| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| LCADNNJD_00001 | 3.9e-108 | yorS | 3.1.3.5 | S | 5' nucleotidase, deoxy (Pyrimidine), cytosolic type C protein (NT5C) | |
| LCADNNJD_00002 | 1.4e-168 | K | Psort location Cytoplasmic, score | |||
| LCADNNJD_00003 | 2.6e-242 | G | Bacterial extracellular solute-binding protein | |||
| LCADNNJD_00004 | 3.5e-155 | P | Binding-protein-dependent transport system inner membrane component | |||
| LCADNNJD_00005 | 1.5e-141 | P | Binding-protein-dependent transport system inner membrane component | |||
| LCADNNJD_00006 | 0.0 | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family | |
| LCADNNJD_00007 | 2.5e-210 | vbsD | V | MatE | ||
| LCADNNJD_00008 | 1.2e-154 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
| LCADNNJD_00009 | 1.8e-58 | yyaH | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
| LCADNNJD_00010 | 1.9e-83 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
| LCADNNJD_00011 | 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 | ||
| LCADNNJD_00012 | 0.0 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
| LCADNNJD_00013 | 1e-36 | csoR | S | Metal-sensitive transcriptional repressor | ||
| LCADNNJD_00014 | 5.2e-155 | rmuC | S | RmuC family | ||
| LCADNNJD_00015 | 2.1e-110 | pyrE | 2.4.2.10 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
| LCADNNJD_00016 | 4.1e-148 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
| LCADNNJD_00017 | 5.1e-16 | M | domain protein | |||
| LCADNNJD_00018 | 2e-35 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
| LCADNNJD_00019 | 2.3e-287 | gatA | 6.3.5.6, 6.3.5.7 | F | Allows the formation of correctly charged Gln-tRNA(Gln) through the transamidation of misacylated Glu-tRNA(Gln) in organisms which lack glutaminyl-tRNA synthetase. The reaction takes place in the presence of glutamine and ATP through an activated gamma-phospho-Glu-tRNA(Gln) | |
| LCADNNJD_00020 | 1.2e-285 | gatB | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
| LCADNNJD_00021 | 6.4e-152 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
| LCADNNJD_00022 | 1.7e-51 | S | Protein of unknown function (DUF2469) | |||
| LCADNNJD_00023 | 6.4e-293 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
| LCADNNJD_00024 | 2.1e-269 | 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 | ||
| LCADNNJD_00025 | 3.1e-63 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
| LCADNNJD_00026 | 1.4e-268 | S | domain protein | |||
| LCADNNJD_00027 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
| LCADNNJD_00028 | 4e-223 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
| LCADNNJD_00030 | 4.2e-124 | 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 | |
| LCADNNJD_00031 | 9.3e-130 | KT | Transcriptional regulatory protein, C terminal | |||
| LCADNNJD_00032 | 5.6e-98 | |||||
| LCADNNJD_00033 | 5.3e-96 | mntP | P | Probably functions as a manganese efflux pump | ||
| LCADNNJD_00034 | 8.9e-92 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
| LCADNNJD_00035 | 0.0 | glgE | 2.4.99.16 | GH13 | G | Maltosyltransferase that uses maltose 1-phosphate (M1P) as the sugar donor to elongate linear or branched alpha-(1- 4)- glucans. Is involved in a branched alpha-glucan biosynthetic pathway from trehalose, together with TreS, Mak and GlgB |
| LCADNNJD_00036 | 2e-175 | ansA | 3.5.1.1 | EJ | Asparaginase | |
| LCADNNJD_00037 | 1.7e-261 | E | aromatic amino acid transport protein AroP K03293 | |||
| LCADNNJD_00040 | 3.4e-208 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
| LCADNNJD_00041 | 2.2e-140 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
| LCADNNJD_00042 | 5e-29 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
| LCADNNJD_00043 | 1e-45 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
| LCADNNJD_00044 | 7.7e-141 | atpH | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
| LCADNNJD_00045 | 1.1e-303 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
| LCADNNJD_00046 | 2.1e-155 | atpG | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The gamma chain is believed to be important in regulating ATPase activity and the flow of protons through the CF(0) complex | ||
| LCADNNJD_00047 | 7.5e-280 | atpD | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The catalytic sites are hosted primarily by the beta subunits | |
| LCADNNJD_00048 | 1.5e-44 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
| LCADNNJD_00049 | 2.5e-128 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
| LCADNNJD_00050 | 6.5e-138 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
