ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LFBCNLDA_00001 | 3.2e-269 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LFBCNLDA_00002 | 2.7e-167 | L | Excalibur calcium-binding domain | |||
LFBCNLDA_00003 | 4.3e-219 | 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) | |
LFBCNLDA_00004 | 3.4e-242 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_00005 | 2.1e-103 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
LFBCNLDA_00006 | 6.3e-95 | 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) | |
LFBCNLDA_00008 | 1.5e-80 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
LFBCNLDA_00009 | 5.2e-87 | hspR | K | transcriptional regulator, MerR family | ||
LFBCNLDA_00010 | 0.0 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR repeat-like domain | |
LFBCNLDA_00011 | 1.6e-137 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR Asp-box repeat | |
LFBCNLDA_00012 | 2.9e-38 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR Asp-box repeat | |
LFBCNLDA_00013 | 1.1e-242 | 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) | |
LFBCNLDA_00014 | 8e-99 | S | Domain of unknown function (DUF4143) | |||
LFBCNLDA_00015 | 1.9e-65 | S | Domain of unknown function (DUF4143) | |||
LFBCNLDA_00018 | 4.1e-250 | S | Calcineurin-like phosphoesterase | |||
LFBCNLDA_00019 | 2.4e-137 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
LFBCNLDA_00020 | 2.2e-273 | 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 | |
LFBCNLDA_00021 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
LFBCNLDA_00022 | 4.3e-106 | 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 | |
LFBCNLDA_00023 | 2.4e-240 | pbuX | F | Permease family | ||
LFBCNLDA_00025 | 5.8e-45 | 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 | |
LFBCNLDA_00027 | 2.1e-111 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
LFBCNLDA_00028 | 1.1e-40 | |||||
LFBCNLDA_00029 | 1.3e-137 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
LFBCNLDA_00030 | 1.7e-122 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
LFBCNLDA_00031 | 3.2e-42 | csoR | S | Metal-sensitive transcriptional repressor | ||
LFBCNLDA_00032 | 3.2e-213 | rmuC | S | RmuC family | ||
LFBCNLDA_00033 | 5.9e-129 | 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) | |
LFBCNLDA_00034 | 1.7e-157 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
LFBCNLDA_00035 | 1.1e-57 | V | ABC transporter | |||
LFBCNLDA_00036 | 1.7e-47 | V | ABC transporter | |||
LFBCNLDA_00037 | 6.2e-48 | 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) | |
LFBCNLDA_00038 | 9.8e-62 | M | LPXTG cell wall anchor motif | |||
LFBCNLDA_00039 | 2.9e-81 | K | Winged helix DNA-binding domain | |||
LFBCNLDA_00040 | 1.8e-301 | V | ABC transporter, ATP-binding protein | |||
LFBCNLDA_00041 | 0.0 | V | ABC transporter transmembrane region | |||
LFBCNLDA_00042 | 2.2e-81 | |||||
LFBCNLDA_00043 | 2.8e-67 | XK26_04485 | P | Cobalt transport protein | ||
LFBCNLDA_00044 | 3.4e-20 | XK26_04485 | P | Cobalt transport protein | ||
LFBCNLDA_00045 | 1.3e-11 | XK27_08585 | S | Hypothetical bacterial integral membrane protein (Trep_Strep) | ||
LFBCNLDA_00046 | 2.9e-295 | ydfD | EK | Alanine-glyoxylate amino-transferase | ||
LFBCNLDA_00047 | 1e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LFBCNLDA_00048 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
LFBCNLDA_00049 | 6.4e-108 | 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 | ||
LFBCNLDA_00050 | 1.5e-162 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LFBCNLDA_00051 | 8.9e-83 | hsp20 | O | Hsp20/alpha crystallin family | ||
LFBCNLDA_00052 | 4.5e-106 | XK27_02070 | S | Nitroreductase family | ||
LFBCNLDA_00053 | 5.5e-29 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
LFBCNLDA_00054 | 8.1e-59 | V | MacB-like periplasmic core domain | |||
LFBCNLDA_00055 | 2.9e-76 | |||||
LFBCNLDA_00056 | 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 | ||
LFBCNLDA_00057 | 1.1e-76 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LFBCNLDA_00058 | 1.2e-37 | fmdB | S | Putative regulatory protein | ||
LFBCNLDA_00059 | 3.6e-109 | flgA | NO | SAF | ||
LFBCNLDA_00060 | 2.8e-41 | |||||
LFBCNLDA_00061 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
LFBCNLDA_00062 | 1.3e-187 | T | Forkhead associated domain | |||
LFBCNLDA_00063 | 1.1e-231 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LFBCNLDA_00064 | 2.8e-280 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
LFBCNLDA_00065 | 1.7e-142 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
LFBCNLDA_00066 | 2.8e-16 | S | granule-associated protein | |||
LFBCNLDA_00067 | 0.0 | ubiB | S | ABC1 family | ||
LFBCNLDA_00068 | 8.4e-112 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
LFBCNLDA_00069 | 2.7e-157 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
LFBCNLDA_00070 | 3e-76 | 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 | ||
LFBCNLDA_00071 | 9.6e-146 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
LFBCNLDA_00072 | 4.6e-82 | |||||
LFBCNLDA_00073 | 4.7e-14 | |||||
LFBCNLDA_00074 | 1.4e-12 | L | PFAM Integrase catalytic | |||
LFBCNLDA_00076 | 2.1e-128 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
LFBCNLDA_00077 | 0.0 | inlJ | M | domain protein | ||
LFBCNLDA_00078 | 8.1e-280 | M | LPXTG cell wall anchor motif | |||
LFBCNLDA_00079 | 8.7e-27 | thiS | 2.8.1.10 | H | ThiS family | |
LFBCNLDA_00080 | 1.9e-164 | 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 | |
LFBCNLDA_00081 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_00082 | 0.0 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
LFBCNLDA_00083 | 1.2e-49 | 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 | ||
LFBCNLDA_00084 | 2.1e-235 | E | Aminotransferase class I and II | |||
LFBCNLDA_00085 | 2.4e-90 | lrp_3 | K | helix_turn_helix ASNC type | ||
LFBCNLDA_00086 | 5.7e-65 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
LFBCNLDA_00087 | 1.7e-169 | P | Zinc-uptake complex component A periplasmic | |||
LFBCNLDA_00088 | 1.3e-162 | 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 | |
LFBCNLDA_00089 | 1.6e-132 | rpsA | J | Ribosomal protein S1 | ||
LFBCNLDA_00092 | 9.9e-123 | S | HAD hydrolase, family IA, variant 3 | |||
LFBCNLDA_00093 | 2.5e-200 | P | NMT1/THI5 like | |||
LFBCNLDA_00094 | 1.7e-137 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
LFBCNLDA_00095 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LFBCNLDA_00096 | 1.9e-166 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
LFBCNLDA_00097 | 3.1e-31 | ywiC | S | YwiC-like protein | ||
LFBCNLDA_00098 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LFBCNLDA_00099 | 7.6e-83 | K | Helix-turn-helix XRE-family like proteins | |||
LFBCNLDA_00100 | 1.4e-130 | tam | 2.1.1.144, 2.1.1.197 | S | Methyltransferase domain | |
LFBCNLDA_00105 | 3.8e-171 | L | Transposase and inactivated derivatives IS30 family | |||
LFBCNLDA_00106 | 3.1e-24 | |||||
LFBCNLDA_00107 | 3.5e-07 | S | Scramblase | |||
LFBCNLDA_00108 | 9.7e-55 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_00109 | 1.1e-13 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_00110 | 6.4e-145 | gluP | 3.4.21.105 | S | Rhomboid family | |
LFBCNLDA_00111 | 3.4e-35 | |||||
LFBCNLDA_00112 | 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 |
LFBCNLDA_00114 | 8.8e-222 | pbuO | S | Permease family | ||
LFBCNLDA_00115 | 1.4e-12 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_00116 | 6.6e-168 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_00117 | 3.6e-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 | |
LFBCNLDA_00118 | 1.7e-149 | pstA | P | Phosphate transport system permease | ||
LFBCNLDA_00121 | 2.8e-243 | topB | 5.99.1.2 | L | DNA topoisomerase | |
LFBCNLDA_00124 | 1.3e-67 | |||||
LFBCNLDA_00125 | 8e-16 | lemA | S | LemA family | ||
LFBCNLDA_00126 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
LFBCNLDA_00127 | 7.8e-74 | megL | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_00128 | 1.4e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_00129 | 1.2e-91 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_00130 | 8.1e-44 | 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 | |
LFBCNLDA_00131 | 1.4e-84 | argR | K | Regulates arginine biosynthesis genes | ||
LFBCNLDA_00132 | 4.1e-239 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LFBCNLDA_00133 | 1e-178 | L | Phage integrase family | |||
LFBCNLDA_00134 | 1.3e-96 | 3.1.21.3 | V | restriction | ||
LFBCNLDA_00135 | 5e-42 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_00138 | 1.2e-131 | G | Phosphoglycerate mutase family | |||
LFBCNLDA_00139 | 9.6e-69 | S | Protein of unknown function (DUF4235) | |||
LFBCNLDA_00141 | 1.7e-283 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
LFBCNLDA_00142 | 1.7e-134 | smc | D | Required for chromosome condensation and partitioning | ||
LFBCNLDA_00143 | 1.6e-53 | dprA | LU | DNA recombination-mediator protein A | ||
LFBCNLDA_00144 | 6.8e-08 | int | L | Phage integrase, N-terminal SAM-like domain | ||
LFBCNLDA_00145 | 9.7e-30 | |||||
LFBCNLDA_00146 | 1.7e-27 | S | Protein of unknown function (DUF3800) | |||
LFBCNLDA_00147 | 3.1e-194 | int | L | Phage integrase, N-terminal SAM-like domain | ||
LFBCNLDA_00148 | 2.5e-141 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LFBCNLDA_00149 | 3.1e-83 | 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 | |
LFBCNLDA_00150 | 3.1e-203 | 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 | |
LFBCNLDA_00151 | 8.8e-184 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein of unknown function (DUF559) | |
LFBCNLDA_00152 | 6.1e-196 | lacZ | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_00153 | 9.3e-147 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
LFBCNLDA_00154 | 6.9e-178 | 2.7.1.2 | GK | ROK family | ||
LFBCNLDA_00155 | 6.4e-218 | GK | ROK family | |||
LFBCNLDA_00156 | 6.9e-206 | mdsC | 2.7.1.162, 2.7.1.39 | S | Phosphotransferase enzyme family | |
LFBCNLDA_00157 | 9.4e-264 | L | DNA helicase | |||
LFBCNLDA_00158 | 2.9e-229 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
LFBCNLDA_00159 | 8.8e-83 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LFBCNLDA_00160 | 3.5e-48 | M | Lysin motif | |||
LFBCNLDA_00161 | 7.5e-129 | 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 | |
LFBCNLDA_00162 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
LFBCNLDA_00163 | 2.7e-304 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
LFBCNLDA_00164 | 3.6e-82 | |||||
LFBCNLDA_00165 | 5.4e-206 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_00166 | 2.5e-132 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LFBCNLDA_00167 | 6.4e-156 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LFBCNLDA_00168 | 5.6e-62 | 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 | ||
LFBCNLDA_00169 | 7.4e-16 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
LFBCNLDA_00170 | 9.8e-129 | V | ABC transporter | |||
LFBCNLDA_00171 | 1.6e-100 | K | Transcriptional regulator C-terminal region | |||
LFBCNLDA_00172 | 3.1e-32 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
LFBCNLDA_00173 | 6.6e-184 | S | Acetyltransferase (GNAT) domain | |||
LFBCNLDA_00175 | 8.4e-35 | 2.7.7.1, 3.6.1.13, 3.6.1.55 | F | Hydrolase of X-linked nucleoside diphosphate N terminal | ||
LFBCNLDA_00176 | 2.2e-54 | K | Transcriptional regulator | |||
LFBCNLDA_00177 | 4.9e-90 | MA20_25245 | K | FR47-like protein | ||
LFBCNLDA_00178 | 8.6e-121 | ydaF_1 | J | Acetyltransferase (GNAT) domain | ||
LFBCNLDA_00179 | 3.1e-223 | |||||
LFBCNLDA_00180 | 1.8e-306 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_00181 | 1.2e-219 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_00182 | 1.5e-191 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
LFBCNLDA_00183 | 4.6e-135 | sapF | E | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_00184 | 3.5e-115 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
LFBCNLDA_00185 | 5.7e-141 | |||||
LFBCNLDA_00186 | 1.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LFBCNLDA_00187 | 9.9e-127 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
LFBCNLDA_00188 | 6.3e-50 | 3.2.1.97 | GH101 | G | Glycosyl hydrolase 101 beta sandwich domain | |
LFBCNLDA_00189 | 1.2e-191 | 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) | |
LFBCNLDA_00190 | 2.1e-167 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
LFBCNLDA_00191 | 1.1e-89 | rnfE | 2.3.1.243, 4.2.99.18 | C | Part of a membrane complex involved in electron transport | |
LFBCNLDA_00192 | 1.7e-223 | 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 | |
LFBCNLDA_00193 | 3.4e-86 | K | Transcriptional regulator | |||
LFBCNLDA_00195 | 9.5e-74 | |||||
LFBCNLDA_00197 | 6.3e-122 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LFBCNLDA_00198 | 9.7e-67 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | Putative cell wall binding repeat |
LFBCNLDA_00199 | 6.5e-33 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | xyloglucan:xyloglucosyl transferase activity |
LFBCNLDA_00200 | 1.9e-59 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
LFBCNLDA_00201 | 1.8e-300 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
LFBCNLDA_00202 | 3.6e-246 | 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 | ||
LFBCNLDA_00203 | 4.4e-247 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
LFBCNLDA_00204 | 1.2e-130 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
LFBCNLDA_00206 | 9.7e-175 | 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) | |
LFBCNLDA_00208 | 0.0 | L | DEAD DEAH box helicase | |||
LFBCNLDA_00209 | 1.9e-192 | 2.7.4.1 | S | Polyphosphate kinase 2 (PPK2) | ||
LFBCNLDA_00210 | 3.3e-223 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LFBCNLDA_00211 | 1.1e-117 | L | Protein of unknown function (DUF1524) | |||
LFBCNLDA_00212 | 2.9e-170 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
LFBCNLDA_00213 | 5.1e-61 | 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 | ||
LFBCNLDA_00214 | 2.4e-280 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
LFBCNLDA_00215 | 8.1e-217 | 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 | |
LFBCNLDA_00216 | 1.1e-44 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
LFBCNLDA_00217 | 2.1e-43 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
LFBCNLDA_00218 | 8.2e-57 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
LFBCNLDA_00219 | 1.5e-36 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
LFBCNLDA_00220 | 7.9e-285 | pdtaS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
LFBCNLDA_00221 | 1.9e-46 | whiB | K | Acts as a transcriptional regulator. Probably redox- responsive. The apo- but not holo-form probably binds DNA | ||
LFBCNLDA_00222 | 4.8e-57 | D | FtsK/SpoIIIE family | |||
LFBCNLDA_00223 | 8.4e-100 | G | ABC transporter permease | |||
LFBCNLDA_00224 | 2.9e-190 | K | Periplasmic binding protein domain | |||
LFBCNLDA_00225 | 7.7e-21 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
LFBCNLDA_00226 | 1.1e-103 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
LFBCNLDA_00227 | 1.5e-25 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
LFBCNLDA_00228 | 1e-66 | cspB | K | 'Cold-shock' DNA-binding domain | ||
LFBCNLDA_00229 | 7.3e-192 | S | Protein of unknown function (DUF3027) | |||
LFBCNLDA_00230 | 1.8e-184 | uspA | T | Belongs to the universal stress protein A family | ||
LFBCNLDA_00231 | 2.1e-21 | pgl | 3.1.1.31, 3.5.99.6 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LFBCNLDA_00232 | 4.5e-277 | 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 | |
LFBCNLDA_00233 | 8.3e-126 | degU | K | helix_turn_helix, Lux Regulon | ||
LFBCNLDA_00234 | 3e-84 | 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 | |
LFBCNLDA_00235 | 2e-244 | 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 | ||
LFBCNLDA_00238 | 9.9e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
LFBCNLDA_00239 | 4.4e-135 | S | UPF0126 domain | |||
LFBCNLDA_00240 | 2.4e-73 | 3.1.4.37 | T | RNA ligase | ||
LFBCNLDA_00241 | 1.7e-72 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
LFBCNLDA_00242 | 2.3e-179 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LFBCNLDA_00243 | 2.9e-93 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
LFBCNLDA_00244 | 5.4e-228 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
LFBCNLDA_00245 | 9.9e-225 | V | ABC-2 family transporter protein | |||
LFBCNLDA_00246 | 7.2e-186 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_00247 | 4.3e-19 | pacL | 3.6.3.8, 3.6.3.9 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
LFBCNLDA_00248 | 4.7e-125 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
LFBCNLDA_00249 | 7.2e-197 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LFBCNLDA_00250 | 1.8e-33 | 1.1.1.399, 1.1.1.95 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | ||
LFBCNLDA_00251 | 3.2e-106 | aroE | 1.1.1.25 | E | Involved in the biosynthesis of the chorismate, which leads to the biosynthesis of aromatic amino acids. Catalyzes the reversible NADPH linked reduction of 3-dehydroshikimate (DHSA) to yield shikimate (SA) | |
LFBCNLDA_00252 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
LFBCNLDA_00253 | 3e-210 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
LFBCNLDA_00256 | 1.7e-185 | mepA_6 | V | MatE | ||
LFBCNLDA_00257 | 1.7e-111 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LFBCNLDA_00258 | 1.4e-270 | S | zinc finger | |||
LFBCNLDA_00259 | 8.6e-71 | 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 | |
LFBCNLDA_00260 | 1.4e-141 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
LFBCNLDA_00261 | 7.3e-89 | dkgB | S | Oxidoreductase, aldo keto reductase family protein | ||
LFBCNLDA_00263 | 1e-124 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
LFBCNLDA_00264 | 2.8e-119 | F | Domain of unknown function (DUF4916) | |||
LFBCNLDA_00265 | 1.5e-59 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
LFBCNLDA_00266 | 1.3e-179 | S | G5 | |||
LFBCNLDA_00267 | 2.8e-128 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LFBCNLDA_00268 | 1.2e-152 | sapF | E | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_00269 | 5.7e-141 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
LFBCNLDA_00270 | 2.4e-78 | EP | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_00271 | 3.7e-215 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LFBCNLDA_00272 | 2.3e-199 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LFBCNLDA_00273 | 2.3e-96 | M | Bacterial capsule synthesis protein PGA_cap | |||
LFBCNLDA_00275 | 5.6e-14 | 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 | |
LFBCNLDA_00276 | 5.1e-93 | 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 | |
LFBCNLDA_00277 | 2.1e-56 | |||||
LFBCNLDA_00278 | 1.1e-203 | 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 | |
LFBCNLDA_00279 | 3.1e-27 | 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 | |
LFBCNLDA_00280 | 1.5e-56 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
LFBCNLDA_00282 | 1e-91 | |||||
LFBCNLDA_00283 | 3.5e-221 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
LFBCNLDA_00284 | 0.0 | yegQ | O | Peptidase family U32 C-terminal domain | ||
LFBCNLDA_00285 | 3.6e-182 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
LFBCNLDA_00286 | 5.3e-159 | ybeM | S | Carbon-nitrogen hydrolase | ||
LFBCNLDA_00287 | 1.3e-113 | S | Sel1-like repeats. | |||
LFBCNLDA_00288 | 8.2e-190 | 1.1.1.65 | C | Aldo/keto reductase family | ||
LFBCNLDA_00289 | 5.9e-94 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
LFBCNLDA_00290 | 2.9e-64 | S | Helix-turn-helix domain | |||
LFBCNLDA_00292 | 7e-155 | 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 |
LFBCNLDA_00293 | 1.8e-217 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LFBCNLDA_00294 | 9.4e-186 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LFBCNLDA_00295 | 2.3e-94 | 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 | ||
LFBCNLDA_00296 | 1e-159 | S | alpha beta | |||
LFBCNLDA_00297 | 8.3e-263 | rodA | D | Belongs to the SEDS family | ||
LFBCNLDA_00298 | 6.4e-72 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
LFBCNLDA_00299 | 1.6e-160 | K | Bacterial regulatory proteins, lacI family | |||
LFBCNLDA_00302 | 2.4e-118 | cyaA | 4.6.1.1 | S | CYTH | |
LFBCNLDA_00303 | 2.3e-41 | trxA2 | O | Tetratricopeptide repeat | ||
LFBCNLDA_00304 | 9.3e-136 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
LFBCNLDA_00305 | 4.2e-29 | IQ | oxidoreductase activity | |||
LFBCNLDA_00307 | 3.3e-67 | K | AraC-like ligand binding domain | |||
LFBCNLDA_00308 | 3.3e-43 | rutG | F | Permease family | ||
LFBCNLDA_00310 | 3.2e-220 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_00311 | 1.9e-250 | metY | 2.5.1.49 | E | Aminotransferase class-V | |
LFBCNLDA_00312 | 6.6e-52 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LFBCNLDA_00313 | 1.1e-68 | D | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LFBCNLDA_00314 | 1.3e-76 | 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 | ||
LFBCNLDA_00315 | 7.2e-87 | nagLU | 3.1.4.53, 3.2.1.21, 3.2.1.50 | GH3 | G | Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain |
LFBCNLDA_00317 | 1.8e-95 | |||||
LFBCNLDA_00318 | 0.0 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LFBCNLDA_00319 | 4.2e-186 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LFBCNLDA_00320 | 2.3e-142 | pgl | 3.1.1.31 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LFBCNLDA_00321 | 4.5e-277 | 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 | |
LFBCNLDA_00322 | 8.5e-126 | degU | K | helix_turn_helix, Lux Regulon | ||
LFBCNLDA_00323 | 3.2e-181 | tcsS3 | KT | PspC domain | ||
LFBCNLDA_00324 | 1.7e-195 | 3.2.1.18 | GH33 | E | GDSL-like Lipase/Acylhydrolase | |
LFBCNLDA_00325 | 4.7e-140 | S | HAD hydrolase, family IA, variant 3 | |||
LFBCNLDA_00327 | 5.9e-126 | dedA | S | SNARE associated Golgi protein | ||
LFBCNLDA_00328 | 5.4e-149 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LFBCNLDA_00329 | 5.8e-50 | |||||
LFBCNLDA_00330 | 3.3e-112 | |||||
LFBCNLDA_00331 | 4e-184 | ykoD | P | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_00332 | 6.5e-148 | cbiQ | P | Cobalt transport protein | ||
LFBCNLDA_00333 | 1.4e-135 | 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 | |
LFBCNLDA_00334 | 3.1e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LFBCNLDA_00335 | 5.5e-225 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LFBCNLDA_00336 | 3.7e-296 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_00337 | 2.4e-113 | S | Domain of unknown function (DUF4194) | |||
LFBCNLDA_00338 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_00339 | 8.5e-222 | dnaK | O | Heat shock 70 kDa protein | ||
LFBCNLDA_00340 | 1.4e-58 | 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 | ||
LFBCNLDA_00341 | 4.6e-172 | dnaJ1 | O | DnaJ molecular chaperone homology domain | ||
LFBCNLDA_00342 | 5.2e-87 | hspR | K | transcriptional regulator, MerR family | ||
LFBCNLDA_00343 | 0.0 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR repeat-like domain | |
LFBCNLDA_00344 | 0.0 | 3.2.1.18, 3.2.1.51 | GH29,GH33 | G | BNR Asp-box repeat | |
LFBCNLDA_00345 | 1.1e-139 | S | HAD hydrolase, family IA, variant 3 | |||
LFBCNLDA_00347 | 2.7e-126 | dedA | S | SNARE associated Golgi protein | ||
LFBCNLDA_00348 | 4e-168 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LFBCNLDA_00349 | 8.6e-59 | |||||
LFBCNLDA_00350 | 3.6e-130 | |||||
LFBCNLDA_00351 | 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 | |
LFBCNLDA_00352 | 6.6e-79 | K | Transcriptional regulator | |||
LFBCNLDA_00353 | 1.6e-13 | G | Bacterial extracellular solute-binding protein | |||
LFBCNLDA_00354 | 4.3e-50 | xylR | 5.3.1.12 | G | MFS/sugar transport protein | |
LFBCNLDA_00355 | 1.1e-204 | xylR | 5.3.1.12 | G | MFS/sugar transport protein | |
LFBCNLDA_00356 | 3.3e-16 | G | MFS/sugar transport protein | |||
LFBCNLDA_00357 | 1.5e-183 | tatD | L | TatD related DNase | ||
LFBCNLDA_00358 | 0.0 | kup | P | Transport of potassium into the cell | ||
LFBCNLDA_00360 | 3e-164 | S | Glutamine amidotransferase domain | |||
LFBCNLDA_00361 | 1.9e-138 | T | HD domain | |||
LFBCNLDA_00362 | 1.3e-179 | V | ABC transporter | |||
LFBCNLDA_00363 | 8.7e-249 | V | ABC transporter permease | |||
LFBCNLDA_00364 | 0.0 | 2.1.1.107, 2.1.1.294, 2.7.1.181, 2.7.11.1 | H | Protein of unknown function (DUF4012) | ||
LFBCNLDA_00365 | 5.5e-15 | gtrB | GT2 | M | Glycosyl transferase family 2 | |
LFBCNLDA_00366 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_00367 | 1.9e-164 | 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 | |
LFBCNLDA_00368 | 3.3e-26 | thiS | 2.8.1.10 | H | ThiS family | |
LFBCNLDA_00369 | 2.5e-275 | |||||
LFBCNLDA_00370 | 6.9e-209 | S | Glycosyltransferase, group 2 family protein | |||
LFBCNLDA_00371 | 5.5e-53 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
LFBCNLDA_00372 | 1e-91 | |||||
LFBCNLDA_00373 | 6.3e-201 | mutT | 3.6.1.13, 3.6.1.55 | LT | Phosphoglycerate mutase family | |
LFBCNLDA_00374 | 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) | |
LFBCNLDA_00376 | 4.5e-129 | cpaE | D | bacterial-type flagellum organization | ||
LFBCNLDA_00377 | 3.4e-191 | cpaF | U | Type II IV secretion system protein | ||
LFBCNLDA_00378 | 5.7e-121 | U | Type ii secretion system | |||
LFBCNLDA_00379 | 8.6e-80 | gspF | NU | Type II secretion system (T2SS), protein F | ||
LFBCNLDA_00380 | 1.9e-41 | S | Protein of unknown function (DUF4244) | |||
LFBCNLDA_00381 | 4.1e-57 | S | TIGRFAM helicase secretion neighborhood TadE-like protein | |||
LFBCNLDA_00382 | 1.9e-214 | dagK | 2.7.1.107 | I | Diacylglycerol kinase catalytic domain protein | |
