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 | ||
LCADNNJD_00110 | 8.8e-163 | pstA | P | Phosphate transport system permease | ||
LCADNNJD_00111 | 4.7e-148 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
LCADNNJD_00112 | 7.2e-61 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LCADNNJD_00113 | 2e-205 | pbuO | S | Permease family | ||
LCADNNJD_00114 | 1.4e-77 | 3.4.22.70 | M | Sortase family | ||
LCADNNJD_00115 | 1.1e-87 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LCADNNJD_00116 | 3.2e-33 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LCADNNJD_00117 | 8.5e-80 | T | Forkhead associated domain | |||
LCADNNJD_00118 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
LCADNNJD_00119 | 2.9e-25 | |||||
LCADNNJD_00120 | 5.5e-34 | flgA | NO | SAF | ||
LCADNNJD_00121 | 1.7e-27 | fmdB | S | Putative regulatory protein | ||
LCADNNJD_00122 | 2.5e-59 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LCADNNJD_00123 | 5.9e-78 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
LCADNNJD_00124 | 3.6e-77 | |||||
LCADNNJD_00125 | 1.3e-45 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LCADNNJD_00126 | 3.7e-142 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
LCADNNJD_00127 | 0.0 | E | Transglutaminase-like superfamily | |||
LCADNNJD_00128 | 3e-162 | pat | 2.6.1.9 | E | Aminotransferase class I and II | |
LCADNNJD_00132 | 1.9e-25 | rpmG | J | Ribosomal protein L33 | ||
LCADNNJD_00133 | 1.5e-172 | murB | 1.3.1.98 | M | Cell wall formation | |
LCADNNJD_00134 | 1.6e-254 | E | aromatic amino acid transport protein AroP K03293 | |||
LCADNNJD_00135 | 8.5e-59 | fdxA | C | 4Fe-4S binding domain | ||
LCADNNJD_00136 | 2e-198 | dapC | E | Aminotransferase class I and II | ||
LCADNNJD_00137 | 3.1e-216 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
LCADNNJD_00142 | 7.2e-86 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
LCADNNJD_00143 | 2.1e-78 | |||||
LCADNNJD_00144 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
LCADNNJD_00145 | 2.4e-75 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
LCADNNJD_00146 | 5.3e-81 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LCADNNJD_00147 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LCADNNJD_00148 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LCADNNJD_00149 | 6.2e-49 | K | Bacterial regulatory proteins, tetR family | |||
LCADNNJD_00150 | 2.6e-157 | lipA | I | Hydrolase, alpha beta domain protein | ||
LCADNNJD_00151 | 2.3e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LCADNNJD_00152 | 9.7e-115 | rplC | J | One of the primary rRNA binding proteins, it binds directly near the 3'-end of the 23S rRNA, where it nucleates assembly of the 50S subunit | ||
LCADNNJD_00153 | 2.9e-114 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LCADNNJD_00154 | 4.4e-46 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
LCADNNJD_00155 | 2.3e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
LCADNNJD_00156 | 1.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LCADNNJD_00157 | 3.3e-56 | rplV | J | The globular domain of the protein is located near the polypeptide exit tunnel on the outside of the subunit, while an extended beta-hairpin is found that lines the wall of the exit tunnel in the center of the 70S ribosome | ||
LCADNNJD_00158 | 1.3e-95 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LCADNNJD_00159 | 6.8e-77 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LCADNNJD_00160 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LCADNNJD_00161 | 1e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LCADNNJD_00162 | 2.5e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LCADNNJD_00163 | 3.7e-49 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LCADNNJD_00164 | 7.8e-100 | rplE | J | This is 1 of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance. In the 70S ribosome it contacts protein S13 of the 30S subunit (bridge B1b), connecting the 2 subunits | ||
LCADNNJD_00165 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
LCADNNJD_00166 | 4.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
LCADNNJD_00167 | 8.7e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
LCADNNJD_00168 | 7.7e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
LCADNNJD_00169 | 1e-96 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LCADNNJD_00170 | 4.2e-23 | rpmD | J | Ribosomal protein L30p/L7e | ||
LCADNNJD_00171 | 4.4e-69 | rplO | J | binds to the 23S rRNA | ||
LCADNNJD_00172 | 4.3e-242 | secY | U | The central subunit of the protein translocation channel SecYEG. Consists of two halves formed by TMs 1-5 and 6-10. These two domains form a lateral gate at the front which open onto the bilayer between TMs 2 and 7, and are clamped together by SecE at the back. The channel is closed by both a pore ring composed of hydrophobic SecY resides and a short helix (helix 2A) on the extracellular side of the membrane which forms a plug. The plug probably moves laterally to allow the channel to open. The ring and the pore may move independently | ||
LCADNNJD_00173 | 1.6e-94 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
LCADNNJD_00174 | 1.6e-32 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
LCADNNJD_00175 | 6.5e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LCADNNJD_00176 | 1.2e-61 | rpsM | J | Located at the top of the head of the 30S subunit, it contacts several helices of the 16S rRNA. In the 70S ribosome it contacts the 23S rRNA (bridge B1a) and protein L5 of the 50S subunit (bridge B1b), connecting the 2 subunits | ||
LCADNNJD_00177 | 1.5e-65 | rpsK | J | Located on the platform of the 30S subunit, it bridges several disparate RNA helices of the 16S rRNA. Forms part of the Shine-Dalgarno cleft in the 70S ribosome | ||
LCADNNJD_00178 | 2e-183 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LCADNNJD_00179 | 3.4e-59 | rplQ | J | Ribosomal protein L17 | ||
LCADNNJD_00180 | 4.4e-135 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LCADNNJD_00182 | 1.5e-81 | |||||
LCADNNJD_00183 | 3e-182 | nusA | K | Participates in both transcription termination and antitermination | ||
LCADNNJD_00184 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
LCADNNJD_00185 | 2.1e-73 | rbfA | J | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Associates with free 30S ribosomal subunits (but not with 30S subunits that are part of 70S ribosomes or polysomes). Required for efficient processing of 16S rRNA. May interact with the 5'-terminal helix region of 16S rRNA | ||
LCADNNJD_00186 | 5.8e-159 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
LCADNNJD_00187 | 1.2e-204 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
LCADNNJD_00188 | 5.1e-257 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
LCADNNJD_00189 | 7.7e-80 | |||||
LCADNNJD_00191 | 1.3e-235 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LCADNNJD_00192 | 5.9e-126 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LCADNNJD_00193 | 3.3e-120 | tcyL | E | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00194 | 9.1e-150 | tcyK | ET | Bacterial periplasmic substrate-binding proteins | ||
LCADNNJD_00195 | 5.6e-116 | tcyM | E | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00196 | 1.9e-130 | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | ||
LCADNNJD_00197 | 2.5e-239 | EK | Alanine-glyoxylate amino-transferase | |||
LCADNNJD_00198 | 5.4e-178 | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | ||
LCADNNJD_00199 | 3.3e-141 | tcyN | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
LCADNNJD_00200 | 1e-216 | EGP | Major facilitator Superfamily | |||
LCADNNJD_00201 | 1.4e-44 | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | ||
LCADNNJD_00202 | 6.3e-146 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LCADNNJD_00203 | 1.2e-197 | adhB | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | |
LCADNNJD_00204 | 1.4e-72 | K | helix_turn_helix, mercury resistance | |||
LCADNNJD_00205 | 3.6e-21 | |||||
LCADNNJD_00206 | 2.4e-179 | S | Choline/ethanolamine kinase | |||
LCADNNJD_00207 | 1.2e-245 | eat | E | Amino acid permease | ||
LCADNNJD_00208 | 1e-246 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
LCADNNJD_00209 | 6.8e-78 | yidP | K | UTRA | ||
LCADNNJD_00210 | 9.1e-306 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
LCADNNJD_00211 | 0.0 | crr | G | pts system, glucose-specific IIABC component | ||
LCADNNJD_00212 | 7.2e-137 | arbG | K | CAT RNA binding domain | ||
LCADNNJD_00213 | 1.1e-171 | I | Diacylglycerol kinase catalytic domain | |||
LCADNNJD_00214 | 3e-240 | 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) | |
LCADNNJD_00216 | 1.3e-104 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LCADNNJD_00217 | 1.2e-110 | degU | K | helix_turn_helix, Lux Regulon | ||
LCADNNJD_00218 | 9e-189 | tcsS3 | KT | PspC domain | ||
LCADNNJD_00219 | 8.8e-170 | pspC | KT | PspC domain | ||
LCADNNJD_00221 | 5.8e-236 | S | alpha beta | |||
LCADNNJD_00222 | 1.9e-98 | S | Protein of unknown function (DUF4125) | |||
LCADNNJD_00223 | 5.1e-15 | S | Domain of unknown function (DUF4037) | |||
LCADNNJD_00224 | 9.3e-298 | S | Domain of unknown function (DUF4037) | |||
LCADNNJD_00227 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LCADNNJD_00228 | 2.4e-114 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
LCADNNJD_00229 | 3.5e-137 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LCADNNJD_00230 | 7.1e-108 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LCADNNJD_00231 | 1.3e-150 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LCADNNJD_00232 | 7.9e-36 | |||||
LCADNNJD_00233 | 1.8e-214 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | Phosphomannose isomerase type I | |
LCADNNJD_00234 | 5.1e-196 | serC | 2.6.1.52 | E | Catalyzes the reversible conversion of 3- phosphohydroxypyruvate to phosphoserine and of 3-hydroxy-2-oxo-4- phosphonooxybutanoate to phosphohydroxythreonine | |
LCADNNJD_00235 | 3.4e-92 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LCADNNJD_00236 | 6.5e-78 | M | NlpC/P60 family | |||
LCADNNJD_00237 | 2.2e-185 | T | Universal stress protein family | |||
LCADNNJD_00238 | 1.5e-68 | attW | O | OsmC-like protein | ||
LCADNNJD_00239 | 7.1e-161 | 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 | |
LCADNNJD_00240 | 2.2e-125 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
LCADNNJD_00241 | 9.2e-95 | ptpA | 3.1.3.48 | T | low molecular weight | |
LCADNNJD_00243 | 7e-139 | trmB | 2.1.1.297, 2.1.1.33, 2.4.99.12, 2.4.99.13, 2.4.99.14, 2.4.99.15 | GT30 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA |
LCADNNJD_00244 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Alpha amylase, catalytic domain |
LCADNNJD_00245 | 2.7e-14 | S | Domain of unknown function (DUF4190) | |||
LCADNNJD_00249 | 1.4e-12 | |||||
LCADNNJD_00250 | 1.1e-47 | K | WYL domain | |||
LCADNNJD_00251 | 2.1e-200 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
LCADNNJD_00252 | 3.8e-176 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
LCADNNJD_00253 | 1.2e-233 | S | AI-2E family transporter | |||
LCADNNJD_00254 | 1.6e-230 | epsG | M | Glycosyl transferase family 21 | ||
LCADNNJD_00255 | 8.3e-199 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
LCADNNJD_00256 | 4.9e-135 | 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 | |
LCADNNJD_00257 | 7.4e-95 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LCADNNJD_00258 | 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 | ||
LCADNNJD_00259 | 1.9e-136 | folK | 1.13.11.81, 2.5.1.15, 2.6.1.85, 2.7.6.3, 3.5.4.16, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
LCADNNJD_00260 | 6.9e-79 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
LCADNNJD_00261 | 4.4e-115 | folP | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the condensation of para-aminobenzoate (pABA) with 6-hydroxymethyl-7,8-dihydropterin diphosphate (DHPt-PP) to form 7,8-dihydropteroate (H2Pte), the immediate precursor of folate derivatives | |
LCADNNJD_00262 | 5.4e-96 | folK | 1.13.11.81, 2.5.1.15, 2.7.6.3, 3.5.4.16, 3.5.4.39, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
LCADNNJD_00263 | 1e-77 | S | Protein of unknown function (DUF3180) | |||
LCADNNJD_00264 | 1.4e-162 | tesB | I | Thioesterase-like superfamily | ||
LCADNNJD_00265 | 0.0 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
LCADNNJD_00266 | 3.8e-146 | S | Sulfite exporter TauE/SafE | |||
LCADNNJD_00267 | 4.7e-263 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
LCADNNJD_00268 | 0.0 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
LCADNNJD_00269 | 5.9e-119 | S | Pyridoxamine 5'-phosphate oxidase | |||
LCADNNJD_00270 | 4.1e-121 | tenA | 3.5.99.2 | K | Catalyzes an amino-pyrimidine hydrolysis reaction at the C5' of the pyrimidine moiety of thiamine compounds, a reaction that is part of a thiamine salvage pathway. Thus, catalyzes the conversion of 4-amino-5-aminomethyl-2-methylpyrimidine to 4-amino- 5-hydroxymethyl-2-methylpyrimidine (HMP) | |
LCADNNJD_00271 | 0.0 | KL | Domain of unknown function (DUF3427) | |||
LCADNNJD_00272 | 1.3e-63 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
LCADNNJD_00273 | 1.2e-192 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
LCADNNJD_00274 | 3.6e-219 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
LCADNNJD_00275 | 5.6e-194 | panE1 | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
LCADNNJD_00276 | 2.1e-157 | metQ | M | NLPA lipoprotein | ||
LCADNNJD_00277 | 1e-182 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LCADNNJD_00278 | 1.3e-95 | metI | P | Psort location CytoplasmicMembrane, score 9.99 | ||
LCADNNJD_00279 | 1.1e-169 | rarA | L | Recombination factor protein RarA | ||
LCADNNJD_00280 | 1.1e-178 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
LCADNNJD_00281 | 1.2e-141 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, N-terminal domain | |
LCADNNJD_00282 | 5.5e-296 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
LCADNNJD_00283 | 3.9e-245 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
LCADNNJD_00284 | 1.7e-120 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
LCADNNJD_00285 | 3.1e-67 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LCADNNJD_00286 | 3.8e-221 | aspB | E | Aminotransferase class-V | ||
LCADNNJD_00287 | 1.3e-73 | K | Acetyltransferase (GNAT) domain | |||
LCADNNJD_00288 | 3.9e-93 | ywrO | S | Flavodoxin-like fold | ||
LCADNNJD_00289 | 4.8e-61 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
LCADNNJD_00291 | 2e-154 | yocS | S | SBF-like CPA transporter family (DUF4137) | ||
LCADNNJD_00292 | 1.4e-73 | S | EcsC protein family | |||
LCADNNJD_00293 | 5.3e-111 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LCADNNJD_00295 | 1.2e-34 | rpmE | J | Binds the 23S rRNA | ||
LCADNNJD_00296 | 3.4e-192 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LCADNNJD_00297 | 1.2e-147 | prmC | 2.1.1.297 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
LCADNNJD_00298 | 4.8e-93 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
LCADNNJD_00299 | 2.2e-187 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
LCADNNJD_00300 | 5.8e-291 | guaB | 1.1.1.205 | F | Catalyzes the conversion of inosine 5'-phosphate (IMP) to xanthosine 5'-phosphate (XMP), the first committed and rate- limiting step in the de novo synthesis of guanine nucleotides, and therefore plays an important role in the regulation of cell growth | |
LCADNNJD_00301 | 6.1e-299 | putP | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
