ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
DJNALGAK_00001 | 1.9e-208 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
DJNALGAK_00002 | 1.7e-61 | K | Bacterial regulatory proteins, tetR family | |||
DJNALGAK_00003 | 1.9e-114 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
DJNALGAK_00004 | 2e-151 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
DJNALGAK_00005 | 5.6e-69 | dhaL | 2.7.1.121 | S | Dak2 | |
DJNALGAK_00006 | 1.4e-49 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
DJNALGAK_00007 | 8.4e-104 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
DJNALGAK_00008 | 4.9e-176 | yjcE | P | Sodium proton antiporter | ||
DJNALGAK_00009 | 5.4e-53 | 1.14.12.17 | C | Oxidoreductase NAD-binding domain | ||
DJNALGAK_00010 | 9e-102 | qmcA | O | prohibitin homologues | ||
DJNALGAK_00011 | 2.1e-26 | S | protein encoded in hypervariable junctions of pilus gene clusters | |||
DJNALGAK_00012 | 0.0 | O | Belongs to the peptidase S8 family | |||
DJNALGAK_00013 | 1.8e-64 | EGP | Major Facilitator Superfamily | |||
DJNALGAK_00014 | 1.4e-156 | gmuE | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
DJNALGAK_00015 | 3.6e-140 | V | MatE | |||
DJNALGAK_00016 | 1.2e-43 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
DJNALGAK_00017 | 5e-87 | S | Alpha beta hydrolase | |||
DJNALGAK_00018 | 1.6e-94 | 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 | |
DJNALGAK_00019 | 1.9e-174 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
DJNALGAK_00020 | 1e-111 | argE | 3.5.1.18 | E | Peptidase dimerisation domain | |
DJNALGAK_00021 | 1.1e-58 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
DJNALGAK_00022 | 6.5e-158 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
DJNALGAK_00023 | 2.4e-92 | yueF | S | AI-2E family transporter | ||
DJNALGAK_00024 | 2.6e-97 | ygaC | J | Belongs to the UPF0374 family | ||
DJNALGAK_00025 | 6.5e-193 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
DJNALGAK_00026 | 3.4e-69 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
DJNALGAK_00027 | 4e-19 | sigH | K | DNA-templated transcription, initiation | ||
DJNALGAK_00028 | 3.5e-22 | S | Cytochrome B5 | |||
DJNALGAK_00029 | 1.8e-172 | rlmL | 2.1.1.173, 2.1.1.264 | L | Belongs to the methyltransferase superfamily | |
DJNALGAK_00030 | 1.1e-35 | gpsB | D | Divisome component that associates with the complex late in its assembly, after the Z-ring is formed, and is dependent on DivIC and PBP2B for its recruitment to the divisome. Together with EzrA, is a key component of the system that regulates PBP1 localization during cell cycle progression. Its main role could be the removal of PBP1 from the cell pole after pole maturation is completed. Also contributes to the recruitment of PBP1 to the division complex. Not essential for septum formation | ||
DJNALGAK_00032 | 9.2e-88 | murI | 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
DJNALGAK_00033 | 1.2e-171 | patA | 2.6.1.1 | E | Aminotransferase | |
DJNALGAK_00034 | 4.4e-34 | glcR | K | DeoR C terminal sensor domain | ||
DJNALGAK_00035 | 5.8e-117 | cps1D | M | Domain of unknown function (DUF4422) | ||
DJNALGAK_00036 | 8.6e-62 | S | Glycosyltransferase like family 2 | |||
DJNALGAK_00037 | 3.6e-141 | rfbA | 2.7.7.24 | H | Catalyzes the formation of dTDP-glucose, from dTTP and glucose 1-phosphate, as well as its pyrophosphorolysis | |
DJNALGAK_00038 | 9.4e-101 | rfbC | 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 | |
DJNALGAK_00039 | 1.8e-179 | rfbB | 4.2.1.46 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family. dTDP-glucose dehydratase subfamily | |
DJNALGAK_00040 | 2.1e-130 | rfbD | 1.1.1.133, 5.1.3.13 | M | Catalyzes the reduction of dTDP-6-deoxy-L-lyxo-4- hexulose to yield dTDP-L-rhamnose | |
DJNALGAK_00041 | 4.6e-117 | nagZ | 3.2.1.52 | G | Glycosyl hydrolase family 3 N terminal domain | |
DJNALGAK_00042 | 4.4e-27 | S | zinc-ribbon domain | |||
DJNALGAK_00043 | 2.5e-83 | S | response to antibiotic | |||
DJNALGAK_00044 | 2.1e-15 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Alpha-amylase domain |
DJNALGAK_00045 | 0.0 | glgP | 2.4.1.1 | GT35 | G | Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates. However, all known phosphorylases share catalytic and structural properties |
DJNALGAK_00046 | 9.4e-195 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
DJNALGAK_00047 | 4e-119 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
DJNALGAK_00048 | 2.6e-163 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
DJNALGAK_00049 | 8.1e-266 | 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 |
DJNALGAK_00052 | 1.4e-10 | L | Helix-turn-helix domain | |||
DJNALGAK_00053 | 4e-16 | L | hmm pf00665 | |||
DJNALGAK_00054 | 1.9e-48 | L | hmm pf00665 | |||
DJNALGAK_00055 | 1.1e-180 | tetP | J | elongation factor G | ||
DJNALGAK_00056 | 1.3e-15 | ald | 1.4.1.1 | C | Belongs to the AlaDH PNT family | |
DJNALGAK_00057 | 1.1e-166 | potE2 | E | amino acid | ||
DJNALGAK_00060 | 4.6e-116 | 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 | |
DJNALGAK_00061 | 4.5e-129 | mleP2 | S | Sodium Bile acid symporter family | ||
DJNALGAK_00062 | 4.1e-73 | |||||
DJNALGAK_00063 | 1.9e-09 | L | recombinase activity | |||
DJNALGAK_00064 | 3.4e-73 | glnPH2 | P | ABC transporter permease | ||
DJNALGAK_00065 | 2.3e-112 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJNALGAK_00067 | 2.9e-26 | yneF | S | UPF0154 protein | ||
DJNALGAK_00068 | 3.6e-207 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
DJNALGAK_00069 | 6.4e-56 | 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) | ||
DJNALGAK_00070 | 1.6e-108 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
DJNALGAK_00071 | 7e-71 | yacP | S | YacP-like NYN domain | ||
DJNALGAK_00072 | 2.1e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
DJNALGAK_00073 | 2.6e-11 | secE | U | Essential subunit of the Sec protein translocation channel SecYEG. Clamps together the 2 halves of SecY. May contact the channel plug during translocation | ||
DJNALGAK_00074 | 7.7e-84 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
DJNALGAK_00075 | 5e-67 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
DJNALGAK_00076 | 1.6e-115 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
DJNALGAK_00077 | 7.6e-75 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
DJNALGAK_00078 | 2.6e-48 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
DJNALGAK_00079 | 4e-216 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
DJNALGAK_00080 | 4.1e-229 | V | ABC transporter transmembrane region | |||
DJNALGAK_00082 | 2.8e-95 | S | Domain of unknown function DUF87 | |||
DJNALGAK_00083 | 1.7e-147 | scrR | K | helix_turn _helix lactose operon repressor | ||
DJNALGAK_00084 | 3.5e-216 | scrB | 3.2.1.26 | GH32 | G | invertase |
DJNALGAK_00085 | 1e-52 | ddpX | 3.4.13.22 | E | Catalyzes hydrolysis of the D-alanyl-D-alanine dipeptide | |
DJNALGAK_00086 | 9.5e-277 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
DJNALGAK_00087 | 2.1e-36 | M | LysM domain protein | |||
DJNALGAK_00088 | 3.7e-114 | sbcD | L | SbcCD cleaves DNA hairpin structures. These structures can inhibit DNA replication and are intermediates in certain DNA recombination reactions. The complex acts as a 3'- 5' double strand exonuclease that can open hairpins. It also has a 5' single-strand endonuclease activity | ||
DJNALGAK_00089 | 9.8e-89 | pac | DM | Glucan-binding protein C | ||
DJNALGAK_00090 | 6.9e-37 | |||||
DJNALGAK_00091 | 3.4e-92 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
DJNALGAK_00092 | 4.1e-57 | purE | 5.4.99.18 | F | Catalyzes the conversion of N5-carboxyaminoimidazole ribonucleotide (N5-CAIR) to 4-carboxy-5-aminoimidazole ribonucleotide (CAIR) | |
DJNALGAK_00093 | 3.8e-159 | purK | 6.3.4.18 | F | Catalyzes the ATP-dependent conversion of 5- aminoimidazole ribonucleotide (AIR) and HCO(3)(-) to N5- carboxyaminoimidazole ribonucleotide (N5-CAIR) | |
DJNALGAK_00094 | 1.2e-225 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
DJNALGAK_00095 | 5.4e-111 | miaA | 2.5.1.75 | F | Catalyzes the transfer of a dimethylallyl group onto the adenine at position 37 in tRNAs that read codons beginning with uridine, leading to the formation of N6-(dimethylallyl)adenosine (i(6)A) | |
DJNALGAK_00096 | 1.8e-205 | ynbB | 4.4.1.1 | P | aluminum resistance | |
DJNALGAK_00097 | 1.3e-45 | glnR | K | Transcriptional regulator | ||
DJNALGAK_00098 | 2e-247 | glnA | 6.3.1.2 | E | glutamine synthetase | |
DJNALGAK_00100 | 6.8e-73 | gshR | 1.8.1.7 | C | Glutathione reductase | |
DJNALGAK_00101 | 4.9e-179 | proV | E | ABC transporter, ATP-binding protein | ||
DJNALGAK_00102 | 3e-271 | proWX | EM | Periplasmic glycine betaine choline-binding (lipo)protein of an ABC-type transport system (osmoprotectant binding protein) | ||
DJNALGAK_00105 | 3.5e-98 | cadD | P | Cadmium resistance transporter | ||
DJNALGAK_00106 | 1.7e-26 | |||||
DJNALGAK_00107 | 9e-74 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
DJNALGAK_00108 | 9.6e-132 | bacI | V | MacB-like periplasmic core domain | ||
DJNALGAK_00109 | 4.3e-97 | V | ABC transporter | |||
DJNALGAK_00110 | 2e-64 | bacG | M | Belongs to the membrane fusion protein (MFP) (TC 8.A.1) family | ||
DJNALGAK_00111 | 3.5e-70 | mltD | CBM50 | M | NlpC P60 family protein | |
DJNALGAK_00112 | 1.8e-52 | manO | S | Domain of unknown function (DUF956) | ||
DJNALGAK_00113 | 2.1e-147 | manN | G | system, mannose fructose sorbose family IID component | ||
DJNALGAK_00114 | 8e-119 | manY | G | PTS system sorbose-specific iic component | ||
DJNALGAK_00115 | 9e-152 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
DJNALGAK_00116 | 4.1e-80 | rbsB | G | sugar-binding domain protein | ||
DJNALGAK_00117 | 5.1e-99 | baeS | T | Histidine kinase | ||
DJNALGAK_00118 | 3.9e-79 | baeR | K | Bacterial regulatory proteins, luxR family | ||
DJNALGAK_00119 | 1.8e-120 | G | Bacterial extracellular solute-binding protein | |||
DJNALGAK_00120 | 2.2e-190 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
DJNALGAK_00121 | 1.7e-54 | rplI | J | Binds to the 23S rRNA | ||
DJNALGAK_00122 | 2.5e-205 | ywfO | S | HD domain protein | ||
DJNALGAK_00123 | 3.8e-256 | fhs | 6.3.4.3 | F | Belongs to the formate--tetrahydrofolate ligase family | |
DJNALGAK_00124 | 1.5e-22 | S | Family of unknown function (DUF5322) | |||
DJNALGAK_00125 | 2.5e-71 | yqeG | S | HAD phosphatase, family IIIA | ||
DJNALGAK_00126 | 7.7e-53 | 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 | ||
DJNALGAK_00127 | 2.9e-25 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
DJNALGAK_00128 | 1.3e-79 | infC | J | IF-3 binds to the 30S ribosomal subunit and shifts the equilibrum between 70S ribosomes and their 50S and 30S subunits in favor of the free subunits, thus enhancing the availability of 30S subunits on which protein synthesis initiation begins | ||
DJNALGAK_00129 | 1.9e-290 | 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) | |
DJNALGAK_00130 | 2.2e-199 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
DJNALGAK_00131 | 3.5e-125 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
DJNALGAK_00133 | 3.5e-115 | sip | L | Belongs to the 'phage' integrase family | ||
DJNALGAK_00140 | 3.3e-45 | L | Bifunctional DNA primase/polymerase, N-terminal | |||
DJNALGAK_00141 | 3.2e-135 | S | D5 N terminal like | |||
DJNALGAK_00142 | 1.2e-140 | hprA | 1.1.1.29 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJNALGAK_00144 | 1.6e-112 | rssA | S | Phospholipase, patatin family | ||
DJNALGAK_00145 | 6.7e-72 | ywlG | S | Belongs to the UPF0340 family | ||
DJNALGAK_00146 | 1.7e-128 | C | Oxidoreductase | |||
DJNALGAK_00147 | 7.3e-09 | C | pentaerythritol trinitrate reductase activity | |||
DJNALGAK_00148 | 2.4e-178 | L | transposase, IS605 OrfB family | |||
DJNALGAK_00149 | 1.5e-69 | tlpA2 | L | Transposase IS200 like | ||
DJNALGAK_00150 | 1.6e-174 | spoVK | O | PFAM ATPase family associated with various cellular activities (AAA) | ||
DJNALGAK_00151 | 8.9e-44 | S | Domain of unknown function (DUF3841) | |||
DJNALGAK_00152 | 4.9e-56 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
DJNALGAK_00153 | 1.1e-163 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
DJNALGAK_00154 | 0.0 | secA | U | Part of the Sec protein translocase complex. Interacts with the SecYEG preprotein conducting channel. Has a central role in coupling the hydrolysis of ATP to the transfer of proteins into and across the cell membrane, serving as an ATP-driven molecular motor driving the stepwise translocation of polypeptide chains across the membrane | ||
DJNALGAK_00155 | 3.9e-43 | yeaN | P | Major Facilitator Superfamily | ||
DJNALGAK_00156 | 4.7e-81 | S | L,D-transpeptidase catalytic domain | |||
DJNALGAK_00157 | 1.9e-139 | menE | 6.2.1.26 | H | Belongs to the ATP-dependent AMP-binding enzyme family. MenE subfamily | |
DJNALGAK_00158 | 4.3e-144 | menB | 4.1.3.36 | H | Converts o-succinylbenzoyl-CoA (OSB-CoA) to 1,4- dihydroxy-2-naphthoyl-CoA (DHNA-CoA) | |
DJNALGAK_00159 | 4e-65 | accC | 6.3.4.14, 6.4.1.2 | I | Acetyl-CoA carboxylase biotin carboxylase subunit | |
DJNALGAK_00160 | 8e-125 | 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 | |
DJNALGAK_00161 | 5.1e-102 | accA | 2.1.3.15, 6.4.1.2 | I | alpha subunit | |
DJNALGAK_00162 | 1.6e-108 | fabI | 1.3.1.10, 1.3.1.9 | I | Enoyl- acyl-carrier-protein reductase NADH | |
DJNALGAK_00163 | 7.5e-225 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
DJNALGAK_00164 | 7e-152 | V | Pfam:Methyltransf_26 | |||
DJNALGAK_00167 | 0.0 | topA | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
DJNALGAK_00168 | 1.8e-208 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
DJNALGAK_00169 | 6.3e-90 | sirR | K | Helix-turn-helix diphteria tox regulatory element | ||
DJNALGAK_00170 | 4.5e-94 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | J | Responsible for synthesis of pseudouridine from uracil | |
DJNALGAK_00171 | 1.6e-22 | |||||
DJNALGAK_00172 | 1.2e-58 | 3.6.1.27 | I | phosphatase | ||
DJNALGAK_00173 | 2.8e-26 | |||||
DJNALGAK_00174 | 3.6e-66 | I | alpha/beta hydrolase fold | |||
DJNALGAK_00175 | 1.3e-38 | azlD | S | branched-chain amino acid | ||
DJNALGAK_00176 | 1.9e-104 | azlC | E | AzlC protein | ||
DJNALGAK_00177 | 2e-17 | |||||
DJNALGAK_00178 | 8.3e-119 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
DJNALGAK_00179 | 1.3e-172 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
DJNALGAK_00180 | 1.3e-92 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
DJNALGAK_00182 | 1.4e-16 | |||||
DJNALGAK_00183 | 6.9e-198 | oatA | I | Acyltransferase | ||
DJNALGAK_00184 | 2.2e-214 | obg | S | An essential GTPase which binds GTP, GDP and possibly (p)ppGpp with moderate affinity, with high nucleotide exchange rates and a fairly low GTP hydrolysis rate. Plays a role in control of the cell cycle, stress response, ribosome biogenesis and in those bacteria that undergo differentiation, in morphogenesis control | ||
DJNALGAK_00185 | 5.6e-57 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
DJNALGAK_00186 | 1.6e-32 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
DJNALGAK_00187 | 6.8e-26 | ykuJ | S | Protein of unknown function (DUF1797) | ||
DJNALGAK_00188 | 5.1e-113 | yitU | 3.1.3.104 | S | hydrolase | |
DJNALGAK_00189 | 1.5e-60 | speG | J | Acetyltransferase (GNAT) domain | ||
DJNALGAK_00190 | 1.8e-189 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
DJNALGAK_00191 | 1.1e-23 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
DJNALGAK_00192 | 2.2e-56 | 3.1.3.48 | K | Transcriptional regulator | ||
DJNALGAK_00193 | 1.4e-160 | adhB | 1.1.1.1, 1.1.1.14 | E | alcohol dehydrogenase | |
DJNALGAK_00194 | 7e-197 | metY | 2.5.1.49 | E | Catalyzes the formation of L-methionine and acetate from O-acetyl-L-homoserine and methanethiol | |
DJNALGAK_00195 | 4.4e-75 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
DJNALGAK_00196 | 2.4e-129 | yxjG | 2.1.1.14 | E | Cobalamin-independent synthase, Catalytic domain | |
DJNALGAK_00197 | 1e-99 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
DJNALGAK_00198 | 2.8e-81 | S | Belongs to the UPF0246 family | |||
DJNALGAK_00199 | 1.2e-11 | V | CAAX protease self-immunity | |||
DJNALGAK_00200 | 1.6e-59 | coiA | 3.6.4.12 | S | Competence protein | |
DJNALGAK_00201 | 9.2e-48 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
DJNALGAK_00202 | 7.5e-56 | P | Plays a role in the regulation of phosphate uptake | |||
DJNALGAK_00203 | 1.4e-52 | rplQ | J | Ribosomal protein L17 | ||
DJNALGAK_00204 | 1.3e-155 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
DJNALGAK_00205 | 2.3e-63 | 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 | ||