LFBCNLDA_00383 | 0.0 | dnaX | 2.7.7.7 | L | DNA polymerase III subunit gamma tau | |
LFBCNLDA_00384 | 6.7e-110 | 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 | ||
LFBCNLDA_00385 | 5.3e-136 | ask | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
LFBCNLDA_00386 | 2.1e-97 | askB | 1.1.1.3, 2.7.2.4 | E | ACT domain | |
LFBCNLDA_00388 | 4.2e-211 | 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 | |
LFBCNLDA_00389 | 1.7e-116 | |||||
LFBCNLDA_00390 | 1.2e-288 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
LFBCNLDA_00391 | 4.3e-14 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
LFBCNLDA_00392 | 8.7e-278 | S | Calcineurin-like phosphoesterase | |||
LFBCNLDA_00393 | 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) | |
LFBCNLDA_00394 | 0.0 | mrcB | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LFBCNLDA_00395 | 2.4e-233 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
LFBCNLDA_00396 | 4.7e-123 | yplQ | S | Haemolysin-III related | ||
LFBCNLDA_00397 | 0.0 | vpr | M | PA domain | ||
LFBCNLDA_00398 | 3.6e-189 | 3.6.1.27 | I | PAP2 superfamily | ||
LFBCNLDA_00399 | 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 | |
LFBCNLDA_00400 | 4.8e-118 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LFBCNLDA_00401 | 1.4e-212 | holB | 2.7.7.7 | L | DNA polymerase III | |
LFBCNLDA_00402 | 2.4e-198 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_00403 | 1.9e-37 | ptsH | G | PTS HPr component phosphorylation site | ||
LFBCNLDA_00404 | 3.6e-291 | 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) | |
LFBCNLDA_00405 | 1.5e-50 | S | Fic/DOC family | |||
LFBCNLDA_00406 | 6.1e-38 | S | Fic/DOC family | |||
LFBCNLDA_00407 | 1.4e-195 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
LFBCNLDA_00408 | 1.7e-33 | L | Transposase and inactivated derivatives IS30 family | |||
LFBCNLDA_00409 | 0.0 | efeU_1 | P | Iron permease FTR1 family | ||
LFBCNLDA_00410 | 6.4e-109 | tpd | P | Fe2+ transport protein | ||
LFBCNLDA_00411 | 9.2e-234 | S | Predicted membrane protein (DUF2318) | |||
LFBCNLDA_00412 | 1.8e-221 | macB_2 | V | ABC transporter permease | ||
LFBCNLDA_00413 | 2.6e-204 | Z012_06715 | V | FtsX-like permease family | ||
LFBCNLDA_00414 | 5.7e-149 | macB | V | ABC transporter, ATP-binding protein | ||
LFBCNLDA_00415 | 1.3e-70 | S | FMN_bind | |||
LFBCNLDA_00416 | 3.6e-131 | yydK | K | UTRA | ||
LFBCNLDA_00417 | 4.6e-67 | S | haloacid dehalogenase-like hydrolase | |||
LFBCNLDA_00418 | 2.1e-249 | gmuC | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
LFBCNLDA_00419 | 1.2e-48 | celA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
LFBCNLDA_00420 | 7.5e-39 | celC | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIA subunit | |
LFBCNLDA_00421 | 1.4e-294 | bglA | 3.2.1.86 | GT1 | G | Glycosyl hydrolase family 1 |
LFBCNLDA_00422 | 4.7e-35 | Q | phosphatase activity | |||
LFBCNLDA_00423 | 7e-81 | |||||
LFBCNLDA_00424 | 9.5e-239 | S | Putative ABC-transporter type IV | |||
LFBCNLDA_00425 | 6.2e-31 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LFBCNLDA_00426 | 5.2e-118 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LFBCNLDA_00428 | 2.1e-88 | E | IrrE N-terminal-like domain | |||
LFBCNLDA_00429 | 5.8e-43 | L | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_00430 | 3.2e-126 | L | Integrase core domain | |||
LFBCNLDA_00431 | 2.2e-09 | |||||
LFBCNLDA_00432 | 7.7e-82 | K | Winged helix DNA-binding domain | |||
LFBCNLDA_00433 | 1.8e-301 | V | ABC transporter, ATP-binding protein | |||
LFBCNLDA_00434 | 0.0 | V | ABC transporter transmembrane region | |||
LFBCNLDA_00435 | 5.2e-83 | |||||
LFBCNLDA_00436 | 9.8e-88 | XK26_04485 | P | Cobalt transport protein | ||
LFBCNLDA_00438 | 1.4e-305 | pepD | E | Peptidase family C69 | ||
LFBCNLDA_00439 | 0.0 | S | Glycosyl hydrolases related to GH101 family, GH129 | |||
LFBCNLDA_00440 | 6.6e-198 | XK27_01805 | M | Glycosyltransferase like family 2 | ||
LFBCNLDA_00441 | 7.9e-116 | icaR | K | Bacterial regulatory proteins, tetR family | ||
LFBCNLDA_00443 | 2.3e-205 | 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) | ||
LFBCNLDA_00444 | 1.5e-220 | amt | U | Ammonium Transporter Family | ||
LFBCNLDA_00445 | 1e-54 | glnB | K | Nitrogen regulatory protein P-II | ||
LFBCNLDA_00446 | 0.0 | 2.7.7.19, 2.7.7.59 | O | Nucleotidyltransferase domain | ||
LFBCNLDA_00447 | 2.4e-251 | dinF | V | MatE | ||
LFBCNLDA_00448 | 4.9e-257 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LFBCNLDA_00449 | 4.1e-276 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Domain of unknown function (DUF1727) | |
LFBCNLDA_00450 | 2.2e-142 | cobQ | S | CobB/CobQ-like glutamine amidotransferase domain | ||
LFBCNLDA_00451 | 3.5e-19 | S | granule-associated protein | |||
LFBCNLDA_00452 | 0.0 | ubiB | S | ABC1 family | ||
LFBCNLDA_00453 | 0.0 | pacS | 3.6.3.54 | P | E1-E2 ATPase | |
LFBCNLDA_00454 | 9.6e-43 | csoR | S | Metal-sensitive transcriptional repressor | ||
LFBCNLDA_00455 | 1.3e-214 | rmuC | S | RmuC family | ||
LFBCNLDA_00456 | 5.9e-129 | 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) | |
LFBCNLDA_00457 | 6.9e-156 | spoU | 2.1.1.185 | J | RNA methyltransferase TrmH family | |
LFBCNLDA_00458 | 3.6e-39 | V | ABC transporter | |||
LFBCNLDA_00459 | 2.5e-81 | V | ABC transporter | |||
LFBCNLDA_00460 | 6.2e-48 | 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) | |
LFBCNLDA_00461 | 2.4e-289 | 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) | |
LFBCNLDA_00462 | 7.1e-286 | 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) | |
LFBCNLDA_00463 | 5.6e-197 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
LFBCNLDA_00464 | 2.5e-52 | S | Protein of unknown function (DUF2469) | |||
LFBCNLDA_00465 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
LFBCNLDA_00466 | 9.2e-308 | 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 | ||
LFBCNLDA_00467 | 3e-234 | E | Aminotransferase class I and II | |||
LFBCNLDA_00468 | 1.5e-89 | lrp_3 | K | helix_turn_helix ASNC type | ||
LFBCNLDA_00469 | 4.7e-73 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
LFBCNLDA_00470 | 0.0 | S | domain protein | |||
LFBCNLDA_00471 | 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 | |
LFBCNLDA_00472 | 4.3e-294 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LFBCNLDA_00473 | 1.9e-126 | 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 | |
LFBCNLDA_00474 | 2e-135 | KT | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_00475 | 6.2e-105 | |||||
LFBCNLDA_00476 | 1.3e-102 | mntP | P | Probably functions as a manganese efflux pump | ||
LFBCNLDA_00478 | 5.2e-92 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
LFBCNLDA_00479 | 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 |
LFBCNLDA_00480 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
LFBCNLDA_00481 | 4.6e-35 | |||||
LFBCNLDA_00483 | 2e-207 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
LFBCNLDA_00484 | 6e-146 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
LFBCNLDA_00486 | 1.2e-30 | 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 | ||
LFBCNLDA_00487 | 4.6e-62 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
LFBCNLDA_00488 | 1.4e-150 | 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 | ||
LFBCNLDA_00489 | 0.0 | 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 | |
LFBCNLDA_00490 | 2.7e-166 | 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 | ||
LFBCNLDA_00491 | 1.5e-283 | 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 | |
LFBCNLDA_00492 | 8.7e-50 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
LFBCNLDA_00493 | 8e-131 | nucS | L | Cleaves both 3' and 5' ssDNA extremities of branched DNA structures | ||
LFBCNLDA_00494 | 5.9e-146 | QT | PucR C-terminal helix-turn-helix domain | |||
LFBCNLDA_00495 | 0.0 | |||||
LFBCNLDA_00496 | 3.2e-150 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
LFBCNLDA_00497 | 4.2e-93 | bioY | S | BioY family | ||
LFBCNLDA_00498 | 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 | |
LFBCNLDA_00499 | 7.2e-308 | pccB | I | Carboxyl transferase domain | ||
LFBCNLDA_00500 | 0.0 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LFBCNLDA_00501 | 6.5e-99 | 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 | |
LFBCNLDA_00502 | 1.6e-160 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
LFBCNLDA_00504 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
LFBCNLDA_00505 | 1.2e-118 | |||||
LFBCNLDA_00506 | 3e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LFBCNLDA_00507 | 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 | |
LFBCNLDA_00508 | 2.1e-115 | xylR | K | purine nucleotide biosynthetic process | ||
LFBCNLDA_00509 | 3.3e-90 | lemA | S | LemA family | ||
LFBCNLDA_00510 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
LFBCNLDA_00511 | 1.3e-73 | megL | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_00512 | 1.4e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_00513 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_00514 | 1.5e-98 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LFBCNLDA_00515 | 2.2e-41 | nrdH | O | Glutaredoxin | ||
LFBCNLDA_00516 | 5.1e-167 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
LFBCNLDA_00517 | 0.0 | oppD | P | Belongs to the ABC transporter superfamily | ||
LFBCNLDA_00518 | 4.6e-166 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
LFBCNLDA_00519 | 7.9e-177 | appB | EP | Binding-protein-dependent transport system inner membrane component | ||
LFBCNLDA_00520 | 8.6e-187 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
LFBCNLDA_00521 | 7.3e-42 | |||||
LFBCNLDA_00522 | 7.1e-192 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
LFBCNLDA_00523 | 1.7e-198 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
LFBCNLDA_00524 | 5.4e-79 | |||||
LFBCNLDA_00525 | 0.0 | typA | T | Elongation factor G C-terminus | ||
LFBCNLDA_00526 | 3.4e-236 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
LFBCNLDA_00527 | 1.4e-164 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, N-terminal domain | |
LFBCNLDA_00528 | 6.9e-311 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
LFBCNLDA_00529 | 3.7e-251 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
LFBCNLDA_00530 | 8.6e-150 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
LFBCNLDA_00531 | 9.2e-113 | 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 | ||
LFBCNLDA_00532 | 2.5e-150 | 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 | ||
LFBCNLDA_00533 | 2e-151 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LFBCNLDA_00534 | 2.9e-179 | xerD | D | recombinase XerD | ||
LFBCNLDA_00535 | 9.6e-62 | 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 | ||
LFBCNLDA_00536 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
LFBCNLDA_00537 | 1.4e-103 | 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 | ||
LFBCNLDA_00539 | 7.1e-08 | S | Spermine/spermidine synthase domain | |||
LFBCNLDA_00540 | 8e-134 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
LFBCNLDA_00541 | 1e-198 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LFBCNLDA_00542 | 2.4e-92 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
LFBCNLDA_00544 | 2e-180 | 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 | |
LFBCNLDA_00545 | 1.4e-194 | galM | 5.1.3.3 | G | Aldose 1-epimerase | |
LFBCNLDA_00546 | 2e-64 | |||||
LFBCNLDA_00547 | 2.1e-114 | sigH | K | Belongs to the sigma-70 factor family. ECF subfamily | ||
LFBCNLDA_00548 | 4.2e-297 | 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 | |
LFBCNLDA_00549 | 6.8e-192 | V | Acetyltransferase (GNAT) domain | |||
LFBCNLDA_00550 | 2.9e-229 | 2.6.1.33 | M | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
LFBCNLDA_00551 | 8.9e-242 | yxbA | 6.3.1.12 | S | ATP-grasp | |
LFBCNLDA_00552 | 7.4e-129 | racD | 5.1.1.13 | G | Belongs to the aspartate glutamate racemases family | |
LFBCNLDA_00553 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
LFBCNLDA_00554 | 8e-283 | folC | 6.3.2.12, 6.3.2.17 | H | Mur ligase middle domain | |
LFBCNLDA_00556 | 9.6e-97 | 3.6.1.55 | F | NUDIX domain | ||
LFBCNLDA_00557 | 0.0 | pepP | 3.4.11.9 | E | Aminopeptidase P, N-terminal domain | |
LFBCNLDA_00558 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
LFBCNLDA_00559 | 5.1e-191 | dppC | EP | Binding-protein-dependent transport system inner membrane component | ||
LFBCNLDA_00560 | 6.7e-185 | dppB | EP | Binding-protein-dependent transport system inner membrane component | ||
LFBCNLDA_00561 | 2.2e-304 | ddpA | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
LFBCNLDA_00562 | 9.6e-244 | nagA | 3.5.1.25 | G | Amidohydrolase family | |
LFBCNLDA_00563 | 6.6e-153 | nagB | 3.1.1.31, 3.5.99.6 | G | Catalyzes the reversible isomerization-deamination of glucosamine 6-phosphate (GlcN6P) to form fructose 6-phosphate (Fru6P) and ammonium ion | |
LFBCNLDA_00564 | 7.7e-216 | GK | ROK family | |||
LFBCNLDA_00565 | 3.4e-132 | cutC | P | Participates in the control of copper homeostasis | ||
LFBCNLDA_00566 | 1.3e-224 | GK | ROK family | |||
LFBCNLDA_00567 | 1.9e-169 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
LFBCNLDA_00568 | 1.3e-235 | G | Major Facilitator Superfamily | |||
LFBCNLDA_00569 | 1e-85 | 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 | ||
LFBCNLDA_00571 | 4.9e-37 | |||||
LFBCNLDA_00572 | 4.4e-148 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
LFBCNLDA_00573 | 1.1e-292 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
LFBCNLDA_00574 | 1.7e-218 | 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) |
LFBCNLDA_00575 | 9e-224 | ftsW | 2.4.1.227 | GT28 | D | Belongs to the SEDS family |
LFBCNLDA_00576 | 9.5e-264 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LFBCNLDA_00577 | 3.6e-202 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LFBCNLDA_00578 | 1.1e-284 | 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 | |
LFBCNLDA_00579 | 2.8e-180 | 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 | |
LFBCNLDA_00580 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
LFBCNLDA_00581 | 2.5e-59 | 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 | ||
LFBCNLDA_00582 | 1.1e-193 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LFBCNLDA_00583 | 1.3e-90 | mraZ | K | Belongs to the MraZ family | ||
LFBCNLDA_00584 | 0.0 | L | DNA helicase | |||
LFBCNLDA_00585 | 1.1e-228 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
LFBCNLDA_00586 | 7.1e-83 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LFBCNLDA_00587 | 1.1e-49 | M | Lysin motif | |||
LFBCNLDA_00588 | 7.5e-129 | 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 | |
LFBCNLDA_00589 | 2.3e-165 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
LFBCNLDA_00590 | 4.6e-177 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
LFBCNLDA_00591 | 9e-273 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LFBCNLDA_00592 | 1.2e-171 | |||||
LFBCNLDA_00593 | 1.4e-121 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
LFBCNLDA_00594 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
LFBCNLDA_00595 | 1.4e-176 | 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 | |||
LFBCNLDA_00596 | 2.8e-58 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_00597 | 2.1e-252 | S | Domain of unknown function (DUF5067) | |||
LFBCNLDA_00598 | 2.1e-265 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
LFBCNLDA_00599 | 5.4e-283 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
LFBCNLDA_00600 | 1.7e-131 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
LFBCNLDA_00601 | 4.8e-122 | 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 | ||
LFBCNLDA_00602 | 5.9e-113 | |||||
LFBCNLDA_00603 | 3.2e-112 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
LFBCNLDA_00604 | 2.1e-224 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LFBCNLDA_00605 | 1.1e-256 | 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 | |
LFBCNLDA_00606 | 1.2e-180 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_00607 | 3.9e-07 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
LFBCNLDA_00609 | 1.3e-75 | yneG | S | Domain of unknown function (DUF4186) | ||
LFBCNLDA_00610 | 1.7e-173 | dkgA | 1.1.1.346 | C | Aldo/keto reductase family | |
LFBCNLDA_00611 | 5e-156 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
LFBCNLDA_00612 | 1.2e-202 | K | WYL domain | |||
LFBCNLDA_00615 | 0.0 | 4.2.1.53 | S | MCRA family | ||
LFBCNLDA_00616 | 2e-46 | yhbY | J | CRS1_YhbY | ||
LFBCNLDA_00617 | 1.4e-83 | S | zinc-ribbon domain | |||
LFBCNLDA_00618 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
LFBCNLDA_00619 | 3e-39 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LFBCNLDA_00620 | 3.1e-19 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LFBCNLDA_00621 | 2.1e-190 | ywqG | S | Domain of unknown function (DUF1963) | ||
LFBCNLDA_00622 | 1.8e-155 | 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 | |
LFBCNLDA_00623 | 4.6e-143 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LFBCNLDA_00624 | 1.8e-290 | I | acetylesterase activity | |||
LFBCNLDA_00625 | 1e-235 | 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 | |
LFBCNLDA_00626 | 6.4e-221 | 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) | |
LFBCNLDA_00627 | 9.7e-201 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
LFBCNLDA_00629 | 5e-25 | |||||
LFBCNLDA_00630 | 4.1e-46 | |||||
LFBCNLDA_00631 | 5.6e-146 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
LFBCNLDA_00632 | 3e-76 | 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 | ||
LFBCNLDA_00633 | 9.7e-163 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
LFBCNLDA_00634 | 2.4e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
LFBCNLDA_00635 | 2.9e-188 | ftsE | D | Cell division ATP-binding protein FtsE | ||
LFBCNLDA_00636 | 3.7e-202 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LFBCNLDA_00637 | 5.2e-147 | 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 | |
LFBCNLDA_00638 | 6e-63 | |||||
LFBCNLDA_00640 | 3.4e-177 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LFBCNLDA_00641 | 4e-103 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LFBCNLDA_00642 | 9.7e-90 | 3.1.21.3 | V | DivIVA protein | ||
LFBCNLDA_00643 | 2.1e-42 | yggT | S | YGGT family | ||
LFBCNLDA_00644 | 4.3e-80 | 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 | ||
LFBCNLDA_00645 | 7.3e-231 | 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 | ||
LFBCNLDA_00646 | 9.5e-247 | 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 | ||
LFBCNLDA_00647 | 3.9e-300 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
LFBCNLDA_00648 | 0.0 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
LFBCNLDA_00649 | 2.6e-158 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
LFBCNLDA_00650 | 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 | |
LFBCNLDA_00651 | 1.3e-84 | |||||
LFBCNLDA_00652 | 6.9e-231 | O | AAA domain (Cdc48 subfamily) | |||
LFBCNLDA_00653 | 9.2e-164 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
LFBCNLDA_00654 | 4.7e-61 | S | Thiamine-binding protein | |||
LFBCNLDA_00655 | 1.8e-195 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_00656 | 5.5e-66 | S | Protein of unknown function (DUF3052) | |||
LFBCNLDA_00657 | 1.4e-150 | lon | T | Belongs to the peptidase S16 family | ||
LFBCNLDA_00658 | 5.6e-278 | S | Zincin-like metallopeptidase | |||
LFBCNLDA_00659 | 8.1e-282 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
LFBCNLDA_00660 | 7.6e-232 | mphA | S | Aminoglycoside phosphotransferase | ||
LFBCNLDA_00661 | 6.1e-32 | S | Protein of unknown function (DUF3107) | |||
LFBCNLDA_00662 | 2.5e-166 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
LFBCNLDA_00663 | 2e-115 | S | Vitamin K epoxide reductase | |||
LFBCNLDA_00664 | 2.3e-170 | 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 | |
LFBCNLDA_00665 | 1.5e-152 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LFBCNLDA_00666 | 1.2e-167 | S | Patatin-like phospholipase | |||
LFBCNLDA_00667 | 2.2e-293 | V | ABC transporter transmembrane region | |||
LFBCNLDA_00668 | 1.6e-17 | S | Transcription factor WhiB | |||
LFBCNLDA_00670 | 3.5e-154 | 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 |
LFBCNLDA_00671 | 3.4e-199 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LFBCNLDA_00672 | 4.4e-68 | S | Domain of unknown function (DUF4190) | |||
LFBCNLDA_00675 | 8.1e-205 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
LFBCNLDA_00676 | 4.3e-177 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
LFBCNLDA_00677 | 4.3e-273 | S | AI-2E family transporter | |||
LFBCNLDA_00678 | 1.3e-232 | epsG | M | Glycosyl transferase family 21 | ||
LFBCNLDA_00679 | 1.7e-168 | natA | V | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_00680 | 5.6e-308 | |||||
LFBCNLDA_00681 | 1.7e-260 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
LFBCNLDA_00682 | 1.5e-211 | 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 | |
LFBCNLDA_00683 | 4.7e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LFBCNLDA_00684 | 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 | ||
LFBCNLDA_00685 | 4.5e-100 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
LFBCNLDA_00686 | 8.4e-162 | 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 | |
LFBCNLDA_00687 | 4.6e-293 | 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 | |
LFBCNLDA_00688 | 2.8e-75 | S | Protein of unknown function (DUF3180) | |||
LFBCNLDA_00689 | 7.1e-172 | tesB | I | Thioesterase-like superfamily | ||
LFBCNLDA_00690 | 0.0 | 3.2.1.52, 3.2.1.83 | GH16,GH20 | G | hydrolase family 20, catalytic | |
LFBCNLDA_00691 | 2.4e-306 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
LFBCNLDA_00692 | 4e-19 | M | domain, Protein | |||
LFBCNLDA_00693 | 4.7e-48 | M | domain, Protein | |||
LFBCNLDA_00694 | 5.7e-126 | |||||
LFBCNLDA_00696 | 7.4e-115 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
LFBCNLDA_00697 | 4.4e-18 | S | Protein of unknown function (DUF979) | |||
LFBCNLDA_00698 | 7.5e-49 | S | DUF218 domain | |||
LFBCNLDA_00700 | 2.3e-113 | S | Pyridoxamine 5'-phosphate oxidase | |||
LFBCNLDA_00701 | 2.9e-159 | I | alpha/beta hydrolase fold | |||
LFBCNLDA_00702 | 3.5e-49 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_00703 | 2e-278 | S | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_00704 | 6.3e-179 | glkA | 2.7.1.2 | G | ROK family | |
LFBCNLDA_00705 | 5.2e-10 | K | Winged helix DNA-binding domain | |||
LFBCNLDA_00706 | 1.2e-11 | EGP | Major facilitator superfamily | |||
LFBCNLDA_00707 | 3.3e-50 | EGP | Major facilitator superfamily | |||
LFBCNLDA_00708 | 3.4e-252 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LFBCNLDA_00709 | 1.3e-215 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LFBCNLDA_00711 | 1.8e-148 | S | Sulfite exporter TauE/SafE | |||
LFBCNLDA_00712 | 1.6e-149 | V | FtsX-like permease family | |||
LFBCNLDA_00714 | 4.2e-164 | EG | EamA-like transporter family | |||
LFBCNLDA_00715 | 0.0 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
LFBCNLDA_00716 | 4.7e-141 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
LFBCNLDA_00717 | 1.1e-169 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
LFBCNLDA_00718 | 4.9e-104 | |||||
LFBCNLDA_00719 | 7.1e-258 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
LFBCNLDA_00720 | 1.2e-178 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
LFBCNLDA_00721 | 2.6e-163 | glcU | G | Sugar transport protein | ||
LFBCNLDA_00722 | 6.2e-196 | K | helix_turn_helix, arabinose operon control protein | |||
LFBCNLDA_00724 | 3.9e-36 | rpmE | J | Binds the 23S rRNA | ||
LFBCNLDA_00725 | 1.2e-189 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LFBCNLDA_00726 | 3.2e-186 | 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 | |
LFBCNLDA_00727 | 1.2e-54 | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | ||
LFBCNLDA_00728 | 8.9e-116 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
LFBCNLDA_00729 | 1e-191 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
LFBCNLDA_00730 | 1.7e-287 | 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 | |
LFBCNLDA_00731 | 0.0 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
LFBCNLDA_00732 | 2.4e-119 | KT | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_00733 | 2.8e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
LFBCNLDA_00734 | 8.4e-159 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
LFBCNLDA_00735 | 6.1e-271 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
LFBCNLDA_00737 | 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 | |
LFBCNLDA_00738 | 2.4e-170 | |||||
LFBCNLDA_00739 | 1.6e-120 | L | Single-strand binding protein family | |||
LFBCNLDA_00740 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LFBCNLDA_00741 | 3.1e-127 | S | Short repeat of unknown function (DUF308) | |||
LFBCNLDA_00742 | 1.1e-149 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
LFBCNLDA_00743 | 1.1e-250 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
LFBCNLDA_00744 | 5.1e-101 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
LFBCNLDA_00745 | 8.4e-198 | yghZ | C | Aldo/keto reductase family | ||
LFBCNLDA_00746 | 1.7e-79 | EGP | Major Facilitator Superfamily | |||
LFBCNLDA_00747 | 3.6e-93 | K | acetyltransferase | |||
LFBCNLDA_00748 | 0.0 | ctpE | P | E1-E2 ATPase | ||
LFBCNLDA_00749 | 0.0 | macB_2 | V | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_00750 | 5.8e-225 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
LFBCNLDA_00751 | 4.7e-260 | nox | 1.6.3.4 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LFBCNLDA_00752 | 5.7e-233 | metC | 2.5.1.48, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_00753 | 9.9e-244 | 2.5.1.49 | E | Cys/Met metabolism PLP-dependent enzyme | ||
