ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
LFHNALEI_00001 | 2.4e-11 | S | Bacterial mobilisation protein (MobC) | |||
LFHNALEI_00002 | 8.9e-223 | Z012_11675 | L | Arm DNA-binding domain | ||
LFHNALEI_00003 | 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 | ||
LFHNALEI_00004 | 2.2e-39 | yabO | J | Ribosome-associated heat shock protein implicated in the recycling of the 50S subunit (S4 paralog) | ||
LFHNALEI_00005 | 3e-60 | divIC | D | Septum formation initiator | ||
LFHNALEI_00007 | 7.6e-236 | XK27_09285 | 3.5.2.6 | V | Beta-lactamase enzyme family | |
LFHNALEI_00008 | 9.7e-236 | 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 | |
LFHNALEI_00009 | 2e-97 | hpt | 2.4.2.8, 6.3.4.19 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
LFHNALEI_00010 | 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 | ||
LFHNALEI_00011 | 1.9e-77 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
LFHNALEI_00012 | 3.9e-306 | typA | T | GTP-binding protein TypA | ||
LFHNALEI_00013 | 1e-72 | hit | FG | Diadenosine tetraphosphate (Ap4A) hydrolase and other HIT family hydrolases | ||
LFHNALEI_00017 | 3e-96 | yegS | 2.7.1.107 | I | Sphingosine kinase and enzymes related to eukaryotic diacylglycerol kinase | |
LFHNALEI_00018 | 1.6e-31 | S | dextransucrase activity | |||
LFHNALEI_00019 | 6.9e-147 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
LFHNALEI_00020 | 3.7e-08 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
LFHNALEI_00021 | 2.5e-66 | ytxH | S | General stress protein | ||
LFHNALEI_00022 | 5.8e-55 | S | TM2 domain | |||
LFHNALEI_00023 | 2.5e-44 | |||||
LFHNALEI_00025 | 1.5e-219 | metE | 2.1.1.14 | E | Methionine synthase | |
LFHNALEI_00026 | 1.5e-25 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
LFHNALEI_00027 | 6.7e-19 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
LFHNALEI_00028 | 2.7e-277 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
LFHNALEI_00029 | 5.5e-114 | livF | E | COG0410 ABC-type branched-chain amino acid transport systems, ATPase component | ||
LFHNALEI_00030 | 9e-110 | livG | E | COG0411 ABC-type branched-chain amino acid transport systems, ATPase component | ||
LFHNALEI_00031 | 5.9e-159 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | glucose-1-phosphate adenylyltransferase |
LFHNALEI_00032 | 1.8e-89 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
LFHNALEI_00033 | 1.7e-93 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
LFHNALEI_00034 | 5.8e-17 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
LFHNALEI_00035 | 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 | ||
LFHNALEI_00036 | 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 | ||
LFHNALEI_00037 | 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 | ||
LFHNALEI_00038 | 1.3e-134 | stp | 3.1.3.16 | T | phosphatase | |
LFHNALEI_00039 | 2.2e-137 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
LFHNALEI_00040 | 3.3e-56 | ymcA | 3.6.3.21 | S | Belongs to the UPF0342 family | |
LFHNALEI_00041 | 3.1e-69 | argR | K | Regulates arginine biosynthesis genes | ||
LFHNALEI_00042 | 3e-86 | L | COG1943 Transposase and inactivated derivatives | |||
LFHNALEI_00043 | 6.6e-99 | 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 | ||
LFHNALEI_00044 | 1.1e-102 | |||||
LFHNALEI_00045 | 1.7e-170 | scrK | 2.7.1.2, 2.7.1.4 | GK | Fructokinase | |
LFHNALEI_00046 | 9.6e-68 | fecE | 3.6.3.34 | HP | ABC transporter | |
LFHNALEI_00047 | 7.2e-173 | fatB | P | COG0614 ABC-type Fe3 -hydroxamate transport system, periplasmic component | ||
LFHNALEI_00048 | 5e-27 | mmuP | E | amino acid | ||
LFHNALEI_00049 | 3.9e-110 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
LFHNALEI_00050 | 1e-35 | 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 | ||
LFHNALEI_00051 | 8.6e-301 | 3.2.1.26, 3.2.1.65 | GH32 | G | Belongs to the glycosyl hydrolase 32 family | |
LFHNALEI_00052 | 4e-161 | ureD | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
LFHNALEI_00053 | 6.5e-30 | ureG | KO | Facilitates the functional incorporation of the urease nickel metallocenter. This process requires GTP hydrolysis, probably effectuated by UreG | ||
LFHNALEI_00054 | 6.7e-113 | 2.7.6.5 | S | Region found in RelA / SpoT proteins | ||
LFHNALEI_00055 | 4.3e-112 | K | Acetyltransferase (GNAT) family | |||
LFHNALEI_00056 | 6.9e-44 | lmrA2 | V | abc transporter atp-binding protein | ||
LFHNALEI_00057 | 1.2e-164 | O | protein import | |||
LFHNALEI_00058 | 7.9e-67 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
LFHNALEI_00059 | 9.1e-50 | hisE | 3.5.4.19, 3.6.1.31, 5.3.1.16 | E | phosphoribosyl-ATP diphosphatase activity | |
LFHNALEI_00060 | 6.7e-59 | 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 | |
LFHNALEI_00061 | 3.6e-85 | 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 | |
LFHNALEI_00062 | 2.1e-227 | 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 | |
LFHNALEI_00063 | 6.6e-59 | phnA | P | Alkylphosphonate utilization operon protein PhnA | ||
LFHNALEI_00064 | 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 | |
LFHNALEI_00065 | 3.7e-73 | 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 | ||
LFHNALEI_00066 | 0.0 | dex | 3.2.1.11 | GH66 | G | Glycosyl hydrolase family 66 |
LFHNALEI_00067 | 1.9e-236 | 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 | |
LFHNALEI_00068 | 3.5e-48 | 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 | |
LFHNALEI_00069 | 6.1e-302 | dsbD | 1.8.1.8 | CO | Required to facilitate the formation of correct disulfide bonds in some periplasmic proteins and for the assembly of the periplasmic c-type cytochromes. Acts by transferring electrons from cytoplasmic thioredoxin to the periplasm. This transfer involves a cascade of disulfide bond formation and reduction steps | |
LFHNALEI_00070 | 1.4e-07 | 2.7.13.3, 2.7.7.7, 5.4.99.21 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
LFHNALEI_00071 | 4.4e-62 | ygdD | S | Protein of unknown function (DUF423) | ||
LFHNALEI_00072 | 1.4e-67 | yeaL | S | UPF0756 membrane protein | ||
LFHNALEI_00073 | 1.4e-95 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
LFHNALEI_00074 | 7.6e-91 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
LFHNALEI_00075 | 8.6e-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 | ||
LFHNALEI_00076 | 2.6e-100 | yvdD | 3.2.2.10 | S | Belongs to the LOG family | |
LFHNALEI_00077 | 1.6e-51 | rng | J | Ribonuclease G | ||
LFHNALEI_00080 | 4.8e-80 | mdtK | V | Multidrug resistance protein | ||
LFHNALEI_00081 | 4.8e-38 | corA | P | COG0598 Mg2 and Co2 transporters | ||
LFHNALEI_00082 | 1.8e-86 | ycbL | 3.1.2.6 | S | COG0491 Zn-dependent hydrolases, including glyoxylases | |
LFHNALEI_00083 | 1.2e-169 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
LFHNALEI_00084 | 9.4e-33 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
LFHNALEI_00085 | 3.9e-159 | holB | 2.7.7.7 | L | dna polymerase iii | |
LFHNALEI_00086 | 1.1e-110 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
LFHNALEI_00088 | 2.2e-245 | cshA | 3.6.4.13 | JKL | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
LFHNALEI_00089 | 1.4e-16 | dgs | 2.4.1.208 | GT4 | M | Glycosyltransferase, group 1 family protein |
LFHNALEI_00090 | 3.7e-246 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
LFHNALEI_00091 | 3.1e-200 | M | Pilin isopeptide linkage domain protein | |||
LFHNALEI_00092 | 1.7e-60 | DegV | S | DegV family | ||
LFHNALEI_00093 | 2.4e-156 | ypmR | E | COG2755 Lysophospholipase L1 and related esterases | ||
LFHNALEI_00094 | 6.4e-123 | 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 | ||
LFHNALEI_00095 | 3e-24 | tatA | U | protein secretion | ||
LFHNALEI_00096 | 1.4e-65 | msmX | P | Belongs to the ABC transporter superfamily | ||
LFHNALEI_00097 | 3.6e-97 | sdh | 1.1.1.276, 1.1.1.313, 1.1.1.381 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
LFHNALEI_00098 | 4.4e-45 | S | Phage derived protein Gp49-like (DUF891) | |||
LFHNALEI_00099 | 1.7e-45 | K | Helix-turn-helix domain | |||
LFHNALEI_00100 | 2.3e-63 | ftsE | D | cell division ATP-binding protein FtsE | ||
LFHNALEI_00101 | 7.3e-164 | ftsX | D | Part of the ABC transporter FtsEX involved in asymmetric cellular division facilitating the initiation of sporulation | ||
LFHNALEI_00102 | 7.3e-121 | 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 | |
LFHNALEI_00103 | 2e-79 | 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 | |
LFHNALEI_00104 | 5.8e-77 | 3.5.1.19 | Q | hydrolase activity, acting on carbon-nitrogen (but not peptide) bonds, in linear amides | ||
LFHNALEI_00105 | 2.4e-50 | trxA | O | Belongs to the thioredoxin family | ||
LFHNALEI_00106 | 5.1e-142 | S | Macro domain protein | |||
LFHNALEI_00107 | 2.4e-53 | IQ | Thioesterase | |||
LFHNALEI_00108 | 2.3e-100 | yhjX | P | Major Facilitator | ||
LFHNALEI_00109 | 9.2e-43 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
LFHNALEI_00110 | 3.5e-214 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
LFHNALEI_00111 | 8.1e-20 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
LFHNALEI_00112 | 1.6e-257 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
LFHNALEI_00113 | 2.1e-140 | phaB | 5.3.3.14, 5.3.3.18 | I | Belongs to the enoyl-CoA hydratase isomerase family | |
LFHNALEI_00114 | 1.1e-113 | S | HAD hydrolase, family IA, variant 3 | |||
LFHNALEI_00115 | 4.8e-257 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
LFHNALEI_00116 | 3e-192 | asnA | 6.3.1.1 | E | aspartate--ammonia ligase | |
