ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
---|---|---|---|---|---|---|
NEADBANL_00001 | 2e-293 | malQ | 2.4.1.25, 3.2.1.20, 3.2.1.41 | CBM48,GH13,GH31,GH77 | G | Belongs to the glycosyl hydrolase 13 family |
NEADBANL_00002 | 1e-56 | tnp2PF3 | L | Putative transposase of IS4/5 family (DUF4096) | ||
NEADBANL_00003 | 4.6e-82 | tnp2PF3 | L | Transposase DDE domain | ||
NEADBANL_00005 | 5.5e-101 | L | Helix-turn-helix domain of Hin and related proteins, a family of DNA-binding domains unique to bacteria and represented by the Hin protein of Salmonella. The basic HTH domain is a simple fold comprised of three core helices that form a right-handed | |||
NEADBANL_00006 | 3e-78 | |||||
NEADBANL_00007 | 2.9e-108 | |||||
NEADBANL_00008 | 4.1e-39 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
NEADBANL_00009 | 3.6e-29 | relB | L | RelB antitoxin | ||
NEADBANL_00010 | 4.3e-133 | D | CobQ CobB MinD ParA nucleotide binding domain protein | |||
NEADBANL_00012 | 3.3e-131 | repA | S | Replication initiator protein A | ||
NEADBANL_00013 | 1.6e-42 | relB | L | Addiction module antitoxin, RelB DinJ family | ||
NEADBANL_00014 | 8.3e-27 | |||||
NEADBANL_00015 | 1e-114 | S | protein conserved in bacteria | |||
NEADBANL_00016 | 8.9e-41 | |||||
NEADBANL_00017 | 3.2e-27 | |||||
NEADBANL_00018 | 0.0 | traA | L | MobA MobL family protein | ||
NEADBANL_00019 | 1.8e-268 | traI | 5.99.1.2 | L | This gene contains a nucleotide ambiguity which may be the result of a sequencing error | |
NEADBANL_00020 | 2e-32 | |||||
NEADBANL_00021 | 9.6e-195 | L | Psort location Cytoplasmic, score | |||
NEADBANL_00022 | 0.0 | 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 |
NEADBANL_00023 | 3.6e-197 | glgC | 2.7.7.27 | H | Catalyzes the synthesis of ADP-glucose, a sugar donor used in elongation reactions on alpha-glucans | |
NEADBANL_00024 | 1.4e-201 | glgD | 2.4.1.21, 2.7.7.27 | GT5 | G | Nucleotidyl transferase |
NEADBANL_00025 | 8.9e-286 | glgA | 2.4.1.21 | GT5 | F | Synthesizes alpha-1,4-glucan chains using ADP-glucose |
NEADBANL_00026 | 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 |
NEADBANL_00027 | 1.2e-70 | def2 | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins | |
NEADBANL_00028 | 7.9e-227 | N | Uncharacterized conserved protein (DUF2075) | |||
NEADBANL_00029 | 4.5e-203 | pbpX1 | V | Beta-lactamase | ||
NEADBANL_00030 | 0.0 | L | Helicase C-terminal domain protein | |||
NEADBANL_00031 | 1.5e-272 | E | amino acid | |||
NEADBANL_00032 | 2.2e-159 | xth | 3.1.11.2 | L | exodeoxyribonuclease III | |
NEADBANL_00035 | 1.2e-191 | ldhA | 1.1.1.28 | C | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NEADBANL_00036 | 1.3e-151 | 3.1.3.102, 3.1.3.104 | S | haloacid dehalogenase-like hydrolase | ||
NEADBANL_00037 | 0.0 | tetP | J | elongation factor G | ||
NEADBANL_00038 | 1.8e-118 | K | Helix-turn-helix domain | |||
NEADBANL_00039 | 3.6e-83 | |||||
NEADBANL_00041 | 2.7e-74 | M | LysM domain | |||
NEADBANL_00042 | 5.5e-87 | |||||
NEADBANL_00043 | 8.3e-136 | yjjG | 3.1.3.102, 3.1.3.104, 3.1.3.5, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
NEADBANL_00044 | 2.1e-177 | ABC-SBP | S | ABC transporter | ||
NEADBANL_00045 | 2.5e-121 | XK27_08840 | U | Belongs to the binding-protein-dependent transport system permease family | ||
NEADBANL_00046 | 8.1e-137 | XK27_08845 | S | ABC transporter, ATP-binding protein | ||
NEADBANL_00047 | 6.9e-167 | G | Major Facilitator | |||
NEADBANL_00048 | 3.3e-68 | G | Major Facilitator | |||
NEADBANL_00049 | 4.1e-18 | |||||
NEADBANL_00050 | 2e-103 | 3.1.1.5 | E | GDSL-like Lipase/Acylhydrolase | ||
NEADBANL_00051 | 6.4e-177 | K | AI-2E family transporter | |||
NEADBANL_00052 | 0.0 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_00053 | 0.0 | rtpR | 1.1.98.6, 1.17.4.1, 1.17.4.2 | F | ribonucleoside-triphosphate reductase activity | |
NEADBANL_00054 | 4.7e-43 | S | Domain of unknown function (DUF4430) | |||
