ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LLMDOFAF_00001 | 1.6e-77 | sigH | K | DNA-templated transcription, initiation | ||
LLMDOFAF_00002 | 3e-148 | ykuT | M | mechanosensitive ion channel | ||
LLMDOFAF_00003 | 6.4e-219 | 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 | ||
LLMDOFAF_00004 | 4.8e-73 | rpoE | K | Participates in both the initiation and recycling phases of transcription. In the presence of the delta subunit, RNAP displays an increased specificity of transcription, a decreased affinity for nucleic acids, and an increased efficiency of RNA synthesis because of enhanced recycling | ||
LLMDOFAF_00005 | 7.6e-310 | 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 | |
LLMDOFAF_00006 | 1.3e-84 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
LLMDOFAF_00007 | 3.7e-81 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
LLMDOFAF_00008 | 3.7e-179 | prmA | J | Ribosomal protein L11 methyltransferase | ||
LLMDOFAF_00009 | 4.4e-135 | 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 | |
LLMDOFAF_00010 | 0.0 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
LLMDOFAF_00011 | 2.4e-83 | nrdI | F | Belongs to the NrdI family | ||
LLMDOFAF_00012 | 0.0 | relA | 2.7.6.5 | KT | In eubacteria ppGpp (guanosine 3'-diphosphate 5-' diphosphate) is a mediator of the stringent response that coordinates a variety of cellular activities in response to changes in nutritional abundance | |
LLMDOFAF_00013 | 2.3e-75 | 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 | ||
LLMDOFAF_00014 | 1.4e-09 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
LLMDOFAF_00015 | 2e-27 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
LLMDOFAF_00016 | 2.1e-58 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
LLMDOFAF_00017 | 3.9e-46 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
LLMDOFAF_00018 | 1.7e-237 | ilvA | 4.3.1.19 | E | Catalyzes the anaerobic formation of alpha-ketobutyrate and ammonia from threonine in a two-step reaction. The first step involved a dehydration of threonine and a production of enamine intermediates (aminocrotonate), which tautomerizes to its imine form (iminobutyrate). Both intermediates are unstable and short- lived. The second step is the nonenzymatic hydrolysis of the enamine imine intermediates to form 2-ketobutyrate and free ammonia. In the low water environment of the cell, the second step is accelerated by RidA | |
LLMDOFAF_00019 | 3.3e-112 | def | 3.5.1.31, 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 | |
LLMDOFAF_00020 | 1.1e-113 | fnr5 | K | Catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | ||
LLMDOFAF_00021 | 6.5e-202 | yhjX | P | Major Facilitator | ||
LLMDOFAF_00022 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LLMDOFAF_00023 | 5e-94 | V | VanZ like family | |||
LLMDOFAF_00026 | 1e-123 | glnQ | E | abc transporter atp-binding protein | ||
LLMDOFAF_00027 | 1.8e-276 | glnP | P | ABC transporter | ||
LLMDOFAF_00028 | 9.1e-153 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LLMDOFAF_00029 | 2.3e-136 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
LLMDOFAF_00030 | 1.1e-185 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
LLMDOFAF_00031 | 9.5e-144 | sufC | O | ABC-type transport system involved in Fe-S cluster assembly, ATPase component | ||
LLMDOFAF_00032 | 6.3e-235 | sufD | O | assembly protein SufD | ||
LLMDOFAF_00033 | 2.7e-238 | 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 | |
LLMDOFAF_00034 | 1.1e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
LLMDOFAF_00035 | 3.5e-274 | sufB | O | assembly protein SufB | ||
LLMDOFAF_00036 | 2.4e-19 | oppA | E | ABC transporter substrate-binding protein | ||
LLMDOFAF_00037 | 5.4e-99 | oppA | E | ABC transporter substrate-binding protein | ||
LLMDOFAF_00038 | 2.7e-17 | oppA | E | ABC transporter substrate-binding protein | ||
LLMDOFAF_00039 | 4.2e-27 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LLMDOFAF_00040 | 6.6e-11 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LLMDOFAF_00041 | 5.4e-46 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LLMDOFAF_00042 | 5.3e-60 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LLMDOFAF_00043 | 8e-28 | oppD | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_00044 | 2.5e-32 | oppD | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_00045 | 4.8e-67 | oppD | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_00046 | 1.3e-44 | oppD | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_00047 | 9e-170 | oppF | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_00050 | 1.9e-158 | hslO | O | Redox regulated molecular chaperone. Protects both thermally unfolding and oxidatively damaged proteins from irreversible aggregation. Plays an important role in the bacterial defense system toward oxidative stress | ||
LLMDOFAF_00051 | 7.4e-183 | 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 | ||
LLMDOFAF_00052 | 1.9e-209 | EGP | Major facilitator Superfamily | |||
LLMDOFAF_00053 | 3.1e-72 | adcR | K | transcriptional | ||
LLMDOFAF_00054 | 2.2e-136 | adcC | P | ABC transporter, ATP-binding protein | ||
LLMDOFAF_00055 | 5.4e-131 | adcB | P | ABC transporter (Permease | ||
LLMDOFAF_00056 | 4.8e-163 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
LLMDOFAF_00057 | 5.6e-65 | ptsG | 2.7.1.199, 2.7.1.208 | G | pts system | |
LLMDOFAF_00058 | 6e-150 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | pts system | |
LLMDOFAF_00059 | 1.7e-82 | ptsG | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | |
LLMDOFAF_00060 | 1e-150 | rgfB | 3.1.3.90 | L | endonuclease exonuclease phosphatase family protein | |
LLMDOFAF_00061 | 2.8e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LLMDOFAF_00062 | 1.9e-127 | yeeN | K | transcriptional regulatory protein | ||
LLMDOFAF_00063 | 9.8e-50 | yajC | U | protein transport | ||
LLMDOFAF_00064 | 1.1e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
LLMDOFAF_00065 | 1.3e-145 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
LLMDOFAF_00066 | 1.4e-231 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
LLMDOFAF_00067 | 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 | |
LLMDOFAF_00068 | 0.0 | WQ51_06230 | S | ABC transporter substrate binding protein | ||
LLMDOFAF_00069 | 5.2e-142 | cmpC | S | abc transporter atp-binding protein | ||
LLMDOFAF_00070 | 1.3e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LLMDOFAF_00071 | 4.1e-287 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
LLMDOFAF_00072 | 4.4e-37 | L | Transposase | |||
LLMDOFAF_00073 | 6.4e-18 | L | transposase activity | |||
LLMDOFAF_00074 | 1.7e-226 | 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) | |
LLMDOFAF_00075 | 1e-33 | L | Transposase | |||
LLMDOFAF_00076 | 1e-13 | rpmH | J | Ribosomal protein L34 | ||
LLMDOFAF_00077 | 2e-186 | jag | S | RNA-binding protein | ||
LLMDOFAF_00078 | 7.5e-141 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
LLMDOFAF_00079 | 5.9e-55 | rnpA | 3.1.26.5 | J | RNaseP catalyzes the removal of the 5'-leader sequence from pre-tRNA to produce the mature 5'-terminus. It can also cleave other RNA substrates such as 4.5S RNA. The protein component plays an auxiliary but essential role in vivo by binding to the 5'-leader sequence and broadening the substrate specificity of the ribozyme | |
LLMDOFAF_00080 | 1.9e-264 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
LLMDOFAF_00081 | 2e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LLMDOFAF_00082 | 2.1e-282 | gltX | 6.1.1.17, 6.1.1.24 | 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) | |
LLMDOFAF_00083 | 6.7e-81 | amiA | E | transmembrane transport | ||
LLMDOFAF_00084 | 2e-41 | amiA | E | transmembrane transport | ||
LLMDOFAF_00085 | 4.2e-90 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
LLMDOFAF_00086 | 7.8e-28 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
LLMDOFAF_00087 | 4.8e-120 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
LLMDOFAF_00088 | 3.7e-70 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LLMDOFAF_00089 | 9.2e-51 | S | Protein of unknown function (DUF3397) | |||
LLMDOFAF_00090 | 2e-88 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LLMDOFAF_00091 | 9.3e-34 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
LLMDOFAF_00092 | 6.8e-32 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
LLMDOFAF_00093 | 6.2e-12 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
LLMDOFAF_00094 | 1.4e-226 | 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 | ||
LLMDOFAF_00095 | 1.1e-80 | 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 | |
LLMDOFAF_00096 | 4.7e-20 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
LLMDOFAF_00097 | 4.3e-77 | XK27_09620 | S | reductase | ||
LLMDOFAF_00098 | 9e-62 | XK27_09615 | C | reductase | ||
LLMDOFAF_00099 | 1e-141 | XK27_09615 | C | reductase | ||
LLMDOFAF_00100 | 3.2e-62 | fnt | P | Formate nitrite transporter | ||
LLMDOFAF_00101 | 5.5e-64 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
LLMDOFAF_00102 | 2e-186 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
LLMDOFAF_00103 | 5.1e-170 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
LLMDOFAF_00104 | 5.2e-119 | gluP | 3.4.21.105 | O | membrane protein (homolog of Drosophila rhomboid) | |
LLMDOFAF_00105 | 9.1e-95 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
LLMDOFAF_00106 | 7.9e-221 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
LLMDOFAF_00107 | 8.1e-59 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
LLMDOFAF_00108 | 2.7e-48 | S | glycolate biosynthetic process | |||
LLMDOFAF_00109 | 1.5e-64 | S | phosphatase activity | |||
LLMDOFAF_00110 | 6.3e-159 | rrmA | 2.1.1.187 | Q | methyltransferase | |
LLMDOFAF_00113 | 1.2e-91 | tadA | 3.5.4.1, 3.5.4.33 | FJ | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
LLMDOFAF_00114 | 5.1e-66 | ssb_2 | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
LLMDOFAF_00115 | 8.3e-37 | yeeD | O | sulfur carrier activity | ||
LLMDOFAF_00116 | 2.8e-193 | yeeE | S | Sulphur transport | ||
LLMDOFAF_00117 | 7.9e-114 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
LLMDOFAF_00118 | 4.2e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
LLMDOFAF_00119 | 4.1e-09 | S | Domain of unknown function (DUF4651) | |||
LLMDOFAF_00120 | 2e-205 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
LLMDOFAF_00121 | 3.9e-131 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LLMDOFAF_00122 | 1.8e-111 | S | CAAX amino terminal protease family protein | |||
LLMDOFAF_00124 | 5e-67 | V | CAAX protease self-immunity | |||
LLMDOFAF_00125 | 1.4e-33 | V | CAAX protease self-immunity | |||
LLMDOFAF_00126 | 8.8e-27 | lanR | K | sequence-specific DNA binding | ||
LLMDOFAF_00127 | 2.9e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
LLMDOFAF_00128 | 5.9e-177 | ytxK | 2.1.1.72 | L | DNA methylase | |
LLMDOFAF_00129 | 2e-12 | comGF | U | Putative Competence protein ComGF | ||
LLMDOFAF_00130 | 1.5e-71 | comGF | U | Competence protein ComGF | ||
LLMDOFAF_00131 | 1.4e-15 | NU | Type II secretory pathway pseudopilin | |||
LLMDOFAF_00132 | 1.8e-57 | cglD | NU | Competence protein | ||
LLMDOFAF_00133 | 8.5e-43 | comGC | U | Required for transformation and DNA binding | ||
LLMDOFAF_00134 | 1.1e-156 | cglB | U | protein transport across the cell outer membrane | ||
LLMDOFAF_00135 | 4.5e-177 | comGA | NU | Type II secretory pathway, ATPase PulE Tfp pilus assembly pathway, ATPase PilB | ||
LLMDOFAF_00136 | 1e-68 | S | cog cog4699 | |||
LLMDOFAF_00137 | 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 | |
LLMDOFAF_00138 | 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 | |
LLMDOFAF_00139 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LLMDOFAF_00140 | 9.3e-239 | 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) | |
LLMDOFAF_00141 | 1.6e-196 | 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 | |
LLMDOFAF_00142 | 7.7e-77 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
LLMDOFAF_00143 | 0.0 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
LLMDOFAF_00144 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
LLMDOFAF_00145 | 6.3e-202 | 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 | |
LLMDOFAF_00146 | 1.3e-257 | 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 | ||
LLMDOFAF_00147 | 1e-134 | parB | K | Belongs to the ParB family | ||
LLMDOFAF_00148 | 5.6e-185 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
LLMDOFAF_00149 | 1.1e-86 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
LLMDOFAF_00150 | 6.2e-120 | yoaK | S | Psort location CytoplasmicMembrane, score | ||
LLMDOFAF_00154 | 0.0 | XK27_10405 | S | Bacterial membrane protein YfhO | ||
LLMDOFAF_00155 | 6.7e-306 | ybiT | S | abc transporter atp-binding protein | ||
LLMDOFAF_00156 | 1.1e-153 | yvjA | S | membrane | ||
LLMDOFAF_00157 | 8.2e-193 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
LLMDOFAF_00158 | 1.5e-275 | 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 | |
LLMDOFAF_00159 | 5.9e-205 | 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 | ||
LLMDOFAF_00160 | 1.6e-45 | yaaA | S | S4 domain protein YaaA | ||
LLMDOFAF_00161 | 4.8e-235 | ymfF | S | Peptidase M16 | ||
LLMDOFAF_00162 | 1.1e-242 | ymfH | S | Peptidase M16 | ||
LLMDOFAF_00163 | 3.7e-138 | ymfM | S | sequence-specific DNA binding | ||
LLMDOFAF_00164 | 3.1e-90 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LLMDOFAF_00165 | 7.5e-152 | ecfA1 | P | ATP-binding (A) component of a common 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 | ||
LLMDOFAF_00166 | 5.2e-153 | ecfA2 | 3.6.3.55 | P | ATP-binding (A) component of a common 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 | |
LLMDOFAF_00167 | 2e-138 | ecfT | P | Transmembrane (T) component of an 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 | ||
LLMDOFAF_00168 | 3.1e-93 | lytE | M | LysM domain protein | ||
LLMDOFAF_00169 | 1.5e-91 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
LLMDOFAF_00170 | 0.0 | S | Bacterial membrane protein, YfhO | |||
LLMDOFAF_00171 | 3.3e-219 | mnmA | 2.8.1.13 | J | Catalyzes the 2-thiolation of uridine at the wobble position (U34) of tRNA, leading to the formation of s(2)U34 | |
LLMDOFAF_00172 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
LLMDOFAF_00173 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
LLMDOFAF_00174 | 3.9e-70 | rplI | J | binds to the 23S rRNA | ||
LLMDOFAF_00175 | 1.5e-245 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LLMDOFAF_00176 | 8.2e-48 | veg | S | Biofilm formation stimulator VEG | ||
LLMDOFAF_00177 | 9.8e-109 | 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 | ||
LLMDOFAF_00178 | 2.7e-08 | |||||
LLMDOFAF_00179 | 4.8e-55 | ypaA | M | Membrane | ||
LLMDOFAF_00180 | 6.4e-96 | XK27_06935 | K | transcriptional regulator | ||
LLMDOFAF_00181 | 3.9e-161 | XK27_06930 | V | domain protein | ||
LLMDOFAF_00182 | 1.8e-88 | S | Putative adhesin | |||
LLMDOFAF_00183 | 3.1e-19 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
LLMDOFAF_00185 | 1.7e-23 | K | negative regulation of transcription, DNA-templated | |||
LLMDOFAF_00186 | 4e-19 | K | negative regulation of transcription, DNA-templated | |||
LLMDOFAF_00187 | 3.4e-13 | nudL | L | hydrolase | ||
LLMDOFAF_00188 | 7.2e-95 | nudL | L | hydrolase | ||
LLMDOFAF_00189 | 4.9e-12 | K | CsbD-like | |||
LLMDOFAF_00190 | 1.1e-71 | M | Protein conserved in bacteria | |||
LLMDOFAF_00191 | 1.8e-23 | S | Small integral membrane protein | |||
LLMDOFAF_00192 | 3.1e-101 | |||||
LLMDOFAF_00193 | 3.7e-27 | S | Membrane | |||
LLMDOFAF_00195 | 2.7e-95 | S | Hydrophobic domain protein | |||
LLMDOFAF_00196 | 3.1e-20 | yegS | 2.7.1.107 | I | lipid kinase activity | |
LLMDOFAF_00198 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
LLMDOFAF_00199 | 2e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LLMDOFAF_00200 | 9.2e-36 | metE | 2.1.1.14 | E | Methionine synthase | |
LLMDOFAF_00201 | 7.6e-64 | metE | 2.1.1.14 | E | Methionine synthase | |
LLMDOFAF_00202 | 5.7e-52 | metE | 2.1.1.14 | E | Methionine synthase | |
LLMDOFAF_00203 | 1.6e-241 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
LLMDOFAF_00205 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
LLMDOFAF_00206 | 9.9e-169 | XK27_01785 | S | cog cog1284 | ||
LLMDOFAF_00207 | 1.8e-147 | yaaA | S | Belongs to the UPF0246 family | ||
LLMDOFAF_00208 | 3.7e-116 | 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 | |
LLMDOFAF_00209 | 2.6e-91 | XK27_10930 | K | acetyltransferase | ||
LLMDOFAF_00210 | 7.5e-14 | |||||
LLMDOFAF_00211 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
LLMDOFAF_00212 | 2.3e-301 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
LLMDOFAF_00213 | 1.3e-87 | S | Fusaric acid resistance protein-like | |||
LLMDOFAF_00214 | 8.5e-63 | glnR | K | Transcriptional regulator | ||
LLMDOFAF_00215 | 1.5e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
LLMDOFAF_00216 | 2.7e-40 | pscB | M | CHAP domain protein | ||
LLMDOFAF_00217 | 0.0 | rnjA | S | 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 | ||
LLMDOFAF_00218 | 2.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
LLMDOFAF_00219 | 4.3e-121 | yeaZ | 2.3.1.234 | O | COG1214, inactive homolog of metal-dependent proteases | |
LLMDOFAF_00220 | 1.3e-73 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
LLMDOFAF_00221 | 1.1e-186 | 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 | |
LLMDOFAF_00222 | 1.3e-117 | azlC | E | AzlC protein | ||