LFHNALEI_00117 | 2.6e-247 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
LFHNALEI_00118 | 3.7e-137 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
LFHNALEI_00119 | 7.8e-102 | ygaC | J | Belongs to the UPF0374 family | ||
LFHNALEI_00120 | 1.4e-102 | S | Domain of unknown function (DUF1803) | |||
LFHNALEI_00121 | 7.7e-83 | ppaC | 3.6.1.1 | C | inorganic pyrophosphatase | |
LFHNALEI_00122 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
LFHNALEI_00123 | 3.8e-82 | comFC | K | competence protein | ||
LFHNALEI_00124 | 1.5e-135 | lmrA1 | V | abc transporter atp-binding protein | ||
LFHNALEI_00125 | 2e-25 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
LFHNALEI_00126 | 7.2e-181 | XK27_08075 | M | glycosyl transferase family 2 | ||
LFHNALEI_00127 | 6.9e-197 | glgB | 2.4.1.18, 3.2.1.141, 3.2.1.20 | CBM48,GH13,GH31 | G | Catalyzes the formation of the alpha-1,6-glucosidic linkages in glycogen by scission of a 1,4-alpha-linked oligosaccharide from growing alpha-1,4-glucan chains and the subsequent attachment of the oligosaccharide to the alpha-1,6 position |
LFHNALEI_00128 | 5.2e-193 | 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 | |
LFHNALEI_00129 | 3.5e-272 | glnP | P | ABC transporter | ||
LFHNALEI_00130 | 1.7e-96 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
LFHNALEI_00131 | 2e-33 | secG | U | Preprotein translocase subunit SecG | ||
LFHNALEI_00132 | 2.3e-162 | mdtG | EGP | Major facilitator Superfamily | ||
LFHNALEI_00133 | 2.9e-57 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
LFHNALEI_00134 | 9.6e-64 | XK27_02560 | S | cog cog2151 | ||
LFHNALEI_00135 | 8.1e-58 | 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 | ||
LFHNALEI_00136 | 4.5e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
LFHNALEI_00137 | 1.5e-46 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
LFHNALEI_00138 | 7.2e-132 | ydaF_2 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
LFHNALEI_00139 | 5e-63 | WQ51_03320 | S | cog cog4835 | ||
LFHNALEI_00140 | 1e-148 | XK27_08360 | S | EDD domain protein, DegV family | ||
LFHNALEI_00141 | 3.9e-139 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
LFHNALEI_00142 | 2.5e-217 | 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 | |
LFHNALEI_00143 | 0.0 | yfmR | S | abc transporter atp-binding protein | ||
LFHNALEI_00144 | 1.7e-26 | U | response to pH | |||
LFHNALEI_00145 | 9.1e-75 | 3.6.1.13, 3.6.1.55 | F | ADP-ribose pyrophosphatase | ||
LFHNALEI_00146 | 2e-155 | pstS | P | phosphate | ||
LFHNALEI_00147 | 7.7e-199 | 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 | ||
LFHNALEI_00148 | 2.4e-287 | 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 | |
LFHNALEI_00149 | 1.9e-169 | tcdB | S | dextransucrase activity | ||
LFHNALEI_00150 | 3.8e-90 | 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 | |
LFHNALEI_00151 | 3.1e-142 | Z012_04635 | K | sequence-specific DNA binding | ||
LFHNALEI_00152 | 5.4e-77 | 3.4.17.14, 3.5.1.28 | NU | amidase activity | ||
LFHNALEI_00153 | 6.4e-105 | GK | ROK family | |||
LFHNALEI_00154 | 1.6e-145 | map | 3.4.11.18 | E | Removes the N-terminal methionine from nascent proteins. The N-terminal methionine is often cleaved when the second residue in the primary sequence is small and uncharged (Met-Ala-, Cys, Gly, Pro, Ser, Thr, or Val). Requires deformylation of the N(alpha)-formylated initiator methionine before it can be hydrolyzed | |
LFHNALEI_00155 | 2.6e-34 | yebC | M | Membrane | ||
LFHNALEI_00156 | 2.2e-90 | 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 | |
LFHNALEI_00157 | 9.7e-22 | |||||
LFHNALEI_00158 | 1.5e-80 | M | Pilin isopeptide linkage domain protein | |||
LFHNALEI_00159 | 6.5e-96 | 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 | |
LFHNALEI_00160 | 8.9e-130 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
LFHNALEI_00161 | 6.7e-99 | 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 | |
LFHNALEI_00162 | 1.4e-115 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
LFHNALEI_00163 | 1.5e-33 | ykzG | S | Belongs to the UPF0356 family | ||
LFHNALEI_00164 | 2.6e-124 | agrA | KT | phosphorelay signal transduction system | ||
LFHNALEI_00165 | 1.3e-129 | V | Psort location CytoplasmicMembrane, score | |||
LFHNALEI_00166 | 3.7e-100 | skfE | V | abc transporter atp-binding protein | ||
LFHNALEI_00167 | 4.4e-169 | 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 | ||
LFHNALEI_00168 | 1.9e-59 | |||||
LFHNALEI_00169 | 7.9e-199 | 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) | |
LFHNALEI_00170 | 5.2e-119 | yqfA | K | protein, Hemolysin III | ||
LFHNALEI_00171 | 4.1e-29 | pspC | KT | PspC domain protein | ||
LFHNALEI_00172 | 1.8e-87 | S | Protein of unknown function (DUF3114) | |||
LFHNALEI_00173 | 1.3e-57 | fhuR | K | transcriptional regulator (lysR family) | ||
LFHNALEI_00174 | 1.3e-76 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
LFHNALEI_00175 | 1.5e-18 | T | HD domain | |||
LFHNALEI_00176 | 1.9e-144 | ylmH | S | conserved protein, contains S4-like domain | ||
LFHNALEI_00177 | 1.5e-29 | yggT | D | integral membrane protein | ||
LFHNALEI_00178 | 1.2e-28 | sepF | D | cell septum assembly | ||
LFHNALEI_00179 | 2e-65 | yfiB1 | V | abc transporter atp-binding protein | ||
LFHNALEI_00180 | 1.3e-165 | amiD | P | ABC transporter (Permease | ||
LFHNALEI_00181 | 2.5e-113 | S | Plasmid replication protein | |||
LFHNALEI_00183 | 6.2e-32 | livJ | E | COG0683 ABC-type branched-chain amino acid transport systems, periplasmic component | ||
LFHNALEI_00184 | 4.2e-145 | livH | E | Belongs to the binding-protein-dependent transport system permease family | ||
LFHNALEI_00185 | 2.4e-159 | L | Transposase | |||
LFHNALEI_00186 | 3.2e-83 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
LFHNALEI_00187 | 1e-252 | XK27_00765 | ||||
LFHNALEI_00188 | 2.9e-96 | pepF | E | oligoendopeptidase F | ||
LFHNALEI_00189 | 1.5e-200 | 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 | |
LFHNALEI_00190 | 1.6e-117 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
LFHNALEI_00191 | 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 | ||
LFHNALEI_00192 | 8.3e-47 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
LFHNALEI_00193 | 6.8e-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 | ||
LFHNALEI_00194 | 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 | ||
LFHNALEI_00195 | 5.7e-104 | rplD | J | Forms part of the polypeptide exit tunnel | ||
LFHNALEI_00196 | 2.4e-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 | ||
LFHNALEI_00197 | 2.9e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
LFHNALEI_00198 | 3e-187 | 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 | |
LFHNALEI_00199 | 0.0 | XK27_09800 | I | Acyltransferase | ||
LFHNALEI_00200 | 1.3e-79 | dnaE | 2.7.7.7 | L | DNA polymerase | |
LFHNALEI_00201 | 2.1e-54 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
LFHNALEI_00202 | 2.4e-13 | |||||
LFHNALEI_00203 | 1.1e-12 | |||||
LFHNALEI_00204 | 5.5e-217 | 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) | |
LFHNALEI_00205 | 2.8e-185 | 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 | |
LFHNALEI_00206 | 9e-72 | rimI | 2.3.1.128 | K | This enzyme acetylates the N-terminal alanine of ribosomal protein S18 | |
LFHNALEI_00207 | 9.3e-14 | 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 | ||
LFHNALEI_00208 | 1.9e-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 | ||
LFHNALEI_00209 | 1e-58 | yhaI | J | Membrane | ||
LFHNALEI_00210 | 1.3e-61 | yhaI | J | Protein of unknown function (DUF805) | ||
LFHNALEI_00211 | 4.3e-65 | yhaI | S | Protein of unknown function (DUF805) | ||
LFHNALEI_00212 | 2.7e-92 | panT | S | ECF transporter, substrate-specific component | ||
LFHNALEI_00213 | 4.1e-90 | 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 | |
LFHNALEI_00214 | 4.1e-28 | coaB | 4.1.1.36, 6.3.2.5 | H | Phosphopantothenate-cysteine ligase | |
LFHNALEI_00215 | 1.6e-39 | MA20_06245 | S | yiaA/B two helix domain | ||
LFHNALEI_00216 | 5.9e-51 | uup | S | abc transporter atp-binding protein | ||
LFHNALEI_00217 | 1.9e-104 | cinA | 3.5.1.42 | S | Belongs to the CinA family | |
LFHNALEI_00219 | 5.1e-90 | 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) | |
LFHNALEI_00221 | 2.9e-31 | yozG | K | Transcriptional regulator | ||
LFHNALEI_00223 | 1.8e-119 | ansA | 3.5.1.1 | EJ | COG0252 L-asparaginase archaeal Glu-tRNAGln amidotransferase subunit D | |
LFHNALEI_00224 | 2.2e-143 | peb1A | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
LFHNALEI_00225 | 6.8e-145 | ylbM | S | Belongs to the UPF0348 family | ||
LFHNALEI_00226 | 7.6e-39 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
LFHNALEI_00227 | 1.2e-129 | hisA | 5.3.1.16 | E | 1-(5-phosphoribosyl)-5- 5-phosphoribosylamino)methylideneamino imidazole-4-carboxamide isomerase | |
LFHNALEI_00228 | 6.9e-98 | 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 | ||
LFHNALEI_00229 | 3.3e-71 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
LFHNALEI_00230 | 6.4e-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 | ||
LFHNALEI_00231 | 1.2e-50 | S | Protein of unknown function (DUF3397) | |||
LFHNALEI_00232 | 1e-87 | cah | 4.2.1.1 | P | Reversible hydration of carbon dioxide | |
LFHNALEI_00233 | 4.8e-57 | WQ51_05710 | S | Mitochondrial biogenesis AIM24 | ||
LFHNALEI_00234 | 1.7e-30 | 2.4.1.21 | GT5 | M | Right handed beta helix region | |