NEADBANL_00055 | 2.7e-24 | S | Domain of unknown function (DUF4430) | |||
NEADBANL_00056 | 4.7e-54 | S | ECF transporter, substrate-specific component | |||
NEADBANL_00057 | 5.1e-80 | yvqK | 1.2.1.88, 1.5.5.2, 2.5.1.17 | S | cob(I)alamin adenosyltransferase | |
NEADBANL_00058 | 7.4e-146 | S | Putative ABC-transporter type IV | |||
NEADBANL_00059 | 6.5e-07 | S | LPXTG cell wall anchor motif | |||
NEADBANL_00060 | 1.6e-76 | ybaT | E | Amino acid permease | ||
NEADBANL_00062 | 1.4e-24 | WQ51_00220 | K | Helix-turn-helix XRE-family like proteins | ||
NEADBANL_00063 | 8.7e-66 | S | EamA-like transporter family | |||
NEADBANL_00064 | 2e-25 | I | bis(5'-adenosyl)-triphosphatase activity | |||
NEADBANL_00065 | 1.4e-65 | 3.6.1.17 | FG | bis(5'-adenosyl)-triphosphatase activity | ||
NEADBANL_00066 | 2.1e-75 | sufS | 2.8.1.7, 4.4.1.16 | E | PFAM aminotransferase class V | |
NEADBANL_00067 | 3.3e-99 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00068 | 8.8e-29 | |||||
NEADBANL_00071 | 9.8e-74 | L | An automated process has identified a potential problem with this gene model | |||
NEADBANL_00073 | 5.8e-121 | yhiD | S | MgtC family | ||
NEADBANL_00074 | 8.3e-232 | I | Protein of unknown function (DUF2974) | |||
NEADBANL_00075 | 2.4e-16 | |||||
NEADBANL_00077 | 8.7e-167 | scrK | 2.7.1.2, 2.7.1.4 | GK | ROK family | |
NEADBANL_00078 | 1.7e-165 | degV | S | DegV family | ||
NEADBANL_00079 | 6e-166 | phnD | P | ABC transporter, phosphonate, periplasmic substrate-binding protein | ||
NEADBANL_00080 | 6.7e-254 | dnaB | 3.6.4.12 | L | Participates in initiation and elongation during chromosome replication | |
NEADBANL_00081 | 5.7e-69 | rplI | J | Binds to the 23S rRNA | ||
NEADBANL_00082 | 0.0 | yybT | T | signaling protein consisting of a modified GGDEF domain and a DHH domain | ||
NEADBANL_00083 | 1.8e-201 | S | SLAP domain | |||
NEADBANL_00084 | 1.9e-170 | S | Bacteriocin helveticin-J | |||
NEADBANL_00085 | 3.2e-42 | |||||
NEADBANL_00086 | 6e-41 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
NEADBANL_00087 | 1.4e-91 | E | Zn peptidase | |||
NEADBANL_00088 | 1.2e-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 | ||
NEADBANL_00089 | 4.5e-78 | 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 | ||
NEADBANL_00090 | 9.4e-49 | rpsF | J | Binds together with S18 to 16S ribosomal RNA | ||
NEADBANL_00091 | 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 | |
NEADBANL_00092 | 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 | |
NEADBANL_00093 | 2.4e-209 | 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 | ||
NEADBANL_00094 | 2.6e-35 | yaaA | S | S4 domain protein YaaA | ||
NEADBANL_00095 | 9.1e-185 | 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 | |
NEADBANL_00096 | 5.5e-245 | 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 | ||
NEADBANL_00097 | 1.1e-15 | rpmH | J | Belongs to the bacterial ribosomal protein bL34 family | ||
NEADBANL_00098 | 2.7e-61 | 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 | |
NEADBANL_00099 | 8.4e-146 | 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 | ||
NEADBANL_00100 | 1.4e-251 | 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 | ||
NEADBANL_00101 | 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 | ||
NEADBANL_00102 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
NEADBANL_00103 | 2.4e-275 | 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 | |
NEADBANL_00104 | 1.9e-289 | clcA | P | chloride | ||
NEADBANL_00105 | 3.6e-33 | E | Zn peptidase | |||
NEADBANL_00106 | 3.7e-58 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
NEADBANL_00107 | 6.8e-45 | |||||
NEADBANL_00108 | 1.1e-106 | S | Bacteriocin helveticin-J | |||
NEADBANL_00109 | 3.4e-118 | S | SLAP domain | |||
NEADBANL_00110 | 1.9e-211 | |||||
NEADBANL_00111 | 2e-18 | |||||
NEADBANL_00112 | 1.8e-229 | EGP | Sugar (and other) transporter | |||
NEADBANL_00113 | 3e-104 | |||||
