1.1, 2.3.1.35, 2.7.2.8 | E | Catalyzes two activities which are involved in the cyclic version of arginine biosynthesis the synthesis of N- acetylglutamate from glutamate and acetyl-CoA as the acetyl donor, and of ornithine by transacetylation between N(2)-acetylornithine and glutamate | |
EIPGFFGA_00387 | 1.9e-127 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
EIPGFFGA_00388 | 1.6e-143 | tatD | L | Hydrolase, tatd | ||
EIPGFFGA_00389 | 4.1e-52 | S | Domain of unknown function (DUF4300) | |||
EIPGFFGA_00390 | 6.6e-123 | V | CAAX protease self-immunity | |||
EIPGFFGA_00391 | 9.8e-21 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
EIPGFFGA_00392 | 1.6e-93 | 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 | ||
EIPGFFGA_00393 | 5.1e-119 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
EIPGFFGA_00395 | 6.2e-202 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
EIPGFFGA_00396 | 4.1e-18 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
EIPGFFGA_00397 | 1.1e-164 | lytC | 3.4.17.14, 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
EIPGFFGA_00398 | 3.8e-129 | rgpF | GT2,GT4 | M | Glycosyltransferase like family 2 | |
EIPGFFGA_00399 | 1.9e-219 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
EIPGFFGA_00400 | 7.7e-210 | S | phospholipase Carboxylesterase | |||
EIPGFFGA_00401 | 6.6e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
EIPGFFGA_00402 | 1.2e-67 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
EIPGFFGA_00403 | 1.5e-28 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
EIPGFFGA_00404 | 1.6e-94 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
EIPGFFGA_00405 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
EIPGFFGA_00406 | 3.9e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
EIPGFFGA_00407 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
EIPGFFGA_00408 | 3.5e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
EIPGFFGA_00409 | 1.1e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
EIPGFFGA_00410 | 2.1e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
EIPGFFGA_00411 | 7.3e-53 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
EIPGFFGA_00412 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
EIPGFFGA_00413 | 1.5e-152 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
EIPGFFGA_00414 | 2.4e-44 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
EIPGFFGA_00415 | 1.3e-103 | rplD | J | Forms part of the polypeptide exit tunnel | ||
EIPGFFGA_00416 | 2.4e-110 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
EIPGFFGA_00417 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
EIPGFFGA_00418 | 9.1e-189 | XK27_05470 | E | Methionine synthase | ||
EIPGFFGA_00419 | 3.4e-21 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
EIPGFFGA_00420 | 4.6e-12 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
EIPGFFGA_00421 | 3.8e-145 | folP | 2.5.1.15, 2.7.6.3 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
EIPGFFGA_00422 | 5.8e-51 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
EIPGFFGA_00423 | 5.4e-84 | S | membrane | |||
EIPGFFGA_00424 | 7.6e-36 | P | VTC domain | |||
EIPGFFGA_00425 | 1.5e-138 | msmX | P | Belongs to the ABC transporter superfamily | ||
EIPGFFGA_00426 | 3.6e-160 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
EIPGFFGA_00427 | 8.4e-165 | cpsY | K | Transcriptional regulator | ||
EIPGFFGA_00430 | 1.9e-95 | ywlG | S | Belongs to the UPF0340 family | ||
EIPGFFGA_00431 | 1e-218 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
EIPGFFGA_00432 | 1.2e-36 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
EIPGFFGA_00433 | 2.9e-117 | T | response regulator | |||
EIPGFFGA_00435 | 2e-144 | XK27_09825 | V | 'abc transporter, ATP-binding protein | ||
EIPGFFGA_00436 | 1.9e-118 | pepV | 3.5.1.18 | E | Dipeptidase | |
EIPGFFGA_00437 | 3.6e-108 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
EIPGFFGA_00438 | 5.1e-31 | K | transcriptional regulator | |||
EIPGFFGA_00439 | 6.9e-192 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
EIPGFFGA_00441 | 3.9e-51 | L | Transposase | |||
EIPGFFGA_00442 | 3.5e-137 | XK27_00940 | 1.2.1.70, 3.5.1.9 | S | Metal-dependent hydrolase | |
EIPGFFGA_00443 | 2.6e-70 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
EIPGFFGA_00444 | 5.3e-193 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
EIPGFFGA_00445 | 1.9e-65 | bcrA | V | abc transporter atp-binding protein | ||
EIPGFFGA_00446 | 1.2e-124 | S | ABC-2 family transporter protein | |||
EIPGFFGA_00447 | 2.8e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
EIPGFFGA_00448 | 3.6e-117 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
EIPGFFGA_00449 | 1.6e-27 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
EIPGFFGA_00450 | 4.6e-169 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
EIPGFFGA_00452 | 1.2e-41 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
EIPGFFGA_00453 | 6.5e-232 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
EIPGFFGA_00454 | 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 | |
EIPGFFGA_00455 | 2.8e-308 | WQ51_06230 | S | ABC transporter | ||
EIPGFFGA_00456 | 2e-14 | WQ51_06230 | S | ABC transporter | ||
EIPGFFGA_00457 | 1.4e-142 | cmpC | S | abc transporter atp-binding protein | ||
EIPGFFGA_00458 | 4.9e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