LFHNALEI_00235 | 1.7e-151 | gapN | 1.2.1.9 | C | Belongs to the aldehyde dehydrogenase family | |
LFHNALEI_00236 | 9.3e-124 | ygfZ | S | Belongs to the GcvT family | ||
LFHNALEI_00237 | 1.2e-35 | XK27_02060 | S | Transglycosylase associated protein | ||
LFHNALEI_00238 | 7e-121 | pepS | E | COG2309 Leucyl aminopeptidase (aminopeptidase T) | ||
LFHNALEI_00239 | 3.3e-28 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
LFHNALEI_00241 | 2.8e-16 | |||||
LFHNALEI_00243 | 1.5e-129 | mutY | L | A G-specific adenine glycosylase | ||
LFHNALEI_00244 | 1.3e-267 | pflB | 2.3.1.54 | C | formate acetyltransferase' | |
LFHNALEI_00245 | 5.2e-96 | XK27_08140 | K | Bacterial regulatory proteins, tetR family | ||
LFHNALEI_00246 | 1.8e-75 | ctsR | K | Belongs to the CtsR family | ||
LFHNALEI_00248 | 5.2e-104 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
LFHNALEI_00249 | 8e-49 | tetL | EGP | Major Facilitator Superfamily | ||
LFHNALEI_00250 | 2.5e-103 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
LFHNALEI_00251 | 1.8e-17 | S | Protein of unknown function (DUF3021) | |||
LFHNALEI_00252 | 4.5e-19 | uppP | 3.6.1.27 | V | Catalyzes the dephosphorylation of undecaprenyl diphosphate (UPP). Confers resistance to bacitracin | |
LFHNALEI_00253 | 2.5e-119 | yhfC | S | Putative membrane peptidase family (DUF2324) | ||
LFHNALEI_00254 | 1.1e-43 | czrA | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
LFHNALEI_00255 | 2.1e-111 | 3.5.1.28 | M | domain protein | ||
LFHNALEI_00256 | 3.6e-174 | 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 | ||
LFHNALEI_00257 | 3.2e-20 | rpsU | J | Belongs to the bacterial ribosomal protein bS21 family | ||
LFHNALEI_00258 | 1.9e-136 | gltS | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LFHNALEI_00259 | 1.5e-189 | 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 | |
LFHNALEI_00260 | 1.4e-142 | S | von Willebrand factor (vWF) type A domain | |||
LFHNALEI_00261 | 7.6e-168 | D | nuclear chromosome segregation | |||
LFHNALEI_00263 | 1.3e-96 | ytqB | 2.1.1.176 | J | (SAM)-dependent | |
LFHNALEI_00264 | 1.1e-101 | yhcC | S | radical SAM protein | ||
LFHNALEI_00265 | 1.5e-266 | prfC | J | Increases the formation of ribosomal termination complexes and stimulates activities of RF-1 and RF-2. It binds guanine nucleotides and has strong preference for UGA stop codons. It may interact directly with the ribosome. The stimulation of RF- 1 and RF-2 is significantly reduced by GTP and GDP, but not by GMP | ||
LFHNALEI_00266 | 4.4e-141 | proB | 2.7.2.11 | E | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
LFHNALEI_00267 | 5.4e-40 | EGP | Transmembrane secretion effector | |||
LFHNALEI_00269 | 2.6e-71 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LFHNALEI_00270 | 8.5e-179 | 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 | |
LFHNALEI_00271 | 4.2e-33 | hisC | 2.6.1.9 | E | Belongs to the class-II pyridoxal-phosphate-dependent aminotransferase family. Histidinol-phosphate aminotransferase subfamily | |
LFHNALEI_00272 | 3.2e-147 | dnaI | L | Primosomal protein DnaI | ||
LFHNALEI_00273 | 1.4e-207 | scrA | 2.7.1.211 | G | pts system | |
LFHNALEI_00274 | 4.6e-29 | xseB | 3.1.11.6 | L | Bidirectionally degrades single-stranded DNA into large acid-insoluble oligonucleotides, which are then degraded further into small acid-soluble oligonucleotides | |
LFHNALEI_00275 | 4.4e-53 | 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 | |
LFHNALEI_00276 | 2.7e-139 | XK27_00880 | 3.5.1.28 | M | Glycosyl hydrolase, family 25 | |
LFHNALEI_00277 | 4.8e-13 | L | Helix-hairpin-helix DNA-binding motif class 1 | |||
LFHNALEI_00278 | 2.2e-30 | S | Domain of unknown function (DUF1912) | |||
LFHNALEI_00279 | 6e-70 | 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 | |
LFHNALEI_00280 | 1.9e-214 | 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 | ||
LFHNALEI_00281 | 6.6e-240 | metY | 2.5.1.49 | E | o-acetylhomoserine | |
LFHNALEI_00282 | 3.3e-70 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
LFHNALEI_00284 | 3.1e-125 | fruR | K | transcriptional | ||
LFHNALEI_00285 | 1.2e-45 | rny | D | Endoribonuclease that initiates mRNA decay | ||
LFHNALEI_00286 | 3.8e-31 | glnQ | E | abc transporter atp-binding protein | ||
LFHNALEI_00287 | 9.7e-60 | D | nuclear chromosome segregation | |||
LFHNALEI_00288 | 1.4e-174 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
LFHNALEI_00289 | 8e-16 | xylG | 3.6.3.17 | S | ABC transporter, ATP-binding protein | |
LFHNALEI_00290 | 3.5e-45 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
LFHNALEI_00291 | 1.9e-78 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
LFHNALEI_00292 | 4.4e-210 | ascB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
LFHNALEI_00293 | 7.7e-100 | folE | 3.5.4.16 | F | gtp cyclohydrolase | |
LFHNALEI_00294 | 1.3e-212 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
LFHNALEI_00296 | 1.7e-204 | 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 | ||
LFHNALEI_00297 | 1.3e-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 | ||
LFHNALEI_00298 | 6.7e-96 | 3.1.3.18 | S | IA, variant 1 | ||
LFHNALEI_00299 | 7.8e-53 | lrgB | M | cytolysis | ||
LFHNALEI_00300 | 1.8e-63 | cdd | 2.4.2.2, 3.5.4.5 | F | This enzyme scavenges exogenous and endogenous cytidine and 2'-deoxycytidine for UMP synthesis | |
LFHNALEI_00301 | 9.9e-62 | 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 | |
LFHNALEI_00302 | 2.7e-109 | bcrC | 3.6.1.27 | I | Membrane-associated phospholipid phosphatase | |
LFHNALEI_00303 | 1.1e-78 | 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 | ||
LFHNALEI_00304 | 6.8e-178 | yegQ | O | Peptidase U32 | ||
LFHNALEI_00305 | 2.3e-145 | 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 | |
LFHNALEI_00306 | 7.6e-55 | 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 | |
LFHNALEI_00307 | 7.2e-39 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
LFHNALEI_00309 | 1.8e-17 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
LFHNALEI_00310 | 2e-103 | mdlB | V | abc transporter atp-binding protein | ||
LFHNALEI_00313 | 9.6e-72 | oxlT | P | COG0477 Permeases of the major facilitator superfamily | ||
LFHNALEI_00314 | 6.1e-120 | yrrM | 2.1.1.104 | S | O-Methyltransferase | |
LFHNALEI_00315 | 2.1e-114 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
LFHNALEI_00317 | 1.1e-46 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
LFHNALEI_00318 | 2.5e-81 | 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 | ||
LFHNALEI_00319 | 4.1e-139 | vanY | 3.4.17.14 | M | D-alanyl-D-alanine carboxypeptidase | |
LFHNALEI_00320 | 3.1e-68 | ais | G | Phosphoglycerate mutase | ||
LFHNALEI_00322 | 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 | |
LFHNALEI_00323 | 3.7e-75 | ytmP | 2.7.1.89 | M | Phosphotransferase | |
LFHNALEI_00324 | 1.8e-152 | XK27_05675 | S | Esterase | ||
LFHNALEI_00327 | 1.9e-49 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
LFHNALEI_00328 | 4e-47 | ycaO | O | OsmC-like protein | ||
LFHNALEI_00329 | 1.9e-62 | paaI | Q | protein possibly involved in aromatic compounds catabolism | ||
LFHNALEI_00330 | 3e-106 | P | ABC transporter (Permease | |||
LFHNALEI_00331 | 1e-108 | cutC | P | Participates in the control of copper homeostasis | ||
LFHNALEI_00333 | 4.6e-202 | yurR | 1.4.5.1 | E | oxidoreductase | |
LFHNALEI_00334 | 1.6e-81 | amy | 3.2.1.1 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
LFHNALEI_00335 | 9.3e-15 | 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 | ||
LFHNALEI_00336 | 1.2e-89 | cvpA | S | toxin biosynthetic process | ||
LFHNALEI_00337 | 1.6e-37 | S | Bacterial inner membrane protein | |||
LFHNALEI_00338 | 3.9e-145 | XK27_04800 | S | Sucrose-6F-phosphate phosphohydrolase | ||
LFHNALEI_00339 | 3.4e-174 | 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 | |
LFHNALEI_00340 | 3e-102 | 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 | |
LFHNALEI_00342 | 1.3e-35 | ctpE | P | E1-E2 ATPase | ||
LFHNALEI_00343 | 1.1e-59 | |||||
LFHNALEI_00344 | 1.8e-44 | |||||
LFHNALEI_00345 | 2.9e-50 | |||||
LFHNALEI_00346 | 4.4e-132 | ecsA_2 | V | abc transporter atp-binding protein | ||
LFHNALEI_00347 | 2.5e-175 | clpL | O | ATP-dependent Clp protease ATP-binding subunit | ||
LFHNALEI_00348 | 3.5e-129 | sufD | O | assembly protein SufD | ||
LFHNALEI_00350 | 7.2e-38 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
LFHNALEI_00351 | 2.8e-240 | scrB | 3.2.1.26, 3.2.1.80 | GH32 | G | invertase |
LFHNALEI_00352 | 2e-180 | scrR | K | Transcriptional regulator | ||
LFHNALEI_00353 | 8.1e-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 | ||
LFHNALEI_00354 | 1.7e-61 | yqhY | S | protein conserved in bacteria | ||
LFHNALEI_00355 | 7.1e-98 | 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 | ||
LFHNALEI_00356 | 3.3e-85 | comEB | 3.5.4.12 | F | ComE operon protein 2 | |
LFHNALEI_00357 | 7.9e-115 | pepP | 3.4.11.9, 3.4.13.9 | E | Belongs to the peptidase M24B family | |
LFHNALEI_00358 | 1.9e-107 | S | Domain of Unknown Function with PDB structure (DUF3862) | |||
LFHNALEI_00359 | 9.4e-74 | nifU | C | SUF system FeS assembly protein, NifU family | ||
LFHNALEI_00360 | 4.4e-146 | 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 | |
LFHNALEI_00361 | 1.3e-135 | hemN | H | Involved in the biosynthesis of porphyrin-containing compound | ||
LFHNALEI_00362 | 3.3e-77 | K | sequence-specific DNA binding | |||