LCADNNJD_00302 | 1.8e-127 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
LCADNNJD_00304 | 4e-151 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
LCADNNJD_00305 | 6.1e-231 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
LCADNNJD_00306 | 1.3e-60 | |||||
LCADNNJD_00307 | 0.0 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LCADNNJD_00308 | 3.7e-188 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_00309 | 4.4e-129 | S | Protein of unknown function, DUF624 | |||
LCADNNJD_00310 | 1.7e-105 | G | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00311 | 1.1e-179 | G | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00312 | 8.7e-290 | G | Bacterial extracellular solute-binding protein | |||
LCADNNJD_00313 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
LCADNNJD_00314 | 6.8e-57 | L | Single-strand binding protein family | |||
LCADNNJD_00315 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LCADNNJD_00316 | 4.3e-97 | S | Short repeat of unknown function (DUF308) | |||
LCADNNJD_00317 | 1.7e-150 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
LCADNNJD_00318 | 6.2e-246 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
LCADNNJD_00319 | 8.3e-47 | ypaA | S | Protein of unknown function (DUF1304) | ||
LCADNNJD_00320 | 5.2e-128 | dapD | 2.3.1.117 | E | Catalyzes the conversion of the cyclic tetrahydrodipicolinate (THDP) into the acyclic N-succinyl-L-2- amino-6-oxopimelate using succinyl-CoA | |
LCADNNJD_00322 | 2.5e-114 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LCADNNJD_00324 | 1.3e-19 | |||||
LCADNNJD_00325 | 3.9e-74 | |||||
LCADNNJD_00328 | 1.6e-168 | mltE2 | M | Bacteriophage peptidoglycan hydrolase | ||
LCADNNJD_00329 | 6.4e-177 | L | Phage integrase family | |||
LCADNNJD_00330 | 4e-19 | K | Transcriptional regulator | |||
LCADNNJD_00331 | 2.4e-69 | |||||
LCADNNJD_00332 | 5.6e-254 | sdaA | 4.3.1.17 | E | Serine dehydratase alpha chain | |
LCADNNJD_00333 | 2.2e-64 | fkbP | 5.2.1.8 | G | Peptidyl-prolyl cis-trans | |
LCADNNJD_00334 | 4.6e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
LCADNNJD_00335 | 5.4e-124 | yplQ | S | Haemolysin-III related | ||
LCADNNJD_00336 | 3.4e-240 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
LCADNNJD_00337 | 6.4e-47 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
LCADNNJD_00338 | 1.8e-153 | D | FtsK/SpoIIIE family | |||
LCADNNJD_00339 | 4.4e-167 | K | Cell envelope-related transcriptional attenuator domain | |||
LCADNNJD_00340 | 5.4e-187 | K | Cell envelope-related transcriptional attenuator domain | |||
LCADNNJD_00341 | 9.4e-39 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
LCADNNJD_00342 | 0.0 | S | Glycosyl transferase, family 2 | |||
LCADNNJD_00343 | 1.8e-159 | |||||
LCADNNJD_00344 | 4e-57 | MA20_43655 | 2.7.2.8 | S | Zincin-like metallopeptidase | |
LCADNNJD_00345 | 7.4e-128 | cof | 5.2.1.8 | T | Eukaryotic phosphomannomutase | |
LCADNNJD_00346 | 9.7e-45 | ctsW | S | Phosphoribosyl transferase domain | ||
LCADNNJD_00347 | 1.4e-176 | 2.7.7.7 | L | Domain of unknown function (DUF4113) | ||
LCADNNJD_00348 | 1.3e-68 | rulA | 3.4.21.88 | KT | Peptidase S24-like | |
LCADNNJD_00349 | 2.5e-182 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LCADNNJD_00350 | 4.1e-125 | T | Response regulator receiver domain protein | |||
LCADNNJD_00351 | 0.0 | glgB | 2.4.1.18 | CBM48,GH13 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
LCADNNJD_00352 | 2.6e-98 | carD | K | CarD-like/TRCF domain | ||
LCADNNJD_00353 | 2.8e-60 | ispF | 2.1.1.228, 2.7.7.60, 4.6.1.12 | H | Involved in the biosynthesis of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP), two major building blocks of isoprenoid compounds. Catalyzes the conversion of 4- diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-CPP) with a corresponding release of cytidine 5-monophosphate (CMP) | |
LCADNNJD_00354 | 1.2e-125 | znuB | U | ABC 3 transport family | ||
LCADNNJD_00355 | 4.6e-129 | znuC | P | ATPases associated with a variety of cellular activities | ||
LCADNNJD_00356 | 2.2e-111 | P | Zinc-uptake complex component A periplasmic | |||
LCADNNJD_00357 | 1.2e-144 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
LCADNNJD_00358 | 4.9e-239 | rpsA | J | Ribosomal protein S1 | ||
LCADNNJD_00359 | 4.3e-67 | coaE | 2.7.1.24 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
LCADNNJD_00360 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
LCADNNJD_00361 | 4.8e-166 | terC | P | Integral membrane protein, TerC family | ||
LCADNNJD_00362 | 8.1e-271 | pyk | 2.7.1.40 | G | Pyruvate kinase | |
LCADNNJD_00363 | 8.7e-111 | aspA | 3.6.1.13 | L | NUDIX domain | |
LCADNNJD_00364 | 2.2e-149 | 3.6.3.30 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | ||
LCADNNJD_00365 | 8.7e-117 | U | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00366 | 1.1e-127 | U | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00367 | 1.3e-170 | P | Bacterial extracellular solute-binding protein | |||
LCADNNJD_00369 | 2.9e-116 | pdtaR | T | Response regulator receiver domain protein | ||
LCADNNJD_00370 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
LCADNNJD_00371 | 3.1e-140 | yqfO | 3.5.4.16 | L | NIF3 (NGG1p interacting factor 3) | |
LCADNNJD_00372 | 3.9e-93 | 3.6.1.13 | L | NUDIX domain | ||
LCADNNJD_00373 | 0.0 | glgX | 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LCADNNJD_00374 | 1.4e-200 | ykiI | ||||
LCADNNJD_00376 | 3.7e-260 | aroA | 2.5.1.19 | E | Catalyzes the transfer of the enolpyruvyl moiety of phosphoenolpyruvate (PEP) to the 5-hydroxyl of shikimate-3- phosphate (S3P) to produce enolpyruvyl shikimate-3-phosphate and inorganic phosphate | |
LCADNNJD_00378 | 4.8e-232 | ackA | 2.7.2.1, 2.7.2.15 | H | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
LCADNNJD_00379 | 9.3e-311 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LCADNNJD_00380 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
LCADNNJD_00381 | 3.1e-300 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
LCADNNJD_00382 | 6.5e-154 | K | Helix-turn-helix domain, rpiR family | |||
LCADNNJD_00383 | 2.1e-235 | pucG | 2.6.1.112, 2.6.1.44, 2.6.1.45, 2.6.1.51 | E | Aminotransferase class-V | |
LCADNNJD_00384 | 1.8e-245 | amaB | 3.5.1.6, 3.5.1.87, 3.5.3.9 | E | Peptidase dimerisation domain | |
LCADNNJD_00385 | 4.3e-258 | allB | 3.5.2.5 | F | Amidohydrolase family | |
LCADNNJD_00386 | 7.2e-292 | 3.5.1.4, 6.3.5.6, 6.3.5.7 | J | Protein of unknown function (DUF3225) | ||
LCADNNJD_00387 | 1.1e-300 | pucI | FH | Permease for cytosine/purines, uracil, thiamine, allantoin | ||
LCADNNJD_00388 | 6.4e-131 | hyuE | 5.1.99.3 | E | Asp/Glu/Hydantoin racemase | |
LCADNNJD_00389 | 4e-167 | S | beta-lactamase activity | |||
LCADNNJD_00391 | 5.1e-66 | hsdBM | 2.1.1.72 | L | Eco57I restriction-modification methylase | |
LCADNNJD_00392 | 2.3e-95 | K | Psort location Cytoplasmic, score | |||
LCADNNJD_00393 | 3e-167 | 2.1.1.72, 3.1.21.4 | L | restriction endonuclease | ||
LCADNNJD_00394 | 0.0 | KL | type III restriction enzyme, res subunit | |||
LCADNNJD_00395 | 5.9e-169 | S | Protein of unknown function DUF262 | |||
LCADNNJD_00396 | 1.2e-43 | V | Abi-like protein | |||
LCADNNJD_00398 | 3.9e-192 | |||||
LCADNNJD_00399 | 3.8e-29 | gepA | S | Protein of unknown function (DUF4065) | ||
LCADNNJD_00400 | 1.7e-308 | S | ATPases associated with a variety of cellular activities | |||
LCADNNJD_00401 | 1.3e-244 | EGP | Major facilitator Superfamily | |||
LCADNNJD_00402 | 1e-28 | feoA | P | iron ion homeostasis | ||
LCADNNJD_00403 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
LCADNNJD_00404 | 1.4e-09 | |||||
LCADNNJD_00405 | 7.2e-132 | S | Putative ABC-transporter type IV | |||
LCADNNJD_00406 | 1.5e-107 | mpg | 3.2.2.21 | L | Methylpurine-DNA glycosylase (MPG) | |
LCADNNJD_00407 | 1e-176 | V | ATPases associated with a variety of cellular activities | |||
LCADNNJD_00408 | 1.2e-201 | V | ABC-2 family transporter protein | |||
LCADNNJD_00409 | 9e-205 | V | ABC-2 family transporter protein | |||
LCADNNJD_00410 | 1e-88 | K | acetyltransferase | |||
LCADNNJD_00411 | 6.9e-66 | arsC | 1.20.4.1 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
LCADNNJD_00412 | 0.0 | S | TerB-C domain | |||
LCADNNJD_00413 | 5.1e-270 | P | P-loop Domain of unknown function (DUF2791) | |||
LCADNNJD_00414 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
LCADNNJD_00415 | 1e-281 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LCADNNJD_00416 | 6.7e-239 | pbuX | F | Permease family | ||
LCADNNJD_00417 | 1.1e-104 | xpt | 2.4.2.22, 2.4.2.7 | F | Converts the preformed base xanthine, a product of nucleic acid breakdown, to xanthosine 5'-monophosphate (XMP), so it can be reused for RNA or DNA synthesis | |
LCADNNJD_00418 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
LCADNNJD_00419 | 7.5e-81 | KT | Transcriptional regulatory protein, C terminal | |||
LCADNNJD_00420 | 1.1e-89 | T | PhoQ Sensor | |||
LCADNNJD_00421 | 2.4e-68 | apl | 3.1.3.1 | S | SNARE associated Golgi protein | |
LCADNNJD_00422 | 3.1e-102 | rpsD | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the body of the 30S subunit | ||
LCADNNJD_00423 | 0.0 | uvrA3 | L | nucleotide-excision repair | ||
LCADNNJD_00424 | 1.7e-52 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
LCADNNJD_00425 | 2.6e-130 | oatA | I | Psort location CytoplasmicMembrane, score 9.99 | ||
LCADNNJD_00426 | 9e-103 | pgm3 | G | Phosphoglycerate mutase family | ||
LCADNNJD_00427 | 2.5e-50 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
LCADNNJD_00428 | 1.3e-29 | |||||
LCADNNJD_00429 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
LCADNNJD_00430 | 7.4e-59 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LCADNNJD_00431 | 1.2e-171 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LCADNNJD_00432 | 1.1e-209 | aroC | 4.2.3.5 | E | Catalyzes the anti-1,4-elimination of the C-3 phosphate and the C-6 proR hydrogen from 5-enolpyruvylshikimate-3-phosphate (EPSP) to yield chorismate, which is the branch point compound that serves as the starting substrate for the three terminal pathways of aromatic amino acid biosynthesis. This reaction introduces a second double bond into the aromatic ring system | |
LCADNNJD_00433 | 9.6e-279 | aroK | 2.7.1.71, 4.2.3.4 | H | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
LCADNNJD_00434 | 3.1e-75 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
LCADNNJD_00435 | 0.0 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | M | Aamy_C |
LCADNNJD_00436 | 1.2e-283 | amy | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | Aamy_C |
LCADNNJD_00437 | 0.0 | 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 | |
LCADNNJD_00438 | 2.7e-285 | sufB | O | FeS assembly protein SufB | ||
LCADNNJD_00439 | 5.6e-215 | sufD | O | FeS assembly protein SufD | ||
LCADNNJD_00440 | 3.9e-142 | sufC | O | FeS assembly ATPase SufC | ||
LCADNNJD_00441 | 1.7e-235 | sufS | 2.8.1.7, 4.4.1.16 | E | Catalyzes the removal of elemental sulfur and selenium atoms from L-cysteine, L-cystine, L-selenocysteine, and L- selenocystine to produce L-alanine | |
LCADNNJD_00442 | 3.3e-101 | iscU | C | SUF system FeS assembly protein, NifU family | ||
LCADNNJD_00443 | 1.3e-95 | yitW | S | Iron-sulfur cluster assembly protein | ||
LCADNNJD_00444 | 1.6e-149 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
LCADNNJD_00445 | 2.2e-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 | |
LCADNNJD_00447 | 7e-56 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
LCADNNJD_00448 | 2.6e-180 | phoH | T | PhoH-like protein | ||
LCADNNJD_00449 | 6.3e-86 | 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 | |
LCADNNJD_00451 | 2.9e-215 | corC | S | CBS domain | ||
LCADNNJD_00452 | 3.5e-164 | 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 | ||
LCADNNJD_00453 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LCADNNJD_00454 | 7.7e-163 | pntAA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
LCADNNJD_00455 | 2.5e-42 | pntAA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
LCADNNJD_00456 | 3.5e-234 | pntB | 1.6.1.2 | C | The transhydrogenation between NADH and NADP is coupled to respiration and ATP hydrolysis and functions as a proton pump across the membrane | |
LCADNNJD_00457 | 1.3e-118 | S | alpha beta | |||
LCADNNJD_00458 | 5.1e-92 | ctc | J | This is one of the proteins that binds to the 5S RNA in the ribosome where it forms part of the central protuberance | ||
LCADNNJD_00459 | 4.5e-224 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
LCADNNJD_00460 | 6.9e-101 | S | UPF0126 domain | |||
LCADNNJD_00461 | 2.1e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
LCADNNJD_00462 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
LCADNNJD_00463 | 4.8e-164 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LCADNNJD_00464 | 3.5e-82 | maa | 2.3.1.18, 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | |
LCADNNJD_00465 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
LCADNNJD_00466 | 1.3e-290 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
LCADNNJD_00467 | 1.6e-58 | |||||
LCADNNJD_00468 | 1.8e-36 | M | Peptidase family M23 | |||
LCADNNJD_00469 | 8.3e-154 | G | ABC transporter substrate-binding protein | |||
LCADNNJD_00470 | 1.6e-232 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
LCADNNJD_00471 | 6.5e-183 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
LCADNNJD_00472 | 1.5e-14 | |||||
LCADNNJD_00473 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
LCADNNJD_00474 | 1.1e-78 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
LCADNNJD_00475 | 5.6e-136 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LCADNNJD_00476 | 1.1e-145 | tsf | J | Associates with the EF-Tu.GDP complex and induces the exchange of GDP to GTP. It remains bound to the aminoacyl-tRNA.EF- Tu.GTP complex up to the GTP hydrolysis stage on the ribosome | ||
LCADNNJD_00477 | 4.3e-127 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LCADNNJD_00478 | 2.4e-90 | frr | J | Responsible for the release of ribosomes from messenger RNA at the termination of protein biosynthesis. May increase the efficiency of translation by recycling ribosomes from one round of translation to another | ||
LCADNNJD_00479 | 1.8e-144 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
LCADNNJD_00480 | 1.1e-204 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LCADNNJD_00481 | 8.5e-134 | hisF | 4.1.3.27 | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisF subunit catalyzes the cyclization activity that produces IGP and AICAR from PRFAR using the ammonia provided by the HisH subunit | |
LCADNNJD_00482 | 3.9e-64 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
LCADNNJD_00483 | 4.7e-280 | trpE | 4.1.3.27 | E | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
LCADNNJD_00484 | 0.0 | trpB | 4.2.1.20 | E | The beta subunit is responsible for the synthesis of L- tryptophan from indole and L-serine | |
LCADNNJD_00485 | 8.4e-146 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
LCADNNJD_00486 | 2.3e-159 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
LCADNNJD_00487 | 8.9e-96 | rpe | 5.1.3.1 | G | Ribulose-phosphate 3-epimerase | |
LCADNNJD_00488 | 3.5e-39 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP pyrophosphohydrolase | |
LCADNNJD_00489 | 1.9e-150 | hisG | 2.4.2.17 | F | ATP phosphoribosyltransferase | |
LCADNNJD_00490 | 2e-85 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LCADNNJD_00491 | 1.1e-132 | S | Bacterial protein of unknown function (DUF881) | |||