LLMDOFAF_00223 | 2e-47 | azlD | E | branched-chain amino acid | ||
LLMDOFAF_00224 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
LLMDOFAF_00225 | 1.3e-113 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LLMDOFAF_00226 | 4.7e-160 | rnhC | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LLMDOFAF_00227 | 2.3e-13 | zapA | D | Activator of cell division through the inhibition of FtsZ GTPase activity, therefore promoting FtsZ assembly into bundles of protofilaments necessary for the formation of the division Z ring. It is recruited early at mid-cell but it is not essential for cell division | ||
LLMDOFAF_00228 | 1e-93 | cvpA | S | toxin biosynthetic process | ||
LLMDOFAF_00229 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
LLMDOFAF_00230 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
LLMDOFAF_00236 | 2.5e-230 | mutY | L | A G-specific adenine glycosylase | ||
LLMDOFAF_00237 | 3.6e-41 | XK27_05745 | ||||
LLMDOFAF_00238 | 3.9e-47 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LLMDOFAF_00239 | 2.7e-91 | ssb | L | Plays an important role in DNA replication, recombination and repair. Binds to ssDNA and to an array of partner proteins to recruit them to their sites of action during DNA metabolism | ||
LLMDOFAF_00240 | 9.7e-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 | ||
LLMDOFAF_00242 | 3.1e-124 | XK27_01040 | S | Pfam PF06570 | ||
LLMDOFAF_00243 | 2e-169 | corA | P | COG0598 Mg2 and Co2 transporters | ||
LLMDOFAF_00244 | 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 | ||
LLMDOFAF_00247 | 3.8e-58 | V | 'abc transporter, ATP-binding protein | |||
LLMDOFAF_00248 | 8e-44 | V | 'abc transporter, ATP-binding protein | |||
LLMDOFAF_00250 | 5e-193 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
LLMDOFAF_00251 | 3.7e-84 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
LLMDOFAF_00252 | 1.2e-97 | 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 | ||
LLMDOFAF_00253 | 3.4e-62 | yqhY | S | protein conserved in bacteria | ||
LLMDOFAF_00254 | 2.1e-73 | 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 | ||
LLMDOFAF_00255 | 7.5e-180 | scrR | K | Transcriptional | ||
LLMDOFAF_00256 | 5.4e-291 | scrB | 3.2.1.26 | GH32 | G | invertase |
LLMDOFAF_00257 | 0.0 | scrA | 2.7.1.211 | G | pts system | |
LLMDOFAF_00258 | 4.1e-172 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
LLMDOFAF_00259 | 3e-189 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
LLMDOFAF_00261 | 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 | ||
LLMDOFAF_00262 | 3.8e-198 | aroF | 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) | |
LLMDOFAF_00263 | 1.1e-197 | aroF | 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) | |
LLMDOFAF_00264 | 3.1e-62 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
LLMDOFAF_00265 | 1.8e-185 | alr | 5.1.1.1, 5.1.1.5 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
LLMDOFAF_00266 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
LLMDOFAF_00268 | 2.1e-185 | V | Abi-like protein | |||
LLMDOFAF_00271 | 2.9e-31 | yozG | K | Transcriptional regulator | ||
LLMDOFAF_00272 | 9.2e-284 | V | ABC transporter transmembrane region | |||
LLMDOFAF_00273 | 1.9e-158 | K | Helix-turn-helix XRE-family like proteins | |||
LLMDOFAF_00274 | 4.9e-15 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
LLMDOFAF_00275 | 1.4e-29 | S | Domain of unknown function (DUF1912) | |||
LLMDOFAF_00276 | 1.2e-177 | mmuM | 1.5.1.20, 2.1.1.10 | H | Homocysteine | |
LLMDOFAF_00277 | 5.2e-251 | mmuP | E | amino acid | ||
LLMDOFAF_00278 | 3e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
LLMDOFAF_00279 | 2.6e-225 | 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 | ||
LLMDOFAF_00280 | 9.7e-22 | |||||
LLMDOFAF_00281 | 1.4e-92 | folA | 1.5.1.3, 1.5.1.47, 2.1.1.45, 3.5.4.12 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
LLMDOFAF_00282 | 2.2e-167 | 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 | |
LLMDOFAF_00283 | 1.7e-218 | mvaS | 2.3.3.10 | I | synthase | |
LLMDOFAF_00284 | 2.7e-233 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
LLMDOFAF_00285 | 1e-25 | K | hmm pf08876 | |||
LLMDOFAF_00286 | 1.5e-118 | yqfA | K | protein, Hemolysin III | ||
LLMDOFAF_00287 | 1.2e-22 | S | Protein of unknown function (DUF3114) | |||
LLMDOFAF_00288 | 8.6e-167 | S | Protein of unknown function (DUF3114) | |||
LLMDOFAF_00289 | 9.4e-71 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
LLMDOFAF_00290 | 8.9e-57 | S | hydrolase activity, acting on ester bonds | |||
LLMDOFAF_00291 | 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) | |
LLMDOFAF_00292 | 4.9e-21 | XK27_13030 | ||||
LLMDOFAF_00293 | 1.8e-248 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
LLMDOFAF_00294 | 1.1e-192 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
LLMDOFAF_00296 | 2.1e-50 | U | protein secretion | |||
LLMDOFAF_00297 | 3.5e-07 | U | protein secretion | |||
LLMDOFAF_00299 | 2e-118 | 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 | |
LLMDOFAF_00300 | 2.5e-21 | |||||
LLMDOFAF_00301 | 1e-96 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
LLMDOFAF_00302 | 5.1e-254 | 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 | |
LLMDOFAF_00303 | 8.9e-192 | fni | 1.1.1.88, 5.3.3.2 | C | Involved in the biosynthesis of isoprenoids. Catalyzes the 1,3-allylic rearrangement of the homoallylic substrate isopentenyl (IPP) to its allylic isomer, dimethylallyl diphosphate (DMAPP) | |
LLMDOFAF_00304 | 4.6e-180 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | GHMP kinases N terminal domain | |
LLMDOFAF_00305 | 6e-174 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
LLMDOFAF_00306 | 2.5e-142 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
LLMDOFAF_00307 | 4.6e-105 | GBS0088 | J | protein conserved in bacteria | ||
LLMDOFAF_00308 | 6.1e-249 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LLMDOFAF_00309 | 1.7e-46 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
LLMDOFAF_00310 | 3.4e-17 | ald | 1.4.1.1 | E | alanine dehydrogenase activity | |
LLMDOFAF_00311 | 8e-221 | hipO | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
LLMDOFAF_00312 | 8.8e-133 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LLMDOFAF_00313 | 8.7e-114 | S | VIT family | |||
LLMDOFAF_00314 | 2.8e-145 | deoD_1 | 2.4.2.3 | F | Phosphorylase superfamily | |
LLMDOFAF_00315 | 1.1e-22 | |||||
LLMDOFAF_00316 | 8e-28 | XK27_00085 | K | Transcriptional | ||
LLMDOFAF_00317 | 2.4e-197 | yceA | S | Belongs to the UPF0176 family | ||
LLMDOFAF_00318 | 5.4e-122 | sagI | S | ABC-2 type transporter | ||
LLMDOFAF_00319 | 2.8e-168 | V | ABC transporter | |||
LLMDOFAF_00320 | 7.1e-214 | 2.7.7.73, 2.7.7.80 | H | Dinucleotide-utilizing enzymes involved in molybdopterin and thiamine biosynthesis family 2 | ||
LLMDOFAF_00321 | 2.5e-132 | rr02 | KT | response regulator | ||
LLMDOFAF_00322 | 3.3e-215 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
LLMDOFAF_00323 | 5e-125 | 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 | |
LLMDOFAF_00324 | 4.6e-199 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
LLMDOFAF_00325 | 0.0 | lmrA | V | abc transporter atp-binding protein | ||
LLMDOFAF_00326 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
LLMDOFAF_00328 | 0.0 | M | the current gene model (or a revised gene model) may contain a | |||
LLMDOFAF_00329 | 6.5e-50 | M | YSIRK type signal peptide | |||
LLMDOFAF_00330 | 3e-92 | S | MucBP domain | |||
LLMDOFAF_00333 | 1.9e-13 | |||||
LLMDOFAF_00334 | 3e-133 | budA | 4.1.1.5 | H | Belongs to the alpha-acetolactate decarboxylase family | |
LLMDOFAF_00335 | 0.0 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
LLMDOFAF_00336 | 6.6e-61 | EGP | Major facilitator Superfamily | |||
LLMDOFAF_00337 | 3.9e-136 | speB | 3.5.3.11 | E | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amidines | |
LLMDOFAF_00338 | 1.3e-212 | pqqE | C | radical SAM domain protein | ||
LLMDOFAF_00341 | 1.8e-156 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
LLMDOFAF_00342 | 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 | ||
LLMDOFAF_00343 | 3.9e-19 | IQ | Acetoin reductase | |||
LLMDOFAF_00344 | 1.8e-51 | IQ | Acetoin reductase | |||
LLMDOFAF_00345 | 2.7e-48 | pspE | P | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | ||
LLMDOFAF_00346 | 1.7e-75 | ndk | 2.7.4.6 | F | Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate | |
LLMDOFAF_00347 | 1.1e-152 | XK27_05470 | E | Methionine synthase | ||
LLMDOFAF_00348 | 6.6e-259 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
LLMDOFAF_00349 | 1.3e-249 | T | PhoQ Sensor | |||
LLMDOFAF_00350 | 2.2e-122 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LLMDOFAF_00351 | 3.6e-154 | S | TraX protein | |||
LLMDOFAF_00352 | 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 | |
LLMDOFAF_00353 | 8.3e-159 | dprA | LU | DNA protecting protein DprA | ||
LLMDOFAF_00354 | 8.2e-168 | GK | ROK family | |||
LLMDOFAF_00355 | 5.3e-136 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
LLMDOFAF_00356 | 1.1e-158 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
LLMDOFAF_00357 | 9.6e-129 | K | DNA-binding helix-turn-helix protein | |||
LLMDOFAF_00358 | 6e-91 | niaR | S | small molecule binding protein (contains 3H domain) | ||
LLMDOFAF_00359 | 2.4e-87 | niaX | ||||
LLMDOFAF_00360 | 5.9e-275 | 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 | |
LLMDOFAF_00361 | 1.1e-53 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
LLMDOFAF_00362 | 2e-126 | gntR1 | K | transcriptional | ||
LLMDOFAF_00363 | 3.9e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
LLMDOFAF_00364 | 1.1e-19 | sthIM | 2.1.1.72 | L | Adenine specific DNA methylase Mod | |
LLMDOFAF_00365 | 4.2e-113 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
LLMDOFAF_00366 | 8e-58 | adhP | 1.1.1.1 | C | alcohol dehydrogenase | |
LLMDOFAF_00367 | 2.1e-07 | |||||
LLMDOFAF_00368 | 1.2e-146 | uvrX | 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 | |
LLMDOFAF_00369 | 1.1e-158 | aatB | ET | ABC transporter substrate-binding protein | ||
LLMDOFAF_00370 | 1.8e-113 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LLMDOFAF_00371 | 2.4e-105 | artQ | P | ABC transporter (Permease | ||
LLMDOFAF_00372 | 2.5e-58 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
LLMDOFAF_00373 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
LLMDOFAF_00374 | 2.6e-166 | cpsY | K | Transcriptional regulator | ||
LLMDOFAF_00375 | 3.2e-35 | L | transposase activity | |||
LLMDOFAF_00376 | 5.1e-117 | mur1 | NU | muramidase | ||
LLMDOFAF_00377 | 1.2e-172 | yeiH | S | Membrane | ||
LLMDOFAF_00379 | 1.7e-08 | |||||
LLMDOFAF_00380 | 9.2e-297 | adcA | P | Belongs to the bacterial solute-binding protein 9 family | ||
LLMDOFAF_00381 | 2.2e-101 | XK27_10720 | D | peptidase activity | ||
LLMDOFAF_00382 | 5.9e-79 | hsdM | 2.1.1.72 | V | HsdM N-terminal domain | |
LLMDOFAF_00383 | 1.8e-08 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
LLMDOFAF_00384 | 3.7e-157 | glcU | U | Glucose uptake | ||
LLMDOFAF_00385 | 1.7e-111 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
LLMDOFAF_00386 | 3.7e-54 | hsdS | 2.1.1.72, 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
LLMDOFAF_00387 | 3.7e-44 | L | Transposase | |||
LLMDOFAF_00388 | 0.0 | yfmR | S | abc transporter atp-binding protein | ||
LLMDOFAF_00389 | 1.9e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
LLMDOFAF_00390 | 3e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LLMDOFAF_00391 | 3.6e-74 | XK27_08360 | S | EDD domain protein, DegV family | ||
LLMDOFAF_00392 | 6.4e-61 | XK27_08360 | S | EDD domain protein, DegV family | ||
LLMDOFAF_00393 | 2.6e-64 | WQ51_03320 | S | cog cog4835 | ||
LLMDOFAF_00394 | 7.7e-134 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
LLMDOFAF_00395 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
LLMDOFAF_00396 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
LLMDOFAF_00397 | 6.4e-29 | 2.3.1.128 | K | acetyltransferase | ||
LLMDOFAF_00398 | 7.2e-258 | gtf2 | M | A stabilizing protein that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon. Stabilizes the glycosylation activity of Gtf1 | ||
LLMDOFAF_00399 | 2.2e-295 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
LLMDOFAF_00400 | 2.9e-229 | thiI | 2.8.1.4 | H | Catalyzes the ATP-dependent transfer of a sulfur to tRNA to produce 4-thiouridine in position 8 of tRNAs, which functions as a near-UV photosensor. Also catalyzes the transfer of sulfur to the sulfur carrier protein ThiS, forming ThiS-thiocarboxylate. This is a step in the synthesis of thiazole, in the thiamine biosynthesis pathway. The sulfur is donated as persulfide by IscS | |
LLMDOFAF_00401 | 6.1e-213 | iscS2 | 2.8.1.7 | E | Cysteine sulfinate desulfinase cysteine desulfurase and related enzymes | |
LLMDOFAF_00403 | 2.4e-242 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
LLMDOFAF_00404 | 1.4e-261 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LLMDOFAF_00405 | 5.3e-35 | fruA | 2.7.1.202 | G | phosphotransferase system | |
LLMDOFAF_00406 | 5.1e-145 | fruA | 2.7.1.202 | G | phosphotransferase system | |
LLMDOFAF_00407 | 8e-98 | fruA | 2.7.1.202 | G | phosphotransferase system | |
LLMDOFAF_00408 | 2.6e-166 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
LLMDOFAF_00409 | 5.6e-114 | fruR | K | transcriptional | ||
LLMDOFAF_00410 | 1.8e-84 | L | Transposase | |||
LLMDOFAF_00411 | 1.1e-202 | rny | D | Endoribonuclease that initiates mRNA decay | ||
LLMDOFAF_00412 | 1.4e-65 | tnp | L | Transposase | ||
LLMDOFAF_00413 | 4.7e-90 | 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) | |
LLMDOFAF_00414 | 3e-139 | accA | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. First, biotin carboxylase catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the carboxyltransferase to acetyl-CoA to form malonyl-CoA | |
LLMDOFAF_00415 | 4.1e-161 | accD | 2.1.3.15, 6.4.1.2 | I | Component of the acetyl coenzyme A carboxylase (ACC) complex. Biotin carboxylase (BC) catalyzes the carboxylation of biotin on its carrier protein (BCCP) and then the CO(2) group is transferred by the transcarboxylase to acetyl-CoA to form malonyl- CoA | |
LLMDOFAF_00416 | 7.5e-258 | accC | 6.3.4.14, 6.4.1.2 | I | An AccC homodimer forms the biotin carboxylase subunit of the acetyl CoA carboxylase, an enzyme that catalyzes the formation of malonyl-CoA, which in turn controls the rate of fatty acid metabolism | |
LLMDOFAF_00417 | 1.5e-71 | fabZ | 3.5.1.108, 4.2.1.59 | I | Involved in unsaturated fatty acids biosynthesis. Catalyzes the dehydration of short chain beta-hydroxyacyl-ACPs and long chain saturated and unsaturated beta-hydroxyacyl-ACPs | |
LLMDOFAF_00418 | 7e-57 | accB | 2.3.1.12, 4.1.1.3 | I | first, biotin carboxylase catalyzes the carboxylation of the carrier protein and then the transcarboxylase transfers the carboxyl group to form malonyl-CoA | |
LLMDOFAF_00419 | 1.5e-233 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
LLMDOFAF_00420 | 1.6e-126 | IQ | reductase | |||
LLMDOFAF_00421 | 8.5e-165 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
LLMDOFAF_00422 | 6.8e-173 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
LLMDOFAF_00423 | 3.3e-30 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
LLMDOFAF_00424 | 2.3e-173 | fabH | 2.3.1.180 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP. Catalyzes the first condensation reaction which initiates fatty acid synthesis and may therefore play a role in governing the total rate of fatty acid production. Possesses both acetoacetyl-ACP synthase and acetyl transacylase activities. Its substrate specificity determines the biosynthesis of branched- chain and or straight-chain of fatty acids | |
LLMDOFAF_00425 | 4e-72 | marR | K | Transcriptional regulator, MarR family | ||
LLMDOFAF_00426 | 2.4e-139 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
LLMDOFAF_00427 | 1.9e-115 | S | Haloacid dehalogenase-like hydrolase | |||
LLMDOFAF_00428 | 2.4e-256 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
LLMDOFAF_00429 | 8e-193 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
LLMDOFAF_00430 | 6.7e-259 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LLMDOFAF_00431 | 1.2e-130 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
LLMDOFAF_00432 | 1.3e-101 | ygaC | J | Belongs to the UPF0374 family | ||
LLMDOFAF_00433 | 6.4e-108 | S | Domain of unknown function (DUF1803) | |||
LLMDOFAF_00434 | 2.1e-166 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
LLMDOFAF_00442 | 1.1e-278 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
LLMDOFAF_00443 | 1.2e-188 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
LLMDOFAF_00444 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
LLMDOFAF_00445 | 1.4e-152 | sua5 | 2.7.7.87 | J | Belongs to the SUA5 family | |
LLMDOFAF_00446 | 3.1e-112 | 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 | |
LLMDOFAF_00447 | 6.8e-275 | 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 | |
LLMDOFAF_00448 | 2.5e-43 | ysdA | L | Membrane | ||
LLMDOFAF_00449 | 6.6e-190 | 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 | |
LLMDOFAF_00450 | 3.4e-291 | 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) | |
LLMDOFAF_00451 | 4.6e-131 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LLMDOFAF_00452 | 2.5e-180 | pyrD | 1.3.1.14, 1.3.98.1 | F | Catalyzes the conversion of dihydroorotate to orotate | |
LLMDOFAF_00454 | 2.8e-39 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