LFHNALEI_00363 | 3.3e-83 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
LFHNALEI_00364 | 2e-71 | lytE | M | LysM domain protein | ||
LFHNALEI_00365 | 2.1e-62 | isaA | GH23 | M | Immunodominant staphylococcal antigen A | |
LFHNALEI_00366 | 2.4e-311 | S | Bacterial membrane protein, YfhO | |||
LFHNALEI_00367 | 1.9e-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 | |
LFHNALEI_00368 | 1.2e-98 | yvbG | U | UPF0056 membrane protein | ||
LFHNALEI_00369 | 4.7e-168 | K | transcriptional regulator (lysR family) | |||
LFHNALEI_00370 | 5.3e-110 | rsmG | 2.1.1.170 | J | Ribosomal RNA small subunit methyltransferase G | |
LFHNALEI_00371 | 1.6e-22 | cglB | NU | type II secretion system | ||
LFHNALEI_00372 | 2.2e-43 | comGC | U | Required for transformation and DNA binding | ||
LFHNALEI_00373 | 8.4e-70 | cglD | NU | Competence protein | ||
LFHNALEI_00374 | 3.1e-15 | NU | Type II secretory pathway pseudopilin | |||
LFHNALEI_00375 | 4.5e-71 | comGF | U | Competence protein ComGF | ||
LFHNALEI_00376 | 2e-12 | comGF | U | Putative Competence protein ComGF | ||
LFHNALEI_00377 | 5e-176 | ytxK | 2.1.1.72 | L | DNA methylase | |
LFHNALEI_00378 | 8.3e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
LFHNALEI_00379 | 1.5e-26 | lanR | K | sequence-specific DNA binding | ||
LFHNALEI_00380 | 3.9e-79 | V | CAAX protease self-immunity | |||
LFHNALEI_00382 | 4e-169 | fruA | 3.2.1.1, 3.2.1.26, 3.2.1.65, 3.2.1.80 | GH13,GH32 | G | Belongs to the glycosyl hydrolase 32 family |
LFHNALEI_00383 | 1.1e-24 | nylA | 3.5.1.4 | J | Belongs to the amidase family | |
LFHNALEI_00384 | 1.3e-148 | yckB | ET | Belongs to the bacterial solute-binding protein 3 family | ||
LFHNALEI_00385 | 6.8e-142 | rgpC | GM | Transport permease protein | ||
LFHNALEI_00386 | 3.9e-130 | pepC | 3.4.22.40 | E | aminopeptidase | |
LFHNALEI_00387 | 1.9e-33 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LFHNALEI_00388 | 2.5e-73 | S | dextransucrase activity | |||
LFHNALEI_00389 | 4.6e-64 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LFHNALEI_00390 | 2.9e-59 | glnP | P | ABC-type amino acid transport signal transduction systems periplasmic component domain | ||
LFHNALEI_00391 | 1.4e-13 | MU | outer membrane autotransporter barrel domain protein | |||
LFHNALEI_00392 | 3.7e-34 | yozE | S | Belongs to the UPF0346 family | ||
LFHNALEI_00393 | 4.1e-37 | metB | 2.5.1.48, 4.4.1.8 | E | cystathionine | |
LFHNALEI_00395 | 8.8e-232 | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | ||
LFHNALEI_00396 | 5.1e-273 | 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) | |
LFHNALEI_00397 | 0.0 | amiA | E | ABC transporter, substrate-binding protein, family 5 | ||
LFHNALEI_00398 | 3e-51 | yhaI | L | Membrane | ||
LFHNALEI_00399 | 9.6e-107 | S | Domain of unknown function (DUF4173) | |||
LFHNALEI_00400 | 1.1e-69 | K | LytTr DNA-binding domain | |||
LFHNALEI_00401 | 2.3e-19 | glgA | 2.4.1.21 | GT5 | G | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
LFHNALEI_00404 | 2.6e-10 | |||||
LFHNALEI_00412 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
LFHNALEI_00413 | 7.1e-150 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
LFHNALEI_00414 | 6.8e-15 | gdhA | 1.4.1.4 | E | Belongs to the Glu Leu Phe Val dehydrogenases family | |
LFHNALEI_00415 | 4.6e-112 | mleP2 | S | Transporter, auxin efflux carrier (AEC) family protein | ||
LFHNALEI_00416 | 5.4e-81 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
LFHNALEI_00417 | 2e-129 | mccF | V | LD-carboxypeptidase | ||
LFHNALEI_00418 | 1.2e-98 | saeS | 2.7.13.3 | T | ATPase histidine kinase DNA gyrase B HSP90 domain protein | |
LFHNALEI_00419 | 3.6e-163 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
LFHNALEI_00420 | 4.9e-105 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
LFHNALEI_00422 | 1.3e-63 | yugI | 5.3.1.9 | J | RNA binding protein, contains ribosomal protein S1 domain | |
LFHNALEI_00423 | 4.2e-112 | 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 | |
LFHNALEI_00425 | 1.2e-53 | yeiH | S | Membrane | ||
LFHNALEI_00426 | 3.9e-66 | spxA_2 | 1.20.4.1 | P | Belongs to the ArsC family | |
LFHNALEI_00427 | 1.5e-36 | 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 | ||
LFHNALEI_00428 | 5.9e-32 | fliF | 2.1.1.72 | N | bacterial-type flagellum-dependent cell motility | |
LFHNALEI_00429 | 3.6e-91 | S | double-stranded DNA endodeoxyribonuclease activity | |||
LFHNALEI_00430 | 1e-34 | ykuJ | S | protein conserved in bacteria | ||
LFHNALEI_00431 | 4.6e-14 | M | Putative cell wall binding repeat | |||
LFHNALEI_00432 | 4.1e-136 | P | COG0168 Trk-type K transport systems, membrane components | |||
LFHNALEI_00433 | 1.9e-141 | L | PFAM transposase IS116 IS110 IS902 family | |||
LFHNALEI_00434 | 1.3e-06 | |||||
LFHNALEI_00435 | 0.0 | |||||
LFHNALEI_00436 | 0.0 | bcsA | 2.4.1.12 | GT2 | M | COG1215 Glycosyltransferases, probably involved in cell wall biogenesis |
LFHNALEI_00437 | 1.6e-120 | 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 | |
LFHNALEI_00438 | 5.1e-306 | ybiT | S | abc transporter atp-binding protein | ||
LFHNALEI_00439 | 7.1e-153 | yvjA | S | membrane | ||
LFHNALEI_00440 | 1.2e-191 | trpS | 6.1.1.2 | J | Tryptophanyl-tRNA synthetase | |
LFHNALEI_00441 | 5.6e-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 | |
LFHNALEI_00442 | 5.5e-27 | XK27_07105 | K | transcriptional | ||
LFHNALEI_00443 | 9.2e-28 | |||||
LFHNALEI_00444 | 4.5e-74 | potC | P | ABC-type spermidine putrescine transport system, permease component II | ||
LFHNALEI_00445 | 1.7e-108 | 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 | ||
LFHNALEI_00446 | 6.5e-232 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
LFHNALEI_00447 | 7.2e-144 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
LFHNALEI_00448 | 5.3e-141 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
LFHNALEI_00449 | 7.7e-47 | yajC | U | protein transport | ||
LFHNALEI_00450 | 6.1e-126 | yeeN | K | transcriptional regulatory protein | ||
LFHNALEI_00451 | 4.3e-77 | V | ABC transporter | |||
LFHNALEI_00452 | 1.4e-98 | 2.3.1.128 | K | Acetyltransferase GNAT Family | ||
LFHNALEI_00453 | 1.4e-34 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
LFHNALEI_00454 | 1.4e-218 | norN | V | Mate efflux family protein | ||
LFHNALEI_00455 | 1.4e-57 | asp | S | cog cog1302 | ||
LFHNALEI_00456 | 9.3e-303 | yloV | S | kinase related to dihydroxyacetone kinase | ||
LFHNALEI_00457 | 0.0 | ilvD | 4.2.1.9 | E | Belongs to the IlvD Edd family | |
LFHNALEI_00458 | 1.1e-87 | artQ | P | ABC transporter (Permease | ||
LFHNALEI_00459 | 7.2e-26 | epuA | S | DNA-directed RNA polymerase subunit beta | ||
LFHNALEI_00460 | 1.1e-46 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LFHNALEI_00461 | 8.3e-136 | adcC | P | ABC transporter, ATP-binding protein | ||
LFHNALEI_00462 | 2.2e-70 | adcR | K | transcriptional | ||
LFHNALEI_00463 | 2.8e-182 | 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 | ||
LFHNALEI_00464 | 2.1e-157 | 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 | ||
LFHNALEI_00465 | 1.4e-25 | |||||
LFHNALEI_00466 | 2.9e-273 | sufB | O | assembly protein SufB | ||
LFHNALEI_00467 | 2.7e-105 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
LFHNALEI_00468 | 6.9e-10 | S | Protein of unknown function (DUF1146) | |||
LFHNALEI_00469 | 4.9e-142 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
LFHNALEI_00470 | 5.9e-46 | 3.2.2.21 | S | YCII-related domain | ||
LFHNALEI_00471 | 6e-25 | yjdF | S | Protein of unknown function (DUF2992) | ||
LFHNALEI_00472 | 1.6e-08 | |||||
LFHNALEI_00473 | 3e-60 | ykoD | P | abc transporter atp-binding protein | ||
LFHNALEI_00474 | 8.7e-78 | mccF | V | LD-carboxypeptidase | ||
LFHNALEI_00475 | 5.3e-43 | S | Sugar efflux transporter for intercellular exchange | |||
LFHNALEI_00476 | 6.1e-25 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
LFHNALEI_00477 | 2.2e-38 | 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 | |
LFHNALEI_00478 | 1.5e-171 | malQ | 2.4.1.25 | GH77 | G | 4-alpha-glucanotransferase |
LFHNALEI_00479 | 1.2e-91 | pepV | 3.5.1.18 | E | Dipeptidase | |
LFHNALEI_00480 | 1e-117 | yxeN | P | ABC transporter (Permease | ||
LFHNALEI_00481 | 1.4e-130 | tcyN | 3.6.3.21 | E | abc transporter atp-binding protein | |
LFHNALEI_00482 | 5e-10 | S | Protein of unknown function (DUF4059) | |||
LFHNALEI_00483 | 2.1e-171 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
LFHNALEI_00484 | 1.5e-92 | rsmD | 2.1.1.171 | L | Methyltransferase | |
LFHNALEI_00485 | 1e-87 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
LFHNALEI_00486 | 4.6e-186 | ylbL | T | Belongs to the peptidase S16 family | ||
LFHNALEI_00487 | 4.6e-76 | 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) | |
LFHNALEI_00489 | 5.4e-87 | yeiH | S | membrane | ||
LFHNALEI_00490 | 6.5e-142 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
LFHNALEI_00491 | 8.2e-57 | P | FtsX-like permease family | |||
LFHNALEI_00492 | 1.5e-42 | S | Sugar efflux transporter for intercellular exchange | |||
LFHNALEI_00493 | 2.2e-151 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
LFHNALEI_00494 | 9.2e-78 | 4.1.1.37 | H | Uroporphyrinogen decarboxylase (URO-D) | ||
LFHNALEI_00495 | 5.5e-83 | 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 | |
LFHNALEI_00496 | 4.5e-180 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
LFHNALEI_00497 | 1.3e-91 | vex1 | V | Efflux ABC transporter, permease protein | ||
LFHNALEI_00498 | 2.4e-08 | S | Enterocin A Immunity | |||