LCADNNJD_00492 | 8.1e-33 | sbp | S | Protein of unknown function (DUF1290) | ||
LCADNNJD_00493 | 1.6e-109 | S | Bacterial protein of unknown function (DUF881) | |||
LCADNNJD_00494 | 1.7e-70 | garA | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LCADNNJD_00495 | 2.3e-82 | K | helix_turn_helix, mercury resistance | |||
LCADNNJD_00498 | 4.8e-28 | L | DNA integration | |||
LCADNNJD_00499 | 2.7e-35 | 3.4.22.70 | M | Sortase family | ||
LCADNNJD_00500 | 1.2e-32 | M | domain protein | |||
LCADNNJD_00501 | 3.4e-33 | nrdH | O | Glutaredoxin | ||
LCADNNJD_00502 | 3.8e-104 | KT | Transcriptional regulatory protein, C terminal | |||
LCADNNJD_00503 | 0.0 | T | Osmosensitive K+ channel His kinase sensor domain | |||
LCADNNJD_00504 | 6.9e-70 | kdpC | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit acts as a catalytic chaperone that increases the ATP- binding affinity of the ATP-hydrolyzing subunit KdpB by the formation of a transient KdpB KdpC ATP ternary complex | |
LCADNNJD_00505 | 0.0 | kdpB | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit is responsible for energy coupling to the transport system | |
LCADNNJD_00506 | 3.7e-259 | kdpA | 3.6.3.12 | P | Part of the high-affinity ATP-driven potassium transport (or Kdp) system, which catalyzes the hydrolysis of ATP coupled with the electrogenic transport of potassium into the cytoplasm. This subunit binds and transports the potassium across the cytoplasmic membrane | |
LCADNNJD_00509 | 1.5e-16 | S | Putative ABC-transporter type IV | |||
LCADNNJD_00519 | 5.8e-116 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
LCADNNJD_00520 | 4.1e-59 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
LCADNNJD_00521 | 0.0 | helY | L | DEAD DEAH box helicase | ||
LCADNNJD_00522 | 9.5e-15 | |||||
LCADNNJD_00523 | 0.0 | pafB | K | WYL domain | ||
LCADNNJD_00524 | 7.6e-234 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
LCADNNJD_00526 | 0.0 | der | 1.1.1.399, 1.1.1.95, 2.7.4.25 | F | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
LCADNNJD_00527 | 6.1e-140 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LCADNNJD_00528 | 1.5e-72 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LCADNNJD_00529 | 5.6e-22 | |||||
LCADNNJD_00530 | 3.7e-288 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LCADNNJD_00531 | 1.6e-146 | |||||
LCADNNJD_00532 | 1.1e-156 | sucD | 6.2.1.5 | C | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The alpha subunit of the enzyme binds the substrates coenzyme A and phosphate, while succinate binding and nucleotide specificity is provided by the beta subunit | |
LCADNNJD_00533 | 4.9e-205 | sucC | 6.2.1.5 | F | Succinyl-CoA synthetase functions in the citric acid cycle (TCA), coupling the hydrolysis of succinyl-CoA to the synthesis of either ATP or GTP and thus represents the only step of substrate-level phosphorylation in the TCA. The beta subunit provides nucleotide specificity of the enzyme and binds the substrate succinate, while the binding sites for coenzyme A and phosphate are found in the alpha subunit | |
LCADNNJD_00534 | 3.3e-90 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
LCADNNJD_00535 | 9.9e-14 | yajC | U | Preprotein translocase subunit | ||
LCADNNJD_00536 | 2.8e-183 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
LCADNNJD_00537 | 4.1e-86 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
LCADNNJD_00538 | 1.1e-93 | ruvC | 3.1.22.4 | L | Nuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves the cruciform structure in supercoiled DNA by nicking to strands with the same polarity at sites symmetrically opposed at the junction in the homologous arms and leaves a 5'-terminal phosphate and a 3'-terminal hydroxyl group | |
LCADNNJD_00539 | 3.8e-118 | yebC | K | transcriptional regulatory protein | ||
LCADNNJD_00540 | 1.5e-180 | pimA | 2.4.1.345 | GT4 | M | Glycosyl transferases group 1 |
LCADNNJD_00541 | 4.1e-144 | htrB | 2.3.1.241, 2.3.1.265 | M | Bacterial lipid A biosynthesis acyltransferase | |
LCADNNJD_00542 | 9.1e-89 | pgsA1 | 2.7.8.11, 2.7.8.5 | I | CDP-alcohol phosphatidyltransferase | |
LCADNNJD_00543 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
LCADNNJD_00548 | 1.8e-126 | S | PAC2 family | |||
LCADNNJD_00550 | 2.2e-67 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
LCADNNJD_00551 | 7.5e-153 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LCADNNJD_00552 | 1.1e-152 | G | Fructosamine kinase | |||
LCADNNJD_00553 | 1.5e-190 | dnaJ | O | ATP binding to DnaK triggers the release of the substrate protein, thus completing the reaction cycle. Several rounds of ATP-dependent interactions between DnaJ, DnaK and GrpE are required for fully efficient folding. Also involved, together with DnaK and GrpE, in the DNA replication of plasmids through activation of initiation proteins | ||
LCADNNJD_00554 | 3.8e-164 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LCADNNJD_00556 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
LCADNNJD_00557 | 3.7e-199 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LCADNNJD_00558 | 2.1e-245 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
LCADNNJD_00559 | 9.8e-140 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LCADNNJD_00560 | 2.6e-34 | secG | U | Preprotein translocase SecG subunit | ||
LCADNNJD_00561 | 5.8e-133 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
LCADNNJD_00562 | 1.2e-219 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
LCADNNJD_00563 | 1.2e-167 | whiA | K | May be required for sporulation | ||
LCADNNJD_00564 | 3.9e-157 | rapZ | S | Displays ATPase and GTPase activities | ||
LCADNNJD_00565 | 4.5e-122 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
LCADNNJD_00566 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
LCADNNJD_00567 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
LCADNNJD_00568 | 1.9e-300 | ybiT | S | ABC transporter | ||
LCADNNJD_00569 | 4.9e-120 | E | GDSL-like Lipase/Acylhydrolase family | |||
LCADNNJD_00570 | 2.1e-43 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
LCADNNJD_00572 | 9.8e-12 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
LCADNNJD_00574 | 1.8e-81 | 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 | ||
LCADNNJD_00575 | 3.5e-35 | |||||
LCADNNJD_00576 | 9.9e-232 | V | MatE | |||
LCADNNJD_00577 | 3.2e-126 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
LCADNNJD_00578 | 9.7e-270 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
LCADNNJD_00579 | 2e-198 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
LCADNNJD_00581 | 6.1e-147 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
LCADNNJD_00582 | 7.7e-216 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LCADNNJD_00583 | 3e-201 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LCADNNJD_00584 | 1.8e-204 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
LCADNNJD_00585 | 9.9e-115 | yqeC | 6.3.2.10, 6.3.2.13 | M | Catalyzes the addition of meso-diaminopimelic acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
LCADNNJD_00586 | 6.1e-268 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
LCADNNJD_00587 | 6.8e-46 | ftsL | D | Essential cell division protein. May link together the upstream cell division proteins, which are predominantly cytoplasmic, with the downstream cell division proteins, which are predominantly periplasmic | ||
LCADNNJD_00588 | 6.7e-164 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LCADNNJD_00589 | 3.4e-73 | mraZ | K | Belongs to the MraZ family | ||
LCADNNJD_00590 | 0.0 | L | DNA helicase | |||
LCADNNJD_00591 | 1.7e-216 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
LCADNNJD_00592 | 1.1e-80 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LCADNNJD_00593 | 5.2e-23 | M | Lysin motif | |||
LCADNNJD_00594 | 8.3e-110 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
LCADNNJD_00595 | 9.2e-141 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
LCADNNJD_00596 | 1.2e-174 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
LCADNNJD_00597 | 1.4e-239 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LCADNNJD_00598 | 7.4e-103 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
LCADNNJD_00599 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
LCADNNJD_00600 | 3.6e-150 | M | Converts alpha-N-acetylneuranimic acid (Neu5Ac) to the beta-anomer, accelerating the equilibrium between the alpha- and beta-anomers. Probably facilitates sialidase-negative bacteria to compete sucessfully for limited amounts of extracellular Neu5Ac, which is likely taken up in the beta-anomer. In addition, the rapid removal of sialic acid from solution might be advantageous to the bacterium to damp down host responses | |||
LCADNNJD_00601 | 2.4e-187 | EGP | Major facilitator Superfamily | |||
LCADNNJD_00602 | 7.5e-263 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
LCADNNJD_00603 | 1.4e-125 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
LCADNNJD_00604 | 4.7e-109 | hisH | E | IGPS catalyzes the conversion of PRFAR and glutamine to IGP, AICAR and glutamate. The HisH subunit provides the glutamine amidotransferase activity that produces the ammonia necessary to HisF for the synthesis of IGP and AICAR | ||
LCADNNJD_00605 | 1.6e-71 | |||||
LCADNNJD_00606 | 5.6e-109 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
LCADNNJD_00607 | 2.6e-219 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LCADNNJD_00608 | 8.1e-252 | hisD | 1.1.1.23, 1.1.1.308 | E | Catalyzes the sequential NAD-dependent oxidations of L- histidinol to L-histidinaldehyde and then to L-histidine | |
LCADNNJD_00609 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
LCADNNJD_00610 | 2.2e-168 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LCADNNJD_00611 | 5.6e-60 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LCADNNJD_00612 | 5.5e-70 | GT2,GT4 | D | DivIVA protein | ||
LCADNNJD_00613 | 9.7e-27 | yggT | S | YGGT family | ||
LCADNNJD_00614 | 1.4e-49 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
LCADNNJD_00615 | 1.1e-165 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
LCADNNJD_00616 | 1.4e-239 | 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 | ||
LCADNNJD_00617 | 1.8e-300 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
LCADNNJD_00618 | 9.8e-43 | mshJ | NU | Type II secretion system (T2SS), protein M | ||
LCADNNJD_00619 | 4.7e-20 | pilN | NU | PFAM Fimbrial assembly family protein | ||
LCADNNJD_00620 | 9.6e-26 | pilN | NU | PFAM Fimbrial assembly family protein | ||
LCADNNJD_00621 | 1.2e-97 | pilM | NU | Type IV pilus assembly protein PilM; | ||
LCADNNJD_00622 | 5.6e-97 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
LCADNNJD_00626 | 6.5e-33 | ppdC | NU | Prokaryotic N-terminal methylation motif | ||
LCADNNJD_00627 | 2.6e-32 | |||||
LCADNNJD_00628 | 3.7e-105 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
LCADNNJD_00629 | 0.0 | thiC | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Catalyzes the synthesis of the hydroxymethylpyrimidine phosphate (HMP-P) moiety of thiamine from aminoimidazole ribotide (AIR) in a radical S-adenosyl-L-methionine (SAM)-dependent reaction | |
LCADNNJD_00630 | 4e-137 | 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) | |
LCADNNJD_00631 | 1.3e-61 | S | Thiamine-binding protein | |||
LCADNNJD_00633 | 2.8e-132 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_00634 | 2.5e-149 | uppS | 2.5.1.31, 2.5.1.86, 2.5.1.88 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
LCADNNJD_00635 | 2.9e-120 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LCADNNJD_00636 | 3.8e-273 | I | acetylesterase activity | |||
LCADNNJD_00637 | 1.6e-211 | ispG | 1.17.7.1, 1.17.7.3 | I | Converts 2C-methyl-D-erythritol 2,4-cyclodiphosphate (ME-2,4cPP) into 1-hydroxy-2-methyl-2-(E)-butenyl 4-diphosphate | |
LCADNNJD_00638 | 7.3e-209 | dxr | 1.1.1.267 | I | Catalyzes the NADP-dependent rearrangement and reduction of 1-deoxy-D-xylulose-5-phosphate (DXP) to 2-C-methyl-D-erythritol 4-phosphate (MEP) | |
LCADNNJD_00639 | 6.5e-124 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
LCADNNJD_00641 | 1e-72 | S | Protein of unknown function (DUF3052) | |||
LCADNNJD_00642 | 9.1e-113 | lon | T | Belongs to the peptidase S16 family | ||
LCADNNJD_00643 | 9.6e-215 | S | Zincin-like metallopeptidase | |||
LCADNNJD_00644 | 7.5e-243 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
LCADNNJD_00646 | 5.1e-192 | mphA | S | Aminoglycoside phosphotransferase | ||
LCADNNJD_00647 | 4.2e-33 | S | Protein of unknown function (DUF3107) | |||
LCADNNJD_00648 | 1e-106 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
LCADNNJD_00649 | 5.4e-148 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine | |
LCADNNJD_00650 | 3.5e-17 | |||||
LCADNNJD_00652 | 1.7e-129 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LCADNNJD_00653 | 4.9e-147 | S | Patatin-like phospholipase | |||
LCADNNJD_00654 | 4.6e-121 | XK27_08050 | O | prohibitin homologues | ||
LCADNNJD_00655 | 2.9e-151 | mdh | 1.1.1.350 | C | Malate/L-lactate dehydrogenase | |
LCADNNJD_00656 | 6.6e-118 | patA | 2.6.1.1 | E | Aminotransferase class I and II | |
LCADNNJD_00657 | 5e-134 | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | ||
LCADNNJD_00658 | 3.8e-57 | ypeA | 2.3.1.1 | K | Psort location Cytoplasmic, score 8.87 | |
LCADNNJD_00659 | 6.4e-130 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LCADNNJD_00660 | 3.6e-88 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00661 | 8.1e-117 | blpF | P | NLPA lipoprotein | ||
LCADNNJD_00662 | 1e-224 | L | Helix-turn-helix domain | |||
LCADNNJD_00663 | 5.8e-98 | L | Resolvase, N terminal domain | |||
LCADNNJD_00665 | 1.6e-156 | dapE2 | E | Peptidase family M28 | ||
LCADNNJD_00666 | 9.7e-113 | P | ATPases associated with a variety of cellular activities | |||
LCADNNJD_00667 | 5.9e-128 | ssuC2 | U | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00668 | 3.4e-133 | P | NMT1-like family | |||
LCADNNJD_00670 | 9.7e-123 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
LCADNNJD_00671 | 3.3e-114 | 2.1.1.157 | Q | Methyltransferase domain | ||
LCADNNJD_00672 | 1.6e-200 | metK | 2.5.1.6 | H | S-adenosylmethionine synthetase, C-terminal domain | |
LCADNNJD_00673 | 1.2e-08 | metK | 2.5.1.6 | H | S-adenosylmethionine synthetase, C-terminal domain | |
LCADNNJD_00675 | 3.8e-229 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LCADNNJD_00678 | 1.5e-178 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
LCADNNJD_00679 | 4e-179 | yghZ | C | Aldo/keto reductase family | ||
LCADNNJD_00681 | 1.9e-56 | yccF | S | Inner membrane component domain | ||
LCADNNJD_00682 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
LCADNNJD_00683 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
LCADNNJD_00684 | 0.0 | V | ABC transporter transmembrane region | |||
LCADNNJD_00685 | 0.0 | V | ABC transporter, ATP-binding protein | |||
LCADNNJD_00686 | 2.6e-58 | K | MarR family | |||
LCADNNJD_00687 | 3.3e-156 | lmrB | U | Major Facilitator Superfamily | ||
LCADNNJD_00688 | 0.0 | bglB | 3.2.1.21 | GH3 | G | Glycosyl hydrolase family 3 N-terminal domain protein |
LCADNNJD_00689 | 9.4e-247 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
LCADNNJD_00690 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LCADNNJD_00691 | 8.9e-44 | yfeO | P | Chloride transporter, ClC family | ||
LCADNNJD_00692 | 3.8e-136 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
LCADNNJD_00693 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
LCADNNJD_00694 | 2.6e-215 | xseA | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