DJNALGAK_00206 | 4.4e-56 | 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 | ||
DJNALGAK_00207 | 2.5e-13 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
DJNALGAK_00208 | 4.8e-34 | infA | J | One of the essential components for the initiation of protein synthesis. Stabilizes the binding of IF-2 and IF-3 on the 30S subunit to which N-formylmethionyl-tRNA(fMet) subsequently binds. Helps modulate mRNA selection, yielding the 30S pre- initiation complex (PIC). Upon addition of the 50S ribosomal subunit IF-1, IF-2 and IF-3 are released leaving the mature 70S translation initation complex | ||
DJNALGAK_00209 | 1.1e-293 | ponA | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein 1A |
DJNALGAK_00210 | 6e-161 | purD | 6.3.4.13 | F | Belongs to the GARS family | |
DJNALGAK_00211 | 1.2e-202 | purH | 2.1.2.3, 3.5.4.10 | F | Bifunctional purine biosynthesis protein PurH | |
DJNALGAK_00212 | 3e-58 | 3.5.1.28 | M | N-acetylmuramoyl-L-alanine amidase | ||
DJNALGAK_00213 | 0.0 | typA | T | GTP-binding protein TypA | ||
DJNALGAK_00214 | 3.5e-148 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
DJNALGAK_00215 | 7e-115 | manY | G | PTS system | ||
DJNALGAK_00216 | 3.3e-148 | manN | G | system, mannose fructose sorbose family IID component | ||
DJNALGAK_00217 | 3e-101 | ftsW | D | Belongs to the SEDS family | ||
DJNALGAK_00218 | 0.0 | pyc | 6.4.1.1 | C | Catalyzes a 2-step reaction, involving the ATP-dependent carboxylation of the covalently attached biotin in the first step and the transfer of the carboxyl group to pyruvate in the second | |
DJNALGAK_00219 | 3.3e-134 | S | interspecies interaction between organisms | |||
DJNALGAK_00220 | 6.7e-206 | G | glycerol-3-phosphate transporter | |||
DJNALGAK_00221 | 9.8e-72 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
DJNALGAK_00222 | 5.9e-130 | htrA | 3.4.21.107 | O | serine protease | |
DJNALGAK_00223 | 1.9e-181 | L | Transposase DDE domain group 1 | |||
DJNALGAK_00224 | 8.5e-184 | pepT | 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
DJNALGAK_00225 | 6.3e-103 | yqfO | 3.5.4.16 | S | Belongs to the GTP cyclohydrolase I type 2 NIF3 family | |
DJNALGAK_00226 | 7.8e-78 | trmK | 2.1.1.217 | S | SAM-dependent methyltransferase | |
DJNALGAK_00227 | 4.3e-149 | EGP | Sugar (and other) transporter | |||
DJNALGAK_00228 | 4.6e-45 | L | Primase C terminal 1 (PriCT-1) | |||
DJNALGAK_00233 | 1.4e-142 | 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 | ||
DJNALGAK_00234 | 1e-44 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
DJNALGAK_00235 | 1.5e-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 | ||
DJNALGAK_00236 | 5.2e-116 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
DJNALGAK_00237 | 3.1e-72 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
DJNALGAK_00238 | 9e-24 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
DJNALGAK_00239 | 8e-39 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
DJNALGAK_00240 | 5.1e-60 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
DJNALGAK_00241 | 7e-47 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
DJNALGAK_00242 | 1.3e-91 | 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 | ||
DJNALGAK_00243 | 4.4e-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 | ||
DJNALGAK_00244 | 2.5e-65 | 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 | ||
DJNALGAK_00245 | 3.2e-87 | rplF | J | This protein binds to the 23S rRNA, and is important in its secondary structure. It is located near the subunit interface in the base of the L7 L12 stalk, and near the tRNA binding site of the peptidyltransferase center | ||
DJNALGAK_00246 | 9.6e-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 | ||
DJNALGAK_00247 | 1.3e-82 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
DJNALGAK_00248 | 2.1e-22 | rpmD | J | Ribosomal protein L30 | ||
DJNALGAK_00249 | 1e-67 | rplO | J | Binds to the 23S rRNA | ||
DJNALGAK_00250 | 4.4e-207 | 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 | ||
DJNALGAK_00251 | 2.1e-19 | M | domain protein | |||
DJNALGAK_00252 | 3e-124 | yvgN | C | Aldo keto reductase | ||
DJNALGAK_00253 | 3e-105 | yraQ | S | Predicted permease | ||
DJNALGAK_00254 | 6.9e-62 | yeeE | S | Sulphur transport | ||
DJNALGAK_00255 | 3.5e-16 | yeeD | O | Belongs to the sulfur carrier protein TusA family | ||
DJNALGAK_00256 | 2.2e-116 | ynjE | 2.8.1.11 | P | Rhodanese Homology Domain | |
DJNALGAK_00258 | 1.1e-120 | adhC | 1.1.1.90 | C | Zn-dependent alcohol dehydrogenases, class III | |
DJNALGAK_00259 | 3.9e-48 | fucU | 5.1.3.29 | G | RbsD / FucU transport protein family | |
DJNALGAK_00260 | 3.5e-180 | xylB | 2.7.1.17 | GH19 | EGP | Major facilitator Superfamily |
DJNALGAK_00261 | 3e-125 | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | ||
DJNALGAK_00262 | 5.4e-85 | dps | P | Ferritin-like domain | ||
DJNALGAK_00263 | 1.1e-14 | tnp | L | Transposase IS66 family | ||
DJNALGAK_00265 | 1.6e-159 | mgtE | P | Acts as a magnesium transporter | ||
DJNALGAK_00266 | 5.4e-92 | rluD | 5.4.99.23, 5.4.99.28, 5.4.99.29 | G | Responsible for synthesis of pseudouridine from uracil | |
DJNALGAK_00267 | 7.6e-117 | nadK | 2.7.1.23 | F | Involved in the regulation of the intracellular balance of NAD and NADP, and is a key enzyme in the biosynthesis of NADP. Catalyzes specifically the phosphorylation on 2'-hydroxyl of the adenosine moiety of NAD to yield NADP | |
DJNALGAK_00268 | 2.5e-94 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
DJNALGAK_00269 | 1.1e-17 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
DJNALGAK_00270 | 1e-72 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
DJNALGAK_00271 | 4e-49 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
DJNALGAK_00272 | 1.8e-131 | ylbL | T | Belongs to the peptidase S16 family | ||
DJNALGAK_00273 | 2.9e-96 | purC | 4.1.1.21, 4.3.2.2, 6.3.2.6 | F | Belongs to the SAICAR synthetase family | |
DJNALGAK_00274 | 4.8e-30 | purS | 6.3.2.6, 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJNALGAK_00275 | 1.2e-102 | purQ | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJNALGAK_00276 | 4.2e-151 | yfeX | P | Peroxidase | ||
DJNALGAK_00277 | 4e-279 | 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 | ||
DJNALGAK_00278 | 1.5e-63 | ymfM | S | Helix-turn-helix domain | ||
DJNALGAK_00279 | 2.4e-90 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
DJNALGAK_00280 | 2.4e-149 | ymfH | S | Peptidase M16 | ||
DJNALGAK_00281 | 3.5e-54 | ymfF | S | Peptidase M16 inactive domain protein | ||
DJNALGAK_00282 | 4.7e-43 | L | Protein of unknown function (DUF3991) | |||
DJNALGAK_00283 | 2.3e-213 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
DJNALGAK_00284 | 3e-44 | tkt | 2.2.1.1 | H | Catalyzes the transfer of a two-carbon ketol group from a ketose donor to an aldose acceptor, via a covalent intermediate with the cofactor thiamine pyrophosphate | |
DJNALGAK_00285 | 6.6e-87 | tal | 2.2.1.2 | F | Transaldolase is important for the balance of metabolites in the pentose-phosphate pathway | |
DJNALGAK_00286 | 2.8e-167 | gutB | 1.1.1.1, 1.1.1.14 | E | Dehydrogenase | |
DJNALGAK_00287 | 5.6e-120 | gatD | 1.1.1.14 | E | Alcohol dehydrogenase GroES-like domain | |
DJNALGAK_00288 | 1.3e-181 | gatC | G | PTS system sugar-specific permease component | ||
DJNALGAK_00289 | 3.6e-79 | S | Sucrose-6F-phosphate phosphohydrolase | |||
DJNALGAK_00290 | 1.9e-34 | trxA | O | Belongs to the thioredoxin family | ||
DJNALGAK_00291 | 9.4e-22 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
DJNALGAK_00292 | 1.3e-20 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
DJNALGAK_00293 | 3.3e-65 | degV | S | Uncharacterised protein, DegV family COG1307 | ||
DJNALGAK_00295 | 4.3e-54 | queT | S | QueT transporter | ||
DJNALGAK_00296 | 3.9e-34 | XK27_01315 | S | Protein of unknown function (DUF2829) | ||
DJNALGAK_00297 | 7.2e-65 | yxeH | S | hydrolase | ||
DJNALGAK_00299 | 3.4e-78 | rapL | 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | |
DJNALGAK_00300 | 1.2e-21 | rapL | 4.3.1.12 | E | Ornithine cyclodeaminase/mu-crystallin family | |
DJNALGAK_00302 | 2.6e-17 | pre | D | Plasmid recombination enzyme | ||
DJNALGAK_00303 | 4.6e-72 | catB | 2.3.1.28 | V | This enzyme is an effector of chloramphenicol resistance in bacteria | |
DJNALGAK_00304 | 4.1e-41 | L | Replication initiation factor | |||
DJNALGAK_00305 | 4.1e-240 | tetL | EGP | Major Facilitator Superfamily | ||
DJNALGAK_00306 | 0.0 | tetP | J | Elongation factor G, domain IV | ||
DJNALGAK_00307 | 1e-182 | queA | 2.4.99.17 | J | Transfers and isomerizes the ribose moiety from AdoMet to the 7-aminomethyl group of 7-deazaguanine (preQ1-tRNA) to give epoxyqueuosine (oQ-tRNA) | |
DJNALGAK_00308 | 1.1e-152 | 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 | |
DJNALGAK_00309 | 4.3e-72 | 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 | |
DJNALGAK_00310 | 1.1e-98 | 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 | ||
DJNALGAK_00313 | 3.9e-127 | mltG | S | Functions as a peptidoglycan terminase that cleaves nascent peptidoglycan strands endolytically to terminate their elongation | ||
DJNALGAK_00314 | 1.8e-97 | udk | 2.7.1.48 | F | Cytidine monophosphokinase | |
DJNALGAK_00315 | 1.7e-68 | 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 | ||
DJNALGAK_00316 | 4.1e-15 | ywzB | S | Protein of unknown function (DUF1146) | ||
DJNALGAK_00317 | 4.9e-196 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
DJNALGAK_00319 | 1.2e-192 | clpB | O | Belongs to the ClpA ClpB family | ||
DJNALGAK_00320 | 4.2e-61 | marR | K | Transcriptional regulator, MarR family | ||
DJNALGAK_00321 | 9.8e-66 | 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 | |
DJNALGAK_00322 | 1.1e-100 | rnc | 3.1.26.3 | J | Digests double-stranded RNA. Involved in the processing of primary rRNA transcript to yield the immediate precursors to the large and small rRNAs (23S and 16S). Processes some mRNAs, and tRNAs when they are encoded in the rRNA operon. Processes pre- crRNA and tracrRNA of type II CRISPR loci if present in the organism | |
DJNALGAK_00323 | 4.6e-25 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
DJNALGAK_00324 | 1.6e-140 | 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 | |
DJNALGAK_00325 | 4e-247 | 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) | |
DJNALGAK_00326 | 1.3e-238 | yloV | S | DAK2 domain fusion protein YloV | ||
DJNALGAK_00327 | 4.5e-53 | asp | S | Asp23 family, cell envelope-related function | ||
DJNALGAK_00328 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
DJNALGAK_00329 | 3.8e-58 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
DJNALGAK_00330 | 3.5e-77 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
DJNALGAK_00331 | 4.7e-71 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
DJNALGAK_00332 | 5.1e-49 | rsfS | J | Functions as a ribosomal silencing factor. Interacts with ribosomal protein L14 (rplN), blocking formation of intersubunit bridge B8. Prevents association of the 30S and 50S ribosomal subunits and the formation of functional ribosomes, thus repressing translation | ||
DJNALGAK_00333 | 5.5e-82 | H | Nodulation protein S (NodS) | |||
DJNALGAK_00334 | 1.7e-105 | manA | 1.14.13.81, 5.3.1.8, 5.4.2.8 | G | MucBP domain | |
DJNALGAK_00335 | 3e-311 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
DJNALGAK_00337 | 5.6e-57 | spoVK | O | ATPase family associated with various cellular activities (AAA) | ||
DJNALGAK_00338 | 3.6e-24 | L | Eco57I restriction-modification methylase | |||
DJNALGAK_00339 | 1.6e-38 | M | Glycosyl transferase family 8 | |||
DJNALGAK_00340 | 1.2e-55 | nss | M | transferase activity, transferring glycosyl groups | ||
DJNALGAK_00342 | 5.7e-13 | arbx | M | family 8 | ||
DJNALGAK_00343 | 3.4e-268 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
DJNALGAK_00344 | 9.7e-184 | asd | 1.2.1.11, 1.2.1.12 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
DJNALGAK_00345 | 8.2e-154 | yacL | S | domain protein | ||
DJNALGAK_00346 | 1.6e-223 | 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 | ||
DJNALGAK_00347 | 4e-36 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
DJNALGAK_00348 | 3.7e-212 | yfnA | E | Amino Acid | ||
DJNALGAK_00349 | 1.1e-60 | hrtB | V | ABC transporter permease | ||
DJNALGAK_00350 | 3.4e-86 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
DJNALGAK_00351 | 5.2e-67 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
DJNALGAK_00352 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
DJNALGAK_00353 | 2.8e-230 | 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 | |
DJNALGAK_00354 | 1.2e-63 | C | FMN binding | |||
DJNALGAK_00355 | 6.7e-206 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
DJNALGAK_00356 | 3.2e-45 | yjcF | K | protein acetylation | ||
DJNALGAK_00357 | 3.8e-07 | |||||
DJNALGAK_00360 | 4.2e-29 | M | CHAP domain | |||
DJNALGAK_00362 | 2.2e-191 | U | type IV secretory pathway VirB4 | |||
DJNALGAK_00363 | 3.8e-12 | polC | 2.7.7.7 | L | BRCA1 C Terminus (BRCT) domain | |
DJNALGAK_00364 | 5.7e-20 | |||||
DJNALGAK_00367 | 2.1e-119 | rarA | L | recombination factor protein RarA | ||
DJNALGAK_00368 | 1.1e-100 | EG | EamA-like transporter family | |||
DJNALGAK_00369 | 3.6e-150 | S | Tetratricopeptide repeat protein | |||
DJNALGAK_00370 | 3.4e-204 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
DJNALGAK_00371 | 8.7e-299 | 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) | |
DJNALGAK_00372 | 2.1e-54 | bioY | S | BioY family | ||
DJNALGAK_00373 | 1.3e-183 | lmrB | EGP | Major facilitator Superfamily | ||
DJNALGAK_00374 | 9.5e-34 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
DJNALGAK_00375 | 1.6e-191 | 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 | ||
DJNALGAK_00376 | 3.4e-180 | ftsZ | D | Essential cell division protein that forms a contractile ring structure (Z ring) at the future cell division site. The regulation of the ring assembly controls the timing and the location of cell division. One of the functions of the FtsZ ring is to recruit other cell division proteins to the septum to produce a new cell wall between the dividing cells. Binds GTP and shows GTPase activity | ||
DJNALGAK_00377 | 5e-33 | sepF | D | Cell division protein that is part of the divisome complex and is recruited early to the Z-ring. Probably stimulates Z-ring formation, perhaps through the cross-linking of FtsZ protofilaments. Its function overlaps with FtsA | ||
DJNALGAK_00378 | 3e-19 | yggT | S | YGGT family | ||
DJNALGAK_00379 | 1.2e-82 | ylmH | S | S4 domain protein | ||
DJNALGAK_00380 | 3.9e-62 | divIVA | D | DivIVA domain protein | ||
DJNALGAK_00381 | 3.2e-57 | salK | 2.7.13.3 | T | Histidine kinase | |
DJNALGAK_00382 | 4.4e-77 | desR | K | helix_turn_helix, Lux Regulon | ||
DJNALGAK_00383 | 1.6e-71 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
DJNALGAK_00384 | 1.5e-51 | lssY | 3.6.1.27 | I | phosphatidate phosphatase activity | |
DJNALGAK_00385 | 1.2e-13 | 2.3.1.128 | J | COG1670 acetyltransferases, including N-acetylases of ribosomal proteins | ||
DJNALGAK_00386 | 8.6e-272 | alsS | 2.2.1.6 | EH | Belongs to the TPP enzyme family | |
DJNALGAK_00387 | 3.1e-69 | budA | 4.1.1.5 | Q | Alpha-acetolactate decarboxylase | |
DJNALGAK_00388 | 5.5e-243 | lysP | E | amino acid | ||
DJNALGAK_00389 | 3.6e-190 | 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) | |
DJNALGAK_00390 | 6.9e-76 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
DJNALGAK_00391 | 3.4e-48 | ndoA | L | Toxic component of a toxin-antitoxin (TA) module | ||
DJNALGAK_00392 | 5.4e-13 | |||||
DJNALGAK_00393 | 1.5e-144 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
DJNALGAK_00394 | 6.3e-09 | topA2 | 5.99.1.2 | L | Releases the supercoiling and torsional tension of DNA, which is introduced during the DNA replication and transcription, by transiently cleaving and rejoining one strand of the DNA duplex. Introduces a single-strand break via transesterification at a target site in duplex DNA. The scissile phosphodiester is attacked by the catalytic tyrosine of the enzyme, resulting in the formation of a DNA-(5'-phosphotyrosyl)-enzyme intermediate and the expulsion of a 3'-OH DNA strand. The free DNA strand then undergoes passage around the unbroken strand, thus removing DNA supercoils. Finally, in the religation step, the DNA 3'-OH attacks the covalent intermediate to expel the active-site tyrosine and restore the DNA phosphodiester backbone | |
DJNALGAK_00396 | 1.5e-63 | secY2 | U | Part of the accessory SecA2 SecY2 system specifically required for export of | ||
DJNALGAK_00397 | 9.2e-90 | asp1 | S | Accessory Sec system protein Asp1 | ||
DJNALGAK_00398 | 7.5e-105 | asp2 | 3.4.11.5 | S | Accessory Sec system protein Asp2 | |