LFHNALEI_00499 | 5.3e-142 | S | hydrolases or acyltransferases (alpha beta hydrolase superfamily) | |||
LFHNALEI_00500 | 2.1e-77 | T | Histidine kinase | |||
LFHNALEI_00502 | 7.6e-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 | ||
LFHNALEI_00503 | 1.1e-80 | ygaC | J | Belongs to the UPF0374 family | ||
LFHNALEI_00504 | 2.1e-82 | acoB | 1.2.4.1, 1.2.4.4 | C | COG0022 Pyruvate 2-oxoglutarate dehydrogenase complex, dehydrogenase (E1) component, eukaryotic type, beta subunit | |
LFHNALEI_00505 | 1.1e-110 | vraR | K | Response regulator containing a CheY-like receiver domain and an HTH DNA-binding domain | ||
LFHNALEI_00507 | 7.8e-135 | P | cobalt transport protein | |||
LFHNALEI_00508 | 7.5e-29 | cbiM | P | PDGLE domain | ||
LFHNALEI_00509 | 8.1e-168 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
LFHNALEI_00510 | 5.8e-222 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
LFHNALEI_00511 | 3e-87 | S | Fusaric acid resistance protein-like | |||
LFHNALEI_00512 | 2.5e-62 | glnR | K | Transcriptional regulator | ||
LFHNALEI_00513 | 5.2e-264 | glnA | 6.3.1.2 | E | glutamine synthetase | |
LFHNALEI_00515 | 5.5e-24 | |||||
LFHNALEI_00517 | 3.6e-140 | modF | 3.6.3.21, 3.6.3.34 | P | abc transporter atp-binding protein | |
LFHNALEI_00518 | 3.8e-238 | hlyX | S | COG1253 Hemolysins and related proteins containing CBS domains | ||
LFHNALEI_00519 | 3.7e-31 | NT | Putative ABC-transporter type IV | |||
LFHNALEI_00520 | 5.8e-230 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
LFHNALEI_00521 | 7.1e-264 | argH | 4.3.2.1 | E | Argininosuccinate lyase | |
LFHNALEI_00522 | 3.8e-54 | 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 | |
LFHNALEI_00523 | 9.7e-147 | 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 | ||
LFHNALEI_00524 | 1.6e-238 | 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) | |
LFHNALEI_00525 | 0.0 | pbp1B | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LFHNALEI_00526 | 1.3e-69 | rpoB | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFHNALEI_00527 | 4.8e-157 | 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 | ||
LFHNALEI_00528 | 1e-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 | |
LFHNALEI_00529 | 3.9e-85 | 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 | ||
LFHNALEI_00530 | 3.6e-77 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
LFHNALEI_00531 | 1.4e-122 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
LFHNALEI_00532 | 2.4e-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 | ||
LFHNALEI_00533 | 1.4e-41 | S | RteC protein | |||
LFHNALEI_00534 | 1.6e-89 | T | COG COG0664 cAMP-binding proteins - catabolite gene activator and regulatory subunit of cAMP-dependent protein kinases | |||
LFHNALEI_00535 | 8.5e-146 | rlmJ | 2.1.1.266 | S | COG COG2961 Protein involved in catabolism of external DNA | |
LFHNALEI_00536 | 2.5e-57 | S | RteC protein | |||
LFHNALEI_00537 | 2.6e-53 | S | Helix-turn-helix domain | |||
LFHNALEI_00538 | 8.2e-97 | |||||
LFHNALEI_00540 | 7.8e-288 | ahpF | O | alkyl hydroperoxide reductase | ||
LFHNALEI_00541 | 2.4e-106 | ahpC | 1.11.1.15 | O | alkyl hydroperoxide reductase | |
LFHNALEI_00542 | 7.4e-138 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
LFHNALEI_00543 | 1e-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 | ||
LFHNALEI_00544 | 0.0 | ftsI | 3.4.16.4 | M | penicillin-binding protein | |
LFHNALEI_00545 | 4e-45 | ftsL | D | cell division protein FtsL | ||
LFHNALEI_00546 | 4.4e-172 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
LFHNALEI_00547 | 3.7e-08 | |||||
LFHNALEI_00548 | 6.8e-95 | ureI | S | AmiS/UreI family transporter | ||
LFHNALEI_00549 | 7.6e-46 | ureA | 3.5.1.5 | E | Belongs to the urease gamma subunit family | |
LFHNALEI_00550 | 7.8e-54 | ureB | 3.5.1.5 | E | Belongs to the urease beta subunit family | |
LFHNALEI_00551 | 0.0 | ureC | 3.5.1.5 | E | Belongs to the metallo-dependent hydrolases superfamily. Urease alpha subunit family | |
LFHNALEI_00552 | 6.6e-78 | ureE | O | enzyme active site formation | ||
LFHNALEI_00553 | 6.9e-130 | ureF | O | Required for maturation of urease via the functional incorporation of the urease nickel metallocenter | ||
LFHNALEI_00554 | 3.3e-112 | cysE | 2.3.1.30 | E | serine acetyltransferase | |
LFHNALEI_00555 | 1e-139 | S | SseB protein N-terminal domain | |||
LFHNALEI_00556 | 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 | |
LFHNALEI_00559 | 4.3e-95 | ywlG | S | Belongs to the UPF0340 family | ||
LFHNALEI_00560 | 2.3e-125 | treR | K | trehalose operon | ||
LFHNALEI_00561 | 6.9e-136 | thiD | 2.7.1.35, 2.7.1.49, 2.7.4.7 | H | phosphomethylpyrimidine kinase | |
LFHNALEI_00562 | 2e-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 | |
LFHNALEI_00563 | 4.2e-193 | 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 | ||
LFHNALEI_00564 | 8.9e-180 | dnaK | O | Heat shock 70 kDa protein | ||
LFHNALEI_00565 | 7.7e-88 | XK27_09675 | K | histone acetyltransferase HPA2 and related acetyltransferases | ||
LFHNALEI_00566 | 2.3e-256 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
LFHNALEI_00567 | 9.6e-23 | |||||
LFHNALEI_00568 | 4e-139 | snf | 2.7.11.1 | L | Superfamily II DNA RNA helicases, SNF2 family' | |
LFHNALEI_00569 | 9.5e-203 | 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 | |
LFHNALEI_00570 | 6.1e-35 | |||||
LFHNALEI_00571 | 1.5e-152 | yxeM | ET | ABC-type amino acid transport signal transduction systems, periplasmic component domain | ||
LFHNALEI_00572 | 1.2e-255 | 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 | ||
LFHNALEI_00573 | 7.7e-135 | parB | K | Belongs to the ParB family | ||
LFHNALEI_00574 | 9.2e-207 | htrA | 3.4.21.107 | O | Trypsin-like serine proteases, typically periplasmic, contain C-terminal PDZ domain' | |
LFHNALEI_00575 | 1.6e-28 | ynzC | S | UPF0291 protein | ||
LFHNALEI_00576 | 6e-255 | cycA | E | permease | ||
LFHNALEI_00577 | 5e-07 | uvrX | 2.7.7.7 | L | impB/mucB/samB family | |
LFHNALEI_00578 | 4.6e-35 | XK27_09620 | S | FMN reductase (NADPH) activity | ||
LFHNALEI_00579 | 2.3e-229 | XK27_09615 | C | reductase | ||
LFHNALEI_00580 | 1.8e-139 | fnt | P | Formate nitrite transporter | ||
LFHNALEI_00581 | 1.3e-94 | XK27_08585 | S | Psort location CytoplasmicMembrane, score | ||
LFHNALEI_00582 | 1.3e-70 | 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 | ||
LFHNALEI_00583 | 5.2e-229 | 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 | ||
LFHNALEI_00584 | 9.6e-139 | ykuT | M | mechanosensitive ion channel | ||
LFHNALEI_00585 | 3.9e-87 | sigH | K | DNA-templated transcription, initiation | ||
LFHNALEI_00588 | 8.8e-22 | |||||
LFHNALEI_00589 | 4e-08 | sraP | UW | domain, Protein | ||
LFHNALEI_00590 | 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 | ||
LFHNALEI_00591 | 1.3e-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 | ||
LFHNALEI_00592 | 1.9e-23 | rpmD | J | ribosomal protein l30 | ||
LFHNALEI_00593 | 5.7e-58 | rplO | J | binds to the 23S rRNA | ||
LFHNALEI_00594 | 2.1e-230 | 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 | ||
LFHNALEI_00595 | 2.1e-114 | 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 | |
LFHNALEI_00596 | 2.2e-73 | rplI | J | binds to the 23S rRNA | ||
LFHNALEI_00597 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
LFHNALEI_00598 | 5.3e-256 | 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 | ||
LFHNALEI_00599 | 6.9e-168 | manL | 2.7.1.191 | G | pts system | |
LFHNALEI_00600 | 1.8e-131 | manY | G | pts system | ||
LFHNALEI_00601 | 5.3e-159 | manN | G | PTS system mannose fructose sorbose family IID component | ||
LFHNALEI_00602 | 1e-66 | manO | S | Protein conserved in bacteria | ||
LFHNALEI_00603 | 6e-91 | yacP | S | RNA-binding protein containing a PIN domain | ||
LFHNALEI_00604 | 3.7e-134 | trmH | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LFHNALEI_00606 | 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) | ||
LFHNALEI_00607 | 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 | |
LFHNALEI_00608 | 3.1e-81 | folK | 2.7.6.3, 4.1.2.25 | H | 2-amino-4-hydroxy-6-hydroxymethyldihydropteridine pyrophosphokinase | |
LFHNALEI_00609 | 6.3e-179 | murB | 1.3.1.98 | M | cell wall formation | |
LFHNALEI_00610 | 2.6e-211 | 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 | |
LFHNALEI_00611 | 1.5e-121 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LFHNALEI_00612 | 9.3e-231 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
LFHNALEI_00613 | 3.5e-258 | clpC | O | Belongs to the ClpA ClpB family | ||
LFHNALEI_00614 | 8e-42 | ylxQ | J | ribosomal protein | ||
LFHNALEI_00615 | 3e-47 | ylxR | K | Nucleic-acid-binding protein implicated in transcription termination | ||
LFHNALEI_00616 | 2.4e-196 | nusA | K | Participates in both transcription termination and antitermination | ||
LFHNALEI_00617 | 3.5e-12 | rimP | S | Required for maturation of 30S ribosomal subunits | ||
LFHNALEI_00618 | 4.4e-121 | macB | V | ABC transporter, ATP-binding protein | ||
LFHNALEI_00619 | 2.3e-181 | acrA | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
LFHNALEI_00620 | 1e-111 | 2.1.1.223 | S | Putative SAM-dependent methyltransferase | ||
LFHNALEI_00621 | 1.2e-76 | ydiB | 2.7.1.221, 5.1.1.1 | M | ATPase or kinase | |
LFHNALEI_00622 | 1.6e-247 | pbuO | S | permease | ||
LFHNALEI_00623 | 3.5e-154 | yitU | 3.1.3.104 | S | hydrolases of the HAD superfamily | |
LFHNALEI_00624 | 2.3e-198 | 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) | ||