LCADNNJD_00695 | 2.5e-36 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
LCADNNJD_00696 | 7.6e-157 | S | Endonuclease/Exonuclease/phosphatase family | |||
LCADNNJD_00697 | 2.4e-150 | S | zinc finger | |||
LCADNNJD_00698 | 6.9e-108 | def | 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
LCADNNJD_00699 | 2.5e-253 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LCADNNJD_00701 | 2.3e-102 | mmyX | 5.3.1.12 | F | Cytidylate kinase-like family | |
LCADNNJD_00702 | 0.0 | 1.1.1.1, 1.1.1.202 | CE | Amino acid permease | ||
LCADNNJD_00703 | 1.1e-82 | phnO | K | Acetyltransferase (GNAT) family | ||
LCADNNJD_00704 | 1.2e-260 | gabT | 2.6.1.19, 2.6.1.22 | E | Aminotransferase class-III | |
LCADNNJD_00705 | 3.4e-56 | S | Protein of unknown function DUF86 | |||
LCADNNJD_00706 | 1.9e-66 | S | Nucleotidyltransferase domain | |||
LCADNNJD_00707 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
LCADNNJD_00708 | 0.0 | rnj | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
LCADNNJD_00709 | 7e-164 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LCADNNJD_00710 | 7e-125 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LCADNNJD_00711 | 3.8e-214 | G | Major Facilitator Superfamily | |||
LCADNNJD_00712 | 5.1e-133 | K | -acetyltransferase | |||
LCADNNJD_00713 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
LCADNNJD_00714 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
LCADNNJD_00715 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LCADNNJD_00716 | 0.0 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LCADNNJD_00718 | 1.8e-71 | |||||
LCADNNJD_00719 | 3.2e-121 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
LCADNNJD_00720 | 9.2e-111 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LCADNNJD_00721 | 1.3e-202 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LCADNNJD_00722 | 1.3e-158 | ftsE | D | Cell division ATP-binding protein FtsE | ||
LCADNNJD_00723 | 1e-154 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
LCADNNJD_00724 | 2.3e-124 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
LCADNNJD_00726 | 4.3e-75 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
LCADNNJD_00727 | 3.5e-140 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LCADNNJD_00728 | 4.6e-150 | pknD | ET | ABC transporter, substrate-binding protein, family 3 | ||
LCADNNJD_00729 | 4.2e-117 | yecS | E | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00730 | 6.7e-140 | tcyC | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | |
LCADNNJD_00732 | 9.6e-184 | 2.7.13.3 | T | Histidine kinase | ||
LCADNNJD_00733 | 7.5e-121 | K | helix_turn_helix, Lux Regulon | |||
LCADNNJD_00734 | 5.8e-173 | V | N-Acetylmuramoyl-L-alanine amidase | |||
LCADNNJD_00735 | 1.4e-14 | |||||
LCADNNJD_00736 | 7.6e-147 | |||||
LCADNNJD_00737 | 3.9e-71 | |||||
LCADNNJD_00738 | 1.3e-90 | |||||
LCADNNJD_00739 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
LCADNNJD_00740 | 1.4e-140 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
LCADNNJD_00741 | 8.5e-158 | K | Periplasmic binding protein domain | |||
LCADNNJD_00742 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LCADNNJD_00743 | 8.1e-239 | G | Bacterial extracellular solute-binding protein | |||
LCADNNJD_00744 | 2.3e-227 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
LCADNNJD_00745 | 2.6e-138 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
LCADNNJD_00746 | 1.5e-279 | E | ABC transporter, substrate-binding protein, family 5 | |||
LCADNNJD_00747 | 4.2e-146 | P | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00748 | 1.2e-110 | EP | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00749 | 3.9e-102 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
LCADNNJD_00750 | 7e-100 | sapF | E | ATPases associated with a variety of cellular activities | ||
LCADNNJD_00751 | 5.1e-182 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LCADNNJD_00752 | 8.8e-173 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LCADNNJD_00753 | 2.2e-190 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
LCADNNJD_00754 | 5.7e-222 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LCADNNJD_00755 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LCADNNJD_00756 | 1.4e-95 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LCADNNJD_00757 | 6e-96 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
LCADNNJD_00758 | 2.7e-91 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
LCADNNJD_00759 | 4.4e-267 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
LCADNNJD_00760 | 7.4e-258 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LCADNNJD_00761 | 4.9e-235 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
LCADNNJD_00762 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LCADNNJD_00763 | 8.4e-171 | pabC | 2.6.1.42, 4.1.3.38 | EH | Amino-transferase class IV | |
LCADNNJD_00764 | 1.3e-148 | S | Protein of unknown function (DUF1445) | |||
LCADNNJD_00765 | 5.6e-136 | lamB | S | LamB/YcsF family | ||
LCADNNJD_00766 | 5e-311 | ybgK | E | Allophanate hydrolase subunit 2 | ||
LCADNNJD_00767 | 0.0 | bccA | 6.3.4.14, 6.4.1.2, 6.4.1.3 | I | Biotin carboxylase C-terminal domain | |
LCADNNJD_00768 | 3.6e-180 | 4.2.1.48 | S | Domain of unknown function (DUF4392) | ||
LCADNNJD_00769 | 2.9e-128 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
LCADNNJD_00770 | 6.4e-282 | V | Beta-lactamase | |||
LCADNNJD_00771 | 0.0 | G | Alpha-L-arabinofuranosidase C-terminal domain | |||
LCADNNJD_00772 | 2.2e-197 | ybiR | P | Citrate transporter | ||
LCADNNJD_00774 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
LCADNNJD_00775 | 3.1e-84 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
LCADNNJD_00776 | 5.3e-220 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
LCADNNJD_00777 | 5.8e-65 | zur | P | Belongs to the Fur family | ||
LCADNNJD_00778 | 5.3e-114 | P | Zinc-uptake complex component A periplasmic | |||
LCADNNJD_00780 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
LCADNNJD_00781 | 1.9e-256 | S | Putative esterase | |||
LCADNNJD_00782 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LCADNNJD_00783 | 1.2e-236 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
LCADNNJD_00784 | 4.6e-183 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
LCADNNJD_00785 | 9.8e-291 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LCADNNJD_00786 | 3.4e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LCADNNJD_00788 | 5.3e-07 | |||||
LCADNNJD_00789 | 9.4e-143 | 3.2.1.4 | GH5,GH9 | G | CBD_II | |
LCADNNJD_00790 | 4.5e-11 | S | HicB family | |||
LCADNNJD_00795 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
LCADNNJD_00796 | 1.6e-129 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
LCADNNJD_00797 | 9.6e-226 | purT | 2.1.2.2 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
LCADNNJD_00798 | 5.2e-210 | M | Glycosyl transferase 4-like domain | |||
LCADNNJD_00799 | 1.3e-75 | NU | general secretion pathway protein | |||
LCADNNJD_00800 | 9.3e-245 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Aldehyde dehydrogenase family | |
LCADNNJD_00801 | 1.5e-70 | asnC | K | helix_turn_helix ASNC type | ||
LCADNNJD_00802 | 5.1e-162 | potA | 3.6.3.31 | E | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
LCADNNJD_00803 | 1.7e-166 | potB | U | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00804 | 5.6e-133 | potC | U | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00805 | 7.3e-196 | E | Bacterial extracellular solute-binding protein | |||
LCADNNJD_00806 | 3.7e-273 | 5.4.3.8 | H | Aminotransferase class-III | ||
LCADNNJD_00809 | 2.7e-61 | rpsL | J | Interacts with and stabilizes bases of the 16S rRNA that are involved in tRNA selection in the A site and with the mRNA backbone. Located at the interface of the 30S and 50S subunits, it traverses the body of the 30S subunit contacting proteins on the other side and probably holding the rRNA structure together. The combined cluster of proteins S8, S12 and S17 appears to hold together the shoulder and platform of the 30S subunit | ||
LCADNNJD_00810 | 3.3e-80 | rpsG | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA where it nucleates assembly of the head domain of the 30S subunit. Is located at the subunit interface close to the decoding center, probably blocks exit of the E-site tRNA | ||
LCADNNJD_00811 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
LCADNNJD_00812 | 8.9e-231 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LCADNNJD_00813 | 5.8e-189 | 1.1.3.46 | C | FMN-dependent dehydrogenase | ||
LCADNNJD_00814 | 2.4e-101 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
LCADNNJD_00815 | 5.8e-72 | nusB | K | Involved in transcription antitermination. Required for transcription of ribosomal RNA (rRNA) genes. Binds specifically to the boxA antiterminator sequence of the ribosomal RNA (rrn) operons | ||
LCADNNJD_00816 | 2.2e-224 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
LCADNNJD_00817 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
LCADNNJD_00818 | 1.5e-156 | pyrF | 2.4.2.10, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LCADNNJD_00819 | 2.9e-92 | gmk | 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LCADNNJD_00820 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
LCADNNJD_00821 | 2.5e-46 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
LCADNNJD_00822 | 7.9e-227 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
LCADNNJD_00823 | 2.8e-254 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
LCADNNJD_00824 | 0.0 | priA | L | Involved in the restart of stalled replication forks. Recognizes and binds the arrested nascent DNA chain at stalled replication forks. It can open the DNA duplex, via its helicase activity, and promote assembly of the primosome and loading of the major replicative helicase DnaB onto DNA | ||
LCADNNJD_00825 | 1.3e-42 | yunC | S | Domain of unknown function (DUF1805) | ||
LCADNNJD_00826 | 1.8e-111 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LCADNNJD_00827 | 4.6e-169 | fmt | 2.1.1.176, 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
LCADNNJD_00828 | 9e-111 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
LCADNNJD_00829 | 2.5e-98 | apl | 3.1.3.1 | S | SNARE associated Golgi protein | |
LCADNNJD_00830 | 1.6e-225 | arc | O | AAA ATPase forming ring-shaped complexes | ||
LCADNNJD_00831 | 3e-258 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
LCADNNJD_00832 | 6.1e-154 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
LCADNNJD_00834 | 6.2e-221 | pafA | 6.3.1.19 | O | Catalyzes the covalent attachment of the prokaryotic ubiquitin-like protein modifier Pup to the proteasomal substrate proteins, thereby targeting them for proteasomal degradation. This tagging system is termed pupylation. The ligation reaction involves the side-chain carboxylate of the C-terminal glutamate of Pup and the side-chain amino group of a substrate lysine | |
LCADNNJD_00835 | 5.6e-35 | hup | L | Belongs to the bacterial histone-like protein family | ||
LCADNNJD_00836 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
LCADNNJD_00837 | 1.8e-265 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
LCADNNJD_00838 | 3e-162 | S | PGAP1-like protein | |||
LCADNNJD_00840 | 4.5e-21 | |||||
LCADNNJD_00841 | 4.1e-120 | S | von Willebrand factor (vWF) type A domain | |||
LCADNNJD_00842 | 2.5e-147 | S | von Willebrand factor (vWF) type A domain | |||
LCADNNJD_00843 | 1.5e-55 | |||||
LCADNNJD_00844 | 1e-131 | S | Protein of unknown function DUF58 | |||
LCADNNJD_00845 | 5.8e-173 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
LCADNNJD_00846 | 3.5e-125 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
LCADNNJD_00847 | 8e-53 | S | LytR cell envelope-related transcriptional attenuator | |||
LCADNNJD_00848 | 1.3e-28 | cspA | K | 'Cold-shock' DNA-binding domain | ||
LCADNNJD_00849 | 1.6e-291 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
LCADNNJD_00851 | 4e-49 | |||||
LCADNNJD_00852 | 7.2e-130 | KT | Response regulator receiver domain protein | |||
LCADNNJD_00853 | 2.2e-271 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
LCADNNJD_00854 | 3.6e-64 | cspB | K | 'Cold-shock' DNA-binding domain | ||
LCADNNJD_00855 | 5.6e-136 | S | Protein of unknown function (DUF3027) | |||
LCADNNJD_00856 | 8.8e-152 | uspA | T | Belongs to the universal stress protein A family | ||
LCADNNJD_00857 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
LCADNNJD_00858 | 3.4e-208 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
LCADNNJD_00859 | 3.4e-258 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
LCADNNJD_00860 | 0.0 | aspS | 6.1.1.12 | J | Aspartyl-tRNA synthetase with relaxed tRNA specificity since it is able to aspartylate not only its cognate tRNA(Asp) but also tRNA(Asn). Reaction proceeds in two steps L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp Asn) | |
LCADNNJD_00861 | 1.7e-132 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
LCADNNJD_00862 | 2.8e-154 | gluB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LCADNNJD_00863 | 1.1e-113 | gluC | E | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00864 | 5e-178 | gluD | E | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_00865 | 8.7e-51 | S | Aminoacyl-tRNA editing domain | |||
LCADNNJD_00866 | 5.8e-25 | S | Aminoacyl-tRNA editing domain | |||
LCADNNJD_00867 | 3.1e-174 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
LCADNNJD_00868 | 0.0 | L | DEAD DEAH box helicase | |||
LCADNNJD_00869 | 1.9e-230 | rarA | L | Recombination factor protein RarA | ||
LCADNNJD_00870 | 2.7e-46 | yhbY | J | CRS1_YhbY | ||
LCADNNJD_00871 | 1.8e-209 | macA | 1.1.1.61, 1.3.1.32 | C | Iron-containing alcohol dehydrogenase | |
LCADNNJD_00872 | 1.6e-108 | 1.1.1.65 | C | Aldo/keto reductase family | ||
LCADNNJD_00873 | 8.9e-243 | yhjX | EGP | Major facilitator Superfamily | ||
LCADNNJD_00874 | 4.5e-95 | 1.5.1.40 | S | NADP oxidoreductase coenzyme F420-dependent | ||
LCADNNJD_00875 | 7.6e-54 | K | HxlR-like helix-turn-helix | |||
LCADNNJD_00876 | 1.6e-66 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
LCADNNJD_00877 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
LCADNNJD_00878 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
LCADNNJD_00879 | 1.4e-116 | S | Fic/DOC family | |||
LCADNNJD_00881 | 1.1e-191 | livK | E | Receptor family ligand binding region | ||
LCADNNJD_00882 | 6.6e-117 | U | Belongs to the binding-protein-dependent transport system permease family | |||
LCADNNJD_00883 | 6.5e-183 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
LCADNNJD_00884 | 5.2e-148 | E | Branched-chain amino acid ATP-binding cassette transporter | |||
LCADNNJD_00885 | 1.6e-123 | livF | E | ATPases associated with a variety of cellular activities | ||
LCADNNJD_00886 | 6.3e-37 | ywhH | S | Cys-tRNA(Pro) hydrolase activity | ||
LCADNNJD_00888 | 1.1e-227 | G | MFS/sugar transport protein | |||
LCADNNJD_00889 | 3.8e-72 | K | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_00890 | 3.9e-232 | pip | S | YhgE Pip domain protein | ||
LCADNNJD_00891 | 9.9e-304 | pip | S | YhgE Pip domain protein | ||
LCADNNJD_00897 | 2e-208 | S | Putative ABC-transporter type IV | |||
LCADNNJD_00898 | 6.9e-41 | pilA | NU | Prokaryotic N-terminal methylation motif | ||
LCADNNJD_00899 | 1.9e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LCADNNJD_00900 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LCADNNJD_00901 | 2.5e-72 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LCADNNJD_00902 | 2.9e-32 | nrdH | O | Glutaredoxin | ||
