| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| EAJPHFHB_00008 | 5.5e-08 | |||||
| EAJPHFHB_00018 | 1.3e-90 | traP | 1.14.99.57, 6.2.1.3 | S | enzyme involved in biosynthesis of extracellular polysaccharides | |
| EAJPHFHB_00019 | 2.2e-139 | yhfI | S | Metallo-beta-lactamase superfamily | ||
| EAJPHFHB_00020 | 2.7e-67 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
| EAJPHFHB_00021 | 2.2e-131 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
| EAJPHFHB_00022 | 1.2e-202 | coiA | 3.6.4.12 | S | Competence protein | |
| EAJPHFHB_00023 | 0.0 | pepF | E | oligoendopeptidase F | ||
| EAJPHFHB_00024 | 3.6e-114 | yjbH | Q | Thioredoxin | ||
| EAJPHFHB_00025 | 2.7e-120 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
| EAJPHFHB_00026 | 4.7e-151 | nadK | 2.7.1.23 | F | 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 | |
| EAJPHFHB_00027 | 9.8e-174 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
| EAJPHFHB_00028 | 5.1e-116 | cutC | P | Participates in the control of copper homeostasis | ||
| EAJPHFHB_00029 | 7.4e-194 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
| EAJPHFHB_00030 | 3.9e-57 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
| EAJPHFHB_00031 | 4.3e-206 | XK27_05220 | S | AI-2E family transporter | ||
| EAJPHFHB_00032 | 8.6e-41 | 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 | ||
| EAJPHFHB_00033 | 5.3e-161 | rrmA | 2.1.1.187 | H | Methyltransferase | |
| EAJPHFHB_00035 | 4.8e-209 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
| EAJPHFHB_00036 | 3.1e-113 | ywnB | S | NAD(P)H-binding | ||
| EAJPHFHB_00037 | 1.8e-95 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
| EAJPHFHB_00038 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
| EAJPHFHB_00039 | 4.2e-175 | corA | P | CorA-like Mg2+ transporter protein | ||
| EAJPHFHB_00040 | 1.9e-62 | S | Protein of unknown function (DUF3397) | |||
| EAJPHFHB_00041 | 1.4e-77 | mraZ | K | Belongs to the MraZ family | ||
| EAJPHFHB_00042 | 5.5e-175 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
| EAJPHFHB_00043 | 7.5e-54 | ftsL | D | Cell division protein FtsL | ||
| EAJPHFHB_00044 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
| EAJPHFHB_00045 | 8.3e-179 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
| EAJPHFHB_00046 | 2.3e-259 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
| EAJPHFHB_00047 | 1.5e-197 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
| EAJPHFHB_00048 | 1.1e-161 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
| EAJPHFHB_00049 | 5.5e-245 | 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 | ||
| EAJPHFHB_00050 | 1.4e-229 | 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 | ||
| EAJPHFHB_00051 | 3.3e-71 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
| EAJPHFHB_00052 | 1.2e-36 | yggT | S | YGGT family | ||
| EAJPHFHB_00053 | 9.9e-146 | ylmH | S | S4 domain protein | ||
| EAJPHFHB_00054 | 1.2e-86 | divIVA | D | DivIVA domain protein | ||
| EAJPHFHB_00055 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
| EAJPHFHB_00056 | 8.8e-79 | cylA | V | abc transporter atp-binding protein | ||
| EAJPHFHB_00057 | 2.7e-80 | cylB | U | ABC-2 type transporter | ||
| EAJPHFHB_00058 | 2.9e-36 | K | LytTr DNA-binding domain | |||
| EAJPHFHB_00059 | 9e-18 | S | Protein of unknown function (DUF3021) | |||
| EAJPHFHB_00060 | 1.1e-189 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
| EAJPHFHB_00061 | 1.9e-95 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
| EAJPHFHB_00062 | 4.6e-28 | |||||
| EAJPHFHB_00063 | 1.8e-122 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
| EAJPHFHB_00064 | 7.1e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
| EAJPHFHB_00065 | 4.9e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
| EAJPHFHB_00066 | 9e-225 | 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 | |