LFHNALEI_00625 | 6e-146 | XK27_02985 | S | overlaps another CDS with the same product name | ||
LFHNALEI_00626 | 1.4e-147 | supH | S | overlaps another CDS with the same product name | ||
LFHNALEI_00627 | 2.5e-63 | S | sequence-specific DNA binding | |||
LFHNALEI_00628 | 1.5e-89 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
LFHNALEI_00629 | 4.1e-150 | 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 | ||
LFHNALEI_00630 | 4.7e-154 | 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 | |
LFHNALEI_00631 | 2.8e-132 | 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 | ||
LFHNALEI_00632 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
LFHNALEI_00633 | 3.7e-12 | treC | 3.2.1.93 | GH13 | G | COG0366 Glycosidases |
LFHNALEI_00634 | 2.3e-153 | vicX | 3.1.26.11 | S | Metal-dependent hydrolases of the beta-lactamase superfamily I | |
LFHNALEI_00635 | 1e-235 | vicK | 2.7.13.3 | T | Histidine kinase | |
LFHNALEI_00636 | 3.8e-128 | KT | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LFHNALEI_00637 | 3.1e-49 | Z012_09305 | 3.4.21.72 | MU | Autotransporter beta-domain | |
LFHNALEI_00638 | 1.1e-203 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
LFHNALEI_00639 | 1.1e-29 | yyzM | S | Protein conserved in bacteria | ||
LFHNALEI_00640 | 3.5e-138 | 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 | |
LFHNALEI_00641 | 8.2e-61 | K | helix_turn_helix gluconate operon transcriptional repressor | |||
LFHNALEI_00642 | 2.9e-20 | copY | K | Copper transport repressor, CopY TcrY family | ||
LFHNALEI_00643 | 3.7e-66 | silP | 1.9.3.1, 3.6.3.54 | S | cog cog4633 | |
LFHNALEI_00644 | 2.6e-308 | copA | 3.6.3.54 | P | P-type ATPase | |
LFHNALEI_00645 | 2.3e-76 | copA | 3.6.3.54 | P | P-type ATPase | |
LFHNALEI_00646 | 3.1e-12 | spxB | 1.2.3.3, 1.2.5.1 | C | Pyruvate flavodoxin/ferredoxin oxidoreductase, thiamine diP-bdg | |
LFHNALEI_00647 | 1.9e-118 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
LFHNALEI_00648 | 8.2e-60 | XK27_04120 | S | Putative amino acid metabolism | ||
LFHNALEI_00649 | 9.2e-206 | iscS | 2.8.1.7 | E | Cysteine desulfurase | |
LFHNALEI_00650 | 6.7e-159 | 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) | |
LFHNALEI_00651 | 1.8e-29 | acpP1 | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
LFHNALEI_00652 | 3.5e-183 | 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 | |
LFHNALEI_00653 | 1.6e-140 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
LFHNALEI_00654 | 1.1e-217 | araT | 2.6.1.1 | E | Aminotransferase | |
LFHNALEI_00655 | 1.9e-53 | glnB | K | Belongs to the P(II) protein family | ||
LFHNALEI_00656 | 3.3e-228 | amt | P | Ammonium Transporter | ||
LFHNALEI_00657 | 1.8e-156 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
LFHNALEI_00658 | 1.2e-54 | yabA | L | Involved in initiation control of chromosome replication | ||
LFHNALEI_00659 | 9.5e-32 | yaaT | S | stage 0 sporulation protein | ||
LFHNALEI_00660 | 2.4e-12 | S | PcfK-like protein | |||
LFHNALEI_00661 | 4.3e-17 | |||||
LFHNALEI_00662 | 3.1e-72 | S | Region found in RelA / SpoT proteins | |||
LFHNALEI_00664 | 1.8e-99 | K | transcriptional regulator, MerR family | |||
LFHNALEI_00665 | 0.0 | V | ABC transporter (Permease | |||
LFHNALEI_00666 | 2.4e-19 | V | abc transporter atp-binding protein | |||
LFHNALEI_00667 | 9.5e-46 | cbf | S | 3'-5' exoribonuclease yhaM | ||
LFHNALEI_00668 | 4e-142 | purR | 2.4.2.7 | F | operon repressor | |
LFHNALEI_00669 | 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 | ||
LFHNALEI_00670 | 3.9e-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 | ||
LFHNALEI_00671 | 6.2e-99 | 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) | |
LFHNALEI_00673 | 8.6e-240 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
LFHNALEI_00674 | 1.1e-31 | 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | ||
LFHNALEI_00675 | 2.1e-79 | 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 | |
LFHNALEI_00676 | 3.3e-30 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
LFHNALEI_00677 | 4.4e-172 | fabK | 1.3.1.9 | S | 2-Nitropropane dioxygenase | |
LFHNALEI_00678 | 7.2e-164 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
LFHNALEI_00679 | 2.2e-42 | |||||
LFHNALEI_00680 | 2.6e-214 | L | COG3547 Transposase and inactivated derivatives | |||
LFHNALEI_00681 | 1.7e-11 | 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 | |
LFHNALEI_00682 | 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 | |
LFHNALEI_00683 | 5.4e-256 | 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 | |
LFHNALEI_00684 | 5e-159 | 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 | |
LFHNALEI_00685 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
LFHNALEI_00686 | 2.5e-62 | manO | S | protein conserved in bacteria | ||
LFHNALEI_00687 | 3.3e-169 | manN | G | PTS system mannose fructose sorbose family IID component | ||
LFHNALEI_00688 | 1.3e-116 | manM | G | pts system | ||
LFHNALEI_00689 | 5.7e-110 | manL | 2.7.1.191 | G | pts system | |
LFHNALEI_00690 | 7.7e-109 | yvyE | 3.4.13.9 | S | YigZ family | |
LFHNALEI_00691 | 6.3e-168 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
LFHNALEI_00692 | 6e-112 | acuB | S | CBS domain | ||
LFHNALEI_00693 | 6.5e-151 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
LFHNALEI_00694 | 8.7e-78 | yueI | S | Protein of unknown function (DUF1694) | ||
LFHNALEI_00695 | 7.4e-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 | |
LFHNALEI_00696 | 2e-22 | WQ51_00785 | ||||
LFHNALEI_00697 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
LFHNALEI_00698 | 2.8e-24 | secE | U | Belongs to the SecE SEC61-gamma family | ||
LFHNALEI_00699 | 8.4e-96 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
LFHNALEI_00702 | 3.6e-257 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
LFHNALEI_00703 | 1.4e-204 | 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 | ||
LFHNALEI_00704 | 1.6e-148 | estA | CE1 | S | Esterase | |
LFHNALEI_00705 | 8e-126 | XK27_08875 | O | Zinc-dependent metalloprotease | ||
LFHNALEI_00707 | 6.2e-08 | L | Psort location Cytoplasmic, score 8.96 | |||
LFHNALEI_00708 | 7.4e-88 | L | COG1943 Transposase and inactivated derivatives | |||
LFHNALEI_00709 | 2.5e-167 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFHNALEI_00710 | 3.9e-50 | rplQ | J | ribosomal protein l17 | ||
LFHNALEI_00711 | 2.7e-241 | 6.3.2.2 | H | gamma-glutamylcysteine synthetase | ||
LFHNALEI_00712 | 5.4e-56 | hpk9 | 2.7.13.3 | T | protein histidine kinase activity | |
LFHNALEI_00713 | 8e-225 | fasC | 2.7.13.3 | T | protein histidine kinase activity | |
LFHNALEI_00714 | 7.2e-130 | fasA | KT | Response regulator of the LytR AlgR family | ||
LFHNALEI_00715 | 0.0 | rpoC | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
LFHNALEI_00716 | 1.8e-213 | macB_2 | V | FtsX-like permease family | ||
LFHNALEI_00717 | 4.3e-121 | yhcA | V | abc transporter atp-binding protein | ||
LFHNALEI_00718 | 4.9e-309 | 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 | |
LFHNALEI_00719 | 3.8e-84 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
LFHNALEI_00720 | 3.2e-75 | mutT3 | 3.6.1.13, 3.6.1.55 | L | NUDIX domain | |
LFHNALEI_00721 | 1.1e-124 | agrA | KT | LytTr DNA-binding domain | ||
LFHNALEI_00722 | 3.4e-215 | blpH | 2.7.13.3 | T | signal transduction protein with a C-terminal ATPase domain | |
LFHNALEI_00726 | 3.3e-239 | O | MreB/Mbl protein | |||
LFHNALEI_00728 | 5.8e-146 | V | Psort location CytoplasmicMembrane, score | |||
LFHNALEI_00729 | 1.7e-137 | V | abc transporter atp-binding protein | |||
LFHNALEI_00730 | 0.0 | V | abc transporter atp-binding protein | |||
LFHNALEI_00731 | 3.6e-82 | 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) | |
LFHNALEI_00732 | 5e-201 | 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) | |
LFHNALEI_00733 | 9.9e-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 | |
LFHNALEI_00734 | 4.8e-199 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
LFHNALEI_00735 | 1.1e-98 | XK27_07830 | 2.3.1.128 | J | Acetyltransferase GNAT Family | |
LFHNALEI_00736 | 2.6e-32 | sitB | 3.6.3.35 | P | ABC transporter, ATP-binding protein | |
LFHNALEI_00737 | 4.6e-133 | mtsC | P | ABC-type Mn2 Zn2 transport systems, permease components | ||
LFHNALEI_00738 | 4.7e-171 | sitA | P | Belongs to the bacterial solute-binding protein 9 family | ||
LFHNALEI_00739 | 2.5e-118 | sirR | K | iron dependent repressor | ||
LFHNALEI_00740 | 4.6e-24 | htpX | O | Belongs to the peptidase M48B family | ||
LFHNALEI_00741 | 4.4e-74 | K | DNA-binding transcription factor activity | |||
LFHNALEI_00742 | 6e-70 | def_1 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
LFHNALEI_00743 | 1e-99 | S | Psort location CytoplasmicMembrane, score | |||
LFHNALEI_00744 | 4.4e-110 | XK27_06930 | V | domain protein | ||
LFHNALEI_00745 | 4.4e-107 | S | Putative adhesin | |||
LFHNALEI_00746 | 7.8e-63 | XK27_06920 | S | Protein of unknown function (DUF1700) | ||
LFHNALEI_00747 | 6.3e-54 | K | transcriptional regulator, PadR family | |||
LFHNALEI_00748 | 2.7e-124 | ftsW | D | Belongs to the SEDS family | ||
LFHNALEI_00749 | 1.6e-224 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
LFHNALEI_00750 | 2.2e-119 | S | Nucleotidyl transferase AbiEii toxin, Type IV TA system | |||
LFHNALEI_00751 | 7.5e-106 | abiGI | K | Transcriptional regulator, AbiEi antitoxin | ||
LFHNALEI_00752 | 9.2e-25 | XK27_01300 | P | Protein conserved in bacteria | ||
