| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| EIFNAJPL_00001 | 3.4e-39 | S | COG NOG14552 non supervised orthologous group | |||
| EIFNAJPL_00002 | 2.8e-63 | L | Replication protein | |||
| EIFNAJPL_00003 | 1.6e-76 | L | Molecular Function DNA binding, Biological Process DNA recombination | |||
| EIFNAJPL_00004 | 2.7e-137 | nfrA | 1.5.1.38, 1.5.1.39 | C | Oxidoreductase | |
| EIFNAJPL_00005 | 9.8e-214 | rodA | D | Belongs to the SEDS family | ||
| EIFNAJPL_00006 | 1e-82 | ysnE | K | acetyltransferase | ||
| EIFNAJPL_00007 | 1e-38 | ywcE | S | Required for proper spore morphogenesis. Important for spore germination | ||
| EIFNAJPL_00008 | 2e-64 | qoxD | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
| EIFNAJPL_00009 | 8.1e-111 | qoxC | 1.10.3.12, 1.9.3.1 | C | quinol oxidase, subunit | |
| EIFNAJPL_00010 | 0.0 | qoxB | 1.10.3.12, 1.9.3.1 | C | Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1- 3 form the functional core of the enzyme complex. CO I is the catalytic subunit of the enzyme. Electrons originating in cytochrome c are transferred via the copper A center of subunit 2 and heme A of subunit 1 to the bimetallic center formed by heme A3 and copper B | |
| EIFNAJPL_00011 | 8.3e-179 | cyoA | 1.10.3.10, 1.10.3.12 | C | Catalyzes quinol oxidation with the concomitant reduction of oxygen to water. Subunit II transfers the electrons from a quinol to the binuclear center of the catalytic subunit I | |
| EIFNAJPL_00012 | 8.4e-27 | ywzA | S | membrane | ||
| EIFNAJPL_00013 | 4.3e-302 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
| EIFNAJPL_00014 | 5.7e-230 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
| EIFNAJPL_00015 | 1.9e-63 | gtcA | S | GtrA-like protein | ||
| EIFNAJPL_00016 | 8.7e-113 | ywcC | K | Bacterial regulatory proteins, tetR family | ||
| EIFNAJPL_00018 | 1.9e-129 | H | Methionine biosynthesis protein MetW | |||
| EIFNAJPL_00019 | 2.6e-134 | S | Streptomycin biosynthesis protein StrF | |||
| EIFNAJPL_00020 | 5.5e-112 | ywbO | Q | dithiol-disulfide isomerase involved in polyketide biosynthesis | ||
| EIFNAJPL_00021 | 1.1e-244 | ywbN | P | Dyp-type peroxidase family protein | ||
| EIFNAJPL_00022 | 9.1e-116 | thiE | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Condenses 4-methyl-5-(beta-hydroxyethyl)thiazole monophosphate (THZ-P) and 2-methyl-4-amino-5-hydroxymethyl pyrimidine pyrophosphate (HMP-PP) to form thiamine monophosphate (TMP) | |
| EIFNAJPL_00023 | 6e-138 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
| EIFNAJPL_00024 | 8.2e-152 | ywbI | K | Transcriptional regulator | ||
| EIFNAJPL_00025 | 2.5e-57 | ywbH | S | Increases the activity of extracellular murein hydrolases possibly by mediating their export via hole formation. Inhibited by the antiholin-like proteins LrgAB. In an unstressed cell, the LrgAB products probably inhibit the function of the CidA protein. When a cell is stressed by the addition of antibiotics or by other factors in the environment, CidA possibly oligomerizes within the bacterial cell membrane, creating lesions that disrupt the proton motive force, which in turn results in loss of cell viability. These lesions are also hypothesized to regulate the subsequent cell lysis by either allowing the murein hydrolases access to the cell wall substrate and or regulating their activity by a | ||
| EIFNAJPL_00026 | 1.5e-110 | ywbG | M | effector of murein hydrolase | ||
| EIFNAJPL_00027 | 1.8e-27 | ywbE | S | Uncharacterized conserved protein (DUF2196) | ||