LCADNNJD_00903 | 3.7e-274 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
LCADNNJD_00904 | 3e-142 | pgl | 3.1.1.31 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LCADNNJD_00905 | 1.7e-17 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | |||
LCADNNJD_00906 | 9.2e-181 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LCADNNJD_00907 | 6e-304 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LCADNNJD_00908 | 1.1e-125 | 3.2.2.9 | F | Phosphorylase superfamily | ||
LCADNNJD_00910 | 1.2e-42 | XAC3035 | O | Glutaredoxin | ||
LCADNNJD_00911 | 1.8e-111 | E | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_00912 | 6.9e-126 | tcyA | ET | Bacterial periplasmic substrate-binding proteins | ||
LCADNNJD_00913 | 2e-132 | 3.6.3.21 | E | ATPases associated with a variety of cellular activities | ||
LCADNNJD_00914 | 4.6e-311 | pepD | E | Peptidase family C69 | ||
LCADNNJD_00915 | 4.9e-192 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
LCADNNJD_00916 | 1.6e-109 | icaR | K | Bacterial regulatory proteins, tetR family | ||
LCADNNJD_00919 | 2.5e-154 | ftsY | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Acts as a receptor for the complex formed by the signal recognition particle (SRP) and the ribosome-nascent chain (RNC) | ||
LCADNNJD_00920 | 5.8e-193 | napA | P | Sodium/hydrogen exchanger family | ||
LCADNNJD_00921 | 2.5e-237 | amt | U | Ammonium Transporter Family | ||
LCADNNJD_00922 | 1.9e-210 | amt | U | Ammonium Transporter Family | ||
LCADNNJD_00923 | 1.3e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
LCADNNJD_00924 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
LCADNNJD_00925 | 1.1e-262 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LCADNNJD_00926 | 4.1e-231 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
LCADNNJD_00927 | 6.8e-150 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
LCADNNJD_00928 | 6.4e-29 | S | granule-associated protein | |||
LCADNNJD_00929 | 1.4e-286 | ubiB | S | ABC1 family | ||
LCADNNJD_00930 | 1.2e-186 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
LCADNNJD_00931 | 1.3e-114 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
LCADNNJD_00932 | 1.6e-84 | |||||
LCADNNJD_00933 | 2e-181 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
LCADNNJD_00935 | 0.0 | ppk | 2.7.4.1 | P | Catalyzes the reversible transfer of the terminal phosphate of ATP to form a long-chain polyphosphate (polyP) | |
LCADNNJD_00937 | 3.2e-106 | cpaE | D | bacterial-type flagellum organization | ||
LCADNNJD_00939 | 1.4e-175 | cpaF | U | Type II IV secretion system protein | ||
LCADNNJD_00940 | 6.4e-67 | U | Type ii secretion system | |||
LCADNNJD_00941 | 1.4e-53 | gspF | NU | Type II secretion system (T2SS), protein F | ||
LCADNNJD_00942 | 4.8e-29 | S | Protein of unknown function (DUF4244) | |||
LCADNNJD_00943 | 2.1e-33 | U | TadE-like protein | |||
LCADNNJD_00944 | 5.1e-10 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
LCADNNJD_00945 | 1.6e-310 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
LCADNNJD_00946 | 2.7e-103 | recR | L | May play a role in DNA repair. It seems to be involved in an RecBC-independent recombinational process of DNA repair. It may act with RecF and RecO | ||
LCADNNJD_00947 | 9.1e-136 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
LCADNNJD_00948 | 1.6e-92 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
LCADNNJD_00949 | 5.3e-214 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
LCADNNJD_00950 | 2.1e-188 | 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) | |
LCADNNJD_00951 | 2.3e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LCADNNJD_00952 | 3.3e-62 | ssb1 | L | Single-stranded DNA-binding protein | ||
LCADNNJD_00953 | 2e-36 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
LCADNNJD_00954 | 1.1e-69 | rplI | J | Binds to the 23S rRNA | ||
LCADNNJD_00955 | 3.5e-91 | pgdA | 3.5.1.104 | G | Polysaccharide deacetylase | |
LCADNNJD_00956 | 8e-158 | 3.6.1.27 | I | PAP2 superfamily | ||
LCADNNJD_00957 | 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 | |
LCADNNJD_00958 | 1.1e-90 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LCADNNJD_00959 | 5.4e-193 | holB | 2.7.7.7 | L | DNA polymerase III | |
LCADNNJD_00960 | 6.4e-124 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_00961 | 5.5e-32 | ptsH | G | PTS HPr component phosphorylation site | ||
LCADNNJD_00962 | 2.7e-286 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
LCADNNJD_00963 | 3.5e-100 | S | Phosphatidylethanolamine-binding protein | |||
LCADNNJD_00964 | 7.6e-310 | pepD | E | Peptidase family C69 | ||
LCADNNJD_00965 | 1.2e-285 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
LCADNNJD_00967 | 3.9e-154 | pilT | NU | Type II/IV secretion system protein | ||
LCADNNJD_00968 | 1.9e-56 | S | Macrophage migration inhibitory factor (MIF) | |||
LCADNNJD_00970 | 3.6e-73 | S | GtrA-like protein | |||
LCADNNJD_00971 | 4.5e-207 | EGP | Major facilitator Superfamily | |||
LCADNNJD_00972 | 3.3e-102 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LCADNNJD_00973 | 5.2e-50 | |||||
LCADNNJD_00974 | 1.7e-22 | S | Protein of unknown function (DUF805) | |||
LCADNNJD_00975 | 9.2e-297 | gltX | 6.1.1.17 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
LCADNNJD_00978 | 3.3e-218 | S | Calcineurin-like phosphoesterase | |||
LCADNNJD_00979 | 9.1e-134 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
LCADNNJD_00980 | 5.3e-267 | leuC | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
LCADNNJD_00981 | 1.9e-129 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
LCADNNJD_00982 | 7.5e-18 | leuD | 4.2.1.33, 4.2.1.35 | E | Catalyzes the isomerization between 2-isopropylmalate and 3-isopropylmalate, via the formation of 2-isopropylmaleate | |
LCADNNJD_00983 | 1.4e-68 | frataxin | S | Domain of unknown function (DU1801) | ||
LCADNNJD_00984 | 9.1e-199 | pyrD | 1.3.1.14 | F | Dihydroorotate dehydrogenase | |
LCADNNJD_00985 | 7e-156 | L | Excalibur calcium-binding domain | |||
LCADNNJD_00986 | 9.2e-253 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LCADNNJD_00987 | 3.8e-302 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
LCADNNJD_00988 | 4.1e-160 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LCADNNJD_00989 | 8.1e-174 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LCADNNJD_00990 | 8.3e-174 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
LCADNNJD_00991 | 1.4e-209 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
LCADNNJD_00992 | 4.7e-143 | S | CAAX protease self-immunity | |||
LCADNNJD_00993 | 5.8e-122 | M | Mechanosensitive ion channel | |||
LCADNNJD_00994 | 2e-189 | CP_0417 | 3.1.1.3 | S | Protein of unknown function (DUF2974) | |
LCADNNJD_00995 | 3e-100 | K | Bacterial regulatory proteins, tetR family | |||
LCADNNJD_00996 | 8.2e-119 | S | Putative ABC-transporter type IV | |||
LCADNNJD_00997 | 3.6e-259 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
LCADNNJD_00998 | 4.1e-187 | yxiO | S | Vacuole effluxer Atg22 like | ||
LCADNNJD_00999 | 1.4e-179 | yegV | G | pfkB family carbohydrate kinase | ||
LCADNNJD_01000 | 4e-32 | rpmB | J | Ribosomal L28 family | ||
LCADNNJD_01001 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
LCADNNJD_01002 | 7.2e-104 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
LCADNNJD_01003 | 1.1e-101 | XK27_02070 | S | Nitroreductase family | ||
LCADNNJD_01004 | 1.3e-92 | K | helix_turn_helix, Lux Regulon | |||
LCADNNJD_01006 | 4e-130 | 3.2.1.8 | S | alpha beta | ||
LCADNNJD_01007 | 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 | ||
LCADNNJD_01008 | 7.9e-111 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
LCADNNJD_01010 | 9.6e-84 | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | ||
LCADNNJD_01011 | 6.8e-166 | iunH1 | 3.2.2.1 | F | nucleoside hydrolase | |
LCADNNJD_01012 | 1.9e-171 | P | NMT1/THI5 like | |||
LCADNNJD_01013 | 2.1e-106 | yijF | S | Domain of unknown function (DUF1287) | ||
LCADNNJD_01014 | 8.7e-113 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
LCADNNJD_01015 | 0.0 | S | Uncharacterised protein family (UPF0182) | |||
LCADNNJD_01016 | 5.7e-138 | ybbL | V | ATPases associated with a variety of cellular activities | ||
LCADNNJD_01017 | 1.1e-132 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
LCADNNJD_01018 | 2.1e-222 | rutG | F | Permease family | ||
LCADNNJD_01019 | 8.2e-159 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LCADNNJD_01020 | 2.6e-92 | M | L,D-transpeptidase catalytic domain | |||
LCADNNJD_01022 | 4.1e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LCADNNJD_01023 | 1.5e-141 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LCADNNJD_01024 | 3.1e-259 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
LCADNNJD_01025 | 0.0 | tcsS2 | T | Histidine kinase | ||
LCADNNJD_01026 | 1.4e-277 | S | Predicted membrane protein (DUF2207) | |||
LCADNNJD_01027 | 2.7e-94 | S | Predicted membrane protein (DUF2207) | |||
LCADNNJD_01028 | 4.6e-124 | K | helix_turn_helix, Lux Regulon | |||
LCADNNJD_01029 | 0.0 | MV | MacB-like periplasmic core domain | |||
LCADNNJD_01030 | 1.2e-141 | V | ABC transporter, ATP-binding protein | |||
LCADNNJD_01031 | 8.8e-89 | P | Cobalt transport protein | |||
LCADNNJD_01032 | 4.8e-208 | 3.6.3.24 | P | AAA domain, putative AbiEii toxin, Type IV TA system | ||
LCADNNJD_01033 | 3.7e-88 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
LCADNNJD_01034 | 2.2e-288 | E | ABC transporter, substrate-binding protein, family 5 | |||
LCADNNJD_01035 | 5.3e-253 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
LCADNNJD_01036 | 6.4e-157 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
LCADNNJD_01037 | 1.9e-52 | yraN | L | Belongs to the UPF0102 family | ||
LCADNNJD_01038 | 1.3e-234 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
LCADNNJD_01039 | 1.6e-158 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
LCADNNJD_01040 | 1.1e-48 | ybaZ | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
LCADNNJD_01041 | 5.6e-296 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
LCADNNJD_01042 | 1.2e-132 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
LCADNNJD_01043 | 2.3e-66 | safC | S | O-methyltransferase | ||
LCADNNJD_01044 | 1.9e-122 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
LCADNNJD_01045 | 4.8e-215 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
LCADNNJD_01047 | 1.1e-212 | clpX | O | ATP-dependent specificity component of the Clp protease. It directs the protease to specific substrates. Can perform chaperone functions in the absence of ClpP | ||
LCADNNJD_01048 | 4.4e-118 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
LCADNNJD_01049 | 9.7e-112 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
LCADNNJD_01050 | 1.3e-225 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
LCADNNJD_01051 | 1.7e-214 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
LCADNNJD_01052 | 4e-54 | S | Protein of unknown function (DUF3000) | |||
LCADNNJD_01053 | 1e-165 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
LCADNNJD_01054 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
LCADNNJD_01055 | 1.1e-29 | |||||
LCADNNJD_01056 | 0.0 | nadE | 6.3.1.5, 6.3.5.1 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses L-glutamine as a nitrogen source | |
LCADNNJD_01057 | 4.1e-217 | S | Peptidase dimerisation domain | |||
LCADNNJD_01058 | 5.1e-117 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01059 | 1.8e-201 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LCADNNJD_01060 | 2.7e-159 | metQ | P | NLPA lipoprotein | ||
LCADNNJD_01061 | 1.4e-155 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LCADNNJD_01062 | 1.3e-101 | ppiA | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
LCADNNJD_01063 | 0.0 | relA | 2.7.6.5, 3.1.7.2 | 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 | |
LCADNNJD_01064 | 5.4e-78 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | This enzyme is involved in nucleotide metabolism it produces dUMP, the immediate precursor of thymidine nucleotides and it decreases the intracellular concentration of dUTP so that uracil cannot be incorporated into DNA | |
LCADNNJD_01065 | 1.2e-43 | S | Domain of unknown function (DUF4193) | |||
LCADNNJD_01066 | 8e-115 | S | Protein of unknown function (DUF3071) | |||
LCADNNJD_01067 | 4.4e-185 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
LCADNNJD_01068 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LCADNNJD_01069 | 1.1e-220 | G | Major Facilitator Superfamily | |||
LCADNNJD_01070 | 8.1e-35 | yozG | K | Cro/C1-type HTH DNA-binding domain | ||
LCADNNJD_01071 | 1.8e-62 | S | Protein of unknown function (DUF2975) | |||
LCADNNJD_01072 | 4.8e-248 | ftsZ | M | Domain of unknown function (DUF4173) | ||
LCADNNJD_01073 | 1.3e-215 | 2.4.1.345 | GT4 | M | Glycosyl transferase 4-like domain | |
LCADNNJD_01074 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LCADNNJD_01075 | 3.4e-179 | 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 | ||
LCADNNJD_01076 | 3.7e-95 | |||||
LCADNNJD_01077 | 1.4e-137 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
LCADNNJD_01078 | 2.2e-294 | pknL | 2.7.11.1 | KLT | PASTA | |
LCADNNJD_01079 | 1.2e-121 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LCADNNJD_01080 | 1.3e-33 | |||||
LCADNNJD_01081 | 1.6e-183 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
LCADNNJD_01082 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
LCADNNJD_01083 | 2.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LCADNNJD_01084 | 3.6e-65 | recX | S | Modulates RecA activity | ||
LCADNNJD_01085 | 7.8e-187 | recA | L | Can catalyze the hydrolysis of ATP in the presence of single-stranded DNA, the ATP-dependent uptake of single-stranded DNA by duplex DNA, and the ATP-dependent hybridization of homologous single-stranded DNAs. It interacts with LexA causing its activation and leading to its autocatalytic cleavage | ||
LCADNNJD_01086 | 2.8e-35 | S | Protein of unknown function (DUF3046) | |||
LCADNNJD_01087 | 3.2e-68 | K | Helix-turn-helix XRE-family like proteins | |||
LCADNNJD_01088 | 1.8e-69 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LCADNNJD_01089 | 3.1e-105 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LCADNNJD_01090 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
LCADNNJD_01091 | 8.8e-177 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
LCADNNJD_01092 | 3.4e-269 | miaB | 2.8.4.3 | H | Catalyzes the methylthiolation of N6- (dimethylallyl)adenosine (i(6)A), leading to the formation of 2- methylthio-N6-(dimethylallyl)adenosine (ms(2)i(6)A) at position 37 in tRNAs that read codons beginning with uridine | |
LCADNNJD_01093 | 8.1e-113 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
LCADNNJD_01094 | 9.5e-276 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 3.5.99.2 | H | Phosphomethylpyrimidine kinase | |
LCADNNJD_01095 | 3.7e-134 | ydeD | EG | EamA-like transporter family | ||
LCADNNJD_01096 | 1.1e-108 | ybhL | S | Belongs to the BI1 family | ||
LCADNNJD_01097 | 3.2e-87 | |||||
LCADNNJD_01098 | 1.3e-296 | S | Protein of unknown function DUF262 | |||
LCADNNJD_01099 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
LCADNNJD_01100 | 0.0 | ctpE | P | E1-E2 ATPase | ||
LCADNNJD_01101 | 2.3e-143 | rlrG | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LCADNNJD_01102 | 0.0 | 4.2.1.53 | S | MCRA family | ||
LCADNNJD_01103 | 2.4e-163 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
LCADNNJD_01104 | 8.8e-86 | |||||