LFBCNLDA_00754 | 1.8e-127 | XK27_08050 | O | prohibitin homologues | ||
LFBCNLDA_00755 | 3.2e-275 | aldH | 1.2.1.3, 1.2.1.5 | C | Aldehyde dehydrogenase family | |
LFBCNLDA_00756 | 5e-55 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
LFBCNLDA_00757 | 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) | |
LFBCNLDA_00759 | 0.0 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
LFBCNLDA_00760 | 1.4e-17 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
LFBCNLDA_00761 | 2.9e-190 | K | Periplasmic binding protein domain | |||
LFBCNLDA_00762 | 1.3e-42 | G | ABC transporter permease | |||
LFBCNLDA_00763 | 9.4e-56 | G | ABC transporter permease | |||
LFBCNLDA_00764 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_00765 | 2.3e-69 | G | carbohydrate transport | |||
LFBCNLDA_00766 | 8.8e-278 | G | Bacterial extracellular solute-binding protein | |||
LFBCNLDA_00767 | 3.6e-143 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
LFBCNLDA_00768 | 4.6e-310 | E | ABC transporter, substrate-binding protein, family 5 | |||
LFBCNLDA_00769 | 5.5e-170 | P | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_00770 | 1.4e-162 | EP | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_00771 | 4e-142 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
LFBCNLDA_00772 | 2e-155 | sapF | E | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_00773 | 1e-187 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LFBCNLDA_00774 | 1.2e-135 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
LFBCNLDA_00775 | 2.1e-128 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
LFBCNLDA_00776 | 3.4e-50 | |||||
LFBCNLDA_00777 | 7.6e-60 | |||||
LFBCNLDA_00778 | 2.2e-94 | J | tRNA 5'-leader removal | |||
LFBCNLDA_00780 | 6.9e-118 | cyaA | 4.6.1.1 | S | CYTH | |
LFBCNLDA_00781 | 8.5e-163 | trxA2 | O | Tetratricopeptide repeat | ||
LFBCNLDA_00782 | 7.9e-180 | |||||
LFBCNLDA_00783 | 1.3e-188 | |||||
LFBCNLDA_00784 | 1.2e-164 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
LFBCNLDA_00785 | 6.1e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
LFBCNLDA_00786 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LFBCNLDA_00787 | 6.4e-128 | |||||
LFBCNLDA_00788 | 2.1e-131 | K | Bacterial regulatory proteins, tetR family | |||
LFBCNLDA_00789 | 8.2e-225 | G | Transmembrane secretion effector | |||
LFBCNLDA_00790 | 9.8e-255 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LFBCNLDA_00791 | 2.6e-219 | pyrD | 1.3.1.14 | F | Dihydroorotate dehydrogenase | |
LFBCNLDA_00792 | 5.6e-179 | S | CAAX protease self-immunity | |||
LFBCNLDA_00794 | 0.0 | snf | 2.7.11.1 | KL | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_00795 | 3.8e-133 | 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 | |
LFBCNLDA_00796 | 2.2e-273 | 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 | |
LFBCNLDA_00797 | 2.2e-138 | ltbR | K | Transcriptional regulator, IclR family, C-terminal domain protein | ||
LFBCNLDA_00798 | 1.3e-251 | S | Calcineurin-like phosphoesterase | |||
LFBCNLDA_00801 | 4.4e-72 | S | Domain of unknown function (DUF4143) | |||
LFBCNLDA_00802 | 4.9e-276 | 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) | |
LFBCNLDA_00804 | 3.1e-124 | S | HAD hydrolase, family IA, variant 3 | |||
LFBCNLDA_00805 | 3.3e-200 | P | NMT1/THI5 like | |||
LFBCNLDA_00806 | 1.7e-137 | ytlD1 | 2.7.1.50 | P | Binding-protein-dependent transport system inner membrane component | |
LFBCNLDA_00807 | 7.8e-142 | |||||
LFBCNLDA_00808 | 3.6e-125 | 3.1.3.3, 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_00809 | 6.2e-263 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_00810 | 2.6e-97 | S | GtrA-like protein | |||
LFBCNLDA_00811 | 1.3e-62 | S | Macrophage migration inhibitory factor (MIF) | |||
LFBCNLDA_00812 | 8.5e-287 | fhs | 1.5.1.5, 3.5.4.9, 6.3.4.3 | F | Formate-tetrahydrofolate ligase | |
LFBCNLDA_00813 | 0.0 | pepD | E | Peptidase family C69 | ||
LFBCNLDA_00814 | 1.3e-107 | S | Phosphatidylethanolamine-binding protein | |||
LFBCNLDA_00815 | 0.0 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
LFBCNLDA_00816 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
LFBCNLDA_00817 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
LFBCNLDA_00818 | 5.9e-94 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
LFBCNLDA_00819 | 8.2e-190 | 1.1.1.65 | C | Aldo/keto reductase family | ||
LFBCNLDA_00820 | 7.7e-79 | M | Belongs to the glycosyl hydrolase 30 family | |||
LFBCNLDA_00821 | 5.8e-26 | M | Belongs to the glycosyl hydrolase 30 family | |||
LFBCNLDA_00823 | 0.0 | cas9 | L | CRISPR (clustered regularly interspaced short palindromic repeat) is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). In type II CRISPR systems correct processing of pre-crRNA requires a trans-encoded small RNA (tracrRNA), endogenous ribonuclease 3 (rnc) and this protein. The tracrRNA serves as a guide for ribonuclease 3-aided processing of pre-crRNA. Subsequently Cas9 crRNA tracrRNA endonucleolytically cleaves linear or circular dsDNA target complementary to the spacer | ||
LFBCNLDA_00824 | 2.6e-126 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
LFBCNLDA_00825 | 2.6e-78 | S | CRISPR-associated protein (Cas_Csn2) | |||
LFBCNLDA_00826 | 4.2e-23 | L | Transposase, Mutator family | |||
LFBCNLDA_00827 | 5.2e-85 | |||||
LFBCNLDA_00828 | 2.7e-10 | sprF | 4.6.1.1 | M | Cell surface antigen C-terminus | |
LFBCNLDA_00829 | 2.9e-86 | |||||
LFBCNLDA_00830 | 2.1e-41 | XAC3035 | O | Glutaredoxin | ||
LFBCNLDA_00831 | 5.7e-159 | S | Virulence factor BrkB | |||
LFBCNLDA_00832 | 9.3e-95 | bcp | 1.11.1.15 | O | Redoxin | |
LFBCNLDA_00833 | 1.2e-39 | E | ABC transporter | |||
LFBCNLDA_00834 | 3e-116 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
LFBCNLDA_00835 | 8.6e-84 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
LFBCNLDA_00836 | 0.0 | V | FtsX-like permease family | |||
LFBCNLDA_00837 | 2.6e-129 | V | ABC transporter | |||
LFBCNLDA_00838 | 2.4e-101 | K | Transcriptional regulator C-terminal region | |||
LFBCNLDA_00839 | 3.4e-272 | aroP | E | aromatic amino acid transport protein AroP K03293 | ||
LFBCNLDA_00840 | 0.0 | lacZ | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_00842 | 2e-183 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein of unknown function (DUF559) | |
LFBCNLDA_00843 | 3e-127 | 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 | |
LFBCNLDA_00844 | 2.5e-22 | |||||
LFBCNLDA_00845 | 6.1e-53 | L | transposase activity | |||
LFBCNLDA_00846 | 9.8e-89 | tnp7109-21 | L | Integrase core domain | ||
LFBCNLDA_00847 | 6.7e-77 | T | protein histidine kinase activity | |||
LFBCNLDA_00848 | 1.9e-89 | K | LytTr DNA-binding domain | |||
LFBCNLDA_00849 | 1e-47 | S | Protein of unknown function (DUF3073) | |||
LFBCNLDA_00850 | 6.5e-204 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFBCNLDA_00851 | 7.4e-194 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_00852 | 2.7e-178 | S | Amidohydrolase family | |||
LFBCNLDA_00853 | 0.0 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LFBCNLDA_00854 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LFBCNLDA_00855 | 4.3e-239 | yhjX | EGP | Major facilitator Superfamily | ||
LFBCNLDA_00856 | 1.9e-308 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LFBCNLDA_00857 | 0.0 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
LFBCNLDA_00858 | 2.9e-107 | ahpC | 1.11.1.15 | O | C-terminal domain of 1-Cys peroxiredoxin | |
LFBCNLDA_00859 | 7.6e-118 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LFBCNLDA_00860 | 6.3e-53 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_00861 | 1.2e-241 | ytfL | P | Transporter associated domain | ||
LFBCNLDA_00862 | 2.2e-188 | yddG | EG | EamA-like transporter family | ||
LFBCNLDA_00863 | 1.9e-83 | dps | P | Belongs to the Dps family | ||
LFBCNLDA_00864 | 2.8e-134 | S | Protein of unknown function DUF45 | |||
LFBCNLDA_00865 | 5.2e-252 | ulaA | 2.7.1.194 | S | PTS system sugar-specific permease component | |
LFBCNLDA_00866 | 3.3e-40 | ulaC | 2.7.1.194 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
LFBCNLDA_00867 | 7.3e-77 | ulaC | 2.7.1.194, 2.7.1.197, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |
LFBCNLDA_00868 | 2.3e-190 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_00869 | 0.0 | G | Glycosyl hydrolase family 20, domain 2 | |||
LFBCNLDA_00872 | 0.0 | 3.2.1.55 | GH51 | G | arabinose metabolic process | |
LFBCNLDA_00873 | 2.5e-50 | 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 | ||
LFBCNLDA_00874 | 2.5e-124 | gntR | K | FCD | ||
LFBCNLDA_00875 | 2.3e-259 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LFBCNLDA_00876 | 1.9e-24 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LFBCNLDA_00879 | 3.4e-18 | S | Domain of unknown function (DUF4160) | |||
LFBCNLDA_00880 | 9.6e-42 | S | Protein of unknown function (DUF2442) | |||
LFBCNLDA_00881 | 6.7e-09 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_00882 | 2.3e-228 | I | Serine aminopeptidase, S33 | |||
LFBCNLDA_00883 | 2.7e-187 | K | Periplasmic binding protein domain | |||
LFBCNLDA_00884 | 7.9e-187 | G | Glycosyl hydrolases family 43 | |||
LFBCNLDA_00886 | 1.3e-14 | abfA1 | 3.2.1.55 | GH51 | G | arabinose metabolic process |
LFBCNLDA_00887 | 1.2e-73 | S | Transmembrane domain of unknown function (DUF3566) | |||
LFBCNLDA_00888 | 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 | |
LFBCNLDA_00889 | 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 | |
LFBCNLDA_00890 | 3.1e-88 | S | Protein of unknown function (DUF721) | |||
LFBCNLDA_00891 | 2.6e-239 | 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 | ||
LFBCNLDA_00892 | 6e-205 | 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 | |
LFBCNLDA_00893 | 4.1e-300 | 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 | ||
LFBCNLDA_00894 | 4.5e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
LFBCNLDA_00895 | 7.4e-170 | yidC | U | Membrane protein insertase, YidC Oxa1 family | ||
LFBCNLDA_00896 | 1.5e-92 | jag | S | Putative single-stranded nucleic acids-binding domain | ||
LFBCNLDA_00897 | 1.9e-124 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
LFBCNLDA_00898 | 8.5e-179 | parA | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LFBCNLDA_00899 | 3e-243 | parB | K | Belongs to the ParB family | ||
LFBCNLDA_00900 | 2e-203 | trxB | 1.8.1.9, 4.3.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LFBCNLDA_00901 | 0.0 | murJ | KLT | MviN-like protein | ||
LFBCNLDA_00902 | 0.0 | M | Conserved repeat domain | |||
LFBCNLDA_00903 | 5.2e-124 | deoC | 3.6.1.13, 3.6.1.17, 3.6.1.55, 3.6.1.61 | L | Belongs to the Nudix hydrolase family | |
LFBCNLDA_00904 | 1e-278 | cca | 2.7.7.19, 2.7.7.72 | J | Probable RNA and SrmB- binding site of polymerase A | |
LFBCNLDA_00905 | 6.7e-113 | S | LytR cell envelope-related transcriptional attenuator | |||
LFBCNLDA_00906 | 1.3e-166 | 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 | |
LFBCNLDA_00907 | 4.8e-171 | 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 | |
LFBCNLDA_00908 | 8.1e-213 | S | G5 | |||
LFBCNLDA_00910 | 2.4e-150 | O | Thioredoxin | |||
LFBCNLDA_00911 | 0.0 | KLT | Protein tyrosine kinase | |||
LFBCNLDA_00912 | 3.4e-174 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_00913 | 4.3e-211 | ugpC | E | Belongs to the ABC transporter superfamily | ||
LFBCNLDA_00914 | 8e-102 | L | Helix-turn-helix domain | |||
LFBCNLDA_00915 | 7.1e-162 | |||||
LFBCNLDA_00916 | 2.8e-188 | nusA | K | Participates in both transcription termination and antitermination | ||
LFBCNLDA_00917 | 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 | ||
LFBCNLDA_00918 | 4.7e-84 | 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 | ||
LFBCNLDA_00919 | 5.3e-237 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
LFBCNLDA_00920 | 6.9e-234 | ribF | 2.7.1.26, 2.7.7.2 | H | riboflavin kinase | |
LFBCNLDA_00921 | 7.9e-255 | 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 | ||
LFBCNLDA_00922 | 1.2e-106 | |||||
LFBCNLDA_00924 | 5.4e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LFBCNLDA_00925 | 3.8e-204 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LFBCNLDA_00926 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
LFBCNLDA_00927 | 2.6e-261 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LFBCNLDA_00928 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
LFBCNLDA_00929 | 4.6e-74 | M | Spy0128-like isopeptide containing domain | |||
LFBCNLDA_00930 | 6.8e-43 | M | Spy0128-like isopeptide containing domain | |||
LFBCNLDA_00931 | 0.0 | crr | G | pts system, glucose-specific IIABC component | ||
LFBCNLDA_00932 | 1.3e-151 | arbG | K | CAT RNA binding domain | ||
LFBCNLDA_00933 | 5e-215 | I | Diacylglycerol kinase catalytic domain | |||
LFBCNLDA_00934 | 0.0 | nucH | 3.1.3.5 | F | 5'-nucleotidase, C-terminal domain | |
LFBCNLDA_00935 | 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) | |
LFBCNLDA_00937 | 0.0 | nagLU | 3.1.4.53, 3.2.1.21, 3.2.1.50 | GH3 | G | Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain |
LFBCNLDA_00939 | 1.8e-95 | |||||
LFBCNLDA_00940 | 0.0 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LFBCNLDA_00941 | 4.2e-186 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LFBCNLDA_00942 | 2.3e-142 | pgl | 3.1.1.31 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LFBCNLDA_00944 | 4.5e-277 | 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 | |
LFBCNLDA_00945 | 1.9e-125 | degU | K | helix_turn_helix, Lux Regulon | ||
LFBCNLDA_00946 | 1.3e-255 | tcsS3 | KT | PspC domain | ||
LFBCNLDA_00947 | 5.9e-292 | pspC | KT | PspC domain | ||
LFBCNLDA_00948 | 3.2e-130 | |||||
LFBCNLDA_00949 | 6.1e-111 | S | Protein of unknown function (DUF4125) | |||
LFBCNLDA_00950 | 0.0 | S | Domain of unknown function (DUF4037) | |||
LFBCNLDA_00951 | 5.6e-217 | araJ | EGP | Major facilitator Superfamily | ||
LFBCNLDA_00953 | 0.0 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LFBCNLDA_00954 | 1.1e-173 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
LFBCNLDA_00955 | 1.3e-153 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LFBCNLDA_00956 | 1.4e-09 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_00957 | 1.7e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LFBCNLDA_00958 | 1.6e-217 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LFBCNLDA_00959 | 2.6e-39 | |||||
LFBCNLDA_00960 | 4.2e-214 | 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 | |
LFBCNLDA_00961 | 6.3e-177 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LFBCNLDA_00962 | 6e-106 | M | NlpC/P60 family | |||
LFBCNLDA_00963 | 1.6e-191 | T | Universal stress protein family | |||
LFBCNLDA_00964 | 3.2e-71 | attW | O | OsmC-like protein | ||
LFBCNLDA_00965 | 1.9e-174 | 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 | |
LFBCNLDA_00966 | 7.8e-128 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
LFBCNLDA_00967 | 1.8e-95 | ptpA | 3.1.3.48 | T | low molecular weight | |
LFBCNLDA_00968 | 3.7e-196 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
LFBCNLDA_00969 | 9.4e-23 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
LFBCNLDA_00970 | 1.7e-31 | vex2 | V | ABC transporter, ATP-binding protein | ||
LFBCNLDA_00971 | 2.9e-234 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LFBCNLDA_00974 | 1.7e-243 | 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 | ||
LFBCNLDA_00975 | 1.2e-126 | 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 | |
LFBCNLDA_00976 | 1.1e-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 | |
LFBCNLDA_00977 | 1.6e-255 | clcA_2 | P | Voltage gated chloride channel | ||
LFBCNLDA_00978 | 3.4e-234 | 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 | ||
LFBCNLDA_00979 | 1.6e-246 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
LFBCNLDA_00980 | 5.9e-111 | S | Protein of unknown function (DUF3000) | |||
LFBCNLDA_00981 | 3.9e-175 | 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 | |
LFBCNLDA_00982 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
LFBCNLDA_00983 | 6.4e-40 | |||||
LFBCNLDA_00984 | 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 | |
LFBCNLDA_00985 | 5e-223 | S | Peptidase dimerisation domain | |||
LFBCNLDA_00986 | 2.4e-87 | P | ABC-type metal ion transport system permease component | |||
LFBCNLDA_00987 | 3.8e-167 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LFBCNLDA_00988 | 8.4e-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 | |
LFBCNLDA_00989 | 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 | |
LFBCNLDA_00990 | 2.2e-84 | 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 | |
LFBCNLDA_00991 | 1.4e-47 | S | Domain of unknown function (DUF4193) | |||
LFBCNLDA_00992 | 2e-173 | S | Protein of unknown function (DUF3071) | |||
LFBCNLDA_00993 | 8.6e-237 | S | Type I phosphodiesterase / nucleotide pyrophosphatase | |||
LFBCNLDA_00994 | 0.0 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LFBCNLDA_00995 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
LFBCNLDA_00996 | 5.9e-42 | S | Protein of unknown function (DUF2975) | |||
LFBCNLDA_00997 | 4.9e-276 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
LFBCNLDA_00998 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LFBCNLDA_00999 | 6.3e-181 | 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 | ||
LFBCNLDA_01000 | 7.2e-121 | |||||
LFBCNLDA_01001 | 1.5e-200 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
LFBCNLDA_01002 | 0.0 | pknL | 2.7.11.1 | KLT | PASTA | |
LFBCNLDA_01003 | 1e-133 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LFBCNLDA_01004 | 4.3e-109 | |||||
LFBCNLDA_01005 | 1.1e-192 | 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) | |
LFBCNLDA_01006 | 3.6e-25 | 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 | ||
LFBCNLDA_01007 | 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 | ||
LFBCNLDA_01008 | 6.7e-111 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LFBCNLDA_01010 | 1.1e-86 | recX | S | Modulates RecA activity | ||
LFBCNLDA_01011 | 8e-216 | 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 | ||
LFBCNLDA_01012 | 3.7e-40 | S | Protein of unknown function (DUF3046) | |||
LFBCNLDA_01013 | 1.4e-79 | K | Helix-turn-helix XRE-family like proteins | |||
LFBCNLDA_01014 | 1.3e-96 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LFBCNLDA_01015 | 9.2e-124 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LFBCNLDA_01016 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
LFBCNLDA_01017 | 3.5e-137 | fic | D | Fic/DOC family | ||
LFBCNLDA_01018 | 3.1e-185 | 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) | |
LFBCNLDA_01019 | 5.7e-280 | 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 | |
LFBCNLDA_01020 | 3.5e-120 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
LFBCNLDA_01021 | 2.4e-170 | ydeD | EG | EamA-like transporter family | ||
LFBCNLDA_01022 | 6.6e-132 | ybhL | S | Belongs to the BI1 family | ||
LFBCNLDA_01023 | 1e-97 | S | Domain of unknown function (DUF5067) | |||
LFBCNLDA_01024 | 1.9e-267 | T | Histidine kinase | |||
LFBCNLDA_01025 | 9.1e-116 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_01026 | 0.0 | S | Protein of unknown function DUF262 | |||
LFBCNLDA_01027 | 2e-302 | gmk | 2.4.2.10, 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LFBCNLDA_01028 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
LFBCNLDA_01029 | 3e-93 | T | Forkhead associated domain | |||
LFBCNLDA_01030 | 2.8e-57 | B | Belongs to the OprB family | |||
LFBCNLDA_01031 | 6.3e-165 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
LFBCNLDA_01032 | 0.0 | E | Transglutaminase-like superfamily | |||
LFBCNLDA_01033 | 5.2e-224 | S | Protein of unknown function DUF58 | |||
LFBCNLDA_01034 | 8.2e-230 | S | ATPase family associated with various cellular activities (AAA) | |||
LFBCNLDA_01035 | 0.0 | S | Fibronectin type 3 domain | |||
LFBCNLDA_01036 | 7.5e-269 | KLT | Protein tyrosine kinase | |||
LFBCNLDA_01037 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
LFBCNLDA_01038 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
LFBCNLDA_01039 | 2.4e-153 | K | -acetyltransferase | |||
LFBCNLDA_01040 | 2.2e-249 | G | Major Facilitator Superfamily | |||
LFBCNLDA_01041 | 6.4e-24 | relB | L | RelB antitoxin | ||
LFBCNLDA_01042 | 7.4e-58 | L | Transposase | |||
LFBCNLDA_01043 | 1e-132 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LFBCNLDA_01044 | 9.4e-161 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LFBCNLDA_01045 | 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 | ||
LFBCNLDA_01046 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
LFBCNLDA_01047 | 3.7e-251 | O | Subtilase family | |||
LFBCNLDA_01048 | 1.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LFBCNLDA_01049 | 1.2e-123 | 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 | |
LFBCNLDA_01050 | 3.6e-271 | S | zinc finger | |||
LFBCNLDA_01051 | 9e-113 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LFBCNLDA_01052 | 2.9e-229 | aspB | E | Aminotransferase class-V | ||
LFBCNLDA_01053 | 1.8e-157 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LFBCNLDA_01054 | 1e-131 | tmp1 | S | Domain of unknown function (DUF4391) | ||
LFBCNLDA_01055 | 9.8e-149 | moeB | 2.7.7.80 | H | ThiF family | |
LFBCNLDA_01056 | 1e-254 | cdr | OP | Sulfurtransferase TusA | ||
LFBCNLDA_01057 | 3.1e-181 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LFBCNLDA_01060 | 1.9e-172 | S | Endonuclease/Exonuclease/phosphatase family | |||
LFBCNLDA_01061 | 7.8e-43 | 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 | |
LFBCNLDA_01062 | 8.5e-273 | 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 | |
LFBCNLDA_01063 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
LFBCNLDA_01064 | 1.2e-139 | 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 | |
LFBCNLDA_01066 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LFBCNLDA_01067 | 4.5e-166 | |||||
LFBCNLDA_01068 | 1.7e-256 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
LFBCNLDA_01069 | 0.0 | plyA3 | 3.2.1.18 | GH33 | M | Parallel beta-helix repeats |
LFBCNLDA_01071 | 2.9e-88 | K | MarR family | |||
LFBCNLDA_01072 | 0.0 | V | ABC transporter, ATP-binding protein | |||
LFBCNLDA_01073 | 7.7e-45 | V | ABC transporter transmembrane region | |||
LFBCNLDA_01074 | 1.8e-43 | tnp7109-21 | L | Integrase core domain | ||
LFBCNLDA_01075 | 1e-50 | L | DNA-dependent DNA replication | |||
LFBCNLDA_01076 | 3.6e-74 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_01077 | 2e-73 | I | Sterol carrier protein | |||
LFBCNLDA_01078 | 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 |
LFBCNLDA_01079 | 5.8e-35 | |||||
LFBCNLDA_01080 | 6.4e-145 | gluP | 3.4.21.105 | S | Rhomboid family | |
LFBCNLDA_01081 | 6.7e-120 | L | HTH-like domain | |||
LFBCNLDA_01082 | 4.4e-255 | L | ribosomal rna small subunit methyltransferase | |||
LFBCNLDA_01083 | 2.6e-71 | crgA | D | Involved in cell division | ||
LFBCNLDA_01084 | 3.5e-143 | S | Bacterial protein of unknown function (DUF881) | |||
LFBCNLDA_01085 | 2.6e-233 | srtA | 3.4.22.70 | M | Sortase family | |
LFBCNLDA_01086 | 3.4e-120 | trpG | 2.6.1.85 | EH | para-aminobenzoate synthase glutamine amidotransferase component II | |
LFBCNLDA_01087 | 0.0 | pknB | 2.7.11.1 | KLT | Protein tyrosine kinase | |
LFBCNLDA_01088 | 2e-183 | T | Protein tyrosine kinase | |||
LFBCNLDA_01089 | 2.4e-262 | pbpA | M | penicillin-binding protein | ||
LFBCNLDA_01090 | 1.1e-262 | rodA | D | Belongs to the SEDS family | ||
LFBCNLDA_01091 | 4.7e-259 | pstP | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | |
LFBCNLDA_01092 | 1.3e-93 | fhaB | T | Inner membrane component of T3SS, cytoplasmic domain | ||
LFBCNLDA_01093 | 1e-130 | fhaA | T | Protein of unknown function (DUF2662) | ||
LFBCNLDA_01094 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
LFBCNLDA_01095 | 0.0 | pip | S | YhgE Pip domain protein | ||
LFBCNLDA_01096 | 0.0 | pip | S | YhgE Pip domain protein | ||
LFBCNLDA_01097 | 3.3e-205 | pldB | 3.1.1.5 | I | Serine aminopeptidase, S33 | |
LFBCNLDA_01098 | 5.3e-165 | yicL | EG | EamA-like transporter family | ||
LFBCNLDA_01099 | 4.5e-103 | |||||
LFBCNLDA_01101 | 1.6e-196 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
LFBCNLDA_01103 | 0.0 | KL | Domain of unknown function (DUF3427) | |||
LFBCNLDA_01104 | 2.5e-89 | nudG | 3.6.1.55, 3.6.1.65 | L | NUDIX domain | |
LFBCNLDA_01105 | 5.7e-36 | D | DivIVA domain protein | |||
LFBCNLDA_01107 | 9.3e-53 | ybjQ | S | Putative heavy-metal-binding | ||
LFBCNLDA_01108 | 3.1e-158 | I | Serine aminopeptidase, S33 | |||
LFBCNLDA_01109 | 2.2e-87 | yjcF | Q | Acetyltransferase (GNAT) domain | ||
LFBCNLDA_01111 | 4.9e-259 | 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) | |
LFBCNLDA_01112 | 3.9e-244 | degP | O | Domain present in PSD-95, Dlg, and ZO-1/2. | ||
LFBCNLDA_01113 | 0.0 | cadA | P | E1-E2 ATPase | ||
LFBCNLDA_01114 | 5e-273 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LFBCNLDA_01115 | 4.9e-168 | htpX | O | Belongs to the peptidase M48B family | ||
LFBCNLDA_01117 | 0.0 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LFBCNLDA_01118 | 1.9e-42 | S | Bacterial mobilisation protein (MobC) | |||
LFBCNLDA_01119 | 2.3e-127 | S | Domain of unknown function (DUF4417) | |||
LFBCNLDA_01121 | 1.9e-61 | |||||
LFBCNLDA_01122 | 2e-64 | |||||
LFBCNLDA_01123 | 3e-50 | E | Zn peptidase | |||
LFBCNLDA_01124 | 2e-12 | E | IrrE N-terminal-like domain | |||
LFBCNLDA_01125 | 4.9e-57 | K | Cro/C1-type HTH DNA-binding domain | |||
LFBCNLDA_01126 | 3.8e-251 | 3.5.1.104 | G | Polysaccharide deacetylase | ||
LFBCNLDA_01127 | 3.3e-200 | fbaA | 4.1.2.13 | G | Fructose-bisphosphate aldolase class-II | |