DJNALGAK_00399 | 1e-32 | asp3 | S | Accessory Sec system protein Asp3 | ||
DJNALGAK_00402 | 1.6e-08 | 2.3.1.19 | K | Cro/C1-type HTH DNA-binding domain | ||
DJNALGAK_00403 | 7.5e-39 | 2.7.1.191 | G | PTS system fructose IIA component | ||
DJNALGAK_00404 | 3.2e-123 | G | PTS system mannose/fructose/sorbose family IID component | |||
DJNALGAK_00405 | 4.4e-101 | G | PTS system sorbose-specific iic component | |||
DJNALGAK_00406 | 4.5e-64 | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | ||
DJNALGAK_00407 | 8.7e-81 | metAA | 2.3.1.46 | E | Transfers an acetyl group from acetyl-CoA to | |
DJNALGAK_00408 | 8.6e-141 | cysK | 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
DJNALGAK_00409 | 4.3e-184 | oppA2 | E | Bacterial extracellular solute-binding proteins, family 5 Middle | ||
DJNALGAK_00411 | 2.2e-49 | pepL | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
DJNALGAK_00412 | 1.1e-58 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
DJNALGAK_00413 | 2e-76 | L | Belongs to the 'phage' integrase family | |||
DJNALGAK_00414 | 9e-179 | murF | 6.3.2.10 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
DJNALGAK_00415 | 3.4e-208 | cshA | 3.6.4.13 | F | DEAD-box RNA helicase possibly involved in RNA degradation. Unwinds dsRNA in both 5'- and 3'-directions, has RNA- dependent ATPase activity | |
DJNALGAK_00416 | 1.7e-37 | gatC | 6.3.5.6, 6.3.5.7 | J | Allows the formation of correctly charged Asn-tRNA(Asn) or Gln-tRNA(Gln) through the transamidation of misacylated Asp- tRNA(Asn) or Glu-tRNA(Gln) in organisms which lack either or both of asparaginyl-tRNA or glutaminyl-tRNA synthetases. The reaction takes place in the presence of glutamine and ATP through an activated phospho-Asp-tRNA(Asn) or phospho-Glu-tRNA(Gln) | |
DJNALGAK_00417 | 1.6e-234 | 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) | |
DJNALGAK_00418 | 5.6e-256 | 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) | |
DJNALGAK_00419 | 9.8e-146 | yegS | 2.7.1.107 | G | Lipid kinase | |
DJNALGAK_00420 | 7.6e-210 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
DJNALGAK_00421 | 6.4e-36 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
DJNALGAK_00423 | 2e-120 | L | Mrr N-terminal domain | |||
DJNALGAK_00424 | 7.3e-18 | |||||
DJNALGAK_00425 | 5.2e-137 | purR | 2.4.2.7 | F | pur operon repressor | |
DJNALGAK_00426 | 3.1e-50 | comEA | L | Competence protein ComEA | ||
DJNALGAK_00427 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
DJNALGAK_00428 | 1.6e-60 | yiiE | S | Protein of unknown function (DUF1211) | ||
DJNALGAK_00429 | 1.6e-40 | mscL | M | Channel that opens in response to stretch forces in the membrane lipid bilayer. May participate in the regulation of osmotic pressure changes within the cell | ||
DJNALGAK_00430 | 2.5e-101 | 4.1.2.17 | G | Class II Aldolase and Adducin N-terminal domain | ||
DJNALGAK_00431 | 4.8e-158 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
DJNALGAK_00432 | 3.2e-86 | S | (CBS) domain | |||
DJNALGAK_00433 | 1.4e-141 | panE | 1.1.1.169 | H | Catalyzes the NADPH-dependent reduction of ketopantoate into pantoic acid | |
DJNALGAK_00434 | 3.3e-283 | fruA | 2.7.1.202 | GT | Phosphotransferase System | |
DJNALGAK_00435 | 4.1e-151 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
DJNALGAK_00436 | 9e-88 | fruR | K | DeoR C terminal sensor domain | ||
DJNALGAK_00437 | 4.2e-240 | sufB | O | assembly protein SufB | ||
DJNALGAK_00438 | 4.9e-41 | nifU | C | SUF system FeS assembly protein, NifU family | ||
DJNALGAK_00439 | 2.1e-111 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
DJNALGAK_00440 | 2.4e-125 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
DJNALGAK_00441 | 1e-90 | rfbP | M | Bacterial sugar transferase | ||
DJNALGAK_00442 | 1.7e-117 | M | Core-2/I-Branching enzyme | |||
DJNALGAK_00443 | 2.1e-194 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
DJNALGAK_00444 | 5.5e-24 | 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 | |
DJNALGAK_00445 | 0.0 | valS | 6.1.1.9 | J | amino acids such as threonine, to avoid such errors, it has a posttransfer editing activity that hydrolyzes mischarged Thr-tRNA(Val) in a tRNA-dependent manner | |
DJNALGAK_00447 | 2.4e-31 | M | Glycosyltransferase like family 2 | |||
DJNALGAK_00448 | 1.9e-161 | L | Probable transposase | |||
DJNALGAK_00449 | 1.4e-17 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
DJNALGAK_00450 | 2e-219 | dltA | 6.1.1.13 | H | Catalyzes the first step in the D-alanylation of lipoteichoic acid (LTA), the activation of D-alanine and its transfer onto the D-alanyl carrier protein (Dcp) DltC. In an ATP- dependent two-step reaction, forms a high energy D-alanyl-AMP intermediate, followed by transfer of the D-alanyl residue as a thiol ester to the phosphopantheinyl prosthetic group of the Dcp. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
DJNALGAK_00451 | 2.6e-07 | dltX | S | D-Ala-teichoic acid biosynthesis protein | ||
DJNALGAK_00452 | 1.5e-90 | recO | L | Involved in DNA repair and RecF pathway recombination | ||
DJNALGAK_00453 | 1e-154 | era | S | An essential GTPase that binds both GDP and GTP, with rapid nucleotide exchange. Plays a role in 16S rRNA processing and 30S ribosomal subunit biogenesis and possibly also in cell cycle regulation and energy metabolism | ||
DJNALGAK_00454 | 1.1e-29 | dgkA | 2.7.1.107, 2.7.1.66 | M | Diacylglycerol kinase | |
DJNALGAK_00455 | 3e-60 | ybeY | 2.6.99.2, 3.5.4.5 | S | Single strand-specific metallo-endoribonuclease involved in late-stage 70S ribosome quality control and in maturation of the 3' terminus of the 16S rRNA | |
DJNALGAK_00456 | 2.5e-125 | phoH | T | phosphate starvation-inducible protein PhoH | ||
DJNALGAK_00457 | 6.2e-163 | oxlT | P | Major Facilitator Superfamily | ||
DJNALGAK_00458 | 1.8e-271 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
DJNALGAK_00459 | 2.4e-33 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
DJNALGAK_00460 | 1e-64 | 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 | |
DJNALGAK_00461 | 1.7e-46 | 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 | |
DJNALGAK_00462 | 2.1e-195 | fabF | 2.3.1.179 | I | Catalyzes the condensation reaction of fatty acid synthesis by the addition to an acyl acceptor of two carbons from malonyl-ACP | |
DJNALGAK_00463 | 1.1e-98 | IQ | reductase | |||
DJNALGAK_00464 | 5e-104 | fabD | 2.3.1.39 | I | Malonyl CoA-acyl carrier protein transacylase | |
DJNALGAK_00465 | 2.2e-27 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
DJNALGAK_00466 | 0.0 | lacL | 3.2.1.23 | G | -beta-galactosidase | |
DJNALGAK_00467 | 6.5e-197 | argG | 6.3.4.5 | E | Belongs to the argininosuccinate synthase family. Type 1 subfamily | |
DJNALGAK_00468 | 2.2e-201 | argH | 4.3.2.1 | E | argininosuccinate lyase | |
DJNALGAK_00469 | 3e-155 | amtB | P | ammonium transporter | ||
DJNALGAK_00470 | 9e-116 | ispE | 2.1.1.182, 2.7.1.148 | F | Catalyzes the phosphorylation of the position 2 hydroxy group of 4-diphosphocytidyl-2C-methyl-D-erythritol | |
DJNALGAK_00471 | 6.6e-46 | argR | K | Regulates arginine biosynthesis genes | ||
DJNALGAK_00472 | 1.7e-138 | arcT | 2.6.1.1 | E | Cys/Met metabolism PLP-dependent enzyme | |
DJNALGAK_00473 | 8.3e-90 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
DJNALGAK_00474 | 1.2e-22 | veg | S | Biofilm formation stimulator VEG | ||
DJNALGAK_00475 | 7e-132 | 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 | |
DJNALGAK_00476 | 3.4e-87 | 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 | |
DJNALGAK_00477 | 9.2e-104 | tatD | L | hydrolase, TatD family | ||
DJNALGAK_00478 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
DJNALGAK_00479 | 2.6e-69 | smpB | J | the 2 termini fold to resemble tRNA(Ala) and it encodes a tag peptide , a short internal open reading frame. During trans-translation Ala- aminoacylated tmRNA acts like a tRNA, entering the A-site of stalled ribosomes, displacing the stalled mRNA. The ribosome then switches to translate the ORF on the tmRNA | ||
DJNALGAK_00480 | 3.1e-42 | yxjI | ||||
DJNALGAK_00481 | 1.8e-116 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
DJNALGAK_00482 | 6.8e-106 | ung | 3.2.2.27 | L | Excises uracil residues from the DNA which can arise as a result of misincorporation of dUMP residues by DNA polymerase or due to deamination of cytosine | |
DJNALGAK_00483 | 1.3e-142 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
DJNALGAK_00484 | 2.5e-56 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
DJNALGAK_00485 | 3e-69 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
DJNALGAK_00486 | 3.7e-168 | glyQ | 6.1.1.14 | J | glycyl-tRNA synthetase alpha subunit | |
DJNALGAK_00487 | 2.1e-280 | glyS | 6.1.1.14 | J | Glycyl-tRNA synthetase beta subunit | |
DJNALGAK_00488 | 6.4e-13 | 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 | |
DJNALGAK_00489 | 1.2e-16 | 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 | |
DJNALGAK_00490 | 1.4e-82 | ispA | 2.5.1.1, 2.5.1.10, 2.5.1.29, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
DJNALGAK_00491 | 4.4e-120 | rrmJ | 2.1.1.226, 2.1.1.227 | J | Ribosomal RNA large subunit methyltransferase J | |
DJNALGAK_00492 | 6.6e-49 | argR | K | Regulates arginine biosynthesis genes | ||
DJNALGAK_00493 | 9.3e-178 | recN | L | May be involved in recombinational repair of damaged DNA | ||
DJNALGAK_00494 | 9.5e-38 | S | CAAX protease self-immunity | |||
DJNALGAK_00495 | 1.6e-88 | yvyE | 3.4.13.9 | S | YigZ family | |
DJNALGAK_00496 | 3.9e-58 | S | Haloacid dehalogenase-like hydrolase | |||
DJNALGAK_00497 | 2.6e-154 | EGP | Major facilitator Superfamily | |||
DJNALGAK_00498 | 4.4e-94 | XK27_00825 | S | Sulfite exporter TauE/SafE | ||
DJNALGAK_00499 | 7e-144 | 5.1.1.4 | E | Proline racemase | ||
DJNALGAK_00500 | 2.7e-66 | 3.5.1.1 | EJ | Glycine/sarcosine/betaine reductase component B subunits | ||
DJNALGAK_00501 | 4.7e-73 | prdD | S | An automated process has identified a potential problem with this gene model | ||
DJNALGAK_00502 | 4.3e-31 | S | the current gene model (or a revised gene model) may contain a premature stop | |||
DJNALGAK_00503 | 5.8e-66 | prdB | 1.21.4.1, 1.21.4.2 | S | the current gene model (or a revised gene model) may contain a premature stop | |
DJNALGAK_00504 | 3.2e-26 | S | Psort location Cytoplasmic, score | |||
DJNALGAK_00505 | 9.5e-235 | prdA | 1.21.4.1 | EJ | Glycine/sarcosine/betaine reductase component B subunits | |
DJNALGAK_00506 | 1.7e-09 | S | Helix-turn-helix domain | |||
DJNALGAK_00507 | 7.5e-43 | S | Phage regulatory protein Rha (Phage_pRha) | |||
DJNALGAK_00516 | 1.9e-42 | ybl78 | L | DnaD domain protein | ||
DJNALGAK_00517 | 4.8e-09 | |||||
DJNALGAK_00520 | 9.7e-91 | licT | K | CAT RNA binding domain | ||
DJNALGAK_00521 | 6.9e-214 | G | phosphotransferase system | |||
DJNALGAK_00522 | 1.2e-221 | bglH | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
DJNALGAK_00523 | 4.7e-294 | lai | 4.2.1.53 | S | Myosin-crossreactive antigen | |
DJNALGAK_00524 | 3.5e-33 | nmtR | K | helix_turn_helix, Arsenical Resistance Operon Repressor | ||
DJNALGAK_00525 | 1.1e-193 | cadA | 3.6.3.3, 3.6.3.5 | P | P-type ATPase | |
DJNALGAK_00526 | 6e-24 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
DJNALGAK_00528 | 4.3e-113 | xerD | D | recombinase XerD | ||
DJNALGAK_00529 | 1.1e-124 | cvfB | S | S1 domain | ||
DJNALGAK_00530 | 2.4e-51 | yeaL | S | Protein of unknown function (DUF441) | ||
DJNALGAK_00531 | 4.5e-58 | 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 | |||
DJNALGAK_00532 | 1.4e-12 | yajC | U | Preprotein translocase | ||
DJNALGAK_00533 | 4.5e-99 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
DJNALGAK_00534 | 2.5e-11 | ftsL | D | cell division protein FtsL | ||
DJNALGAK_00535 | 4e-282 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
DJNALGAK_00536 | 1.9e-135 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
DJNALGAK_00537 | 1.5e-186 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
DJNALGAK_00538 | 1.4e-153 | murG | 2.4.1.227, 6.3.2.8 | GT28 | M | Cell wall formation. Catalyzes the transfer of a GlcNAc subunit on undecaprenyl-pyrophosphoryl-MurNAc-pentapeptide (lipid intermediate I) to form undecaprenyl-pyrophosphoryl-MurNAc- (pentapeptide)GlcNAc (lipid intermediate II) |
DJNALGAK_00539 | 1.2e-09 | selB | J | Elongation factor SelB, winged helix | ||
DJNALGAK_00540 | 8.8e-111 | sufS | 2.8.1.7, 4.4.1.16 | E | Serine hydroxymethyltransferase | |
DJNALGAK_00541 | 1.7e-80 | FbpA | K | Fibronectin-binding protein | ||
DJNALGAK_00542 | 1.7e-127 | parC | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
DJNALGAK_00543 | 1.4e-06 | |||||
DJNALGAK_00549 | 5.1e-08 | |||||
DJNALGAK_00556 | 2.2e-136 | T | PhoQ Sensor | |||
DJNALGAK_00557 | 1.7e-119 | yxaA | S | membrane transporter protein | ||
DJNALGAK_00558 | 2.6e-32 | ywjH | S | Protein of unknown function (DUF1634) | ||
DJNALGAK_00559 | 7e-126 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
DJNALGAK_00560 | 2.8e-27 | 2.7.13.3 | T | GHKL domain | ||
DJNALGAK_00561 | 4.3e-56 | K | LytTr DNA-binding domain | |||
DJNALGAK_00564 | 1.1e-221 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
DJNALGAK_00565 | 1.9e-237 | sftA | D | Belongs to the FtsK SpoIIIE SftA family | ||
DJNALGAK_00566 | 2.3e-53 | sip | L | Belongs to the 'phage' integrase family | ||
DJNALGAK_00567 | 3.4e-83 | qorB | 1.6.5.2 | GM | NmrA-like family | |
DJNALGAK_00568 | 8e-40 | K | Transcriptional regulator | |||
DJNALGAK_00569 | 1.4e-31 | S | CHY zinc finger | |||
DJNALGAK_00571 | 3.2e-181 | pbuG | S | permease | ||
DJNALGAK_00572 | 3.8e-267 | rnjB | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
DJNALGAK_00573 | 1.8e-116 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
DJNALGAK_00574 | 5.6e-40 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
DJNALGAK_00575 | 1.8e-32 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
DJNALGAK_00576 | 7.9e-102 | rbsK | 2.7.1.15 | H | Catalyzes the phosphorylation of ribose at O-5 in a reaction requiring ATP and magnesium. The resulting D-ribose-5- phosphate can then be used either for sythesis of nucleotides, histidine, and tryptophan, or as a component of the pentose phosphate pathway | |
DJNALGAK_00577 | 1.5e-119 | yebC | K | Transcriptional regulatory protein | ||
DJNALGAK_00578 | 1.7e-15 | S | VanZ like family | |||
DJNALGAK_00579 | 5.3e-68 | ybbR | S | YbbR-like protein | ||
DJNALGAK_00580 | 8.5e-127 | 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 | |
DJNALGAK_00581 | 5.8e-101 | XK27_05435 | 1.1.1.100 | S | Enoyl-(Acyl carrier protein) reductase | |
DJNALGAK_00582 | 1.1e-251 | L | helicase activity | |||
DJNALGAK_00583 | 2.8e-98 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
DJNALGAK_00586 | 6e-34 | L | Helix-turn-helix domain | |||
DJNALGAK_00587 | 1.4e-67 | spx4 | 1.20.4.1 | P | ArsC family | |
DJNALGAK_00588 | 5.9e-146 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
DJNALGAK_00589 | 2.9e-230 | baeS | 2.7.13.3 | T | Histidine kinase | |
DJNALGAK_00590 | 5e-117 | K | response regulator | |||
DJNALGAK_00591 | 1.5e-33 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
DJNALGAK_00592 | 4.8e-16 | 3.2.1.23 | S | Domain of unknown function DUF302 | ||
DJNALGAK_00593 | 2.4e-40 | S | membrane protein (DUF2078) | |||
DJNALGAK_00594 | 0.0 | 3.6.3.4 | P | haloacid dehalogenase-like hydrolase | ||
DJNALGAK_00595 | 4.5e-58 | copY | K | Penicillinase repressor | ||
DJNALGAK_00598 | 1.5e-284 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
DJNALGAK_00599 | 2e-47 | pts33BCA | 2.7.1.193, 2.7.1.199, 2.7.1.201, 2.7.1.208, 2.7.1.211 | G | Pts system | |
DJNALGAK_00601 | 1.2e-44 | K | Copper transport repressor CopY TcrY | |||
DJNALGAK_00602 | 6.1e-60 | T | Belongs to the universal stress protein A family | |||
DJNALGAK_00603 | 2.6e-41 | K | Bacterial regulatory proteins, tetR family | |||
DJNALGAK_00604 | 3.1e-56 | K | transcriptional | |||
DJNALGAK_00607 | 7e-22 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
DJNALGAK_00608 | 0.0 | uvrB | L | damaged site, the DNA wraps around one UvrB monomer. DNA wrap is dependent on ATP binding by UvrB and probably causes local melting of the DNA helix, facilitating insertion of UvrB beta-hairpin between the DNA strands. Then UvrB probes one DNA strand for the presence of a lesion. If a lesion is found the UvrA subunits dissociate and the UvrB-DNA preincision complex is formed. This complex is subsequently bound by UvrC and the second UvrB is released. If no lesion is found, the DNA wraps around the other UvrB subunit that will check the other stand for damage | ||
DJNALGAK_00609 | 6.1e-273 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
DJNALGAK_00610 | 1.1e-112 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