LLMDOFAF_00455 | 2.1e-84 | ypmS | S | Protein conserved in bacteria | ||
LLMDOFAF_00456 | 1.3e-143 | ypmR | E | lipolytic protein G-D-S-L family | ||
LLMDOFAF_00457 | 1e-148 | DegV | S | DegV family | ||
LLMDOFAF_00458 | 5.8e-305 | recN | L | May be involved in recombinational repair of damaged DNA | ||
LLMDOFAF_00459 | 3.7e-73 | argR | K | Regulates arginine biosynthesis genes | ||
LLMDOFAF_00460 | 5e-159 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LLMDOFAF_00461 | 3e-159 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
LLMDOFAF_00462 | 3.5e-29 | xseB | 3.1.11.6 | L | exodeoxyribonuclease VII activity | |
LLMDOFAF_00463 | 1.2e-247 | 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 | |
LLMDOFAF_00466 | 3.4e-120 | 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 | |
LLMDOFAF_00467 | 2.9e-125 | dnaD | ||||
LLMDOFAF_00468 | 9.3e-183 | metA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to L- homoserine, forming acetyl-L-homoserine | |
LLMDOFAF_00469 | 2e-94 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
LLMDOFAF_00470 | 0.0 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
LLMDOFAF_00471 | 6.7e-139 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
LLMDOFAF_00472 | 9.2e-175 | rnz | 3.1.26.11 | S | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
LLMDOFAF_00473 | 4.2e-118 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
LLMDOFAF_00474 | 1.4e-223 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LLMDOFAF_00475 | 5.4e-197 | L | transposase, IS4 family | |||
LLMDOFAF_00476 | 5.6e-240 | rodA | D | Belongs to the SEDS family | ||
LLMDOFAF_00477 | 1.8e-50 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | Phosphoribosyl-ATP | |
LLMDOFAF_00478 | 5.5e-61 | hisI | 3.5.4.19, 3.5.4.25, 3.6.1.31, 5.3.1.16 | E | Catalyzes the hydrolysis of the adenine ring of phosphoribosyl-AMP | |
LLMDOFAF_00479 | 9.6e-138 | hisF | 3.5.4.19, 3.6.1.31 | 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 | |
LLMDOFAF_00480 | 1.7e-131 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
LLMDOFAF_00481 | 3.2e-112 | 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 | ||
LLMDOFAF_00482 | 3.9e-107 | hisB | 1.1.1.23, 2.6.1.9, 3.1.3.15, 4.2.1.19 | E | imidazoleglycerol-phosphate dehydratase | |
LLMDOFAF_00483 | 1.1e-234 | 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 | |
LLMDOFAF_00484 | 2.7e-117 | hisG | 2.4.2.17 | E | Catalyzes the condensation of ATP and 5-phosphoribose 1- diphosphate to form N'-(5'-phosphoribosyl)-ATP (PR-ATP). Has a crucial role in the pathway because the rate of histidine biosynthesis seems to be controlled primarily by regulation of HisG enzymatic activity | |
LLMDOFAF_00485 | 1.5e-183 | hisZ | 2.4.2.17, 6.1.1.21 | E | Required for the first step of histidine biosynthesis. May allow the feedback regulation of ATP phosphoribosyltransferase activity by histidine | |
LLMDOFAF_00486 | 1.5e-197 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LLMDOFAF_00488 | 1.6e-32 | L | Integrase core domain protein | |||
LLMDOFAF_00489 | 3.6e-230 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
LLMDOFAF_00490 | 1.7e-35 | dltC | 6.1.1.13 | IQ | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
LLMDOFAF_00491 | 4.6e-238 | dltB | M | Membrane protein involved in D-alanine export | ||
LLMDOFAF_00492 | 1.4e-297 | dltA | 6.1.1.13 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
LLMDOFAF_00493 | 1.7e-09 | S | D-Ala-teichoic acid biosynthesis protein | |||
LLMDOFAF_00494 | 0.0 | XK27_10035 | V | abc transporter atp-binding protein | ||
LLMDOFAF_00495 | 0.0 | yfiB1 | V | abc transporter atp-binding protein | ||
LLMDOFAF_00496 | 6e-106 | pvaA | M | lytic transglycosylase activity | ||
LLMDOFAF_00497 | 1.2e-177 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
LLMDOFAF_00498 | 1.8e-234 | glyA | 2.1.2.1 | E | Catalyzes the reversible interconversion of serine and glycine with tetrahydrofolate (THF) serving as the one-carbon carrier. This reaction serves as the major source of one-carbon groups required for the biosynthesis of purines, thymidylate, methionine, and other important biomolecules. Also exhibits THF- independent aldolase activity toward beta-hydroxyamino acids, producing glycine and aldehydes, via a retro-aldol mechanism | |
LLMDOFAF_00499 | 9.7e-109 | ywlC | 2.7.7.87, 3.1.3.48 | J | Required for the formation of a threonylcarbamoyl group on adenosine at position 37 (t(6)A37) in tRNAs that read codons beginning with adenine | |
LLMDOFAF_00500 | 1.2e-154 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
LLMDOFAF_00501 | 3e-193 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
LLMDOFAF_00502 | 4.5e-111 | tdk | 2.7.1.21 | F | thymidine kinase | |
LLMDOFAF_00503 | 1.6e-188 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
LLMDOFAF_00504 | 2.4e-155 | gst | O | Glutathione S-transferase | ||
LLMDOFAF_00505 | 1e-184 | nrnA | 3.1.13.3, 3.1.3.7 | S | domain protein | |
LLMDOFAF_00506 | 9.8e-177 | 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 | |
LLMDOFAF_00507 | 2e-45 | rpmE2 | J | 50S ribosomal protein L31 | ||
LLMDOFAF_00508 | 3.2e-231 | mntH | P | Mn2 and Fe2 transporters of the NRAMP family | ||
LLMDOFAF_00509 | 1.3e-10 | |||||
LLMDOFAF_00510 | 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) | |
LLMDOFAF_00511 | 1.8e-135 | divIVA | D | Cell division protein DivIVA | ||
LLMDOFAF_00512 | 4.2e-144 | ylmH | T | S4 RNA-binding domain | ||
LLMDOFAF_00513 | 2e-34 | yggT | D | integral membrane protein | ||
LLMDOFAF_00514 | 1.4e-96 | sepF | D | cell septum assembly | ||
LLMDOFAF_00515 | 2.7e-123 | ylmE | S | Pyridoxal 5'-phosphate (PLP)-binding protein, which is involved in PLP homeostasis | ||
LLMDOFAF_00516 | 5.4e-237 | 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 | ||
LLMDOFAF_00517 | 8e-252 | ftsA | D | Cell division protein that is involved in the assembly of the Z ring. May serve as a membrane anchor for the Z ring | ||
LLMDOFAF_00518 | 6.7e-172 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
LLMDOFAF_00519 | 1e-201 | murG | 2.4.1.227 | 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) |
LLMDOFAF_00520 | 1.6e-252 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LLMDOFAF_00522 | 0.0 | typA | T | GTP-binding protein TypA | ||
LLMDOFAF_00523 | 2.2e-179 | glk | 2.7.1.2 | G | Glucokinase | |
LLMDOFAF_00524 | 8.4e-28 | yqgQ | S | protein conserved in bacteria | ||
LLMDOFAF_00525 | 1.1e-80 | perR | P | Belongs to the Fur family | ||
LLMDOFAF_00526 | 3.2e-92 | dps | P | Belongs to the Dps family | ||
LLMDOFAF_00527 | 1.5e-115 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
LLMDOFAF_00528 | 4.8e-196 | 3.5.2.6 | V | D-alanyl-D-alanine carboxypeptidase | ||
LLMDOFAF_00529 | 1.8e-237 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
LLMDOFAF_00530 | 2.8e-154 | thrB | 2.7.1.39 | E | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
LLMDOFAF_00531 | 5.5e-153 | rarD | S | Transporter | ||
LLMDOFAF_00532 | 2.2e-15 | T | peptidase | |||
LLMDOFAF_00533 | 8.9e-14 | coiA | 3.6.4.12 | S | Competence protein | |
LLMDOFAF_00534 | 6.6e-147 | S | COG1853 Conserved protein domain typically associated with flavoprotein oxygenases, DIM6 NTAB family | |||
LLMDOFAF_00535 | 8.3e-75 | 2.3.1.128, 5.2.1.8 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
LLMDOFAF_00536 | 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 | |
LLMDOFAF_00537 | 3.2e-16 | 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 | ||
LLMDOFAF_00538 | 4.3e-124 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
LLMDOFAF_00539 | 3.3e-78 | atpF | C | ATP synthase F(0) sector subunit b | ||
LLMDOFAF_00540 | 9.3e-87 | 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 | ||
LLMDOFAF_00541 | 3.8e-279 | 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 | |
LLMDOFAF_00542 | 2.5e-158 | 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 | ||
LLMDOFAF_00543 | 2.7e-263 | 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 | |
LLMDOFAF_00544 | 5.2e-67 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
LLMDOFAF_00545 | 2.8e-230 | ftsW | D | Belongs to the SEDS family | ||
LLMDOFAF_00546 | 9.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LLMDOFAF_00547 | 1.4e-136 | 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) | |
LLMDOFAF_00548 | 1.7e-111 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LLMDOFAF_00549 | 6.4e-162 | holB | 2.7.7.7 | L | dna polymerase iii | |
LLMDOFAF_00550 | 1.2e-135 | yaaT | S | stage 0 sporulation protein | ||
LLMDOFAF_00551 | 9.5e-55 | yabA | L | Involved in initiation control of chromosome replication | ||
LLMDOFAF_00552 | 2.7e-160 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LLMDOFAF_00553 | 2.6e-233 | amt | P | Ammonium Transporter | ||
LLMDOFAF_00554 | 1.1e-53 | glnB | K | Belongs to the P(II) protein family | ||
LLMDOFAF_00555 | 4.9e-106 | mur1 | NU | mannosyl-glycoprotein | ||
LLMDOFAF_00556 | 5.8e-149 | XK27_04800 | S | Sucrose-6F-phosphate phosphohydrolase | ||
LLMDOFAF_00557 | 2.9e-68 | nptA | P | sodium-dependent phosphate transmembrane transporter activity | ||
LLMDOFAF_00558 | 1.9e-222 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
LLMDOFAF_00559 | 1.8e-53 | |||||
LLMDOFAF_00560 | 7.5e-26 | |||||
LLMDOFAF_00561 | 1.5e-59 | |||||
LLMDOFAF_00562 | 6.1e-63 | S | membrane | |||
LLMDOFAF_00563 | 4.8e-176 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
LLMDOFAF_00564 | 0.0 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
LLMDOFAF_00565 | 4.5e-39 | ynzC | S | UPF0291 protein | ||
LLMDOFAF_00566 | 1.8e-254 | cycA | E | permease | ||
LLMDOFAF_00567 | 2.4e-09 | uvrX | 2.7.7.7 | L | impB/mucB/samB family | |
LLMDOFAF_00568 | 5.8e-71 | pts33BCA | G | pts system | ||
LLMDOFAF_00569 | 3.5e-143 | pts33BCA | G | pts system | ||
LLMDOFAF_00570 | 3.2e-141 | ppiA | 5.2.1.8 | O | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
LLMDOFAF_00571 | 1.2e-165 | L | integrase core domain | |||
LLMDOFAF_00572 | 8.5e-113 | sodA | 1.15.1.1 | C | radicals which are normally produced within the cells and which are toxic to biological systems | |
LLMDOFAF_00573 | 1.9e-184 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
LLMDOFAF_00574 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LLMDOFAF_00575 | 6.2e-56 | S | Domain of unknown function (DUF4430) | |||
LLMDOFAF_00576 | 1.8e-73 | S | Psort location CytoplasmicMembrane, score | |||
LLMDOFAF_00577 | 6.4e-133 | htpX | O | Belongs to the peptidase M48B family | ||
LLMDOFAF_00578 | 9e-93 | lemA | S | LemA family | ||
LLMDOFAF_00579 | 9.9e-90 | spd | F | DNA RNA non-specific endonuclease | ||
LLMDOFAF_00580 | 1e-36 | spd | F | DNA RNA non-specific endonuclease | ||
LLMDOFAF_00581 | 5.9e-22 | S | PD-(D/E)XK nuclease family transposase | |||
LLMDOFAF_00582 | 6.6e-306 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
LLMDOFAF_00583 | 1e-136 | S | Protein conserved in bacteria | |||
LLMDOFAF_00584 | 2.2e-105 | |||||
LLMDOFAF_00585 | 2.8e-221 | hsdS | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
LLMDOFAF_00587 | 1.2e-216 | S | Bacteriophage abortive infection AbiH | |||
LLMDOFAF_00588 | 0.0 | hsdR | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
LLMDOFAF_00589 | 7.6e-71 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
LLMDOFAF_00590 | 8.7e-45 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
LLMDOFAF_00591 | 9.1e-27 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
LLMDOFAF_00592 | 1.4e-23 | MA20_36090 | S | Protein of unknown function (DUF2974) | ||
LLMDOFAF_00593 | 1.6e-114 | 1.14.14.5 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
LLMDOFAF_00594 | 2.7e-27 | P | Hemerythrin HHE cation binding domain protein | |||
LLMDOFAF_00595 | 2.8e-155 | XK27_00880 | 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
LLMDOFAF_00596 | 7.9e-82 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
LLMDOFAF_00597 | 6.6e-116 | pgm6 | 5.4.2.11, 5.4.2.12 | G | phosphoglycerate mutase | |
LLMDOFAF_00598 | 2.3e-175 | S | hydrolase | |||
LLMDOFAF_00599 | 7.6e-16 | |||||
LLMDOFAF_00600 | 1e-163 | M | LysM domain | |||
LLMDOFAF_00601 | 9.9e-288 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LLMDOFAF_00602 | 4.2e-117 | |||||
LLMDOFAF_00603 | 7.7e-238 | dcm | 2.1.1.37 | L | Belongs to the class I-like SAM-binding methyltransferase superfamily. C5-methyltransferase family | |
LLMDOFAF_00604 | 1.9e-12 | |||||
LLMDOFAF_00605 | 7.8e-236 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
LLMDOFAF_00606 | 1.1e-33 | XK27_12190 | S | protein conserved in bacteria | ||
LLMDOFAF_00608 | 1.5e-89 | bioY | S | biotin synthase | ||
LLMDOFAF_00609 | 3.4e-252 | yegQ | O | Peptidase U32 | ||
LLMDOFAF_00610 | 4.4e-177 | yegQ | O | Peptidase U32 | ||
LLMDOFAF_00612 | 5.5e-69 | ytxH | S | General stress protein | ||
LLMDOFAF_00614 | 4e-147 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
LLMDOFAF_00615 | 1e-170 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
LLMDOFAF_00616 | 9.9e-42 | pspC | KT | PspC domain | ||
LLMDOFAF_00617 | 0.0 | yhgF | K | Transcriptional accessory protein | ||
LLMDOFAF_00619 | 1.7e-157 | XK27_03015 | S | permease | ||
LLMDOFAF_00620 | 1.3e-148 | ycgQ | S | TIGR03943 family | ||
LLMDOFAF_00621 | 2.3e-198 | S | CRISPR-associated protein Csn2 subfamily St | |||
LLMDOFAF_00622 | 1.8e-53 | cas2 | 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 sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
LLMDOFAF_00623 | 1.1e-172 | 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 | ||
LLMDOFAF_00624 | 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 | ||
LLMDOFAF_00625 | 4.4e-93 | |||||
LLMDOFAF_00626 | 1.5e-25 | estA | E | GDSL-like Lipase/Acylhydrolase | ||
LLMDOFAF_00627 | 7.8e-50 | dam | 2.1.1.72 | L | D12 class N6 adenine-specific DNA methyltransferase | |
LLMDOFAF_00628 | 1e-31 | K | Cro/C1-type HTH DNA-binding domain | |||
LLMDOFAF_00629 | 3.2e-46 | |||||
LLMDOFAF_00630 | 8.9e-20 | |||||
LLMDOFAF_00631 | 1.7e-257 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LLMDOFAF_00632 | 3.5e-97 | mip | S | hydroperoxide reductase activity | ||
LLMDOFAF_00633 | 2.4e-203 | I | acyl-CoA dehydrogenase | |||
LLMDOFAF_00634 | 3.5e-150 | ydiA | P | C4-dicarboxylate transporter malic acid transport protein | ||
LLMDOFAF_00635 | 2.6e-253 | msrR | K | Transcriptional regulator | ||
LLMDOFAF_00636 | 2.3e-153 | pheA | 4.2.1.51 | E | Prephenate dehydratase | |
LLMDOFAF_00637 | 1.7e-87 | aroK | 1.1.1.25, 2.7.1.71, 4.2.1.10, 4.2.3.4 | F | Catalyzes the specific phosphorylation of the 3-hydroxyl group of shikimic acid using ATP as a cosubstrate | |
LLMDOFAF_00638 | 2.6e-236 | aroA | 1.3.1.12, 1.3.1.43, 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 | |
LLMDOFAF_00639 | 3e-173 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
LLMDOFAF_00640 | 3.2e-53 | yheA | S | Belongs to the UPF0342 family | ||
LLMDOFAF_00641 | 2.2e-207 | tyrA | 1.3.1.12, 1.3.1.43 | E | prephenate dehydrogenase | |
LLMDOFAF_00642 | 4.5e-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 | |
LLMDOFAF_00643 | 3.5e-202 | aroB | 2.7.1.71, 4.2.3.4 | E | Catalyzes the conversion of 3-deoxy-D-arabino- heptulosonate 7-phosphate (DAHP) to dehydroquinate (DHQ) | |
LLMDOFAF_00644 | 1.7e-162 | 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) | |
LLMDOFAF_00645 | 8.6e-122 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
LLMDOFAF_00646 | 6.9e-220 | ywbD | 2.1.1.191 | J | Methyltransferase | |
LLMDOFAF_00647 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
LLMDOFAF_00648 | 2e-25 | WQ51_00785 | ||||
LLMDOFAF_00649 | 9.6e-247 | eno | 4.2.1.11 | G | Catalyzes the reversible conversion of 2- phosphoglycerate into phosphoenolpyruvate. It is essential for the degradation of carbohydrates via glycolysis | |
LLMDOFAF_00650 | 1e-78 | yueI | S | Protein of unknown function (DUF1694) | ||
LLMDOFAF_00651 | 1.3e-207 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
LLMDOFAF_00652 | 6.6e-101 | yyaQ | V | Protein conserved in bacteria | ||
LLMDOFAF_00653 | 2.8e-28 | yyaQ | S | YjbR | ||
LLMDOFAF_00654 | 4.4e-183 | ccpA | K | Catabolite control protein A | ||
LLMDOFAF_00655 | 4.2e-211 | pepQ | 3.4.13.9 | E | Belongs to the peptidase M24B family | |
LLMDOFAF_00656 | 1.7e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
LLMDOFAF_00657 | 9.6e-277 | ppiB | 5.2.1.8 | G | PPIases accelerate the folding of proteins. It catalyzes the cis-trans isomerization of proline imidic peptide bonds in oligopeptides | |
LLMDOFAF_00658 | 1.1e-80 | smpB | O | 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 | ||
LLMDOFAF_00659 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
LLMDOFAF_00660 | 2.6e-33 | secG | U | Preprotein translocase subunit SecG | ||
LLMDOFAF_00661 | 9.5e-74 | mdtG | EGP | Major facilitator Superfamily | ||
LLMDOFAF_00662 | 6e-133 | mdtG | EGP | Major facilitator Superfamily | ||
LLMDOFAF_00663 | 1.3e-105 | coaE | 2.7.1.24, 3.2.2.23, 4.2.99.18 | GH23 | H | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A |
LLMDOFAF_00664 | 1.9e-155 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
LLMDOFAF_00665 | 1.3e-165 | era | M | 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 | ||
LLMDOFAF_00666 | 1.7e-64 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
LLMDOFAF_00667 | 5.9e-88 | 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 | |
LLMDOFAF_00668 | 6.8e-53 | licT | K | transcriptional antiterminator | ||
