| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| NOJDNIFM_00002 | 1.3e-67 | IQ | KR domain | |||
| NOJDNIFM_00003 | 1.3e-70 | S | membrane transporter protein | |||
| NOJDNIFM_00004 | 8.7e-35 | yobS | K | transcriptional regulator | ||
| NOJDNIFM_00005 | 2.2e-120 | Q | Methyltransferase domain | |||
| NOJDNIFM_00006 | 2.4e-129 | |||||
| NOJDNIFM_00007 | 1.8e-198 | xerS | L | Belongs to the 'phage' integrase family | ||
| NOJDNIFM_00008 | 6.7e-67 | 3.6.1.55 | F | NUDIX domain | ||
| NOJDNIFM_00009 | 1.4e-98 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
| NOJDNIFM_00010 | 1.3e-81 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
| NOJDNIFM_00011 | 1.6e-100 | zmp1 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
| NOJDNIFM_00012 | 6.4e-168 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
| NOJDNIFM_00013 | 1.4e-181 | K | Transcriptional regulator | |||
| NOJDNIFM_00014 | 0.0 | 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 | |
| NOJDNIFM_00015 | 0.0 | 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 | |
| NOJDNIFM_00016 | 3.2e-99 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
| NOJDNIFM_00017 | 1.7e-167 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
| NOJDNIFM_00018 | 8.9e-262 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
| NOJDNIFM_00019 | 1.8e-93 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
| NOJDNIFM_00020 | 2.9e-176 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
| NOJDNIFM_00021 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
| NOJDNIFM_00022 | 3.5e-163 | dprA | LU | DNA protecting protein DprA | ||
| NOJDNIFM_00023 | 1.6e-135 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
| NOJDNIFM_00024 | 3.6e-157 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
| NOJDNIFM_00027 | 8.2e-120 | |||||
| NOJDNIFM_00028 | 2.9e-136 | K | sugar-binding domain protein | |||
| NOJDNIFM_00029 | 1.8e-265 | 2.7.1.17 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
| NOJDNIFM_00030 | 7.4e-178 | S | Domain of unknown function (DUF4432) | |||
| NOJDNIFM_00031 | 3.5e-239 | fucP | G | Major Facilitator Superfamily | ||
| NOJDNIFM_00032 | 5.8e-35 | yozE | S | Belongs to the UPF0346 family | ||
| NOJDNIFM_00033 | 6.5e-105 | ypmS | S | Uncharacterized protein conserved in bacteria (DUF2140) | ||
| NOJDNIFM_00034 | 1.2e-161 | ypmR | E | GDSL-like Lipase/Acylhydrolase | ||
| NOJDNIFM_00035 | 3e-148 | DegV | S | EDD domain protein, DegV family | ||
| NOJDNIFM_00036 | 2.8e-114 | hlyIII | S | protein, hemolysin III | ||
| NOJDNIFM_00037 | 4.3e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
| NOJDNIFM_00038 | 9e-186 | 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 | |
| NOJDNIFM_00039 | 0.0 | yfmR | S | ABC transporter, ATP-binding protein | ||
| NOJDNIFM_00040 | 1.9e-220 | 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 | |
| NOJDNIFM_00041 | 1.3e-171 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
| NOJDNIFM_00042 | 5.3e-234 | S | Tetratricopeptide repeat protein | |||
| NOJDNIFM_00043 | 1.5e-40 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
| NOJDNIFM_00044 | 6.7e-248 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
| NOJDNIFM_00045 | 3.2e-210 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
| NOJDNIFM_00046 | 6.4e-117 | 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 | |
| NOJDNIFM_00047 | 8e-26 | M | Lysin motif | |||
| NOJDNIFM_00048 | 8.3e-252 | recQ1 | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
| NOJDNIFM_00049 | 3.3e-181 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
| NOJDNIFM_00050 | 3.2e-93 | U | Mediates riboflavin uptake, may also transport FMN and roseoflavin. Probably a riboflavin-binding protein that interacts with the 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. The substrates themselves are bound by transmembrane, not extracytoplasmic soluble proteins | |||
| NOJDNIFM_00051 | 2.7e-129 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
| NOJDNIFM_00052 | 8.8e-102 | 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 | ||