DJNALGAK_00611 | 7.4e-132 | hprK | F | Catalyzes the ATP- as well as the pyrophosphate- dependent phosphorylation of a specific serine residue in HPr, a phosphocarrier protein of the phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS). HprK P also catalyzes the pyrophosphate-producing, inorganic phosphate-dependent dephosphorylation (phosphorolysis) of seryl-phosphorylated HPr (P- Ser-HPr). The two antagonistic activities of HprK P are regulated by several intracellular metabolites, which change their concentration in response to the absence or presence of rapidly metabolisable carbon sources (glucose, fructose, etc.) in the growth medium. Therefore, by controlling the phosphorylation state of HPr, HPrK P is a sensor enzyme that plays a major role in the regulation of carbon metabolism and sugar transport it mediates carbon catabolite repression (CCR), and regulates PTS-catalyzed carbohydrate uptake and inducer exclusion | ||
DJNALGAK_00612 | 1.1e-12 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
DJNALGAK_00613 | 6.1e-66 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
DJNALGAK_00615 | 4.3e-83 | L | Phage terminase, small subunit | |||
DJNALGAK_00616 | 0.0 | S | Phage Terminase | |||
DJNALGAK_00618 | 6.7e-207 | S | Phage portal protein | |||
DJNALGAK_00619 | 4.2e-119 | clpP | 3.4.21.92 | OU | Belongs to the peptidase S14 family | |
DJNALGAK_00620 | 4.4e-222 | S | Phage capsid family | |||
DJNALGAK_00621 | 4.8e-22 | S | Phage gp6-like head-tail connector protein | |||
DJNALGAK_00622 | 4.2e-59 | S | Phage head-tail joining protein | |||
DJNALGAK_00623 | 1.9e-65 | S | Bacteriophage HK97-gp10, putative tail-component | |||
DJNALGAK_00624 | 5.4e-65 | S | Protein of unknown function (DUF806) | |||
DJNALGAK_00625 | 6.1e-123 | S | Phage tail tube protein | |||
DJNALGAK_00626 | 8.2e-54 | S | Phage tail assembly chaperone proteins, TAC | |||
DJNALGAK_00628 | 9.6e-62 | |||||
DJNALGAK_00629 | 7.6e-136 | pflA | 1.97.1.4 | C | Activation of pyruvate formate-lyase under anaerobic conditions by generation of an organic free radical, using S- adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
DJNALGAK_00630 | 0.0 | pflB | 2.3.1.54 | C | Pyruvate formate lyase-like | |
DJNALGAK_00631 | 1.2e-44 | S | VIT family | |||
DJNALGAK_00632 | 1e-148 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
DJNALGAK_00633 | 8.2e-07 | fhaB | M | Rib/alpha-like repeat | ||
DJNALGAK_00634 | 1.2e-103 | pfoS | S | Phosphotransferase system, EIIC | ||
DJNALGAK_00635 | 2.9e-126 | ldhD | 1.1.1.28 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJNALGAK_00636 | 2.9e-143 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
DJNALGAK_00637 | 2.7e-94 | pstS | P | T5orf172 | ||
DJNALGAK_00638 | 4.8e-258 | yeeB | L | DEAD-like helicases superfamily | ||
DJNALGAK_00639 | 1.9e-210 | yeeA | V | Type II restriction enzyme, methylase subunits | ||
DJNALGAK_00640 | 1.2e-14 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
DJNALGAK_00641 | 0.0 | mapA | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
DJNALGAK_00642 | 2.4e-84 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
DJNALGAK_00643 | 2.7e-44 | thiT | S | Thiamine transporter protein (Thia_YuaJ) | ||
DJNALGAK_00644 | 1.1e-286 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
DJNALGAK_00645 | 2.2e-111 | dat | 2.6.1.21 | EH | PFAM aminotransferase, class IV | |
DJNALGAK_00646 | 5.1e-08 | S | SdpI/YhfL protein family | |||
DJNALGAK_00647 | 3.9e-41 | yjbH | Q | Thioredoxin | ||
DJNALGAK_00648 | 1e-34 | pepF | E | Oligopeptidase F | ||
DJNALGAK_00649 | 2.7e-171 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
DJNALGAK_00650 | 4.5e-228 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
DJNALGAK_00651 | 5.5e-29 | |||||
DJNALGAK_00652 | 2.5e-78 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
DJNALGAK_00653 | 3.5e-99 | rpiA | 2.7.1.12, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
DJNALGAK_00654 | 3.3e-311 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
DJNALGAK_00655 | 1.5e-43 | S | zinc-ribbon domain | |||
DJNALGAK_00656 | 4.4e-102 | 2.1.1.72, 3.1.21.3 | V | N-6 DNA Methylase | ||
DJNALGAK_00657 | 1.4e-21 | K | helix_turn_helix multiple antibiotic resistance protein | |||
DJNALGAK_00658 | 5.1e-225 | pipD | E | Dipeptidase | ||
DJNALGAK_00659 | 2.9e-102 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
DJNALGAK_00660 | 1.9e-217 | ybeC | E | amino acid | ||
DJNALGAK_00661 | 9.3e-168 | ilvE | 2.6.1.42 | E | Branched-chain amino acid aminotransferase | |
DJNALGAK_00662 | 6.2e-210 | glnP | P | ABC transporter | ||
DJNALGAK_00664 | 3.5e-100 | M | Prophage endopeptidase tail | |||
DJNALGAK_00665 | 7.7e-274 | rny | D | peptidase | ||
DJNALGAK_00666 | 2.5e-141 | S | Phage tail protein | |||
DJNALGAK_00667 | 3.2e-82 | ybhF_2 | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
DJNALGAK_00668 | 3e-70 | lepB | 3.4.21.89 | U | Signal peptidase, peptidase S26 | |
DJNALGAK_00669 | 5.5e-40 | 6.3.3.2 | S | ASCH | ||
DJNALGAK_00670 | 8.3e-187 | 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 | |
DJNALGAK_00672 | 8.1e-116 | sufC | O | FeS assembly ATPase SufC | ||
DJNALGAK_00673 | 2.1e-145 | sufD | O | FeS assembly protein SufD | ||
DJNALGAK_00674 | 4.8e-43 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
DJNALGAK_00675 | 1.7e-156 | nrnB | S | DHHA1 domain | ||
DJNALGAK_00676 | 3.7e-90 | yunF | F | Protein of unknown function DUF72 | ||
DJNALGAK_00679 | 9.5e-246 | yhcA | V | ABC transporter, ATP-binding protein | ||
DJNALGAK_00681 | 1.5e-41 | S | Phosphoesterase | |||
DJNALGAK_00682 | 1.5e-72 | 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 | |
DJNALGAK_00683 | 1.1e-60 | yslB | S | Protein of unknown function (DUF2507) | ||
DJNALGAK_00684 | 9.9e-41 | trxA | O | Belongs to the thioredoxin family | ||
DJNALGAK_00685 | 2.4e-254 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
DJNALGAK_00686 | 3.3e-105 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
DJNALGAK_00687 | 6.6e-157 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
DJNALGAK_00688 | 2.8e-125 | rapZ | S | Displays ATPase and GTPase activities | ||
DJNALGAK_00689 | 8.2e-153 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
DJNALGAK_00690 | 1.2e-74 | purN | 2.1.2.2 | F | Catalyzes the transfer of a formyl group from 10- formyltetrahydrofolate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR) and tetrahydrofolate | |
DJNALGAK_00691 | 1.9e-21 | purM | 6.3.3.1, 6.3.4.13 | F | Phosphoribosylformylglycinamidine cyclo-ligase | |
DJNALGAK_00692 | 7.8e-198 | 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 | ||
DJNALGAK_00693 | 3.9e-249 | gnd | 1.1.1.343, 1.1.1.44 | H | Catalyzes the oxidative decarboxylation of 6- phosphogluconate to ribulose 5-phosphate and CO(2), with concomitant reduction of NADP to NADPH | |
DJNALGAK_00694 | 1.9e-300 | rnjA | J | An RNase that has 5'-3' exonuclease and possibly endonuclease activity. Involved in maturation of rRNA and in some organisms also mRNA maturation and or decay | ||
DJNALGAK_00695 | 5e-23 | ykzG | S | Belongs to the UPF0356 family | ||
DJNALGAK_00696 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
DJNALGAK_00697 | 6.1e-99 | fabK | 1.3.1.9 | S | Nitronate monooxygenase | |
DJNALGAK_00698 | 3e-162 | ytbD | EGP | Major facilitator Superfamily | ||
DJNALGAK_00699 | 0.0 | parE | 5.99.1.3 | L | Topoisomerase IV is essential for chromosome segregation. It relaxes supercoiled DNA. Performs the decatenation events required during the replication of a circular DNA molecule | |
DJNALGAK_00700 | 3.2e-83 | plsY | 2.3.1.15, 3.5.1.104 | I | Catalyzes the transfer of an acyl group from acyl- phosphate (acyl-PO(4)) to glycerol-3-phosphate (G3P) to form lysophosphatidic acid (LPA). This enzyme utilizes acyl-phosphate as fatty acyl donor, but not acyl-CoA or acyl-ACP | |
DJNALGAK_00701 | 7.7e-135 | 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 | |
DJNALGAK_00702 | 9.9e-85 | prmB | 2.1.1.297, 2.1.1.298 | J | Methylates the class 1 translation termination release factors RF1 PrfA and RF2 PrfB on the glutamine residue of the universally conserved GGQ motif | |
DJNALGAK_00703 | 1e-177 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
DJNALGAK_00704 | 6.8e-86 | tdk | 2.7.1.21 | F | thymidine kinase | |
DJNALGAK_00705 | 3.7e-49 | cps3F | ||||
DJNALGAK_00711 | 4.7e-133 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
DJNALGAK_00712 | 1.5e-18 | 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 | ||
DJNALGAK_00713 | 2.5e-161 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
DJNALGAK_00714 | 7.2e-82 | 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 | ||
DJNALGAK_00715 | 6.3e-115 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
DJNALGAK_00716 | 1.6e-40 | manO | S | Domain of unknown function (DUF956) | ||
DJNALGAK_00717 | 1.4e-290 | ybiT | S | ABC transporter, ATP-binding protein | ||
DJNALGAK_00718 | 1.5e-62 | bCE_4747 | S | Beta-lactamase superfamily domain | ||
DJNALGAK_00719 | 1.3e-99 | birA | 6.3.4.15 | H | Acts both as a biotin-- acetyl-CoA-carboxylase ligase and a repressor | |
DJNALGAK_00720 | 6.5e-75 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
DJNALGAK_00721 | 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 | ||
DJNALGAK_00724 | 1e-86 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
DJNALGAK_00725 | 2.1e-67 | XK27_09705 | 6.1.1.14 | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | |
DJNALGAK_00726 | 6.9e-43 | yodB | K | Transcriptional regulator, HxlR family | ||
DJNALGAK_00727 | 7.4e-173 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
DJNALGAK_00728 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
DJNALGAK_00729 | 2.4e-221 | gdhA | 1.4.1.4 | E | Glutamate/Leucine/Phenylalanine/Valine dehydrogenase | |
DJNALGAK_00730 | 6.7e-219 | XK27_08635 | S | UPF0210 protein | ||
DJNALGAK_00731 | 4.1e-27 | gcvR | T | Belongs to the UPF0237 family | ||
DJNALGAK_00732 | 1.1e-09 | cps3I | G | Acyltransferase family | ||
DJNALGAK_00733 | 1.2e-148 | iunH | 3.2.2.1 | F | Inosine-uridine preferring nucleoside hydrolase | |
DJNALGAK_00734 | 1.2e-39 | 2.7.7.65 | T | phosphorelay sensor kinase activity | ||
DJNALGAK_00735 | 5.4e-157 | XK27_09615 | S | reductase | ||
DJNALGAK_00736 | 1.9e-67 | XK27_09620 | S | NADPH-dependent FMN reductase | ||
DJNALGAK_00738 | 1.5e-188 | iolF | EGP | Major facilitator Superfamily | ||
DJNALGAK_00739 | 5.8e-216 | rhaB | 2.7.1.5, 5.3.1.14 | F | Involved in the catabolism of L-rhamnose (6-deoxy-L- mannose). Catalyzes the transfer of the gamma-phosphate group from ATP to the 1-hydroxyl group of L-rhamnulose to yield L-rhamnulose 1-phosphate | |
DJNALGAK_00740 | 4e-40 | rhaM | 5.1.3.32 | G | Involved in the anomeric conversion of L-rhamnose | |
DJNALGAK_00741 | 4.8e-219 | rhaA | 2.7.1.5, 5.3.1.14 | G | L-rhamnose isomerase (RhaA) | |
DJNALGAK_00742 | 6.9e-110 | rhaD | 4.1.2.17, 4.1.2.19 | H | Catalyzes the reversible cleavage of L-rhamnulose-1- phosphate to dihydroxyacetone phosphate (DHAP) and L-lactaldehyde | |
DJNALGAK_00743 | 7.2e-259 | 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 | ||
DJNALGAK_00744 | 2e-131 | 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 | ||
DJNALGAK_00745 | 3.6e-169 | 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 | ||
DJNALGAK_00746 | 5.1e-260 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
DJNALGAK_00747 | 7.2e-11 | S | Putative Competence protein ComGF | |||
DJNALGAK_00749 | 5.6e-13 | |||||
DJNALGAK_00750 | 1.2e-27 | comGC | U | competence protein ComGC | ||
DJNALGAK_00751 | 5.7e-98 | comGB | NU | type II secretion system | ||
DJNALGAK_00752 | 3.1e-120 | comGA | NU | Type II IV secretion system protein | ||
DJNALGAK_00753 | 8.7e-144 | iunH2 | 3.2.2.1 | F | nucleoside hydrolase | |
DJNALGAK_00754 | 1.7e-42 | XK27_03960 | S | Protein of unknown function (DUF3013) | ||
DJNALGAK_00756 | 2.8e-09 | S | Protein of unknown function (DUF805) | |||
DJNALGAK_00758 | 4.3e-203 | 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 | |
DJNALGAK_00759 | 4.7e-148 | mepA | V | MATE efflux family protein | ||
DJNALGAK_00760 | 1.6e-152 | lsa | S | ABC transporter | ||
DJNALGAK_00761 | 8.2e-232 | 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 | |
DJNALGAK_00762 | 5e-121 | malT | G | Transporter, major facilitator family protein | ||
DJNALGAK_00763 | 2.1e-196 | ade | 3.5.4.2 | F | Belongs to the metallo-dependent hydrolases superfamily. Adenine deaminase family | |
DJNALGAK_00764 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
DJNALGAK_00765 | 1.7e-87 | S | hydrolase | |||
DJNALGAK_00766 | 1.2e-23 | ydcZ | S | Putative inner membrane exporter, YdcZ | ||
DJNALGAK_00767 | 1.7e-111 | endA | F | DNA RNA non-specific endonuclease | ||
DJNALGAK_00768 | 6.4e-69 | G | Transporter, major facilitator family protein | |||
DJNALGAK_00769 | 2.6e-223 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
DJNALGAK_00770 | 1.7e-219 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
DJNALGAK_00771 | 1.1e-83 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
DJNALGAK_00772 | 5.9e-80 | ylbE | GM | NAD dependent epimerase dehydratase family protein | ||
DJNALGAK_00773 | 7.5e-83 | L | COG1961 Site-specific recombinases, DNA invertase Pin homologs | |||
DJNALGAK_00774 | 1.1e-71 | S | Recombinase | |||
DJNALGAK_00775 | 2.3e-295 | L | Recombinase | |||
DJNALGAK_00776 | 1.6e-32 | K | Cro/C1-type HTH DNA-binding domain | |||
DJNALGAK_00777 | 3.1e-164 | L | Nucleotidyltransferase domain | |||
DJNALGAK_00778 | 6.8e-141 | Q | Protein of unknown function (DUF1698) | |||
DJNALGAK_00779 | 3.8e-167 | aadK | G | adenylyltransferase | ||
DJNALGAK_00780 | 4.4e-63 | mraZ | K | Belongs to the MraZ family | ||
DJNALGAK_00781 | 2.2e-07 | S | Protein of unknown function (DUF3397) | |||
DJNALGAK_00782 | 1.2e-155 | dapG | 1.1.1.3, 2.7.2.4 | E | Amino acid kinase family | |
DJNALGAK_00783 | 2.9e-91 | K | response regulator | |||
DJNALGAK_00784 | 3.3e-142 | hpk31 | 2.7.13.3 | T | Histidine kinase | |
DJNALGAK_00785 | 3.7e-134 | K | Transcriptional regulator | |||
DJNALGAK_00786 | 2e-88 | pyrE | 2.4.2.10, 4.1.1.23 | F | Catalyzes the transfer of a ribosyl phosphate group from 5-phosphoribose 1-diphosphate to orotate, leading to the formation of orotidine monophosphate (OMP) | |
DJNALGAK_00787 | 2.3e-85 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
DJNALGAK_00788 | 2.7e-43 | sip | L | Belongs to the 'phage' integrase family | ||
DJNALGAK_00789 | 8.9e-73 | yjjH | S | Calcineurin-like phosphoesterase | ||
DJNALGAK_00790 | 1.8e-95 | EG | EamA-like transporter family | |||
DJNALGAK_00791 | 1.3e-74 | natB | CP | ABC-type Na efflux pump, permease component | ||
DJNALGAK_00792 | 7.1e-295 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
DJNALGAK_00793 | 1.3e-55 | 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 | ||
DJNALGAK_00794 | 2.5e-51 | yvfR | V | ABC transporter | ||
DJNALGAK_00796 | 2.7e-66 | |||||
DJNALGAK_00797 | 1.5e-199 | L | Transposase DDE domain group 1 | |||
DJNALGAK_00798 | 1.6e-121 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
DJNALGAK_00799 | 3.9e-187 | cshB | 3.6.4.13 | JKL | DEAD-box RNA helicase. May work in conjunction with the cold shock proteins to ensure proper initiation of transcription at low and optimal temperatures | |
DJNALGAK_00800 | 0.0 | alaS | 6.1.1.7 | J | Catalyzes the attachment of alanine to tRNA(Ala) in a two-step reaction alanine is first activated by ATP to form Ala- AMP and then transferred to the acceptor end of tRNA(Ala). Also edits incorrectly charged Ser-tRNA(Ala) and Gly-tRNA(Ala) via its editing domain | |
DJNALGAK_00801 | 2.1e-36 | yrzL | S | Belongs to the UPF0297 family | ||
DJNALGAK_00802 | 2.3e-59 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
DJNALGAK_00803 | 1.9e-33 | yrzB | S | Belongs to the UPF0473 family | ||
DJNALGAK_00804 | 1.4e-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 | ||
DJNALGAK_00809 | 1.5e-69 | S | RRXRR protein | |||
DJNALGAK_00812 | 8.3e-48 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
DJNALGAK_00813 | 1e-27 | ysxB | J | Cysteine protease Prp | ||
DJNALGAK_00814 | 1.6e-42 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
DJNALGAK_00815 | 2.7e-204 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
DJNALGAK_00816 | 2.2e-76 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
DJNALGAK_00817 | 1.1e-207 | 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) | |
DJNALGAK_00818 | 7.2e-53 | perR | P | Belongs to the Fur family | ||
DJNALGAK_00819 | 3.8e-08 | E | Amino acid permease | |||
DJNALGAK_00820 | 1.6e-55 | ctsR | K | Belongs to the CtsR family | ||