LFHNALEI_00753 | 2.7e-230 | 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 | |
LFHNALEI_00754 | 1.3e-62 | XK27_05710 | K | Acetyltransferase (GNAT) domain | ||
LFHNALEI_00755 | 2.8e-77 | 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 | |
LFHNALEI_00756 | 2e-109 | 3.4.17.14, 3.5.1.28 | M | GBS Bsp-like repeat | ||
LFHNALEI_00757 | 3.7e-134 | agrA | KT | response regulator | ||
LFHNALEI_00759 | 8.5e-113 | capA | M | Bacterial capsule synthesis protein | ||
LFHNALEI_00760 | 1e-38 | gcvR | T | UPF0237 protein | ||
LFHNALEI_00761 | 2.3e-243 | XK27_08635 | S | UPF0210 protein | ||
LFHNALEI_00762 | 2.7e-83 | mreD | M | rod shape-determining protein MreD | ||
LFHNALEI_00763 | 7.3e-107 | mreC | M | Involved in formation and maintenance of cell shape | ||
LFHNALEI_00767 | 5e-27 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LFHNALEI_00768 | 3.1e-78 | feoA | P | FeoA domain protein | ||
LFHNALEI_00769 | 0.0 | S | bacteriocin-associated integral membrane protein | |||
LFHNALEI_00770 | 2.1e-19 | S | Bacteriocin (Lactococcin_972) | |||
LFHNALEI_00771 | 3.4e-132 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
LFHNALEI_00772 | 1.4e-13 | yidD | M | Could be involved in insertion of integral membrane proteins into the membrane | ||
LFHNALEI_00773 | 4.2e-259 | trkH | P | Cation transport protein | ||
LFHNALEI_00774 | 1.5e-33 | trkA | P | Potassium transporter peripheral membrane component | ||
LFHNALEI_00775 | 1.9e-112 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
LFHNALEI_00776 | 7.6e-09 | S | NTF2 fold immunity protein | |||
LFHNALEI_00777 | 9.4e-55 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
LFHNALEI_00778 | 3.5e-08 | XK27_10305 | S | Domain of unknown function (DUF4651) | ||
LFHNALEI_00781 | 2.4e-158 | rrmA | 2.1.1.187 | Q | methyltransferase | |
LFHNALEI_00782 | 1.6e-140 | S | HAD hydrolase, family IA, variant | |||
LFHNALEI_00783 | 2.4e-245 | 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 | ||
LFHNALEI_00784 | 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) | |
LFHNALEI_00785 | 1.3e-137 | tcyC2 | 3.6.3.21 | E | abc transporter atp-binding protein | |
LFHNALEI_00786 | 1.1e-113 | yxeN | P | ABC transporter, permease protein | ||
LFHNALEI_00787 | 1.1e-111 | ytmL | P | ABC transporter (Permease | ||
LFHNALEI_00788 | 2.8e-72 | ET | ABC transporter substrate-binding protein | |||
LFHNALEI_00789 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | G | Belongs to the glycosyl hydrolase 68 family |
LFHNALEI_00790 | 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 | |
LFHNALEI_00791 | 2.5e-43 | M | Glycosyl transferase family 2 | |||
LFHNALEI_00792 | 2.3e-234 | spsC | 2.6.1.102 | E | Belongs to the DegT DnrJ EryC1 family | |
LFHNALEI_00793 | 1.7e-102 | bplG | M | Bacterial sugar transferase | ||
LFHNALEI_00794 | 0.0 | WQ51_06230 | S | ABC transporter | ||
LFHNALEI_00795 | 6e-45 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
LFHNALEI_00796 | 1.9e-164 | 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 | ||
LFHNALEI_00797 | 1.2e-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 | ||
LFHNALEI_00798 | 1.1e-22 | mltG | ADL | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
LFHNALEI_00799 | 8e-238 | 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 | ||
LFHNALEI_00800 | 6.7e-179 | gap | 1.2.1.12 | C | Glyceraldehyde 3-phosphate dehydrogenase, C-terminal domain | |
LFHNALEI_00801 | 4e-130 | deoD | 2.4.2.1, 2.4.2.28 | F | purine nucleoside phosphorylase | |
LFHNALEI_00802 | 1.9e-132 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
LFHNALEI_00803 | 6e-155 | clcA_2 | P | Chloride transporter, ClC family | ||
LFHNALEI_00804 | 1.3e-105 | 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 | |
LFHNALEI_00805 | 1.7e-211 | T | signal transduction protein with a C-terminal ATPase domain | |||
LFHNALEI_00806 | 1.3e-96 | rr02 | KT | response regulator | ||
LFHNALEI_00807 | 8.3e-73 | argR | K | Regulates arginine biosynthesis genes | ||
LFHNALEI_00808 | 2.9e-148 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
LFHNALEI_00809 | 1.9e-181 | ccpA | K | Catabolite control protein A | ||
LFHNALEI_00811 | 1.7e-18 | S | Domain of unknown function (DUF4649) | |||
LFHNALEI_00812 | 2.8e-177 | XK27_08835 | S | ABC transporter substrate binding protein | ||
LFHNALEI_00815 | 1.2e-160 | 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 | |
LFHNALEI_00816 | 2.3e-119 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
LFHNALEI_00817 | 6.6e-176 | coiA | 3.6.4.12 | S | Competence protein | |
LFHNALEI_00818 | 5.9e-280 | T | PhoQ Sensor | |||
LFHNALEI_00819 | 7.9e-123 | T | Response regulators consisting of a CheY-like receiver domain and a winged-helix DNA-binding domain | |||
LFHNALEI_00820 | 3.2e-137 | yxkH | G | deacetylase | ||
LFHNALEI_00821 | 4.6e-205 | argD | 2.6.1.11, 2.6.1.17 | E | acetylornithine aminotransferase | |
LFHNALEI_00822 | 1.5e-247 | merA | 1.16.1.1 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LFHNALEI_00823 | 3e-142 | E | Alpha beta hydrolase | |||
LFHNALEI_00825 | 2.2e-92 | 2.7.7.65 | T | Psort location CytoplasmicMembrane, score | ||
LFHNALEI_00826 | 1.7e-140 | S | Phenazine biosynthesis protein | |||
LFHNALEI_00827 | 4.5e-29 | K | Helix-turn-helix domain | |||
LFHNALEI_00828 | 9.6e-21 | |||||
LFHNALEI_00829 | 7.3e-65 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
LFHNALEI_00830 | 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 | ||
LFHNALEI_00831 | 1.5e-20 | gltJ | P | ABC transporter (Permease | ||
LFHNALEI_00832 | 2.9e-111 | tcyB_2 | P | ABC transporter (permease) | ||
LFHNALEI_00833 | 1.6e-140 | glnQ | 3.6.3.21 | E | abc transporter atp-binding protein | |
LFHNALEI_00834 | 5.8e-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 | ||
LFHNALEI_00835 | 1.8e-47 | veg | S | Biofilm formation stimulator VEG | ||
LFHNALEI_00836 | 2.7e-230 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
LFHNALEI_00837 | 1.9e-186 | 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) | |
LFHNALEI_00838 | 2.6e-175 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
LFHNALEI_00841 | 7.8e-140 | 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 | |
LFHNALEI_00842 | 2.5e-59 | pts33BCA | G | pts system | ||
LFHNALEI_00843 | 1.7e-265 | pacL | 3.6.3.8, 3.6.3.9 | P | cation transport ATPase | |
LFHNALEI_00844 | 3e-179 | trpD | 2.4.2.18, 4.1.3.27 | F | Catalyzes the transfer of the phosphoribosyl group of 5- phosphorylribose-1-pyrophosphate (PRPP) to anthranilate to yield N-(5'-phosphoribosyl)-anthranilate (PRA) | |
LFHNALEI_00845 | 2.7e-105 | trpG | 2.4.2.18, 2.6.1.85, 4.1.3.27 | EH | anthranilate | |
LFHNALEI_00846 | 1.2e-106 | trpE | 4.1.3.27 | EH | Part of a heterotetrameric complex that catalyzes the two-step biosynthesis of anthranilate, an intermediate in the biosynthesis of L-tryptophan. In the first step, the glutamine- binding beta subunit (TrpG) of anthranilate synthase (AS) provides the glutamine amidotransferase activity which generates ammonia as a substrate that, along with chorismate, is used in the second step, catalyzed by the large alpha subunit of AS (TrpE) to produce anthranilate. In the absence of TrpG, TrpE can synthesize anthranilate directly from chorismate and high concentrations of ammonia | |
LFHNALEI_00849 | 1.9e-164 | metQ | M | Belongs to the NlpA lipoprotein family | ||
LFHNALEI_00850 | 5.1e-142 | ET | amino acid transport | |||
LFHNALEI_00851 | 1e-20 | metI | P | ABC transporter (Permease | ||
LFHNALEI_00852 | 6.1e-211 | sstT | E | Involved in the import of serine and threonine into the cell, with the concomitant import of sodium (symport system) | ||
LFHNALEI_00853 | 0.0 | ltaS | 2.7.8.20 | M | Belongs to the LTA synthase family | |
LFHNALEI_00854 | 8.6e-139 | 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 | |
LFHNALEI_00855 | 3.9e-98 | XK27_09740 | S | Phosphoesterase | ||
LFHNALEI_00856 | 8.3e-87 | ykuL | S | CBS domain | ||
LFHNALEI_00857 | 1.1e-112 | 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 | |
LFHNALEI_00858 | 2.4e-161 | rfbA | 2.7.7.24 | M | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
LFHNALEI_00859 | 7.4e-54 | S | phospholipase Carboxylesterase | |||
LFHNALEI_00860 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
LFHNALEI_00862 | 3.1e-259 | XK27_03190 | S | hydrolases of the HAD superfamily | ||
LFHNALEI_00863 | 2.9e-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 | |
LFHNALEI_00864 | 2.5e-144 | tatD | L | Hydrolase, tatd | ||
LFHNALEI_00865 | 9.4e-74 | yccU | S | CoA-binding protein | ||
LFHNALEI_00866 | 2.5e-138 | hisK | 3.1.3.15 | E | Histidinol phosphatase and related hydrolases of the PHP family | |
LFHNALEI_00867 | 7.1e-118 | ylfI | S | tigr01906 | ||
LFHNALEI_00868 | 8.3e-93 | ypsA | S | Belongs to the UPF0398 family | ||
LFHNALEI_00869 | 4.3e-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 | ||
LFHNALEI_00870 | 1.3e-13 | |||||
LFHNALEI_00871 | 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) | |
LFHNALEI_00872 | 2.6e-297 | ptsG | 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | pts system | |
LFHNALEI_00873 | 3.1e-220 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
LFHNALEI_00874 | 1e-104 | wecD | M | Acetyltransferase (GNAT) domain | ||
LFHNALEI_00875 | 2.5e-49 | 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 | |
LFHNALEI_00876 | 7.6e-148 | nodB3 | G | deacetylase | ||