EIPGFFGA_00459 | 1.5e-59 | 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 | ||
EIPGFFGA_00460 | 2.6e-144 | desK | 2.7.13.3 | T | Histidine kinase | |
EIPGFFGA_00461 | 6.7e-113 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
EIPGFFGA_00462 | 3.7e-199 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | COG0366 Glycosidases |
EIPGFFGA_00463 | 6.2e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
EIPGFFGA_00464 | 5.2e-75 | S | oxidoreductase | |||
EIPGFFGA_00465 | 5.5e-217 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
EIPGFFGA_00466 | 3.8e-182 | L | the current gene model (or a revised gene model) may contain a | |||
EIPGFFGA_00467 | 9.1e-53 | vraS | 2.7.13.3 | T | Histidine kinase | |
EIPGFFGA_00468 | 4.3e-83 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
EIPGFFGA_00469 | 1.8e-156 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
EIPGFFGA_00470 | 7.4e-35 | rlpA | M | LysM domain protein | ||
EIPGFFGA_00471 | 3.2e-228 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
EIPGFFGA_00473 | 8.2e-165 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
EIPGFFGA_00474 | 2.5e-98 | mdlA | V | abc transporter atp-binding protein | ||
EIPGFFGA_00475 | 7.8e-120 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
EIPGFFGA_00476 | 2.3e-47 | supH | S | overlaps another CDS with the same product name | ||
EIPGFFGA_00477 | 7.1e-147 | XK27_02985 | S | overlaps another CDS with the same product name | ||
EIPGFFGA_00478 | 3.3e-200 | yurR | 1.4.5.1 | E | oxidoreductase | |
EIPGFFGA_00479 | 1.9e-169 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
EIPGFFGA_00480 | 5.1e-21 | sumf2 | S | PEGA domain | ||
EIPGFFGA_00481 | 1.7e-131 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
EIPGFFGA_00482 | 4.2e-187 | ylbL | T | Belongs to the peptidase S16 family | ||
EIPGFFGA_00483 | 6e-17 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
EIPGFFGA_00484 | 4e-30 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
EIPGFFGA_00485 | 5.8e-24 | U | response to pH | |||
EIPGFFGA_00486 | 1.1e-107 | yfmR | S | abc transporter atp-binding protein | ||
EIPGFFGA_00487 | 1.3e-129 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
EIPGFFGA_00489 | 4.6e-120 | ydaO | E | amino acid | ||
EIPGFFGA_00490 | 2.6e-216 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
EIPGFFGA_00491 | 1.2e-47 | |||||
EIPGFFGA_00492 | 4.8e-42 | |||||
EIPGFFGA_00493 | 3.1e-197 | yceA | S | Belongs to the UPF0176 family | ||
EIPGFFGA_00494 | 8.5e-193 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
EIPGFFGA_00495 | 2e-136 | fliF | 2.1.1.72 | N | bacterial-type flagellum-dependent cell motility | |
EIPGFFGA_00496 | 1.2e-17 | S | Protein of unknown function (DUF3021) | |||
EIPGFFGA_00497 | 2.5e-50 | L | transposase and inactivated derivatives, IS30 family | |||
EIPGFFGA_00498 | 1.8e-104 | L | Integrase | |||
EIPGFFGA_00499 | 1.1e-25 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
EIPGFFGA_00500 | 1.6e-85 | manL | 2.7.1.191 | G | pts system | |
EIPGFFGA_00501 | 4.6e-97 | 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 | |
EIPGFFGA_00502 | 1.6e-122 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
EIPGFFGA_00505 | 3.9e-42 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
EIPGFFGA_00506 | 1.9e-189 | 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 | |
EIPGFFGA_00508 | 3.5e-99 | V | CAAX protease self-immunity | |||
EIPGFFGA_00509 | 4.4e-58 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
EIPGFFGA_00510 | 3e-14 | coiA | 3.6.4.12 | S | Competence protein | |
EIPGFFGA_00511 | 1.2e-13 | |||||
EIPGFFGA_00512 | 4.9e-103 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
EIPGFFGA_00513 | 3.2e-44 | yrzB | S | Belongs to the UPF0473 family | ||
EIPGFFGA_00514 | 7.3e-33 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
EIPGFFGA_00515 | 1.6e-19 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
EIPGFFGA_00516 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
EIPGFFGA_00517 | 1.3e-81 | Z012_10770 | M | Domain of unknown function (DUF1919) | ||
EIPGFFGA_00518 | 1.4e-189 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
EIPGFFGA_00519 | 8.7e-75 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
EIPGFFGA_00520 | 1.4e-87 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
EIPGFFGA_00521 | 1.4e-178 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
EIPGFFGA_00522 | 6.1e-56 | 3.5.1.28 | M | domain protein | ||
EIPGFFGA_00523 | 1.8e-42 | htpX | O | Belongs to the peptidase M48B family | ||
EIPGFFGA_00524 | 5e-119 | sirR | K | iron dependent repressor | ||
EIPGFFGA_00525 | 4.4e-90 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
EIPGFFGA_00526 | 4.6e-59 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
EIPGFFGA_00527 | 4.4e-32 | ftsE | D | cell division ATP-binding protein FtsE | ||
EIPGFFGA_00528 | 8.4e-198 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
EIPGFFGA_00529 | 4.1e-59 | sitB | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
EIPGFFGA_00530 | 2.6e-74 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
EIPGFFGA_00531 | 1.2e-206 | 2.7.13.3 | T | GHKL domain | ||
EIPGFFGA_00532 | 5.2e-119 | yqfA | K | protein, Hemolysin III | ||
EIPGFFGA_00533 | 4.1e-29 | pspC | KT | PspC domain protein | ||
EIPGFFGA_00534 | 5.1e-55 | yaaT | S | stage 0 sporulation protein | ||