LCADNNJD_01105 | 1.4e-55 | gloA3 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
LCADNNJD_01106 | 2.1e-143 | arsB | P | PFAM Bile acid sodium symporter | ||
LCADNNJD_01107 | 1.3e-29 | arsR | K | regulatory protein, arsR | ||
LCADNNJD_01108 | 5.7e-231 | trmA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LCADNNJD_01109 | 5.4e-114 | S | Protein of unknown function (DUF3159) | |||
LCADNNJD_01110 | 1.4e-122 | S | Protein of unknown function (DUF3710) | |||
LCADNNJD_01111 | 1.9e-146 | cobB2 | K | Sir2 family | ||
LCADNNJD_01112 | 3.2e-229 | tdcB | 4.3.1.19 | E | Pyridoxal-phosphate dependent enzyme | |
LCADNNJD_01113 | 0.0 | 3.2.1.10 | GH13 | G | Alpha amylase, catalytic domain protein | |
LCADNNJD_01114 | 0.0 | rafA | 3.2.1.22 | G | Raffinose synthase or seed imbibition protein Sip1 | |
LCADNNJD_01115 | 4.1e-201 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
LCADNNJD_01116 | 9.7e-128 | G | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01117 | 6e-80 | G | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01118 | 6.1e-146 | G | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01119 | 4.2e-167 | G | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01120 | 2.2e-243 | msmE7 | G | Bacterial extracellular solute-binding protein | ||
LCADNNJD_01121 | 2.2e-232 | nagC | GK | ROK family | ||
LCADNNJD_01122 | 4.9e-64 | S | Domain of unknown function (DUF5067) | |||
LCADNNJD_01123 | 1.8e-177 | T | Histidine kinase | |||
LCADNNJD_01124 | 1.2e-118 | K | helix_turn_helix, Lux Regulon | |||
LCADNNJD_01125 | 2.8e-138 | S | membrane transporter protein | |||
LCADNNJD_01126 | 0.0 | 3.2.1.22 | G | Glycosyl hydrolase family 36 N-terminal domain | ||
LCADNNJD_01127 | 8.8e-72 | tadA | 3.5.4.1, 3.5.4.33, 3.8.1.5, 6.3.4.19 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
LCADNNJD_01128 | 0.0 | yjcE | P | Sodium/hydrogen exchanger family | ||
LCADNNJD_01129 | 6.3e-134 | ypfH | S | Phospholipase/Carboxylesterase | ||
LCADNNJD_01130 | 6.8e-91 | |||||
LCADNNJD_01131 | 0.0 | pacL2 | 3.6.3.8 | P | Cation transporter/ATPase, N-terminus | |
LCADNNJD_01132 | 1.5e-170 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LCADNNJD_01133 | 1.5e-259 | KLT | Domain of unknown function (DUF4032) | |||
LCADNNJD_01134 | 6.9e-209 | ugpC | E | Belongs to the ABC transporter superfamily | ||
LCADNNJD_01136 | 1.1e-221 | KLT | Protein tyrosine kinase | |||
LCADNNJD_01137 | 8.2e-89 | O | Thioredoxin | |||
LCADNNJD_01139 | 7.4e-177 | S | G5 | |||
LCADNNJD_01140 | 2.7e-129 | ksgA | 2.1.1.182, 2.1.1.184 | 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 | |
LCADNNJD_01141 | 1.8e-106 | 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 | |
LCADNNJD_01142 | 2.9e-92 | S | LytR cell envelope-related transcriptional attenuator | |||
LCADNNJD_01143 | 2.5e-243 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
LCADNNJD_01144 | 2.4e-113 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
LCADNNJD_01145 | 6.2e-225 | |||||
LCADNNJD_01146 | 0.0 | murJ | KLT | MviN-like protein | ||
LCADNNJD_01147 | 2.8e-139 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LCADNNJD_01149 | 8.2e-128 | parB | K | Belongs to the ParB family | ||
LCADNNJD_01150 | 1.5e-153 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LCADNNJD_01152 | 1.9e-100 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
LCADNNJD_01153 | 2.9e-83 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
LCADNNJD_01154 | 2.2e-166 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
LCADNNJD_01155 | 5.9e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
LCADNNJD_01156 | 1.9e-243 | dnaA | L | it binds specifically double-stranded DNA at a 9 bp consensus (dnaA box) 5'-TTATC CA A CA A-3'. DnaA binds to ATP and to acidic phospholipids | ||
LCADNNJD_01157 | 2.9e-191 | dnaN | 2.7.7.7 | L | Confers DNA tethering and processivity to DNA polymerases and other proteins. Acts as a clamp, forming a ring around DNA (a reaction catalyzed by the clamp-loading complex) which diffuses in an ATP-independent manner freely and bidirectionally along dsDNA. Initially characterized for its ability to contact the catalytic subunit of DNA polymerase III (Pol III), a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria | |
LCADNNJD_01158 | 3.6e-157 | recF | L | it is required for DNA replication and normal SOS inducibility. RecF binds preferentially to single-stranded, linear DNA. It also seems to bind ATP | ||
LCADNNJD_01159 | 3.9e-68 | S | Protein of unknown function (DUF721) | |||
LCADNNJD_01160 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
LCADNNJD_01161 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
LCADNNJD_01162 | 9.8e-62 | S | Transmembrane domain of unknown function (DUF3566) | |||
LCADNNJD_01163 | 8.8e-202 | I | Serine aminopeptidase, S33 | |||
LCADNNJD_01164 | 4.7e-179 | V | VanZ like family | |||
LCADNNJD_01165 | 6.4e-254 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LCADNNJD_01166 | 1e-41 | 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 | ||
LCADNNJD_01169 | 1e-125 | S | SOS response associated peptidase (SRAP) | |||
LCADNNJD_01170 | 1.4e-128 | S | Protein of unknown function DUF45 | |||
LCADNNJD_01171 | 3e-238 | ytfL | P | Transporter associated domain | ||
LCADNNJD_01172 | 9.8e-98 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LCADNNJD_01174 | 5e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
LCADNNJD_01175 | 1e-307 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
LCADNNJD_01176 | 7.2e-18 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
LCADNNJD_01177 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LCADNNJD_01178 | 4.5e-288 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LCADNNJD_01179 | 2e-111 | dcd | 3.5.4.13 | F | Belongs to the dCTP deaminase family | |
LCADNNJD_01180 | 2.7e-227 | malY | 4.4.1.8 | E | Aminotransferase, class I II | |
LCADNNJD_01181 | 1.1e-23 | |||||
LCADNNJD_01182 | 2.6e-194 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
LCADNNJD_01183 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
LCADNNJD_01184 | 1.7e-125 | fhaA | T | Protein of unknown function (DUF2662) | ||
LCADNNJD_01185 | 4.7e-59 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LCADNNJD_01186 | 4.8e-243 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
LCADNNJD_01187 | 8.6e-230 | rodA | D | Belongs to the SEDS family | ||
LCADNNJD_01188 | 2.3e-241 | pbpA | M | penicillin-binding protein | ||
LCADNNJD_01189 | 1.2e-178 | T | Protein tyrosine kinase | |||
LCADNNJD_01190 | 3.5e-304 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
LCADNNJD_01191 | 2.2e-107 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
LCADNNJD_01193 | 7.7e-191 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
LCADNNJD_01194 | 8e-148 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
LCADNNJD_01195 | 5.3e-185 | exeA | S | Peptidase_C39 like family | ||
LCADNNJD_01196 | 3.3e-274 | P | Oligopeptide/dipeptide transporter, C-terminal region | |||
LCADNNJD_01197 | 4.3e-146 | EP | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01198 | 1.5e-167 | U | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01199 | 4.1e-279 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LCADNNJD_01200 | 1.2e-241 | codA | 3.5.4.1 | F | Amidohydrolase family | |
LCADNNJD_01201 | 4e-281 | U | Permease for cytosine/purines, uracil, thiamine, allantoin | |||
LCADNNJD_01202 | 3.5e-278 | purR | QT | Purine catabolism regulatory protein-like family | ||
LCADNNJD_01203 | 6.8e-256 | codA | 3.5.4.1, 3.5.4.21 | F | Amidohydrolase family | |
LCADNNJD_01204 | 1e-277 | EK | Alanine-glyoxylate amino-transferase | |||
LCADNNJD_01205 | 3.4e-249 | 3.2.1.58 | G | Belongs to the glycosyl hydrolase 5 (cellulase A) family | ||
LCADNNJD_01206 | 6.9e-241 | M | Glycosyltransferase like family 2 | |||
LCADNNJD_01207 | 3.2e-151 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LCADNNJD_01208 | 7.3e-112 | pdxT | 4.3.3.6 | H | Catalyzes the hydrolysis of glutamine to glutamate and ammonia as part of the biosynthesis of pyridoxal 5'-phosphate. The resulting ammonia molecule is channeled to the active site of PdxS | |
LCADNNJD_01209 | 2.8e-157 | pdxS | 4.3.3.6 | H | Catalyzes the formation of pyridoxal 5'-phosphate from ribose 5-phosphate (RBP), glyceraldehyde 3-phosphate (G3P) and ammonia. The ammonia is provided by the PdxT subunit. Can also use ribulose 5-phosphate and dihydroxyacetone phosphate as substrates, resulting from enzyme-catalyzed isomerization of RBP and G3P, respectively | |
LCADNNJD_01211 | 0.0 | cadA | P | E1-E2 ATPase | ||
LCADNNJD_01212 | 8.7e-70 | gepA | S | Protein of unknown function (DUF4065) | ||
LCADNNJD_01213 | 3.1e-195 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
LCADNNJD_01214 | 2.5e-283 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LCADNNJD_01215 | 7.4e-175 | htpX | O | Belongs to the peptidase M48B family | ||
LCADNNJD_01216 | 2.5e-54 | ybjG | 3.6.1.27 | I | Psort location CytoplasmicMembrane, score | |
LCADNNJD_01217 | 2.1e-67 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LCADNNJD_01218 | 1.3e-166 | yddG | EG | EamA-like transporter family | ||
LCADNNJD_01221 | 5.9e-135 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
LCADNNJD_01222 | 5.2e-198 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
LCADNNJD_01223 | 1.1e-196 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
LCADNNJD_01224 | 0.0 | L | SNF2 family N-terminal domain | |||
LCADNNJD_01225 | 7e-67 | S | Domain of unknown function (DUF4391) | |||
LCADNNJD_01226 | 5.1e-178 | 2.1.1.72 | L | DNA methylase | ||
LCADNNJD_01227 | 2.2e-114 | S | Psort location Cytoplasmic, score | |||
LCADNNJD_01228 | 0.0 | res | 3.1.21.5 | V | Type III restriction enzyme, res subunit | |
LCADNNJD_01229 | 2.3e-256 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
LCADNNJD_01230 | 1.7e-72 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LCADNNJD_01231 | 1.2e-49 | crcB | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LCADNNJD_01232 | 2.8e-288 | clcA | P | Voltage gated chloride channel | ||
LCADNNJD_01234 | 1e-209 | U | Belongs to the binding-protein-dependent transport system permease family | |||
LCADNNJD_01235 | 1.6e-153 | livM | U | Belongs to the binding-protein-dependent transport system permease family | ||
LCADNNJD_01236 | 1e-196 | natA | E | Branched-chain amino acid ATP-binding cassette transporter | ||
LCADNNJD_01237 | 5.7e-142 | livF | E | ATPases associated with a variety of cellular activities | ||
LCADNNJD_01238 | 9.5e-202 | natB | E | Receptor family ligand binding region | ||
LCADNNJD_01239 | 7.8e-84 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LCADNNJD_01240 | 3.6e-50 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LCADNNJD_01241 | 2.5e-142 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_01242 | 3.1e-123 | K | FCD | |||
LCADNNJD_01243 | 5.2e-209 | C | Acetamidase/Formamidase family | |||
LCADNNJD_01244 | 3.6e-225 | clcA_2 | P | Voltage gated chloride channel | ||
LCADNNJD_01245 | 7.2e-27 | S | Protein of unknown function (DUF1653) | |||
LCADNNJD_01246 | 2.3e-284 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
LCADNNJD_01247 | 3.4e-262 | G | Transporter major facilitator family protein | |||
LCADNNJD_01248 | 4.8e-249 | yhjE | EGP | Sugar (and other) transporter | ||
LCADNNJD_01249 | 4.2e-200 | ilvC | 1.1.1.86 | H | Involved in the biosynthesis of branched-chain amino acids (BCAA). Catalyzes an alkyl-migration followed by a ketol- acid reduction of (S)-2-acetolactate (S2AL) to yield (R)-2,3- dihydroxy-isovalerate. In the isomerase reaction, S2AL is rearranged via a Mg-dependent methyl migration to produce 3- hydroxy-3-methyl-2-ketobutyrate (HMKB). In the reductase reaction, this 2-ketoacid undergoes a metal-dependent reduction by NADPH to yield (R)-2,3-dihydroxy-isovalerate | |
LCADNNJD_01250 | 3.9e-54 | E | GDSL-like Lipase/Acylhydrolase family | |||
LCADNNJD_01251 | 2.1e-170 | 3.1.1.53 | E | Carbohydrate esterase, sialic acid-specific acetylesterase | ||
LCADNNJD_01252 | 7.8e-146 | E | GDSL-like Lipase/Acylhydrolase family | |||
LCADNNJD_01253 | 5.1e-198 | bglA | 3.2.1.21 | G | Glycosyl hydrolase family 1 | |
LCADNNJD_01255 | 1.2e-197 | G | Bacterial extracellular solute-binding protein | |||
LCADNNJD_01256 | 3.6e-124 | U | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01257 | 2.9e-133 | malG | U | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01258 | 0.0 | 3.2.1.25 | G | beta-mannosidase | ||
LCADNNJD_01259 | 3.5e-159 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_01260 | 6.8e-47 | S | Protein of unknown function, DUF624 | |||
LCADNNJD_01261 | 2.6e-52 | |||||
LCADNNJD_01262 | 1.3e-119 | natA | V | ATPases associated with a variety of cellular activities | ||
LCADNNJD_01263 | 2e-167 | |||||
LCADNNJD_01265 | 1.9e-191 | yihS | 5.1.3.11 | G | N-acylglucosamine 2-epimerase (GlcNAc 2-epimerase) | |
LCADNNJD_01266 | 1.6e-256 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
LCADNNJD_01267 | 9e-10 | K | Transcriptional regulator C-terminal region | |||
LCADNNJD_01268 | 6.7e-15 | K | Transcriptional regulator C-terminal region | |||
LCADNNJD_01269 | 6.3e-99 | S | Protein of unknown function, DUF624 | |||
LCADNNJD_01270 | 0.0 | malQ | 2.4.1.18, 2.4.1.25, 3.2.1.196, 5.4.99.15 | CBM48,GH13,GH77 | G | 4-alpha-glucanotransferase |
LCADNNJD_01271 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LCADNNJD_01272 | 6.6e-154 | malG | G | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01273 | 2.1e-231 | malF | G | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01274 | 8.3e-203 | malE | G | Bacterial extracellular solute-binding protein | ||
LCADNNJD_01275 | 1.9e-289 | malL | 3.2.1.1, 5.4.99.16 | GH13 | G | Alpha-amylase domain |
LCADNNJD_01276 | 1.6e-113 | S | HAD-hyrolase-like | |||
LCADNNJD_01277 | 4.9e-113 | traX | S | TraX protein | ||
LCADNNJD_01278 | 2.2e-174 | K | Psort location Cytoplasmic, score | |||
LCADNNJD_01279 | 2.5e-74 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
LCADNNJD_01280 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
LCADNNJD_01281 | 1e-62 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
LCADNNJD_01282 | 7.9e-156 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
LCADNNJD_01283 | 4.2e-82 | hspR | K | transcriptional regulator, MerR family | ||
LCADNNJD_01284 | 3.6e-89 | S | HAD hydrolase, family IA, variant 3 | |||
LCADNNJD_01285 | 7.4e-113 | mgtC | S | MgtC family | ||
LCADNNJD_01287 | 8.1e-130 | dedA | S | SNARE associated Golgi protein | ||
LCADNNJD_01288 | 5.5e-285 | pmt | 2.4.1.109 | GT39 | O | C-terminal four TMM region of protein-O-mannosyltransferase |
LCADNNJD_01289 | 2.4e-165 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LCADNNJD_01290 | 2.7e-17 | |||||
LCADNNJD_01291 | 1.6e-58 | |||||
LCADNNJD_01292 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
LCADNNJD_01293 | 1.7e-187 | K | NAD-dependent protein deacetylase, SIR2 family | |||
LCADNNJD_01294 | 3.6e-160 | S | Appr-1'-p processing enzyme | |||
LCADNNJD_01295 | 6e-109 | S | NAD(P)H-binding | |||
LCADNNJD_01296 | 4.3e-56 | ydeP | K | HxlR-like helix-turn-helix | ||
LCADNNJD_01297 | 3.3e-251 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LCADNNJD_01298 | 1e-171 | tatD | L | TatD related DNase | ||
LCADNNJD_01299 | 0.0 | kup | P | Transport of potassium into the cell | ||
LCADNNJD_01300 | 7.1e-153 | S | Glutamine amidotransferase domain | |||
LCADNNJD_01301 | 7.2e-135 | T | HD domain | |||
LCADNNJD_01302 | 1e-119 | V | ABC transporter | |||