| NOJDNIFM_00053 | 1.2e-130 | 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 | ||
| NOJDNIFM_00054 | 3.1e-71 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
| NOJDNIFM_00055 | 2.2e-165 | xerD | D | recombinase XerD | ||
| NOJDNIFM_00056 | 6e-168 | cvfB | S | S1 domain | ||
| NOJDNIFM_00057 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
| NOJDNIFM_00058 | 1.8e-125 | tal | 2.2.1.2 | H | Transaldolase/Fructose-6-phosphate aldolase | |
| NOJDNIFM_00059 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
| NOJDNIFM_00060 | 0.0 | clpB | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
| NOJDNIFM_00061 | 6.2e-235 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
| NOJDNIFM_00062 | 3.1e-155 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
| NOJDNIFM_00063 | 8.7e-125 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
| NOJDNIFM_00064 | 0.0 | ydgH | S | MMPL family | ||
| NOJDNIFM_00065 | 3e-87 | K | Transcriptional regulator | |||
| NOJDNIFM_00066 | 4.6e-197 | 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 | ||
| NOJDNIFM_00067 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
| NOJDNIFM_00068 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
| NOJDNIFM_00069 | 1.5e-177 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
| NOJDNIFM_00070 | 3.3e-149 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
| NOJDNIFM_00071 | 1.5e-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 | ||
| NOJDNIFM_00072 | 1.7e-61 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
| NOJDNIFM_00073 | 8.5e-79 | 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 | |
| NOJDNIFM_00074 | 1.6e-180 | phoH | T | phosphate starvation-inducible protein PhoH | ||
| NOJDNIFM_00075 | 7e-72 | yqeY | S | YqeY-like protein | ||
| NOJDNIFM_00076 | 2.4e-65 | hxlR | K | Transcriptional regulator, HxlR family | ||
| NOJDNIFM_00077 | 5.5e-189 | qor | 1.1.1.1, 1.6.5.5 | C | Belongs to the zinc-containing alcohol dehydrogenase family. Quinone oxidoreductase subfamily | |
| NOJDNIFM_00078 | 1.3e-22 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
| NOJDNIFM_00079 | 4.8e-151 | 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 | |
| NOJDNIFM_00080 | 4.7e-171 | 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 | |
| NOJDNIFM_00081 | 5.7e-241 | tagF1 | 2.7.8.12, 2.7.8.45 | M | glycerophosphotransferase | |
| NOJDNIFM_00082 | 8e-151 | tagG | U | Transport permease protein | ||
| NOJDNIFM_00083 | 7.2e-188 | tagB | 2.7.8.14, 2.7.8.44, 2.7.8.47 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |
| NOJDNIFM_00084 | 3.8e-162 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
| NOJDNIFM_00085 | 2.8e-96 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
| NOJDNIFM_00086 | 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) | |
| NOJDNIFM_00087 | 8.7e-248 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
| NOJDNIFM_00088 | 2.4e-95 | |||||
| NOJDNIFM_00089 | 3e-156 | lytH | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | |
| NOJDNIFM_00090 | 5.2e-164 | yniA | G | Fructosamine kinase | ||
| NOJDNIFM_00091 | 2.1e-114 | 3.1.3.18 | S | HAD-hyrolase-like | ||
| NOJDNIFM_00092 | 1.1e-74 | 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 | ||
| NOJDNIFM_00093 | 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 | |
| NOJDNIFM_00094 | 1.8e-59 | |||||
| NOJDNIFM_00095 | 7e-133 | 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 | |
| NOJDNIFM_00096 | 9.1e-178 | prmA | J | Ribosomal protein L11 methyltransferase | ||
| NOJDNIFM_00097 | 1.2e-54 | |||||
| NOJDNIFM_00098 | 1.3e-26 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
| NOJDNIFM_00099 | 5.3e-62 | |||||
| NOJDNIFM_00101 | 7.5e-13 | |||||
| NOJDNIFM_00102 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
| NOJDNIFM_00103 | 4.3e-36 | ykuJ | S | Protein of unknown function (DUF1797) | ||
| NOJDNIFM_00104 | 4.1e-184 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms |
Showing 1 to 100 of 2,469 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)