LFHNALEI_00877 | 6.9e-133 | 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 | |
LFHNALEI_00878 | 2.6e-68 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
LFHNALEI_00879 | 8.1e-168 | L | Transposase | |||
LFHNALEI_00880 | 5.7e-36 | cmpC | S | abc transporter atp-binding protein | ||
LFHNALEI_00881 | 4.9e-42 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
LFHNALEI_00882 | 8.8e-204 | 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 | |
LFHNALEI_00883 | 2.8e-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) | |
LFHNALEI_00884 | 3.4e-14 | rpmH | J | Ribosomal protein L34 | ||
LFHNALEI_00885 | 2.2e-66 | 1.6.5.2 | S | NADPH-quinone reductase (modulator of drug activity B) | ||
LFHNALEI_00886 | 1.6e-152 | corA | P | CorA-like protein | ||
LFHNALEI_00887 | 3.3e-62 | yjqA | S | Bacterial PH domain | ||
LFHNALEI_00888 | 1.7e-99 | thiT | S | Thiamine transporter | ||
LFHNALEI_00889 | 5.4e-104 | rsmC | 2.1.1.172 | J | Methyltransferase small domain protein | |
LFHNALEI_00890 | 5e-232 | 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 | |
LFHNALEI_00891 | 1.1e-200 | I | acyl-CoA dehydrogenase | |||
LFHNALEI_00892 | 2e-97 | mip | S | hydroperoxide reductase activity | ||
LFHNALEI_00894 | 2e-149 | srtB | 3.4.22.70 | S | Sortase family | |
LFHNALEI_00895 | 2.4e-267 | ilvB | 2.2.1.6 | EH | Acetolactate synthase | |
LFHNALEI_00896 | 2.2e-76 | ilvN | 2.2.1.6 | E | Acetolactate synthase | |
LFHNALEI_00897 | 1.3e-17 | |||||
LFHNALEI_00898 | 7.8e-52 | L | single-stranded DNA binding | |||
LFHNALEI_00899 | 1.8e-19 | |||||
LFHNALEI_00900 | 1.6e-76 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
LFHNALEI_00901 | 1.5e-186 | trxB1 | 1.18.1.2, 1.19.1.1 | C | Ferredoxin--NADP reductase | |
LFHNALEI_00902 | 0.0 | dnaG | L | RNA polymerase that catalyzes the synthesis of short RNA molecules used as primers for DNA polymerase during DNA replication | ||
LFHNALEI_00903 | 1.8e-92 | 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) | |
LFHNALEI_00904 | 1e-273 | 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) | |
LFHNALEI_00905 | 6.2e-165 | pepA | 3.4.11.7 | G | COG1363 Cellulase M and related proteins | |
LFHNALEI_00906 | 1.7e-129 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
LFHNALEI_00907 | 3.3e-58 | S | CAAX amino terminal protease family protein | |||
LFHNALEI_00908 | 1.5e-77 | ccl | S | cog cog4708 | ||
LFHNALEI_00909 | 2.7e-48 | nudF | 3.6.1.13 | L | AdP-ribose pyrophosphatase | |
LFHNALEI_00910 | 9.2e-24 | |||||
LFHNALEI_00911 | 7.7e-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 | |
LFHNALEI_00912 | 3.2e-20 | WQ51_02665 | S | Protein of unknown function (DUF3042) | ||
LFHNALEI_00915 | 1.1e-56 | 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 | ||
LFHNALEI_00916 | 1.3e-91 | XK27_05110 | P | Chloride transporter ClC family | ||
LFHNALEI_00917 | 5.6e-34 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
LFHNALEI_00920 | 1.4e-130 | rlmN | 2.1.1.192 | J | Specifically methylates position 2 of adenine 2503 in 23S rRNA and position 2 of adenine 37 in tRNAs | |
LFHNALEI_00921 | 1e-109 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
LFHNALEI_00923 | 1.3e-223 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
LFHNALEI_00924 | 1.1e-184 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
LFHNALEI_00925 | 2.1e-88 | acmA | 3.2.1.17, 3.4.17.14, 3.5.1.28 | NU | Muramidase (Flagellum-specific) | |
LFHNALEI_00926 | 3.5e-82 | 3.5.1.28 | M | domain protein | ||
LFHNALEI_00927 | 1.1e-251 | 2.4.1.5 | GH13 | M | KxYKxGKxW signal domain protein | |
LFHNALEI_00928 | 2.9e-265 | 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 | |
LFHNALEI_00929 | 2e-208 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
LFHNALEI_00930 | 1.6e-36 | yneF | S | UPF0154 protein | ||
LFHNALEI_00931 | 1.8e-90 | K | transcriptional regulator | |||
LFHNALEI_00932 | 1.9e-55 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LFHNALEI_00933 | 1.1e-34 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
LFHNALEI_00934 | 7.3e-94 | XK27_09705 | 6.1.1.14 | S | HD superfamily hydrolase | |
LFHNALEI_00935 | 2.2e-101 | ybhL | S | Belongs to the BI1 family | ||
LFHNALEI_00937 | 2.2e-66 | dapE | 3.5.1.18 | E | COG0624, acetylornithine deacetylase succinyl-diaminopimelate desuccinylase and related deacylases | |
LFHNALEI_00938 | 1.9e-187 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
LFHNALEI_00939 | 6.5e-87 | lysA | 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
LFHNALEI_00940 | 3.2e-113 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
LFHNALEI_00941 | 1.3e-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 | |
LFHNALEI_00942 | 2.4e-18 | 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 | |
LFHNALEI_00943 | 1.2e-141 | L | Transposase and inactivated derivatives | |||
LFHNALEI_00944 | 5.3e-74 | L | Transposase | |||
LFHNALEI_00945 | 1.7e-76 | 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 | |
LFHNALEI_00946 | 2.6e-156 | L | Replication initiation factor | |||
LFHNALEI_00947 | 1.9e-18 | S | Domain of unknown function (DUF3173) | |||
LFHNALEI_00948 | 1.7e-215 | int | L | Phage integrase family | ||
LFHNALEI_00950 | 3.7e-235 | rarA | L | ATPase related to the helicase subunit of the Holliday junction resolvase | ||
LFHNALEI_00951 | 8.4e-27 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
LFHNALEI_00952 | 6.3e-44 | yrzL | S | Belongs to the UPF0297 family | ||
LFHNALEI_00953 | 2.3e-69 | yqgF | L | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
LFHNALEI_00954 | 2.1e-43 | yrzB | S | Belongs to the UPF0473 family | ||
LFHNALEI_00955 | 6.4e-296 | ccs | S | the current gene model (or a revised gene model) may contain a frame shift | ||
LFHNALEI_00956 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
LFHNALEI_00957 | 7.5e-14 | |||||
LFHNALEI_00958 | 4.2e-46 | ylbG | S | UPF0298 protein | ||
LFHNALEI_00959 | 4.4e-74 | ylbF | S | Belongs to the UPF0342 family | ||
LFHNALEI_00960 | 5.5e-77 | 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 | |
LFHNALEI_00961 | 3e-78 | K | hmm pf08876 | |||
LFHNALEI_00962 | 1.6e-222 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
LFHNALEI_00963 | 1e-16 | rafG | P | sugar transport system permease | ||
LFHNALEI_00964 | 1.3e-57 | XK27_00915 | C | COG2141 Coenzyme F420-dependent N5,N10-methylene tetrahydromethanopterin reductase and related flavin-dependent oxidoreductases | ||
LFHNALEI_00965 | 2.2e-17 | yjdB | S | Domain of unknown function (DUF4767) | ||
LFHNALEI_00966 | 9.1e-83 | tehB | 2.1.1.265 | PQ | tellurite resistance protein tehb | |
LFHNALEI_00968 | 1.1e-104 | recJ | L | Single-strand DNA-specific exonuclease, C terminal domain | ||
LFHNALEI_00969 | 6.4e-93 | 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 | |
LFHNALEI_00970 | 1.1e-84 | fruA | 2.7.1.202 | G | phosphotransferase system | |
LFHNALEI_00971 | 4e-78 | gor | 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
LFHNALEI_00972 | 3.7e-78 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
LFHNALEI_00973 | 5.7e-166 | 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 | |
LFHNALEI_00974 | 5.2e-237 | ymfH | S | Peptidase M16 | ||
LFHNALEI_00975 | 4.1e-30 | 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 | |
LFHNALEI_00976 | 5.1e-110 | tdk | 2.7.1.21 | F | thymidine kinase | |
LFHNALEI_00977 | 4e-165 | S | hmm pf01594 | |||
LFHNALEI_00978 | 1.4e-53 | ndpA | S | 37-kD nucleoid-associated bacterial protein | ||
LFHNALEI_00979 | 1.9e-99 | pvaA | M | lytic transglycosylase activity | ||
LFHNALEI_00980 | 8.5e-08 | N | PFAM Uncharacterised protein family UPF0150 | |||
LFHNALEI_00981 | 4e-151 | EG | Permeases of the drug metabolite transporter (DMT) superfamily | |||
LFHNALEI_00983 | 2.5e-170 | rmuC | S | RmuC domain protein | ||
LFHNALEI_00984 | 3e-142 | trpA | 4.2.1.20 | E | The alpha subunit is responsible for the aldol cleavage of indoleglycerol phosphate to indole and glyceraldehyde 3- phosphate | |
LFHNALEI_00985 | 6.7e-87 | yciE | S | cellular response to DNA damage stimulus | ||
LFHNALEI_00986 | 2.1e-80 | yciF | S | cellular response to DNA damage stimulus | ||
LFHNALEI_00988 | 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 | ||
LFHNALEI_00989 | 4.2e-83 | XK27_03610 | K | Gnat family | ||
LFHNALEI_00990 | 4.6e-91 | yybC | ||||
LFHNALEI_00991 | 1.6e-206 | mapZ | D | Early cell division protein that marks the future cell division site and supports proper FtsZ ring positioning | ||
LFHNALEI_00992 | 3.8e-105 | mdlB | V | abc transporter atp-binding protein | ||
LFHNALEI_00993 | 2.7e-152 | cylA | V | abc transporter atp-binding protein | ||
LFHNALEI_00994 | 6.9e-69 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
LFHNALEI_00995 | 1.2e-13 | S | oxidoreductase | |||
LFHNALEI_00996 | 6.2e-48 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
LFHNALEI_00997 | 6.3e-84 | mutT | 3.5.4.33, 3.6.1.13, 3.6.1.55 | L | Belongs to the Nudix hydrolase family | |
LFHNALEI_00998 | 3e-96 | clpE | O | Belongs to the ClpA ClpB family | ||
LFHNALEI_00999 | 1.1e-49 | |||||
LFHNALEI_01000 | 8.7e-60 | |||||
LFHNALEI_01001 | 5.9e-55 | |||||
LFHNALEI_01002 | 1.5e-36 | 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 | |
LFHNALEI_01003 | 3.2e-133 | srtA | 3.4.22.70 | M | Sortase (surface protein transpeptidase) | |
LFHNALEI_01004 | 2e-101 | 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 |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)