LCADNNJD_01303 | 4.6e-205 | V | ABC transporter permease | |||
LCADNNJD_01304 | 0.0 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LCADNNJD_01305 | 1.1e-39 | 2.7.11.1 | S | RDD family | ||
LCADNNJD_01306 | 4.1e-88 | L | Transposase and inactivated derivatives IS30 family | |||
LCADNNJD_01307 | 5.9e-208 | mgtA | 3.6.3.2 | P | PFAM E1-E2 ATPase-associated domain protein, Haloacid dehalogenase domain protein hydrolase, cation transporting ATPase domain protein | |
LCADNNJD_01308 | 4.8e-75 | IQ | KR domain | |||
LCADNNJD_01309 | 5.9e-296 | araA | 5.3.1.4 | G | Catalyzes the conversion of L-arabinose to L-ribulose | |
LCADNNJD_01310 | 6.3e-124 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
LCADNNJD_01311 | 1.9e-255 | araB | 2.7.1.16 | G | FGGY family of carbohydrate kinases, C-terminal domain | |
LCADNNJD_01312 | 6.4e-207 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_01313 | 1.5e-124 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LCADNNJD_01314 | 9.8e-149 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LCADNNJD_01315 | 6.6e-75 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
LCADNNJD_01316 | 0.0 | opuAB | P | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01317 | 1.1e-271 | abcT3 | P | ATPases associated with a variety of cellular activities | ||
LCADNNJD_01318 | 2.2e-158 | L | Transposase and inactivated derivatives IS30 family | |||
LCADNNJD_01319 | 1.4e-21 | L | Phage integrase, N-terminal SAM-like domain | |||
LCADNNJD_01321 | 2.6e-112 | |||||
LCADNNJD_01322 | 7.3e-89 | bcp | 1.11.1.15 | O | Redoxin | |
LCADNNJD_01323 | 3.9e-160 | S | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_01324 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_01325 | 3.6e-83 | S | Domain of unknown function (DUF4194) | |||
LCADNNJD_01326 | 1e-239 | S | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_01327 | 5e-191 | cat | P | Cation efflux family | ||
LCADNNJD_01328 | 1.4e-83 | hsp20 | O | Hsp20/alpha crystallin family | ||
LCADNNJD_01331 | 1.5e-149 | S | Calcineurin-like phosphoesterase | |||
LCADNNJD_01332 | 0.0 | leuA | 2.3.3.13 | E | Catalyzes the condensation of the acetyl group of acetyl-CoA with 3-methyl-2-oxobutanoate (2-oxoisovalerate) to form 3-carboxy-3-hydroxy-4-methylpentanoate (2-isopropylmalate) | |
LCADNNJD_01333 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LCADNNJD_01334 | 2.7e-216 | ino1 | 5.5.1.4 | I | Myo-inositol-1-phosphate synthase | |
LCADNNJD_01335 | 3.9e-231 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
LCADNNJD_01336 | 3e-120 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LCADNNJD_01338 | 1.3e-97 | |||||
LCADNNJD_01339 | 5.2e-153 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LCADNNJD_01340 | 2.3e-124 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
LCADNNJD_01341 | 2.1e-35 | acyP | 3.6.1.7 | C | Acylphosphatase | |
LCADNNJD_01342 | 3.3e-72 | 3.4.21.105 | M | Sortase family | ||
LCADNNJD_01343 | 2.9e-85 | |||||
LCADNNJD_01344 | 7.2e-83 | 3.4.21.105 | M | Sortase family | ||
LCADNNJD_01345 | 7.9e-138 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_01346 | 2.8e-11 | bga1 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LCADNNJD_01347 | 2e-32 | |||||
LCADNNJD_01348 | 7.2e-48 | |||||
LCADNNJD_01351 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
LCADNNJD_01352 | 2.7e-81 | ribU | 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 | ||
LCADNNJD_01353 | 1.3e-169 | S | Glycosyltransferase, group 2 family protein | |||
LCADNNJD_01354 | 2e-138 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
LCADNNJD_01355 | 6.9e-183 | E | Aminotransferase class I and II | |||
LCADNNJD_01356 | 3.5e-106 | bioM | P | ATPases associated with a variety of cellular activities | ||
LCADNNJD_01357 | 1e-248 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LCADNNJD_01358 | 0.0 | S | Tetratricopeptide repeat | |||
LCADNNJD_01359 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
LCADNNJD_01360 | 3.1e-197 | mrp | D | Binds and transfers iron-sulfur (Fe-S) clusters to target apoproteins. Can hydrolyze ATP | ||
LCADNNJD_01361 | 4.1e-237 | int | L | Phage integrase, N-terminal SAM-like domain | ||
LCADNNJD_01362 | 9.3e-08 | |||||
LCADNNJD_01365 | 1.3e-243 | L | Phage integrase family | |||
LCADNNJD_01366 | 0.0 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
LCADNNJD_01368 | 9.8e-94 | S | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_01369 | 3e-38 | S | Type II restriction endonuclease EcoO109I | |||
LCADNNJD_01370 | 1.3e-214 | sinIM | 2.1.1.37 | H | C-5 cytosine-specific DNA methylase | |
LCADNNJD_01373 | 3.8e-38 | |||||
LCADNNJD_01374 | 3.5e-282 | glnA | 6.3.1.2 | E | glutamine synthetase | |
LCADNNJD_01375 | 3.2e-144 | S | Domain of unknown function (DUF4191) | |||
LCADNNJD_01376 | 5.4e-270 | lpdA | 1.16.1.1, 1.8.1.4 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LCADNNJD_01377 | 5.7e-88 | S | Protein of unknown function (DUF3043) | |||
LCADNNJD_01378 | 8e-260 | argE | E | Peptidase dimerisation domain | ||
LCADNNJD_01379 | 3.6e-106 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LCADNNJD_01380 | 6.4e-104 | ykoE | S | ABC-type cobalt transport system, permease component | ||
LCADNNJD_01381 | 0.0 | cbiQ | P | ATPases associated with a variety of cellular activities | ||
LCADNNJD_01384 | 5.4e-101 | ywlG | S | Protein of unknown function (DUF436) | ||
LCADNNJD_01385 | 6.7e-162 | IV02_28330 | 2.1.1.185, 2.1.1.34 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LCADNNJD_01386 | 3.5e-202 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LCADNNJD_01387 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LCADNNJD_01388 | 3.4e-45 | |||||
LCADNNJD_01389 | 4.2e-195 | 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 | |
LCADNNJD_01390 | 7.9e-208 | 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 | |
LCADNNJD_01391 | 1.8e-173 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LCADNNJD_01392 | 5.3e-229 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
LCADNNJD_01393 | 1.6e-182 | 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 | |
LCADNNJD_01394 | 1.9e-68 | argR | K | Regulates arginine biosynthesis genes | ||
LCADNNJD_01395 | 5e-237 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LCADNNJD_01396 | 1.3e-263 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
LCADNNJD_01397 | 1.6e-75 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LCADNNJD_01398 | 9.4e-99 | S | Putative ABC-transporter type IV | |||
LCADNNJD_01400 | 1.6e-244 | tyrS | 6.1.1.1 | J | Catalyzes the attachment of tyrosine to tRNA(Tyr) in a two-step reaction tyrosine is first activated by ATP to form Tyr- AMP and then transferred to the acceptor end of tRNA(Tyr) | |
LCADNNJD_01401 | 8.8e-141 | L | Tetratricopeptide repeat | |||
LCADNNJD_01402 | 1.8e-142 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
LCADNNJD_01404 | 5.1e-102 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LCADNNJD_01406 | 6.1e-77 | trkA | P | TrkA-N domain | ||
LCADNNJD_01407 | 8.2e-14 | trkA | P | TrkA-N domain | ||
LCADNNJD_01408 | 2.4e-123 | trkB | P | Cation transport protein | ||
LCADNNJD_01409 | 1.7e-62 | trkB | P | Cation transport protein | ||
LCADNNJD_01410 | 6e-150 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
LCADNNJD_01411 | 2.5e-245 | recN | L | May be involved in recombinational repair of damaged DNA | ||
LCADNNJD_01412 | 8.9e-116 | S | Haloacid dehalogenase-like hydrolase | |||
LCADNNJD_01413 | 3.5e-51 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
LCADNNJD_01414 | 5e-284 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
LCADNNJD_01415 | 8.3e-230 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
LCADNNJD_01416 | 2.9e-79 | |||||
LCADNNJD_01417 | 2e-127 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LCADNNJD_01418 | 1e-190 | 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) | |
LCADNNJD_01419 | 2.3e-73 | QT | Purine catabolism regulatory protein-like family | |||
LCADNNJD_01420 | 8.7e-192 | gabT | 2.6.1.19 | H | Aminotransferase class-III | |
LCADNNJD_01421 | 3.9e-128 | EP | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01422 | 3.4e-102 | EP | Binding-protein-dependent transport system inner membrane component | |||
LCADNNJD_01423 | 1.8e-124 | oppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
LCADNNJD_01424 | 3.5e-107 | P | ATPase activity | |||
LCADNNJD_01425 | 2.9e-208 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LCADNNJD_01426 | 4.2e-249 | gatA3 | 3.5.1.4, 6.3.5.6, 6.3.5.7 | J | Amidase | |
LCADNNJD_01427 | 3.8e-232 | S | Amidohydrolase family | |||
LCADNNJD_01428 | 1.6e-138 | 1.1.1.14 | C | Zinc-binding dehydrogenase | ||
LCADNNJD_01429 | 4e-60 | S | Phosphotransferase enzyme family | |||
LCADNNJD_01430 | 3.2e-160 | gabT | 2.6.1.19, 2.6.1.22 | H | Aminotransferase class-III | |
LCADNNJD_01431 | 5.2e-121 | smlA | P | Major facilitator Superfamily | ||
LCADNNJD_01432 | 9.7e-110 | L | Transposase and inactivated derivatives IS30 family | |||
LCADNNJD_01434 | 4.2e-60 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
LCADNNJD_01435 | 5.9e-62 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
LCADNNJD_01436 | 3e-60 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain protein | ||
LCADNNJD_01437 | 2e-113 | L | Phage integrase family | |||
LCADNNJD_01438 | 1.7e-80 | 3.1.21.3 | L | PFAM Type I restriction modification DNA specificity domain | ||
LCADNNJD_01439 | 2.5e-69 | V | Restriction endonuclease | |||
LCADNNJD_01440 | 3.9e-227 | hsdM | 2.1.1.72 | V | modification (methylase) protein of type I restriction-modification system K03427 | |
LCADNNJD_01441 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LCADNNJD_01443 | 7.2e-212 | G | Major Facilitator Superfamily | |||
LCADNNJD_01444 | 1.4e-167 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
LCADNNJD_01445 | 1.7e-216 | GK | ROK family | |||
LCADNNJD_01446 | 2e-64 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LCADNNJD_01447 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
LCADNNJD_01448 | 3e-87 | 3.6.1.55 | F | NUDIX domain | ||
LCADNNJD_01449 | 2.3e-277 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
LCADNNJD_01450 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
LCADNNJD_01451 | 5.8e-233 | 6.3.1.12 | S | ATP-grasp | ||
LCADNNJD_01452 | 5e-258 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
LCADNNJD_01453 | 2.6e-130 | dnaQ2 | 2.7.7.7 | L | Exonuclease | |
LCADNNJD_01454 | 1.1e-103 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
LCADNNJD_01455 | 2.4e-50 | |||||
LCADNNJD_01456 | 4e-162 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
LCADNNJD_01457 | 3.5e-168 | ispH | 1.17.7.4, 2.7.4.25 | IM | Catalyzes the conversion of 1-hydroxy-2-methyl-2-(E)- butenyl 4-diphosphate (HMBPP) into a mixture of isopentenyl diphosphate (IPP) and dimethylallyl diphosphate (DMAPP). Acts in the terminal step of the DOXP MEP pathway for isoprenoid precursor biosynthesis | |
LCADNNJD_01458 | 5.1e-90 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
LCADNNJD_01459 | 3e-198 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LCADNNJD_01460 | 1.2e-114 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
LCADNNJD_01461 | 8.1e-99 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
LCADNNJD_01462 | 1.3e-25 | rpmI | J | Ribosomal protein L35 | ||
LCADNNJD_01463 | 9e-60 | rplT | J | Binds directly to 23S ribosomal RNA and is necessary for the in vitro assembly process of the 50S ribosomal subunit. It is not involved in the protein synthesizing functions of that subunit | ||
LCADNNJD_01464 | 4.7e-142 | xerD | D | recombinase XerD | ||
LCADNNJD_01465 | 5.1e-147 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LCADNNJD_01466 | 6.1e-91 | 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 | ||
LCADNNJD_01467 | 3.3e-65 | 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 | ||
LCADNNJD_01468 | 0.0 | typA | T | Elongation factor G C-terminus | ||
LCADNNJD_01469 | 1.3e-69 | |||||
LCADNNJD_01470 | 1.7e-140 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
LCADNNJD_01471 | 8e-151 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
LCADNNJD_01473 | 3.2e-28 | |||||
LCADNNJD_01474 | 1.5e-123 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
LCADNNJD_01475 | 2.8e-296 | E | ABC transporter, substrate-binding protein, family 5 | |||
LCADNNJD_01476 | 4.1e-151 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01477 | 1.7e-168 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
LCADNNJD_01478 | 0.0 | dppD | EP | Oligopeptide/dipeptide transporter, C-terminal region | ||
LCADNNJD_01479 | 3e-164 | exoA | 3.1.11.2 | L | Endonuclease/Exonuclease/phosphatase family | |
LCADNNJD_01480 | 3e-235 | S | UPF0210 protein | |||
LCADNNJD_01481 | 2.5e-40 | gcvR | T | Belongs to the UPF0237 family | ||
LCADNNJD_01482 | 2.1e-209 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
LCADNNJD_01483 | 6.6e-248 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
LCADNNJD_01484 | 5.8e-133 | glpR | K | DeoR C terminal sensor domain | ||
LCADNNJD_01485 | 1e-120 | ppm1 | 2.4.1.83 | GT2 | S | Glycosyl transferase family 2 |
LCADNNJD_01486 | 5.9e-216 | pyrD | 1.3.1.14, 1.3.5.2, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate with quinone as electron acceptor | |
LCADNNJD_01488 | 3.3e-164 | KLT | Protein tyrosine kinase | |||
LCADNNJD_01489 | 0.0 | S | Fibronectin type 3 domain | |||
LCADNNJD_01490 | 5.7e-166 | S | ATPase family associated with various cellular activities (AAA) | |||
LCADNNJD_01491 | 1.9e-175 | S | Protein of unknown function DUF58 | |||
LCADNNJD_01492 | 0.0 | E | Transglutaminase-like superfamily | |||
LCADNNJD_01493 | 8.5e-202 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
LCADNNJD_01494 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LCADNNJD_01495 | 7.2e-127 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
LCADNNJD_01497 | 1e-143 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
LCADNNJD_01498 | 1.3e-29 | J | TM2 domain | |||
LCADNNJD_01499 | 1.2e-191 | leuB | 1.1.1.85 | CE | Catalyzes the oxidation of 3-carboxy-2-hydroxy-4- methylpentanoate (3-isopropylmalate) to 3-carboxy-4-methyl-2- oxopentanoate. The product decarboxylates to 4-methyl-2 oxopentanoate | |
LCADNNJD_01500 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
LCADNNJD_01501 | 2.6e-211 | S | Uncharacterized conserved protein (DUF2183) | |||
LCADNNJD_01502 | 1.7e-64 | gcvH | E | The glycine cleavage system catalyzes the degradation of glycine. The H protein shuttles the methylamine group of glycine from the P protein to the T protein | ||
LCADNNJD_01503 | 2.9e-243 | enhA_2 | S | L,D-transpeptidase catalytic domain | ||
LCADNNJD_01504 | 5.1e-180 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
LCADNNJD_01505 | 6e-122 | mhpC | I | Alpha/beta hydrolase family | ||
LCADNNJD_01506 | 2e-112 | F | Domain of unknown function (DUF4916) | |||
LCADNNJD_01507 | 3.7e-49 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
LCADNNJD_01508 | 1.1e-165 | S | G5 | |||
LCADNNJD_01509 | 3.5e-69 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LCADNNJD_01510 | 3.9e-75 | |||||
LCADNNJD_01511 | 3.9e-190 | wcoI | DM | Psort location CytoplasmicMembrane, score | ||
LCADNNJD_01512 | 5.8e-37 | |||||
LCADNNJD_01513 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LCADNNJD_01514 | 0.0 | glfT | 2.4.1.288 | GT2 | S | Glycosyltransferase like family 2 |
LCADNNJD_01515 | 2.1e-297 | |||||