LFBCNLDA_01128 | 1.7e-251 | 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 | |
LFBCNLDA_01129 | 6.9e-162 | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | |||
LFBCNLDA_01130 | 4.3e-59 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
LFBCNLDA_01131 | 8.4e-193 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_01132 | 4.8e-78 | gtfA | 2.4.1.329, 2.4.1.7 | GH13 | G | Domain of unknown function (DUF1964) |
LFBCNLDA_01133 | 7e-298 | scrT | G | Transporter major facilitator family protein | ||
LFBCNLDA_01134 | 5e-254 | yhjE | EGP | Sugar (and other) transporter | ||
LFBCNLDA_01136 | 1.4e-173 | K | Putative sugar-binding domain | |||
LFBCNLDA_01137 | 4e-213 | gatC | G | PTS system sugar-specific permease component | ||
LFBCNLDA_01138 | 2.9e-295 | 2.7.1.53 | G | FGGY family of carbohydrate kinases, C-terminal domain | ||
LFBCNLDA_01139 | 1.1e-172 | ulaE | 5.1.3.22 | G | Xylose isomerase-like TIM barrel | |
LFBCNLDA_01140 | 1.1e-129 | araD | 4.1.2.17, 5.1.3.4 | G | Class II Aldolase and Adducin N-terminal domain | |
LFBCNLDA_01141 | 5.6e-62 | 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 | ||
LFBCNLDA_01142 | 1.8e-158 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LFBCNLDA_01143 | 1.2e-131 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LFBCNLDA_01144 | 6.4e-207 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_01145 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_01146 | 6.9e-156 | 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 | |
LFBCNLDA_01147 | 4.8e-111 | 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 | |
LFBCNLDA_01150 | 5.7e-170 | G | Glycosyl hydrolases family 43 | |||
LFBCNLDA_01151 | 6.5e-107 | G | Glycosyl hydrolases family 43 | |||
LFBCNLDA_01152 | 8.1e-202 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_01153 | 2.9e-170 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
LFBCNLDA_01154 | 1.7e-122 | L | Protein of unknown function (DUF1524) | |||
LFBCNLDA_01155 | 2.5e-226 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LFBCNLDA_01156 | 1.5e-305 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_01157 | 5.7e-225 | |||||
LFBCNLDA_01158 | 1.3e-179 | S | G5 | |||
LFBCNLDA_01159 | 1.5e-59 | trxA | 1.8.1.8, 1.8.1.9 | O | Belongs to the thioredoxin family | |
LFBCNLDA_01160 | 4.1e-118 | F | Domain of unknown function (DUF4916) | |||
LFBCNLDA_01161 | 1e-159 | mhpC | I | Alpha/beta hydrolase family | ||
LFBCNLDA_01162 | 1.1e-206 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
LFBCNLDA_01163 | 0.0 | enhA_2 | S | L,D-transpeptidase catalytic domain | ||
LFBCNLDA_01164 | 3.7e-72 | 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 | ||
LFBCNLDA_01165 | 4.1e-240 | S | Uncharacterized conserved protein (DUF2183) | |||
LFBCNLDA_01166 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
LFBCNLDA_01167 | 9.2e-192 | 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 | |
LFBCNLDA_01168 | 2.2e-232 | lplA | 6.3.1.20 | H | Biotin/lipoate A/B protein ligase family | |
LFBCNLDA_01169 | 1.6e-134 | glxR | K | helix_turn_helix, cAMP Regulatory protein | ||
LFBCNLDA_01170 | 0.0 | pon1 | 2.4.1.129, 3.4.16.4 | GT51 | M | Transglycosylase |
LFBCNLDA_01171 | 1.9e-219 | namA | 1.6.99.1 | C | NADH:flavin oxidoreductase / NADH oxidase family | |
LFBCNLDA_01172 | 6.7e-227 | 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 | |
LFBCNLDA_01173 | 3.1e-139 | glpR | K | DeoR C terminal sensor domain | ||
LFBCNLDA_01174 | 3.3e-252 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
LFBCNLDA_01175 | 9.9e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
LFBCNLDA_01176 | 5.6e-242 | EGP | Sugar (and other) transporter | |||
LFBCNLDA_01177 | 4.2e-43 | gcvR | T | Belongs to the UPF0237 family | ||
LFBCNLDA_01178 | 9.4e-253 | S | UPF0210 protein | |||
LFBCNLDA_01179 | 3.3e-72 | |||||
LFBCNLDA_01181 | 6.3e-122 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LFBCNLDA_01182 | 1.1e-62 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | Putative cell wall binding repeat |
LFBCNLDA_01183 | 5.5e-185 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
LFBCNLDA_01184 | 1.9e-102 | |||||
LFBCNLDA_01185 | 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 | |
LFBCNLDA_01186 | 3.5e-285 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFBCNLDA_01187 | 3.7e-159 | S | Domain of unknown function (DUF4357) | |||
LFBCNLDA_01188 | 9.6e-94 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
LFBCNLDA_01189 | 1.4e-178 | L | Phage integrase family | |||
LFBCNLDA_01190 | 4.1e-239 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LFBCNLDA_01191 | 1.1e-84 | argR | K | Regulates arginine biosynthesis genes | ||
LFBCNLDA_01192 | 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 | |
LFBCNLDA_01193 | 1.9e-247 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
LFBCNLDA_01194 | 1.7e-179 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LFBCNLDA_01195 | 7.9e-216 | 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 | |
LFBCNLDA_01196 | 5.9e-205 | 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 | |
LFBCNLDA_01197 | 1.3e-87 | |||||
LFBCNLDA_01198 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LFBCNLDA_01199 | 7e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LFBCNLDA_01200 | 1.3e-159 | 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 | |
LFBCNLDA_01201 | 4.5e-135 | ybbL | V | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_01202 | 2.5e-136 | ybbM | V | Uncharacterised protein family (UPF0014) | ||
LFBCNLDA_01203 | 6.8e-53 | IQ | oxidoreductase activity | |||
LFBCNLDA_01205 | 6.8e-93 | K | AraC-like ligand binding domain | |||
LFBCNLDA_01206 | 1.4e-237 | rutG | F | Permease family | ||
LFBCNLDA_01207 | 8.9e-158 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_01208 | 3.5e-62 | S | Phospholipase/Carboxylesterase | |||
LFBCNLDA_01209 | 1.6e-186 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
LFBCNLDA_01210 | 9.6e-144 | rlrG | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LFBCNLDA_01211 | 1.1e-115 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
LFBCNLDA_01212 | 1.7e-290 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
LFBCNLDA_01214 | 0.0 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
LFBCNLDA_01215 | 6.1e-125 | ypfH | S | Phospholipase/Carboxylesterase | ||
LFBCNLDA_01216 | 1.3e-72 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LFBCNLDA_01217 | 1.9e-24 | |||||
LFBCNLDA_01218 | 1.2e-34 | yhcC | S | Nucleic-acid-binding protein containing Zn-ribbon domain (DUF2082) | ||
LFBCNLDA_01219 | 2.8e-66 | S | Zincin-like metallopeptidase | |||
LFBCNLDA_01220 | 1e-86 | S | Helix-turn-helix | |||
LFBCNLDA_01221 | 2.5e-199 | S | Short C-terminal domain | |||
LFBCNLDA_01222 | 1e-21 | |||||
LFBCNLDA_01223 | 5e-12 | |||||
LFBCNLDA_01225 | 4.5e-79 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_01226 | 4.1e-258 | KLT | Protein tyrosine kinase | |||
LFBCNLDA_01227 | 2.6e-63 | S | Cupin 2, conserved barrel domain protein | |||
LFBCNLDA_01228 | 3.6e-157 | ksgA | 2.1.1.182 | J | Methyltransferase domain | |
LFBCNLDA_01229 | 5.6e-59 | yccF | S | Inner membrane component domain | ||
LFBCNLDA_01230 | 1.1e-119 | E | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_01231 | 5.2e-248 | XK27_00240 | K | Fic/DOC family | ||
LFBCNLDA_01232 | 1.4e-201 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LFBCNLDA_01233 | 1.7e-229 | mtnE | 2.6.1.83 | E | Aminotransferase class I and II | |
LFBCNLDA_01234 | 2.9e-93 | metI | P | Binding-protein-dependent transport system inner membrane component | ||
LFBCNLDA_01235 | 2e-203 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LFBCNLDA_01236 | 1.1e-181 | 1.2.4.1 | C | Pyruvate 2-oxoglutarate dehydrogenase complex dehydrogenase (E1) component eukaryotic type beta subunit | ||
LFBCNLDA_01237 | 3.6e-185 | acoA | 1.2.4.1 | C | Dehydrogenase E1 component | |
LFBCNLDA_01238 | 1.4e-147 | P | NLPA lipoprotein | |||
LFBCNLDA_01239 | 4.9e-168 | iaaA | 3.4.19.5, 3.5.1.1 | E | Asparaginase | |
LFBCNLDA_01240 | 1.5e-144 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LFBCNLDA_01241 | 1.4e-264 | pip | 3.4.11.5 | S | alpha/beta hydrolase fold | |
LFBCNLDA_01242 | 0.0 | tcsS2 | T | Histidine kinase | ||
LFBCNLDA_01243 | 6.1e-132 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_01244 | 0.0 | phoN | I | PAP2 superfamily | ||
LFBCNLDA_01245 | 3.5e-146 | KT | RESPONSE REGULATOR receiver | |||
LFBCNLDA_01246 | 2.2e-193 | V | VanZ like family | |||
LFBCNLDA_01247 | 2.3e-110 | ycaK | 1.6.5.2 | S | NADPH-dependent FMN reductase | |
LFBCNLDA_01248 | 1.9e-95 | ypjC | S | Putative ABC-transporter type IV | ||
LFBCNLDA_01249 | 1.2e-158 | |||||
LFBCNLDA_01251 | 3.4e-118 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_01252 | 1.3e-163 | rpoC | M | heme binding | ||
LFBCNLDA_01253 | 1.6e-79 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
LFBCNLDA_01254 | 7.2e-124 | |||||
LFBCNLDA_01255 | 1.9e-132 | S | SOS response associated peptidase (SRAP) | |||
LFBCNLDA_01256 | 2.9e-184 | S | Acetyltransferase (GNAT) domain | |||
LFBCNLDA_01258 | 4.5e-68 | |||||
LFBCNLDA_01260 | 2.4e-43 | 2.7.7.1, 3.6.1.13, 3.6.1.55 | F | Hydrolase of X-linked nucleoside diphosphate N terminal | ||
LFBCNLDA_01261 | 1.2e-55 | K | Transcriptional regulator | |||
LFBCNLDA_01262 | 3.7e-90 | MA20_25245 | K | FR47-like protein | ||
LFBCNLDA_01263 | 8.4e-119 | ydaF_1 | J | Acetyltransferase (GNAT) domain | ||
LFBCNLDA_01264 | 2.6e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
LFBCNLDA_01265 | 2.1e-162 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
LFBCNLDA_01266 | 1.7e-282 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_01267 | 2.3e-110 | S | Domain of unknown function (DUF4194) | |||
LFBCNLDA_01268 | 0.0 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_01269 | 1.5e-299 | E | Serine carboxypeptidase | |||
LFBCNLDA_01270 | 3.6e-162 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_01271 | 3.7e-171 | corA | P | CorA-like Mg2+ transporter protein | ||
LFBCNLDA_01272 | 1.7e-168 | ET | Bacterial periplasmic substrate-binding proteins | |||
LFBCNLDA_01273 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFBCNLDA_01274 | 1.7e-87 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
LFBCNLDA_01275 | 0.0 | comE | S | Competence protein | ||
LFBCNLDA_01276 | 4.8e-182 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LFBCNLDA_01277 | 1.7e-119 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
LFBCNLDA_01278 | 1.3e-159 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
LFBCNLDA_01279 | 3.1e-104 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
LFBCNLDA_01280 | 1.4e-195 | 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 | |
LFBCNLDA_01282 | 6.5e-132 | M | Peptidase family M23 | |||
LFBCNLDA_01283 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_01284 | 6.4e-277 | G | ABC transporter substrate-binding protein | |||
LFBCNLDA_01285 | 3.3e-241 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
LFBCNLDA_01286 | 2.5e-200 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
LFBCNLDA_01287 | 5.7e-91 | |||||
LFBCNLDA_01288 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
LFBCNLDA_01289 | 1.7e-87 | 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 | |
LFBCNLDA_01290 | 1.4e-145 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LFBCNLDA_01291 | 4.8e-146 | 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 | ||
LFBCNLDA_01292 | 1e-127 | 3.2.1.8 | S | alpha beta | ||
LFBCNLDA_01293 | 2.4e-133 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LFBCNLDA_01294 | 2.4e-93 | 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 | ||
LFBCNLDA_01295 | 1.8e-176 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
LFBCNLDA_01296 | 8.3e-229 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LFBCNLDA_01297 | 1.4e-139 | 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 | |
LFBCNLDA_01298 | 3.5e-73 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
LFBCNLDA_01299 | 7.1e-308 | 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 | |
LFBCNLDA_01300 | 6.9e-245 | G | Bacterial extracellular solute-binding protein | |||
LFBCNLDA_01301 | 1.1e-173 | G | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_01302 | 1e-168 | G | ABC transporter permease | |||
LFBCNLDA_01303 | 2.2e-135 | pgm3 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_01304 | 3.8e-64 | WQ51_05790 | S | Bacterial protein of unknown function (DUF948) | ||
LFBCNLDA_01305 | 1.1e-36 | |||||
LFBCNLDA_01306 | 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 | |
LFBCNLDA_01307 | 3e-75 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LFBCNLDA_01308 | 7.1e-188 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LFBCNLDA_01309 | 1.3e-47 | 3.4.23.43 | S | Type IV leader peptidase family | ||
LFBCNLDA_01310 | 3.5e-219 | 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 | |
LFBCNLDA_01311 | 0.0 | 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) | |
LFBCNLDA_01312 | 2.2e-78 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
LFBCNLDA_01313 | 3.4e-15 | |||||
LFBCNLDA_01314 | 1.7e-120 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_01315 | 2.6e-07 | 3.4.22.70 | M | Sortase family | ||
LFBCNLDA_01316 | 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 | |
LFBCNLDA_01317 | 3.6e-290 | sufB | O | FeS assembly protein SufB | ||
LFBCNLDA_01318 | 1.5e-233 | sufD | O | FeS assembly protein SufD | ||
LFBCNLDA_01319 | 1.4e-144 | sufC | O | FeS assembly ATPase SufC | ||
LFBCNLDA_01320 | 4.1e-242 | 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 | |
LFBCNLDA_01321 | 1.5e-100 | iscU | C | SUF system FeS assembly protein, NifU family | ||
LFBCNLDA_01322 | 1.2e-108 | yitW | S | Iron-sulfur cluster assembly protein | ||
LFBCNLDA_01323 | 4.7e-243 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
LFBCNLDA_01324 | 4e-164 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
LFBCNLDA_01326 | 1.4e-134 | 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 | |
LFBCNLDA_01327 | 4.4e-58 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
LFBCNLDA_01328 | 2e-197 | phoH | T | PhoH-like protein | ||
LFBCNLDA_01329 | 7.4e-100 | 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 | |
LFBCNLDA_01330 | 2.4e-251 | corC | S | CBS domain | ||
LFBCNLDA_01331 | 1.5e-186 | 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 | ||
LFBCNLDA_01332 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_01333 | 7e-201 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
LFBCNLDA_01334 | 4.4e-44 | pntA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
LFBCNLDA_01335 | 6.7e-233 | 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 | |
LFBCNLDA_01336 | 2.8e-190 | S | alpha beta | |||
LFBCNLDA_01337 | 3.9e-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 | ||
LFBCNLDA_01338 | 2.4e-225 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
LFBCNLDA_01339 | 2.8e-120 | 3.1.4.37 | T | RNA ligase | ||
LFBCNLDA_01340 | 6.6e-23 | 3.1.4.37 | T | RNA ligase | ||
LFBCNLDA_01341 | 4.4e-135 | S | UPF0126 domain | |||
LFBCNLDA_01342 | 9.9e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
LFBCNLDA_01343 | 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 | ||
LFBCNLDA_01344 | 3.7e-244 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LFBCNLDA_01345 | 4e-13 | S | Membrane | |||
LFBCNLDA_01346 | 4.3e-289 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
LFBCNLDA_01347 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
LFBCNLDA_01348 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
LFBCNLDA_01349 | 2.7e-304 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
LFBCNLDA_01350 | 3.6e-82 | |||||
LFBCNLDA_01351 | 5.6e-244 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
LFBCNLDA_01352 | 8.9e-164 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
LFBCNLDA_01353 | 1.7e-151 | ybeM | S | Carbon-nitrogen hydrolase | ||
LFBCNLDA_01354 | 3e-50 | S | Sel1-like repeats. | |||
LFBCNLDA_01355 | 7.3e-103 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
LFBCNLDA_01356 | 7.5e-34 | |||||
LFBCNLDA_01358 | 1.3e-153 | E | Transglutaminase/protease-like homologues | |||
LFBCNLDA_01359 | 0.0 | gcs2 | S | A circularly permuted ATPgrasp | ||
LFBCNLDA_01360 | 6.4e-173 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LFBCNLDA_01361 | 0.0 | 3.2.1.52 | GH20 | G | hydrolase family 20, catalytic | |
LFBCNLDA_01362 | 2.8e-64 | rplQ | J | Ribosomal protein L17 | ||
LFBCNLDA_01363 | 8.9e-184 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFBCNLDA_01364 | 1.1e-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 | ||
LFBCNLDA_01365 | 3.3e-62 | 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 | ||
LFBCNLDA_01366 | 6.5e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LFBCNLDA_01367 | 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 | ||
LFBCNLDA_01368 | 3.8e-99 | 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 | |
LFBCNLDA_01369 | 4.7e-249 | 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 | ||
LFBCNLDA_01370 | 6.1e-63 | rplO | J | binds to the 23S rRNA | ||
LFBCNLDA_01371 | 1e-24 | rpmD | J | Ribosomal protein L30p/L7e | ||
LFBCNLDA_01372 | 1.5e-100 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LFBCNLDA_01373 | 1.1e-57 | 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 | ||
LFBCNLDA_01374 | 2.1e-94 | 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 | ||
LFBCNLDA_01375 | 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 | ||
LFBCNLDA_01376 | 9.2e-18 | 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 | ||
LFBCNLDA_01377 | 2.2e-102 | 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 | ||
LFBCNLDA_01378 | 3.5e-52 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LFBCNLDA_01379 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LFBCNLDA_01380 | 3.5e-42 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LFBCNLDA_01381 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LFBCNLDA_01382 | 5.8e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LFBCNLDA_01383 | 7.5e-96 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LFBCNLDA_01384 | 4.3e-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 | ||
LFBCNLDA_01385 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LFBCNLDA_01386 | 4.2e-155 | 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 | ||
LFBCNLDA_01387 | 2.6e-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 | ||
LFBCNLDA_01388 | 3.9e-119 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LFBCNLDA_01389 | 4.2e-118 | 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 | ||
LFBCNLDA_01390 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LFBCNLDA_01391 | 1.6e-19 | ywiC | S | YwiC-like protein | ||
LFBCNLDA_01392 | 4.2e-08 | ywiC | S | YwiC-like protein | ||
LFBCNLDA_01393 | 8.7e-167 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
LFBCNLDA_01394 | 3.3e-149 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LFBCNLDA_01395 | 1.7e-11 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LFBCNLDA_01396 | 3.9e-119 | K | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_01397 | 1.9e-223 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
LFBCNLDA_01398 | 4.6e-180 | lacR | K | Transcriptional regulator, LacI family | ||
LFBCNLDA_01399 | 0.0 | lacL | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_01400 | 3.5e-46 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
LFBCNLDA_01401 | 3.5e-35 | lacS | G | Psort location CytoplasmicMembrane, score 10.00 | ||
LFBCNLDA_01402 | 1.1e-176 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LFBCNLDA_01405 | 6.4e-174 | S | Auxin Efflux Carrier | |||
LFBCNLDA_01406 | 1.1e-116 | 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 | |
LFBCNLDA_01407 | 2.1e-134 | 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 | |
LFBCNLDA_01408 | 7.5e-247 | 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 | |
LFBCNLDA_01410 | 7.6e-92 | ilvN | 2.2.1.6 | E | ACT domain | |
LFBCNLDA_01411 | 0.0 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
LFBCNLDA_01412 | 6.1e-140 | 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 | |
LFBCNLDA_01413 | 2.3e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LFBCNLDA_01414 | 1e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
LFBCNLDA_01415 | 1.6e-107 | |||||
LFBCNLDA_01416 | 1.7e-81 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LFBCNLDA_01417 | 2e-58 | S | Protein of unknown function (DUF3039) | |||
LFBCNLDA_01418 | 0.0 | yjjK | S | ABC transporter | ||
LFBCNLDA_01419 | 2.3e-136 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
LFBCNLDA_01420 | 0.0 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFBCNLDA_01421 | 4.2e-164 | P | Cation efflux family | |||
LFBCNLDA_01422 | 2.4e-271 | 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 | |
LFBCNLDA_01423 | 1.9e-222 | S | Endonuclease/Exonuclease/phosphatase family | |||
LFBCNLDA_01424 | 1.3e-93 | argO | S | LysE type translocator | ||
LFBCNLDA_01425 | 4.2e-294 | ydfD | EK | Alanine-glyoxylate amino-transferase | ||
LFBCNLDA_01426 | 1e-54 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LFBCNLDA_01427 | 1.8e-34 | CP_0960 | S | Belongs to the UPF0109 family | ||
LFBCNLDA_01428 | 6.4e-108 | 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 | ||
LFBCNLDA_01429 | 4.3e-162 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LFBCNLDA_01430 | 3.8e-81 | hsp20 | O | Hsp20/alpha crystallin family | ||
LFBCNLDA_01431 | 6.3e-108 | XK27_02070 | S | Nitroreductase family | ||
LFBCNLDA_01432 | 6.4e-120 | rsmD | 2.1.1.171 | L | Conserved hypothetical protein 95 | |
LFBCNLDA_01433 | 7.6e-249 | U | Sodium:dicarboxylate symporter family | |||
LFBCNLDA_01434 | 0.0 | |||||
LFBCNLDA_01437 | 1e-219 | steT | E | amino acid | ||
LFBCNLDA_01438 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
LFBCNLDA_01439 | 1.4e-29 | rpmB | J | Ribosomal L28 family | ||
LFBCNLDA_01440 | 4.2e-200 | yegV | G | pfkB family carbohydrate kinase | ||
LFBCNLDA_01442 | 3.8e-243 | yxiO | S | Vacuole effluxer Atg22 like | ||
LFBCNLDA_01443 | 3.8e-131 | K | helix_turn_helix, mercury resistance | |||
LFBCNLDA_01444 | 5e-60 | T | Toxic component of a toxin-antitoxin (TA) module | |||
LFBCNLDA_01445 | 3.3e-07 | tonB | M | Interacts with outer membrane receptor proteins that carry out high-affinity binding and energy dependent uptake into the periplasmic space of specific substrates. It could act to transduce energy from the cytoplasmic membrane to specific energy- requiring processes in the outer membrane, resulting in the release into the periplasm of ligands bound by these outer membrane proteins | ||
LFBCNLDA_01446 | 2.4e-92 | ybaK | J | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
LFBCNLDA_01447 | 1e-198 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LFBCNLDA_01448 | 8e-134 | 2.7.6.2 | H | Thiamin pyrophosphokinase, vitamin B1 binding domain | ||
LFBCNLDA_01449 | 7.1e-08 | S | Spermine/spermidine synthase domain | |||
LFBCNLDA_01451 | 1.4e-103 | 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 | ||
LFBCNLDA_01452 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
LFBCNLDA_01453 | 9.6e-62 | 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 | ||
LFBCNLDA_01454 | 2.9e-179 | xerD | D | recombinase XerD | ||
LFBCNLDA_01455 | 2e-151 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LFBCNLDA_01456 | 2.5e-150 | 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 | ||
LFBCNLDA_01457 | 9.2e-113 | 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 | ||
LFBCNLDA_01458 | 8.6e-150 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
LFBCNLDA_01459 | 3.7e-251 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
LFBCNLDA_01460 | 6.9e-311 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
LFBCNLDA_01461 | 1.4e-164 | nadC | 1.4.3.16, 2.4.2.19 | H | Quinolinate phosphoribosyl transferase, N-terminal domain | |
LFBCNLDA_01462 | 3.4e-236 | iscS1 | 2.8.1.7 | E | Aminotransferase class-V | |
LFBCNLDA_01463 | 0.0 | typA | T | Elongation factor G C-terminus | ||
LFBCNLDA_01464 | 5.4e-79 | |||||
LFBCNLDA_01465 | 1.7e-198 | pheA | 1.3.1.12, 4.2.1.51, 5.4.99.5 | E | Prephenate dehydratase | |
LFBCNLDA_01466 | 7.1e-192 | tyrA | 1.3.1.12, 1.3.1.43 | E | Prephenate dehydrogenase | |
LFBCNLDA_01467 | 7.3e-42 | |||||
LFBCNLDA_01468 | 8.6e-187 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
LFBCNLDA_01469 | 7.9e-177 | appB | EP | Binding-protein-dependent transport system inner membrane component | ||
LFBCNLDA_01470 | 4.6e-166 | dppC | EP | N-terminal TM domain of oligopeptide transport permease C | ||
LFBCNLDA_01471 | 0.0 | oppD | P | Belongs to the ABC transporter superfamily | ||
LFBCNLDA_01472 | 1.1e-173 | menA | 2.5.1.74 | H | Belongs to the MenA family. Type 1 subfamily | |
LFBCNLDA_01473 | 1.3e-153 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LFBCNLDA_01474 | 1.4e-09 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_01475 | 1.7e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LFBCNLDA_01476 | 1.6e-217 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |||
LFBCNLDA_01477 | 2.6e-39 | |||||
LFBCNLDA_01478 | 4.2e-214 | 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 | |
LFBCNLDA_01479 | 6.3e-177 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LFBCNLDA_01480 | 6e-106 | M | NlpC/P60 family | |||
LFBCNLDA_01481 | 1.6e-191 | T | Universal stress protein family | |||
LFBCNLDA_01482 | 3.2e-71 | attW | O | OsmC-like protein | ||
LFBCNLDA_01483 | 1.9e-174 | 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 | |
LFBCNLDA_01484 | 7.8e-128 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