| LCADNNJD_00051 | 5.8e-116 | |||||
| LCADNNJD_00052 | 2.4e-160 | |||||
| LCADNNJD_00053 | 8.4e-139 | trxA2 | O | Tetratricopeptide repeat | ||
| LCADNNJD_00056 | 0.0 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
| LCADNNJD_00057 | 2.8e-61 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
| LCADNNJD_00058 | 1.6e-237 | mmuP | E | amino acid | ||
| LCADNNJD_00059 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
| LCADNNJD_00060 | 2.5e-284 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
| LCADNNJD_00061 | 3.8e-235 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
| LCADNNJD_00062 | 3.6e-169 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
| LCADNNJD_00063 | 3e-260 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
| LCADNNJD_00064 | 2e-156 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
| LCADNNJD_00065 | 1.3e-210 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
| LCADNNJD_00066 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
| LCADNNJD_00067 | 1.1e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
| LCADNNJD_00068 | 4.4e-39 | rpmA | J | Ribosomal L27 protein | ||
| LCADNNJD_00069 | 2.9e-275 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
| LCADNNJD_00070 | 4.7e-197 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
| LCADNNJD_00071 | 8.7e-226 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
| LCADNNJD_00073 | 4.8e-29 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
| LCADNNJD_00074 | 1.5e-118 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
| LCADNNJD_00075 | 2e-71 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
| LCADNNJD_00076 | 1.4e-122 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
| LCADNNJD_00078 | 2.1e-124 | QT | PucR C-terminal helix-turn-helix domain | |||
| LCADNNJD_00079 | 2.8e-307 | |||||
| LCADNNJD_00080 | 2.1e-136 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
| LCADNNJD_00081 | 1.3e-84 | bioY | S | BioY family | ||
| LCADNNJD_00082 | 0.0 | accA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Carbamoyl-phosphate synthase L chain, ATP binding domain protein | |
| LCADNNJD_00083 | 4.5e-286 | pccB | I | Carboxyl transferase domain | ||
| LCADNNJD_00084 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
| LCADNNJD_00085 | 3.6e-146 | S | CAAX protease self-immunity | |||
| LCADNNJD_00086 | 5.8e-50 | acpS | 2.7.8.7, 3.2.1.52 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
| LCADNNJD_00087 | 0.0 | ams | 2.4.1.4, 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha amylase, catalytic domain |
| LCADNNJD_00089 | 3.3e-97 | |||||
| LCADNNJD_00090 | 1.9e-40 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
| LCADNNJD_00091 | 0.0 | pnp | 2.7.7.8 | J | Involved in mRNA degradation. Catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3'- to 5'-direction | |
| LCADNNJD_00093 | 2.2e-86 | lemA | S | LemA family | ||
| LCADNNJD_00094 | 7.1e-234 | S | Predicted membrane protein (DUF2207) | |||
| LCADNNJD_00095 | 7.1e-28 | S | Predicted membrane protein (DUF2207) | |||
| LCADNNJD_00096 | 2e-171 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
| LCADNNJD_00097 | 2.4e-268 | yegQ | O | Peptidase family U32 C-terminal domain | ||
| LCADNNJD_00098 | 6.8e-176 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
| LCADNNJD_00099 | 1.3e-125 | ispD | 1.1.1.405, 2.7.7.40, 2.7.7.60, 4.6.1.12 | I | Catalyzes the formation of 4-diphosphocytidyl-2-C- methyl-D-erythritol from CTP and 2-C-methyl-D-erythritol 4- phosphate (MEP) | |
| LCADNNJD_00100 | 1.7e-112 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
| LCADNNJD_00101 | 8.8e-28 | D | nuclear chromosome segregation | |||
| LCADNNJD_00102 | 3.1e-256 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
| LCADNNJD_00103 | 5.5e-214 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
| LCADNNJD_00104 | 1e-224 | aroG | 2.5.1.54 | E | Stereospecific condensation of phosphoenolpyruvate (PEP) and D-erythrose-4-phosphate (E4P) giving rise to 3-deoxy-D- arabino-heptulosonate-7-phosphate (DAHP) | |
| LCADNNJD_00105 | 5.5e-116 | 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 | |
| LCADNNJD_00106 | 2.8e-162 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
| LCADNNJD_00107 | 9.5e-124 | KT | Transcriptional regulatory protein, C terminal | |||
| LCADNNJD_00108 | 3.8e-191 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
| LCADNNJD_00109 | 6.1e-150 | pstC | P | probably responsible for the translocation of the substrate across the membrane |
Showing 1 to 100 of 1,536 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)