LCADNNJD_01516 | 3.3e-164 | M | Glycosyltransferase like family 2 | |||
LCADNNJD_01517 | 4.4e-285 | GT2,GT4 | M | Glycosyl transferase family 2 | ||
LCADNNJD_01518 | 7.7e-220 | rgpD | 3.6.3.38 | GM | ABC transporter, ATP-binding protein | |
LCADNNJD_01519 | 2.4e-142 | rgpC | U | Transport permease protein | ||
LCADNNJD_01520 | 0.0 | wbbM | M | Glycosyl transferase family 8 | ||
LCADNNJD_01521 | 2e-60 | |||||
LCADNNJD_01522 | 3.9e-44 | I | Acyltransferase family | |||
LCADNNJD_01525 | 0.0 | amyE | 3.2.1.1, 3.2.1.80 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LCADNNJD_01526 | 1.1e-203 | S | Endonuclease/Exonuclease/phosphatase family | |||
LCADNNJD_01527 | 6.2e-79 | 3.1.3.48 | T | Low molecular weight phosphatase family | ||
LCADNNJD_01528 | 5.8e-223 | rfbP | 2.7.8.6 | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | |
LCADNNJD_01529 | 7e-240 | EGP | Major facilitator Superfamily | |||
LCADNNJD_01530 | 1.9e-196 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LCADNNJD_01531 | 5.7e-102 | L | Protein of unknown function (DUF1524) | |||
LCADNNJD_01533 | 3.4e-186 | natB | E | Receptor family ligand binding region | ||
LCADNNJD_01534 | 1.6e-202 | EK | Bacterial regulatory proteins, gntR family | |||
LCADNNJD_01535 | 1.5e-258 | 2.6.1.55 | E | Aminotransferase class-III | ||
LCADNNJD_01536 | 2.4e-113 | S | Enoyl-(Acyl carrier protein) reductase | |||
LCADNNJD_01537 | 1.9e-275 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
LCADNNJD_01538 | 0.0 | cydD | V | ABC transporter transmembrane region | ||
LCADNNJD_01539 | 3.8e-175 | K | helix_turn _helix lactose operon repressor | |||
LCADNNJD_01540 | 8.1e-111 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LCADNNJD_01541 | 2.6e-100 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LCADNNJD_01542 | 1.2e-58 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
LCADNNJD_01543 | 0.0 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LCADNNJD_01544 | 8.9e-226 | manC | 2.7.7.13, 5.3.1.8 | M | Mannose-6-phosphate isomerase | |
LCADNNJD_01548 | 2.8e-153 | S | Auxin Efflux Carrier | |||
LCADNNJD_01549 | 8.2e-109 | rdgB | 3.6.1.66, 5.1.1.3 | F | Pyrophosphatase that catalyzes the hydrolysis of nucleoside triphosphates to their monophosphate derivatives, with a high preference for the non-canonical purine nucleotides XTP (xanthosine triphosphate), dITP (deoxyinosine triphosphate) and ITP. Seems to function as a house-cleaning enzyme that removes non-canonical purine nucleotides from the nucleotide pool, thus preventing their incorporation into DNA RNA and avoiding chromosomal lesions | |
LCADNNJD_01550 | 1.7e-132 | rph | 2.7.7.56, 3.6.1.66 | J | Phosphorolytic exoribonuclease that removes nucleotide residues following the -CCA terminus of tRNA and adds nucleotides to the ends of RNA molecules by using nucleoside diphosphates as substrates | |
LCADNNJD_01551 | 2.4e-110 | |||||
LCADNNJD_01552 | 7e-245 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
LCADNNJD_01553 | 2.1e-44 | S | Protein of unknown function (DUF3039) | |||
LCADNNJD_01554 | 2.6e-83 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LCADNNJD_01555 | 5.6e-35 | |||||
LCADNNJD_01556 | 7.8e-95 | yceD | S | Uncharacterized ACR, COG1399 | ||
LCADNNJD_01557 | 1.3e-22 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LCADNNJD_01558 | 6.5e-137 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
LCADNNJD_01559 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
LCADNNJD_01560 | 2.4e-90 | ilvN | 2.2.1.6 | E | ACT domain | |
LCADNNJD_01561 | 0.0 | yjjK | S | ABC transporter | ||
LCADNNJD_01562 | 1.3e-131 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
LCADNNJD_01563 | 2.9e-280 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LCADNNJD_01564 | 4.9e-264 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
LCADNNJD_01565 | 3.9e-150 | S | Endonuclease/Exonuclease/phosphatase family | |||
LCADNNJD_01566 | 5.2e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LCADNNJD_01567 | 1.4e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
LCADNNJD_01568 | 1.3e-105 | rimM | J | An accessory protein needed during the final step in the assembly of 30S ribosomal subunit, possibly for assembly of the head region. Probably interacts with S19. Essential for efficient processing of 16S rRNA. May be needed both before and after RbfA during the maturation of 16S rRNA. It has affinity for free ribosomal 30S subunits but not for 70S ribosomes | ||
LCADNNJD_01569 | 7.8e-38 | S | Domain of unknown function (DUF4190) | |||
LCADNNJD_01570 | 3.9e-150 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LCADNNJD_01571 | 9.9e-250 | 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 | |
LCADNNJD_01572 | 1.9e-63 | rsfS | 2.7.7.18 | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | |
LCADNNJD_01573 | 2e-132 | 3.1.3.85 | G | Phosphoglycerate mutase family | ||
LCADNNJD_01574 | 7.6e-234 | S | AMMECR1 | |||
LCADNNJD_01575 | 3e-229 | pflA | 1.97.1.4 | O | Radical SAM superfamily | |
LCADNNJD_01576 | 5.9e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
LCADNNJD_01577 | 2.8e-148 | EG | EamA-like transporter family | |||
LCADNNJD_01578 | 1.5e-111 | S | HAD hydrolase, family IA, variant 3 | |||
LCADNNJD_01579 | 1.7e-45 | |||||
LCADNNJD_01580 | 3.8e-57 | cadD | P | Cadmium resistance transporter | ||
LCADNNJD_01583 | 6.5e-168 | corA | P | CorA-like Mg2+ transporter protein | ||
LCADNNJD_01584 | 1.9e-102 | ET | Bacterial periplasmic substrate-binding proteins | |||
LCADNNJD_01585 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LCADNNJD_01586 | 8.6e-25 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
LCADNNJD_01587 | 4e-145 | comE | S | Competence protein | ||
LCADNNJD_01588 | 1.1e-146 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LCADNNJD_01589 | 9.3e-76 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
LCADNNJD_01590 | 6.1e-120 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
LCADNNJD_01591 | 1.1e-71 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
LCADNNJD_01592 | 1.9e-192 | tsaD | 2.3.1.234 | O | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine. Is involved in the transfer of the threonylcarbamoyl moiety of threonylcarbamoyl-AMP (TC-AMP) to the N6 group of A37, together with TsaE and TsaB. TsaD likely plays a direct catalytic role in this reaction | |
LCADNNJD_01594 | 2.6e-115 | tnp3503b | 2.7.7.7 | L | Transposase and inactivated derivatives | |
LCADNNJD_01595 | 9.3e-69 | S | zinc finger | |||
LCADNNJD_01596 | 2.1e-13 | CP_1020 | S | zinc finger | ||
LCADNNJD_01599 | 8.6e-110 | 3.1.1.3 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
LCADNNJD_01600 | 9.9e-224 | nnrD | 4.2.1.136, 5.1.99.6 | H | Catalyzes the dehydration of the S-form of NAD(P)HX at the expense of ADP, which is converted to AMP. Together with NAD(P)HX epimerase, which catalyzes the epimerization of the S- and R-forms, the enzyme 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 | |
LCADNNJD_01601 | 1e-48 | S | Protein of unknown function (DUF4232) | |||
LCADNNJD_01602 | 1.2e-81 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LCADNNJD_01603 | 8e-171 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LCADNNJD_01604 | 4.6e-118 | 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_01605 | 7.7e-177 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
LCADNNJD_01606 | 5.1e-145 | pyrK | 1.18.1.2, 1.19.1.1, 1.4.1.13, 1.4.1.14 | C | Iron-sulfur cluster binding domain of dihydroorotate dehydrogenase B | |
LCADNNJD_01607 | 5.4e-162 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
LCADNNJD_01608 | 4.9e-260 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
LCADNNJD_01609 | 1.2e-73 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
LCADNNJD_01610 | 1.1e-181 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LCADNNJD_01611 | 0.0 | glnE | 2.7.7.42, 2.7.7.89 | H | Involved in the regulation of glutamine synthetase GlnA, a key enzyme in the process to assimilate ammonia. When cellular nitrogen levels are high, the C-terminal adenylyl transferase (AT) inactivates GlnA by covalent transfer of an adenylyl group from ATP to specific tyrosine residue of GlnA, thus reducing its activity. Conversely, when nitrogen levels are low, the N-terminal adenylyl removase (AR) activates GlnA by removing the adenylyl group by phosphorolysis, increasing its activity. The regulatory region of GlnE binds the signal transduction protein PII (GlnB) which indicates the nitrogen status of the cell | |
LCADNNJD_01614 | 1.9e-158 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
LCADNNJD_01615 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
LCADNNJD_01616 | 4.7e-81 | sixA | T | Phosphoglycerate mutase family | ||
LCADNNJD_01617 | 2.6e-163 | trmI | 2.1.1.219, 2.1.1.220 | J | Catalyzes the S-adenosyl-L-methionine-dependent formation of N(1)-methyladenine at position 58 (m1A58) in tRNA | |
LCADNNJD_01618 | 9.6e-144 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
LCADNNJD_01619 | 3.6e-46 | ybjQ | S | Putative heavy-metal-binding | ||
LCADNNJD_01621 | 2.5e-47 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
LCADNNJD_01622 | 4e-118 | azlC | E | AzlC protein | ||
LCADNNJD_01623 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
LCADNNJD_01624 | 1.1e-86 | phzB | S | Phenazine biosynthesis protein A/B | ||
LCADNNJD_01625 | 2.1e-25 | thiS | 2.8.1.10 | H | ThiS family | |
LCADNNJD_01626 | 6e-126 | thiF | 2.7.7.73, 2.7.7.80 | H | ThiF family | |
LCADNNJD_01627 | 1.9e-161 | thiG | 2.8.1.10 | H | Catalyzes the rearrangement of 1-deoxy-D-xylulose 5- phosphate (DXP) to produce the thiazole phosphate moiety of thiamine. Sulfur is provided by the thiocarboxylate moiety of the carrier protein ThiS. In vitro, sulfur can be provided by H(2)S | |
LCADNNJD_01628 | 9.4e-23 | cycA | E | Amino acid permease | ||
LCADNNJD_01629 | 9.3e-268 | cycA | E | Amino acid permease | ||
LCADNNJD_01630 | 5.5e-48 | S | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_01631 | 1.2e-112 | M | domain protein | |||
LCADNNJD_01632 | 1.4e-162 | inlJ | M | domain protein | ||
LCADNNJD_01633 | 2e-52 | inlJ | M | domain protein | ||
LCADNNJD_01634 | 5.5e-112 | 3.4.22.70 | M | Sortase family | ||
LCADNNJD_01635 | 1.5e-51 | S | Psort location Cytoplasmic, score 8.87 | |||
LCADNNJD_01638 | 1.8e-126 | |||||
LCADNNJD_01639 | 4.4e-65 | S | HicB family | |||
LCADNNJD_01640 | 7.4e-258 | amyE | G | Bacterial extracellular solute-binding protein | ||
LCADNNJD_01641 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
LCADNNJD_01642 | 2.1e-180 | K | Periplasmic binding protein-like domain | |||
LCADNNJD_01643 | 6.8e-253 | P | Sodium/hydrogen exchanger family | |||
LCADNNJD_01644 | 1.9e-63 | M | NlpC/P60 family | |||
LCADNNJD_01645 | 7.5e-122 | ykoT | 2.4.1.83 | GT2 | M | Glycosyl transferase family 2 |
LCADNNJD_01646 | 1.7e-143 | lytC | 3.2.1.17, 3.2.1.4, 3.2.1.96, 3.2.1.97 | GH101,GH5,GH9 | M | Glycosyl hydrolases family 25 |
LCADNNJD_01647 | 3.1e-68 | |||||
LCADNNJD_01648 | 8.4e-175 | 3.6.4.12 | ||||
LCADNNJD_01649 | 1.3e-179 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
LCADNNJD_01652 | 4.9e-43 | F | Permease family | |||
LCADNNJD_01653 | 2.7e-07 | J | cysteine-tRNA ligase activity | |||
LCADNNJD_01654 | 1.4e-75 | S | AAA domain, putative AbiEii toxin, Type IV TA system | |||
LCADNNJD_01655 | 7.2e-148 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LCADNNJD_01656 | 1.2e-266 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
LCADNNJD_01657 | 6.7e-195 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LCADNNJD_01658 | 1.9e-110 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
LCADNNJD_01659 | 1.2e-169 | srtA | 3.4.22.70 | M | Sortase family | |
LCADNNJD_01660 | 8.2e-94 | S | Bacterial protein of unknown function (DUF881) | |||
LCADNNJD_01661 | 5.3e-58 | crgA | D | Involved in cell division | ||
LCADNNJD_01662 | 5.2e-165 | L | ribosomal rna small subunit methyltransferase | |||
LCADNNJD_01663 | 8.8e-106 | gluP | 3.4.21.105 | S | Rhomboid family | |
LCADNNJD_01664 | 2.5e-27 | |||||
LCADNNJD_01665 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
LCADNNJD_01666 | 1.3e-70 | I | Sterol carrier protein | |||
LCADNNJD_01667 | 4.3e-200 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LCADNNJD_01668 | 1.5e-59 | S | Protein of unknown function (DUF3073) | |||
LCADNNJD_01669 | 1.4e-50 | K | helix_turn_helix, Lux Regulon | |||
LCADNNJD_01670 | 8.9e-27 | 2.7.13.3 | T | Histidine kinase | ||
LCADNNJD_01671 | 2.5e-09 | S | VanZ like family | |||
LCADNNJD_01672 | 3.4e-19 | |||||
LCADNNJD_01673 | 3.5e-132 | tgt | 2.4.2.29 | F | Catalyzes the base-exchange of a guanine (G) residue with the queuine precursor 7-aminomethyl-7-deazaguanine (PreQ1) at position 34 (anticodon wobble position) in tRNAs with GU(N) anticodons (tRNA-Asp, -Asn, -His and -Tyr). Catalysis occurs through a double-displacement mechanism. The nucleophile active site attacks the C1' of nucleotide 34 to detach the guanine base from the RNA, forming a covalent enzyme-RNA intermediate. The proton acceptor active site deprotonates the incoming PreQ1, allowing a nucleophilic attack on the C1' of the ribose to form the product. After dissociation, two additional enzymatic reactions on the tRNA convert PreQ1 to queuine (Q), resulting in the hypermodified nucleoside queuosine (7-(((4,5-cis-dihydroxy-2- cyclopenten-1-yl)amino)methyl)-7-deazaguanosine) | |
LCADNNJD_01674 | 1.8e-27 | K | helix_turn_helix, Lux Regulon | |||
LCADNNJD_01675 | 3.4e-77 | |||||
LCADNNJD_01677 | 1.8e-245 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
LCADNNJD_01678 | 1.7e-57 | divIC | D | Septum formation initiator | ||
LCADNNJD_01679 | 4.9e-95 | ppx2 | 3.6.1.11, 3.6.1.40 | S | Protein of unknown function (DUF501) | |
LCADNNJD_01680 | 6.6e-174 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LCADNNJD_01684 | 2.1e-57 | ydhQ | 2.7.11.1 | MU | cell adhesion | |
LCADNNJD_01689 | 9.8e-37 | S | Helix-turn-helix domain | |||
LCADNNJD_01690 | 1.1e-23 | |||||
LCADNNJD_01691 | 8.3e-16 | G | Fic/DOC family | |||
LCADNNJD_01694 | 2.1e-13 | |||||
LCADNNJD_01696 | 1e-71 | yvgN | S | Aldo/keto reductase family | ||
LCADNNJD_01697 | 1.8e-152 | EGP | Major facilitator Superfamily | |||
LCADNNJD_01698 | 8.9e-40 | |||||
LCADNNJD_01699 | 3.4e-122 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
LCADNNJD_01700 | 2.1e-11 | S | Protein of unknown function (DUF4235) | |||
LCADNNJD_01701 | 9.2e-112 | G | Phosphoglycerate mutase family | |||
LCADNNJD_01702 | 6.4e-230 | amyE | G | Bacterial extracellular solute-binding protein | ||
LCADNNJD_01703 | 3.5e-159 | K | Psort location Cytoplasmic, score | |||
LCADNNJD_01704 | 8.5e-151 | msmF | G | Binding-protein-dependent transport system inner membrane component | ||
LCADNNJD_01705 | 8.8e-156 | rafG | G | ABC transporter permease | ||
LCADNNJD_01706 | 6.2e-55 | |||||
LCADNNJD_01708 | 3.8e-83 | V | Abi-like protein | |||
LCADNNJD_01709 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
LCADNNJD_01710 | 8.9e-34 | copZ | P | Heavy-metal-associated domain | ||
LCADNNJD_01711 | 2e-46 | D | Di-iron-containing protein involved in the repair of iron-sulfur clusters | |||
LCADNNJD_01712 | 2.1e-109 | flp | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | Crp-like helix-turn-helix domain | |
LCADNNJD_01714 | 2e-137 | draG | O | ADP-ribosylglycohydrolase | ||
LCADNNJD_01717 | 7e-40 | |||||
LCADNNJD_01718 | 1e-114 | L | Psort location Cytoplasmic, score |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)