LFBCNLDA_01485 | 1.8e-95 | ptpA | 3.1.3.48 | T | low molecular weight | |
LFBCNLDA_01486 | 3.7e-196 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
LFBCNLDA_01487 | 9.4e-23 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
LFBCNLDA_01488 | 6.4e-111 | vex2 | V | ABC transporter, ATP-binding protein | ||
LFBCNLDA_01489 | 4.7e-211 | vex1 | V | Efflux ABC transporter, permease protein | ||
LFBCNLDA_01490 | 1.1e-219 | vex3 | V | ABC transporter permease | ||
LFBCNLDA_01491 | 1.7e-11 | S | Psort location CytoplasmicMembrane, score 9.99 | |||
LFBCNLDA_01492 | 3.9e-119 | K | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_01493 | 1.9e-223 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |||
LFBCNLDA_01494 | 4.6e-180 | lacR | K | Transcriptional regulator, LacI family | ||
LFBCNLDA_01495 | 1.1e-45 | |||||
LFBCNLDA_01496 | 1.8e-139 | nfrA | 1.5.1.38, 1.5.1.39 | C | Nitroreductase family | |
LFBCNLDA_01497 | 2.6e-68 | S | Protein of unknown function (DUF4235) | |||
LFBCNLDA_01498 | 4.6e-131 | G | Phosphoglycerate mutase family | |||
LFBCNLDA_01501 | 2.9e-190 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_01502 | 0.0 | phoA | 3.1.3.1, 3.1.3.39 | P | Alkaline phosphatase homologues | |
LFBCNLDA_01503 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
LFBCNLDA_01504 | 1.4e-58 | 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 | ||
LFBCNLDA_01505 | 1e-157 | lytC | 2.1.1.197, 3.2.1.17, 3.2.1.96 | M | Glycosyl hydrolases family 25 | |
LFBCNLDA_01506 | 1.3e-279 | L | PFAM Integrase catalytic | |||
LFBCNLDA_01507 | 2.3e-123 | L | IstB-like ATP binding protein | |||
LFBCNLDA_01508 | 6.1e-75 | L | PFAM Integrase catalytic | |||
LFBCNLDA_01509 | 5e-258 | L | HTH-like domain | |||
LFBCNLDA_01510 | 1.6e-143 | L | PFAM Integrase catalytic | |||
LFBCNLDA_01511 | 2.6e-102 | 1.1.1.399, 1.1.1.95 | C | D-isomer specific 2-hydroxyacid dehydrogenase NAD-binding protein | ||
LFBCNLDA_01512 | 5.5e-52 | XK27_05505 | S | Domain of unknown function (DUF4956) | ||
LFBCNLDA_01513 | 1.8e-225 | ilvE | 2.6.1.42 | E | Amino-transferase class IV | |
LFBCNLDA_01514 | 1.2e-113 | S | phosphoesterase or phosphohydrolase | |||
LFBCNLDA_01515 | 1.4e-22 | 3.1.4.37 | T | RNA ligase | ||
LFBCNLDA_01516 | 2.2e-134 | S | UPF0126 domain | |||
LFBCNLDA_01517 | 9.9e-34 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
LFBCNLDA_01518 | 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 | ||
LFBCNLDA_01519 | 3.7e-244 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LFBCNLDA_01521 | 1.1e-236 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase, class I II | |
LFBCNLDA_01522 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
LFBCNLDA_01523 | 0.0 | gltB | 1.4.1.13, 1.4.1.14, 1.4.7.1 | E | glutamate synthase NADPH large subunit | |
LFBCNLDA_01524 | 2.7e-304 | gltD | 1.4.1.13, 1.4.1.14 | C | Dihydroprymidine dehydrogenase domain II, 4Fe-4S cluster | |
LFBCNLDA_01525 | 7.9e-82 | |||||
LFBCNLDA_01526 | 2.1e-243 | glgA | 2.4.1.342 | GT4 | G | Starch synthase catalytic domain |
LFBCNLDA_01527 | 3.6e-182 | modF | 3.6.3.21, 3.6.3.34 | P | ATPases associated with a variety of cellular activities | |
LFBCNLDA_01528 | 6.2e-163 | ybeM | S | Carbon-nitrogen hydrolase | ||
LFBCNLDA_01529 | 4.9e-66 | S | Sel1-like repeats. | |||
LFBCNLDA_01530 | 2.1e-271 | 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) | |
LFBCNLDA_01531 | 2.9e-193 | 2.3.1.57 | J | Acetyltransferase (GNAT) domain | ||
LFBCNLDA_01532 | 3.7e-51 | S | Protein of unknown function (DUF2469) | |||
LFBCNLDA_01533 | 0.0 | 5.4.99.9 | H | Flavin containing amine oxidoreductase | ||
LFBCNLDA_01534 | 1.1e-303 | 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 | ||
LFBCNLDA_01535 | 1.8e-234 | E | Aminotransferase class I and II | |||
LFBCNLDA_01536 | 2.4e-90 | lrp_3 | K | helix_turn_helix ASNC type | ||
LFBCNLDA_01537 | 3.9e-72 | tyrA | 5.4.99.5 | E | Chorismate mutase type II | |
LFBCNLDA_01538 | 0.0 | S | domain protein | |||
LFBCNLDA_01539 | 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 | |
LFBCNLDA_01540 | 4.8e-293 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | |||
LFBCNLDA_01541 | 1.3e-119 | 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 | |
LFBCNLDA_01542 | 5.9e-132 | KT | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_01543 | 1.4e-125 | |||||
LFBCNLDA_01544 | 7.2e-101 | mntP | P | Probably functions as a manganese efflux pump | ||
LFBCNLDA_01546 | 0.0 | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase | |
LFBCNLDA_01547 | 3.5e-82 | ghrA | EH | D-isomer specific 2-hydroxyacid dehydrogenase, NAD binding domain | ||
LFBCNLDA_01548 | 6e-188 | K | Periplasmic binding protein domain | |||
LFBCNLDA_01549 | 6e-36 | G | ABC transporter permease | |||
LFBCNLDA_01550 | 0.0 | lacZ5 | 3.2.1.23 | G | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_01551 | 1.5e-55 | G | carbohydrate transport | |||
LFBCNLDA_01552 | 4.1e-275 | G | Bacterial extracellular solute-binding protein | |||
LFBCNLDA_01553 | 3.6e-143 | coaX | 2.7.1.33 | H | Catalyzes the phosphorylation of pantothenate (Pan), the first step in CoA biosynthesis | |
LFBCNLDA_01554 | 9.6e-308 | E | ABC transporter, substrate-binding protein, family 5 | |||
LFBCNLDA_01555 | 1.2e-169 | P | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_01556 | 1.4e-162 | EP | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_01557 | 7.6e-138 | oppD | EP | oligopeptide transport protein of the ABC superfamily, ATP-binding component | ||
LFBCNLDA_01558 | 3.1e-153 | sapF | E | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_01559 | 2.1e-185 | MA20_16500 | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LFBCNLDA_01560 | 2.3e-105 | |||||
LFBCNLDA_01562 | 5.4e-127 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LFBCNLDA_01563 | 4.1e-203 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LFBCNLDA_01564 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
LFBCNLDA_01565 | 1.4e-259 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LFBCNLDA_01566 | 0.0 | pgm | 5.4.2.2 | G | Phosphoglucomutase/phosphomannomutase, alpha/beta/alpha domain II | |
LFBCNLDA_01569 | 3e-35 | crr | G | pts system, glucose-specific IIABC component | ||
LFBCNLDA_01570 | 4.3e-25 | crr | G | pts system, glucose-specific IIABC component | ||
LFBCNLDA_01571 | 2.1e-24 | crr | G | pts system, glucose-specific IIABC component | ||
LFBCNLDA_01572 | 2.3e-23 | crr | G | pts system, glucose-specific IIABC component | ||
LFBCNLDA_01573 | 0.0 | nagLU | 3.1.4.53, 3.2.1.21, 3.2.1.50 | GH3 | G | Alpha-N-acetylglucosaminidase (NAGLU) tim-barrel domain |
LFBCNLDA_01575 | 5.3e-95 | |||||
LFBCNLDA_01576 | 0.0 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
LFBCNLDA_01577 | 1.6e-185 | opcA | G | Glucose-6-phosphate dehydrogenase subunit | ||
LFBCNLDA_01578 | 5.6e-141 | pgl | 3.1.1.31 | G | Glucosamine-6-phosphate isomerases/6-phosphogluconolactonase | |
LFBCNLDA_01579 | 2.2e-276 | 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 | |
LFBCNLDA_01580 | 8.5e-126 | degU | K | helix_turn_helix, Lux Regulon | ||
LFBCNLDA_01581 | 6.4e-182 | tcsS3 | KT | PspC domain | ||
LFBCNLDA_01582 | 7.6e-111 | M | Spy0128-like isopeptide containing domain | |||
LFBCNLDA_01583 | 5.7e-68 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LFBCNLDA_01584 | 8.3e-168 | |||||
LFBCNLDA_01585 | 3.1e-121 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
LFBCNLDA_01586 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
LFBCNLDA_01587 | 1.2e-126 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LFBCNLDA_01588 | 5e-99 | 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 | |
LFBCNLDA_01589 | 1.6e-160 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
LFBCNLDA_01591 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
LFBCNLDA_01592 | 4.9e-117 | |||||
LFBCNLDA_01593 | 3e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LFBCNLDA_01594 | 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 | |
LFBCNLDA_01595 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LFBCNLDA_01596 | 1.6e-123 | S | Short repeat of unknown function (DUF308) | |||
LFBCNLDA_01597 | 4.2e-149 | map | 3.4.11.18 | E | Methionine aminopeptidase | |
LFBCNLDA_01598 | 1.1e-250 | gltA | 2.3.3.1 | C | Citrate synthase, C-terminal domain | |
LFBCNLDA_01599 | 5.1e-101 | dnaQ | 2.7.7.7 | L | Exonuclease, DNA polymerase III, epsilon subunit family | |
LFBCNLDA_01600 | 7.8e-196 | yghZ | C | Aldo/keto reductase family | ||
LFBCNLDA_01601 | 2.6e-55 | racA | K | MerR, DNA binding | ||
LFBCNLDA_01602 | 1.5e-91 | K | acetyltransferase | |||
LFBCNLDA_01603 | 1.6e-211 | ctpE | P | E1-E2 ATPase | ||
LFBCNLDA_01604 | 3e-76 | nadB | 1.3.5.4, 1.4.3.16, 2.4.2.19 | H | Catalyzes the oxidation of L-aspartate to iminoaspartate | |
LFBCNLDA_01605 | 3.7e-251 | nadA | 2.5.1.72 | H | Catalyzes the condensation of iminoaspartate with dihydroxyacetone phosphate to form quinolinate | |
LFBCNLDA_01606 | 1.5e-152 | nrtR | 3.6.1.55 | F | NUDIX hydrolase | |
LFBCNLDA_01607 | 5.4e-113 | 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 | ||
LFBCNLDA_01608 | 1e-148 | 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 | ||
LFBCNLDA_01609 | 5.9e-151 | soj | D | CobQ CobB MinD ParA nucleotide binding domain protein | ||
LFBCNLDA_01610 | 8.4e-179 | xerD | D | recombinase XerD | ||
LFBCNLDA_01611 | 2.4e-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 | ||
LFBCNLDA_01612 | 2.1e-25 | rpmI | J | Ribosomal protein L35 | ||
LFBCNLDA_01613 | 2.4e-192 | 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 | |
LFBCNLDA_01614 | 0.0 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
LFBCNLDA_01615 | 2.3e-226 | S | Uncharacterized conserved protein (DUF2183) | |||
LFBCNLDA_01616 | 2.8e-165 | 3.1.3.16 | T | Sigma factor PP2C-like phosphatases | ||
LFBCNLDA_01617 | 1.4e-67 | B | Belongs to the OprB family | |||
LFBCNLDA_01618 | 1.3e-96 | T | Forkhead associated domain | |||
LFBCNLDA_01619 | 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 | |
LFBCNLDA_01621 | 2.3e-287 | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 | |
LFBCNLDA_01622 | 1.3e-116 | 3.1.3.27 | E | haloacid dehalogenase-like hydrolase | ||
LFBCNLDA_01623 | 3.7e-67 | rlrG | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LFBCNLDA_01625 | 1.6e-154 | 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 |
LFBCNLDA_01626 | 2.6e-199 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LFBCNLDA_01627 | 4e-58 | S | Domain of unknown function (DUF4190) | |||
LFBCNLDA_01630 | 4.9e-77 | tal | 2.2.1.2 | H | Transaldolase | |
LFBCNLDA_01631 | 3.8e-186 | ftsE | D | Cell division ATP-binding protein FtsE | ||
LFBCNLDA_01632 | 1.8e-201 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LFBCNLDA_01633 | 8.3e-13 | |||||
LFBCNLDA_01634 | 5.8e-21 | KLT | Protein tyrosine kinase | |||
LFBCNLDA_01635 | 3.3e-136 | |||||
LFBCNLDA_01636 | 8.3e-154 | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | ||
LFBCNLDA_01637 | 2.5e-52 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
LFBCNLDA_01638 | 6.9e-178 | 2.7.1.2 | GK | ROK family | ||
LFBCNLDA_01639 | 1.6e-216 | GK | ROK family | |||
LFBCNLDA_01640 | 7.5e-14 | L | Transposase and inactivated derivatives IS30 family | |||
LFBCNLDA_01641 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding protein, transpeptidase domain protein | |
LFBCNLDA_01642 | 6.5e-60 | 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 | ||
LFBCNLDA_01643 | 2.6e-35 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LFBCNLDA_01644 | 2.1e-263 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LFBCNLDA_01645 | 2.3e-27 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LFBCNLDA_01646 | 2.8e-38 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_01647 | 1.6e-45 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_01648 | 1.7e-276 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
LFBCNLDA_01649 | 4.4e-58 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
LFBCNLDA_01650 | 4.1e-81 | V | N-Acetylmuramoyl-L-alanine amidase | |||
LFBCNLDA_01651 | 7.7e-106 | ytrE | V | ABC transporter | ||
LFBCNLDA_01652 | 1.4e-169 | |||||
LFBCNLDA_01653 | 1.9e-64 | ohr | O | OsmC-like protein | ||
LFBCNLDA_01654 | 9.1e-141 | L | Phage integrase family | |||
LFBCNLDA_01655 | 1.8e-136 | L | IstB-like ATP binding protein | |||
LFBCNLDA_01656 | 9.8e-288 | L | PFAM Integrase catalytic | |||
LFBCNLDA_01657 | 3.8e-42 | S | Protein of unknown function (DUF3801) | |||
LFBCNLDA_01658 | 2.3e-164 | glkA | 2.7.1.2 | G | ROK family | |
LFBCNLDA_01659 | 5.2e-10 | K | Winged helix DNA-binding domain | |||
LFBCNLDA_01660 | 1.2e-11 | EGP | Major facilitator superfamily | |||
LFBCNLDA_01661 | 3.3e-50 | EGP | Major facilitator superfamily | |||
LFBCNLDA_01662 | 1.2e-120 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LFBCNLDA_01663 | 4.5e-181 | ftsK | D | FtsK SpoIIIE family protein | ||
LFBCNLDA_01664 | 2.2e-47 | glpT | G | glycerol-3-phosphate transporter | ||
LFBCNLDA_01665 | 1.8e-73 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LFBCNLDA_01666 | 1e-131 | tmp1 | S | Domain of unknown function (DUF4391) | ||
LFBCNLDA_01667 | 9.8e-149 | moeB | 2.7.7.80 | H | ThiF family | |
LFBCNLDA_01668 | 1e-254 | cdr | OP | Sulfurtransferase TusA | ||
LFBCNLDA_01669 | 3.1e-181 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LFBCNLDA_01672 | 1.9e-172 | S | Endonuclease/Exonuclease/phosphatase family | |||
LFBCNLDA_01673 | 7.8e-43 | 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 | |
LFBCNLDA_01674 | 8.5e-273 | 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 | |
LFBCNLDA_01675 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
LFBCNLDA_01676 | 1.2e-139 | 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 | |
LFBCNLDA_01678 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LFBCNLDA_01679 | 4.5e-166 | |||||
LFBCNLDA_01680 | 1.7e-256 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
LFBCNLDA_01681 | 0.0 | plyA3 | 3.2.1.18 | GH33 | M | Parallel beta-helix repeats |
LFBCNLDA_01683 | 2.9e-88 | K | MarR family | |||
LFBCNLDA_01684 | 0.0 | V | ABC transporter, ATP-binding protein | |||
LFBCNLDA_01685 | 0.0 | V | ABC transporter transmembrane region | |||
LFBCNLDA_01686 | 1.2e-167 | S | Patatin-like phospholipase | |||
LFBCNLDA_01687 | 1.5e-152 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LFBCNLDA_01688 | 2.3e-170 | 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 | |
LFBCNLDA_01689 | 2e-115 | S | Vitamin K epoxide reductase | |||
LFBCNLDA_01690 | 2.5e-166 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
LFBCNLDA_01691 | 6.1e-32 | S | Protein of unknown function (DUF3107) | |||
LFBCNLDA_01692 | 7.6e-232 | mphA | S | Aminoglycoside phosphotransferase | ||
LFBCNLDA_01693 | 8.1e-282 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
LFBCNLDA_01694 | 5.6e-278 | S | Zincin-like metallopeptidase | |||
LFBCNLDA_01695 | 1.4e-150 | lon | T | Belongs to the peptidase S16 family | ||
LFBCNLDA_01696 | 5.5e-66 | S | Protein of unknown function (DUF3052) | |||
LFBCNLDA_01697 | 1.8e-195 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_01698 | 4.7e-61 | S | Thiamine-binding protein | |||
LFBCNLDA_01699 | 9.2e-164 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
LFBCNLDA_01700 | 6.9e-231 | O | AAA domain (Cdc48 subfamily) | |||
LFBCNLDA_01701 | 1.3e-84 | |||||
LFBCNLDA_01702 | 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 | |
LFBCNLDA_01703 | 2.6e-158 | thiM | 2.7.1.50 | H | Catalyzes the phosphorylation of the hydroxyl group of 4-methyl-5-beta-hydroxyethylthiazole (THZ) | |
LFBCNLDA_01704 | 0.0 | lacZ | 3.2.1.23 | G | Domain of unknown function (DUF4982) | |
LFBCNLDA_01705 | 3.9e-300 | glyQS | 6.1.1.14 | J | Catalyzes the attachment of glycine to tRNA(Gly) | |
LFBCNLDA_01706 | 9.5e-247 | 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 | ||
LFBCNLDA_01707 | 7.3e-231 | 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 | ||
LFBCNLDA_01708 | 4.3e-80 | 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 | ||
LFBCNLDA_01709 | 2.1e-42 | yggT | S | YGGT family | ||
LFBCNLDA_01710 | 9.7e-90 | 3.1.21.3 | V | DivIVA protein | ||
LFBCNLDA_01711 | 4e-103 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LFBCNLDA_01712 | 3.4e-177 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LFBCNLDA_01714 | 6e-63 | |||||
LFBCNLDA_01715 | 5.2e-147 | 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 | |
LFBCNLDA_01716 | 3.7e-202 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LFBCNLDA_01717 | 2.9e-188 | ftsE | D | Cell division ATP-binding protein FtsE | ||
LFBCNLDA_01718 | 2.4e-159 | ftsX | D | Part of the ABC transporter FtsEX involved in cellular division | ||
LFBCNLDA_01719 | 9.7e-163 | usp | 3.5.1.28 | CBM50 | D | CHAP domain protein |
LFBCNLDA_01720 | 3e-76 | 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 | ||
LFBCNLDA_01721 | 5.6e-146 | rluA | 5.4.99.28, 5.4.99.29 | J | RNA pseudouridylate synthase | |
LFBCNLDA_01722 | 4.1e-46 | |||||
LFBCNLDA_01723 | 5e-25 | |||||
LFBCNLDA_01725 | 9.7e-201 | 2.7.11.1 | NU | Tfp pilus assembly protein FimV | ||
LFBCNLDA_01726 | 6.4e-221 | 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) | |
LFBCNLDA_01727 | 1e-235 | 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 | |
LFBCNLDA_01728 | 1.8e-290 | I | acetylesterase activity | |||
LFBCNLDA_01729 | 4.6e-143 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LFBCNLDA_01730 | 1.8e-155 | 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 | |
LFBCNLDA_01731 | 2.1e-190 | ywqG | S | Domain of unknown function (DUF1963) | ||
LFBCNLDA_01732 | 3.1e-19 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LFBCNLDA_01733 | 3e-39 | cscA | 3.2.1.26 | GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LFBCNLDA_01734 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase III alpha subunit | |
LFBCNLDA_01735 | 1.4e-83 | S | zinc-ribbon domain | |||
LFBCNLDA_01736 | 2e-46 | yhbY | J | CRS1_YhbY | ||
LFBCNLDA_01737 | 0.0 | 4.2.1.53 | S | MCRA family | ||
LFBCNLDA_01740 | 1.2e-202 | K | WYL domain | |||
LFBCNLDA_01741 | 5e-156 | yvgN | 1.1.1.346 | S | Aldo/keto reductase family | |
LFBCNLDA_01742 | 1.7e-173 | dkgA | 1.1.1.346 | C | Aldo/keto reductase family | |
LFBCNLDA_01743 | 1.3e-75 | yneG | S | Domain of unknown function (DUF4186) | ||
LFBCNLDA_01745 | 3.9e-07 | pbpB | 2.7.11.1, 3.4.16.4 | S | PASTA domain | |
LFBCNLDA_01746 | 1.2e-180 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_01747 | 1.1e-256 | 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 | |
LFBCNLDA_01748 | 2.1e-224 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LFBCNLDA_01749 | 3.2e-112 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
LFBCNLDA_01750 | 5.9e-113 | |||||
LFBCNLDA_01751 | 4.8e-122 | 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 | ||
LFBCNLDA_01752 | 1.7e-131 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
LFBCNLDA_01753 | 5.4e-283 | S | Uncharacterized protein conserved in bacteria (DUF2252) | |||
LFBCNLDA_01754 | 2.1e-265 | glnA2 | 6.3.1.2 | E | glutamine synthetase | |
LFBCNLDA_01755 | 2.1e-252 | S | Domain of unknown function (DUF5067) | |||
LFBCNLDA_01756 | 2.8e-58 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_01757 | 1.4e-176 | 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 | |||
LFBCNLDA_01758 | 0.0 | hrpA | 3.6.4.13 | L | Helicase associated domain (HA2) Add an annotation | |
LFBCNLDA_01759 | 1.4e-121 | rsmC | 2.1.1.172 | J | Ribosomal protein L11 methyltransferase (PrmA) | |
LFBCNLDA_01760 | 1.2e-171 | |||||
LFBCNLDA_01761 | 9e-273 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LFBCNLDA_01762 | 4.6e-177 | ldh | 1.1.1.27, 1.1.1.37 | C | Belongs to the LDH MDH superfamily. LDH family | |
LFBCNLDA_01763 | 2.3e-165 | czcD | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
LFBCNLDA_01764 | 7.5e-129 | 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 | |
LFBCNLDA_01765 | 1.1e-49 | M | Lysin motif | |||
LFBCNLDA_01766 | 7.1e-83 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LFBCNLDA_01767 | 1.1e-228 | serA | 1.1.1.399, 1.1.1.95 | EH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
LFBCNLDA_01768 | 0.0 | L | DNA helicase | |||
LFBCNLDA_01769 | 1.3e-90 | mraZ | K | Belongs to the MraZ family | ||
LFBCNLDA_01770 | 1.1e-193 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LFBCNLDA_01771 | 1.2e-25 | |||||
LFBCNLDA_01772 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_01773 | 2e-22 | K | Transcriptional regulator | |||
LFBCNLDA_01775 | 3.2e-15 | |||||
LFBCNLDA_01776 | 4.2e-233 | yhdR | 2.6.1.1 | E | Psort location Cytoplasmic, score 8.87 | |
LFBCNLDA_01777 | 5.5e-239 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LFBCNLDA_01778 | 1.7e-119 | K | Bacterial regulatory proteins, tetR family | |||
LFBCNLDA_01779 | 3e-131 | M | Mechanosensitive ion channel | |||
LFBCNLDA_01780 | 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 | ||
LFBCNLDA_01781 | 5.6e-30 | 2.1.1.72 | S | Protein conserved in bacteria | ||
LFBCNLDA_01782 | 4.2e-155 | fahA | Q | Fumarylacetoacetate (FAA) hydrolase family | ||
LFBCNLDA_01783 | 9.1e-78 | S | Domain of unknown function (DUF4854) | |||
LFBCNLDA_01784 | 3.8e-210 | 3.4.22.70 | M | Sortase family | ||
LFBCNLDA_01785 | 5.1e-282 | M | LPXTG cell wall anchor motif | |||
LFBCNLDA_01786 | 0.0 | inlJ | M | domain protein | ||
LFBCNLDA_01787 | 3.6e-53 | acyP | 3.6.1.7 | C | Acylphosphatase | |
LFBCNLDA_01788 | 8.5e-148 | yggS | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
LFBCNLDA_01789 | 3.1e-186 | gluQ | 6.1.1.17 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFBCNLDA_01790 | 1.3e-129 | M | Protein of unknown function (DUF3152) | |||
LFBCNLDA_01791 | 1.1e-130 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LFBCNLDA_01793 | 1e-69 | E | Domain of unknown function (DUF5011) | |||
LFBCNLDA_01794 | 6.5e-46 | S | Parallel beta-helix repeats | |||
LFBCNLDA_01795 | 1.9e-14 | S | Parallel beta-helix repeats | |||
LFBCNLDA_01797 | 6.6e-70 | rplI | J | Binds to the 23S rRNA | ||
LFBCNLDA_01798 | 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 | ||
LFBCNLDA_01799 | 1.1e-79 | ssb1 | L | Single-stranded DNA-binding protein | ||
LFBCNLDA_01800 | 6.1e-48 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LFBCNLDA_01801 | 4.5e-172 | T | Pfam Adenylate and Guanylate cyclase catalytic domain | |||
LFBCNLDA_01802 | 4.3e-116 | |||||
LFBCNLDA_01803 | 0.0 | ftsK | 2.7.11.1, 2.7.7.7, 3.4.21.110, 4.2.1.2 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |
LFBCNLDA_01804 | 6.9e-192 | 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) | |
LFBCNLDA_01805 | 0.0 | 3.2.1.97 | GH101 | G | Glycosyl hydrolase 101 beta sandwich domain | |
LFBCNLDA_01806 | 1.4e-200 | ugpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
LFBCNLDA_01807 | 2.4e-217 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
LFBCNLDA_01808 | 2.5e-178 | gpsA | 1.1.1.94 | I | NAD-dependent glycerol-3-phosphate dehydrogenase C-terminus | |
LFBCNLDA_01809 | 2.8e-173 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LFBCNLDA_01810 | 5.5e-110 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
LFBCNLDA_01811 | 4.7e-32 | 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 | ||
LFBCNLDA_01813 | 1.7e-229 | aspC | E | DegT/DnrJ/EryC1/StrS aminotransferase family | ||
LFBCNLDA_01814 | 4.1e-201 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LFBCNLDA_01815 | 1.4e-298 | 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 | ||
LFBCNLDA_01816 | 3.7e-215 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_01817 | 3.1e-40 | rpmA | J | Ribosomal L27 protein | ||
LFBCNLDA_01818 | 9.2e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
LFBCNLDA_01819 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
LFBCNLDA_01820 | 7.6e-241 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
LFBCNLDA_01821 | 9.3e-167 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
LFBCNLDA_01822 | 3.3e-256 | V | Efflux ABC transporter, permease protein | |||
LFBCNLDA_01823 | 2.4e-164 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_01824 | 6.1e-58 | |||||
LFBCNLDA_01825 | 1.6e-64 | |||||
LFBCNLDA_01826 | 4.7e-279 | maf | 1.1.1.25, 2.1.1.190, 3.6.1.55, 3.6.1.67 | DF | Maf-like protein | |
LFBCNLDA_01827 | 3.5e-188 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
LFBCNLDA_01828 | 5.2e-240 | hom | 1.1.1.3 | E | Homoserine dehydrogenase | |
LFBCNLDA_01829 | 2.9e-290 | nagE | 2.7.1.193, 2.7.1.199 | G | phosphotransferase system, EIIB | |
LFBCNLDA_01830 | 1.9e-81 | 2.7.1.208 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
LFBCNLDA_01831 | 1.1e-303 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LFBCNLDA_01832 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
LFBCNLDA_01833 | 3.4e-180 | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | ||
LFBCNLDA_01834 | 5.2e-63 | psp1 | 3.5.99.10 | J | Endoribonuclease L-PSP | |
LFBCNLDA_01835 | 2.2e-156 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
LFBCNLDA_01836 | 4.4e-109 | |||||
LFBCNLDA_01837 | 1.7e-190 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
LFBCNLDA_01838 | 7.7e-219 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_01839 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LFBCNLDA_01840 | 3.9e-92 | 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) | |
LFBCNLDA_01841 | 3.6e-31 | J | Acetyltransferase (GNAT) domain | |||
LFBCNLDA_01842 | 2.9e-101 | cysE | 2.3.1.178 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | |
LFBCNLDA_01843 | 7.5e-269 | yhdG | E | aromatic amino acid transport protein AroP K03293 | ||