| EIFNAJPL_00028 | 2.2e-142 | mta | K | transcriptional | ||
| EIFNAJPL_00029 | 1.2e-171 | yjfC | O | Predicted Zn-dependent protease (DUF2268) | ||
| EIFNAJPL_00030 | 5.5e-225 | ywbD | 2.1.1.191 | J | Methyltransferase | |
| EIFNAJPL_00031 | 9e-68 | ywbC | 4.4.1.5 | E | glyoxalase | |
| EIFNAJPL_00032 | 2.4e-245 | celB | 2.7.1.207 | 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 | |
| EIFNAJPL_00033 | 7e-269 | epr | 3.4.21.62 | O | Belongs to the peptidase S8 family | |
| EIFNAJPL_00034 | 5.2e-164 | gspA | M | General stress | ||
| EIFNAJPL_00035 | 7.8e-117 | ywaC | 2.7.6.5 | S | protein conserved in bacteria | |
| EIFNAJPL_00036 | 1.3e-168 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
| EIFNAJPL_00037 | 6.1e-12 | S | D-Ala-teichoic acid biosynthesis protein | |||
| EIFNAJPL_00038 | 4.2e-294 | 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 | |
| EIFNAJPL_00039 | 3.7e-229 | dltB | M | membrane protein involved in D-alanine export | ||
| EIFNAJPL_00040 | 1.5e-36 | 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 | |
| EIFNAJPL_00041 | 3.7e-229 | dltD | M | COG3966 Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
| EIFNAJPL_00042 | 4e-206 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
| EIFNAJPL_00043 | 9.2e-253 | licH | 3.2.1.86 | GT4 | G | COG1486 Alpha-galactosidases 6-phospho-beta-glucosidases, family 4 of glycosyl hydrolases |
| EIFNAJPL_00044 | 7.8e-52 | licA | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
| EIFNAJPL_00045 | 2.6e-250 | licC | 2.7.1.207 | 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 | |
| EIFNAJPL_00046 | 1.2e-49 | licB | 2.7.1.196, 2.7.1.205 | G | transporter subunit IIB | |
| EIFNAJPL_00047 | 0.0 | licR | 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
| EIFNAJPL_00048 | 1.1e-112 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
| EIFNAJPL_00049 | 4.3e-173 | fhuB3 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
| EIFNAJPL_00050 | 6.1e-180 | fhuG1 | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
| EIFNAJPL_00051 | 3e-167 | cbrA3 | P | Periplasmic binding protein | ||
| EIFNAJPL_00052 | 3.7e-60 | arsR | K | transcriptional | ||
| EIFNAJPL_00053 | 1.4e-229 | arsB | P | Involved in arsenical resistance. Thought to form the channel of an arsenite pump | ||
| EIFNAJPL_00054 | 6.9e-50 | ydhM | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
| EIFNAJPL_00055 | 1.4e-50 | ydhN3 | 2.7.1.196, 2.7.1.205 | G | phosphotransferase system | |
| EIFNAJPL_00056 | 3.7e-230 | celB | 2.7.1.207 | 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 | |
| EIFNAJPL_00057 | 7.1e-288 | ydhP | 3.2.1.21, 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
| EIFNAJPL_00058 | 4.2e-169 | gmuE | 2.7.1.2, 2.7.1.4 | GK | COG1940 Transcriptional regulator sugar kinase | |
| EIFNAJPL_00059 | 8.4e-192 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
| EIFNAJPL_00060 | 4.4e-213 | gmuG | 3.2.1.78 | GH26 | G | Belongs to the glycosyl hydrolase 26 family |
| EIFNAJPL_00061 | 0.0 | katX | 1.11.1.6 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
| EIFNAJPL_00062 | 6.5e-195 | yxeI | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
| EIFNAJPL_00063 | 4.2e-253 | yxlA | F | Belongs to the purine-cytosine permease (2.A.39) family | ||
| EIFNAJPL_00064 | 7e-158 | nnrD | 4.2.1.136, 5.1.99.6 | G | Bifunctional enzyme that catalyzes the epimerization of the S- and R-forms of NAD(P)HX and the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. This allows the repair of both epimers of NAD(P)HX, a damaged form of NAD(P)H that is a result of enzymatic or heat-dependent hydration | |
