ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
EHOHLJFL_00001 | 3.1e-36 | LV | site-specific DNA-methyltransferase (adenine-specific) activity | |||
EHOHLJFL_00002 | 6.2e-79 | fic | D | Fic/DOC family | ||
EHOHLJFL_00003 | 3.8e-66 | S | Protein of unknown function (DUF1093) | |||
EHOHLJFL_00004 | 5.3e-37 | |||||
EHOHLJFL_00005 | 7.3e-112 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
EHOHLJFL_00006 | 2.9e-87 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
EHOHLJFL_00007 | 3.6e-174 | prmA | J | Ribosomal protein L11 methyltransferase | ||
EHOHLJFL_00008 | 5.9e-132 | 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 | |
EHOHLJFL_00009 | 3.8e-43 | |||||
EHOHLJFL_00010 | 0.0 | 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 | |
EHOHLJFL_00011 | 4.2e-77 | dtd | J | rejects L-amino acids rather than detecting D-amino acids in the active site. By recycling D-aminoacyl-tRNA to D-amino acids and free tRNA molecules, this enzyme counteracts the toxicity associated with the formation of D-aminoacyl-tRNA entities in vivo and helps enforce protein L-homochirality | ||
EHOHLJFL_00012 | 5.9e-117 | 3.1.3.18 | J | HAD-hyrolase-like | ||
EHOHLJFL_00013 | 2e-244 | lytH | 3.5.1.28, 6.1.1.12 | M | N-acetylmuramoyl-L-alanine amidase | |
EHOHLJFL_00014 | 1.8e-83 | FG | adenosine 5'-monophosphoramidase activity | |||
EHOHLJFL_00015 | 1.6e-157 | V | ABC transporter | |||
EHOHLJFL_00016 | 2.4e-273 | |||||
EHOHLJFL_00017 | 1.5e-34 | XK27_04345 | 3.6.1.1 | C | Inorganic pyrophosphatase | |
EHOHLJFL_00018 | 4.4e-244 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
EHOHLJFL_00019 | 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) | |
EHOHLJFL_00020 | 6.4e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
EHOHLJFL_00021 | 7.4e-169 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
EHOHLJFL_00022 | 3.1e-164 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
EHOHLJFL_00023 | 1.2e-154 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
EHOHLJFL_00024 | 2.9e-21 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
EHOHLJFL_00025 | 6.1e-68 | yqeY | S | YqeY-like protein | ||
EHOHLJFL_00027 | 5.9e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
EHOHLJFL_00028 | 2e-82 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
EHOHLJFL_00029 | 3.1e-63 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
EHOHLJFL_00030 | 4e-63 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
EHOHLJFL_00031 | 9.5e-169 | era | S | 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 | ||
EHOHLJFL_00032 | 4.7e-140 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
EHOHLJFL_00033 | 2.5e-52 | |||||
EHOHLJFL_00034 | 2e-41 | |||||
EHOHLJFL_00035 | 2e-171 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
EHOHLJFL_00036 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
EHOHLJFL_00037 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
EHOHLJFL_00038 | 4.7e-190 | 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 | ||
EHOHLJFL_00039 | 2.3e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
EHOHLJFL_00040 | 6e-151 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
EHOHLJFL_00041 | 3.5e-25 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
EHOHLJFL_00042 | 8.2e-60 | yitW | S | Iron-sulfur cluster assembly protein | ||
EHOHLJFL_00043 | 1.3e-142 | |||||
EHOHLJFL_00044 | 1.6e-174 | |||||
EHOHLJFL_00045 | 1.4e-264 | rsmF | 2.1.1.176 | J | NOL1 NOP2 sun family protein | |
EHOHLJFL_00046 | 1.4e-192 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
EHOHLJFL_00047 | 2.3e-179 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
EHOHLJFL_00048 | 4.2e-167 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
EHOHLJFL_00049 | 0.0 | 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. This subunit has 5' - 3' nuclease activity | |
EHOHLJFL_00050 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