EIPGFFGA_00535 | 1.2e-54 | yabA | L | Involved in initiation control of chromosome replication | ||
EIPGFFGA_00537 | 1.7e-24 | I | acyl-CoA dehydrogenase | |||
EIPGFFGA_00538 | 7.4e-137 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
EIPGFFGA_00539 | 1.2e-79 | glnA | 6.3.1.2 | E | glutamine synthetase | |
EIPGFFGA_00540 | 6.2e-114 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
EIPGFFGA_00542 | 2.4e-30 | yozG | K | Transcriptional regulator | ||
EIPGFFGA_00544 | 4.4e-147 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
EIPGFFGA_00545 | 1.1e-197 | aroF | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
EIPGFFGA_00546 | 3.9e-67 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
EIPGFFGA_00547 | 7.7e-55 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
EIPGFFGA_00548 | 1.8e-75 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
EIPGFFGA_00549 | 6.4e-168 | 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 | ||
EIPGFFGA_00550 | 1.7e-44 | K | WHG domain | |||
EIPGFFGA_00551 | 5.1e-45 | V | abc transporter atp-binding protein | |||
EIPGFFGA_00552 | 1.6e-64 | V | abc transporter atp-binding protein | |||
EIPGFFGA_00553 | 1.6e-29 | |||||
EIPGFFGA_00555 | 1.1e-49 | |||||
EIPGFFGA_00556 | 2e-146 | murB | 1.3.1.98 | M | cell wall formation | |
EIPGFFGA_00557 | 2.2e-108 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
EIPGFFGA_00559 | 8.4e-70 | K | LytTr DNA-binding domain | |||
EIPGFFGA_00560 | 1.2e-79 | S | Protein of unknown function (DUF3021) | |||
EIPGFFGA_00561 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
EIPGFFGA_00562 | 1.1e-56 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
EIPGFFGA_00563 | 6.9e-69 | argR | K | Regulates arginine biosynthesis genes | ||
EIPGFFGA_00564 | 0.0 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
EIPGFFGA_00565 | 1.2e-64 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
EIPGFFGA_00566 | 2e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
EIPGFFGA_00567 | 2.9e-134 | fatB | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
EIPGFFGA_00568 | 3.7e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
EIPGFFGA_00569 | 7.9e-191 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
EIPGFFGA_00570 | 1.2e-45 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
EIPGFFGA_00571 | 1.6e-97 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
EIPGFFGA_00572 | 2.4e-102 | T | Histidine kinase | |||
EIPGFFGA_00574 | 1.4e-16 | csbD | S | CsbD-like | ||
EIPGFFGA_00575 | 8.2e-73 | S | Protein of unknown function (DUF421) | |||
EIPGFFGA_00577 | 3.5e-74 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
EIPGFFGA_00578 | 1.2e-103 | 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 | |
EIPGFFGA_00579 | 2.2e-79 | 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 | |
EIPGFFGA_00580 | 5.9e-52 | U | protein secretion | |||
EIPGFFGA_00581 | 8e-112 | lrgB | M | cytolysis | ||
EIPGFFGA_00582 | 2.6e-65 | M | Pfam SNARE associated Golgi protein | |||
EIPGFFGA_00584 | 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 | ||
EIPGFFGA_00585 | 1e-35 | XK27_05110 | P | chloride | ||
EIPGFFGA_00586 | 8.6e-93 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
EIPGFFGA_00587 | 7.9e-140 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
EIPGFFGA_00588 | 5.7e-197 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
EIPGFFGA_00589 | 7e-192 | rgpF | GT2,GT4 | M | Glycosyltransferase like family 2 | |
EIPGFFGA_00590 | 2.1e-32 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
EIPGFFGA_00591 | 9.1e-19 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
EIPGFFGA_00592 | 5.3e-74 | L | Transposase | |||
EIPGFFGA_00593 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
EIPGFFGA_00594 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
EIPGFFGA_00595 | 5.9e-67 | manO | S | Protein conserved in bacteria | ||
EIPGFFGA_00596 | 3.5e-83 | manN | G | PTS system mannose fructose sorbose family IID component | ||
EIPGFFGA_00597 | 2.9e-179 | 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 | ||
EIPGFFGA_00598 | 2.9e-47 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
EIPGFFGA_00599 | 1.5e-97 | XK27_09740 | S | Phosphoesterase | ||
EIPGFFGA_00600 | 2.4e-73 | soj1 | D | chromosome partitioning | ||
EIPGFFGA_00601 | 1.4e-151 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
EIPGFFGA_00602 | 9.3e-15 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
EIPGFFGA_00603 | 7.4e-92 | cvpA | S | toxin biosynthetic process | ||
EIPGFFGA_00604 | 6.5e-54 | 3.1.3.18 | S | IA, variant 1 | ||
EIPGFFGA_00605 | 7.2e-148 | yeiH | S | Psort location CytoplasmicMembrane, score 10.00 | ||
EIPGFFGA_00606 | 2.7e-169 | 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 | ||
EIPGFFGA_00607 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
EIPGFFGA_00608 | 5.1e-72 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
EIPGFFGA_00609 | 1.5e-141 | 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 | |
EIPGFFGA_00610 | 3.1e-107 | 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 | |
EIPGFFGA_00611 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
EIPGFFGA_00612 | 7.2e-101 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
EIPGFFGA_00613 | 3e-63 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
EIPGFFGA_00614 | 5.2e-31 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