DJNALGAK_00822 | 7.3e-119 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
DJNALGAK_00823 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
DJNALGAK_00824 | 6.3e-159 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
DJNALGAK_00825 | 1.4e-186 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
DJNALGAK_00826 | 3.4e-120 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
DJNALGAK_00828 | 9.2e-16 | |||||
DJNALGAK_00830 | 1.2e-74 | phoR | 2.7.13.3 | T | Histidine kinase | |
DJNALGAK_00831 | 4.1e-08 | KT | PspC domain protein | |||
DJNALGAK_00832 | 1.6e-26 | yvlD | S | Mycobacterial 4 TMS phage holin, superfamily IV | ||
DJNALGAK_00833 | 4.1e-38 | M | group 2 family protein | |||
DJNALGAK_00834 | 1.5e-98 | M | Glycosyl transferase family 8 | |||
DJNALGAK_00835 | 2.1e-94 | 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 | ||
DJNALGAK_00836 | 3.7e-46 | yqhY | S | Asp23 family, cell envelope-related function | ||
DJNALGAK_00837 | 4.2e-36 | 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 | ||
DJNALGAK_00838 | 1e-103 | 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 | |
DJNALGAK_00839 | 3.2e-26 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
DJNALGAK_00840 | 2.3e-139 | ansA | 3.5.1.1 | EJ | Asparaginase | |
DJNALGAK_00841 | 4.1e-69 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
DJNALGAK_00842 | 4.3e-28 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
DJNALGAK_00843 | 6.4e-161 | tsaD | 2.3.1.234 | 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. 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 | |
DJNALGAK_00844 | 1.5e-117 | uup | S | ABC transporter, ATP-binding protein | ||
DJNALGAK_00845 | 3.9e-157 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
DJNALGAK_00847 | 2.7e-143 | L | Probable transposase | |||
DJNALGAK_00848 | 7.3e-94 | C | Luciferase-like monooxygenase | |||
DJNALGAK_00849 | 1.3e-24 | 1.5.1.38 | S | FMN reductase | ||
DJNALGAK_00850 | 4.3e-26 | 1.5.1.38 | S | NADPH-dependent FMN reductase | ||
DJNALGAK_00851 | 1.5e-117 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
DJNALGAK_00852 | 3.9e-76 | L | haloacid dehalogenase-like hydrolase | |||
DJNALGAK_00853 | 3.1e-61 | EG | EamA-like transporter family | |||
DJNALGAK_00854 | 1.2e-117 | K | AI-2E family transporter | |||
DJNALGAK_00855 | 2.4e-172 | malY | 4.4.1.8 | E | Aminotransferase, class I | |
DJNALGAK_00857 | 1.6e-38 | |||||
DJNALGAK_00859 | 7.3e-13 | |||||
DJNALGAK_00860 | 8.9e-19 | L | nuclease | |||
DJNALGAK_00861 | 9.6e-28 | S | Short C-terminal domain | |||
DJNALGAK_00862 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
DJNALGAK_00863 | 2.8e-96 | nrdG | 1.97.1.4 | O | Activation of anaerobic ribonucleoside-triphosphate reductase under anaerobic conditions by generation of an organic free radical, using S-adenosylmethionine and reduced flavodoxin as cosubstrates to produce 5'-deoxy-adenosine | |
DJNALGAK_00864 | 8.8e-58 | spxA | 1.20.4.1 | K | Interferes with activator-stimulated transcription by interaction with the RNA polymerase alpha-CTD. May function to globally reduce transcription of genes involved in growth- and development-promoting processes and to increase transcription of genes involved in thiol homeostasis, during periods of extreme stress | |
DJNALGAK_00865 | 7.5e-178 | merA | 1.16.1.1, 1.8.1.7 | C | Pyridine nucleotide-disulfide oxidoreductase | |
DJNALGAK_00866 | 2.6e-295 | fucI | 5.3.1.25, 5.3.1.3 | G | Converts the aldose L-fucose into the corresponding ketose L-fuculose | |
DJNALGAK_00867 | 3.4e-167 | mbl | D | Cell shape determining protein MreB Mrl | ||
DJNALGAK_00868 | 9e-27 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
DJNALGAK_00869 | 1.3e-13 | S | Protein of unknown function (DUF2969) | |||
DJNALGAK_00870 | 2.6e-182 | rny | S | Endoribonuclease that initiates mRNA decay | ||
DJNALGAK_00871 | 2.3e-159 | 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 | ||
DJNALGAK_00872 | 3.3e-32 | ykuL | S | CBS domain | ||
DJNALGAK_00873 | 3e-61 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
DJNALGAK_00874 | 2.4e-177 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
DJNALGAK_00875 | 6.4e-48 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
DJNALGAK_00876 | 7.6e-275 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
DJNALGAK_00877 | 2.6e-120 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
DJNALGAK_00878 | 2.2e-75 | cas3 | L | CRISPR-associated helicase cas3 | ||
DJNALGAK_00879 | 1.5e-74 | cas3 | L | CRISPR-associated helicase cas3 | ||
DJNALGAK_00880 | 5.1e-16 | |||||
DJNALGAK_00882 | 3.3e-27 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
DJNALGAK_00883 | 1.7e-116 | vicX | 3.1.26.11 | S | domain protein | |
DJNALGAK_00884 | 6.8e-30 | yyaQ | S | YjbR | ||
DJNALGAK_00885 | 2.1e-79 | yycI | S | YycH protein | ||
DJNALGAK_00886 | 1.3e-102 | yycH | S | YycH protein | ||
DJNALGAK_00887 | 1.5e-272 | vicK | 2.7.13.3 | T | Histidine kinase | |
DJNALGAK_00888 | 9e-114 | K | response regulator | |||
DJNALGAK_00889 | 3.3e-09 | bta | 1.8.1.8 | CO | transport accessory protein | |
DJNALGAK_00890 | 4.9e-115 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
DJNALGAK_00891 | 1.7e-82 | cas2 | 2.7.7.7 | L | CRISPR-associated protein (Cas_Cas2CT1978) | |
DJNALGAK_00892 | 1.6e-118 | cas1 | L | CRISPR (clustered regularly interspaced short palindromic repeat), is an adaptive immune system that provides protection against mobile genetic elements (viruses, transposable elements and conjugative plasmids). CRISPR clusters contain spacers, sequences complementary to antecedent mobile elements, and target invading nucleic acids. CRISPR clusters are transcribed and processed into CRISPR RNA (crRNA). Acts as a dsDNA endonuclease. Involved in the integration of spacer DNA into the CRISPR cassette | ||
DJNALGAK_00893 | 6.2e-61 | casE | S | CRISPR_assoc | ||
DJNALGAK_00894 | 5.6e-60 | casD | S | CRISPR-associated protein (Cas_Cas5) | ||
DJNALGAK_00895 | 1.5e-112 | casC | L | CT1975-like protein | ||
DJNALGAK_00896 | 8.1e-22 | casB | S | CRISPR-associated protein Cse2 (CRISPR_cse2) | ||
DJNALGAK_00897 | 1.9e-167 | pfkA | 2.7.1.11 | F | Catalyzes the phosphorylation of D-fructose 6-phosphate to fructose 1,6-bisphosphate by ATP, the first committing step of glycolysis | |
DJNALGAK_00898 | 3.7e-310 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
DJNALGAK_00899 | 4.5e-08 | S | Protein of unknown function (DUF3343) | |||
DJNALGAK_00900 | 4.9e-105 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
DJNALGAK_00901 | 5.1e-102 | cdsA | 2.7.7.41 | S | Belongs to the CDS family | |
DJNALGAK_00902 | 4.1e-157 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
DJNALGAK_00903 | 1.7e-259 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
DJNALGAK_00904 | 5.1e-167 | arlS | 2.7.13.3 | T | Histidine kinase | |
DJNALGAK_00905 | 2.2e-85 | K | response regulator | |||
DJNALGAK_00906 | 3.4e-16 | queD | 4.1.2.50, 4.2.3.12 | H | 6-pyruvoyl tetrahydropterin synthase | |
DJNALGAK_00907 | 1.4e-120 | ica2 | GT2 | M | Glycosyl transferase family group 2 | |
DJNALGAK_00908 | 1.7e-44 | |||||
DJNALGAK_00909 | 3.3e-92 | M | 4-amino-4-deoxy-L-arabinose transferase and related glycosyltransferases of PMT family | |||
DJNALGAK_00912 | 2.7e-66 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
DJNALGAK_00913 | 4.8e-170 | nusA | K | Participates in both transcription termination and antitermination | ||
DJNALGAK_00914 | 1.4e-39 | ylxR | K | Protein of unknown function (DUF448) | ||
DJNALGAK_00915 | 6.9e-26 | ylxQ | J | ribosomal protein | ||
DJNALGAK_00917 | 9.1e-263 | ydaO | E | amino acid | ||
DJNALGAK_00918 | 1.6e-157 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
DJNALGAK_00919 | 2.4e-81 | yabB | 2.1.1.223 | L | Methyltransferase small domain | |
DJNALGAK_00920 | 1.5e-27 | yazA | L | GIY-YIG catalytic domain protein | ||
DJNALGAK_00921 | 7.2e-128 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
DJNALGAK_00922 | 3.6e-128 | 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 | ||
DJNALGAK_00923 | 7.7e-60 | sip | L | Belongs to the 'phage' integrase family | ||
DJNALGAK_00924 | 9.9e-223 | lmrA | V | ABC transporter, ATP-binding protein | ||
DJNALGAK_00925 | 3.9e-254 | yfiC | V | ABC transporter | ||
DJNALGAK_00927 | 3.5e-144 | purK2 | 6.3.4.18 | F | Involved in the de novo purine biosynthesis. Catalyzes the transfer of formate to 5-phospho-ribosyl-glycinamide (GAR), producing 5-phospho-ribosyl-N-formylglycinamide (FGAR). Formate is provided by PurU via hydrolysis of 10-formyl-tetrahydrofolate | |
DJNALGAK_00928 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
DJNALGAK_00929 | 2.3e-279 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
DJNALGAK_00930 | 7.1e-161 | camS | S | sex pheromone | ||
DJNALGAK_00931 | 8.5e-28 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
DJNALGAK_00932 | 5.3e-79 | radC | L | DNA repair protein | ||
DJNALGAK_00933 | 4.5e-21 | K | Cold shock | |||
DJNALGAK_00934 | 3.6e-156 | mreB | D | cell shape determining protein MreB | ||
DJNALGAK_00935 | 2.1e-88 | mreC | M | Involved in formation and maintenance of cell shape | ||
DJNALGAK_00936 | 1.5e-54 | mreD | M | rod shape-determining protein MreD | ||
DJNALGAK_00937 | 8.3e-77 | minC | D | Cell division inhibitor that blocks the formation of polar Z ring septums. Rapidly oscillates between the poles of the cell to destabilize FtsZ filaments that have formed before they mature into polar Z rings. Prevents FtsZ polymerization | ||
DJNALGAK_00938 | 1.8e-126 | minD | D | Belongs to the ParA family | ||
DJNALGAK_00939 | 1.9e-94 | glnP | P | ABC transporter permease | ||
DJNALGAK_00940 | 5.7e-32 | dnaD | L | DnaD domain protein | ||
DJNALGAK_00941 | 1.5e-83 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
DJNALGAK_00942 | 2.6e-78 | msrA | 1.8.4.11, 1.8.4.12 | O | Has an important function as a repair enzyme for proteins that have been inactivated by oxidation. Catalyzes the reversible oxidation-reduction of methionine sulfoxide in proteins to methionine | |
DJNALGAK_00943 | 9.6e-126 | yitT | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
DJNALGAK_00944 | 6.2e-92 | M | transferase activity, transferring glycosyl groups | |||
DJNALGAK_00945 | 1.9e-75 | K | Helix-turn-helix domain, rpiR family | |||
DJNALGAK_00946 | 3.3e-92 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
DJNALGAK_00947 | 1.3e-127 | nanA | 4.1.3.3, 4.3.3.7 | EM | Neu5Ac) to form pyruvate and N-acetylmannosamine (ManNAc) via a Schiff base intermediate | |
DJNALGAK_00948 | 6.5e-90 | nanK | GK | ROK family | ||
DJNALGAK_00949 | 1.1e-53 | ndk | 2.7.4.6 | F | Belongs to the NDK family | |
DJNALGAK_00950 | 1.5e-56 | ohrR | K | helix_turn_helix multiple antibiotic resistance protein | ||
DJNALGAK_00951 | 2.6e-31 | azlD | S | Branched-chain amino acid transport protein (AzlD) | ||
DJNALGAK_00952 | 5.1e-77 | azlC | E | branched-chain amino acid | ||
DJNALGAK_00953 | 2.7e-58 | 2.4.2.6 | F | Nucleoside 2-deoxyribosyltransferase | ||
DJNALGAK_00956 | 1.6e-140 | K | Phage regulatory protein | |||
DJNALGAK_00957 | 1.7e-10 | K | Helix-turn-helix XRE-family like proteins | |||
DJNALGAK_00958 | 7.6e-199 | dinG | 3.1.12.1, 3.6.4.12 | KL | DEAD_2 | |
DJNALGAK_00959 | 1.1e-146 | XK27_08315 | M | Sulfatase | ||
DJNALGAK_00960 | 3.8e-93 | yihY | S | Belongs to the UPF0761 family | ||
DJNALGAK_00961 | 4.7e-12 | mltD | CBM50 | M | Lysin motif | |
DJNALGAK_00962 | 3.6e-56 | S | CAAX protease self-immunity | |||
DJNALGAK_00963 | 2.4e-46 | C | Flavodoxin | |||
DJNALGAK_00964 | 1.1e-55 | yphH | S | Cupin domain | ||
DJNALGAK_00965 | 1.4e-45 | yphJ | 4.1.1.44 | S | decarboxylase | |
DJNALGAK_00966 | 1e-143 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
DJNALGAK_00967 | 7.4e-107 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
DJNALGAK_00968 | 1.5e-149 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
DJNALGAK_00969 | 9.6e-68 | metI | P | ABC transporter permease | ||
DJNALGAK_00970 | 8.8e-135 | argE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
DJNALGAK_00971 | 3e-84 | drgA | C | nitroreductase | ||
DJNALGAK_00972 | 3.9e-84 | adc | 4.1.1.4 | Q | Acetoacetate decarboxylase (ADC) | |
DJNALGAK_00973 | 2.3e-106 | fadB4 | 1.1.1.157 | I | 3-hydroxyacyl-CoA dehydrogenase | |
DJNALGAK_00974 | 1.3e-172 | npr | 1.11.1.1 | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | |
DJNALGAK_00975 | 3.3e-265 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
DJNALGAK_00978 | 9.9e-11 | S | Predicted membrane protein (DUF2207) | |||
DJNALGAK_00979 | 1.4e-19 | |||||
DJNALGAK_00980 | 4.4e-37 | M | Glycosyltransferase group 2 family protein | |||
DJNALGAK_00981 | 7.4e-54 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
DJNALGAK_00982 | 2.8e-58 | ktrA | P | TrkA-N domain | ||
DJNALGAK_00983 | 1.2e-114 | ntpJ | P | Potassium uptake protein | ||
DJNALGAK_00984 | 1.6e-236 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
DJNALGAK_00987 | 5e-132 | 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 | |
DJNALGAK_00988 | 2e-86 | 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 | |
DJNALGAK_00989 | 7.7e-12 | M | Lysin motif | |||
DJNALGAK_00990 | 5.5e-145 | L | transposase, IS605 OrfB family | |||
DJNALGAK_00991 | 0.0 | ileS | 6.1.1.5 | J | amino acids such as valine, to avoid such errors it has two additional distinct tRNA(Ile)-dependent editing activities. One activity is designated as 'pretransfer' editing and involves the hydrolysis of activated Val-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Val-tRNA(Ile) | |
DJNALGAK_00992 | 1.3e-68 | pts13C | G | The phosphoenolpyruvate-dependent sugar phosphotransferase system (PTS), a major carbohydrate active - transport system, catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | ||
DJNALGAK_00993 | 1.7e-83 | comEC | S | Competence protein ComEC | ||
DJNALGAK_00994 | 9.1e-29 | yaaL | S | Protein of unknown function (DUF2508) | ||
DJNALGAK_00995 | 2.2e-97 | 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 | ||
DJNALGAK_00996 | 7e-34 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
DJNALGAK_00997 | 5.1e-211 | dnaX | 2.7.7.7 | L | DNA polymerase III is a complex, multichain enzyme responsible for most of the replicative synthesis in bacteria. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
DJNALGAK_00998 | 3.3e-62 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
DJNALGAK_00999 | 3.2e-75 | rsmC | 2.1.1.172 | J | Methyltransferase | |
DJNALGAK_01000 | 2.7e-27 | nrdH | O | Glutaredoxin | ||
DJNALGAK_01001 | 6.3e-45 | nrdI | F | NrdI Flavodoxin like | ||
DJNALGAK_01002 | 0.0 | nrdE | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
DJNALGAK_01003 | 1e-160 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
DJNALGAK_01004 | 5.5e-46 | cps3F | ||||
DJNALGAK_01005 | 2.1e-83 | S | Membrane | |||
DJNALGAK_01006 | 9.5e-234 | 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 | |
DJNALGAK_01007 | 2.3e-128 | tpiA | 2.7.2.3, 5.3.1.1 | G | Involved in the gluconeogenesis. Catalyzes stereospecifically the conversion of dihydroxyacetone phosphate (DHAP) to D-glyceraldehyde-3-phosphate (G3P) | |
DJNALGAK_01008 | 1.3e-208 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
DJNALGAK_01009 | 6.1e-180 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
DJNALGAK_01010 | 2.9e-137 | cggR | K | Putative sugar-binding domain | ||
DJNALGAK_01011 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
DJNALGAK_01012 | 3.5e-110 | cobQ | S | glutamine amidotransferase | ||
DJNALGAK_01013 | 1e-219 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
DJNALGAK_01014 | 1.1e-75 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
DJNALGAK_01015 | 9.2e-16 | psiE | S | Phosphate-starvation-inducible E | ||
DJNALGAK_01016 | 5.4e-208 | mmuP | E | amino acid | ||
DJNALGAK_01017 | 6.9e-114 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
DJNALGAK_01018 | 5.3e-40 | K | LytTr DNA-binding domain | |||
DJNALGAK_01019 | 7.8e-18 | S | Protein of unknown function (DUF3021) | |||
DJNALGAK_01020 | 7.4e-177 | metK | 2.5.1.6 | H | Catalyzes the formation of S-adenosylmethionine (AdoMet) from methionine and ATP. The overall synthetic reaction is composed of two sequential steps, AdoMet formation and the subsequent tripolyphosphate hydrolysis which occurs prior to release of AdoMet from the enzyme | |
DJNALGAK_01021 | 1.2e-135 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
DJNALGAK_01022 | 9.4e-109 | L | Initiator Replication protein | |||
DJNALGAK_01023 | 7.4e-115 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
DJNALGAK_01025 | 3.4e-24 | S | Domain of unknown function (DUF4828) | |||
DJNALGAK_01026 | 1.6e-127 | mocA | S | Oxidoreductase | ||