LLMDOFAF_00669 | 9.2e-43 | licT | K | transcriptional antiterminator | ||
LLMDOFAF_00671 | 2.2e-105 | 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 | ||
LLMDOFAF_00672 | 0.0 | pbp2b | 3.4.16.4 | M | penicillin-binding protein | |
LLMDOFAF_00673 | 3.2e-150 | 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 | |
LLMDOFAF_00674 | 2.1e-157 | 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 | |
LLMDOFAF_00675 | 7.5e-23 | I | Alpha/beta hydrolase family | |||
LLMDOFAF_00676 | 1.5e-35 | yugF | I | carboxylic ester hydrolase activity | ||
LLMDOFAF_00677 | 2.2e-45 | K | sequence-specific DNA binding | |||
LLMDOFAF_00678 | 2.4e-104 | 1.1.1.133, 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | ||
LLMDOFAF_00679 | 1.5e-07 | |||||
LLMDOFAF_00680 | 0.0 | feoB | P | transporter of a GTP-driven Fe(2 ) uptake system | ||
LLMDOFAF_00681 | 1.1e-78 | feoA | P | FeoA domain protein | ||
LLMDOFAF_00682 | 2.2e-131 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LLMDOFAF_00683 | 7.5e-118 | WQ51_01820 | P | Binding-protein-dependent transport system inner membrane component | ||
LLMDOFAF_00684 | 1.3e-34 | ykuJ | S | protein conserved in bacteria | ||
LLMDOFAF_00685 | 1.3e-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 | |
LLMDOFAF_00686 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
LLMDOFAF_00687 | 1.8e-86 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
LLMDOFAF_00688 | 7.4e-49 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
LLMDOFAF_00689 | 2.4e-66 | S | oxidoreductase | |||
LLMDOFAF_00690 | 1.5e-50 | S | oxidoreductase | |||
LLMDOFAF_00691 | 6.8e-234 | murN | 2.3.2.10, 2.3.2.16 | V | FemAB family | |
LLMDOFAF_00692 | 1.7e-63 | M | Pfam SNARE associated Golgi protein | |||
LLMDOFAF_00693 | 1.5e-30 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
LLMDOFAF_00694 | 1e-29 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
LLMDOFAF_00697 | 6.4e-205 | rpsA | 1.17.7.4 | J | ribosomal protein S1 | |
LLMDOFAF_00700 | 4.8e-16 | S | Protein of unknown function (DUF2969) | |||
LLMDOFAF_00701 | 2.4e-200 | ilvE | 2.6.1.42 | E | Aminotransferase | |
LLMDOFAF_00702 | 0.0 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
LLMDOFAF_00703 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
LLMDOFAF_00704 | 1.2e-101 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
LLMDOFAF_00705 | 2.1e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LLMDOFAF_00706 | 4.4e-123 | comFC | S | Competence protein | ||
LLMDOFAF_00707 | 1.3e-254 | comFA | L | Superfamily II DNA RNA helicase required for DNA uptake (late competence protein) | ||
LLMDOFAF_00708 | 6.3e-111 | yvyE | 3.4.13.9 | S | YigZ family | |
LLMDOFAF_00709 | 2.2e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
LLMDOFAF_00710 | 3.3e-43 | acuB | S | IMP dehydrogenase activity | ||
LLMDOFAF_00711 | 1.1e-69 | acuB | S | IMP dehydrogenase activity | ||
LLMDOFAF_00712 | 9.6e-124 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
LLMDOFAF_00713 | 9.6e-138 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
LLMDOFAF_00714 | 1.4e-138 | livM | E | Belongs to the binding-protein-dependent transport system permease family | ||
LLMDOFAF_00715 | 1.9e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
LLMDOFAF_00716 | 1.1e-212 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
LLMDOFAF_00717 | 7.1e-46 | ylbG | S | UPF0298 protein | ||
LLMDOFAF_00718 | 3.4e-74 | ylbF | S | Belongs to the UPF0342 family | ||
LLMDOFAF_00719 | 2.9e-105 | clpP | 3.4.21.92 | OU | 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 | |
LLMDOFAF_00720 | 4.4e-112 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
LLMDOFAF_00721 | 1.2e-08 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | G | Belongs to the glycosyl hydrolase 68 family |
LLMDOFAF_00723 | 1e-223 | malY | 4.4.1.8 | E | COG1168 Bifunctional PLP-dependent enzyme with beta-cystathionase and maltose regulon repressor activities | |
LLMDOFAF_00724 | 4.7e-202 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
LLMDOFAF_00725 | 3.3e-96 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
LLMDOFAF_00726 | 4.5e-283 | ytgP | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
LLMDOFAF_00727 | 4.9e-276 | murE | 6.3.2.13, 6.3.2.7 | M | to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
LLMDOFAF_00728 | 3.2e-214 | femA | 2.3.2.10, 2.3.2.16, 2.3.2.17, 2.3.2.18 | V | protein involved in methicillin resistance | |
LLMDOFAF_00729 | 3.4e-37 | yvdD | 3.2.2.10 | L | Belongs to the LOG family | |
LLMDOFAF_00730 | 2e-22 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
LLMDOFAF_00731 | 1.7e-57 | 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 | ||
LLMDOFAF_00732 | 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 | ||
LLMDOFAF_00733 | 1.4e-41 | ylxQ | J | ribosomal protein | ||
LLMDOFAF_00734 | 1e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
LLMDOFAF_00735 | 3.1e-212 | nusA | K | Participates in both transcription termination and antitermination | ||
LLMDOFAF_00736 | 3.9e-81 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
LLMDOFAF_00737 | 2.5e-220 | brpA | K | Transcriptional | ||
LLMDOFAF_00738 | 2.4e-92 | XK27_05885 | 2.3.1.82 | M | Acetyltransferase GNAT Family | |
LLMDOFAF_00739 | 1.4e-77 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
LLMDOFAF_00740 | 1.9e-248 | pbuO | S | permease | ||
LLMDOFAF_00741 | 1e-153 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
LLMDOFAF_00742 | 1.5e-140 | XK27_00940 | 1.2.1.70, 3.5.1.9 | S | Metal-dependent hydrolase | |
LLMDOFAF_00743 | 1.3e-174 | manL | 2.7.1.191 | G | pts system | |
LLMDOFAF_00744 | 7e-118 | manM | G | pts system | ||
LLMDOFAF_00745 | 1.9e-169 | manN | G | PTS system mannose fructose sorbose family IID component | ||
LLMDOFAF_00746 | 6.5e-63 | manO | S | protein conserved in bacteria | ||
LLMDOFAF_00747 | 1.5e-231 | 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) | |
LLMDOFAF_00748 | 1.2e-34 | |||||
LLMDOFAF_00750 | 2e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
LLMDOFAF_00751 | 5.2e-167 | dnaI | L | Primosomal protein DnaI | ||
LLMDOFAF_00752 | 6.5e-218 | dnaB | L | Replication initiation and membrane attachment | ||
LLMDOFAF_00753 | 4.7e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
LLMDOFAF_00754 | 2.8e-282 | T | PhoQ Sensor | |||
LLMDOFAF_00755 | 1.8e-122 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LLMDOFAF_00756 | 2.1e-91 | yceD | K | metal-binding, possibly nucleic acid-binding protein | ||
LLMDOFAF_00757 | 1.1e-130 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
LLMDOFAF_00758 | 5.2e-243 | P | COG0168 Trk-type K transport systems, membrane components | |||
LLMDOFAF_00759 | 1.4e-121 | ktrA | P | COG0569 K transport systems, NAD-binding component | ||
LLMDOFAF_00760 | 9.7e-13 | ulaG | S | L-ascorbate 6-phosphate lactonase | ||
LLMDOFAF_00761 | 0.0 | tkt | 2.2.1.1 | G | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
LLMDOFAF_00762 | 1.2e-149 | cbiQ | P | cobalt transport | ||
LLMDOFAF_00763 | 0.0 | ykoD | P | abc transporter atp-binding protein | ||
LLMDOFAF_00764 | 9.4e-95 | S | UPF0397 protein | |||
LLMDOFAF_00765 | 2.9e-159 | salL | 2.5.1.63, 2.5.1.94 | S | S-adenosyl-l-methionine hydroxide adenosyltransferase | |
LLMDOFAF_00766 | 2.7e-211 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
LLMDOFAF_00767 | 3e-98 | metI | P | ABC transporter (Permease | ||
LLMDOFAF_00768 | 1.5e-189 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LLMDOFAF_00769 | 1e-63 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase activity | |
LLMDOFAF_00770 | 1.4e-62 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase activity | |
LLMDOFAF_00771 | 7.1e-86 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
LLMDOFAF_00772 | 3.7e-165 | metQ | M | Belongs to the NlpA lipoprotein family | ||
LLMDOFAF_00773 | 5.3e-153 | ET | amino acid transport | |||
LLMDOFAF_00774 | 3.8e-205 | EGP | Transmembrane secretion effector | |||
LLMDOFAF_00775 | 0.0 | 3.3.1.1, 3.6.1.55, 3.6.1.67 | F | NUDIX domain | ||
LLMDOFAF_00776 | 0.0 | Q | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |||
LLMDOFAF_00777 | 3.3e-118 | ET | amino acid transport | |||
LLMDOFAF_00778 | 5.8e-62 | L | PFAM Integrase, catalytic core | |||
LLMDOFAF_00779 | 1.3e-165 | fba | 4.1.2.13, 4.1.2.29 | G | aldolase | |
LLMDOFAF_00781 | 6.7e-110 | 6.3.2.2 | H | ergothioneine biosynthetic process | ||
LLMDOFAF_00782 | 9.6e-65 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
LLMDOFAF_00783 | 7.2e-12 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
LLMDOFAF_00784 | 3.3e-09 | L | PFAM Integrase, catalytic core | |||
LLMDOFAF_00785 | 1.8e-111 | L | PFAM Integrase, catalytic core | |||
LLMDOFAF_00786 | 3.3e-62 | rplQ | J | ribosomal protein l17 | ||
LLMDOFAF_00787 | 4.8e-171 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LLMDOFAF_00788 | 9.6e-62 | 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 | ||
LLMDOFAF_00789 | 4e-57 | 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 | ||
LLMDOFAF_00790 | 6e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
LLMDOFAF_00791 | 2.7e-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 | ||
LLMDOFAF_00792 | 9.2e-121 | 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 | |
LLMDOFAF_00793 | 2.3e-232 | 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 | ||
LLMDOFAF_00794 | 4.4e-58 | rplO | J | binds to the 23S rRNA | ||
LLMDOFAF_00795 | 2.5e-23 | rpmD | J | ribosomal protein l30 | ||
LLMDOFAF_00796 | 1.7e-79 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
LLMDOFAF_00797 | 1.9e-56 | rplR | J | This is one of the proteins that binds and probably mediates the attachment of the 5S RNA into the large ribosomal subunit, where it forms part of the central protuberance | ||
LLMDOFAF_00798 | 2.3e-93 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
LLMDOFAF_00799 | 1.2e-67 | 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 | ||
LLMDOFAF_00800 | 1.5e-28 | 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 | ||
LLMDOFAF_00801 | 1.6e-94 | 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 | ||
LLMDOFAF_00802 | 1.4e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LLMDOFAF_00803 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
LLMDOFAF_00804 | 6e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
LLMDOFAF_00805 | 2.7e-26 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
LLMDOFAF_00806 | 7.2e-71 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
LLMDOFAF_00807 | 2.1e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LLMDOFAF_00808 | 7.3e-53 | 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 | ||
LLMDOFAF_00809 | 4.9e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LLMDOFAF_00810 | 8.8e-153 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
LLMDOFAF_00811 | 2.4e-44 | 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 | ||
LLMDOFAF_00812 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LLMDOFAF_00813 | 1.1e-110 | 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 | ||
LLMDOFAF_00814 | 1.3e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LLMDOFAF_00815 | 7.8e-188 | 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 | |
LLMDOFAF_00816 | 0.0 | XK27_09800 | I | Acyltransferase | ||
LLMDOFAF_00817 | 1.7e-35 | XK27_09805 | S | MORN repeat protein | ||
LLMDOFAF_00818 | 1e-80 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
LLMDOFAF_00819 | 4.1e-250 | 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 | |
LLMDOFAF_00820 | 8.8e-83 | adk | 2.7.4.3 | F | topology modulation protein | |
LLMDOFAF_00821 | 3.1e-172 | yxaM | EGP | Major facilitator Superfamily | ||
LLMDOFAF_00822 | 1.9e-197 | 2.7.7.73, 2.7.7.80 | H | Involved in molybdopterin and thiamine biosynthesis, family 2 | ||
LLMDOFAF_00823 | 0.0 | 3.6.3.8 | P | cation transport ATPase | ||
LLMDOFAF_00824 | 0.0 | pabB | 2.6.1.85, 4.1.3.27, 4.1.3.38 | EH | component I | |
LLMDOFAF_00826 | 3e-44 | ymbI | L | transposase activity | ||
LLMDOFAF_00827 | 4e-22 | L | Belongs to the 'phage' integrase family | |||
LLMDOFAF_00828 | 1.4e-66 | S | tRNA_anti-like | |||
LLMDOFAF_00829 | 2e-103 | |||||
LLMDOFAF_00831 | 5e-12 | |||||
LLMDOFAF_00833 | 2e-296 | S | DNA primase | |||
LLMDOFAF_00834 | 3e-164 | KL | Phage plasmid primase P4 family | |||
LLMDOFAF_00835 | 6.9e-22 | |||||
LLMDOFAF_00836 | 9.2e-13 | |||||
LLMDOFAF_00841 | 1.3e-17 | K | Cro/C1-type HTH DNA-binding domain | |||
LLMDOFAF_00843 | 1.1e-220 | sip | L | Belongs to the 'phage' integrase family | ||
LLMDOFAF_00845 | 0.0 | metE | 2.1.1.14 | E | Catalyzes the transfer of a methyl group from 5- methyltetrahydrofolate to homocysteine resulting in methionine formation | |
LLMDOFAF_00846 | 7.3e-166 | metF | 1.5.1.20 | E | reductase | |
LLMDOFAF_00847 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase | |
LLMDOFAF_00848 | 1.7e-94 | panT | S | ECF transporter, substrate-specific component | ||
LLMDOFAF_00849 | 4.8e-94 | coaBC | 4.1.1.36, 6.3.2.5 | H | Catalyzes two steps in the biosynthesis of coenzyme A. In the first step cysteine is conjugated to 4'-phosphopantothenate to form 4-phosphopantothenoylcysteine, in the latter compound is decarboxylated to form 4'-phosphopantotheine | |
LLMDOFAF_00850 | 1.2e-120 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
LLMDOFAF_00851 | 0.0 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
LLMDOFAF_00852 | 6.4e-66 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LLMDOFAF_00853 | 2.8e-40 | T | PhoQ Sensor | |||
LLMDOFAF_00854 | 1.7e-43 | T | PhoQ Sensor | |||
LLMDOFAF_00855 | 5.8e-79 | T | PhoQ Sensor | |||
LLMDOFAF_00856 | 2.2e-61 | rlpA | M | LysM domain protein | ||
LLMDOFAF_00857 | 8e-191 | phoH | T | phosphate starvation-inducible protein PhoH | ||
LLMDOFAF_00861 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
LLMDOFAF_00862 | 1.8e-167 | K | transcriptional regulator (lysR family) | |||
LLMDOFAF_00863 | 1.4e-186 | coiA | 3.6.4.12 | S | Competence protein | |
LLMDOFAF_00864 | 0.0 | pepF | E | oligoendopeptidase F | ||
LLMDOFAF_00865 | 5.4e-127 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
LLMDOFAF_00866 | 4.6e-168 | prsA | 3.1.3.16, 5.2.1.8 | O | peptidyl-prolyl cis-trans isomerase activity | |
LLMDOFAF_00867 | 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 | |
LLMDOFAF_00868 | 7.9e-24 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
LLMDOFAF_00869 | 6.9e-179 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
LLMDOFAF_00870 | 1.8e-30 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
LLMDOFAF_00871 | 7.1e-89 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
LLMDOFAF_00872 | 1.2e-146 | cnhA | 3.5.1.3 | S | Nitrilase cyanide hydratase and apolipoprotein N-acyltransferase | |
LLMDOFAF_00873 | 5.3e-228 | mtnE | 2.6.1.83 | E | mutations do not affect methionine salvage in vivo however | |
LLMDOFAF_00874 | 1.5e-191 | 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 | |
LLMDOFAF_00875 | 1.5e-222 | 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 | |
LLMDOFAF_00876 | 1.9e-130 | argB | 2.7.2.8 | E | Belongs to the acetylglutamate kinase family. ArgB subfamily | |
LLMDOFAF_00877 | 1.6e-210 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
LLMDOFAF_00878 | 8.5e-142 | yxkH | G | deacetylase | ||
LLMDOFAF_00879 | 2.3e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
LLMDOFAF_00880 | 4.7e-205 | 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 | ||
LLMDOFAF_00881 | 1e-232 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LLMDOFAF_00882 | 6.4e-107 | tag | 3.2.2.20 | L | 3-methyladenine DNA glycosylase | |
LLMDOFAF_00883 | 7.8e-103 | 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 | |
LLMDOFAF_00885 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
LLMDOFAF_00887 | 6.5e-63 | KT | phosphorelay signal transduction system | |||
LLMDOFAF_00888 | 1.9e-80 | S | Protein of unknown function (DUF3021) | |||
LLMDOFAF_00889 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
LLMDOFAF_00890 | 1e-57 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
LLMDOFAF_00891 | 8.2e-70 | argR | K | Regulates arginine biosynthesis genes | ||
LLMDOFAF_00892 | 0.0 | argS | 6.1.1.19 | J | Catalyzes a two-step reaction, first charging an arginine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
LLMDOFAF_00893 | 8.7e-248 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
LLMDOFAF_00894 | 9.2e-141 | 1.1.1.169 | H | Ketopantoate reductase | ||
LLMDOFAF_00895 | 2.2e-204 | 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) | |
LLMDOFAF_00896 | 4.9e-76 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
LLMDOFAF_00897 | 3.4e-241 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
LLMDOFAF_00898 | 2.3e-161 | S | CHAP domain | |||
LLMDOFAF_00899 | 2e-32 | L | Integrase core domain protein | |||
LLMDOFAF_00900 | 3.5e-50 | L | transposition | |||
LLMDOFAF_00901 | 1.4e-20 | L | transposase activity | |||
LLMDOFAF_00908 | 5.3e-11 | |||||
LLMDOFAF_00914 | 1.3e-140 | mreC | M | Involved in formation and maintenance of cell shape | ||
LLMDOFAF_00915 | 8.2e-88 | mreD | M | Involved in formation of the rod shape of the cell. May also contribute to regulation of formation of penicillin-binding proteins | ||
LLMDOFAF_00916 | 8.9e-102 | usp | 3.5.1.28 | CBM50 | S | CHAP domain |
LLMDOFAF_00917 | 4.3e-175 | 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) | |
LLMDOFAF_00918 | 2.5e-26 | |||||
LLMDOFAF_00919 | 5.9e-219 | araT | 2.6.1.1 | E | Aminotransferase | |