EIPGFFGA_00615 | 1.8e-87 | yvqF | S | Membrane | ||
EIPGFFGA_00616 | 1e-54 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
EIPGFFGA_00617 | 5.8e-49 | |||||
EIPGFFGA_00618 | 8.5e-78 | K | TetR family transcriptional regulator | |||
EIPGFFGA_00619 | 1.9e-143 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
EIPGFFGA_00620 | 1.8e-53 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
EIPGFFGA_00621 | 6.2e-67 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
EIPGFFGA_00622 | 2.3e-111 | 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 | ||
EIPGFFGA_00623 | 3.4e-166 | era | M | 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 | ||
EIPGFFGA_00624 | 7.7e-92 | lemA | S | LemA family | ||
EIPGFFGA_00625 | 8.4e-182 | 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 | |
EIPGFFGA_00626 | 3.9e-114 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
EIPGFFGA_00627 | 3.6e-49 | 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 | |
EIPGFFGA_00628 | 3e-181 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
EIPGFFGA_00629 | 5.3e-167 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
EIPGFFGA_00630 | 5.8e-118 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
EIPGFFGA_00631 | 4.4e-52 | |||||
EIPGFFGA_00633 | 3.9e-27 | yqeB | S | Pyrimidine dimer DNA glycosylase | ||
EIPGFFGA_00634 | 7e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
EIPGFFGA_00635 | 1.3e-15 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
EIPGFFGA_00636 | 2.1e-151 | 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 | |
EIPGFFGA_00637 | 1e-84 | endA | F | DNA RNA non-specific endonuclease | ||
EIPGFFGA_00638 | 1e-54 | tcyB_2 | P | ABC transporter (permease) | ||
EIPGFFGA_00639 | 1.7e-41 | L | Phage integrase, N-terminal SAM-like domain | |||
EIPGFFGA_00640 | 6.2e-120 | yoaK | S | Protein of unknown function (DUF1275) | ||
EIPGFFGA_00642 | 2.6e-166 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
EIPGFFGA_00643 | 1e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
EIPGFFGA_00644 | 4.1e-07 | |||||
EIPGFFGA_00645 | 8.6e-57 | 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 | ||
EIPGFFGA_00646 | 1.6e-24 | 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 | ||
EIPGFFGA_00647 | 2.9e-168 | corA | P | COG0598 Mg2 and Co2 transporters | ||
EIPGFFGA_00648 | 1e-19 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
EIPGFFGA_00649 | 4.9e-102 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
EIPGFFGA_00650 | 2e-155 | pstS | P | phosphate | ||
EIPGFFGA_00651 | 5.6e-172 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
EIPGFFGA_00652 | 2.5e-33 | S | Domain of unknown function (DUF5123) | |||
EIPGFFGA_00653 | 1.2e-132 | lmrA | V | abc transporter atp-binding protein | ||
EIPGFFGA_00654 | 3.9e-128 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
EIPGFFGA_00658 | 1.4e-47 | L | PFAM Integrase, catalytic core | |||
EIPGFFGA_00659 | 2.6e-73 | L | PFAM Integrase, catalytic core | |||
EIPGFFGA_00660 | 4e-34 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
EIPGFFGA_00661 | 2.3e-51 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
EIPGFFGA_00662 | 3.3e-26 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
EIPGFFGA_00663 | 7.9e-56 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
EIPGFFGA_00664 | 4.2e-28 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
EIPGFFGA_00665 | 1.9e-46 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | adenylyltransferase | |
EIPGFFGA_00666 | 6.7e-45 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
EIPGFFGA_00667 | 1e-96 | hscC | O | Belongs to the heat shock protein 70 family | ||
EIPGFFGA_00669 | 1.6e-169 | pyrP | F | uracil Permease | ||
EIPGFFGA_00670 | 5.7e-50 | XK27_01300 | S | ASCH | ||
EIPGFFGA_00671 | 6e-93 | leuS | 6.1.1.4 | J | Leucyl-tRNA synthetase, Domain 2 | |
EIPGFFGA_00672 | 5.5e-24 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
EIPGFFGA_00673 | 3.6e-79 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
EIPGFFGA_00674 | 1.7e-156 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
EIPGFFGA_00675 | 4.4e-214 | amiC | P | ABC transporter (Permease | ||
EIPGFFGA_00676 | 3.8e-165 | amiD | P | ABC transporter (Permease | ||
EIPGFFGA_00677 | 7.9e-202 | oppD | P | Belongs to the ABC transporter superfamily | ||
EIPGFFGA_00678 | 3.3e-172 | oppF | P | Belongs to the ABC transporter superfamily | ||
EIPGFFGA_00679 | 3.2e-128 | V | Psort location CytoplasmicMembrane, score | |||
EIPGFFGA_00680 | 3.5e-118 | skfE | V | abc transporter atp-binding protein | ||
EIPGFFGA_00681 | 2.8e-45 | yvoA_1 | K | Transcriptional | ||
EIPGFFGA_00682 | 1.4e-158 | rgfB | 3.1.3.90 | L | Endonuclease/Exonuclease/phosphatase family | |
EIPGFFGA_00683 | 0.0 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
EIPGFFGA_00684 | 2.4e-162 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
EIPGFFGA_00685 | 8.7e-129 | adcB | P | ABC transporter (Permease | ||
EIPGFFGA_00686 | 9.2e-135 | adcC | P | ABC transporter, ATP-binding protein | ||
EIPGFFGA_00687 | 2.3e-298 | O | MreB/Mbl protein | |||
EIPGFFGA_00689 | 5.8e-146 | V | Psort location CytoplasmicMembrane, score | |||
EIPGFFGA_00693 | 8.9e-14 | |||||
EIPGFFGA_00694 | 1.2e-120 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
EIPGFFGA_00695 | 7.3e-150 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