LFBCNLDA_01844 | 2e-263 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LFBCNLDA_01845 | 2.5e-247 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
LFBCNLDA_01846 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LFBCNLDA_01847 | 3.3e-158 | K | Helix-turn-helix domain, rpiR family | |||
LFBCNLDA_01848 | 7.9e-227 | K | Putative ATP-dependent DNA helicase recG C-terminal | |||
LFBCNLDA_01849 | 1.2e-43 | S | Memo-like protein | |||
LFBCNLDA_01851 | 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) | |
LFBCNLDA_01852 | 1.9e-178 | adh3 | C | Zinc-binding dehydrogenase | ||
LFBCNLDA_01853 | 1.4e-84 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
LFBCNLDA_01854 | 2.4e-228 | 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) | |
LFBCNLDA_01855 | 1.6e-72 | zur | P | Belongs to the Fur family | ||
LFBCNLDA_01856 | 5.4e-43 | |||||
LFBCNLDA_01857 | 2.6e-154 | S | TIGRFAM TIGR03943 family protein | |||
LFBCNLDA_01858 | 2e-200 | ycgR | S | Predicted permease | ||
LFBCNLDA_01859 | 2.3e-23 | J | Ribosomal L32p protein family | |||
LFBCNLDA_01860 | 7e-14 | rpmJ | J | Ribosomal protein L36 | ||
LFBCNLDA_01861 | 7.4e-42 | rpmE2 | J | Ribosomal protein L31 | ||
LFBCNLDA_01862 | 7.5e-49 | 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 | ||
LFBCNLDA_01863 | 3.4e-46 | rpmB | J | Ribosomal L28 family | ||
LFBCNLDA_01864 | 1.1e-136 | S | cobalamin synthesis protein | |||
LFBCNLDA_01865 | 3.9e-162 | P | Zinc-uptake complex component A periplasmic | |||
LFBCNLDA_01867 | 0.0 | lysX | S | Uncharacterised conserved protein (DUF2156) | ||
LFBCNLDA_01868 | 1e-246 | S | Putative esterase | |||
LFBCNLDA_01869 | 0.0 | XK27_08315 | M | Psort location CytoplasmicMembrane, score 9.26 | ||
LFBCNLDA_01870 | 5e-240 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
LFBCNLDA_01871 | 4.9e-185 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
LFBCNLDA_01872 | 1.3e-292 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LFBCNLDA_01873 | 4.4e-302 | umuC | 2.7.7.7 | L | DNA-damage repair protein (DNA polymerase IV) K00961 | |
LFBCNLDA_01874 | 2e-32 | |||||
LFBCNLDA_01875 | 1.8e-68 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
LFBCNLDA_01876 | 8.4e-23 | K | DNA-binding transcription factor activity | |||
LFBCNLDA_01877 | 1.7e-98 | mug | 3.2.2.28 | L | Uracil DNA glycosylase superfamily | |
LFBCNLDA_01878 | 9e-97 | S | Protein of unknown function (DUF4230) | |||
LFBCNLDA_01879 | 2.1e-104 | |||||
LFBCNLDA_01880 | 0.0 | purL | 6.3.5.3 | F | CobB/CobQ-like glutamine amidotransferase domain | |
LFBCNLDA_01881 | 3.8e-139 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
LFBCNLDA_01882 | 7.8e-233 | 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 | |
LFBCNLDA_01883 | 0.0 | M | Parallel beta-helix repeats | |||
LFBCNLDA_01884 | 1.2e-227 | M | Glycosyl transferase 4-like domain | |||
LFBCNLDA_01885 | 5.9e-199 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
LFBCNLDA_01887 | 9.3e-62 | 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 | ||
LFBCNLDA_01888 | 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 | ||
LFBCNLDA_01889 | 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 | ||
LFBCNLDA_01890 | 3.9e-186 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LFBCNLDA_01891 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
LFBCNLDA_01892 | 5.6e-142 | yijF | S | Domain of unknown function (DUF1287) | ||
LFBCNLDA_01893 | 5e-133 | C | Putative TM nitroreductase | |||
LFBCNLDA_01894 | 1.2e-108 | |||||
LFBCNLDA_01896 | 3.2e-255 | nplT | 3.2.1.1 | GH13 | G | Alpha amylase, catalytic domain |
LFBCNLDA_01897 | 1.3e-78 | S | Bacterial PH domain | |||
LFBCNLDA_01898 | 6e-137 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_01899 | 1.2e-68 | 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 | |
LFBCNLDA_01900 | 1.6e-263 | 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 | |
LFBCNLDA_01902 | 9.1e-192 | 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) | |
LFBCNLDA_01903 | 1.2e-143 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LFBCNLDA_01904 | 2.6e-92 | |||||
LFBCNLDA_01905 | 1e-235 | 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 | |
LFBCNLDA_01906 | 1.9e-283 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
LFBCNLDA_01907 | 5.3e-122 | S | ABC-2 family transporter protein | |||
LFBCNLDA_01908 | 3.7e-126 | S | ABC-2 family transporter protein | |||
LFBCNLDA_01909 | 1.3e-176 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_01910 | 2.4e-57 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
LFBCNLDA_01911 | 2.6e-123 | S | Haloacid dehalogenase-like hydrolase | |||
LFBCNLDA_01912 | 2.9e-294 | recN | L | May be involved in recombinational repair of damaged DNA | ||
LFBCNLDA_01913 | 7.3e-183 | 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 | |
LFBCNLDA_01914 | 3.3e-235 | trkB | P | Cation transport protein | ||
LFBCNLDA_01915 | 6.8e-116 | trkA | P | TrkA-N domain | ||
LFBCNLDA_01916 | 1.3e-101 | |||||
LFBCNLDA_01917 | 3.6e-137 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LFBCNLDA_01919 | 3.3e-189 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
LFBCNLDA_01920 | 3.6e-159 | L | Tetratricopeptide repeat | |||
LFBCNLDA_01921 | 1.7e-254 | 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) | |
LFBCNLDA_01922 | 4.6e-143 | S | Putative ABC-transporter type IV | |||
LFBCNLDA_01923 | 7.2e-109 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LFBCNLDA_01924 | 1.4e-281 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
LFBCNLDA_01925 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LFBCNLDA_01926 | 6.5e-274 | 3.6.4.12 | K | Putative DNA-binding domain | ||
LFBCNLDA_01927 | 4.7e-74 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
LFBCNLDA_01928 | 0.0 | hsdM | 2.1.1.72 | V | modification (methylase) protein of type I restriction-modification system K03427 | |
LFBCNLDA_01929 | 3.7e-159 | S | Domain of unknown function (DUF4357) | |||
LFBCNLDA_01930 | 9.6e-94 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | ||
LFBCNLDA_01931 | 1.4e-178 | L | Phage integrase family | |||
LFBCNLDA_01932 | 4.1e-239 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LFBCNLDA_01933 | 1.1e-84 | argR | K | Regulates arginine biosynthesis genes | ||
LFBCNLDA_01934 | 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 | |
LFBCNLDA_01935 | 1.9e-247 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
LFBCNLDA_01936 | 1.7e-179 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LFBCNLDA_01937 | 7.9e-216 | 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 | |
LFBCNLDA_01938 | 5.9e-205 | 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 | |
LFBCNLDA_01939 | 1.3e-87 | |||||
LFBCNLDA_01940 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LFBCNLDA_01941 | 7e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LFBCNLDA_01942 | 2.8e-105 | 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 | |
LFBCNLDA_01943 | 1.1e-207 | pknL | 2.7.11.1 | KLT | PASTA | |
LFBCNLDA_01944 | 1e-133 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LFBCNLDA_01945 | 4.3e-109 | |||||
LFBCNLDA_01946 | 1.1e-192 | 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) | |
LFBCNLDA_01947 | 3.6e-25 | 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 | ||
LFBCNLDA_01948 | 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 | ||
LFBCNLDA_01949 | 6.7e-111 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LFBCNLDA_01951 | 1.1e-86 | recX | S | Modulates RecA activity | ||
LFBCNLDA_01952 | 8e-216 | 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 | ||
LFBCNLDA_01953 | 3.7e-40 | S | Protein of unknown function (DUF3046) | |||
LFBCNLDA_01954 | 1.4e-79 | K | Helix-turn-helix XRE-family like proteins | |||
LFBCNLDA_01955 | 1.3e-96 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LFBCNLDA_01956 | 9.2e-124 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LFBCNLDA_01957 | 0.0 | ftsK | D | FtsK SpoIIIE family protein | ||
LFBCNLDA_01958 | 3.5e-137 | fic | D | Fic/DOC family | ||
LFBCNLDA_01959 | 3.1e-185 | 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) | |
LFBCNLDA_01960 | 5.7e-280 | 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 | |
LFBCNLDA_01961 | 3.5e-120 | relA2 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | |
LFBCNLDA_01962 | 2.4e-170 | ydeD | EG | EamA-like transporter family | ||
LFBCNLDA_01963 | 6.6e-132 | ybhL | S | Belongs to the BI1 family | ||
LFBCNLDA_01964 | 1e-97 | S | Domain of unknown function (DUF5067) | |||
LFBCNLDA_01965 | 1.9e-267 | T | Histidine kinase | |||
LFBCNLDA_01966 | 9.1e-116 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_01967 | 0.0 | S | Protein of unknown function DUF262 | |||
LFBCNLDA_01968 | 2e-302 | gmk | 2.4.2.10, 2.7.4.8, 4.1.1.23 | F | Essential for recycling GMP and indirectly, cGMP | |
LFBCNLDA_01969 | 0.0 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
LFBCNLDA_01970 | 1e-237 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
LFBCNLDA_01971 | 7.3e-89 | 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 | ||
LFBCNLDA_01972 | 3.3e-103 | 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 | ||
LFBCNLDA_01974 | 1.1e-190 | EGP | Transmembrane secretion effector | |||
LFBCNLDA_01975 | 0.0 | S | Esterase-like activity of phytase | |||
LFBCNLDA_01976 | 2e-17 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LFBCNLDA_01977 | 5.3e-158 | gnpA | 2.4.1.211 | S | Lacto-N-biose phosphorylase C-terminal domain | |
LFBCNLDA_01978 | 1.5e-177 | 2.7.1.2 | GK | ROK family | ||
LFBCNLDA_01979 | 6.4e-218 | GK | ROK family | |||
LFBCNLDA_01980 | 2.8e-207 | mdsC | 2.7.1.162, 2.7.1.39 | S | Phosphotransferase enzyme family | |
LFBCNLDA_01981 | 1.1e-307 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
LFBCNLDA_01982 | 1.4e-197 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LFBCNLDA_01983 | 8.9e-303 | ybiT | S | ABC transporter | ||
LFBCNLDA_01984 | 4.5e-140 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
LFBCNLDA_01985 | 4.3e-232 | qseC | 2.7.13.3 | T | HAMP (Histidine kinases, Adenylyl cyclases, Methyl binding proteins, Phosphatases) domain | |
LFBCNLDA_01986 | 3.3e-118 | K | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_01987 | 7.1e-28 | V | MacB-like periplasmic core domain | |||
LFBCNLDA_01988 | 2.1e-77 | |||||
LFBCNLDA_01989 | 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 | ||
LFBCNLDA_01990 | 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 | ||
LFBCNLDA_01991 | 4.3e-183 | aroE | 1.1.1.25 | E | Shikimate dehydrogenase substrate binding domain | |
LFBCNLDA_01992 | 1.5e-177 | rapZ | S | Displays ATPase and GTPase activities | ||
LFBCNLDA_01993 | 3.1e-173 | whiA | K | May be required for sporulation | ||
LFBCNLDA_01994 | 2e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
LFBCNLDA_01995 | 5.3e-147 | 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) | |
LFBCNLDA_01996 | 8e-33 | secG | U | Preprotein translocase SecG subunit | ||
LFBCNLDA_01997 | 3.1e-178 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
LFBCNLDA_01998 | 6.1e-162 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LFBCNLDA_01999 | 1.2e-239 | mepA_6 | V | MatE | ||
LFBCNLDA_02001 | 7.5e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
LFBCNLDA_02002 | 1.2e-143 | yoaK | S | Protein of unknown function (DUF1275) | ||
LFBCNLDA_02003 | 1e-201 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LFBCNLDA_02004 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
LFBCNLDA_02005 | 2.3e-221 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LFBCNLDA_02006 | 3.4e-211 | 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 | ||
LFBCNLDA_02007 | 7.1e-160 | G | Fructosamine kinase | |||
LFBCNLDA_02008 | 2.5e-167 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LFBCNLDA_02009 | 2.8e-156 | S | PAC2 family | |||
LFBCNLDA_02013 | 1.7e-90 | dkgB | S | Oxidoreductase, aldo keto reductase family protein | ||
LFBCNLDA_02014 | 3.8e-142 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
LFBCNLDA_02015 | 0.0 | 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 | |
LFBCNLDA_02016 | 1.5e-123 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LFBCNLDA_02017 | 1.2e-171 | cpsY | K | Bacterial regulatory helix-turn-helix protein, lysR family | ||
LFBCNLDA_02018 | 9.2e-89 | T | Domain of unknown function (DUF4234) | |||
LFBCNLDA_02019 | 1.9e-101 | K | Bacterial regulatory proteins, tetR family | |||
LFBCNLDA_02020 | 1.2e-18 | |||||
LFBCNLDA_02021 | 2.6e-48 | tam | 2.1.1.144, 2.1.1.197 | FG | trans-aconitate 2-methyltransferase activity | |
LFBCNLDA_02022 | 3.7e-41 | K | Helix-turn-helix | |||
LFBCNLDA_02023 | 8.5e-223 | hipA | 2.7.11.1 | S | HipA N-terminal domain | |
LFBCNLDA_02024 | 4.3e-67 | 4.1.1.44 | S | Cupin domain | ||
LFBCNLDA_02025 | 4.4e-175 | S | Membrane transport protein | |||
LFBCNLDA_02026 | 1e-93 | laaE | K | Transcriptional regulator PadR-like family | ||
LFBCNLDA_02027 | 7.9e-134 | magIII | L | endonuclease III | ||
LFBCNLDA_02028 | 9.6e-132 | S | Enoyl-(Acyl carrier protein) reductase | |||
LFBCNLDA_02029 | 1.1e-240 | vbsD | V | MatE | ||
LFBCNLDA_02030 | 0.0 | uvrA3 | 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 | ||
LFBCNLDA_02031 | 2e-15 | KLT | Protein tyrosine kinase | |||
LFBCNLDA_02032 | 1.3e-16 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_02033 | 1.1e-137 | |||||
LFBCNLDA_02034 | 7.6e-194 | 1.1.1.1, 1.1.1.14 | C | Zinc-binding dehydrogenase | ||
LFBCNLDA_02035 | 6.5e-125 | 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) | |
LFBCNLDA_02036 | 1.1e-178 | pyrD | 1.3.1.14 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
LFBCNLDA_02037 | 6.5e-156 | 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 | |
LFBCNLDA_02038 | 8.9e-181 | pyrF | 2.4.2.10, 4.1.1.23 | F | Belongs to the OMP decarboxylase family. Type 2 subfamily | |
LFBCNLDA_02039 | 2.9e-281 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
LFBCNLDA_02040 | 2e-73 | pyrI | 2.1.3.2 | F | Aspartate carbamoyltransferase regulatory chain, allosteric domain protein | |
LFBCNLDA_02041 | 6.4e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LFBCNLDA_02042 | 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 | |
LFBCNLDA_02044 | 6.2e-162 | metF | 1.5.1.20 | E | Methylenetetrahydrofolate reductase | |
LFBCNLDA_02045 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
LFBCNLDA_02046 | 1.2e-100 | sixA | T | Phosphoglycerate mutase family | ||
LFBCNLDA_02047 | 7.4e-208 | 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 | |
LFBCNLDA_02048 | 8.8e-178 | I | alpha/beta hydrolase fold | |||
LFBCNLDA_02049 | 1.4e-23 | rarD | S | EamA-like transporter family | ||
LFBCNLDA_02050 | 8.1e-72 | rarD | 3.4.17.13 | E | Rard protein | |
LFBCNLDA_02051 | 1.1e-29 | |||||
LFBCNLDA_02052 | 2.4e-271 | L | Uncharacterized conserved protein (DUF2075) | |||
LFBCNLDA_02054 | 5.4e-54 | KLT | Associated with various cellular activities | |||
LFBCNLDA_02055 | 4e-128 | bla1 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
LFBCNLDA_02056 | 1.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LFBCNLDA_02057 | 2.4e-139 | |||||
LFBCNLDA_02058 | 2.3e-92 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
LFBCNLDA_02059 | 5.4e-121 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LFBCNLDA_02060 | 3.2e-38 | fmdB | S | Putative regulatory protein | ||
LFBCNLDA_02061 | 3.6e-109 | flgA | NO | SAF | ||
LFBCNLDA_02062 | 9.6e-42 | |||||
LFBCNLDA_02063 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
LFBCNLDA_02064 | 1e-248 | T | Forkhead associated domain | |||
LFBCNLDA_02066 | 1.3e-37 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LFBCNLDA_02067 | 2.1e-88 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LFBCNLDA_02068 | 5.6e-186 | xynB2 | 1.1.1.169 | E | lipolytic protein G-D-S-L family | |
LFBCNLDA_02069 | 0.0 | guxA1 | 3.2.1.18, 3.2.1.91 | GH33,GH6 | G | BNR repeat-like domain |
LFBCNLDA_02071 | 8.8e-222 | pbuO | S | Permease family | ||
LFBCNLDA_02072 | 1.4e-12 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_02073 | 3e-170 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_02074 | 3.6e-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 | |
LFBCNLDA_02075 | 6.2e-180 | pstA | P | Phosphate transport system permease | ||
LFBCNLDA_02076 | 3.8e-171 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LFBCNLDA_02077 | 3e-172 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
LFBCNLDA_02078 | 1.3e-128 | KT | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_02079 | 1.5e-242 | senX3 | 2.7.13.3 | T | His Kinase A (phosphoacceptor) domain | |
LFBCNLDA_02080 | 1.9e-124 | 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 | |
LFBCNLDA_02081 | 2.4e-239 | 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) | |
LFBCNLDA_02084 | 1.9e-25 | rpmG | J | Ribosomal protein L33 | ||
LFBCNLDA_02085 | 4.5e-214 | murB | 1.3.1.98 | M | Cell wall formation | |
LFBCNLDA_02086 | 9e-61 | fdxA | C | 4Fe-4S binding domain | ||
LFBCNLDA_02087 | 1.2e-224 | dapC | E | Aminotransferase class I and II | ||
LFBCNLDA_02088 | 3.3e-239 | 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 | |
LFBCNLDA_02090 | 3.1e-256 | M | Bacterial capsule synthesis protein PGA_cap | |||
LFBCNLDA_02091 | 2.4e-113 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
LFBCNLDA_02092 | 8.9e-112 | |||||
LFBCNLDA_02093 | 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 |
LFBCNLDA_02094 | 3.5e-79 | 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 | ||
LFBCNLDA_02095 | 8.8e-68 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LFBCNLDA_02096 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LFBCNLDA_02097 | 9.7e-233 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
LFBCNLDA_02098 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LFBCNLDA_02099 | 8.7e-167 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
LFBCNLDA_02100 | 4.2e-08 | ywiC | S | YwiC-like protein | ||
LFBCNLDA_02101 | 1.6e-19 | ywiC | S | YwiC-like protein | ||
LFBCNLDA_02102 | 5.2e-50 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LFBCNLDA_02103 | 4.2e-118 | 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 | ||
LFBCNLDA_02104 | 3.9e-119 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LFBCNLDA_02105 | 2.6e-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 | ||
LFBCNLDA_02106 | 4.2e-155 | 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 | ||
LFBCNLDA_02107 | 3.7e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LFBCNLDA_02108 | 4.3e-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 | ||
LFBCNLDA_02109 | 2.7e-98 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LFBCNLDA_02110 | 1.4e-30 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LFBCNLDA_02111 | 5.1e-167 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
LFBCNLDA_02112 | 2.2e-41 | nrdH | O | Glutaredoxin | ||
LFBCNLDA_02113 | 1.5e-98 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LFBCNLDA_02114 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_02115 | 1.4e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_02116 | 1.3e-73 | megL | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_02117 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
LFBCNLDA_02118 | 3.3e-90 | lemA | S | LemA family | ||
LFBCNLDA_02119 | 2.1e-115 | xylR | K | purine nucleotide biosynthetic process | ||
LFBCNLDA_02120 | 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 | |
LFBCNLDA_02121 | 3e-41 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LFBCNLDA_02122 | 1.2e-118 | |||||
LFBCNLDA_02123 | 0.0 | nagH | 3.2.1.35, 3.2.1.52 | GH20 | G | beta-N-acetylglucosaminidase |
LFBCNLDA_02125 | 1.6e-160 | birA | 2.7.1.33, 6.3.4.15 | H | Biotin/lipoate A/B protein ligase family | |
LFBCNLDA_02126 | 6.5e-99 | 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 | |
LFBCNLDA_02127 | 2.3e-273 | fas | 2.3.1.179 | I | Beta-ketoacyl synthase, C-terminal domain | |
LFBCNLDA_02128 | 1.2e-259 | |||||
LFBCNLDA_02131 | 2.2e-250 | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | |||
LFBCNLDA_02132 | 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) | |
LFBCNLDA_02133 | 0.0 | 3.2.1.52 | GH20 | M | Glycosyl hydrolase family 20, catalytic domain | |
LFBCNLDA_02134 | 1e-131 | yebC | K | transcriptional regulatory protein | ||
LFBCNLDA_02135 | 1.8e-99 | 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 | |
LFBCNLDA_02136 | 2.5e-104 | 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 | |
LFBCNLDA_02137 | 1.8e-201 | 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 | |
LFBCNLDA_02138 | 2.6e-44 | yajC | U | Preprotein translocase subunit | ||
LFBCNLDA_02139 | 5.5e-101 | apt | 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
LFBCNLDA_02140 | 1.9e-225 | 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 | |
LFBCNLDA_02141 | 1.1e-167 | 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 | |
LFBCNLDA_02142 | 5e-246 | |||||
LFBCNLDA_02143 | 0.0 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LFBCNLDA_02144 | 5.7e-30 | |||||
LFBCNLDA_02145 | 1.8e-103 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LFBCNLDA_02146 | 7.5e-146 | rluB | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LFBCNLDA_02148 | 1.3e-78 | |||||
LFBCNLDA_02149 | 1.2e-64 | D | MobA/MobL family | |||
LFBCNLDA_02150 | 8.6e-48 | L | Transposase | |||
LFBCNLDA_02151 | 5.9e-182 | tnp7109-21 | L | Integrase core domain | ||
LFBCNLDA_02152 | 2.4e-26 | 2.1.1.72 | S | Adenine-specific methyltransferase EcoRI | ||
LFBCNLDA_02153 | 6.4e-38 | |||||
LFBCNLDA_02154 | 8.1e-111 | pncA | 2.7.11.1, 3.5.1.19 | Q | Isochorismatase family | |
LFBCNLDA_02156 | 6.7e-90 | 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 | |
LFBCNLDA_02157 | 2e-17 | 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 | |
LFBCNLDA_02158 | 1.4e-11 | 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 | |
LFBCNLDA_02160 | 3.7e-241 | pbuX | F | Permease family | ||
LFBCNLDA_02161 | 3e-107 | 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 | |
LFBCNLDA_02162 | 0.0 | yrhL | I | Psort location CytoplasmicMembrane, score 9.99 | ||
LFBCNLDA_02163 | 0.0 | pcrA | 3.6.4.12 | L | DNA helicase | |
LFBCNLDA_02164 | 4.8e-64 | S | Domain of unknown function (DUF4418) | |||
LFBCNLDA_02165 | 3.2e-212 | V | FtsX-like permease family | |||
LFBCNLDA_02166 | 1.9e-128 | lolD | V | ABC transporter | ||
LFBCNLDA_02167 | 1e-108 | 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 | ||
LFBCNLDA_02168 | 2.2e-237 | oatA | I | Psort location CytoplasmicMembrane, score 9.99 | ||
LFBCNLDA_02169 | 1.2e-127 | oatA | I | Psort location CytoplasmicMembrane, score 9.99 | ||
LFBCNLDA_02170 | 3.6e-81 | 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 | |
LFBCNLDA_02171 | 2.4e-122 | glpR | K | DeoR C terminal sensor domain | ||
LFBCNLDA_02172 | 1.8e-250 | galT | 2.7.7.12 | C | Galactose-1-phosphate uridyl transferase, N-terminal domain | |
LFBCNLDA_02173 | 9.9e-233 | galK | 2.7.1.6, 2.7.7.12 | G | Belongs to the GHMP kinase family. GalK subfamily | |
LFBCNLDA_02174 | 5.6e-242 | EGP | Sugar (and other) transporter | |||
LFBCNLDA_02175 | 4.2e-43 | gcvR | T | Belongs to the UPF0237 family | ||
LFBCNLDA_02176 | 9.4e-253 | S | UPF0210 protein | |||
LFBCNLDA_02177 | 3.3e-72 | |||||
LFBCNLDA_02179 | 6.3e-122 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LFBCNLDA_02180 | 1.1e-62 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | Putative cell wall binding repeat |
LFBCNLDA_02181 | 5.5e-185 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
LFBCNLDA_02182 | 1.9e-102 | |||||
LFBCNLDA_02183 | 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 | |
LFBCNLDA_02184 | 3.5e-285 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFBCNLDA_02185 | 7.2e-37 | V | ABC-2 family transporter protein | |||
LFBCNLDA_02186 | 9.2e-28 | V | ABC-2 family transporter protein | |||
LFBCNLDA_02187 | 8.1e-227 | V | ABC-2 family transporter protein | |||
LFBCNLDA_02188 | 2e-183 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_02189 | 9.9e-42 | pacL | 3.6.3.8, 3.6.3.9 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
LFBCNLDA_02190 | 2.1e-233 | T | Histidine kinase | |||
LFBCNLDA_02191 | 1.7e-120 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_02192 | 1.1e-115 | MA20_27875 | P | Protein of unknown function DUF47 | ||
LFBCNLDA_02193 | 1.5e-189 | pit | P | Phosphate transporter family | ||
LFBCNLDA_02194 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
LFBCNLDA_02195 | 8.7e-303 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
LFBCNLDA_02196 | 1e-24 | |||||
LFBCNLDA_02197 | 2.1e-185 | |||||
LFBCNLDA_02198 | 1.1e-30 | L | Transposase | |||
LFBCNLDA_02199 | 3e-69 | L | Integrase core domain | |||
LFBCNLDA_02201 | 1.5e-191 | S | Protein of unknown function DUF262 | |||
LFBCNLDA_02202 | 5.7e-118 | S | Protein of unknown function (DUF3800) | |||
LFBCNLDA_02203 | 0.0 | yegQ | O | Peptidase family U32 C-terminal domain | ||
LFBCNLDA_02204 | 3.5e-188 | yfiH | Q | Multi-copper polyphenol oxidoreductase laccase | ||
LFBCNLDA_02205 | 3.2e-144 | 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) | |
LFBCNLDA_02206 | 8e-128 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
LFBCNLDA_02207 | 2.2e-45 | D | nuclear chromosome segregation | |||
LFBCNLDA_02208 | 3.2e-269 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
LFBCNLDA_02209 | 3.4e-170 | L | Excalibur calcium-binding domain | |||
LFBCNLDA_02210 | 1.5e-219 | 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) | |
LFBCNLDA_02211 | 5.8e-242 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_02212 | 1e-105 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
