| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| GJNGAHFB_00001 | 3e-292 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
| GJNGAHFB_00002 | 3.5e-188 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
| GJNGAHFB_00003 | 1.2e-163 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
| GJNGAHFB_00004 | 0.0 | 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 | ||
| GJNGAHFB_00005 | 1.7e-96 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
| GJNGAHFB_00006 | 3.8e-254 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
| GJNGAHFB_00007 | 3.1e-74 | yabR | J | RNA binding | ||
| GJNGAHFB_00008 | 1.1e-63 | divIC | D | Septum formation initiator | ||
| GJNGAHFB_00010 | 2.2e-42 | yabO | J | S4 domain protein | ||
| GJNGAHFB_00011 | 3.3e-289 | yabM | S | Polysaccharide biosynthesis protein | ||
| GJNGAHFB_00012 | 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 | ||
| GJNGAHFB_00013 | 4.5e-100 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
| GJNGAHFB_00014 | 1e-176 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
| GJNGAHFB_00015 | 1.4e-264 | S | Putative peptidoglycan binding domain | |||
| GJNGAHFB_00016 | 8.1e-114 | S | (CBS) domain | |||
| GJNGAHFB_00017 | 4.1e-84 | S | QueT transporter | |||
| GJNGAHFB_00018 | 9.4e-189 | argF | 2.1.3.3 | E | Reversibly catalyzes the transfer of the carbamoyl group from carbamoyl phosphate (CP) to the N(epsilon) atom of ornithine (ORN) to produce L-citrulline | |
| GJNGAHFB_00019 | 3.8e-218 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine | |
| GJNGAHFB_00020 | 9.4e-130 | argB | 2.7.2.8 | F | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
| GJNGAHFB_00021 | 6.9e-231 | 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 | |
| GJNGAHFB_00022 | 2.7e-188 | 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 | |
| GJNGAHFB_00023 | 7.5e-205 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
| GJNGAHFB_00024 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
| GJNGAHFB_00025 | 3.9e-44 | kup | P | Transport of potassium into the cell | ||
| GJNGAHFB_00026 | 1.5e-305 | kup | P | Transport of potassium into the cell | ||
| GJNGAHFB_00027 | 2.3e-63 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
| GJNGAHFB_00028 | 1.7e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
| GJNGAHFB_00029 | 1e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
| GJNGAHFB_00030 | 6.6e-258 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
| GJNGAHFB_00031 | 5.6e-261 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
| GJNGAHFB_00032 | 2e-146 | |||||
| GJNGAHFB_00033 | 2.1e-139 | htpX | O | Belongs to the peptidase M48B family | ||
| GJNGAHFB_00034 | 1.7e-91 | lemA | S | LemA family | ||
| GJNGAHFB_00035 | 9.2e-127 | srtA | 3.4.22.70 | M | sortase family | |
| GJNGAHFB_00036 | 3.2e-214 | J | translation release factor activity | |||
| GJNGAHFB_00037 | 7.8e-41 | rpmE2 | J | Ribosomal protein L31 | ||
| GJNGAHFB_00038 | 3e-240 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
| GJNGAHFB_00039 | 3.6e-238 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
| GJNGAHFB_00040 | 2.5e-26 | |||||
| GJNGAHFB_00041 | 6.4e-131 | S | YheO-like PAS domain | |||
| GJNGAHFB_00042 | 7.6e-158 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
| GJNGAHFB_00043 | 3.7e-122 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
| GJNGAHFB_00044 | 3.1e-229 | tdcC | E | amino acid | ||
| GJNGAHFB_00045 | 1e-245 | 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) | |
| GJNGAHFB_00046 | 3.4e-310 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
| GJNGAHFB_00047 | 4e-46 | 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 | ||
| GJNGAHFB_00048 | 3.8e-78 | ywiB | S | Domain of unknown function (DUF1934) | ||
| GJNGAHFB_00049 | 3.3e-155 | lipL | 2.3.1.200, 2.3.1.204 | H | biotin lipoate A B protein ligase | |