EIPGFFGA_00696 | 8.5e-43 | comGC | U | Required for transformation and DNA binding | ||
EIPGFFGA_00697 | 8.4e-70 | cglD | NU | Competence protein | ||
EIPGFFGA_00698 | 3.1e-15 | NU | Type II secretory pathway pseudopilin | |||
EIPGFFGA_00699 | 4.5e-71 | comGF | U | Competence protein ComGF | ||
EIPGFFGA_00700 | 2e-12 | comGF | U | Putative Competence protein ComGF | ||
EIPGFFGA_00701 | 1.1e-175 | ytxK | 2.1.1.72 | L | DNA methylase | |
EIPGFFGA_00702 | 2.9e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
EIPGFFGA_00703 | 3.8e-110 | 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 | |
EIPGFFGA_00704 | 5.9e-82 | nrdI | F | Belongs to the NrdI family | ||
EIPGFFGA_00705 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
EIPGFFGA_00706 | 1.4e-30 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
EIPGFFGA_00707 | 1.6e-52 | K | transcriptional regulator, PadR family | |||
EIPGFFGA_00708 | 1e-70 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
EIPGFFGA_00709 | 2.2e-106 | S | Putative adhesin | |||
EIPGFFGA_00710 | 1.6e-159 | XK27_06930 | V | domain protein | ||
EIPGFFGA_00711 | 9.9e-97 | XK27_06935 | K | transcriptional regulator | ||
EIPGFFGA_00712 | 5e-45 | ypaA | M | Membrane | ||
EIPGFFGA_00713 | 1.7e-117 | S | CAAX protease self-immunity | |||
EIPGFFGA_00714 | 5.1e-113 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
EIPGFFGA_00715 | 7.6e-09 | S | NTF2 fold immunity protein | |||
EIPGFFGA_00716 | 5.1e-53 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
EIPGFFGA_00717 | 3.5e-08 | XK27_10305 | S | Domain of unknown function (DUF4651) | ||
EIPGFFGA_00718 | 1.1e-198 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
EIPGFFGA_00719 | 1.1e-113 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
EIPGFFGA_00720 | 1.1e-23 | S | CAAX amino terminal protease family protein | |||
EIPGFFGA_00721 | 1e-268 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
EIPGFFGA_00722 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
EIPGFFGA_00723 | 1e-246 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
EIPGFFGA_00724 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
EIPGFFGA_00725 | 5.8e-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 | ||
EIPGFFGA_00726 | 1.9e-10 | |||||
EIPGFFGA_00727 | 7.5e-14 | |||||
EIPGFFGA_00728 | 1.6e-88 | XK27_10930 | K | acetyltransferase | ||
EIPGFFGA_00729 | 8.2e-116 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
EIPGFFGA_00730 | 4e-122 | yaaA | S | Belongs to the UPF0246 family | ||
EIPGFFGA_00731 | 9.3e-167 | XK27_01785 | S | cog cog1284 | ||
EIPGFFGA_00732 | 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) | |
EIPGFFGA_00733 | 1.8e-19 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
EIPGFFGA_00734 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
EIPGFFGA_00736 | 3.6e-137 | cbf | S | 3'-5' exoribonuclease yhaM | ||
EIPGFFGA_00737 | 6.9e-142 | purR | 2.4.2.7 | F | operon repressor | |
EIPGFFGA_00738 | 2.3e-69 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
EIPGFFGA_00739 | 3.9e-81 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
EIPGFFGA_00740 | 7.3e-33 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
EIPGFFGA_00741 | 3.3e-33 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
EIPGFFGA_00742 | 1.6e-28 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
EIPGFFGA_00743 | 2e-255 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
EIPGFFGA_00744 | 3.9e-159 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
EIPGFFGA_00745 | 5.1e-139 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
EIPGFFGA_00746 | 4.7e-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) | |
EIPGFFGA_00747 | 3.3e-112 | 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 | |
EIPGFFGA_00748 | 1.5e-236 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
EIPGFFGA_00749 | 5.3e-275 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
EIPGFFGA_00750 | 8.4e-64 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
EIPGFFGA_00751 | 0.0 | S | Bacterial membrane protein, YfhO | |||
EIPGFFGA_00752 | 9.6e-219 | 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 | |
EIPGFFGA_00753 | 5.4e-99 | yvbG | U | UPF0056 membrane protein | ||
EIPGFFGA_00754 | 3.1e-41 | yaaA | S | S4 domain protein YaaA | ||
EIPGFFGA_00755 | 5.7e-200 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
EIPGFFGA_00756 | 5.6e-275 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
EIPGFFGA_00757 | 4.5e-191 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
EIPGFFGA_00758 | 2.7e-249 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
EIPGFFGA_00759 | 1.1e-142 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
EIPGFFGA_00760 | 3.6e-94 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
EIPGFFGA_00761 | 1.4e-125 | K | transcriptional regulator, MerR family | |||
EIPGFFGA_00762 | 0.0 | V | ABC transporter (Permease | |||
EIPGFFGA_00763 | 6.9e-19 | V | abc transporter atp-binding protein | |||
EIPGFFGA_00764 | 5.4e-93 | asp1 | S | Accessory Sec system protein Asp1 | ||
EIPGFFGA_00765 | 4.7e-211 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
EIPGFFGA_00766 | 0.0 | M | family 8 | |||
EIPGFFGA_00767 | 1.7e-19 | M | family 8 | |||
EIPGFFGA_00768 | 1.5e-100 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