LFBCNLDA_02214 | 1.6e-142 | pgp | 3.1.3.18 | S | HAD-hyrolase-like | |
LFBCNLDA_02215 | 8.7e-62 | rbpA | K | Binds to RNA polymerase (RNAP), stimulating transcription from principal, but not alternative sigma factor promoters | ||
LFBCNLDA_02216 | 0.0 | helY | L | DEAD DEAH box helicase | ||
LFBCNLDA_02217 | 1e-51 | |||||
LFBCNLDA_02218 | 0.0 | pafB | K | WYL domain | ||
LFBCNLDA_02219 | 7.4e-288 | ugpA | 2.7.7.9 | G | UTP-glucose-1-phosphate uridylyltransferase | |
LFBCNLDA_02221 | 0.0 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LFBCNLDA_02222 | 2.5e-140 | 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 | |
LFBCNLDA_02223 | 0.0 | nrdD | 1.1.98.6 | F | Anaerobic ribonucleoside-triphosphate reductase | |
LFBCNLDA_02224 | 2.5e-272 | 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 | |
LFBCNLDA_02225 | 7.8e-43 | 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 | |
LFBCNLDA_02226 | 1.5e-172 | S | Endonuclease/Exonuclease/phosphatase family | |||
LFBCNLDA_02229 | 1.4e-181 | iunH1 | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
LFBCNLDA_02230 | 3.2e-253 | cdr | OP | Sulfurtransferase TusA | ||
LFBCNLDA_02231 | 4.4e-149 | moeB | 2.7.7.80 | H | ThiF family | |
LFBCNLDA_02232 | 4.5e-132 | tmp1 | S | Domain of unknown function (DUF4391) | ||
LFBCNLDA_02233 | 3.9e-57 | ppx | 3.6.1.11, 3.6.1.40 | FP | Ppx/GppA phosphatase family | |
LFBCNLDA_02234 | 2.9e-229 | aspB | E | Aminotransferase class-V | ||
LFBCNLDA_02235 | 1.3e-111 | vsr | L | May nick specific sequences that contain T G mispairs resulting from m5C-deamination | ||
LFBCNLDA_02236 | 2.3e-270 | S | zinc finger | |||
LFBCNLDA_02237 | 2.6e-123 | 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 | |
LFBCNLDA_02238 | 1.1e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LFBCNLDA_02239 | 8.7e-246 | O | Subtilase family | |||
LFBCNLDA_02240 | 0.0 | pepN | 3.4.11.2 | E | Peptidase family M1 domain | |
LFBCNLDA_02241 | 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 | ||
LFBCNLDA_02242 | 1.2e-160 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LFBCNLDA_02243 | 1e-132 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LFBCNLDA_02244 | 5e-54 | L | Transposase | |||
LFBCNLDA_02245 | 6.4e-24 | relB | L | RelB antitoxin | ||
LFBCNLDA_02246 | 4.7e-27 | 2.1.1.72 | L | Belongs to the N(4) N(6)-methyltransferase family | ||
LFBCNLDA_02247 | 1.4e-65 | gsiA | P | ATPase activity | ||
LFBCNLDA_02248 | 4.2e-256 | G | Major Facilitator Superfamily | |||
LFBCNLDA_02249 | 5.1e-135 | K | -acetyltransferase | |||
LFBCNLDA_02250 | 0.0 | uvrD2 | 3.6.4.12 | L | Belongs to the helicase family. UvrD subfamily | |
LFBCNLDA_02251 | 0.0 | uvrD | 3.6.4.12 | L | PD-(D/E)XK nuclease superfamily | |
LFBCNLDA_02252 | 3.7e-268 | KLT | Protein tyrosine kinase | |||
LFBCNLDA_02253 | 0.0 | S | Fibronectin type 3 domain | |||
LFBCNLDA_02254 | 1.3e-227 | S | ATPase family associated with various cellular activities (AAA) | |||
LFBCNLDA_02255 | 3e-227 | S | Protein of unknown function DUF58 | |||
LFBCNLDA_02256 | 1.6e-38 | E | Transglutaminase-like superfamily | |||
LFBCNLDA_02257 | 3.8e-63 | E | Transglutaminase-like superfamily | |||
LFBCNLDA_02258 | 1.2e-205 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
LFBCNLDA_02260 | 1.1e-163 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_02261 | 1.3e-42 | S | enterobacterial common antigen metabolic process | |||
LFBCNLDA_02262 | 3.9e-170 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LFBCNLDA_02263 | 4.6e-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 | |
LFBCNLDA_02264 | 7.7e-199 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LFBCNLDA_02265 | 1.6e-12 | L | Transposase, Mutator family | |||
LFBCNLDA_02266 | 1.8e-61 | L | PFAM Integrase catalytic | |||
LFBCNLDA_02267 | 1.7e-131 | L | IstB-like ATP binding protein | |||
LFBCNLDA_02268 | 2.4e-33 | L | Transposase | |||
LFBCNLDA_02269 | 8.9e-195 | L | Transposase | |||
LFBCNLDA_02270 | 0.0 | ilvD | 4.2.1.9 | H | Belongs to the IlvD Edd family | |
LFBCNLDA_02271 | 1.1e-53 | 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 | |
LFBCNLDA_02272 | 8.5e-221 | 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 | |
LFBCNLDA_02273 | 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 | ||
LFBCNLDA_02274 | 5.4e-135 | 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
LFBCNLDA_02275 | 9.6e-183 | 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 | |
LFBCNLDA_02276 | 1.9e-138 | serB | 3.1.3.3 | E | haloacid dehalogenase-like hydrolase | |
LFBCNLDA_02277 | 0.0 | arc | O | AAA ATPase forming ring-shaped complexes | ||
LFBCNLDA_02278 | 0.0 | dop | 3.5.1.119, 6.3.1.19 | S | Pup-ligase protein | |
LFBCNLDA_02279 | 3e-161 | hisN | 3.1.3.25 | G | Inositol monophosphatase family | |
LFBCNLDA_02280 | 1.6e-10 | pup | S | Protein modifier that is covalently attached to lysine residues of substrate proteins, thereby targeting them for proteasomal degradation. The tagging system is termed pupylation | ||
LFBCNLDA_02281 | 6.5e-276 | 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 | |
LFBCNLDA_02282 | 8.1e-42 | hup | L | Belongs to the bacterial histone-like protein family | ||
LFBCNLDA_02283 | 0.0 | S | Lysylphosphatidylglycerol synthase TM region | |||
LFBCNLDA_02284 | 8.6e-281 | purB | 4.3.2.2 | F | Adenylosuccinate lyase C-terminal | |
LFBCNLDA_02285 | 1.2e-288 | S | PGAP1-like protein | |||
LFBCNLDA_02287 | 4e-73 | |||||
LFBCNLDA_02288 | 7.6e-146 | S | von Willebrand factor (vWF) type A domain | |||
LFBCNLDA_02289 | 2e-189 | S | von Willebrand factor (vWF) type A domain | |||
LFBCNLDA_02290 | 6.4e-94 | |||||
LFBCNLDA_02291 | 8.7e-176 | S | Protein of unknown function DUF58 | |||
LFBCNLDA_02292 | 7.2e-181 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
LFBCNLDA_02293 | 4e-31 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_02294 | 3.5e-111 | S | Domain of unknown function (DUF4194) | |||
LFBCNLDA_02295 | 3.3e-283 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_02296 | 3.7e-162 | nfo | 3.1.21.2 | L | Endonuclease IV plays a role in DNA repair. It cleaves phosphodiester bonds at apurinic or apyrimidinic sites (AP sites) to produce new 5'-ends that are base-free deoxyribose 5-phosphate residues. It preferentially attacks modified AP sites created by bleomycin and neocarzinostatin | |
LFBCNLDA_02297 | 1.5e-64 | yeaO | K | Protein of unknown function, DUF488 | ||
LFBCNLDA_02298 | 1.5e-115 | ydaF_1 | J | Acetyltransferase (GNAT) domain | ||
LFBCNLDA_02300 | 2.2e-100 | XK27_07525 | 3.6.1.55 | F | Hydrolase of X-linked nucleoside diphosphate N terminal | |
LFBCNLDA_02301 | 1.8e-31 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
LFBCNLDA_02303 | 7.7e-185 | S | Acetyltransferase (GNAT) domain | |||
LFBCNLDA_02304 | 3e-148 | |||||
LFBCNLDA_02305 | 4e-101 | ytrE | V | ABC transporter | ||
LFBCNLDA_02306 | 8.1e-159 | V | Putative peptidoglycan binding domain | |||
LFBCNLDA_02307 | 9.4e-100 | |||||
LFBCNLDA_02308 | 1.9e-39 | |||||
LFBCNLDA_02309 | 1.5e-102 | K | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_02310 | 2.3e-136 | qseC | 2.7.13.3 | T | GHKL domain | |
LFBCNLDA_02311 | 2.1e-48 | |||||
LFBCNLDA_02312 | 3.1e-78 | MA20_22310 | 4.4.1.5 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |
LFBCNLDA_02313 | 4.6e-161 | rpoC | M | heme binding | ||
LFBCNLDA_02314 | 1.6e-32 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_02315 | 4.1e-156 | |||||
LFBCNLDA_02316 | 2.4e-95 | ypjC | S | Putative ABC-transporter type IV | ||
LFBCNLDA_02317 | 5.1e-110 | ycaK | 1.6.5.2 | S | NADPH-dependent FMN reductase | |
LFBCNLDA_02318 | 2.2e-193 | V | VanZ like family | |||
LFBCNLDA_02319 | 7.9e-146 | KT | RESPONSE REGULATOR receiver | |||
LFBCNLDA_02320 | 2.7e-70 | pdxH | S | Pfam:Pyridox_oxidase | ||
LFBCNLDA_02321 | 1.1e-138 | yijF | S | Domain of unknown function (DUF1287) | ||
LFBCNLDA_02322 | 5.1e-139 | gluA | 3.6.3.21 | E | ATP-binding protein of ABC transporter for glutamate K02028 | |
LFBCNLDA_02323 | 7.3e-95 | S | Aminoacyl-tRNA editing domain | |||
LFBCNLDA_02325 | 3.2e-20 | S | Aminoacyl-tRNA editing domain | |||
LFBCNLDA_02326 | 7.7e-83 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_02327 | 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) | |
LFBCNLDA_02328 | 1.1e-261 | hisS | 6.1.1.21 | J | Histidyl-tRNA synthetase | |
LFBCNLDA_02329 | 1.8e-209 | 3.1.26.12, 3.2.1.8 | S | Domain of Unknown Function (DUF349) | ||
LFBCNLDA_02334 | 0.0 | clpC | O | ATPase family associated with various cellular activities (AAA) | ||
LFBCNLDA_02335 | 1.8e-184 | uspA | T | Belongs to the universal stress protein A family | ||
LFBCNLDA_02336 | 3.6e-175 | S | Protein of unknown function (DUF3027) | |||
LFBCNLDA_02337 | 2.3e-66 | cspB | K | 'Cold-shock' DNA-binding domain | ||
LFBCNLDA_02338 | 0.0 | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | ||
LFBCNLDA_02339 | 9e-133 | KT | Response regulator receiver domain protein | |||
LFBCNLDA_02340 | 3.4e-171 | |||||
LFBCNLDA_02341 | 1.7e-10 | S | Proteins of 100 residues with WXG | |||
LFBCNLDA_02342 | 2.7e-291 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
LFBCNLDA_02343 | 5.2e-30 | cspA | K | 'Cold-shock' DNA-binding domain | ||
LFBCNLDA_02344 | 2.7e-68 | S | LytR cell envelope-related transcriptional attenuator | |||
LFBCNLDA_02345 | 1.8e-144 | 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 | |
LFBCNLDA_02347 | 4.4e-89 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
LFBCNLDA_02348 | 3.1e-239 | icd | 1.1.1.42 | C | Belongs to the isocitrate and isopropylmalate dehydrogenases family | |
LFBCNLDA_02349 | 2.4e-263 | G | ABC transporter substrate-binding protein | |||
LFBCNLDA_02350 | 0.0 | fadD1 | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_02351 | 2.5e-131 | M | Peptidase family M23 | |||
LFBCNLDA_02353 | 1.4e-195 | 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 | |
LFBCNLDA_02354 | 9.7e-98 | rimI | 2.3.1.128, 2.3.1.234 | K | FR47-like protein | |
LFBCNLDA_02355 | 3e-159 | yeaZ | 2.3.1.234 | O | Glycoprotease family | |
LFBCNLDA_02356 | 5e-119 | ydiB | 2.7.1.221, 5.1.1.1 | S | Threonylcarbamoyl adenosine biosynthesis protein TsaE | |
LFBCNLDA_02357 | 1.8e-181 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LFBCNLDA_02358 | 0.0 | comE | S | Competence protein | ||
LFBCNLDA_02359 | 3e-89 | comEA | 2.4.1.21 | GT5 | L | Helix-hairpin-helix motif |
LFBCNLDA_02360 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFBCNLDA_02361 | 9.2e-167 | ET | Bacterial periplasmic substrate-binding proteins | |||
LFBCNLDA_02362 | 4.8e-171 | corA | P | CorA-like Mg2+ transporter protein | ||
LFBCNLDA_02363 | 7.9e-157 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_02364 | 1.2e-296 | E | Serine carboxypeptidase | |||
LFBCNLDA_02365 | 2.6e-08 | S | Psort location Cytoplasmic, score 8.87 | |||
LFBCNLDA_02366 | 6.5e-250 | recN | L | May be involved in recombinational repair of damaged DNA | ||
LFBCNLDA_02367 | 8.9e-124 | S | Haloacid dehalogenase-like hydrolase | |||
LFBCNLDA_02368 | 3.7e-58 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
LFBCNLDA_02369 | 1.9e-175 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_02370 | 1.9e-122 | S | ABC-2 family transporter protein | |||
LFBCNLDA_02371 | 2.5e-116 | S | ABC-2 family transporter protein | |||
LFBCNLDA_02372 | 1.5e-283 | thrC | 4.2.3.1 | E | Threonine synthase N terminus | |
LFBCNLDA_02373 | 2.4e-237 | 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 | |
LFBCNLDA_02374 | 2.6e-89 | |||||
LFBCNLDA_02375 | 1.6e-145 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LFBCNLDA_02376 | 1.5e-191 | 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) | |
LFBCNLDA_02378 | 1e-262 | 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 | |
LFBCNLDA_02379 | 1.2e-68 | 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 | |
LFBCNLDA_02380 | 1.8e-136 | 3.1.3.85, 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_02381 | 1.1e-77 | S | Bacterial PH domain | |||
LFBCNLDA_02382 | 7.1e-255 | nplT | 3.2.1.1 | GH13 | G | Alpha amylase, catalytic domain |
LFBCNLDA_02383 | 3.3e-139 | S | Protein conserved in bacteria | |||
LFBCNLDA_02386 | 5.1e-39 | D | FtsK/SpoIIIE family | |||
LFBCNLDA_02389 | 2.9e-75 | L | Phage integrase family | |||
LFBCNLDA_02390 | 6.1e-85 | S | Protein of unknown function (DUF3071) | |||
LFBCNLDA_02391 | 1.4e-47 | S | Domain of unknown function (DUF4193) | |||
LFBCNLDA_02392 | 8.5e-84 | 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 | |
LFBCNLDA_02393 | 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 | |
LFBCNLDA_02394 | 8e-28 | |||||
LFBCNLDA_02395 | 3.9e-68 | T | Toxic component of a toxin-antitoxin (TA) module | |||
LFBCNLDA_02396 | 1.1e-49 | relB | L | RelB antitoxin | ||
LFBCNLDA_02397 | 7.1e-103 | 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 | |
LFBCNLDA_02398 | 5.5e-166 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LFBCNLDA_02399 | 1.3e-55 | P | ABC-type metal ion transport system permease component | |||
LFBCNLDA_02400 | 2.3e-223 | S | Peptidase dimerisation domain | |||
LFBCNLDA_02401 | 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 | |
LFBCNLDA_02402 | 6.4e-40 | |||||
LFBCNLDA_02403 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
LFBCNLDA_02404 | 3.9e-175 | 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 | |
LFBCNLDA_02405 | 1.6e-111 | S | Protein of unknown function (DUF3000) | |||
LFBCNLDA_02406 | 1.3e-248 | rnd | 3.1.13.5 | J | 3'-5' exonuclease | |
LFBCNLDA_02407 | 1.8e-235 | 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 | ||
LFBCNLDA_02408 | 1.3e-252 | clcA_2 | P | Voltage gated chloride channel | ||
LFBCNLDA_02410 | 1.2e-87 | L | Transposase and inactivated derivatives | |||
LFBCNLDA_02412 | 8.5e-153 | E | Transglutaminase/protease-like homologues | |||
LFBCNLDA_02413 | 0.0 | gcs2 | S | A circularly permuted ATPgrasp | ||
LFBCNLDA_02414 | 6.4e-173 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LFBCNLDA_02415 | 0.0 | 3.2.1.52 | GH20 | G | hydrolase family 20, catalytic | |
LFBCNLDA_02416 | 8.1e-64 | rplQ | J | Ribosomal protein L17 | ||
LFBCNLDA_02417 | 8.9e-184 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFBCNLDA_02418 | 1.1e-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 | ||
LFBCNLDA_02419 | 3.3e-62 | 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 | ||
LFBCNLDA_02420 | 6.5e-14 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LFBCNLDA_02421 | 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 | ||
LFBCNLDA_02422 | 6.5e-99 | 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 | |
LFBCNLDA_02423 | 2.3e-248 | 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 | ||
LFBCNLDA_02424 | 2.7e-63 | rplO | J | binds to the 23S rRNA | ||
LFBCNLDA_02425 | 1e-24 | rpmD | J | Ribosomal protein L30p/L7e | ||
LFBCNLDA_02426 | 1.3e-99 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LFBCNLDA_02427 | 1.1e-57 | 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 | ||
LFBCNLDA_02428 | 2.1e-94 | 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 | ||
LFBCNLDA_02429 | 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 | ||
LFBCNLDA_02430 | 9.2e-18 | 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 | ||
LFBCNLDA_02431 | 2.2e-102 | 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 | ||
LFBCNLDA_02432 | 3.5e-52 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LFBCNLDA_02433 | 6.6e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LFBCNLDA_02434 | 3.5e-42 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LFBCNLDA_02435 | 5e-38 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LFBCNLDA_02436 | 5.8e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LFBCNLDA_02439 | 1.9e-25 | rpmG | J | Ribosomal protein L33 | ||
LFBCNLDA_02440 | 6.5e-213 | murB | 1.3.1.98 | M | Cell wall formation | |
LFBCNLDA_02441 | 9e-61 | fdxA | C | 4Fe-4S binding domain | ||
LFBCNLDA_02442 | 3.6e-224 | dapC | E | Aminotransferase class I and II | ||
LFBCNLDA_02443 | 6.2e-238 | 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 | |
LFBCNLDA_02444 | 1.6e-127 | S | EamA-like transporter family | |||
LFBCNLDA_02446 | 1.4e-256 | M | Bacterial capsule synthesis protein PGA_cap | |||
LFBCNLDA_02447 | 1.1e-113 | yigZ | 2.1.1.45, 3.4.13.9 | S | Uncharacterized protein family UPF0029 | |
LFBCNLDA_02448 | 4.6e-108 | |||||
LFBCNLDA_02449 | 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 |
LFBCNLDA_02450 | 3.5e-79 | 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 | ||
LFBCNLDA_02451 | 8.8e-68 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LFBCNLDA_02452 | 0.0 | glgX | 3.2.1.196, 3.2.1.68 | CBM48,GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LFBCNLDA_02453 | 9e-231 | 2.7.1.2 | GK | transcriptional repressor of nag (N-acetylglucosamine) operon K02565 | ||
LFBCNLDA_02454 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LFBCNLDA_02455 | 1.3e-165 | budA | 4.1.1.5 | H | Alpha-acetolactate decarboxylase | |
LFBCNLDA_02456 | 4.6e-25 | pyrD | 1.3.1.14 | F | Dihydroorotate dehydrogenase | |
LFBCNLDA_02457 | 3.7e-254 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LFBCNLDA_02458 | 2.6e-38 | G | Transmembrane secretion effector | |||
LFBCNLDA_02459 | 3e-85 | G | Transmembrane secretion effector | |||
LFBCNLDA_02460 | 8.5e-120 | |||||
LFBCNLDA_02461 | 2.3e-72 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LFBCNLDA_02462 | 6.1e-123 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
LFBCNLDA_02464 | 1.4e-165 | fkbB | 5.2.1.8 | M | FKBP-type peptidyl-prolyl cis-trans isomerase | |
LFBCNLDA_02465 | 2.1e-186 | |||||
LFBCNLDA_02466 | 3.3e-178 | |||||
LFBCNLDA_02467 | 2.3e-160 | trxA2 | O | Tetratricopeptide repeat | ||
LFBCNLDA_02468 | 3.4e-117 | cyaA | 4.6.1.1 | S | CYTH | |
LFBCNLDA_02470 | 2.5e-181 | K | Bacterial regulatory proteins, lacI family | |||
LFBCNLDA_02471 | 2.7e-32 | 4.2.1.68 | M | Enolase C-terminal domain-like | ||
LFBCNLDA_02472 | 1.9e-62 | IQ | KR domain | |||
LFBCNLDA_02473 | 2.6e-186 | G | Bacterial extracellular solute-binding protein | |||
LFBCNLDA_02474 | 6.5e-120 | U | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_02475 | 3.5e-126 | G | Binding-protein-dependent transport systems inner membrane component | |||
LFBCNLDA_02477 | 1.7e-183 | fucA | 3.2.1.51 | GH29 | G | Alpha-L-fucosidase |
LFBCNLDA_02479 | 4.1e-239 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LFBCNLDA_02480 | 7.1e-84 | argR | K | Regulates arginine biosynthesis genes | ||
LFBCNLDA_02481 | 1.9e-183 | 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 | |
LFBCNLDA_02482 | 8.1e-246 | argD | 2.6.1.11, 2.6.1.17 | E | Aminotransferase class-III | |
LFBCNLDA_02483 | 1.7e-179 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LFBCNLDA_02484 | 1.3e-215 | 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 | |
LFBCNLDA_02485 | 7.7e-205 | 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 | |
LFBCNLDA_02486 | 3.3e-86 | |||||
LFBCNLDA_02487 | 0.0 | pheT | 6.1.1.20 | J | Phenylalanyl-tRNA synthetase beta | |
LFBCNLDA_02488 | 3.1e-203 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LFBCNLDA_02489 | 8.6e-159 | 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 | |
LFBCNLDA_02490 | 5.9e-51 | L | PFAM Integrase catalytic | |||
LFBCNLDA_02491 | 1.4e-47 | yueD | S | Enoyl-(Acyl carrier protein) reductase | ||
LFBCNLDA_02492 | 2.6e-19 | S | Enoyl-(Acyl carrier protein) reductase | |||
LFBCNLDA_02494 | 4e-237 | rutG | F | Permease family | ||
LFBCNLDA_02495 | 3.1e-158 | 3.1.3.73 | G | Phosphoglycerate mutase family | ||
LFBCNLDA_02496 | 3.5e-62 | S | Phospholipase/Carboxylesterase | |||
LFBCNLDA_02497 | 3.2e-187 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
LFBCNLDA_02498 | 5.7e-167 | S | Patatin-like phospholipase | |||
LFBCNLDA_02499 | 2.5e-152 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LFBCNLDA_02500 | 1.2e-168 | 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 | |
LFBCNLDA_02501 | 3.8e-114 | S | Vitamin K epoxide reductase | |||
LFBCNLDA_02502 | 6.9e-164 | PPA1328 | 3.1.3.97 | S | DNA polymerase alpha chain like domain | |
LFBCNLDA_02503 | 6.1e-32 | S | Protein of unknown function (DUF3107) | |||
LFBCNLDA_02504 | 7.9e-237 | mphA | S | Aminoglycoside phosphotransferase | ||
LFBCNLDA_02505 | 3.1e-281 | uvrD2 | 3.6.4.12 | L | DNA helicase | |
LFBCNLDA_02506 | 1.5e-286 | S | Zincin-like metallopeptidase | |||
LFBCNLDA_02507 | 6e-149 | lon | T | Belongs to the peptidase S16 family | ||
LFBCNLDA_02508 | 5.7e-47 | S | Protein of unknown function (DUF3052) | |||
LFBCNLDA_02509 | 7.6e-194 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_02510 | 1.2e-61 | S | Thiamine-binding protein | |||
LFBCNLDA_02511 | 5e-162 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
LFBCNLDA_02512 | 6.9e-231 | O | AAA domain (Cdc48 subfamily) | |||
LFBCNLDA_02513 | 1.3e-84 | |||||
LFBCNLDA_02514 | 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 | |
LFBCNLDA_02515 | 1.9e-74 | fthC | 6.3.3.2 | H | 5-formyltetrahydrofolate cyclo-ligase family | |
LFBCNLDA_02516 | 3.2e-38 | fmdB | S | Putative regulatory protein | ||
LFBCNLDA_02517 | 2.8e-109 | flgA | NO | SAF | ||
LFBCNLDA_02518 | 9.6e-42 | |||||
LFBCNLDA_02519 | 0.0 | L | Superfamily I DNA and RNA helicases and helicase subunits | |||
LFBCNLDA_02520 | 2.2e-240 | T | Forkhead associated domain | |||
LFBCNLDA_02522 | 2.9e-36 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LFBCNLDA_02523 | 2.1e-88 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LFBCNLDA_02524 | 1.5e-183 | xynB2 | 1.1.1.169 | E | lipolytic protein G-D-S-L family | |
LFBCNLDA_02527 | 8.8e-222 | pbuO | S | Permease family | ||
LFBCNLDA_02528 | 9e-146 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_02529 | 3.6e-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 | |
LFBCNLDA_02530 | 6.2e-180 | pstA | P | Phosphate transport system permease | ||
LFBCNLDA_02531 | 3.8e-171 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LFBCNLDA_02532 | 9.8e-171 | pstS | P | Part of the ABC transporter complex PstSACB involved in phosphate import | ||
LFBCNLDA_02533 | 3.7e-128 | KT | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_02534 | 5.9e-20 | pgk | 2.7.2.3, 5.3.1.1 | F | Phosphoglycerate kinase | |
LFBCNLDA_02535 | 1.5e-146 | 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) | |
LFBCNLDA_02536 | 8e-33 | secG | U | Preprotein translocase SecG subunit | ||
LFBCNLDA_02537 | 2.9e-176 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
LFBCNLDA_02538 | 3e-161 | S | Sucrose-6F-phosphate phosphohydrolase | |||
LFBCNLDA_02539 | 5.2e-243 | mepA_6 | V | MatE | ||
LFBCNLDA_02541 | 2.6e-253 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
LFBCNLDA_02542 | 1.1e-142 | yoaK | S | Protein of unknown function (DUF1275) | ||
LFBCNLDA_02543 | 1e-201 | tal | 2.2.1.2 | H | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
LFBCNLDA_02544 | 0.0 | tkt | 2.2.1.1 | H | Belongs to the transketolase family | |
LFBCNLDA_02545 | 4.3e-220 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LFBCNLDA_02546 | 3.4e-211 | 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 | ||
LFBCNLDA_02547 | 7.1e-160 | G | Fructosamine kinase | |||
LFBCNLDA_02548 | 5e-168 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LFBCNLDA_02549 | 3.7e-156 | S | PAC2 family | |||
LFBCNLDA_02553 | 7.4e-129 | 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 | |
LFBCNLDA_02554 | 2.1e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LFBCNLDA_02555 | 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 | ||
LFBCNLDA_02556 | 4.5e-100 | folE | 2.7.6.3, 3.5.4.16 | H | GTP cyclohydrolase | |
LFBCNLDA_02557 | 4.9e-162 | 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 | |
LFBCNLDA_02558 | 7.9e-293 | 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 | |
LFBCNLDA_02559 | 5.7e-76 | S | Protein of unknown function (DUF3180) | |||
LFBCNLDA_02560 | 7.1e-172 | tesB | I | Thioesterase-like superfamily | ||
LFBCNLDA_02561 | 0.0 | 3.2.1.52, 3.2.1.83 | GH16,GH20 | G | hydrolase family 20, catalytic | |
LFBCNLDA_02562 | 2.4e-306 | yjjK | S | ATP-binding cassette protein, ChvD family | ||
LFBCNLDA_02564 | 3.3e-115 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
LFBCNLDA_02565 | 1.5e-156 | S | Protein of unknown function (DUF979) | |||
LFBCNLDA_02566 | 2.8e-110 | S | Protein of unknown function (DUF969) | |||
LFBCNLDA_02568 | 4.1e-59 | guaB | 1.1.1.205 | F | IMP dehydrogenase family protein | |
LFBCNLDA_02569 | 6.3e-90 | |||||
LFBCNLDA_02570 | 0.0 | fadD3 | 6.2.1.3 | I | long-chain-fatty acid CoA ligase | |
LFBCNLDA_02571 | 1.7e-87 | 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 | |
LFBCNLDA_02572 | 4.6e-141 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LFBCNLDA_02573 | 4.8e-146 | 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 | ||
LFBCNLDA_02574 | 2.8e-125 | 3.2.1.8 | S | alpha beta | ||
LFBCNLDA_02575 | 4.1e-133 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LFBCNLDA_02576 | 2.4e-93 | 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 | ||
LFBCNLDA_02577 | 1.8e-176 | cdsA | 2.7.7.41, 2.7.7.67 | I | Cytidylyltransferase family | |
LFBCNLDA_02578 | 1.2e-227 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LFBCNLDA_02579 | 1.4e-139 | 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 | |
LFBCNLDA_02580 | 1.3e-72 | hisI | 3.5.4.19, 3.6.1.31 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
LFBCNLDA_02581 | 9.6e-305 | 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 | |
LFBCNLDA_02582 | 6.1e-233 | G | Bacterial extracellular solute-binding protein | |||