DJNALGAK_01027 | 2e-159 | yfmL | L | DEAD DEAH box helicase | ||
DJNALGAK_01028 | 2e-20 | S | Domain of unknown function (DUF3284) | |||
DJNALGAK_01030 | 1e-279 | kup | P | Transport of potassium into the cell | ||
DJNALGAK_01031 | 4.1e-81 | 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 | |
DJNALGAK_01032 | 1.1e-61 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
DJNALGAK_01033 | 9.7e-63 | ytgP | S | Polysaccharide biosynthesis protein | ||
DJNALGAK_01034 | 8.9e-289 | lacS | G | Transporter | ||
DJNALGAK_01035 | 9.4e-236 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
DJNALGAK_01036 | 1.5e-107 | 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 | |
DJNALGAK_01037 | 1.4e-40 | yabA | L | Involved in initiation control of chromosome replication | ||
DJNALGAK_01038 | 3.2e-92 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
DJNALGAK_01039 | 4.2e-56 | ytsP | 1.8.4.14 | T | GAF domain-containing protein | |
DJNALGAK_01040 | 7.5e-101 | 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 | ||
DJNALGAK_01041 | 6.7e-301 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
DJNALGAK_01042 | 3e-57 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
DJNALGAK_01043 | 1e-196 | yfnA | E | amino acid | ||
DJNALGAK_01044 | 3.3e-90 | stp | 3.1.3.16 | T | phosphatase | |
DJNALGAK_01045 | 4.4e-36 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
DJNALGAK_01046 | 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 | |
DJNALGAK_01047 | 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 | |
DJNALGAK_01048 | 3.3e-23 | pilD | 3.4.23.43 | NOU | aspartic-type endopeptidase activity | |
DJNALGAK_01049 | 2.2e-120 | 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 | |
DJNALGAK_01050 | 2.5e-21 | rpoZ | 2.7.7.6 | K | Promotes RNA polymerase assembly. Latches the N- and C- terminal regions of the beta' subunit thereby facilitating its interaction with the beta and alpha subunits | |
DJNALGAK_01051 | 1.1e-102 | gmk | 2.7.4.8 | F | Essential for recycling GMP and indirectly, cGMP | |
DJNALGAK_01052 | 2.1e-153 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
DJNALGAK_01053 | 4.7e-220 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
DJNALGAK_01054 | 3.1e-246 | sfcA | 1.1.1.38, 4.1.1.101 | C | Malic enzyme | |
DJNALGAK_01055 | 2.9e-86 | S | overlaps another CDS with the same product name | |||
DJNALGAK_01056 | 8.3e-91 | S | overlaps another CDS with the same product name | |||
DJNALGAK_01057 | 5.4e-156 | sigA | K | Sigma factors are initiation factors that promote the attachment of RNA polymerase to specific initiation sites and are then released. This sigma factor is the primary sigma factor during exponential growth | ||
DJNALGAK_01058 | 7.3e-149 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
DJNALGAK_01059 | 3e-210 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
DJNALGAK_01060 | 1.1e-52 | gtcA | S | Teichoic acid glycosylation protein | ||
DJNALGAK_01061 | 5.1e-54 | fld | C | Flavodoxin | ||
DJNALGAK_01062 | 1.2e-143 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
DJNALGAK_01063 | 4.5e-227 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
DJNALGAK_01064 | 1.9e-167 | mdtG | EGP | Major facilitator Superfamily | ||
DJNALGAK_01066 | 1.7e-53 | K | LysR substrate binding domain | |||
DJNALGAK_01067 | 1.5e-122 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
DJNALGAK_01068 | 1.1e-199 | nupG | F | Nucleoside | ||
DJNALGAK_01069 | 1.8e-76 | 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 | ||
DJNALGAK_01070 | 6.3e-188 | nhaC | C | Na H antiporter NhaC | ||
DJNALGAK_01072 | 4.3e-61 | uspA | T | universal stress protein | ||
DJNALGAK_01073 | 1.5e-22 | infB | UW | LPXTG-motif cell wall anchor domain protein | ||
DJNALGAK_01074 | 1.4e-51 | |||||
DJNALGAK_01075 | 1.8e-82 | L | Transposase, IS116 IS110 IS902 family | |||
DJNALGAK_01076 | 1.8e-27 | S | Protein of unknown function (DUF3290) | |||
DJNALGAK_01077 | 2.3e-279 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
DJNALGAK_01078 | 1.7e-155 | thyA | 2.1.1.45 | F | Catalyzes the reductive methylation of 2'-deoxyuridine- 5'-monophosphate (dUMP) to 2'-deoxythymidine-5'-monophosphate (dTMP) while utilizing 5,10-methylenetetrahydrofolate (mTHF) as the methyl donor and reductant in the reaction, yielding dihydrofolate (DHF) as a by-product. This enzymatic reaction provides an intracellular de novo source of dTMP, an essential precursor for DNA biosynthesis | |
DJNALGAK_01079 | 2.2e-276 | yfmR | S | ABC transporter, ATP-binding protein | ||
DJNALGAK_01081 | 2.1e-65 | H | Methyltransferase domain | |||
DJNALGAK_01082 | 1.7e-41 | cps2D | 5.1.3.2 | M | RmlD substrate binding domain | |
DJNALGAK_01083 | 1.6e-133 | yvgN | C | Aldo keto reductase | ||
DJNALGAK_01084 | 4.2e-35 | K | helix_turn_helix, mercury resistance | |||
DJNALGAK_01085 | 3.5e-113 | S | Aldo keto reductase | |||
DJNALGAK_01086 | 4.5e-252 | L | Transposase DDE domain group 1 | |||
DJNALGAK_01087 | 2.6e-30 | 1.1.1.27 | C | L-malate dehydrogenase activity | ||
DJNALGAK_01088 | 1.2e-24 | yktA | S | Belongs to the UPF0223 family | ||
DJNALGAK_01089 | 6.3e-76 | suhB | 3.1.3.25 | G | Belongs to the inositol monophosphatase superfamily | |
DJNALGAK_01090 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
DJNALGAK_01091 | 6.9e-285 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
DJNALGAK_01092 | 9.7e-37 | ptsH | G | phosphocarrier protein HPR | ||
DJNALGAK_01093 | 1.5e-15 | |||||
DJNALGAK_01094 | 2e-26 | clpE | O | Belongs to the ClpA ClpB family | ||
DJNALGAK_01095 | 7.1e-35 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
DJNALGAK_01096 | 1.7e-74 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
DJNALGAK_01099 | 8.9e-100 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
DJNALGAK_01100 | 2.4e-44 | S | Repeat protein | |||
DJNALGAK_01101 | 1.8e-07 | |||||
DJNALGAK_01102 | 1.8e-65 | yxkH | G | Polysaccharide deacetylase | ||
DJNALGAK_01103 | 2.7e-127 | guaC | 1.1.1.205, 1.7.1.7 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
DJNALGAK_01104 | 3.6e-40 | glnP | P | ABC transporter | ||
DJNALGAK_01105 | 2.6e-119 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJNALGAK_01106 | 1.5e-31 | |||||
DJNALGAK_01107 | 4.7e-93 | ampC | V | Beta-lactamase | ||
DJNALGAK_01108 | 7.1e-187 | XK27_11280 | S | Psort location CytoplasmicMembrane, score | ||
DJNALGAK_01109 | 8.5e-161 | nhaC | C | Na H antiporter NhaC | ||
DJNALGAK_01110 | 1.5e-130 | dapF | 5.1.1.7 | E | Catalyzes the stereoinversion of LL-2,6- diaminoheptanedioate (L,L-DAP) to meso-diaminoheptanedioate (meso- DAP), a precursor of L-lysine and an essential component of the bacterial peptidoglycan | |
DJNALGAK_01111 | 5.8e-81 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
DJNALGAK_01115 | 3.7e-26 | radC | L | DNA repair protein | ||
DJNALGAK_01117 | 2.1e-11 | EGP | Transmembrane secretion effector | |||
DJNALGAK_01118 | 2.5e-192 | glmU | 2.3.1.157, 2.7.7.23 | M | Catalyzes the last two sequential reactions in the de novo biosynthetic pathway for UDP-N-acetylglucosamine (UDP- GlcNAc). The C-terminal domain catalyzes the transfer of acetyl group from acetyl coenzyme A to glucosamine-1-phosphate (GlcN-1-P) to produce N-acetylglucosamine-1-phosphate (GlcNAc-1-P), which is converted into UDP-GlcNAc by the transfer of uridine 5- monophosphate (from uridine 5-triphosphate), a reaction catalyzed by the N-terminal domain | |
DJNALGAK_01119 | 6.3e-49 | S | Threonine/Serine exporter, ThrE | |||
DJNALGAK_01120 | 4.3e-82 | thrE | S | Putative threonine/serine exporter | ||
DJNALGAK_01121 | 0.0 | res | 2.1.1.72, 3.1.21.5 | L | Type III restriction enzyme, res subunit | |
DJNALGAK_01122 | 1.1e-210 | K | DNA binding | |||
DJNALGAK_01123 | 5.4e-52 | L | Psort location Cytoplasmic, score | |||
DJNALGAK_01124 | 3.3e-39 | KLT | serine threonine protein kinase | |||
DJNALGAK_01125 | 1.4e-28 | dltC | 6.1.1.13 | J | Carrier protein involved in the D-alanylation of lipoteichoic acid (LTA). The loading of thioester-linked D-alanine onto DltC is catalyzed by D-alanine--D-alanyl carrier protein ligase DltA. The DltC-carried D-alanyl group is further transferred to cell membrane phosphatidylglycerol (PG) by forming an ester bond, probably catalyzed by DltD. D-alanylation of LTA plays an important role in modulating the properties of the cell wall in Gram-positive bacteria, influencing the net charge of the cell wall | |
DJNALGAK_01126 | 2.5e-120 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
DJNALGAK_01129 | 2.7e-21 | S | Bacteriophage holin of superfamily 6 (Holin_LLH) | |||
DJNALGAK_01130 | 4.8e-115 | S | N-acetylmuramoyl-L-alanine amidase activity | |||
DJNALGAK_01131 | 2e-204 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
DJNALGAK_01132 | 4.3e-109 | K | Primase C terminal 1 (PriCT-1) | |||
DJNALGAK_01133 | 1.1e-15 | S | Pfam:DUF955 | |||
DJNALGAK_01134 | 2.9e-23 | 3.4.21.88 | K | Helix-turn-helix domain | ||
DJNALGAK_01135 | 6.1e-70 | 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 | ||
DJNALGAK_01136 | 1.3e-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 | ||
DJNALGAK_01137 | 0.0 | fusA | J | Catalyzes the GTP-dependent ribosomal translocation step during translation elongation. During this step, the ribosome changes from the pre-translocational (PRE) to the post- translocational (POST) state as the newly formed A-site-bound peptidyl-tRNA and P-site-bound deacylated tRNA move to the P and E sites, respectively. Catalyzes the coordinated movement of the two tRNA molecules, the mRNA and conformational changes in the ribosome | ||
DJNALGAK_01138 | 9.4e-84 | cobB | K | NAD-dependent protein deacetylase which modulates the activities of several enzymes which are inactive in their acetylated form | ||
DJNALGAK_01139 | 3.4e-89 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
DJNALGAK_01140 | 1.1e-99 | clpP | 3.4.21.92 | O | Cleaves peptides in various proteins in a process that requires ATP hydrolysis. Has a chymotrypsin-like activity. Plays a major role in the degradation of misfolded proteins | |
DJNALGAK_01141 | 1.1e-96 | whiA | K | May be required for sporulation | ||
DJNALGAK_01142 | 3.9e-207 | nanT | E | Belongs to the sodium solute symporter (SSF) (TC 2.A.21) family | ||
DJNALGAK_01143 | 6.1e-103 | V | domain protein | |||
DJNALGAK_01144 | 4e-16 | |||||
DJNALGAK_01146 | 7.6e-210 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
DJNALGAK_01147 | 6.7e-47 | hmpT | S | ECF-type riboflavin transporter, S component | ||
DJNALGAK_01148 | 6.6e-71 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
DJNALGAK_01149 | 8e-61 | |||||
DJNALGAK_01150 | 1.4e-40 | rpmE2 | J | Ribosomal protein L31 | ||
DJNALGAK_01151 | 4.1e-189 | rho | K | Facilitates transcription termination by a mechanism that involves Rho binding to the nascent RNA, activation of Rho's RNA-dependent ATPase activity, and release of the mRNA from the DNA template | ||
DJNALGAK_01152 | 1.6e-201 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
DJNALGAK_01154 | 2.3e-54 | ypuA | S | Protein of unknown function (DUF1002) | ||
DJNALGAK_01155 | 4.7e-66 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
DJNALGAK_01156 | 4.9e-96 | gntR1 | K | UbiC transcription regulator-associated domain protein | ||
DJNALGAK_01157 | 4.6e-90 | proC | 1.5.1.2 | E | Catalyzes the reduction of 1-pyrroline-5-carboxylate (PCA) to L-proline | |
DJNALGAK_01159 | 1.1e-07 | |||||
DJNALGAK_01160 | 2.4e-27 | S | Calcineurin-like phosphoesterase | |||
DJNALGAK_01161 | 7.1e-12 | N | Bacterial Ig-like domain 2 | |||
DJNALGAK_01166 | 4.8e-12 | dnaB | L | replication initiation and membrane attachment | ||
DJNALGAK_01169 | 2.4e-28 | D | COG1674 DNA segregation ATPase FtsK SpoIIIE and related proteins | |||
DJNALGAK_01172 | 3.3e-79 | L | Replication protein | |||
DJNALGAK_01173 | 1.1e-115 | yqfL | 2.7.11.33, 2.7.4.28 | F | Bifunctional serine threonine kinase and phosphorylase involved in the regulation of the pyruvate, phosphate dikinase (PPDK) by catalyzing its phosphorylation dephosphorylation | |
DJNALGAK_01180 | 1e-197 | 2.1.1.72 | V | site-specific DNA-methyltransferase (adenine-specific) activity | ||
DJNALGAK_01181 | 1.8e-27 | rsmF | 2.1.1.176, 2.1.1.178 | J | NOL1 NOP2 sun family protein | |
DJNALGAK_01182 | 1.1e-41 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
DJNALGAK_01183 | 0.0 | S | Bacterial membrane protein YfhO | |||
DJNALGAK_01184 | 3.3e-61 | pat | 2.3.1.183 | M | Acetyltransferase (GNAT) domain | |
DJNALGAK_01185 | 1.9e-114 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
DJNALGAK_01186 | 2.9e-11 | 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 | ||
DJNALGAK_01187 | 2.2e-204 | G | PTS system Galactitol-specific IIC component | |||
DJNALGAK_01188 | 2e-93 | M | Exporter of polyketide antibiotics | |||
DJNALGAK_01189 | 9.5e-48 | M | Exporter of polyketide antibiotics | |||
DJNALGAK_01190 | 1.2e-46 | comFC | S | Competence protein | ||
DJNALGAK_01191 | 5e-127 | comFA | L | Helicase C-terminal domain protein | ||
DJNALGAK_01192 | 1.1e-161 | mgs | 2.4.1.337 | GT4 | M | Glycosyltransferase, group 1 family protein |
DJNALGAK_01193 | 4.5e-179 | cfa | 2.1.1.317, 2.1.1.79 | M | cyclopropane-fatty-acyl-phospholipid synthase | |
DJNALGAK_01194 | 3.9e-30 | S | Enterocin A Immunity | |||
DJNALGAK_01195 | 5.8e-223 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
DJNALGAK_01196 | 4.3e-19 | HA62_12640 | S | GCN5-related N-acetyl-transferase | ||
DJNALGAK_01197 | 2.5e-136 | pfoS | S | Phosphotransferase system, EIIC | ||
DJNALGAK_01198 | 6.9e-153 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
DJNALGAK_01199 | 9.7e-24 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
DJNALGAK_01200 | 8e-188 | cycA | E | Amino acid permease | ||
DJNALGAK_01201 | 6.1e-163 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
DJNALGAK_01203 | 4.1e-11 | |||||
DJNALGAK_01204 | 1.2e-261 | U | COG3505 Type IV secretory pathway, VirD4 components | |||
DJNALGAK_01205 | 5.4e-44 | MA20_27270 | S | mazG nucleotide pyrophosphohydrolase | ||
DJNALGAK_01206 | 3.4e-73 | usp6 | T | universal stress protein | ||
DJNALGAK_01207 | 3.8e-54 | tag | 3.2.2.20 | L | glycosylase | |
DJNALGAK_01208 | 1.4e-45 | yqhL | P | Rhodanese-like protein | ||
DJNALGAK_01209 | 4.7e-158 | glk | 2.7.1.2 | G | Glucokinase | |
DJNALGAK_01210 | 1.5e-25 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
DJNALGAK_01211 | 2.8e-52 | yutD | S | Protein of unknown function (DUF1027) | ||
DJNALGAK_01212 | 2.9e-113 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
DJNALGAK_01213 | 1.9e-117 | ldhA | 1.1.1.28 | CH | D-isomer specific 2-hydroxyacid dehydrogenase, catalytic domain | |
DJNALGAK_01214 | 7.2e-52 | cadA | P | P-type ATPase | ||
DJNALGAK_01215 | 1.8e-254 | E | Amino acid permease | |||
DJNALGAK_01216 | 3.4e-41 | S | Protein of unknown function (DUF1211) | |||
DJNALGAK_01217 | 7.3e-105 | |||||
DJNALGAK_01220 | 4.3e-101 | sip | L | Belongs to the 'phage' integrase family | ||
DJNALGAK_01221 | 1.7e-221 | mntH | P | H( )-stimulated, divalent metal cation uptake system | ||
DJNALGAK_01222 | 4.9e-60 | ypbB | 5.1.3.1 | S | Helix-turn-helix domain | |
DJNALGAK_01223 | 5e-127 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
DJNALGAK_01224 | 3.1e-240 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
DJNALGAK_01229 | 5.5e-57 | 1.1.1.1 | C | Zinc-binding dehydrogenase | ||
DJNALGAK_01231 | 1.2e-159 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
DJNALGAK_01232 | 1.9e-32 | purL | 6.3.5.3 | F | Part of the phosphoribosylformylglycinamidine synthase complex involved in the purines biosynthetic pathway. Catalyzes the ATP-dependent conversion of formylglycinamide ribonucleotide (FGAR) and glutamine to yield formylglycinamidine ribonucleotide (FGAM) and glutamate. The FGAM synthase complex is composed of three subunits. PurQ produces an ammonia molecule by converting glutamine to glutamate. PurL transfers the ammonia molecule to FGAR to form FGAM in an ATP-dependent manner. PurS interacts with PurQ and PurL and is thought to assist in the transfer of the ammonia molecule from PurQ to PurL | |
DJNALGAK_01233 | 5.5e-227 | purF | 2.4.2.14 | F | Catalyzes the formation of phosphoribosylamine from phosphoribosylpyrophosphate (PRPP) and glutamine | |
DJNALGAK_01234 | 5.1e-68 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
DJNALGAK_01235 | 3.9e-68 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
DJNALGAK_01236 | 5.1e-81 | XK27_07525 | 3.6.1.55 | F | Hydrolase, nudix family | |
DJNALGAK_01238 | 1.7e-182 | cycA | E | Amino acid permease | ||
DJNALGAK_01239 | 0.0 | gidA | D | NAD-binding protein involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA-cmnm(5)s(2)U34 | ||