EIPGFFGA_00769 | 1.4e-189 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
EIPGFFGA_00770 | 6.4e-276 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
EIPGFFGA_00771 | 1.6e-102 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
EIPGFFGA_00772 | 2.6e-233 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
EIPGFFGA_00773 | 1.8e-125 | IQ | reductase | |||
EIPGFFGA_00774 | 3e-162 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
EIPGFFGA_00775 | 9.9e-172 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
EIPGFFGA_00776 | 1.8e-105 | artQ | P | ABC transporter (Permease | ||
EIPGFFGA_00777 | 4.4e-112 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
EIPGFFGA_00778 | 4.6e-157 | aatB | ET | ABC transporter substrate-binding protein | ||
EIPGFFGA_00779 | 3.7e-268 | uvrX | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
EIPGFFGA_00780 | 1.8e-38 | gcvR | T | UPF0237 protein | ||
EIPGFFGA_00781 | 6.6e-243 | XK27_08635 | S | UPF0210 protein | ||
EIPGFFGA_00782 | 6.2e-131 | ais | G | Phosphoglycerate mutase | ||
EIPGFFGA_00783 | 5.3e-139 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
EIPGFFGA_00784 | 7.2e-101 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
EIPGFFGA_00785 | 5.4e-129 | S | sequence-specific DNA binding | |||
EIPGFFGA_00786 | 3.5e-233 | ymfH | S | Peptidase M16 | ||
EIPGFFGA_00787 | 9.3e-231 | ymfF | S | Peptidase M16 | ||
EIPGFFGA_00788 | 6.6e-90 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
EIPGFFGA_00792 | 3.3e-155 | rrmA | 2.1.1.187 | Q | methyltransferase | |
EIPGFFGA_00793 | 2.6e-135 | S | HAD hydrolase, family IA, variant | |||
EIPGFFGA_00794 | 2.6e-106 | K | transcriptional regulator (lysR family) | |||
EIPGFFGA_00795 | 9.8e-64 | S | reductase | |||
EIPGFFGA_00796 | 4.6e-74 | S | reductase | |||
EIPGFFGA_00797 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
EIPGFFGA_00798 | 2.5e-62 | manO | S | protein conserved in bacteria | ||
EIPGFFGA_00799 | 2.3e-156 | manN | G | PTS system mannose fructose sorbose family IID component | ||
EIPGFFGA_00800 | 2e-117 | manM | G | pts system | ||
EIPGFFGA_00801 | 3.1e-173 | manL | 2.7.1.191 | G | pts system | |
EIPGFFGA_00802 | 0.0 | pepF | E | oligoendopeptidase F | ||
EIPGFFGA_00803 | 6.4e-131 | coiA | 3.6.4.12 | S | Competence protein | |
EIPGFFGA_00804 | 7.5e-175 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
EIPGFFGA_00805 | 1.2e-112 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
EIPGFFGA_00806 | 1.3e-66 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
EIPGFFGA_00807 | 1.2e-183 | tcsA | S | membrane | ||
EIPGFFGA_00808 | 4.5e-152 | degV | S | DegV family | ||
EIPGFFGA_00809 | 6e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
EIPGFFGA_00810 | 3.7e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
EIPGFFGA_00812 | 3.4e-179 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | glucose-1-phosphate adenylyltransferase |
EIPGFFGA_00813 | 1.4e-188 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
EIPGFFGA_00814 | 2.1e-238 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
EIPGFFGA_00815 | 3.3e-155 | S | CHAP domain | |||
EIPGFFGA_00816 | 4.3e-200 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
EIPGFFGA_00817 | 5.9e-202 | 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) | |
EIPGFFGA_00818 | 7.7e-160 | 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) | |
EIPGFFGA_00819 | 2e-115 | 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 | |
EIPGFFGA_00820 | 7.7e-163 | ywbD | 2.1.1.191 | J | Methyltransferase | |
EIPGFFGA_00821 | 6.3e-199 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
EIPGFFGA_00822 | 3e-192 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
EIPGFFGA_00823 | 4.8e-210 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
EIPGFFGA_00824 | 7.6e-178 | jag | S | RNA-binding protein | ||
EIPGFFGA_00825 | 9.9e-98 | K | Transcriptional regulator | |||
EIPGFFGA_00826 | 4.2e-98 | 1.6.5.2 | S | NADPH-quinone reductase (modulator of drug activity B) | ||
EIPGFFGA_00827 | 3.4e-14 | rpmH | J | Ribosomal protein L34 | ||
EIPGFFGA_00828 | 4.4e-155 | V | ABC transporter | |||
EIPGFFGA_00829 | 6.1e-126 | yeeN | K | transcriptional regulatory protein | ||
EIPGFFGA_00830 | 8.5e-46 | yajC | U | protein transport | ||
EIPGFFGA_00831 | 5.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
EIPGFFGA_00832 | 9.9e-280 | ybiT | S | abc transporter atp-binding protein | ||
EIPGFFGA_00833 | 1.1e-64 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
EIPGFFGA_00834 | 1.7e-71 | S | QueT transporter | |||
EIPGFFGA_00836 | 2.1e-111 | yfjR | K | regulation of single-species biofilm formation | ||
EIPGFFGA_00837 | 1e-207 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
EIPGFFGA_00838 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
EIPGFFGA_00839 | 4e-181 | S | Protein of unknown function (DUF3114) | |||
EIPGFFGA_00840 | 1.3e-140 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
EIPGFFGA_00841 | 4.5e-293 | 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) | |
EIPGFFGA_00842 | 9.3e-231 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
EIPGFFGA_00843 | 1.5e-36 | ylqC | L | Belongs to the UPF0109 family | ||
EIPGFFGA_00844 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
EIPGFFGA_00846 | 4.6e-266 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
EIPGFFGA_00847 | 2.6e-209 | macB_2 | V | FtsX-like permease family | ||