LLMDOFAF_00920 | 1.6e-143 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LLMDOFAF_00921 | 1.3e-179 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
LLMDOFAF_00922 | 4.2e-34 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
LLMDOFAF_00923 | 5.2e-130 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
LLMDOFAF_00924 | 0.0 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
LLMDOFAF_00925 | 1.3e-276 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LLMDOFAF_00926 | 4.8e-185 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
LLMDOFAF_00927 | 1.4e-101 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
LLMDOFAF_00928 | 6.6e-295 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
LLMDOFAF_00929 | 4.2e-44 | yrzB | S | Belongs to the UPF0473 family | ||
LLMDOFAF_00930 | 1.2e-70 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LLMDOFAF_00931 | 2.8e-44 | yrzL | S | Belongs to the UPF0297 family | ||
LLMDOFAF_00932 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
LLMDOFAF_00933 | 5.2e-237 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
LLMDOFAF_00935 | 3.5e-216 | int | L | Belongs to the 'phage' integrase family | ||
LLMDOFAF_00936 | 1.9e-18 | S | Domain of unknown function (DUF3173) | |||
LLMDOFAF_00937 | 1.4e-107 | L | Replication initiation factor | |||
LLMDOFAF_00938 | 1e-36 | L | Replication initiation factor | |||
LLMDOFAF_00939 | 1.7e-90 | K | sequence-specific DNA binding | |||
LLMDOFAF_00940 | 3.9e-287 | V | ABC transporter transmembrane region | |||
LLMDOFAF_00941 | 3.4e-191 | C | Radical SAM | |||
LLMDOFAF_00943 | 1.4e-127 | Z012_04635 | K | sequence-specific DNA binding | ||
LLMDOFAF_00944 | 2.1e-280 | V | ABC transporter | |||
LLMDOFAF_00945 | 0.0 | KLT | serine threonine protein kinase | |||
LLMDOFAF_00946 | 3.4e-155 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
LLMDOFAF_00948 | 1.4e-231 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LLMDOFAF_00949 | 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 | |
LLMDOFAF_00950 | 6.9e-144 | S | SseB protein N-terminal domain | |||
LLMDOFAF_00951 | 1.1e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
LLMDOFAF_00952 | 1.7e-259 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LLMDOFAF_00953 | 2.7e-67 | mrnC | J | Involved in correct processing of both the 5' and 3' ends of 23S rRNA precursor. Processes 30S rRNA precursor transcript even in absence of ribonuclease 3 (Rnc) | ||
LLMDOFAF_00956 | 5.7e-135 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LLMDOFAF_00957 | 3.5e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
LLMDOFAF_00958 | 3.4e-155 | degV | S | DegV family | ||
LLMDOFAF_00959 | 1.8e-31 | K | helix-turn-helix | |||
LLMDOFAF_00960 | 1.6e-182 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
LLMDOFAF_00961 | 2e-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 | ||
LLMDOFAF_00962 | 9.5e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LLMDOFAF_00963 | 1.5e-35 | K | sequence-specific DNA binding | |||
LLMDOFAF_00965 | 0.0 | |||||
LLMDOFAF_00966 | 3.8e-173 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
LLMDOFAF_00967 | 4.3e-261 | XK27_03190 | 5.2.1.8 | S | hydrolases of the HAD superfamily | |
LLMDOFAF_00968 | 2.9e-18 | yebC | M | Membrane | ||
LLMDOFAF_00969 | 2.6e-80 | yebC | M | Membrane | ||
LLMDOFAF_00970 | 3.6e-66 | KT | response to antibiotic | |||
LLMDOFAF_00971 | 5.2e-75 | XK27_02470 | K | LytTr DNA-binding domain | ||
LLMDOFAF_00972 | 2.6e-121 | liaI | S | membrane | ||
LLMDOFAF_00973 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination | |
LLMDOFAF_00974 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
LLMDOFAF_00975 | 1.6e-11 | S | Protein of unknown function (DUF554) | |||
LLMDOFAF_00976 | 8.5e-32 | S | Protein of unknown function (DUF554) | |||
LLMDOFAF_00977 | 2.5e-47 | S | Protein of unknown function (DUF554) | |||
LLMDOFAF_00978 | 1.4e-133 | ecsA_2 | V | abc transporter atp-binding protein | ||
LLMDOFAF_00979 | 6.2e-288 | XK27_00765 | ||||
LLMDOFAF_00980 | 4.4e-141 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LLMDOFAF_00981 | 9e-226 | 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 | |
LLMDOFAF_00982 | 1.3e-08 | D | nuclear chromosome segregation | |||
LLMDOFAF_00983 | 9.7e-32 | yhaI | J | Protein of unknown function (DUF805) | ||
LLMDOFAF_00985 | 2.6e-30 | |||||
LLMDOFAF_00986 | 7.4e-27 | |||||
LLMDOFAF_00987 | 1.6e-65 | |||||
LLMDOFAF_00988 | 3.9e-173 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LLMDOFAF_00989 | 4.3e-47 | ftsL | D | cell division protein FtsL | ||
LLMDOFAF_00990 | 0.0 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
LLMDOFAF_00991 | 6.3e-185 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LLMDOFAF_00992 | 1.4e-221 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
LLMDOFAF_00994 | 1.3e-270 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
LLMDOFAF_00995 | 3.6e-70 | yutD | J | protein conserved in bacteria | ||
LLMDOFAF_00996 | 7.9e-224 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LLMDOFAF_00997 | 1.7e-93 | XK27_09885 | V | Glycopeptide antibiotics resistance protein | ||
LLMDOFAF_00999 | 9.1e-303 | mdlA | V | abc transporter atp-binding protein | ||
LLMDOFAF_01000 | 0.0 | mdlB | V | abc transporter atp-binding protein | ||
LLMDOFAF_01001 | 0.0 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
LLMDOFAF_01002 | 7.3e-237 | mesE | M | Transport protein ComB | ||
LLMDOFAF_01004 | 3.4e-239 | blpH | 2.7.13.3 | T | protein histidine kinase activity | |
LLMDOFAF_01005 | 7.4e-135 | agrA | KT | phosphorelay signal transduction system | ||
LLMDOFAF_01009 | 6.7e-26 | S | Bacteriocin class II with double-glycine leader peptide | |||
LLMDOFAF_01016 | 6.7e-98 | blpT | ||||
LLMDOFAF_01017 | 2.9e-28 | blpT | ||||
LLMDOFAF_01018 | 3e-47 | spiA | K | sequence-specific DNA binding | ||
LLMDOFAF_01021 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
LLMDOFAF_01022 | 2.3e-164 | gla | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
LLMDOFAF_01023 | 5e-44 | V | CAAX protease self-immunity | |||
LLMDOFAF_01024 | 4.6e-140 | cppA | E | CppA N-terminal | ||
LLMDOFAF_01025 | 4.5e-185 | ampC | V | COG1680 Beta-lactamase class C and other penicillin binding proteins | ||
LLMDOFAF_01026 | 1.2e-117 | ybbL | S | abc transporter atp-binding protein | ||
LLMDOFAF_01027 | 1.5e-127 | ybbM | S | transport system, permease component | ||
LLMDOFAF_01028 | 2.9e-87 | D | nuclear chromosome segregation | |||
LLMDOFAF_01029 | 1e-44 | hsdS_1 | 3.1.21.3 | V | type I restriction modification DNA specificity domain | |
LLMDOFAF_01030 | 2.1e-85 | yjcF | S | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
LLMDOFAF_01031 | 1.8e-147 | cah | 4.2.1.1 | P | carbonic anhydrase | |
LLMDOFAF_01032 | 0.0 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
LLMDOFAF_01033 | 1.4e-206 | 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 | |
LLMDOFAF_01035 | 1.2e-152 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
LLMDOFAF_01036 | 4.7e-163 | yxeN | P | ABC transporter (Permease | ||
LLMDOFAF_01037 | 4.5e-132 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
LLMDOFAF_01038 | 1.9e-09 | S | Protein of unknown function (DUF4059) | |||
LLMDOFAF_01039 | 1.9e-172 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LLMDOFAF_01040 | 5.1e-93 | rsmD | 2.1.1.171 | L | Methyltransferase | |
LLMDOFAF_01041 | 2.7e-88 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LLMDOFAF_01042 | 2.2e-196 | ylbL | T | Belongs to the peptidase S16 family | ||
LLMDOFAF_01043 | 1.3e-184 | yhcC | S | radical SAM protein | ||
LLMDOFAF_01044 | 1.4e-98 | ytqB | 2.1.1.176 | J | (SAM)-dependent | |
LLMDOFAF_01046 | 0.0 | yjcE | P | NhaP-type Na H and K H antiporters | ||
LLMDOFAF_01047 | 2.4e-144 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
LLMDOFAF_01048 | 2e-239 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
LLMDOFAF_01049 | 2e-157 | 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 | |
LLMDOFAF_01052 | 2.4e-75 | XK27_03180 | T | universal stress protein | ||
LLMDOFAF_01053 | 3.7e-240 | alaA | 2.6.1.2, 2.6.1.66 | E | Aminotransferase | |
LLMDOFAF_01054 | 1.2e-140 | codY | K | DNA-binding protein that represses the expression of many genes that are induced as cells make the transition from rapid exponential growth to stationary phase. It is a GTP-binding protein that senses the intracellular GTP concentration as an indicator of nutritional limitations. At low GTP concentration it no longer binds GTP and stop to act as a transcriptional repressor | ||
LLMDOFAF_01055 | 6.8e-101 | pncA | Q | isochorismatase | ||
LLMDOFAF_01056 | 1.6e-154 | hlpA | M | Belongs to the NlpA lipoprotein family | ||
LLMDOFAF_01057 | 6.7e-95 | 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 | |
LLMDOFAF_01058 | 1.3e-251 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
LLMDOFAF_01059 | 1.4e-47 | 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) | |
LLMDOFAF_01060 | 2.4e-270 | gatA | 6.3.5.6, 6.3.5.7 | J | 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) | |
LLMDOFAF_01061 | 7.8e-274 | gatB | 6.1.1.12, 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) | |
LLMDOFAF_01062 | 3.5e-13 | |||||
LLMDOFAF_01063 | 5.8e-24 | |||||
LLMDOFAF_01064 | 1.1e-153 | yicL | EG | COG0697 Permeases of the drug metabolite transporter (DMT) superfamily | ||
LLMDOFAF_01065 | 1.8e-98 | yqeG | S | hydrolase of the HAD superfamily | ||
LLMDOFAF_01066 | 1.7e-215 | yqeH | S | in Bacillus subtilis this enzyme appears to be involved in 30S ribosomal RNA subunit biogenesis | ||
LLMDOFAF_01067 | 3.5e-49 | yhbY | J | RNA-binding protein | ||
LLMDOFAF_01068 | 3.1e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
LLMDOFAF_01069 | 1.4e-107 | nadD | 2.7.6.3, 2.7.7.18 | H | HD superfamily hydrolase involved in NAD metabolism | |
LLMDOFAF_01070 | 6e-58 | rsfS | 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 | ||
LLMDOFAF_01071 | 2e-140 | yqeM | Q | Methyltransferase domain protein | ||
LLMDOFAF_01072 | 6.9e-206 | ylbM | S | Belongs to the UPF0348 family | ||
LLMDOFAF_01073 | 0.0 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
LLMDOFAF_01074 | 3.2e-110 | |||||
LLMDOFAF_01075 | 1.3e-56 | S | CD20-like family | |||
LLMDOFAF_01076 | 6e-11 | |||||
LLMDOFAF_01077 | 3.9e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
LLMDOFAF_01078 | 2.3e-133 | ecsA | V | abc transporter atp-binding protein | ||
LLMDOFAF_01079 | 2.7e-183 | ecsB | U | ABC transporter | ||
LLMDOFAF_01080 | 1.2e-151 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
LLMDOFAF_01081 | 3.1e-121 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
LLMDOFAF_01083 | 7.7e-227 | ytfP | S | Flavoprotein | ||
LLMDOFAF_01084 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
LLMDOFAF_01085 | 7.4e-64 | XK27_02560 | S | cog cog2151 | ||
LLMDOFAF_01086 | 1.2e-41 | WQ51_02910 | S | Protein of unknown function, DUF536 | ||
LLMDOFAF_01087 | 1.3e-105 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
LLMDOFAF_01088 | 1.4e-81 | K | transcriptional regulator, MerR family | |||
LLMDOFAF_01089 | 5.1e-47 | L | transposase activity | |||
LLMDOFAF_01090 | 1.2e-43 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
LLMDOFAF_01091 | 3.9e-26 | |||||
LLMDOFAF_01092 | 0.0 | ctpE | P | E1-E2 ATPase | ||
LLMDOFAF_01093 | 1.4e-54 | |||||
LLMDOFAF_01094 | 2.1e-30 | rpsT | J | rRNA binding | ||
LLMDOFAF_01095 | 1.9e-172 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
LLMDOFAF_01096 | 1.8e-107 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
LLMDOFAF_01097 | 1.2e-57 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
LLMDOFAF_01098 | 1.3e-97 | pdp | 2.4.2.2, 2.4.2.4 | F | Catalyzes the reversible phosphorolysis of thymidine, deoxyuridine and their analogues to their respective bases and 2-deoxyribose 1-phosphate | |
LLMDOFAF_01099 | 1.4e-22 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
LLMDOFAF_01100 | 4e-63 | deoC | 4.1.2.4, 5.4.2.8 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
LLMDOFAF_01101 | 1.3e-69 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
LLMDOFAF_01102 | 9.5e-192 | tcsA | S | ABC-type transport system, periplasmic component surface lipoprotein | ||
LLMDOFAF_01103 | 3.7e-282 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
LLMDOFAF_01104 | 4.7e-191 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
LLMDOFAF_01105 | 4.8e-171 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
LLMDOFAF_01106 | 8.9e-121 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
LLMDOFAF_01107 | 0.0 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
LLMDOFAF_01108 | 3.1e-81 | ypmB | S | Protein conserved in bacteria | ||
LLMDOFAF_01109 | 6.5e-218 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
LLMDOFAF_01110 | 1.7e-262 | asnS | 6.1.1.22 | J | Catalyzes a two-step reaction, first charging an asparagine molecule by linking its carboxyl group to the alpha-phosphate of ATP, followed by transfer of the aminoacyl-adenylate to its tRNA | |
LLMDOFAF_01111 | 9e-08 | |||||
LLMDOFAF_01112 | 1.3e-54 | bta | 1.8.1.8 | CO | cell redox homeostasis | |
LLMDOFAF_01113 | 3.1e-10 | L | thioesterase | |||
LLMDOFAF_01114 | 7.8e-143 | S | Macro domain protein | |||
LLMDOFAF_01115 | 4.8e-51 | trxA | O | Belongs to the thioredoxin family | ||
LLMDOFAF_01116 | 2.5e-26 | yccU | S | CoA-binding protein | ||
LLMDOFAF_01117 | 1.4e-144 | tatD | L | Hydrolase, tatd | ||
LLMDOFAF_01118 | 8.4e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
LLMDOFAF_01119 | 1.1e-156 | ksgA | 2.1.1.182 | 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 | |
LLMDOFAF_01121 | 2.6e-163 | rsgA | 3.1.3.100 | G | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
LLMDOFAF_01122 | 3e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
LLMDOFAF_01123 | 1.8e-118 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
LLMDOFAF_01124 | 6.9e-173 | rmuC | S | RmuC domain protein | ||
LLMDOFAF_01125 | 1.8e-178 | cbf | S | 3'-5' exoribonuclease yhaM | ||
LLMDOFAF_01126 | 1.1e-142 | purR | 2.4.2.7 | F | operon repressor | |
LLMDOFAF_01127 | 2.3e-69 | 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 | ||
LLMDOFAF_01128 | 6.7e-81 | 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 | ||
LLMDOFAF_01129 | 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 | ||
LLMDOFAF_01130 | 1.4e-189 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
LLMDOFAF_01131 | 7.4e-35 | yozE | S | Belongs to the UPF0346 family | ||
LLMDOFAF_01132 | 5.3e-161 | cvfB | S | Protein conserved in bacteria | ||
LLMDOFAF_01133 | 1.3e-91 | 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 | ||
LLMDOFAF_01134 | 4.9e-131 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LLMDOFAF_01135 | 2.9e-120 | sptS | 2.7.13.3 | T | Histidine kinase | |
LLMDOFAF_01136 | 1.6e-44 | K | Acetyltransferase (GNAT) family | |||
LLMDOFAF_01137 | 0.0 | lmrA2 | V | abc transporter atp-binding protein | ||
LLMDOFAF_01138 | 0.0 | lmrA1 | V | abc transporter atp-binding protein | ||
LLMDOFAF_01139 | 1.9e-77 | K | DNA-binding transcription factor activity | |||
LLMDOFAF_01140 | 1e-69 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LLMDOFAF_01141 | 1.8e-256 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LLMDOFAF_01142 | 2.1e-204 | nadD | 2.7.1.22, 2.7.7.1, 2.7.7.18, 3.6.1.55 | H | adenylyltransferase | |
LLMDOFAF_01143 | 1.1e-141 | 3.6.1.13, 3.6.1.55 | F | AdP-ribose pyrophosphatase | ||
LLMDOFAF_01144 | 1.6e-24 | U | response to pH | |||
LLMDOFAF_01146 | 3.3e-95 | ywlG | S | Belongs to the UPF0340 family | ||
LLMDOFAF_01147 | 1.2e-85 | treR | K | trehalose operon | ||
LLMDOFAF_01148 | 5.8e-21 | treR | K | DNA-binding transcription factor activity | ||
LLMDOFAF_01149 | 1.4e-54 | treB | 2.7.1.201 | G | PTS System | |
LLMDOFAF_01150 | 5.9e-66 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
LLMDOFAF_01151 | 1.2e-69 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
LLMDOFAF_01152 | 2.8e-38 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
LLMDOFAF_01153 | 4e-226 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LLMDOFAF_01154 | 1.7e-133 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LLMDOFAF_01155 | 3.1e-63 | adhE | 1.1.1.1, 1.2.1.10 | C | Dehydrogenase | |
LLMDOFAF_01156 | 6.3e-132 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LLMDOFAF_01157 | 1.1e-65 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LLMDOFAF_01158 | 8e-35 | adhE | 1.1.1.1, 1.2.1.10 | C | hydroxyacid-oxoacid transhydrogenase activity | |
LLMDOFAF_01159 | 5.5e-65 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LLMDOFAF_01160 | 9.2e-278 | thrC | 4.2.3.1 | E | Threonine synthase | |
LLMDOFAF_01161 | 3.2e-226 | norN | V | Mate efflux family protein | ||
LLMDOFAF_01162 | 1.8e-57 | asp | S | cog cog1302 | ||
LLMDOFAF_01163 | 7.6e-305 | yloV | S | kinase related to dihydroxyacetone kinase | ||
LLMDOFAF_01164 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
LLMDOFAF_01165 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LLMDOFAF_01166 | 1.4e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
LLMDOFAF_01167 | 0.0 | mfd | L | Couples transcription and DNA repair by recognizing RNA polymerase (RNAP) stalled at DNA lesions. Mediates ATP-dependent release of RNAP and its truncated transcript from the DNA, and recruitment of nucleotide excision repair machinery to the damaged site | ||
LLMDOFAF_01168 | 1.7e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