DJNALGAK_01240 | 1.4e-224 | mnmE | S | Exhibits a very high intrinsic GTPase hydrolysis rate. Involved in the addition of a carboxymethylaminomethyl (cmnm) group at the wobble position (U34) of certain tRNAs, forming tRNA- cmnm(5)s(2)U34 | ||
DJNALGAK_01241 | 4.1e-54 | 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 | ||
DJNALGAK_01242 | 7.4e-67 | M | ErfK YbiS YcfS YnhG | |||
DJNALGAK_01243 | 1e-107 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
DJNALGAK_01244 | 4.3e-113 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
DJNALGAK_01245 | 7.8e-132 | ABC-SBP | S | ABC transporter | ||
DJNALGAK_01246 | 1.1e-158 | potD | P | ABC transporter | ||
DJNALGAK_01247 | 1.3e-103 | potC | U | Binding-protein-dependent transport system inner membrane component | ||
DJNALGAK_01248 | 9.5e-120 | potB | P | ABC transporter permease | ||
DJNALGAK_01249 | 8.2e-167 | 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 | |
DJNALGAK_01250 | 7.4e-100 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
DJNALGAK_01251 | 1.6e-260 | glpD | 1.1.3.21, 1.1.5.3 | C | C-terminal domain of alpha-glycerophosphate oxidase | |
DJNALGAK_01252 | 1.5e-235 | glpK | 2.7.1.30 | F | Key enzyme in the regulation of glycerol uptake and metabolism. Catalyzes the phosphorylation of glycerol to yield sn- glycerol 3-phosphate | |
DJNALGAK_01253 | 3.9e-13 | S | Enterocin A Immunity | |||
DJNALGAK_01254 | 2.2e-16 | pspC | KT | PspC domain | ||
DJNALGAK_01255 | 7e-200 | L | transposition, DNA-mediated | |||
DJNALGAK_01256 | 9.4e-94 | cca | 2.7.7.19, 2.7.7.72 | J | Aminoglycoside-2''-adenylyltransferase | |
DJNALGAK_01257 | 7.2e-49 | L | PFAM Integrase catalytic region | |||
DJNALGAK_01258 | 2.8e-28 | L | HTH-like domain | |||
DJNALGAK_01259 | 4.5e-30 | L | Helix-turn-helix domain | |||
DJNALGAK_01260 | 2.9e-43 | yjeM | E | Amino Acid | ||
DJNALGAK_01261 | 3e-17 | L | hmm pf00665 | |||
DJNALGAK_01262 | 1.4e-51 | 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 | |
DJNALGAK_01263 | 2.4e-164 | serA | 1.1.1.399, 1.1.1.95 | EH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
DJNALGAK_01264 | 4.1e-75 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
DJNALGAK_01265 | 4e-25 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJNALGAK_01266 | 1.7e-109 | aatB | ET | ABC transporter substrate-binding protein | ||
DJNALGAK_01267 | 9.8e-100 | D | Alpha beta | |||
DJNALGAK_01268 | 5.7e-85 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
DJNALGAK_01270 | 1.8e-116 | degV | S | EDD domain protein, DegV family | ||
DJNALGAK_01271 | 8.1e-122 | pbuO_1 | S | Permease family | ||
DJNALGAK_01273 | 3.8e-23 | secA2 | 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 | ||
DJNALGAK_01274 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
DJNALGAK_01275 | 6.4e-110 | 3.1.4.46 | C | phosphodiesterase | ||
DJNALGAK_01276 | 4.5e-126 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily | |
DJNALGAK_01277 | 4.7e-102 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
DJNALGAK_01278 | 2.8e-82 | noc | K | Belongs to the ParB family | ||
DJNALGAK_01279 | 6.5e-118 | soj | D | Sporulation initiation inhibitor | ||
DJNALGAK_01280 | 4.1e-108 | spo0J | K | Belongs to the ParB family | ||
DJNALGAK_01281 | 9e-24 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
DJNALGAK_01282 | 2.4e-190 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
DJNALGAK_01283 | 1.9e-53 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
DJNALGAK_01284 | 1.4e-94 | S | Bacterial membrane protein, YfhO | |||
DJNALGAK_01285 | 1.4e-49 | I | Alpha/beta hydrolase family | |||
DJNALGAK_01286 | 7.3e-14 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
DJNALGAK_01287 | 1.5e-38 | |||||
DJNALGAK_01288 | 2.7e-104 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
DJNALGAK_01289 | 1e-98 | fhuC | P | ABC transporter | ||
DJNALGAK_01290 | 2.1e-103 | znuB | U | ABC 3 transport family | ||
DJNALGAK_01291 | 1.5e-55 | S | ECF transporter, substrate-specific component | |||
DJNALGAK_01292 | 4.7e-103 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
DJNALGAK_01293 | 1.9e-88 | S | NADPH-dependent FMN reductase | |||
DJNALGAK_01294 | 1.2e-27 | K | helix_turn_helix, mercury resistance | |||
DJNALGAK_01295 | 1.2e-67 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
DJNALGAK_01298 | 2e-208 | yfnA | E | Amino Acid | ||
DJNALGAK_01300 | 1.3e-139 | fmt | 2.1.2.9 | J | Attaches a formyl group to the free amino group of methionyl-tRNA(fMet). The formyl group appears to play a dual role in the initiator identity of N-formylmethionyl-tRNA by promoting its recognition by IF2 and preventing the misappropriation of this tRNA by the elongation apparatus | |
DJNALGAK_01301 | 4.2e-21 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
DJNALGAK_01302 | 1.6e-38 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
DJNALGAK_01303 | 3.1e-40 | K | Transcriptional regulator | |||
DJNALGAK_01304 | 6.9e-80 | |||||
DJNALGAK_01305 | 1.8e-98 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
DJNALGAK_01306 | 1.7e-41 | pstA | P | Phosphate transport system permease protein PstA | ||
DJNALGAK_01307 | 1e-38 | 2.7.1.194, 2.7.1.200, 2.7.1.202 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
DJNALGAK_01308 | 9.5e-259 | treB | G | phosphotransferase system | ||
DJNALGAK_01309 | 4.6e-63 | 3.1.3.73 | G | phosphoglycerate mutase | ||
DJNALGAK_01310 | 2.4e-82 | pncA | Q | isochorismatase | ||
DJNALGAK_01311 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
DJNALGAK_01313 | 2.1e-73 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
DJNALGAK_01314 | 2.4e-31 | metI | U | ABC transporter permease | ||
DJNALGAK_01315 | 2.5e-128 | metQ | M | Belongs to the nlpA lipoprotein family | ||
DJNALGAK_01316 | 2.3e-34 | S | Protein of unknown function (DUF4256) | |||
DJNALGAK_01319 | 4.7e-178 | pdhA | 1.2.4.1, 1.2.4.4 | C | Dehydrogenase E1 component | |
DJNALGAK_01320 | 2.8e-166 | pdhB | 1.2.4.1 | C | Transketolase, C-terminal domain protein | |
DJNALGAK_01321 | 2.9e-179 | pdhC | 2.3.1.12 | C | Dihydrolipoamide acetyltransferase component of pyruvate dehydrogenase complex | |
DJNALGAK_01322 | 4e-230 | lpdA | 1.8.1.4 | C | Dehydrogenase | |
DJNALGAK_01323 | 7.3e-149 | lplA | 6.3.1.20 | H | Lipoate-protein ligase | |
DJNALGAK_01324 | 9.2e-56 | S | Protein of unknown function (DUF975) | |||
DJNALGAK_01325 | 1.1e-76 | E | GDSL-like Lipase/Acylhydrolase family | |||
DJNALGAK_01326 | 1.3e-74 | sdaAB | 4.3.1.17 | E | Serine dehydratase beta chain | |
DJNALGAK_01327 | 4.7e-112 | sdaAA | 4.3.1.17 | E | L-serine dehydratase, iron-sulfur-dependent, alpha subunit | |
DJNALGAK_01328 | 7.7e-41 | S | Iron-sulfur cluster assembly protein | |||
DJNALGAK_01329 | 3.4e-67 | S | Protein of unknown function (DUF1440) | |||
DJNALGAK_01330 | 9.1e-83 | mtnU | 3.5.1.3 | S | Carbon-nitrogen hydrolase | |
DJNALGAK_01331 | 4.5e-187 | mtnE | 2.6.1.83 | E | Aminotransferase | |
DJNALGAK_01332 | 1.1e-41 | gntR1 | K | Transcriptional regulator, GntR family | ||
DJNALGAK_01333 | 3e-95 | V | ABC transporter, ATP-binding protein | |||
DJNALGAK_01334 | 9.7e-08 | |||||
DJNALGAK_01335 | 1.1e-39 | ybjQ | S | Belongs to the UPF0145 family | ||
DJNALGAK_01336 | 7.7e-122 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
DJNALGAK_01337 | 1.5e-104 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
DJNALGAK_01338 | 4.5e-43 | gutM | K | Glucitol operon activator protein (GutM) | ||
DJNALGAK_01339 | 4.8e-83 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
DJNALGAK_01340 | 2.7e-135 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
DJNALGAK_01341 | 3.1e-36 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
DJNALGAK_01342 | 2.2e-64 | tal | 2.2.1.2 | G | Transaldolase/Fructose-6-phosphate aldolase | |
DJNALGAK_01343 | 8.8e-53 | L | Protein involved in initiation of plasmid replication | |||
DJNALGAK_01344 | 5.3e-18 | |||||
DJNALGAK_01347 | 4e-48 | L | Resolvase, N terminal domain | |||
DJNALGAK_01348 | 5.9e-50 | S | Filamentation induced by cAMP protein fic | |||
DJNALGAK_01349 | 2.3e-105 | K | Psort location CytoplasmicMembrane, score | |||
DJNALGAK_01350 | 2.6e-169 | bcrA | V | ABC transporter | ||
DJNALGAK_01351 | 1.7e-126 | S | ABC-2 family transporter protein | |||
DJNALGAK_01353 | 8.3e-25 | yqfZ | 3.2.1.17 | M | hydrolase, family 25 | |
DJNALGAK_01354 | 6.2e-87 | L | Replication initiation factor | |||
DJNALGAK_01355 | 3.1e-29 | L | Single-strand binding protein family | |||
DJNALGAK_01356 | 2.3e-55 | L | Phage integrase, N-terminal SAM-like domain | |||
DJNALGAK_01360 | 9e-76 | L | Lactococcus lactis RepB C-terminus | |||
DJNALGAK_01361 | 1.7e-142 | S | the current gene model (or a revised gene model) may contain a frame shift | |||
DJNALGAK_01362 | 2.2e-190 | yddH | M | NlpC p60 family protein | ||
DJNALGAK_01363 | 1.2e-59 | S | Conjugative transposon protein TcpC | |||
DJNALGAK_01364 | 9.8e-39 | S | Conjugative transposon protein TcpC | |||
DJNALGAK_01365 | 2.3e-163 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
DJNALGAK_01366 | 4.5e-179 | galK | 2.7.1.6 | F | Catalyzes the transfer of the gamma-phosphate of ATP to D-galactose to form alpha-D-galactose-1-phosphate (Gal-1-P) | |
DJNALGAK_01367 | 5.9e-111 | galR | K | Transcriptional regulator | ||
DJNALGAK_01368 | 9.6e-251 | guaB | 1.1.1.205 | F | Catalyzes the irreversible NADPH-dependent deamination of GMP to IMP. It functions in the conversion of nucleobase, nucleoside and nucleotide derivatives of G to A nucleotides, and in maintaining the intracellular balance of A and G nucleotides | |
DJNALGAK_01369 | 0.0 | L | Helicase C-terminal domain protein | |||
DJNALGAK_01370 | 6e-79 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
DJNALGAK_01371 | 2.1e-180 | yhdP | S | Transporter associated domain | ||
DJNALGAK_01372 | 6.8e-69 | rny | D | Peptidase family M23 | ||
DJNALGAK_01374 | 2.3e-138 | tetA | EGP | Major facilitator Superfamily | ||
DJNALGAK_01375 | 1.8e-32 | yvdC | S | MazG nucleotide pyrophosphohydrolase domain | ||
DJNALGAK_01376 | 3.6e-213 | yjeM | E | Amino Acid | ||
DJNALGAK_01377 | 1.9e-15 | mleP | S | Sodium Bile acid symporter family | ||
DJNALGAK_01378 | 3.2e-64 | S | ECF transporter, substrate-specific component | |||
DJNALGAK_01379 | 6.3e-61 | acmC | 3.2.1.96 | NU | mannosyl-glycoprotein | |
DJNALGAK_01380 | 3.3e-74 | 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 | |
DJNALGAK_01381 | 1.7e-193 | pbuX | F | xanthine permease | ||
DJNALGAK_01382 | 3.1e-34 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
DJNALGAK_01383 | 7.3e-41 | M1-874 | K | Domain of unknown function (DUF1836) | ||
DJNALGAK_01384 | 9.4e-84 | S | membrane | |||
DJNALGAK_01385 | 1.1e-79 | S | VIT family | |||
DJNALGAK_01386 | 3.1e-244 | lutB | C | 4Fe-4S dicluster domain | ||
DJNALGAK_01387 | 3.2e-66 | yrjD | S | LUD domain | ||
DJNALGAK_01388 | 8e-147 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
DJNALGAK_01389 | 8e-10 | |||||
DJNALGAK_01390 | 3.8e-27 | ylqC | S | Belongs to the UPF0109 family | ||
DJNALGAK_01391 | 3.6e-42 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
DJNALGAK_01392 | 5e-204 | ffh | 3.6.5.4 | U | Involved in targeting and insertion of nascent membrane proteins into the cytoplasmic membrane. Binds to the hydrophobic signal sequence of the ribosome-nascent chain (RNC) as it emerges from the ribosomes. The SRP-RNC complex is then targeted to the cytoplasmic membrane where it interacts with the SRP receptor FtsY | |
DJNALGAK_01393 | 1.2e-39 | ylxM | S | Might take part in the signal recognition particle (SRP) pathway. This is inferred from the conservation of its genetic proximity to ftsY ffh. May be a regulatory protein | ||
DJNALGAK_01394 | 7.2e-146 | 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) | ||
DJNALGAK_01395 | 1.7e-128 | smc | D | Required for chromosome condensation and partitioning | ||
DJNALGAK_01396 | 4.8e-115 | gtf1 | 2.4.1.52 | GT4 | M | An N-acetylglucosaminyl transferase that is part of the accessory SecA2 SecY2 system specifically required to export serine-rich repeat cell wall proteins usually encoded upstream in the same operon |
DJNALGAK_01397 | 9e-34 | yxaB | 2.4.1.166 | GT2 | M | Glycosyltransferase like family 2 |
DJNALGAK_01398 | 9.6e-109 | 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 | ||
DJNALGAK_01400 | 1.6e-138 | G | Xylose isomerase-like TIM barrel | |||
DJNALGAK_01401 | 4.6e-117 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
DJNALGAK_01402 | 3e-216 | 1.3.5.4 | C | FAD binding domain | ||
DJNALGAK_01403 | 8.4e-138 | aroE | 1.1.1.25, 1.1.1.282, 1.3.5.4 | 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) | |
DJNALGAK_01404 | 4.5e-71 | aroD | 1.1.1.25, 4.2.1.10 | E | Involved in the third step of the chorismate pathway, which leads to the biosynthesis of aromatic amino acids. Catalyzes the cis-dehydration of 3-dehydroquinate (DHQ) and introduces the first double bond of the aromatic ring to yield 3- dehydroshikimate | |
DJNALGAK_01405 | 2.4e-142 | xerS | L | Phage integrase family | ||
DJNALGAK_01407 | 2.4e-185 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
DJNALGAK_01408 | 2.8e-65 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
DJNALGAK_01409 | 3.8e-262 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
DJNALGAK_01410 | 2.2e-107 | terC | P | Integral membrane protein TerC family | ||
DJNALGAK_01411 | 1.6e-38 | K | Transcriptional regulator | |||
DJNALGAK_01412 | 9.8e-96 | tcyA | ET | Belongs to the bacterial solute-binding protein 3 family | ||
DJNALGAK_01413 | 1.6e-100 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJNALGAK_01414 | 4.5e-102 | tcyB | E | ABC transporter | ||
DJNALGAK_01416 | 3.7e-13 | ponA | V | the current gene model (or a revised gene model) may contain a frame shift | ||
DJNALGAK_01417 | 2.3e-187 | nox | S | Pyridine nucleotide-disulphide oxidoreductase, dimerisation domain | ||
DJNALGAK_01418 | 1.8e-244 | 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 | |
DJNALGAK_01419 | 1e-281 | scrA | 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
DJNALGAK_01420 | 2.9e-22 | 3.1.21.3 | V | Type I restriction modification DNA specificity domain | ||
DJNALGAK_01421 | 0.0 | metG | 6.1.1.10, 6.1.1.20 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
DJNALGAK_01422 | 5.6e-127 | |||||
DJNALGAK_01423 | 5.1e-152 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
DJNALGAK_01424 | 1.6e-42 | VPA1512 | ET | Bacterial extracellular solute-binding proteins, family 3 | ||
DJNALGAK_01425 | 7.5e-07 | K | Bacterial regulatory proteins, tetR family | |||
DJNALGAK_01426 | 9.3e-37 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
DJNALGAK_01427 | 3.4e-205 | yflS | P | Sodium:sulfate symporter transmembrane region | ||
DJNALGAK_01428 | 1.4e-198 | frdC | 1.3.5.4 | C | FAD binding domain | |
DJNALGAK_01429 | 1.9e-237 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
DJNALGAK_01430 | 6.5e-81 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
DJNALGAK_01431 | 1.7e-73 | epsB | M | biosynthesis protein | ||
DJNALGAK_01433 | 5.5e-115 | cps2J | S | Polysaccharide biosynthesis protein | ||
DJNALGAK_01435 | 0.0 | cadA | 3.6.3.3, 3.6.3.5 | P | E1-E2 ATPase | |
DJNALGAK_01436 | 9.1e-71 | S | Protein of unknown function (DUF554) | |||
DJNALGAK_01437 | 1e-39 | yaeR | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | ||
DJNALGAK_01438 | 1.9e-32 | merR | K | MerR HTH family regulatory protein | ||
DJNALGAK_01439 | 2.7e-197 | lmrB | EGP | Major facilitator Superfamily | ||
DJNALGAK_01440 | 7e-34 | S | Domain of unknown function (DUF4811) | |||
DJNALGAK_01441 | 4.3e-41 | S | CAAX protease self-immunity | |||
DJNALGAK_01442 | 1.3e-60 | yceE | S | haloacid dehalogenase-like hydrolase | ||
DJNALGAK_01443 | 7.6e-74 | glcR | K | DeoR C terminal sensor domain | ||
DJNALGAK_01444 | 1.2e-07 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
DJNALGAK_01445 | 5e-100 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
DJNALGAK_01446 | 4.5e-97 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
DJNALGAK_01447 | 1.8e-15 | 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 | ||
DJNALGAK_01448 | 2.4e-39 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
DJNALGAK_01449 | 4.1e-58 | 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 | ||
DJNALGAK_01450 | 6.3e-266 | 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 | |
DJNALGAK_01451 | 5.1e-141 | 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 | ||
DJNALGAK_01452 | 1.7e-236 | 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 | |
DJNALGAK_01453 | 3e-48 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