LFBCNLDA_02583 | 1.5e-172 | G | Binding-protein-dependent transport system inner membrane component | |||
LFBCNLDA_02584 | 7.5e-156 | G | ABC transporter permease | |||
LFBCNLDA_02585 | 3.3e-133 | S | Tripartite tricarboxylate transporter family receptor | |||
LFBCNLDA_02586 | 2.3e-177 | pknL | 2.7.11.1 | KLT | PASTA | |
LFBCNLDA_02587 | 6.7e-133 | plsC2 | 2.3.1.51 | I | Phosphate acyltransferases | |
LFBCNLDA_02588 | 7.4e-109 | |||||
LFBCNLDA_02589 | 7.9e-191 | 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) | |
LFBCNLDA_02590 | 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 | ||
LFBCNLDA_02591 | 3.3e-110 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LFBCNLDA_02592 | 1.4e-26 | marR5 | K | Winged helix DNA-binding domain | ||
LFBCNLDA_02593 | 3e-72 | recX | S | Modulates RecA activity | ||
LFBCNLDA_02594 | 8e-216 | 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 | ||
LFBCNLDA_02595 | 3.7e-40 | S | Protein of unknown function (DUF3046) | |||
LFBCNLDA_02596 | 1e-79 | K | Helix-turn-helix XRE-family like proteins | |||
LFBCNLDA_02597 | 1.3e-96 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LFBCNLDA_02598 | 1.9e-121 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LFBCNLDA_02599 | 8.4e-296 | ftsK | D | FtsK SpoIIIE family protein | ||
LFBCNLDA_02600 | 3.4e-183 | rfbP | 2.7.8.6 | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | |
LFBCNLDA_02601 | 3.8e-304 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_02602 | 2.1e-225 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LFBCNLDA_02603 | 2.9e-122 | L | Protein of unknown function (DUF1524) | |||
LFBCNLDA_02604 | 2.9e-170 | dkgA | 1.1.1.346 | S | Oxidoreductase, aldo keto reductase family protein | |
LFBCNLDA_02605 | 1.8e-09 | chiA | 3.1.6.1, 3.2.1.14, 3.2.1.17, 3.2.1.23, 3.2.1.4 | AA10,CBM15,CBM73,GH18,GH5,GH9 | S | chitin catabolic process |
LFBCNLDA_02606 | 4.2e-201 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_02607 | 2.9e-240 | G | Glycosyl hydrolases family 43 | |||
LFBCNLDA_02610 | 1.6e-111 | 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 | |
LFBCNLDA_02611 | 9e-156 | 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 | |
LFBCNLDA_02612 | 0.0 | fadD | 6.2.1.3 | I | AMP-binding enzyme | |
LFBCNLDA_02614 | 2.9e-25 | M | Belongs to the glycosyl hydrolase 30 family | |||
LFBCNLDA_02615 | 6.3e-23 | M | Belongs to the glycosyl hydrolase 30 family | |||
LFBCNLDA_02617 | 1.5e-202 | 1.1.1.65 | C | Aldo/keto reductase family | ||
LFBCNLDA_02618 | 8.3e-42 | S | Protein of unknown function (DUF1778) | |||
LFBCNLDA_02619 | 5.9e-94 | ydgJ | K | helix_turn_helix multiple antibiotic resistance protein | ||
LFBCNLDA_02620 | 0.0 | lmrA1 | V | ABC transporter, ATP-binding protein | ||
LFBCNLDA_02621 | 0.0 | lmrA2 | V | ABC transporter transmembrane region | ||
LFBCNLDA_02622 | 9e-25 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
LFBCNLDA_02623 | 2.2e-16 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
LFBCNLDA_02624 | 0.0 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
LFBCNLDA_02625 | 9.3e-137 | 3.2.1.51 | GH95 | G | Glycosyl hydrolase family 65, N-terminal domain | |
LFBCNLDA_02626 | 1.2e-54 | helY | L | DEAD DEAH box helicase | ||
LFBCNLDA_02627 | 3.2e-256 | rarA | L | Recombination factor protein RarA | ||
LFBCNLDA_02629 | 2.6e-256 | EGP | Major facilitator Superfamily | |||
LFBCNLDA_02630 | 0.0 | ecfA | GP | ABC transporter, ATP-binding protein | ||
LFBCNLDA_02631 | 2.8e-103 | 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 | ||
LFBCNLDA_02632 | 5.1e-139 | ppgK | 2.7.1.2, 2.7.1.63 | GK | ROK family | |
LFBCNLDA_02633 | 2.7e-213 | E | Aminotransferase class I and II | |||
LFBCNLDA_02634 | 3.4e-138 | bioM | P | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_02635 | 2.5e-239 | 2.8.2.22 | S | Arylsulfotransferase Ig-like domain | ||
LFBCNLDA_02636 | 0.0 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
LFBCNLDA_02637 | 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 | |
LFBCNLDA_02638 | 2.5e-90 | |||||
LFBCNLDA_02639 | 1.1e-181 | mutY | 2.1.1.37, 2.1.3.15, 6.4.1.2 | L | FES | |
LFBCNLDA_02640 | 4.9e-36 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | xyloglucan:xyloglucosyl transferase activity |
LFBCNLDA_02641 | 7.9e-42 | exsH | 3.2.1.178, 3.2.1.18, 3.2.1.52 | GH16,GH20,GH33 | G | Putative cell wall binding repeat |
LFBCNLDA_02643 | 3.1e-121 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LFBCNLDA_02644 | 1.9e-45 | |||||
LFBCNLDA_02645 | 1.6e-252 | S | UPF0210 protein | |||
LFBCNLDA_02646 | 4.2e-43 | gcvR | T | Belongs to the UPF0237 family | ||
LFBCNLDA_02647 | 6.2e-241 | EGP | Sugar (and other) transporter | |||
LFBCNLDA_02648 | 3.2e-134 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LFBCNLDA_02649 | 1.2e-280 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
LFBCNLDA_02650 | 1.4e-107 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
LFBCNLDA_02651 | 1e-142 | S | Putative ABC-transporter type IV | |||
LFBCNLDA_02652 | 1.4e-253 | 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) | |
LFBCNLDA_02653 | 7.8e-159 | L | Tetratricopeptide repeat | |||
LFBCNLDA_02654 | 2.3e-190 | yutF | 3.1.3.41 | G | Haloacid dehalogenase-like hydrolase | |
LFBCNLDA_02656 | 1.5e-135 | tlyA | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LFBCNLDA_02657 | 7.5e-102 | |||||
LFBCNLDA_02658 | 2e-115 | trkA | P | TrkA-N domain | ||
LFBCNLDA_02659 | 3.3e-235 | trkB | P | Cation transport protein | ||
LFBCNLDA_02660 | 7.3e-183 | 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 | |
LFBCNLDA_02661 | 7.3e-126 | 3.2.1.10, 3.2.1.20, 3.2.1.93 | GH13,GH31 | G | Alpha-amylase domain | |
LFBCNLDA_02662 | 1.1e-116 | KT | Transcriptional regulatory protein, C terminal | |||
LFBCNLDA_02663 | 2.8e-122 | orn | L | 3'-to-5' exoribonuclease specific for small oligoribonucleotides | ||
LFBCNLDA_02664 | 4e-161 | supH | S | Sucrose-6F-phosphate phosphohydrolase | ||
LFBCNLDA_02665 | 1.5e-269 | recD2 | 3.6.4.12 | L | PIF1-like helicase | |
LFBCNLDA_02666 | 7.4e-39 | GT87 | NU | Tfp pilus assembly protein FimV | ||
LFBCNLDA_02667 | 7.9e-185 | phoN | I | PAP2 superfamily | ||
LFBCNLDA_02668 | 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 | |
LFBCNLDA_02669 | 1.4e-87 | |||||
LFBCNLDA_02670 | 9.4e-50 | L | Single-strand binding protein family | |||
LFBCNLDA_02671 | 1.6e-27 | M | domain protein | |||
LFBCNLDA_02672 | 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 | |
LFBCNLDA_02673 | 3.6e-290 | sufB | O | FeS assembly protein SufB | ||
LFBCNLDA_02674 | 1.5e-228 | sufD | O | FeS assembly protein SufD | ||
LFBCNLDA_02675 | 1.4e-144 | sufC | O | FeS assembly ATPase SufC | ||
LFBCNLDA_02676 | 5.5e-239 | 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 | |
LFBCNLDA_02677 | 8.8e-101 | iscU | C | SUF system FeS assembly protein, NifU family | ||
LFBCNLDA_02678 | 1e-107 | yitW | S | Iron-sulfur cluster assembly protein | ||
LFBCNLDA_02679 | 5.2e-242 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
LFBCNLDA_02680 | 1.2e-163 | spoU | 2.1.1.185 | J | SpoU rRNA Methylase family | |
LFBCNLDA_02682 | 0.0 | M | Parallel beta-helix repeats | |||
LFBCNLDA_02683 | 2.9e-226 | M | Glycosyl transferase 4-like domain | |||
LFBCNLDA_02684 | 3.8e-198 | ltaE | 4.1.2.48 | E | Beta-eliminating lyase | |
LFBCNLDA_02686 | 9.3e-62 | 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 | ||
LFBCNLDA_02687 | 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 | ||
LFBCNLDA_02688 | 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 | ||
LFBCNLDA_02689 | 1.6e-204 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
LFBCNLDA_02690 | 2.3e-303 | guaA | 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
LFBCNLDA_02691 | 1.3e-279 | XK27_07020 | S | Domain of unknown function (DUF1846) | ||
LFBCNLDA_02692 | 0.0 | pta | 1.1.1.40, 2.3.1.19, 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LFBCNLDA_02693 | 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 | |
LFBCNLDA_02694 | 3.5e-274 | 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 | |
LFBCNLDA_02695 | 2.6e-109 | 3.4.13.21 | E | Peptidase family S51 | ||
LFBCNLDA_02697 | 3e-75 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LFBCNLDA_02698 | 6e-187 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LFBCNLDA_02699 | 1.8e-46 | 3.4.23.43 | S | Type IV leader peptidase family | ||
LFBCNLDA_02700 | 1.6e-219 | 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 | |
LFBCNLDA_02701 | 0.0 | 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) | |
LFBCNLDA_02702 | 2.2e-78 | aroQ | 4.2.1.10 | E | Catalyzes a trans-dehydration via an enolate intermediate | |
LFBCNLDA_02703 | 9.1e-67 | |||||
LFBCNLDA_02704 | 1.7e-120 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_02705 | 3.1e-39 | M | Sortase family | |||
LFBCNLDA_02706 | 2.1e-43 | S | Listeria-Bacteroides repeat domain (List_Bact_rpt) | |||
LFBCNLDA_02707 | 1.1e-30 | M | domain protein | |||
LFBCNLDA_02708 | 8.5e-260 | dacB | 3.4.16.4 | M | D-Ala-D-Ala carboxypeptidase 3 (S13) family | |
LFBCNLDA_02709 | 1.2e-305 | |||||
LFBCNLDA_02710 | 6e-166 | natA | V | ATPases associated with a variety of cellular activities | ||
LFBCNLDA_02711 | 1.4e-231 | epsG | M | Glycosyl transferase family 21 | ||
LFBCNLDA_02712 | 9e-271 | S | AI-2E family transporter | |||
LFBCNLDA_02713 | 1.8e-175 | 3.4.14.13 | M | Glycosyltransferase like family 2 | ||
LFBCNLDA_02714 | 8.1e-205 | fucO | 1.1.1.1, 1.1.1.77, 1.1.99.37, 1.2.98.1 | C | Iron-containing alcohol dehydrogenase | |
LFBCNLDA_02715 | 4.6e-33 | S | membrane transporter protein | |||
LFBCNLDA_02716 | 1e-224 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
LFBCNLDA_02717 | 1.3e-122 | V | ABC-2 family transporter protein | |||
LFBCNLDA_02718 | 4.1e-70 | V | ABC-2 family transporter protein | |||
LFBCNLDA_02719 | 2.7e-182 | V | ABC-2 family transporter protein | |||
LFBCNLDA_02720 | 7.2e-186 | V | ATPases associated with a variety of cellular activities | |||
LFBCNLDA_02721 | 1.7e-41 | pacL | 3.6.3.8, 3.6.3.9 | P | ATPase, P-type transporting, HAD superfamily, subfamily IC | |
LFBCNLDA_02722 | 2.1e-233 | T | Histidine kinase | |||
LFBCNLDA_02723 | 8.8e-122 | K | helix_turn_helix, Lux Regulon | |||
LFBCNLDA_02724 | 1.1e-115 | MA20_27875 | P | Protein of unknown function DUF47 | ||
LFBCNLDA_02725 | 1.7e-188 | pit | P | Phosphate transporter family | ||
LFBCNLDA_02726 | 3.2e-98 | xfp | 4.1.2.22, 4.1.2.9 | G | D-xylulose 5-phosphate/D-fructose 6-phosphate phosphoketolase | |
LFBCNLDA_02727 | 2.1e-163 | EG | EamA-like transporter family | |||
LFBCNLDA_02728 | 1.5e-100 | V | ABC transporter, ATP-binding protein | |||
LFBCNLDA_02729 | 3.1e-138 | V | FtsX-like permease family | |||
LFBCNLDA_02730 | 1.7e-146 | S | Sulfite exporter TauE/SafE | |||
LFBCNLDA_02731 | 4.9e-215 | MA20_36090 | S | Psort location Cytoplasmic, score 8.87 | ||
LFBCNLDA_02732 | 7e-250 | metY | 2.5.1.49 | H | Psort location Cytoplasmic, score 9.98 | |
LFBCNLDA_02733 | 1.6e-35 | 1.1.1.122, 1.1.1.65 | C | Aldo/keto reductase family | ||
LFBCNLDA_02734 | 6e-69 | EGP | Major facilitator superfamily | |||
LFBCNLDA_02735 | 1.5e-46 | K | Winged helix DNA-binding domain | |||
LFBCNLDA_02736 | 1.9e-128 | pknL | 2.7.11.1 | KLT | PASTA | |
LFBCNLDA_02737 | 1.4e-198 | crtE | 2.5.1.1, 2.5.1.10, 2.5.1.29 | H | Belongs to the FPP GGPP synthase family | |
LFBCNLDA_02738 | 7.2e-121 | |||||
LFBCNLDA_02739 | 6.2e-181 | 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 | ||
LFBCNLDA_02740 | 0.0 | gyrB2 | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LFBCNLDA_02741 | 7.6e-277 | aspA | 4.3.1.1 | E | Fumarase C C-terminus | |
LFBCNLDA_02742 | 1.9e-178 | gyrA | 5.99.1.3 | L | DNA topoisomerase (ATP-hydrolyzing) | |
LFBCNLDA_02743 | 1.2e-225 | nhaA | P | Na( ) H( ) antiporter that extrudes sodium in exchange for external protons | ||
LFBCNLDA_02744 | 3.2e-158 | fmt2 | 3.2.2.10 | S | Belongs to the LOG family | |
LFBCNLDA_02745 | 1.1e-116 | safC | S | O-methyltransferase | ||
LFBCNLDA_02746 | 4.4e-180 | sdhB | 1.3.5.1, 1.3.5.4 | C | 4Fe-4S dicluster domain | |
LFBCNLDA_02747 | 3e-71 | yraN | L | Belongs to the UPF0102 family | ||
LFBCNLDA_02748 | 6.1e-293 | comM | O | Magnesium chelatase, subunit ChlI C-terminal | ||
LFBCNLDA_02749 | 9.1e-281 | dprA | 5.99.1.2 | LU | DNA recombination-mediator protein A | |
LFBCNLDA_02750 | 1.2e-57 | ybaZ | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
LFBCNLDA_02751 | 3.8e-30 | sdhA | 1.3.5.1, 1.3.5.4 | C | Succinate dehydrogenase flavoprotein subunit | |
LFBCNLDA_02752 | 1.3e-215 | GK | ROK family | |||
LFBCNLDA_02753 | 1.4e-130 | cutC | P | Participates in the control of copper homeostasis | ||
LFBCNLDA_02754 | 4e-223 | GK | ROK family | |||
LFBCNLDA_02755 | 1.9e-169 | 2.7.1.4 | G | pfkB family carbohydrate kinase | ||
LFBCNLDA_02756 | 3.7e-235 | G | Major Facilitator Superfamily | |||
LFBCNLDA_02757 | 1e-85 | 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 | ||
LFBCNLDA_02759 | 1.3e-37 | |||||
LFBCNLDA_02760 | 4.4e-148 | ftsQ | 6.3.2.4 | D | Cell division protein FtsQ | |
LFBCNLDA_02761 | 4.7e-79 | murC | 6.3.2.8 | M | Belongs to the MurCDEF family | |
LFBCNLDA_02762 | 9.4e-214 | 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 | |
LFBCNLDA_02763 | 2e-175 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LFBCNLDA_02764 | 5.1e-105 | M | NlpC/P60 family | |||
LFBCNLDA_02765 | 1.3e-190 | T | Universal stress protein family | |||
LFBCNLDA_02766 | 1e-72 | attW | O | OsmC-like protein | ||
LFBCNLDA_02767 | 1.9e-174 | 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 | |
LFBCNLDA_02768 | 8.6e-127 | folA | 1.5.1.3 | H | dihydrofolate reductase | |
LFBCNLDA_02769 | 1.8e-95 | ptpA | 3.1.3.48 | T | low molecular weight | |
LFBCNLDA_02770 | 5.3e-195 | afr_2 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
LFBCNLDA_02771 | 5.1e-43 | azlD | E | Branched-chain amino acid transport protein (AzlD) | ||
LFBCNLDA_02772 | 9.2e-60 | U | Sodium:dicarboxylate symporter family | |||
LFBCNLDA_02773 | 1e-31 | U | Sodium:dicarboxylate symporter family | |||
LFBCNLDA_02775 | 0.0 | recG | 3.6.4.12 | L | helicase superfamily c-terminal domain | |
LFBCNLDA_02776 | 1.4e-29 | rpmB | J | Ribosomal L28 family | ||
LFBCNLDA_02777 | 4.7e-199 | yegV | G | pfkB family carbohydrate kinase | ||
LFBCNLDA_02779 | 8.9e-240 | yxiO | S | Vacuole effluxer Atg22 like | ||
LFBCNLDA_02780 | 2.9e-181 | cysS | 6.1.1.16 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFBCNLDA_02781 | 4.2e-135 | guaA1 | 6.3.5.2 | F | Peptidase C26 | |
LFBCNLDA_02782 | 0.0 | yjjK | S | ABC transporter | ||
LFBCNLDA_02783 | 2e-58 | S | Protein of unknown function (DUF3039) | |||
LFBCNLDA_02784 | 1.7e-81 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LFBCNLDA_02785 | 1.1e-100 | |||||
LFBCNLDA_02786 | 1e-113 | yceD | S | Uncharacterized ACR, COG1399 | ||
LFBCNLDA_02787 | 2.3e-19 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LFBCNLDA_02788 | 6.1e-140 | 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 | |
LFBCNLDA_02789 | 9.9e-158 | ilvB | 2.2.1.6 | H | Thiamine pyrophosphate enzyme, central domain | |
LFBCNLDA_02790 | 1.8e-74 | xylR | K | purine nucleotide biosynthetic process | ||
LFBCNLDA_02791 | 1e-91 | lemA | S | LemA family | ||
LFBCNLDA_02792 | 0.0 | S | Predicted membrane protein (DUF2207) | |||
LFBCNLDA_02793 | 2.6e-76 | megL | 2.5.1.48, 4.4.1.1, 4.4.1.11, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_02794 | 5.3e-189 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_02796 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LFBCNLDA_02797 | 1.5e-73 | nrdI | F | Probably involved in ribonucleotide reductase function | ||
LFBCNLDA_02798 | 8.4e-201 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
LFBCNLDA_02799 | 4.3e-63 | S | Fic/DOC family | |||
LFBCNLDA_02800 | 1.7e-30 | S | Fic/DOC family | |||
LFBCNLDA_02801 | 1.5e-289 | 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) | |
LFBCNLDA_02802 | 1.9e-37 | ptsH | G | PTS HPr component phosphorylation site | ||
LFBCNLDA_02803 | 7.8e-197 | K | helix_turn _helix lactose operon repressor | |||
LFBCNLDA_02804 | 1.5e-209 | holB | 2.7.7.7 | L | DNA polymerase III | |
LFBCNLDA_02805 | 6.2e-118 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LFBCNLDA_02806 | 8.7e-260 | 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 | |
LFBCNLDA_02807 | 2e-22 | G | MFS/sugar transport protein | |||
LFBCNLDA_02808 | 2.3e-304 | efeU_1 | P | Iron permease FTR1 family | ||
LFBCNLDA_02809 | 5.4e-108 | tpd | P | Fe2+ transport protein | ||
LFBCNLDA_02810 | 1.2e-233 | S | Predicted membrane protein (DUF2318) | |||
LFBCNLDA_02811 | 9.7e-223 | macB_2 | V | ABC transporter permease | ||
LFBCNLDA_02812 | 1.4e-202 | Z012_06715 | V | FtsX-like permease family | ||
LFBCNLDA_02813 | 2.2e-148 | macB | V | ABC transporter, ATP-binding protein | ||
LFBCNLDA_02814 | 1.9e-69 | S | FMN_bind | |||
LFBCNLDA_02815 | 4.9e-12 | Q | phosphatase activity | |||
LFBCNLDA_02816 | 9.1e-08 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
LFBCNLDA_02817 | 4.5e-133 | gmk | 1.1.1.23, 2.7.4.8 | S | Protein conserved in bacteria | |
LFBCNLDA_02818 | 5.5e-256 | 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 | |
LFBCNLDA_02819 | 2.5e-222 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LFBCNLDA_02820 | 1.6e-111 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | Imidazoleglycerol-phosphate dehydratase | |
LFBCNLDA_02821 | 1.9e-111 | |||||
LFBCNLDA_02822 | 1.4e-121 | 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 | ||
LFBCNLDA_02823 | 6.3e-131 | hisA | 5.3.1.16, 5.3.1.24 | E | Histidine biosynthesis protein | |
LFBCNLDA_02824 | 5.2e-92 | ppa | 3.6.1.1 | C | Catalyzes the hydrolysis of inorganic pyrophosphate (PPi) forming two phosphate ions | |
LFBCNLDA_02825 | 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 |
LFBCNLDA_02826 | 0.0 | K | RNA polymerase II activating transcription factor binding | |||
LFBCNLDA_02827 | 1e-39 | |||||
LFBCNLDA_02828 | 1.4e-21 | S | Ribonuclease toxin, BrnT, of type II toxin-antitoxin system | |||
LFBCNLDA_02832 | 2.8e-22 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LFBCNLDA_02833 | 1.4e-298 | 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 | ||
LFBCNLDA_02834 | 1.4e-183 | K | Psort location Cytoplasmic, score | |||
LFBCNLDA_02835 | 3.1e-40 | rpmA | J | Ribosomal L27 protein | ||
LFBCNLDA_02836 | 5.4e-47 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
LFBCNLDA_02837 | 0.0 | rne | 3.1.26.12 | J | Ribonuclease E/G family | |
LFBCNLDA_02838 | 0.0 | dpp4 | 3.4.14.5 | E | Dipeptidyl peptidase IV (DPP IV) N-terminal region | |
LFBCNLDA_02839 | 0.0 | pip | S | YhgE Pip domain protein | ||
LFBCNLDA_02840 | 0.0 | pip | S | YhgE Pip domain protein | ||
LFBCNLDA_02841 | 1.2e-288 | 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 | |
LFBCNLDA_02842 | 1e-191 | tagO | 2.7.8.33, 2.7.8.35 | M | Glycosyl transferase family 4 | |
LFBCNLDA_02843 | 5.2e-116 | ywlC | 2.7.7.87 | J | Belongs to the SUA5 family | |
LFBCNLDA_02844 | 1.3e-53 | 2.3.1.79 | S | Bacterial transferase hexapeptide repeat protein | ||
LFBCNLDA_02845 | 2.7e-185 | 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 | |
LFBCNLDA_02846 | 1.2e-189 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LFBCNLDA_02847 | 3.9e-36 | rpmE | J | Binds the 23S rRNA | ||
LFBCNLDA_02849 | 8.7e-34 | K | Putative ATP-dependent DNA helicase recG C-terminal | |||
LFBCNLDA_02850 | 1.1e-37 | S | Memo-like protein | |||
LFBCNLDA_02852 | 1.4e-99 | S | AMMECR1 | |||
LFBCNLDA_02853 | 7.8e-88 | pflA | 1.97.1.4 | O | Radical SAM superfamily | |
LFBCNLDA_02854 | 3e-22 | pflA | 1.97.1.4 | O | Radical SAM superfamily | |
LFBCNLDA_02856 | 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) | |
LFBCNLDA_02857 | 2.7e-179 | ptrB | 3.4.21.83 | E | Peptidase, S9A B C family, catalytic domain protein | |
LFBCNLDA_02858 | 4.2e-237 | S | Uncharacterized conserved protein (DUF2183) | |||
LFBCNLDA_02859 | 3.7e-72 | 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 | ||
LFBCNLDA_02860 | 0.0 | enhA_2 | S | L,D-transpeptidase catalytic domain | ||
LFBCNLDA_02861 | 2.4e-08 | nudC | 1.3.7.1, 3.6.1.22 | L | NADH pyrophosphatase zinc ribbon domain | |
LFBCNLDA_02862 | 1.4e-113 | mhpC | I | Alpha/beta hydrolase family | ||
LFBCNLDA_02863 | 4e-133 | trxB1 | 1.8.1.9 | C | Thioredoxin domain | |
LFBCNLDA_02864 | 5.8e-236 | yhjX | EGP | Major facilitator Superfamily | ||
LFBCNLDA_02865 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LFBCNLDA_02866 | 7.8e-133 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LFBCNLDA_02867 | 1.8e-46 | deaD | 3.6.4.13 | JKL | helicase superfamily c-terminal domain | |
LFBCNLDA_02868 | 1.4e-140 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
LFBCNLDA_02869 | 1.1e-169 | yeaD | 4.2.1.9, 5.1.3.15 | G | Aldose 1-epimerase | |
LFBCNLDA_02870 | 6.5e-61 | |||||
LFBCNLDA_02871 | 1.6e-254 | cma | 2.1.1.79 | M | Mycolic acid cyclopropane synthetase | |
LFBCNLDA_02872 | 5.9e-46 | iolG | 1.1.1.18, 1.1.1.369 | S | Oxidoreductase family, C-terminal alpha/beta domain | |
LFBCNLDA_02873 | 2.6e-103 | K | helix_turn_helix, arabinose operon control protein | |||
LFBCNLDA_02874 | 7.4e-280 | hgdC | I | CoA enzyme activase uncharacterised domain (DUF2229) | ||
LFBCNLDA_02875 | 4.9e-165 | |||||
LFBCNLDA_02876 | 2.9e-256 | gshA | 6.3.2.2 | H | Glutamate-cysteine ligase family 2(GCS2) | |
LFBCNLDA_02877 | 1e-293 | plyA3 | M | Parallel beta-helix repeats | ||
LFBCNLDA_02878 | 2e-17 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LFBCNLDA_02879 | 2.6e-53 | S | Esterase-like activity of phytase | |||
LFBCNLDA_02880 | 8.9e-188 | EGP | Transmembrane secretion effector | |||
LFBCNLDA_02882 | 3.3e-103 | 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 | ||
LFBCNLDA_02883 | 2.9e-90 | 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 | ||
LFBCNLDA_02884 | 2.5e-236 | carA | 6.3.5.5 | F | Belongs to the CarA family | |
LFBCNLDA_02885 | 1.6e-126 | carB | 6.3.5.5 | EF | Carbamoyl-phosphate synthetase large chain, oligomerisation domain | |
LFBCNLDA_02886 | 0.0 | V | ABC transporter transmembrane region | |||
LFBCNLDA_02887 | 0.0 | V | ABC transporter, ATP-binding protein | |||
LFBCNLDA_02888 | 2.4e-87 | K | MarR family | |||
LFBCNLDA_02889 | 1.4e-91 | plyA3 | 3.2.1.18 | GH33 | M | Parallel beta-helix repeats |
LFBCNLDA_02890 | 5.6e-19 | vpr | M | PA domain | ||
LFBCNLDA_02891 | 0.0 | vpr | M | PA domain | ||
LFBCNLDA_02892 | 1.5e-186 | 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 | ||
LFBCNLDA_02893 | 3.3e-248 | corC | S | CBS domain | ||
LFBCNLDA_02894 | 8.2e-99 | 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 | |
LFBCNLDA_02895 | 5.8e-197 | phoH | T | PhoH-like protein | ||
LFBCNLDA_02896 | 3.7e-57 | hinT | 2.1.1.226, 2.1.1.227 | FG | Scavenger mRNA decapping enzyme C-term binding | |
LFBCNLDA_02897 | 1.6e-83 | 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 | |
LFBCNLDA_02898 | 6.9e-11 | S | Domain of unknown function (DUF4190) | |||
LFBCNLDA_02899 | 4.2e-239 | dapE | 3.5.1.18 | E | Peptidase dimerisation domain | |
LFBCNLDA_02900 | 2.9e-168 | mdcF | S | Transporter, auxin efflux carrier (AEC) family protein | ||
LFBCNLDA_02901 | 7.6e-181 | V | Efflux ABC transporter, permease protein | |||
LFBCNLDA_02902 | 7.7e-286 | cadA | P | E1-E2 ATPase | ||
LFBCNLDA_02903 | 4.2e-272 | fprA | 1.18.1.2, 1.19.1.1 | C | Pyridine nucleotide-disulphide oxidoreductase | |
LFBCNLDA_02904 | 1.8e-170 | htpX | O | Belongs to the peptidase M48B family | ||
LFBCNLDA_02906 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LFBCNLDA_02907 | 1.5e-244 | dgt | 3.1.5.1 | F | Phosphohydrolase-associated domain | |
LFBCNLDA_02908 | 9.8e-174 | alr | 5.1.1.1 | M | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LFBCNLDA_02909 | 2e-93 | rimJ | 2.3.1.128 | J | Acetyltransferase (GNAT) domain | |
LFBCNLDA_02910 | 7.5e-141 | |||||
LFBCNLDA_02911 | 1.5e-46 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LFBCNLDA_02912 | 1.5e-53 | moxR | S | ATPase family associated with various cellular activities (AAA) | ||
LFBCNLDA_02915 | 4e-192 | cbs | 2.5.1.47, 4.2.1.22 | E | Pyridoxal-phosphate dependent enzyme | |
LFBCNLDA_02916 | 2.4e-220 | metB | 2.5.1.48, 4.4.1.1, 4.4.1.8 | E | Cys/Met metabolism PLP-dependent enzyme | |
LFBCNLDA_02917 | 1.3e-111 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
LFBCNLDA_02918 | 8.7e-93 | pntA | 1.6.1.2 | C | NAD(P) transhydrogenase subunit alpha part 1 K00324 | |
LFBCNLDA_02919 | 1.3e-43 | pntA | 1.6.1.2 | C | 4TM region of pyridine nucleotide transhydrogenase, mitoch | |
LFBCNLDA_02920 | 2.6e-232 | 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 | |
LFBCNLDA_02921 | 2.9e-187 | S | alpha beta | |||
LFBCNLDA_02922 | 2.5e-37 | 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 | ||
LFBCNLDA_02923 | 1.1e-233 | patB | 4.4.1.8 | E | Aminotransferase, class I II | |
LFBCNLDA_02926 | 9.4e-242 | 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 | ||
LFBCNLDA_02927 | 1.7e-102 | 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 | |
LFBCNLDA_02928 | 1.8e-210 | S | Amidohydrolase family | |||
LFBCNLDA_02929 | 3.4e-208 | yjjP | S | Threonine/Serine exporter, ThrE | ||
LFBCNLDA_02930 | 2.6e-91 | L | Transposase and inactivated derivatives IS30 family | |||
LFBCNLDA_02931 | 4.6e-168 | 1.1.1.65 | C | Oxidoreductase, aldo keto reductase family protein | ||
LFBCNLDA_02932 | 2.2e-41 | nrdH | O | Glutaredoxin | ||
LFBCNLDA_02933 | 1.8e-173 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | |||
LFBCNLDA_02934 | 6.9e-192 | 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) |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)