LLMDOFAF_01169 | 2.7e-61 | divIC | D | Septum formation initiator | ||
LLMDOFAF_01171 | 1.3e-240 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
LLMDOFAF_01172 | 5e-240 | tilS | 2.4.2.8, 6.3.4.19 | D | 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 | |
LLMDOFAF_01173 | 3.4e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LLMDOFAF_01174 | 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 | ||
LLMDOFAF_01175 | 2.4e-164 | L | Transposase | |||
LLMDOFAF_01176 | 1.2e-42 | capA | M | Bacterial capsule synthesis protein PGA_cap | ||
LLMDOFAF_01177 | 4.3e-109 | capA | M | Bacterial capsule synthesis protein | ||
LLMDOFAF_01178 | 1.5e-55 | capA | M | Bacterial capsule synthesis protein | ||
LLMDOFAF_01179 | 3.6e-39 | gcvR | T | UPF0237 protein | ||
LLMDOFAF_01180 | 1.7e-243 | XK27_08635 | S | UPF0210 protein | ||
LLMDOFAF_01181 | 2.4e-135 | ais | G | Phosphoglycerate mutase | ||
LLMDOFAF_01182 | 2.1e-143 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
LLMDOFAF_01183 | 1.3e-102 | acmA | 3.2.1.17 | NU | amidase activity | |
LLMDOFAF_01184 | 5.3e-198 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LLMDOFAF_01185 | 1.3e-71 | 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 | ||
LLMDOFAF_01186 | 7.5e-298 | dnaK | O | Heat shock 70 kDa protein | ||
LLMDOFAF_01187 | 3.1e-185 | 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 | ||
LLMDOFAF_01188 | 7.7e-140 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
LLMDOFAF_01189 | 1.6e-137 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
LLMDOFAF_01190 | 3.8e-31 | hmpT | S | membrane | ||
LLMDOFAF_01195 | 1.8e-167 | fhuR | K | transcriptional regulator (lysR family) | ||
LLMDOFAF_01196 | 8.8e-78 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LLMDOFAF_01197 | 1e-162 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
LLMDOFAF_01198 | 1.1e-87 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
LLMDOFAF_01199 | 4.9e-227 | pyrP | F | uracil Permease | ||
LLMDOFAF_01200 | 1e-173 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LLMDOFAF_01201 | 1.1e-211 | carA | 6.3.5.5 | F | carbamoyl-phosphate synthetase glutamine chain | |
LLMDOFAF_01202 | 0.0 | carB | 6.3.5.5 | F | carbamoyl-phosphate synthetase ammonia chain | |
LLMDOFAF_01203 | 8.4e-190 | L | Transposase | |||
LLMDOFAF_01204 | 1.7e-28 | potC | P | Binding-protein-dependent transport system inner membrane component | ||
LLMDOFAF_01205 | 8.9e-206 | potD | P | spermidine putrescine ABC transporter | ||
LLMDOFAF_01206 | 3.1e-268 | clcA | P | Chloride transporter, ClC family | ||
LLMDOFAF_01207 | 0.0 | prtS | 3.4.21.96 | O | Belongs to the peptidase S8 family | |
LLMDOFAF_01208 | 3e-63 | tdcF | 3.5.99.10 | J | endoribonuclease L-PSP | |
LLMDOFAF_01209 | 4e-124 | queC | 6.3.4.20 | F | Catalyzes the ATP-dependent conversion of 7-carboxy-7- deazaguanine (CDG) to 7-cyano-7-deazaguanine (preQ(0)) | |
LLMDOFAF_01210 | 2e-82 | queD | 4.1.2.50, 4.2.3.12 | H | synthase | |
LLMDOFAF_01211 | 2.9e-136 | queE | 1.97.1.4, 4.3.99.3 | H | Catalyzes the complex heterocyclic radical-mediated conversion of 6-carboxy-5,6,7,8-tetrahydropterin (CPH4) to 7- carboxy-7-deazaguanine (CDG), a step common to the biosynthetic pathways of all 7-deazapurine-containing compounds | |
LLMDOFAF_01212 | 6.5e-95 | queF | 1.7.1.13 | S | Belongs to the GTP cyclohydrolase I family. QueF type 1 subfamily | |
LLMDOFAF_01213 | 7.7e-20 | D | nuclear chromosome segregation | |||
LLMDOFAF_01214 | 7.4e-138 | yejC | S | cyclic nucleotide-binding protein | ||
LLMDOFAF_01215 | 1.2e-163 | rapZ | S | Displays ATPase and GTPase activities | ||
LLMDOFAF_01216 | 9.6e-183 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
LLMDOFAF_01217 | 8.7e-162 | whiA | K | May be required for sporulation | ||
LLMDOFAF_01218 | 2.8e-90 | pepD | E | Dipeptidase | ||
LLMDOFAF_01219 | 5.8e-41 | pepD | E | dipeptidase activity | ||
LLMDOFAF_01220 | 5.4e-32 | cspD | K | Cold shock protein domain | ||
LLMDOFAF_01221 | 9.4e-43 | K | Cold-Shock Protein | |||
LLMDOFAF_01222 | 1.4e-96 | V | VanZ like family | |||
LLMDOFAF_01223 | 7.6e-70 | supH | 3.1.3.102, 3.1.3.104 | Q | phosphatase activity | |
LLMDOFAF_01224 | 3.5e-29 | G | Belongs to the phosphoglycerate mutase family | |||
LLMDOFAF_01225 | 3.9e-61 | G | Belongs to the phosphoglycerate mutase family | |||
LLMDOFAF_01226 | 1.3e-199 | S | hmm pf01594 | |||
LLMDOFAF_01227 | 2e-18 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
LLMDOFAF_01228 | 3.5e-138 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
LLMDOFAF_01229 | 2.1e-35 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
LLMDOFAF_01230 | 4.9e-39 | S | granule-associated protein | |||
LLMDOFAF_01231 | 2e-294 | S | unusual protein kinase | |||
LLMDOFAF_01232 | 2.6e-15 | estA | E | Lysophospholipase L1 and related esterases | ||
LLMDOFAF_01233 | 6.1e-79 | estA | E | GDSL-like protein | ||
LLMDOFAF_01234 | 1.3e-159 | rssA | S | Phospholipase, patatin family | ||
LLMDOFAF_01235 | 1.3e-125 | 3.4.16.4 | M | Belongs to the peptidase S11 family | ||
LLMDOFAF_01236 | 3.9e-24 | 3.4.16.4 | M | Belongs to the peptidase S11 family | ||
LLMDOFAF_01237 | 3.8e-17 | dacA1 | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LLMDOFAF_01238 | 3e-218 | yeaB | K | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | ||
LLMDOFAF_01239 | 7.7e-128 | 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 | |
LLMDOFAF_01240 | 3.7e-235 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
LLMDOFAF_01241 | 4.4e-66 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
LLMDOFAF_01242 | 1.1e-37 | P | membrane protein (DUF2207) | |||
LLMDOFAF_01243 | 6e-185 | acoA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
LLMDOFAF_01244 | 3.7e-182 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
LLMDOFAF_01245 | 1.1e-200 | acoC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
LLMDOFAF_01246 | 0.0 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
LLMDOFAF_01247 | 6.4e-11 | 3.5.1.28 | NU | amidase activity | ||
LLMDOFAF_01248 | 2.7e-67 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
LLMDOFAF_01249 | 8.6e-187 | 3.5.1.28 | M | GBS Bsp-like repeat | ||
LLMDOFAF_01250 | 1.5e-133 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
LLMDOFAF_01251 | 7.6e-66 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
LLMDOFAF_01252 | 1.7e-60 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
LLMDOFAF_01253 | 3.7e-85 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
LLMDOFAF_01254 | 1.5e-33 | pulA | 3.2.1.1, 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
LLMDOFAF_01255 | 1e-165 | yclN | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
LLMDOFAF_01256 | 5.6e-167 | fatC | P | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
LLMDOFAF_01257 | 6.8e-136 | yclP | 3.6.3.34 | P | abc transporter atp-binding protein | |
LLMDOFAF_01258 | 2e-178 | fatB | P | ABC-type enterochelin transport system, periplasmic component | ||
LLMDOFAF_01259 | 3.2e-153 | ycdO | P | periplasmic lipoprotein involved in iron transport | ||
LLMDOFAF_01260 | 8.7e-234 | ycdB | P | peroxidase | ||
LLMDOFAF_01261 | 7.2e-303 | ywbL | P | COG0672 High-affinity Fe2 Pb2 permease | ||
LLMDOFAF_01262 | 9e-122 | tatC | U | Part of the twin-arginine translocation (Tat) system that transports large folded proteins containing a characteristic twin-arginine motif in their signal peptide across membranes | ||
LLMDOFAF_01263 | 4.6e-25 | tatA | U | protein secretion | ||
LLMDOFAF_01264 | 2.3e-23 | L | Transposase | |||
LLMDOFAF_01265 | 1.2e-304 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
LLMDOFAF_01266 | 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 |
LLMDOFAF_01269 | 2.9e-187 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
LLMDOFAF_01270 | 8.3e-196 | xerS | D | Site-specific tyrosine recombinase, which acts by catalyzing the cutting and rejoining of the recombining DNA molecules. Essential to convert dimers of the bacterial chromosome into monomers to permit their segregation at cell division | ||
LLMDOFAF_01271 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
LLMDOFAF_01272 | 1.9e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LLMDOFAF_01273 | 2.3e-139 | 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 | |
LLMDOFAF_01274 | 1e-150 | 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 | |
LLMDOFAF_01275 | 1.2e-155 | pstA | P | phosphate transport system permease | ||
LLMDOFAF_01276 | 2.5e-156 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LLMDOFAF_01277 | 3.3e-158 | pstS | P | phosphate | ||
LLMDOFAF_01278 | 7.9e-257 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
LLMDOFAF_01279 | 5e-142 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
LLMDOFAF_01280 | 1.9e-43 | yktA | S | Belongs to the UPF0223 family | ||
LLMDOFAF_01281 | 1.4e-71 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
LLMDOFAF_01282 | 5.3e-175 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
LLMDOFAF_01283 | 4.9e-151 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
LLMDOFAF_01284 | 2.6e-49 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
LLMDOFAF_01285 | 1.7e-96 | XK27_04775 | S | hemerythrin HHE cation binding domain | ||
LLMDOFAF_01286 | 1.1e-110 | hsdS2 | 2.1.1.72 | V | Type I restriction modification DNA specificity domain | |
LLMDOFAF_01287 | 3.5e-88 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
LLMDOFAF_01288 | 9.3e-62 | S | haloacid dehalogenase-like hydrolase | |||
LLMDOFAF_01289 | 1.8e-59 | Q | phosphatase activity | |||
LLMDOFAF_01290 | 4.6e-241 | metY | 2.5.1.49 | E | o-acetylhomoserine | |
LLMDOFAF_01291 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
LLMDOFAF_01292 | 1.8e-240 | agcS | E | (Alanine) symporter | ||
LLMDOFAF_01293 | 1.6e-247 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
LLMDOFAF_01294 | 4e-99 | yfiF3 | K | sequence-specific DNA binding | ||
LLMDOFAF_01295 | 9.8e-35 | 3.1.3.6, 3.1.4.16 | F | nucleotide catabolic process | ||
LLMDOFAF_01296 | 8.1e-114 | sasH | 3.1.3.5, 3.6.1.45 | F | Belongs to the 5'-nucleotidase family | |
LLMDOFAF_01298 | 2.3e-20 | yecS | P | amino acid transport | ||
LLMDOFAF_01299 | 1.4e-62 | yecS | P | ABC transporter (Permease | ||
LLMDOFAF_01300 | 1.6e-266 | dtpT | E | transporter | ||
LLMDOFAF_01301 | 7.5e-112 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
LLMDOFAF_01302 | 2.4e-127 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
LLMDOFAF_01303 | 9.5e-32 | csm6 | S | Psort location Cytoplasmic, score | ||
LLMDOFAF_01305 | 2e-205 | csm5 | L | CRISPR-associated RAMP protein, Csm5 family | ||
LLMDOFAF_01306 | 2.3e-167 | csm4 | L | CRISPR-associated RAMP protein, Csm4 family | ||
LLMDOFAF_01307 | 1.6e-117 | csm3 | L | RAMP superfamily | ||
LLMDOFAF_01308 | 2.5e-62 | csm2 | L | Csm2 Type III-A | ||
LLMDOFAF_01309 | 1.2e-210 | csm1 | S | CRISPR-associated protein Csm1 family | ||
LLMDOFAF_01310 | 1.1e-204 | csm1 | S | CRISPR-associated protein Csm1 family | ||
LLMDOFAF_01311 | 6.8e-133 | cas6 | S | CRISPR-associated endoribonuclease Cas6 | ||
LLMDOFAF_01312 | 9.8e-55 | cas2 | 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 sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
LLMDOFAF_01313 | 6e-188 | 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 | ||
LLMDOFAF_01314 | 1.1e-175 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
LLMDOFAF_01315 | 1.3e-148 | pyrK | C | Responsible for channeling the electrons from the oxidation of dihydroorotate from the FMN redox center in the PyrD type B subunit to the ultimate electron acceptor NAD( ) | ||
LLMDOFAF_01316 | 5.9e-97 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1 family | |
LLMDOFAF_01317 | 4.3e-118 | S | TraX protein | |||
LLMDOFAF_01319 | 3.5e-28 | 3.4.13.21 | I | Protein conserved in bacteria | ||
LLMDOFAF_01320 | 8.1e-90 | FNV0100 | F | Belongs to the Nudix hydrolase family | ||
LLMDOFAF_01321 | 3.7e-190 | |||||
LLMDOFAF_01322 | 9.2e-311 | FbpA | K | RNA-binding protein homologous to eukaryotic snRNP | ||
LLMDOFAF_01324 | 3.6e-18 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
LLMDOFAF_01325 | 3.6e-14 | yclQ | P | ABC-type enterochelin transport system, periplasmic component | ||
LLMDOFAF_01326 | 8.3e-119 | gph | 3.1.3.18 | S | HAD hydrolase, family IA, variant 1 | |
LLMDOFAF_01327 | 1.2e-143 | 2.4.2.3 | F | Phosphorylase superfamily | ||
LLMDOFAF_01330 | 4.5e-79 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
LLMDOFAF_01331 | 7.9e-17 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
LLMDOFAF_01332 | 6e-08 | S | Hydrolases of the alpha beta superfamily | |||
LLMDOFAF_01333 | 6.2e-196 | adhB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
LLMDOFAF_01334 | 2.7e-210 | hemH | 4.99.1.1, 4.99.1.9 | H | Catalyzes the ferrous insertion into protoporphyrin IX | |
LLMDOFAF_01335 | 1.8e-159 | czcD | P | cation diffusion facilitator family transporter | ||
LLMDOFAF_01336 | 9e-98 | K | Transcriptional regulator, TetR family | |||
LLMDOFAF_01337 | 1.6e-10 | |||||
LLMDOFAF_01338 | 2.8e-115 | IQ | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
LLMDOFAF_01339 | 6.4e-104 | V | ABC transporter (Permease | |||
LLMDOFAF_01340 | 1.9e-22 | yocD | 3.4.17.13 | V | carboxypeptidase activity | |
LLMDOFAF_01341 | 3.8e-87 | yocD | 3.4.17.13 | V | proteins, homologs of microcin C7 resistance protein MccF | |
LLMDOFAF_01343 | 1.6e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LLMDOFAF_01344 | 1.7e-182 | 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 | ||
LLMDOFAF_01345 | 5.5e-83 | S | Putative small multi-drug export protein | |||
LLMDOFAF_01346 | 1.8e-75 | ctsR | K | Belongs to the CtsR family | ||
LLMDOFAF_01347 | 0.0 | clpC | O | Belongs to the ClpA ClpB family | ||
LLMDOFAF_01348 | 7e-127 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LLMDOFAF_01349 | 1.7e-52 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LLMDOFAF_01350 | 3.5e-97 | S | reductase | |||
LLMDOFAF_01351 | 2.6e-55 | badR | K | DNA-binding transcription factor activity | ||
LLMDOFAF_01352 | 1.9e-36 | XK27_02060 | S | Transglycosylase associated protein | ||
LLMDOFAF_01353 | 2.3e-237 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
LLMDOFAF_01354 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
LLMDOFAF_01359 | 1.9e-07 | |||||
LLMDOFAF_01360 | 1.9e-57 | L | Transposase | |||
LLMDOFAF_01362 | 0.0 | ddpA | E | ABC transporter substrate-binding protein | ||
LLMDOFAF_01363 | 2.8e-188 | dppB | P | COG0601 ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
LLMDOFAF_01364 | 1.8e-141 | dppC | P | N-terminal TM domain of oligopeptide transport permease C | ||
LLMDOFAF_01365 | 0.0 | P | Belongs to the ABC transporter superfamily | |||
LLMDOFAF_01366 | 3e-13 | mesE | M | Transport protein ComB | ||
LLMDOFAF_01367 | 2.6e-95 | cysE | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
LLMDOFAF_01368 | 9.1e-220 | metC | 2.5.1.48, 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
LLMDOFAF_01369 | 2.3e-170 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
LLMDOFAF_01370 | 1.5e-194 | 3.1.21.3 | L | Subunit R is required for both nuclease and ATPase activities, but not for modification | ||
LLMDOFAF_01371 | 3e-52 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LLMDOFAF_01372 | 5.6e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LLMDOFAF_01373 | 8.2e-28 | ytrF | V | efflux transmembrane transporter activity | ||
LLMDOFAF_01374 | 3.1e-31 | V | efflux transmembrane transporter activity | |||
LLMDOFAF_01375 | 3.6e-35 | V | efflux transmembrane transporter activity | |||
LLMDOFAF_01376 | 2.2e-134 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
LLMDOFAF_01377 | 1.8e-127 | tnp | L | Transposase | ||
LLMDOFAF_01378 | 2e-20 | S | phage tail | |||
LLMDOFAF_01379 | 7.1e-130 | S | EcsC protein family | |||
LLMDOFAF_01380 | 2.4e-23 | S | phage tail tape measure protein | |||
LLMDOFAF_01381 | 9.8e-71 | L | Phage integrase family | |||
LLMDOFAF_01383 | 1.9e-225 | nodC | 2.4.1.212 | GT2 | M | Chitin synthase |
LLMDOFAF_01384 | 2.4e-214 | ugd | 1.1.1.22 | M | Belongs to the UDP-glucose GDP-mannose dehydrogenase family | |
LLMDOFAF_01385 | 0.0 | copB | 3.6.3.4 | P | P-type ATPase | |
LLMDOFAF_01386 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
LLMDOFAF_01387 | 8.1e-45 | L | Transposase | |||
LLMDOFAF_01388 | 4.1e-158 | L | COG2801 Transposase and inactivated derivatives | |||
LLMDOFAF_01389 | 1e-23 | oppF | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_01390 | 3.8e-45 | oppF | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_01391 | 1.4e-40 | tatD | L | Hydrolase, tatd | ||
LLMDOFAF_01392 | 6.7e-218 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
LLMDOFAF_01393 | 1e-110 | L | Integrase core domain protein | |||
LLMDOFAF_01394 | 4.3e-23 | L | Transposase | |||
LLMDOFAF_01395 | 8.9e-18 | L | transposase activity | |||
LLMDOFAF_01396 | 8.2e-182 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
LLMDOFAF_01397 | 9.8e-174 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
LLMDOFAF_01398 | 5.4e-150 | nadK | 2.7.1.23 | H | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
LLMDOFAF_01399 | 5.5e-121 | yjbM | 2.7.6.5 | S | Gtp pyrophosphokinase | |
LLMDOFAF_01400 | 1.5e-103 | yjbK | S | Adenylate cyclase | ||
LLMDOFAF_01401 | 1.2e-177 | 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) | |
LLMDOFAF_01402 | 2.4e-206 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
LLMDOFAF_01403 | 3.1e-59 | XK27_04120 | S | Putative amino acid metabolism | ||