EIPGFFGA_00848 | 6.7e-104 | nodB3 | G | deacetylase | ||
EIPGFFGA_00849 | 3.5e-140 | yabB | 2.1.1.223 | L | Methyltransferase | |
EIPGFFGA_00850 | 6.6e-41 | yazA | L | endonuclease containing a URI domain | ||
EIPGFFGA_00851 | 1.9e-244 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
EIPGFFGA_00852 | 5.8e-112 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
EIPGFFGA_00853 | 3e-167 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
EIPGFFGA_00854 | 3e-84 | yxjI | S | LURP-one-related | ||
EIPGFFGA_00855 | 8.4e-94 | F | Shikimate kinase | |||
EIPGFFGA_00856 | 7.6e-55 | 2.3.1.128, 5.2.1.8 | J | Acetyltransferase (GNAT) domain | ||
EIPGFFGA_00857 | 3.3e-101 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
EIPGFFGA_00858 | 2e-92 | S | UPF0397 protein | |||
EIPGFFGA_00859 | 1.9e-308 | ykoD | P | abc transporter atp-binding protein | ||
EIPGFFGA_00861 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 uvrA and 2 uvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by uvrB, the uvrA molecules dissociate | ||
EIPGFFGA_00862 | 7e-127 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
EIPGFFGA_00863 | 1.1e-226 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
EIPGFFGA_00864 | 1.6e-75 | 3.5.1.19 | Q | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | ||
EIPGFFGA_00865 | 1e-78 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
EIPGFFGA_00866 | 2e-144 | 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 | ||
EIPGFFGA_00867 | 1.3e-70 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
EIPGFFGA_00868 | 4.7e-49 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
EIPGFFGA_00869 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
EIPGFFGA_00870 | 2.8e-24 | secE | U | Belongs to the SecE SEC61-gamma family | ||
EIPGFFGA_00871 | 1.6e-293 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
EIPGFFGA_00872 | 2.8e-235 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
EIPGFFGA_00873 | 1.2e-233 | sufD | O | assembly protein SufD | ||
EIPGFFGA_00874 | 1.7e-137 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
EIPGFFGA_00875 | 9.4e-86 | XK27_09675 | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
EIPGFFGA_00876 | 5.2e-256 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
EIPGFFGA_00877 | 9.6e-23 | |||||
EIPGFFGA_00878 | 5.3e-44 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
EIPGFFGA_00879 | 1e-170 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
EIPGFFGA_00880 | 5.7e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
EIPGFFGA_00881 | 7.9e-97 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
EIPGFFGA_00882 | 4.4e-55 | fnt | P | Formate nitrite transporter | ||
EIPGFFGA_00884 | 4.7e-168 | fhuR | K | transcriptional regulator (lysR family) | ||
EIPGFFGA_00885 | 2.6e-77 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
EIPGFFGA_00886 | 1.1e-161 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
EIPGFFGA_00887 | 4.6e-157 | yjjH | S | Calcineurin-like phosphoesterase | ||
EIPGFFGA_00888 | 4.5e-132 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
EIPGFFGA_00889 | 4.3e-68 | pacL | 3.6.3.8 | P | cation transport ATPase | |
EIPGFFGA_00890 | 1.3e-196 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
EIPGFFGA_00891 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
EIPGFFGA_00892 | 6.2e-195 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
EIPGFFGA_00893 | 1.3e-254 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
EIPGFFGA_00894 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
EIPGFFGA_00895 | 1.5e-135 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
EIPGFFGA_00896 | 1.7e-17 | XK27_00735 | ||||
EIPGFFGA_00897 | 9.8e-191 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
EIPGFFGA_00898 | 1.3e-231 | U | protein secretion | |||
EIPGFFGA_00899 | 1.6e-238 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
EIPGFFGA_00900 | 1.3e-193 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
EIPGFFGA_00901 | 3.4e-221 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
EIPGFFGA_00902 | 1.2e-77 | 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 | ||
EIPGFFGA_00903 | 7.2e-161 | 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 | ||
EIPGFFGA_00904 | 2.8e-222 | yfiB1 | V | abc transporter atp-binding protein | ||
EIPGFFGA_00905 | 0.0 | XK27_10035 | V | abc transporter atp-binding protein | ||
EIPGFFGA_00906 | 2.7e-161 | ypuA | S | secreted protein | ||
EIPGFFGA_00907 | 3.7e-72 | yaeR | E | COG0346 Lactoylglutathione lyase and related lyases | ||
EIPGFFGA_00908 | 8.8e-84 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
EIPGFFGA_00909 | 5.3e-84 | 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 | ||
EIPGFFGA_00910 | 3.4e-132 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
EIPGFFGA_00911 | 1.4e-13 | yidD | M | Could be involved in insertion of integral membrane proteins into the membrane | ||
EIPGFFGA_00912 | 3.4e-250 | trkH | P | Cation transport protein | ||
EIPGFFGA_00913 | 4.3e-109 | 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 | ||
EIPGFFGA_00914 | 2.6e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
EIPGFFGA_00915 | 5.7e-112 | |||||
EIPGFFGA_00916 | 7.6e-140 | serS | 6.1.1.11 | J | Catalyzes the attachment of serine to tRNA(Ser). Is also able to aminoacylate tRNA(Sec) with serine, to form the misacylated tRNA L-seryl-tRNA(Sec), which will be further converted into selenocysteinyl-tRNA(Sec) | |