DJNALGAK_01454 | 2.1e-102 | ppx | 3.6.1.11, 3.6.1.40 | FP | exopolyphosphatase | |
DJNALGAK_01455 | 8.8e-171 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
DJNALGAK_01456 | 9.3e-128 | P | Belongs to the cation diffusion facilitator (CDF) transporter (TC 2.A.4) family | |||
DJNALGAK_01457 | 2.2e-270 | helD | 3.6.4.12 | L | DNA helicase | |
DJNALGAK_01459 | 1.3e-114 | htpX | O | Belongs to the peptidase M48B family | ||
DJNALGAK_01460 | 8.7e-72 | lemA | S | LemA family | ||
DJNALGAK_01461 | 1e-64 | napA | P | Belongs to the monovalent cation proton antiporter 2 (CPA2) transporter (TC 2.A.37) family | ||
DJNALGAK_01462 | 9e-29 | yitW | S | Iron-sulfur cluster assembly protein | ||
DJNALGAK_01463 | 2.4e-176 | rnfC | C | RnfC Barrel sandwich hybrid domain | ||
DJNALGAK_01464 | 2.7e-100 | selD | 2.7.9.3 | E | Synthesizes selenophosphate from selenide and ATP | |
DJNALGAK_01465 | 1.3e-24 | |||||
DJNALGAK_01466 | 1.1e-25 | |||||
DJNALGAK_01467 | 2.2e-201 | gshF | 6.3.2.2 | H | Belongs to the glutamate--cysteine ligase type 1 family | |
DJNALGAK_01468 | 5.7e-108 | puuD | S | peptidase C26 | ||
DJNALGAK_01469 | 6.7e-137 | mvaK2 | 2.7.1.36, 2.7.1.43, 2.7.4.2 | I | phosphomevalonate kinase | |
DJNALGAK_01470 | 1.7e-118 | mvaD | 4.1.1.33 | I | diphosphomevalonate decarboxylase | |
DJNALGAK_01471 | 9.5e-95 | mvk | 1.1.1.88, 2.3.3.10, 2.7.1.36 | I | mevalonate kinase | |
DJNALGAK_01472 | 4.3e-89 | thrB | 2.7.1.39 | F | Catalyzes the ATP-dependent phosphorylation of L- homoserine to L-homoserine phosphate | |
DJNALGAK_01473 | 8.8e-168 | hom | 1.1.1.3, 2.7.2.4 | E | homoserine dehydrogenase | |
DJNALGAK_01474 | 3.4e-127 | apbE | 2.7.1.180 | H | Flavin transferase that catalyzes the transfer of the FMN moiety of FAD and its covalent binding to the hydroxyl group of a threonine residue in a target flavoprotein | |
DJNALGAK_01475 | 8.3e-178 | thrC | 4.2.3.1 | E | Threonine synthase | |
DJNALGAK_01476 | 8.2e-75 | 3.2.1.17 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | ||
DJNALGAK_01477 | 1.4e-61 | S | Psort location CytoplasmicMembrane, score | |||
DJNALGAK_01478 | 8.9e-58 | waaB | GT4 | M | Glycosyl transferases group 1 | |
DJNALGAK_01479 | 3.2e-74 | ecfT | U | 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 | ||
DJNALGAK_01480 | 6.5e-126 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
DJNALGAK_01481 | 5.5e-77 | 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 | ||
DJNALGAK_01482 | 1.1e-60 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
DJNALGAK_01483 | 1.8e-30 | |||||
DJNALGAK_01484 | 1.2e-245 | yjbQ | P | TrkA C-terminal domain protein | ||
DJNALGAK_01485 | 7.6e-236 | asnS | 6.1.1.22 | J | Asparaginyl-tRNA synthetase | |
DJNALGAK_01486 | 3.1e-143 | aspB | 2.6.1.1, 2.6.1.14 | E | Aminotransferase | |
DJNALGAK_01487 | 3.1e-36 | ypmB | S | Protein conserved in bacteria | ||
DJNALGAK_01488 | 2.6e-89 | dinG | 2.7.7.7, 3.6.4.12 | L | helicase involved in DNA repair and perhaps also replication | |
DJNALGAK_01489 | 2.6e-70 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
DJNALGAK_01490 | 2.3e-181 | pepS | E | Thermophilic metalloprotease (M29) | ||
DJNALGAK_01491 | 3.1e-131 | S | Putative peptidoglycan binding domain | |||
DJNALGAK_01492 | 2.1e-24 | relB | L | RelB antitoxin | ||
DJNALGAK_01493 | 1.4e-61 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
DJNALGAK_01494 | 2.3e-140 | gldA | 1.1.1.6 | C | Iron-containing alcohol dehydrogenase | |
DJNALGAK_01495 | 1.7e-178 | metC | 4.4.1.1, 4.4.1.2, 4.4.1.8 | E | cystathionine | |
DJNALGAK_01496 | 8.6e-109 | mccA | 2.5.1.134, 2.5.1.47 | E | Belongs to the cysteine synthase cystathionine beta- synthase family | |
DJNALGAK_01497 | 6e-223 | pepF | E | Oligopeptidase F | ||
DJNALGAK_01498 | 3.7e-96 | yicL | EG | EamA-like transporter family | ||
DJNALGAK_01499 | 3e-07 | sbcC | L | Putative exonuclease SbcCD, C subunit | ||
DJNALGAK_01500 | 4.8e-78 | rsmE | 2.1.1.193 | J | Specifically methylates the N3 position of the uracil ring of uridine 1498 (m3U1498) in 16S rRNA. Acts on the fully assembled 30S ribosomal subunit | |
DJNALGAK_01501 | 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 | |
DJNALGAK_01502 | 2.3e-54 | 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 | ||
DJNALGAK_01503 | 5.1e-57 | 3.1.3.18 | J | HAD-hyrolase-like | ||
DJNALGAK_01504 | 3.4e-42 | lspA | 3.4.23.36 | MU | This protein specifically catalyzes the removal of signal peptides from prolipoproteins | |
DJNALGAK_01505 | 1.4e-127 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
DJNALGAK_01506 | 1.3e-75 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
DJNALGAK_01507 | 3.5e-204 | pyrP | F | Permease | ||
DJNALGAK_01509 | 2.2e-66 | sip | L | Belongs to the 'phage' integrase family | ||
DJNALGAK_01510 | 3e-14 | S | Acyltransferase family | |||
DJNALGAK_01511 | 7.5e-195 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
DJNALGAK_01512 | 2.3e-122 | K | LysR substrate binding domain | |||
DJNALGAK_01514 | 2.2e-20 | |||||
DJNALGAK_01515 | 3.1e-202 | oppA | E | ABC transporter, substratebinding protein | ||
DJNALGAK_01516 | 7.9e-142 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
DJNALGAK_01517 | 3.7e-169 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
DJNALGAK_01518 | 1.3e-180 | oppD | P | Belongs to the ABC transporter superfamily | ||
DJNALGAK_01519 | 1.4e-154 | oppF | P | Belongs to the ABC transporter superfamily | ||
DJNALGAK_01520 | 4.5e-60 | ps308 | K | AntA/AntB antirepressor | ||
DJNALGAK_01526 | 3.6e-54 | S | Putative HNHc nuclease | |||
DJNALGAK_01527 | 5.2e-283 | M | Phage tail tape measure protein TP901 | |||
DJNALGAK_01528 | 5.7e-47 | S | Plasmid replication protein | |||
DJNALGAK_01530 | 9.7e-15 | K | Cro/C1-type HTH DNA-binding domain | |||
DJNALGAK_01533 | 2e-77 | S | Siphovirus Gp157 | |||
DJNALGAK_01534 | 5.4e-240 | res | L | Helicase C-terminal domain protein | ||
DJNALGAK_01535 | 5.6e-117 | L | AAA domain | |||
DJNALGAK_01536 | 8.1e-85 | |||||
DJNALGAK_01537 | 2.8e-140 | S | Bifunctional DNA primase/polymerase, N-terminal | |||
DJNALGAK_01538 | 3e-229 | S | Virulence-associated protein E | |||
DJNALGAK_01539 | 1.2e-49 | S | VRR_NUC | |||
DJNALGAK_01543 | 1.4e-32 | arpU | S | Phage transcriptional regulator, ArpU family | ||
DJNALGAK_01544 | 1.4e-08 | T | SpoVT / AbrB like domain | |||
DJNALGAK_01545 | 6.3e-17 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
DJNALGAK_01548 | 5.4e-22 | |||||
DJNALGAK_01549 | 8.7e-26 | V | HNH nucleases | |||
DJNALGAK_01550 | 3.8e-14 | |||||
DJNALGAK_01551 | 6.2e-182 | S | Terminase | |||
DJNALGAK_01552 | 8.5e-82 | S | Phage portal protein | |||
DJNALGAK_01553 | 7.6e-55 | clpP | 3.4.21.92 | OU | Clp protease | |
DJNALGAK_01555 | 1.1e-154 | S | peptidoglycan catabolic process | |||
DJNALGAK_01556 | 8.7e-32 | S | phage tail | |||
DJNALGAK_01557 | 2e-60 | S | Prophage endopeptidase tail | |||
DJNALGAK_01559 | 9.2e-73 | S | Domain of unknown function (DUF2479) | |||
DJNALGAK_01563 | 6.2e-64 | srtA | 3.4.22.70 | M | sortase family | |
DJNALGAK_01564 | 0.0 | addA | 3.6.4.12 | L | ATP-dependent helicase nuclease subunit A | |
DJNALGAK_01565 | 0.0 | rexB | 3.1.21.3, 3.6.4.12 | L | The heterodimer acts as both an ATP-dependent DNA helicase and an ATP-dependent, dual-direction single-stranded exonuclease. Recognizes the chi site generating a DNA molecule suitable for the initiation of homologous recombination. This subunit has 5' - 3' nuclease activity | |
DJNALGAK_01566 | 1.1e-33 | |||||
DJNALGAK_01567 | 1.8e-141 | 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) | |
DJNALGAK_01568 | 1e-157 | proA | 1.2.1.41 | E | Catalyzes the NADPH-dependent reduction of L-glutamate 5-phosphate into L-glutamate 5-semialdehyde and phosphate. The product spontaneously undergoes cyclization to form 1-pyrroline-5- carboxylate | |
DJNALGAK_01569 | 6.6e-97 | proB | 2.7.2.11 | F | Catalyzes the transfer of a phosphate group to glutamate to form L-glutamate 5-phosphate | |
DJNALGAK_01570 | 4.5e-284 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
DJNALGAK_01571 | 1.7e-85 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
DJNALGAK_01572 | 7.5e-99 | rrmA | 2.1.1.187 | H | Methyltransferase | |
DJNALGAK_01573 | 4.3e-248 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
DJNALGAK_01574 | 3.6e-17 | yneR | ||||
DJNALGAK_01575 | 8.7e-231 | murE | 6.3.2.13, 6.3.2.7 | M | Catalyzes the addition of an amino acid to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanyl-D-glutamate (UMAG) in the biosynthesis of bacterial cell-wall peptidoglycan | |
DJNALGAK_01576 | 5.5e-223 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
DJNALGAK_01577 | 9.1e-106 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
DJNALGAK_01578 | 1.7e-152 | mdtG | EGP | Major facilitator Superfamily | ||
DJNALGAK_01579 | 5.9e-15 | K | regulatory protein TetR | |||
DJNALGAK_01580 | 4.8e-109 | glcU | U | sugar transport | ||
DJNALGAK_01581 | 1.6e-167 | yjjP | S | Putative threonine/serine exporter | ||
DJNALGAK_01582 | 1.5e-68 | 2.3.1.178 | J | Acetyltransferase (GNAT) domain | ||
DJNALGAK_01583 | 7.5e-08 | |||||
DJNALGAK_01584 | 7e-67 | D | nuclear chromosome segregation | |||
DJNALGAK_01585 | 0.0 | lepA | M | Required for accurate and efficient protein synthesis under certain stress conditions. May act as a fidelity factor of the translation reaction, by catalyzing a one-codon backward translocation of tRNAs on improperly translocated ribosomes. Back- translocation proceeds from a post-translocation (POST) complex to a pre-translocation (PRE) complex, thus giving elongation factor G a second chance to translocate the tRNAs correctly. Binds to ribosomes in a GTP-dependent manner | ||
DJNALGAK_01586 | 1.2e-160 | 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 | ||
DJNALGAK_01587 | 1.5e-274 | dnaK | O | Heat shock 70 kDa protein | ||
DJNALGAK_01588 | 4.2e-56 | grpE | O | Participates actively in the response to hyperosmotic and heat shock by preventing the aggregation of stress-denatured proteins, in association with DnaK and GrpE. It is the nucleotide exchange factor for DnaK and may function as a thermosensor. Unfolded proteins bind initially to DnaJ | ||
DJNALGAK_01589 | 1.4e-131 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
DJNALGAK_01590 | 1.7e-76 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
DJNALGAK_01591 | 3.9e-208 | V | site-specific DNA-methyltransferase (adenine-specific) activity | |||
DJNALGAK_01594 | 1.6e-25 | |||||
DJNALGAK_01595 | 9.7e-71 | |||||
DJNALGAK_01603 | 3.3e-289 | 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 | |
DJNALGAK_01604 | 9.9e-42 | 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 | ||
DJNALGAK_01605 | 7.1e-17 | ywiB | S | Domain of unknown function (DUF1934) | ||
DJNALGAK_01606 | 4.5e-109 | 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 | ||
DJNALGAK_01607 | 3.7e-48 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
DJNALGAK_01608 | 6.2e-166 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
DJNALGAK_01609 | 6.5e-79 | K | rpiR family | |||
DJNALGAK_01610 | 2.2e-53 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
DJNALGAK_01611 | 8.5e-147 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
DJNALGAK_01612 | 4.9e-21 | K | Acetyltransferase (GNAT) domain | |||
DJNALGAK_01613 | 6.4e-182 | steT | E | amino acid | ||
DJNALGAK_01614 | 9.6e-78 | glnP | P | ABC transporter permease | ||
DJNALGAK_01615 | 1.2e-85 | gluC | P | ABC transporter permease | ||
DJNALGAK_01616 | 1.1e-99 | glnH | ET | ABC transporter | ||
DJNALGAK_01617 | 3.3e-103 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
DJNALGAK_01618 | 1.7e-09 | |||||
DJNALGAK_01619 | 5e-98 | |||||
DJNALGAK_01620 | 3.1e-09 | 3.2.1.14 | GH18 | |||
DJNALGAK_01621 | 2.4e-53 | zur | P | Belongs to the Fur family | ||
DJNALGAK_01622 | 6e-123 | xerC | D | Belongs to the 'phage' integrase family. XerC subfamily | ||
DJNALGAK_01623 | 7e-79 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
DJNALGAK_01624 | 1.9e-216 | hslU | O | this subunit has chaperone activity. The binding of ATP and its subsequent hydrolysis by HslU are essential for unfolding of protein substrates subsequently hydrolyzed by HslV. HslU recognizes the N-terminal part of its protein substrates and unfolds these before they are guided to HslV for hydrolysis | ||
DJNALGAK_01625 | 1.6e-112 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
DJNALGAK_01626 | 4.2e-21 | cutC | P | Participates in the control of copper homeostasis | ||
DJNALGAK_01627 | 2.1e-153 | gltP | U | Belongs to the dicarboxylate amino acid cation symporter (DAACS) (TC 2.A.23) family | ||
DJNALGAK_01628 | 5.7e-64 | D | peptidase | |||
DJNALGAK_01629 | 5.6e-117 | S | Glycosyl transferase family 2 | |||
DJNALGAK_01630 | 5.6e-110 | glxR | 1.1.1.31, 1.1.1.60 | I | Dehydrogenase | |
DJNALGAK_01631 | 6.2e-35 | rpsR | J | Binds as a heterodimer with protein S6 to the central domain of the 16S rRNA, where it helps stabilize the platform of the 30S subunit | ||
DJNALGAK_01632 | 3.3e-63 | 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 | ||
DJNALGAK_01633 | 4.8e-45 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
DJNALGAK_01634 | 0.0 | gyrA | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
DJNALGAK_01635 | 0.0 | gyrB | 5.99.1.3 | L | A type II topoisomerase that negatively supercoils closed circular double-stranded (ds) DNA in an ATP-dependent manner to modulate DNA topology and maintain chromosomes in an underwound state. Negative supercoiling favors strand separation, and DNA replication, transcription, recombination and repair, all of which involve strand separation. Also able to catalyze the interconversion of other topological isomers of dsDNA rings, including catenanes and knotted rings. Type II topoisomerases break and join 2 DNA strands simultaneously in an ATP-dependent manner | |
DJNALGAK_01636 | 8.4e-154 | 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 | ||
DJNALGAK_01637 | 9e-20 | yaaA | S | S4 domain protein YaaA | ||
DJNALGAK_01638 | 8.6e-159 | 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 | |
DJNALGAK_01639 | 2.1e-204 | 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 | ||
DJNALGAK_01640 | 3.4e-14 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
DJNALGAK_01641 | 2.2e-49 | 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 | |
DJNALGAK_01642 | 4.1e-105 | 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 | ||
DJNALGAK_01643 | 2.9e-94 | L | Helicase C-terminal domain protein | |||
DJNALGAK_01644 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
DJNALGAK_01645 | 5.2e-54 | S | Membrane | |||
DJNALGAK_01646 | 5.9e-64 | K | helix_turn_helix, arabinose operon control protein | |||
DJNALGAK_01647 | 4.5e-67 | ybbL | S | ABC transporter | ||
DJNALGAK_01648 | 1.9e-101 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
DJNALGAK_01649 | 3e-41 | ytcD | K | HxlR-like helix-turn-helix | ||
DJNALGAK_01650 | 8.4e-119 | ytbE | S | reductase | ||
DJNALGAK_01651 | 2.3e-68 | E | Glyoxalase/Bleomycin resistance protein/Dioxygenase superfamily | |||
DJNALGAK_01653 | 7e-53 | hit | FG | histidine triad | ||
DJNALGAK_01654 | 9.8e-95 | ecsA | V | ABC transporter, ATP-binding protein | ||
DJNALGAK_01655 | 2.9e-72 | ecsB | U | ABC transporter | ||
DJNALGAK_01656 | 5.9e-98 | ytmP | 2.7.1.89 | M | Choline/ethanolamine kinase | |
DJNALGAK_01657 | 3.9e-100 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
DJNALGAK_01659 | 1e-09 | 3.1.3.48 | D | Lytic transglycosylase with a strong preference for naked glycan strands that lack stem peptides | ||
DJNALGAK_01663 | 1.2e-218 | yifK | E | Amino acid permease | ||
DJNALGAK_01664 | 1.1e-85 | 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 | ||
DJNALGAK_01665 | 5.1e-57 | ybjI | 3.1.3.102, 3.1.3.104, 3.1.3.23 | S | Sucrose-6F-phosphate phosphohydrolase | |
DJNALGAK_01666 | 5e-66 | pgm3 | G | phosphoglycerate mutase family | ||
DJNALGAK_01667 | 2.4e-144 | C | Aldo/keto reductase family | |||
DJNALGAK_01668 | 9.5e-251 | ctpA | 3.6.3.54 | P | P-type ATPase | |
DJNALGAK_01669 | 1.3e-20 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
DJNALGAK_01670 | 1.5e-43 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
DJNALGAK_01671 | 6.7e-151 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
DJNALGAK_01672 | 1.8e-181 | EG | GntP family permease | |||
DJNALGAK_01673 | 5e-116 | KT | Putative sugar diacid recognition | |||
DJNALGAK_01674 | 3.4e-60 | hchA | S | intracellular protease amidase | ||
DJNALGAK_01675 | 3.1e-134 | glpQ | 3.1.4.46 | C | Glycerophosphoryl diester phosphodiesterase family | |
DJNALGAK_01676 | 3.3e-98 | tnp2 | L | Transposase |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)