LLMDOFAF_01404 | 3.3e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
LLMDOFAF_01405 | 7.2e-132 | puuD | T | peptidase C26 | ||
LLMDOFAF_01406 | 1.2e-115 | radC | E | Belongs to the UPF0758 family | ||
LLMDOFAF_01407 | 1.7e-268 | M | Psort location CytoplasmicMembrane, score | |||
LLMDOFAF_01408 | 0.0 | rgpF | M | Rhamnan synthesis protein F | ||
LLMDOFAF_01409 | 2e-305 | GT4 | M | transferase activity, transferring glycosyl groups | ||
LLMDOFAF_01410 | 6.4e-229 | rgpD | 3.6.3.38 | P | Part of the ABC transporter complex TagGH involved in teichoic acids export. Responsible for energy coupling to the transport system | |
LLMDOFAF_01411 | 2.1e-143 | rgpC | GM | Transport permease protein | ||
LLMDOFAF_01412 | 4.9e-176 | rgpB | GT2 | M | Glycosyltransferase, group 2 family protein | |
LLMDOFAF_01413 | 1.8e-228 | rgpA | GT4 | M | Domain of unknown function (DUF1972) | |
LLMDOFAF_01414 | 8.2e-153 | 2.4.1.60 | S | Glycosyltransferase group 2 family protein | ||
LLMDOFAF_01415 | 4.6e-42 | S | Uncharacterized conserved protein (DUF2304) | |||
LLMDOFAF_01416 | 6.9e-130 | arnC | M | group 2 family protein | ||
LLMDOFAF_01417 | 9.5e-183 | cpsIaJ | S | Glycosyltransferase like family 2 | ||
LLMDOFAF_01418 | 9.3e-186 | S | Glycosyltransferase like family 2 | |||
LLMDOFAF_01419 | 9.4e-223 | amrA | S | membrane protein involved in the export of O-antigen and teichoic acid | ||
LLMDOFAF_01420 | 6.9e-161 | rfbD | 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 | |
LLMDOFAF_01421 | 5.3e-237 | S | Predicted membrane protein (DUF2142) | |||
LLMDOFAF_01422 | 1.7e-173 | yfdH | GT2 | M | COG0463, glycosyltransferases involved in cell wall biogenesis | |
LLMDOFAF_01423 | 3.4e-55 | yitW | K | metal-sulfur cluster biosynthetic enzyme | ||
LLMDOFAF_01424 | 1.1e-201 | 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 | ||
LLMDOFAF_01425 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LLMDOFAF_01426 | 5.5e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
LLMDOFAF_01427 | 1.1e-136 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LLMDOFAF_01428 | 1.6e-202 | arcT | 2.6.1.1 | E | Aminotransferase | |
LLMDOFAF_01429 | 6.5e-137 | ET | ABC transporter | |||
LLMDOFAF_01430 | 7.5e-144 | ET | Belongs to the bacterial solute-binding protein 3 family | |||
LLMDOFAF_01431 | 2.9e-84 | mutT | 3.6.1.55 | F | Nudix family | |
LLMDOFAF_01432 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
LLMDOFAF_01433 | 2.5e-56 | V | CAAX protease self-immunity | |||
LLMDOFAF_01434 | 2.4e-33 | S | CAAX amino terminal protease family protein | |||
LLMDOFAF_01435 | 0.0 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
LLMDOFAF_01436 | 6e-137 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LLMDOFAF_01437 | 1.1e-16 | XK27_00735 | ||||
LLMDOFAF_01438 | 1.4e-248 | 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 | ||
LLMDOFAF_01440 | 2.1e-134 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LLMDOFAF_01443 | 5.5e-65 | paaI | Q | protein possibly involved in aromatic compounds catabolism | ||
LLMDOFAF_01444 | 4.7e-51 | ycaO | O | OsmC-like protein | ||
LLMDOFAF_01445 | 1.7e-154 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
LLMDOFAF_01447 | 1.6e-112 | csn2 | S | CRISPR-associated protein (Cas_Csn2) | ||
LLMDOFAF_01448 | 2.6e-55 | cas2 | 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 sequences complementary to antecedent mobile elements and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Functions as a ssRNA-specific endoribonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
LLMDOFAF_01449 | 1.5e-163 | 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 | ||
LLMDOFAF_01450 | 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 | ||
LLMDOFAF_01451 | 6.7e-116 | serB | 3.1.3.3 | E | phosphoserine phosphatase | |
LLMDOFAF_01452 | 3.2e-298 | ezrA | D | modulates the frequency and position of FtsZ ring formation. Inhibits FtsZ ring formation at polar sites. Interacts either with FtsZ or with one of its binding partners to promote depolymerization | ||
LLMDOFAF_01453 | 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 | |
LLMDOFAF_01454 | 2.6e-109 | 3.1.3.18 | S | IA, variant 1 | ||
LLMDOFAF_01455 | 2.2e-117 | lrgB | M | effector of murein hydrolase | ||
LLMDOFAF_01456 | 7.7e-56 | lrgA | S | Effector of murein hydrolase LrgA | ||
LLMDOFAF_01458 | 6.4e-60 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
LLMDOFAF_01459 | 3.1e-56 | ogt | 2.1.1.63, 3.2.2.20 | L | methylated-DNA-[protein]-cysteine S-methyltransferase activity | |
LLMDOFAF_01460 | 1.1e-220 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LLMDOFAF_01461 | 3.9e-104 | wecD | M | Acetyltransferase GNAT family | ||
LLMDOFAF_01462 | 1.3e-209 | 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 | |
LLMDOFAF_01463 | 4.6e-58 | GK | ROK family | |||
LLMDOFAF_01464 | 2.1e-25 | GK | ROK family | |||
LLMDOFAF_01465 | 8.1e-72 | gloA | 4.4.1.5 | E | Lactoylglutathione lyase | |
LLMDOFAF_01466 | 1.7e-47 | XK27_08050 | O | stress-induced mitochondrial fusion | ||
LLMDOFAF_01467 | 1.3e-19 | XK27_08050 | O | HflC and HflK could regulate a protease | ||
LLMDOFAF_01468 | 2.3e-206 | potD | P | spermidine putrescine ABC transporter | ||
LLMDOFAF_01469 | 3e-134 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
LLMDOFAF_01470 | 3.7e-140 | potB | P | ABC-type spermidine putrescine transport system, permease component I | ||
LLMDOFAF_01471 | 1.2e-213 | potA | 3.6.3.30, 3.6.3.31 | P | Part of the ABC transporter complex PotABCD involved in spermidine putrescine import. Responsible for energy coupling to the transport system | |
LLMDOFAF_01472 | 7.8e-171 | murB | 1.3.1.98 | M | cell wall formation | |
LLMDOFAF_01473 | 2.9e-87 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
LLMDOFAF_01474 | 1.2e-61 | folB | 1.13.11.81, 2.5.1.15, 2.7.6.3, 4.1.2.25, 5.1.99.8 | H | Catalyzes the conversion of 7,8-dihydroneopterin to 6- hydroxymethyl-7,8-dihydropterin | |
LLMDOFAF_01475 | 1.2e-298 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LLMDOFAF_01476 | 1.2e-146 | folP | 2.5.1.15, 2.7.6.3 | 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 | |
LLMDOFAF_01477 | 1e-99 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
LLMDOFAF_01478 | 0.0 | ydaO | E | amino acid | ||
LLMDOFAF_01479 | 1.1e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
LLMDOFAF_01480 | 4.1e-37 | ylqC | L | Belongs to the UPF0109 family | ||
LLMDOFAF_01481 | 2.4e-43 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
LLMDOFAF_01482 | 6.9e-172 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
LLMDOFAF_01483 | 8.2e-159 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
LLMDOFAF_01484 | 2.1e-74 | S | QueT transporter | |||
LLMDOFAF_01485 | 2.5e-08 | ribD | 1.1.1.193, 3.5.4.26 | L | Transposase DDE domain | |
LLMDOFAF_01486 | 1.1e-89 | ribD | 1.1.1.193, 3.5.4.26 | L | Transposase DDE domain | |
LLMDOFAF_01487 | 1.9e-186 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
LLMDOFAF_01488 | 1.4e-92 | 3.6.4.12 | K | Divergent AAA domain protein | ||
LLMDOFAF_01489 | 5.9e-24 | 3.6.4.12 | ||||
LLMDOFAF_01490 | 7.7e-112 | EGP | Major facilitator Superfamily | |||
LLMDOFAF_01491 | 4.7e-56 | EGP | Major facilitator Superfamily | |||
LLMDOFAF_01492 | 1.8e-56 | amd | 3.5.1.47 | E | COG1473 Metal-dependent amidase aminoacylase carboxypeptidase | |
LLMDOFAF_01493 | 1.5e-233 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
LLMDOFAF_01494 | 3e-246 | cps1C | S | Polysaccharide biosynthesis protein | ||
LLMDOFAF_01495 | 2e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
LLMDOFAF_01496 | 4.7e-115 | hrtB | V | MacB-like periplasmic core domain | ||
LLMDOFAF_01497 | 1.6e-18 | L | Integrase core domain | |||
LLMDOFAF_01500 | 7e-27 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
LLMDOFAF_01501 | 1.1e-43 | Q | the current gene model (or a revised gene model) may contain a frame shift | |||
LLMDOFAF_01503 | 3.2e-17 | S | Domain of unknown function (DUF4649) | |||
LLMDOFAF_01504 | 3.3e-178 | XK27_08835 | S | ABC transporter substrate binding protein | ||
LLMDOFAF_01505 | 4e-148 | XK27_08840 | S | Belongs to the binding-protein-dependent transport system permease family | ||
LLMDOFAF_01506 | 1.2e-135 | XK27_08845 | S | abc transporter atp-binding protein | ||
LLMDOFAF_01507 | 3.5e-310 | rnjB | S | 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 | ||
LLMDOFAF_01508 | 9.2e-152 | estA | CE1 | S | Putative esterase | |
LLMDOFAF_01509 | 4.7e-126 | XK27_08875 | O | Zinc-dependent metalloprotease | ||
LLMDOFAF_01510 | 5.5e-14 | XK27_08880 | ||||
LLMDOFAF_01511 | 2.3e-75 | fld | C | Flavodoxin | ||
LLMDOFAF_01512 | 6.4e-282 | clcA | P | Chloride transporter, ClC family | ||
LLMDOFAF_01513 | 5.1e-41 | pheA | 1.3.1.12, 2.3.1.79, 4.2.1.51, 5.4.99.5 | E | Chorismate mutase | |
LLMDOFAF_01514 | 3.2e-220 | XK27_05110 | P | chloride | ||
LLMDOFAF_01515 | 8.5e-57 | 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 | ||
LLMDOFAF_01518 | 2.1e-19 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
LLMDOFAF_01519 | 4.2e-164 | miaA | 2.5.1.75 | J | 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) | |
LLMDOFAF_01520 | 1.6e-88 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
LLMDOFAF_01521 | 3.2e-295 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
LLMDOFAF_01522 | 4.2e-175 | birA | 6.3.4.15 | HK | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
LLMDOFAF_01523 | 2.1e-203 | 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 | |
LLMDOFAF_01524 | 0.0 | 5.1.3.2 | GM | Psort location CytoplasmicMembrane, score | ||
LLMDOFAF_01525 | 2.2e-168 | |||||
LLMDOFAF_01526 | 0.0 | S | Uncharacterised protein conserved in bacteria (DUF2194) | |||
LLMDOFAF_01527 | 4.3e-277 | pelF | GT4 | M | Domain of unknown function (DUF3492) | |
LLMDOFAF_01528 | 3.8e-199 | pelG | M | Putative exopolysaccharide Exporter (EPS-E) | ||
LLMDOFAF_01529 | 2.3e-49 | pelG | S | Putative exopolysaccharide Exporter (EPS-E) | ||
LLMDOFAF_01530 | 1.5e-211 | cotH | M | CotH kinase protein | ||
LLMDOFAF_01531 | 8.4e-53 | G | Domain of unknown function (DUF4832) | |||
LLMDOFAF_01532 | 2.2e-21 | G | Domain of unknown function (DUF4832) | |||
LLMDOFAF_01533 | 2.7e-196 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LLMDOFAF_01535 | 7.7e-233 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LLMDOFAF_01536 | 1.2e-25 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
LLMDOFAF_01537 | 2.4e-124 | endA | F | DNA RNA non-specific endonuclease | ||
LLMDOFAF_01538 | 1.7e-111 | tcyB_2 | P | ABC transporter (permease) | ||
LLMDOFAF_01539 | 5.9e-118 | gltJ | P | ABC transporter (Permease | ||
LLMDOFAF_01540 | 3.1e-150 | peb1A | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
LLMDOFAF_01541 | 2.1e-140 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LLMDOFAF_01542 | 9.9e-129 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LLMDOFAF_01543 | 1.5e-247 | vicK | 2.7.13.3 | T | Histidine kinase | |
LLMDOFAF_01544 | 2.1e-154 | vicX | 3.1.26.11 | S | Metal-dependent hydrolases of the beta-lactamase superfamily I | |
LLMDOFAF_01545 | 1.8e-231 | murM | 2.3.2.10, 2.3.2.16 | V | protein involved in methicillin resistance | |
LLMDOFAF_01546 | 1.2e-146 | yidA | S | hydrolases of the HAD superfamily | ||
LLMDOFAF_01547 | 6.3e-51 | XK27_00115 | 2.3.1.128 | K | acetyltransferase | |
LLMDOFAF_01548 | 2.6e-67 | ywiB | S | Domain of unknown function (DUF1934) | ||
LLMDOFAF_01549 | 0.0 | pacL | 3.6.3.8 | P | cation transport ATPase | |
LLMDOFAF_01550 | 5.2e-136 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
LLMDOFAF_01551 | 1.1e-180 | yjjH | S | Calcineurin-like phosphoesterase | ||
LLMDOFAF_01552 | 1.2e-202 | queG | 1.17.99.6 | C | Catalyzes the conversion of epoxyqueuosine (oQ) to queuosine (Q), which is a hypermodified base found in the wobble positions of tRNA(Asp), tRNA(Asn), tRNA(His) and tRNA(Tyr) | |
LLMDOFAF_01553 | 7.4e-183 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
LLMDOFAF_01554 | 2.5e-124 | ftsE | D | cell division ATP-binding protein FtsE | ||
LLMDOFAF_01555 | 3.6e-163 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
LLMDOFAF_01556 | 4.6e-93 | mutX | 3.6.1.55 | F | NTP pyrophosphohydrolases including oxidative damage repair enzymes | |
LLMDOFAF_01557 | 6.2e-176 | yubA | S | permease | ||
LLMDOFAF_01558 | 3.7e-224 | G | COG0457 FOG TPR repeat | |||
LLMDOFAF_01559 | 4.2e-98 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
LLMDOFAF_01560 | 1.4e-234 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
LLMDOFAF_01561 | 2.9e-90 | ebsA | S | Family of unknown function (DUF5322) | ||
LLMDOFAF_01562 | 3.9e-15 | M | LysM domain | |||
LLMDOFAF_01563 | 6.6e-122 | cmk | 1.17.7.4, 2.5.1.19, 2.7.1.26, 2.7.4.25, 2.7.7.2, 6.3.2.1 | F | Belongs to the cytidylate kinase family. Type 1 subfamily | |
LLMDOFAF_01564 | 3.5e-86 | 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 | ||
LLMDOFAF_01565 | 2.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
LLMDOFAF_01566 | 1.5e-56 | 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 | ||
LLMDOFAF_01567 | 4.7e-24 | L | Transposase | |||
LLMDOFAF_01568 | 6.9e-86 | XK27_03610 | K | Gnat family | ||
LLMDOFAF_01569 | 6.4e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
LLMDOFAF_01570 | 2.1e-276 | pepV | 3.5.1.18 | E | Dipeptidase | |
LLMDOFAF_01571 | 2.4e-112 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
LLMDOFAF_01572 | 9.1e-13 | V | Glucan-binding protein C | |||
LLMDOFAF_01574 | 1.7e-122 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
LLMDOFAF_01575 | 3.8e-237 | deoB | 5.4.2.7 | G | Phosphotransfer between the C1 and C5 carbon atoms of pentose | |
LLMDOFAF_01576 | 8.1e-41 | S | Protein of unknown function (DUF1697) | |||
LLMDOFAF_01577 | 4e-150 | punA | 2.4.2.1 | F | The purine nucleoside phosphorylases catalyze the phosphorolytic breakdown of the N-glycosidic bond in the beta- (deoxy)ribonucleoside molecules, with the formation of the corresponding free purine bases and pentose-1-phosphate | |
LLMDOFAF_01578 | 9.4e-66 | clcA_2 | P | chloride | ||
LLMDOFAF_01579 | 3.7e-67 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
LLMDOFAF_01580 | 1.5e-30 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
LLMDOFAF_01581 | 2.4e-130 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
LLMDOFAF_01582 | 8e-258 | cps4A | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
LLMDOFAF_01583 | 4.6e-137 | cpsB | 3.1.3.48 | GM | Capsular polysaccharide biosynthesis protein | |
LLMDOFAF_01584 | 1.9e-116 | cps4C | M | biosynthesis protein | ||
LLMDOFAF_01585 | 9.7e-119 | cpsD | D | COG0489 ATPases involved in chromosome partitioning | ||
LLMDOFAF_01586 | 2.4e-256 | cpsE | M | Exopolysaccharide biosynthesis polyprenyl glycosylphosphotransferase | ||
LLMDOFAF_01587 | 2.4e-31 | rgpAc | GT4 | M | Domain of unknown function (DUF1972) | |
LLMDOFAF_01588 | 3.3e-88 | cpsF | M | Oligosaccharide biosynthesis protein Alg14 like | ||
LLMDOFAF_01589 | 2e-91 | pssE | S | Glycosyltransferase family 28 C-terminal domain | ||
LLMDOFAF_01590 | 4.6e-202 | GT4 | M | Glycosyltransferase, group 1 family protein | ||
LLMDOFAF_01591 | 7.6e-174 | rgpB | GT2 | S | Glycosyl transferase family 2 | |
LLMDOFAF_01592 | 5.8e-202 | cps1B | GT2,GT4 | M | Glycosyl transferases group 1 | |
LLMDOFAF_01594 | 1.1e-183 | M | Glycosyltransferase, group 2 family protein | |||
LLMDOFAF_01595 | 2.8e-93 | pat | 2.3.1.183 | M | acetyltransferase | |
LLMDOFAF_01596 | 7.3e-82 | alkD | L | Dna alkylation repair | ||
LLMDOFAF_01597 | 7.3e-200 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
LLMDOFAF_01598 | 2.3e-173 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LLMDOFAF_01599 | 8.4e-125 | 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 | |
LLMDOFAF_01600 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
LLMDOFAF_01601 | 1.1e-197 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
LLMDOFAF_01602 | 9.9e-94 | paiA | 2.3.1.57 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
LLMDOFAF_01603 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
LLMDOFAF_01605 | 2e-55 | nrdD_1 | 1.1.98.6, 1.17.4.1 | F | Ribonucleoside-triphosphate reductase | |
LLMDOFAF_01606 | 7.7e-241 | XK27_08130 | K | Transcriptional regulators containing a DNA-binding HTH domain and an aminotransferase domain (MocR family) and their eukaryotic orthologs | ||
LLMDOFAF_01608 | 2e-86 | S | ECF-type riboflavin transporter, S component | |||
LLMDOFAF_01609 | 5.5e-42 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
LLMDOFAF_01610 | 9.3e-87 | pdxK | 2.7.1.35 | H | Belongs to the pyridoxine kinase family | |
LLMDOFAF_01611 | 5.6e-84 | XK27_01265 | S | ECF-type riboflavin transporter, S component | ||
LLMDOFAF_01612 | 1.9e-294 | yfmM | S | abc transporter atp-binding protein | ||
LLMDOFAF_01613 | 3.4e-258 | noxE | P | NADH oxidase | ||
LLMDOFAF_01614 | 1.1e-181 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
LLMDOFAF_01615 | 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 | |
LLMDOFAF_01616 | 1.7e-134 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
LLMDOFAF_01617 | 1.4e-71 | yaeR | E | COG0346 Lactoylglutathione lyase and related lyases | ||
LLMDOFAF_01618 | 1.8e-165 | ypuA | S | secreted protein | ||
LLMDOFAF_01619 | 3.3e-26 | L | Transposase (IS116 IS110 IS902 family) | |||
LLMDOFAF_01620 | 4.2e-71 | L | Transposase (IS116 IS110 IS902 family) | |||