EIPGFFGA_00917 | 4.8e-51 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
EIPGFFGA_00918 | 3.3e-198 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
EIPGFFGA_00919 | 8.2e-67 | ctsR | K | Belongs to the CtsR family | ||
EIPGFFGA_00920 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
EIPGFFGA_00921 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
EIPGFFGA_00922 | 6.2e-182 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
EIPGFFGA_00923 | 1e-162 | rapZ | S | Displays ATPase and GTPase activities | ||
EIPGFFGA_00924 | 5e-134 | yejC | S | cyclic nucleotide-binding protein | ||
EIPGFFGA_00925 | 3.2e-65 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
EIPGFFGA_00926 | 2.6e-14 | S | Domain of unknown function (DUF3173) | |||
EIPGFFGA_00927 | 3.5e-142 | |||||
EIPGFFGA_00928 | 9.1e-153 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
EIPGFFGA_00929 | 6.2e-230 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
EIPGFFGA_00930 | 5.4e-175 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
EIPGFFGA_00931 | 2.4e-225 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
EIPGFFGA_00932 | 7.7e-274 | ywbL | P | COG0672 High-affinity Fe2 Pb2 permease | ||
EIPGFFGA_00933 | 9.7e-22 | |||||
EIPGFFGA_00934 | 5.8e-91 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
EIPGFFGA_00935 | 2.2e-167 | 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 | |
EIPGFFGA_00936 | 6.9e-248 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
EIPGFFGA_00937 | 1.7e-63 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
EIPGFFGA_00938 | 7e-56 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
EIPGFFGA_00939 | 1.3e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
EIPGFFGA_00940 | 3.7e-276 | 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 | |
EIPGFFGA_00941 | 2.3e-63 | 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 | ||
EIPGFFGA_00942 | 6.3e-70 | M | Pilin isopeptide linkage domain protein | |||
EIPGFFGA_00943 | 2.4e-172 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
EIPGFFGA_00944 | 2.6e-121 | macB | V | ABC transporter, ATP-binding protein | ||
EIPGFFGA_00945 | 9.1e-178 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
EIPGFFGA_00946 | 7.6e-98 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
EIPGFFGA_00947 | 4.3e-80 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
EIPGFFGA_00948 | 2e-188 | brpA | K | Transcriptional | ||
EIPGFFGA_00949 | 1.3e-90 | XK27_05885 | 2.3.1.82 | M | phosphinothricin N-acetyltransferase activity | |
EIPGFFGA_00950 | 2.6e-65 | trpC | 4.1.1.48, 5.3.1.24 | E | Belongs to the TrpC family | |
EIPGFFGA_00951 | 5.1e-99 | trpF | 4.1.1.48, 4.2.1.160, 4.2.1.20, 5.3.1.24 | E | belongs to the TrpF family | |
EIPGFFGA_00952 | 8.4e-229 | trpB | 4.2.1.20, 5.3.1.24 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
EIPGFFGA_00953 | 1.1e-147 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
EIPGFFGA_00954 | 1e-204 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
EIPGFFGA_00955 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
EIPGFFGA_00956 | 2.3e-131 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
EIPGFFGA_00957 | 1.1e-139 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
EIPGFFGA_00958 | 1.8e-150 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
EIPGFFGA_00959 | 2.7e-26 | |||||
EIPGFFGA_00960 | 2.9e-273 | sufB | O | assembly protein SufB | ||
EIPGFFGA_00961 | 1.1e-30 | nifU | C | SUF system FeS assembly protein, NifU family | ||
EIPGFFGA_00962 | 2.1e-200 | 2.7.13.3 | T | protein histidine kinase activity | ||
EIPGFFGA_00963 | 5.9e-112 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
EIPGFFGA_00964 | 1.1e-298 | 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 | ||
EIPGFFGA_00965 | 2.7e-29 | K | sequence-specific DNA binding | |||
EIPGFFGA_00966 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
EIPGFFGA_00967 | 1.9e-83 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
EIPGFFGA_00968 | 1.9e-80 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
EIPGFFGA_00969 | 1.3e-151 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
EIPGFFGA_00970 | 2.5e-80 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
EIPGFFGA_00971 | 8.4e-279 | 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 | |
EIPGFFGA_00972 | 8.7e-85 | 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 | ||
EIPGFFGA_00973 | 5.1e-45 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
EIPGFFGA_00974 | 1.3e-69 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
EIPGFFGA_00975 | 1.3e-73 | XK27_02470 | K | LytTr DNA-binding domain | ||
EIPGFFGA_00976 | 5.3e-119 | liaI | S | membrane | ||
EIPGFFGA_00977 | 2.9e-193 | mccF | V | LD-carboxypeptidase | ||
EIPGFFGA_00978 | 2.8e-109 | |||||
EIPGFFGA_00979 | 1.8e-276 | L | DNA integration | |||
EIPGFFGA_00980 | 2.7e-302 | yhgF | K | Transcriptional accessory protein | ||
EIPGFFGA_00981 | 3.9e-83 | ydcK | S | Belongs to the SprT family | ||
EIPGFFGA_00982 | 2.2e-41 | pspC | KT | PspC domain | ||
EIPGFFGA_00983 | 5.7e-104 | estA | E | Lysophospholipase L1 and related esterases | ||
EIPGFFGA_00984 | 1e-201 | S | unusual protein kinase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)