| EAJPHFHB_00067 | 1.3e-241 | ktrB | P | Potassium uptake protein | ||
| EAJPHFHB_00068 | 2.6e-115 | ktrA | P | domain protein | ||
| EAJPHFHB_00069 | 2.3e-120 | N | WxL domain surface cell wall-binding | |||
| EAJPHFHB_00070 | 3.7e-193 | S | Bacterial protein of unknown function (DUF916) | |||
| EAJPHFHB_00071 | 3.8e-268 | N | domain, Protein | |||
| EAJPHFHB_00072 | 5.5e-121 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
| EAJPHFHB_00073 | 1.6e-120 | S | Repeat protein | |||
| EAJPHFHB_00074 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
| EAJPHFHB_00075 | 4.4e-172 | 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) | |
| EAJPHFHB_00076 | 4.1e-108 | mltD | CBM50 | M | NlpC P60 family protein | |
| EAJPHFHB_00077 | 1.7e-28 | |||||
| EAJPHFHB_00078 | 5.7e-188 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
| EAJPHFHB_00079 | 0.0 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
| EAJPHFHB_00080 | 3.1e-33 | ykzG | S | Belongs to the UPF0356 family | ||
| EAJPHFHB_00081 | 6.3e-85 | |||||
| EAJPHFHB_00082 | 3.1e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
| EAJPHFHB_00083 | 1.6e-210 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
| EAJPHFHB_00084 | 4.5e-180 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
| EAJPHFHB_00085 | 1.8e-208 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
| EAJPHFHB_00086 | 1.2e-266 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
| EAJPHFHB_00087 | 8.1e-163 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
| EAJPHFHB_00088 | 3.3e-46 | yktA | S | Belongs to the UPF0223 family | ||
| EAJPHFHB_00089 | 3.5e-135 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
| EAJPHFHB_00090 | 0.0 | typA | T | GTP-binding protein TypA | ||
| EAJPHFHB_00091 | 7.7e-244 | |||||
| EAJPHFHB_00092 | 1.6e-205 | ftsW | D | Belongs to the SEDS family | ||
| EAJPHFHB_00093 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
| EAJPHFHB_00094 | 1.5e-49 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
| EAJPHFHB_00095 | 1.1e-101 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
| EAJPHFHB_00096 | 1.4e-84 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
| EAJPHFHB_00097 | 1.6e-196 | ylbL | T | Belongs to the peptidase S16 family | ||
| EAJPHFHB_00098 | 1.3e-120 | comEA | L | Competence protein ComEA | ||
| EAJPHFHB_00099 | 6.4e-79 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
| EAJPHFHB_00100 | 0.0 | comEC | S | Competence protein ComEC | ||
| EAJPHFHB_00101 | 1.1e-187 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
| EAJPHFHB_00102 | 1.5e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
| EAJPHFHB_00103 | 6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
| EAJPHFHB_00104 | 6.9e-177 | mdtG | EGP | Major Facilitator Superfamily | ||
| EAJPHFHB_00105 | 6.2e-157 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
| EAJPHFHB_00106 | 0.0 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
| EAJPHFHB_00107 | 2.2e-157 | S | Tetratricopeptide repeat | |||
| EAJPHFHB_00108 | 6.1e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
| EAJPHFHB_00109 | 4.1e-213 | 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 | ||
| EAJPHFHB_00110 | 3.3e-236 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
| EAJPHFHB_00111 | 5.1e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
| EAJPHFHB_00112 | 2.2e-49 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
| EAJPHFHB_00113 | 9.9e-73 | S | Iron-sulphur cluster biosynthesis | |||
| EAJPHFHB_00114 | 4.3e-22 | |||||
| EAJPHFHB_00115 | 9.2e-270 | glnPH2 | P | ABC transporter permease | ||
| EAJPHFHB_00116 | 1.6e-134 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
| EAJPHFHB_00117 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision |
Showing 1 to 100 of 2,833 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)