LLMDOFAF_01622 | 1.7e-184 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LLMDOFAF_01623 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
LLMDOFAF_01624 | 2.2e-34 | nrdH | O | Glutaredoxin | ||
LLMDOFAF_01625 | 0.0 | acnA | 4.2.1.3 | C | Catalyzes the isomerization of citrate to isocitrate via cis-aconitate | |
LLMDOFAF_01626 | 6.7e-212 | citZ | 2.3.3.1 | C | Belongs to the citrate synthase family | |
LLMDOFAF_01627 | 2.3e-223 | icd | 1.1.1.42 | C | Isocitrate dehydrogenase | |
LLMDOFAF_01628 | 7.9e-39 | ptsH | G | phosphocarrier protein Hpr | ||
LLMDOFAF_01629 | 0.0 | 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) | |
LLMDOFAF_01630 | 1.1e-264 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
LLMDOFAF_01631 | 9.6e-29 | 6.3.2.2, 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | ||
LLMDOFAF_01632 | 9.3e-179 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
LLMDOFAF_01633 | 2.1e-114 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
LLMDOFAF_01634 | 0.0 | uup | S | abc transporter atp-binding protein | ||
LLMDOFAF_01635 | 2.2e-131 | pip | 1.11.1.10 | S | Alpha beta hydrolase | |
LLMDOFAF_01636 | 0.0 | mprF | 2.3.2.3 | J | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | |
LLMDOFAF_01637 | 8.7e-150 | cobQ | S | glutamine amidotransferase | ||
LLMDOFAF_01638 | 7.5e-255 | murD | 3.4.21.10, 6.3.2.13, 6.3.2.9 | M | Mur ligase, middle domain protein | |
LLMDOFAF_01639 | 5.6e-124 | dacA | 2.7.7.85 | S | Catalyzes the condensation of 2 ATP molecules into cyclic di-AMP (c-di-AMP), a second messenger used to regulate differing processes in different bacteria | |
LLMDOFAF_01640 | 6e-169 | ybbR | S | Protein conserved in bacteria | ||
LLMDOFAF_01641 | 1.5e-250 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
LLMDOFAF_01642 | 1.7e-70 | gtrA | S | GtrA-like protein | ||
LLMDOFAF_01643 | 2.7e-123 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
LLMDOFAF_01644 | 9.6e-149 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
LLMDOFAF_01645 | 2.3e-14 | zupT | P | Mediates zinc uptake. May also transport other divalent cations | ||
LLMDOFAF_01646 | 6.4e-29 | zupT | P | transporter | ||
LLMDOFAF_01647 | 1.6e-207 | yurR | 1.4.5.1 | E | oxidoreductase | |
LLMDOFAF_01648 | 1.9e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LLMDOFAF_01649 | 8.3e-113 | rmlC | 1.1.1.133, 5.1.3.13 | M | Catalyzes the epimerization of the C3' and C5'positions of dTDP-6-deoxy-D-xylo-4-hexulose, forming dTDP-6-deoxy-L-lyxo-4- hexulose | |
LLMDOFAF_01650 | 1.9e-205 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LLMDOFAF_01653 | 1.1e-217 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LLMDOFAF_01654 | 6.7e-144 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
LLMDOFAF_01655 | 5.9e-143 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
LLMDOFAF_01656 | 1.1e-121 | ylfI | S | tigr01906 | ||
LLMDOFAF_01657 | 2e-140 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
LLMDOFAF_01658 | 2.3e-09 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
LLMDOFAF_01659 | 5.6e-92 | XK27_08080 | 3.1.1.53 | G | Exopolysaccharide biosynthesis protein | |
LLMDOFAF_01660 | 1.3e-22 | XK27_08085 | ||||
LLMDOFAF_01661 | 5.2e-36 | L | transposase activity | |||
LLMDOFAF_01662 | 1.6e-131 | cbiO | P | ABC transporter | ||
LLMDOFAF_01663 | 1.7e-137 | P | cobalt transport protein | |||
LLMDOFAF_01664 | 2.7e-177 | cbiM | P | PDGLE domain | ||
LLMDOFAF_01665 | 8.9e-161 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
LLMDOFAF_01666 | 9.5e-112 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
LLMDOFAF_01667 | 5.3e-130 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
LLMDOFAF_01668 | 6.6e-78 | ureE | O | enzyme active site formation | ||
LLMDOFAF_01669 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
LLMDOFAF_01670 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
LLMDOFAF_01671 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
LLMDOFAF_01672 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
LLMDOFAF_01673 | 1.4e-54 | S | Domain of unknown function (DUF4173) | |||
LLMDOFAF_01674 | 3.7e-22 | yhaI | L | Membrane | ||
LLMDOFAF_01675 | 6.4e-67 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
LLMDOFAF_01676 | 1.1e-36 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
LLMDOFAF_01677 | 3.4e-62 | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | |||
LLMDOFAF_01678 | 1.6e-32 | V | protein secretion by the type I secretion system | |||
LLMDOFAF_01679 | 2.5e-161 | K | sequence-specific DNA binding | |||
LLMDOFAF_01680 | 8.3e-114 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
LLMDOFAF_01681 | 6.4e-91 | 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 | ||
LLMDOFAF_01682 | 1.6e-96 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
LLMDOFAF_01683 | 1.8e-248 | trkA | P | Potassium transporter peripheral membrane component | ||
LLMDOFAF_01684 | 1.2e-258 | trkH | P | Cation transport protein | ||
LLMDOFAF_01685 | 8.6e-43 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
LLMDOFAF_01686 | 1.6e-140 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LLMDOFAF_01687 | 2.3e-99 | 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 | ||
LLMDOFAF_01688 | 3.1e-122 | 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 | ||
LLMDOFAF_01689 | 3.3e-138 | xerD | L | tyrosine recombinase. Not involved in the cutting and rejoining of the recombining DNA molecules on dif(SL) site | ||
LLMDOFAF_01690 | 5.4e-86 | ykuL | S | CBS domain | ||
LLMDOFAF_01691 | 3.5e-99 | XK27_09740 | S | Phosphoesterase | ||
LLMDOFAF_01692 | 7.1e-186 | 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 | |
LLMDOFAF_01693 | 1.3e-148 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
LLMDOFAF_01694 | 7.6e-36 | yneF | S | UPF0154 protein | ||
LLMDOFAF_01695 | 9.6e-92 | K | transcriptional regulator | |||
LLMDOFAF_01696 | 2.1e-243 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LLMDOFAF_01699 | 1.5e-97 | ybhL | S | Belongs to the BI1 family | ||
LLMDOFAF_01700 | 4.7e-93 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
LLMDOFAF_01701 | 6.4e-131 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LLMDOFAF_01702 | 7e-46 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
LLMDOFAF_01703 | 2.9e-165 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
LLMDOFAF_01704 | 5.3e-89 | L | Integrase core domain protein | |||
LLMDOFAF_01705 | 1.6e-77 | greA | K | Necessary for efficient RNA polymerase transcription elongation past template-encoded arresting sites. The arresting sites in DNA have the property of trapping a certain fraction of elongating RNA polymerases that pass through, resulting in locked ternary complexes. Cleavage of the nascent transcript by cleavage factors such as GreA or GreB allows the resumption of elongation from the new 3'terminus. GreA releases sequences of 2 to 3 nucleotides | ||
LLMDOFAF_01706 | 0.0 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LLMDOFAF_01707 | 9.3e-46 | XK27_09675 | K | -acetyltransferase | ||
LLMDOFAF_01708 | 3.1e-20 | XK27_09675 | K | -acetyltransferase | ||
LLMDOFAF_01709 | 2.6e-255 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
LLMDOFAF_01710 | 2.5e-23 | |||||
LLMDOFAF_01711 | 0.0 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
LLMDOFAF_01712 | 1e-305 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
LLMDOFAF_01713 | 7.9e-224 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
LLMDOFAF_01714 | 5.1e-51 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
LLMDOFAF_01715 | 3.1e-95 | ypsA | S | Belongs to the UPF0398 family | ||
LLMDOFAF_01716 | 2.5e-109 | recU | L | Endonuclease that resolves Holliday junction intermediates in genetic recombination. Cleaves mobile four-strand junctions by introducing symmetrical nicks in paired strands. Promotes annealing of linear ssDNA with homologous dsDNA. Required for DNA repair, homologous recombination and chromosome segregation | ||
LLMDOFAF_01717 | 0.0 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LLMDOFAF_01718 | 4.6e-260 | pepC | 3.4.22.40 | E | aminopeptidase | |
LLMDOFAF_01719 | 1.9e-77 | yhaI | L | Membrane | ||
LLMDOFAF_01720 | 2.1e-151 | nadE | 6.3.1.5 | H | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
LLMDOFAF_01721 | 5.7e-280 | pncB | 6.3.4.21 | H | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
LLMDOFAF_01722 | 1e-139 | S | COG1073 Hydrolases of the alpha beta superfamily | |||
LLMDOFAF_01723 | 2.6e-76 | S | thiolester hydrolase activity | |||
LLMDOFAF_01725 | 3.8e-40 | K | transcriptional | |||
LLMDOFAF_01726 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LLMDOFAF_01727 | 3.9e-21 | glcR | K | transcriptional regulator (DeoR family) | ||
LLMDOFAF_01728 | 2.8e-76 | glcR | K | transcriptional regulator (DeoR family) | ||
LLMDOFAF_01729 | 4e-34 | cof | Q | phosphatase activity | ||
LLMDOFAF_01730 | 6e-55 | cof | Q | phosphatase activity | ||
LLMDOFAF_01731 | 9.3e-86 | 3.1.3.27, 3.1.3.4, 3.1.3.81, 3.6.1.27 | I | phosphatidate phosphatase activity | ||
LLMDOFAF_01732 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
LLMDOFAF_01733 | 5.7e-25 | secE | U | Belongs to the SecE SEC61-gamma family | ||
LLMDOFAF_01734 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LLMDOFAF_01735 | 7.3e-166 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
LLMDOFAF_01736 | 6.8e-56 | S | TM2 domain | |||
LLMDOFAF_01737 | 4.7e-43 | |||||
LLMDOFAF_01740 | 1.1e-278 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
LLMDOFAF_01741 | 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 | ||
LLMDOFAF_01742 | 5.1e-130 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | E | hydrolase | |
LLMDOFAF_01743 | 3.8e-122 | sdaAB | 4.3.1.17 | E | L-serine dehydratase | |
LLMDOFAF_01744 | 9.6e-150 | sdaAA | 4.3.1.17 | E | L-serine dehydratase | |
LLMDOFAF_01745 | 2.3e-27 | |||||
LLMDOFAF_01746 | 7.6e-146 | S | ABC-2 family transporter protein | |||
LLMDOFAF_01747 | 4.1e-150 | S | transport system, permease component | |||
LLMDOFAF_01748 | 1.8e-102 | desR | K | COG2197 Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
LLMDOFAF_01749 | 4.2e-195 | desK | 2.7.13.3 | T | Histidine kinase | |
LLMDOFAF_01750 | 7.4e-135 | yvfS | V | ABC-2 type transporter | ||
LLMDOFAF_01751 | 2.1e-160 | XK27_09825 | V | 'abc transporter, ATP-binding protein | ||
LLMDOFAF_01755 | 2.3e-213 | EGP | Major facilitator Superfamily | |||
LLMDOFAF_01756 | 0.0 | 2.7.7.73, 2.7.7.80 | E | metalloendopeptidase activity | ||
LLMDOFAF_01757 | 1.2e-152 | mutR | K | Transcriptional activator, Rgg GadR MutR family | ||
LLMDOFAF_01758 | 3.9e-41 | 3.6.1.55 | F | NUDIX domain | ||
LLMDOFAF_01760 | 3.7e-122 | S | An automated process has identified a potential problem with this gene model | |||
LLMDOFAF_01761 | 6.1e-26 | XK27_09825 | V | 'abc transporter, ATP-binding protein | ||
LLMDOFAF_01762 | 1.6e-14 | liaI | KT | membrane | ||
LLMDOFAF_01763 | 2.6e-30 | liaI | KT | membrane | ||
LLMDOFAF_01764 | 6e-99 | XK27_05000 | S | Fe-S-cluster oxidoreductase | ||
LLMDOFAF_01765 | 0.0 | V | ABC transporter (permease) | |||
LLMDOFAF_01766 | 5.8e-135 | macB2 | V | ABC transporter, ATP-binding protein | ||
LLMDOFAF_01767 | 6.2e-166 | T | Histidine kinase | |||
LLMDOFAF_01768 | 4.6e-123 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LLMDOFAF_01769 | 5.4e-78 | 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 | |
LLMDOFAF_01771 | 3.3e-69 | pbuX | F | xanthine permease | ||
LLMDOFAF_01772 | 9.2e-119 | pbuX | F | xanthine permease | ||
LLMDOFAF_01773 | 5.3e-248 | norM | V | Multidrug efflux pump | ||
LLMDOFAF_01774 | 4.3e-188 | 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 | |
LLMDOFAF_01775 | 7.8e-236 | brnQ | E | Component of the transport system for branched-chain amino acids | ||
LLMDOFAF_01776 | 2.9e-66 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
LLMDOFAF_01777 | 2.8e-57 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
LLMDOFAF_01778 | 9.6e-26 | csbD | K | CsbD-like | ||
LLMDOFAF_01779 | 1.5e-245 | yfnA | E | amino acid | ||
LLMDOFAF_01780 | 6.1e-111 | XK27_02070 | S | nitroreductase | ||
LLMDOFAF_01781 | 2.1e-154 | 1.13.11.2 | S | glyoxalase | ||
LLMDOFAF_01782 | 3.3e-77 | ywnA | K | Transcriptional regulator | ||
LLMDOFAF_01783 | 6.6e-159 | E | Alpha/beta hydrolase of unknown function (DUF915) | |||
LLMDOFAF_01784 | 2.4e-234 | pts13C | 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 | ||
LLMDOFAF_01785 | 1.3e-111 | drgA | C | Nitroreductase | ||
LLMDOFAF_01786 | 2.4e-75 | yoaK | S | Protein of unknown function (DUF1275) | ||
LLMDOFAF_01787 | 3.1e-161 | yvgN | C | reductase | ||
LLMDOFAF_01788 | 5.6e-103 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LLMDOFAF_01789 | 2.4e-09 | |||||
LLMDOFAF_01790 | 1.6e-140 | S | Abortive infection C-terminus | |||
LLMDOFAF_01791 | 0.0 | L | DEAD-like helicases superfamily | |||
LLMDOFAF_01792 | 1.4e-124 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
LLMDOFAF_01793 | 2.7e-285 | XK27_07020 | S | Belongs to the UPF0371 family | ||
LLMDOFAF_01795 | 1.1e-37 | BP1961 | P | nitric oxide dioxygenase activity | ||
LLMDOFAF_01796 | 1.6e-53 | K | response regulator | |||
LLMDOFAF_01797 | 9.3e-72 | S | Signal peptide protein, YSIRK family | |||
LLMDOFAF_01798 | 4.5e-61 | |||||
LLMDOFAF_01799 | 5.5e-272 | uvrX | 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 | |
LLMDOFAF_01800 | 1.9e-35 | |||||
LLMDOFAF_01801 | 5.3e-12 | IQ | PFAM AMP-dependent synthetase and ligase | |||
LLMDOFAF_01802 | 2.7e-12 | IQ | PFAM AMP-dependent synthetase and ligase | |||
LLMDOFAF_01803 | 5.8e-109 | MA20_06410 | E | LysE type translocator | ||
LLMDOFAF_01804 | 5.6e-08 | |||||
LLMDOFAF_01805 | 2.7e-09 | |||||
LLMDOFAF_01806 | 0.0 | M | family 8 | |||
LLMDOFAF_01808 | 1.1e-151 | V | MatE | |||
LLMDOFAF_01810 | 1.5e-109 | C | Fe-S oxidoreductases | |||
LLMDOFAF_01811 | 1.2e-176 | EGP | Major Facilitator Superfamily | |||
LLMDOFAF_01812 | 5.5e-258 | I | radical SAM domain protein | |||
LLMDOFAF_01814 | 6.5e-159 | Z012_04635 | K | Transcriptional activator, Rgg GadR MutR family | ||
LLMDOFAF_01815 | 1.4e-150 | L | Integrase core domain protein | |||
LLMDOFAF_01816 | 1.8e-87 | L | transposase activity | |||
LLMDOFAF_01818 | 1.5e-61 | |||||
LLMDOFAF_01819 | 0.0 | sbcC | L | ATPase involved in DNA repair | ||
LLMDOFAF_01820 | 5.3e-231 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
LLMDOFAF_01821 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
LLMDOFAF_01822 | 0.0 | lacS | G | transporter | ||
LLMDOFAF_01823 | 2.6e-202 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
LLMDOFAF_01824 | 6.6e-195 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LLMDOFAF_01825 | 8e-290 | galT | 2.7.7.12 | G | UDPglucose--hexose-1-phosphate uridylyltransferase | |
LLMDOFAF_01826 | 5.6e-222 | galK | 2.7.1.6 | G | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
LLMDOFAF_01827 | 1.8e-184 | galR | K | Transcriptional regulator | ||
LLMDOFAF_01828 | 2.7e-08 | L | Integrase core domain protein | |||
LLMDOFAF_01829 | 1.2e-25 | L | transposition | |||
LLMDOFAF_01830 | 3.5e-228 | zmpB | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
LLMDOFAF_01831 | 6.7e-17 | rtxA | M | M26 IgA1-specific Metallo-endopeptidase C-terminal region | ||
LLMDOFAF_01832 | 2.5e-101 | V | abc transporter atp-binding protein | |||
LLMDOFAF_01833 | 4.3e-40 | V | abc transporter atp-binding protein | |||
LLMDOFAF_01834 | 0.0 | gshF | 6.3.2.2, 6.3.2.29, 6.3.2.30, 6.3.2.4 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
LLMDOFAF_01835 | 2.3e-87 | L | Transposase | |||
LLMDOFAF_01836 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
LLMDOFAF_01837 | 1.6e-188 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
LLMDOFAF_01838 | 1.4e-135 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LLMDOFAF_01839 | 5.8e-94 | 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 | ||
LLMDOFAF_01842 | 2.2e-114 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
LLMDOFAF_01843 | 5.8e-175 | vraS | 2.7.13.3 | T | Histidine kinase | |
LLMDOFAF_01844 | 3.7e-120 | yvqF | KT | membrane | ||
LLMDOFAF_01845 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
LLMDOFAF_01846 | 9e-133 | stp | 3.1.3.16 | T | phosphatase | |
LLMDOFAF_01847 | 4e-248 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
LLMDOFAF_01848 | 2.5e-172 | fmt | 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 | |
LLMDOFAF_01849 | 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 | ||
LLMDOFAF_01850 | 2.7e-46 | rpoZ | 2.7.7.6 | K | DNA-directed 5'-3' RNA polymerase activity | |
LLMDOFAF_01851 | 2e-112 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
LLMDOFAF_01852 | 9.7e-213 | 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) | ||
LLMDOFAF_01853 | 1.8e-150 | XK27_02985 | S | overlaps another CDS with the same product name | ||
LLMDOFAF_01854 | 2.1e-148 | supH | S | overlaps another CDS with the same product name | ||
LLMDOFAF_01855 | 8.6e-63 | yvoA_1 | K | Transcriptional | ||
LLMDOFAF_01856 | 9.8e-121 | skfE | V | abc transporter atp-binding protein | ||
LLMDOFAF_01857 | 5.6e-133 | V | ATPase activity | |||
LLMDOFAF_01858 | 4.3e-172 | oppF | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_01859 | 2.2e-204 | oppD | P | Belongs to the ABC transporter superfamily | ||
LLMDOFAF_01860 | 4.9e-168 | amiD | P | ABC transporter (Permease | ||
LLMDOFAF_01861 | 4.2e-278 | amiC | P | ABC transporter (Permease | ||
LLMDOFAF_01862 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)