EHOHLJFL_00051 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
EHOHLJFL_00052 | 1e-11 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
EHOHLJFL_00053 | 2.7e-85 | ypmB | S | Protein conserved in bacteria | ||
EHOHLJFL_00054 | 1e-218 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
EHOHLJFL_00055 | 1.4e-258 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
EHOHLJFL_00056 | 1.8e-113 | dnaD | L | DnaD domain protein | ||
EHOHLJFL_00057 | 4.3e-113 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
EHOHLJFL_00058 | 4.4e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
EHOHLJFL_00059 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
EHOHLJFL_00060 | 8.8e-121 | 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 | ||
EHOHLJFL_00061 | 1.3e-107 | ypsA | S | Belongs to the UPF0398 family | ||
EHOHLJFL_00062 | 2.3e-66 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
EHOHLJFL_00064 | 2.2e-218 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
EHOHLJFL_00065 | 1.2e-174 | pdxB | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | |
EHOHLJFL_00066 | 3.9e-34 | |||||
EHOHLJFL_00067 | 7.4e-194 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
EHOHLJFL_00068 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
EHOHLJFL_00069 | 1.1e-161 | K | Transcriptional regulator | |||
EHOHLJFL_00070 | 2.4e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
EHOHLJFL_00071 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
EHOHLJFL_00072 | 2e-38 | nrdH | O | Glutaredoxin | ||
EHOHLJFL_00073 | 9.3e-275 | S | Mga helix-turn-helix domain | |||
EHOHLJFL_00074 | 1.8e-48 | |||||
EHOHLJFL_00075 | 2.6e-280 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
EHOHLJFL_00076 | 5.7e-109 | XK27_02070 | S | Nitroreductase family | ||
EHOHLJFL_00077 | 1.3e-69 | rnhA | 3.1.26.4 | L | Ribonuclease HI | |
EHOHLJFL_00078 | 1.3e-45 | S | Family of unknown function (DUF5322) | |||
EHOHLJFL_00079 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
EHOHLJFL_00080 | 4.3e-80 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
EHOHLJFL_00081 | 6.1e-171 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
EHOHLJFL_00082 | 1.7e-96 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
EHOHLJFL_00083 | 2.6e-236 | pyrP | F | Permease | ||
EHOHLJFL_00084 | 1.6e-179 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
EHOHLJFL_00085 | 3.9e-237 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
EHOHLJFL_00086 | 1.3e-209 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
EHOHLJFL_00087 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
EHOHLJFL_00088 | 3.4e-155 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
EHOHLJFL_00089 | 9.4e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
EHOHLJFL_00090 | 8.1e-114 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
EHOHLJFL_00091 | 1.4e-148 | pta | 2.3.1.19, 2.3.1.8 | C | Phosphate acetyl/butaryl transferase | |
EHOHLJFL_00092 | 2.5e-203 | buk | 2.7.2.7 | C | Acetokinase family | |
EHOHLJFL_00093 | 1.2e-258 | lpdA | 1.8.1.4 | C | 3-hydroxyacyl-CoA dehydrogenase, NAD binding domain | |
EHOHLJFL_00094 | 2.5e-186 | bfmBAA | 1.2.4.4 | C | Dehydrogenase E1 component | |
EHOHLJFL_00095 | 1.7e-182 | bfmBAB | 1.2.4.1, 1.2.4.4 | C | Transketolase, pyrimidine binding domain | |
EHOHLJFL_00096 | 2.2e-206 | bfmBB | 2.3.1.168, 2.3.1.61 | C | 2-oxoacid dehydrogenases acyltransferase (catalytic domain) | |
EHOHLJFL_00097 | 2e-177 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
EHOHLJFL_00098 | 3.4e-195 | pfoS | S | Phosphotransferase system, EIIC | ||
EHOHLJFL_00099 | 1.2e-49 | S | MazG-like family | |||
EHOHLJFL_00100 | 0.0 | FbpA | K | Fibronectin-binding protein | ||
EHOHLJFL_00101 | 5.9e-160 | degV | S | EDD domain protein, DegV family | ||
EHOHLJFL_00102 | 1.3e-99 | 3.6.1.13 | L | Belongs to the Nudix hydrolase family |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)