| GJNGAHFB_00050 | 9e-264 | ywfO | S | HD domain protein | ||
| GJNGAHFB_00051 | 6.4e-148 | yxeH | S | hydrolase | ||
| GJNGAHFB_00052 | 4.1e-125 | |||||
| GJNGAHFB_00053 | 2.5e-181 | S | DUF218 domain | |||
| GJNGAHFB_00054 | 1.2e-177 | 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) | |
| GJNGAHFB_00055 | 2.2e-151 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
| GJNGAHFB_00056 | 1.2e-207 | 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 | |
| GJNGAHFB_00057 | 8.6e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
| GJNGAHFB_00058 | 2.1e-31 | |||||
| GJNGAHFB_00059 | 6.4e-43 | ankB | S | ankyrin repeats | ||
| GJNGAHFB_00060 | 9.2e-131 | znuB | U | ABC 3 transport family | ||
| GJNGAHFB_00061 | 9.8e-129 | fhuC | 3.6.3.35 | P | ABC transporter | |
| GJNGAHFB_00062 | 5.1e-181 | S | Prolyl oligopeptidase family | |||
| GJNGAHFB_00063 | 3.2e-161 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
| GJNGAHFB_00064 | 3.2e-37 | veg | S | Biofilm formation stimulator VEG | ||
| GJNGAHFB_00065 | 3e-159 | 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 | |
| GJNGAHFB_00066 | 2.3e-96 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
| GJNGAHFB_00067 | 1.5e-146 | tatD | L | hydrolase, TatD family | ||
| GJNGAHFB_00068 | 2.9e-210 | bcr1 | EGP | Major facilitator Superfamily | ||
| GJNGAHFB_00069 | 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 | |
| GJNGAHFB_00070 | 4e-71 | mutT | 3.6.1.55 | F | DNA mismatch repair protein MutT | |
| GJNGAHFB_00071 | 2e-160 | yunF | F | Protein of unknown function DUF72 | ||
| GJNGAHFB_00072 | 3.9e-133 | cobB | K | SIR2 family | ||
| GJNGAHFB_00073 | 3.1e-178 | |||||
| GJNGAHFB_00074 | 6.8e-229 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
| GJNGAHFB_00075 | 8.2e-168 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
| GJNGAHFB_00076 | 3.5e-151 | S | Psort location Cytoplasmic, score | |||
| GJNGAHFB_00077 | 1.1e-206 | |||||
| GJNGAHFB_00078 | 8.1e-191 | dus | J | Catalyzes the synthesis of 5,6-dihydrouridine (D), a modified base found in the D-loop of most tRNAs, via the reduction of the C5-C6 double bond in target uridines | ||
| GJNGAHFB_00079 | 1.2e-132 | K | Helix-turn-helix domain, rpiR family | |||
| GJNGAHFB_00080 | 1e-162 | GK | ROK family | |||
| GJNGAHFB_00081 | 7.3e-296 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
| GJNGAHFB_00082 | 1.3e-249 | chbC | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
| GJNGAHFB_00083 | 2.6e-76 | S | Domain of unknown function (DUF3284) | |||
| GJNGAHFB_00084 | 3.9e-24 | |||||
| GJNGAHFB_00085 | 1.9e-253 | celB | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
| GJNGAHFB_00086 | 9e-130 | K | UbiC transcription regulator-associated domain protein | |||
| GJNGAHFB_00087 | 2.6e-191 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
| GJNGAHFB_00088 | 1e-142 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
| GJNGAHFB_00089 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
| GJNGAHFB_00090 | 1.8e-47 | higA | K | Helix-turn-helix XRE-family like proteins | ||
| GJNGAHFB_00091 | 6.9e-36 | S | RelE-like toxin of type II toxin-antitoxin system HigB | |||
| GJNGAHFB_00092 | 6.7e-114 | S | CAAX protease self-immunity | |||
| GJNGAHFB_00093 | 1.3e-109 | V | CAAX protease self-immunity | |||
| GJNGAHFB_00094 | 4.8e-117 | ypbD | S | CAAX protease self-immunity | ||
| GJNGAHFB_00095 | 1.2e-107 | S | CAAX protease self-immunity | |||
| GJNGAHFB_00096 | 8.9e-243 | mesE | M | Transport protein ComB | ||
| GJNGAHFB_00097 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
| GJNGAHFB_00098 | 6.7e-23 | |||||
| GJNGAHFB_00099 | 6.9e-22 | plnF | ||||
| GJNGAHFB_00100 | 4.8e-129 | S | CAAX protease self-immunity | |||
| GJNGAHFB_00101 | 2.9e-131 | plnD | K | LytTr DNA-binding domain |
Showing 1 to 100 of 2,819 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)