| EIFNAJPL_00065 | 2.2e-294 | cydD | V | ATP-binding protein | ||
| EIFNAJPL_00066 | 0.0 | cydD | V | ATP-binding | ||
| EIFNAJPL_00067 | 4.2e-189 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase, subunit II | |
| EIFNAJPL_00068 | 1.4e-267 | cydA | 1.10.3.14 | C | oxidase, subunit | |
| EIFNAJPL_00069 | 1.5e-215 | cimH | C | COG3493 Na citrate symporter | ||
| EIFNAJPL_00070 | 7.1e-158 | yxkH | G | Polysaccharide deacetylase | ||
| EIFNAJPL_00071 | 2.4e-206 | msmK | P | Belongs to the ABC transporter superfamily | ||
| EIFNAJPL_00072 | 6.5e-170 | lrp | QT | PucR C-terminal helix-turn-helix domain | ||
| EIFNAJPL_00073 | 6.4e-143 | yxkD | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
| EIFNAJPL_00074 | 3.8e-87 | yxkC | S | Domain of unknown function (DUF4352) | ||
| EIFNAJPL_00075 | 2.1e-196 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
| EIFNAJPL_00076 | 6.5e-237 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
| EIFNAJPL_00079 | 1.8e-86 | yxjI | S | LURP-one-related | ||
| EIFNAJPL_00080 | 1.5e-219 | yxjG | 2.1.1.14 | E | Methionine synthase | |
| EIFNAJPL_00081 | 5.6e-166 | rlmA | 2.1.1.187 | Q | Methyltransferase domain | |
| EIFNAJPL_00082 | 3.5e-211 | nupG | F | Belongs to the concentrative nucleoside transporter (CNT) (TC 2.A.41) family | ||
| EIFNAJPL_00083 | 2.7e-75 | T | Domain of unknown function (DUF4163) | |||
| EIFNAJPL_00084 | 1.6e-51 | yxiS | ||||
| EIFNAJPL_00085 | 0.0 | katE | 1.11.1.6, 3.5.1.124 | P | serves to protect cells from the toxic effects of hydrogen peroxide | |
| EIFNAJPL_00086 | 5.6e-223 | citH | C | Citrate transporter | ||
| EIFNAJPL_00087 | 5e-144 | exoK | GH16 | M | licheninase activity | |
| EIFNAJPL_00088 | 1.8e-150 | licT | K | transcriptional antiterminator | ||
| EIFNAJPL_00089 | 2.9e-224 | yxiO | S | COG2270 Permeases of the major facilitator superfamily | ||
| EIFNAJPL_00090 | 1.6e-263 | dbpA | 3.6.4.13 | JKL | DEAD-box RNA helicase involved in the assembly of the 50S ribosomal subunit. Has an RNA-dependent ATPase activity, which is specific for 23S rRNA, and a 3' to 5' RNA helicase activity that uses the energy of ATP hydrolysis to destabilize and unwind short rRNA duplexes | |
| EIFNAJPL_00093 | 2.9e-63 | S | SMI1-KNR4 cell-wall | |||
| EIFNAJPL_00094 | 9.1e-91 | yxiI | S | Protein of unknown function (DUF2716) | ||
| EIFNAJPL_00096 | 3.1e-74 | yxiG | ||||
| EIFNAJPL_00097 | 7.1e-71 | yxxG | ||||
| EIFNAJPL_00099 | 3.7e-204 | pelB | 4.2.2.10, 4.2.2.2 | G | Pectate lyase | |
| EIFNAJPL_00100 | 3.2e-148 | yxxF | EG | EamA-like transporter family | ||
| EIFNAJPL_00101 | 9.8e-74 | yxiE | T | Belongs to the universal stress protein A family | ||
| EIFNAJPL_00102 | 6.4e-281 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
| EIFNAJPL_00103 | 0.0 | bglF | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
| EIFNAJPL_00104 | 0.0 | L | HKD family nuclease | |||
| EIFNAJPL_00105 | 6.5e-66 | nudG | 3.6.1.55, 3.6.1.65 | L | COG0494 NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
| EIFNAJPL_00106 | 1.5e-282 | yxiA | 3.2.1.99 | GH43 | G | Belongs to the glycosyl hydrolase 43 family |
| EIFNAJPL_00107 | 7.7e-79 | hutP | K | Antiterminator that binds to cis-acting regulatory sequences on the mRNA in the presence of histidine, thereby suppressing transcription termination and activating the hut operon for histidine utilization |
Showing 1 to 100 of 3,564 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)