NEADBANL_00114 | 1.7e-106 | flpA | 4.1.99.16, 4.2.3.22, 4.2.3.75 | K | helix_turn_helix, cAMP Regulatory protein | |
NEADBANL_00115 | 0.0 | copA | 3.6.3.54 | P | P-type ATPase | |
NEADBANL_00116 | 2e-48 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
NEADBANL_00117 | 2e-64 | silP | 1.9.3.1, 3.6.3.54 | S | Cupredoxin-like domain | |
NEADBANL_00118 | 9.4e-47 | atkY | K | Penicillinase repressor | ||
NEADBANL_00119 | 5.5e-74 | S | Putative adhesin | |||
NEADBANL_00120 | 8.1e-55 | K | Helix-turn-helix domain | |||
NEADBANL_00121 | 2e-220 | pbuG | S | permease | ||
NEADBANL_00122 | 1.9e-21 | S | haloacid dehalogenase-like hydrolase | |||
NEADBANL_00123 | 1.2e-32 | S | haloacid dehalogenase-like hydrolase | |||
NEADBANL_00124 | 8.8e-232 | pbuG | S | permease | ||
NEADBANL_00125 | 7.3e-127 | K | helix_turn_helix, mercury resistance | |||
NEADBANL_00126 | 1.8e-29 | S | CAAX protease self-immunity | |||
NEADBANL_00128 | 1.1e-148 | S | ABC-2 family transporter protein | |||
NEADBANL_00129 | 1.1e-78 | V | ATPases associated with a variety of cellular activities | |||
NEADBANL_00130 | 8.7e-92 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00131 | 2.8e-230 | pbuG | S | permease | ||
NEADBANL_00132 | 1.2e-141 | cof | S | haloacid dehalogenase-like hydrolase | ||
NEADBANL_00133 | 3.1e-67 | |||||
NEADBANL_00134 | 4.5e-126 | dgk | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
NEADBANL_00135 | 1.9e-118 | dak | 2.7.1.74, 2.7.1.76 | F | deoxynucleoside kinase | |
NEADBANL_00136 | 2.1e-134 | 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 | |
NEADBANL_00137 | 5.7e-160 | yeaE | S | Aldo/keto reductase family | ||
NEADBANL_00138 | 4.8e-171 | yufQ | S | Belongs to the binding-protein-dependent transport system permease family | ||
NEADBANL_00139 | 1.9e-198 | yufP | S | Belongs to the binding-protein-dependent transport system permease family | ||
NEADBANL_00140 | 5.2e-284 | xylG | 3.6.3.17 | S | ABC transporter | |
NEADBANL_00141 | 1.5e-200 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
NEADBANL_00142 | 4.7e-202 | tcsA | S | ABC transporter substrate-binding protein PnrA-like | ||
NEADBANL_00143 | 4.4e-101 | S | ECF transporter, substrate-specific component | |||
NEADBANL_00144 | 0.0 | ppc | 4.1.1.31 | H | Forms oxaloacetate, a four-carbon dicarboxylic acid source for the tricarboxylic acid cycle | |
NEADBANL_00145 | 0.0 | macB_3 | V | ABC transporter, ATP-binding protein | ||
NEADBANL_00146 | 3.6e-194 | S | DUF218 domain | |||
NEADBANL_00147 | 2.4e-121 | S | CAAX protease self-immunity | |||
NEADBANL_00148 | 2e-53 | |||||
NEADBANL_00149 | 9.4e-158 | mutR | K | Helix-turn-helix XRE-family like proteins | ||
NEADBANL_00150 | 1.6e-280 | V | ABC transporter transmembrane region | |||
NEADBANL_00151 | 5.7e-206 | napA | P | Sodium/hydrogen exchanger family | ||
NEADBANL_00152 | 0.0 | cadA | P | P-type ATPase | ||
NEADBANL_00153 | 3.9e-81 | ykuL | S | (CBS) domain | ||
NEADBANL_00154 | 3.4e-216 | ywhK | S | Membrane | ||
NEADBANL_00155 | 4.7e-48 | |||||
NEADBANL_00156 | 4e-19 | S | D-Ala-teichoic acid biosynthesis protein | |||
NEADBANL_00157 | 8.8e-292 | 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 | |
NEADBANL_00158 | 8.6e-237 | dltB | M | MBOAT, membrane-bound O-acyltransferase family | ||
NEADBANL_00159 | 1.7e-35 | 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 | |
NEADBANL_00160 | 6.8e-245 | dltD | M | Protein involved in D-alanine esterification of lipoteichoic acid and wall teichoic acid (D-alanine transfer protein) | ||
NEADBANL_00161 | 1.3e-168 | pbpX2 | V | Beta-lactamase | ||
NEADBANL_00162 | 1.3e-133 | S | Protein of unknown function (DUF975) | |||
NEADBANL_00163 | 2.7e-137 | lysA2 | M | Glycosyl hydrolases family 25 | ||
NEADBANL_00164 | 2.5e-289 | ytgP | S | Polysaccharide biosynthesis protein | ||
NEADBANL_00165 | 1.9e-36 | |||||
NEADBANL_00166 | 0.0 | XK27_06780 | V | ABC transporter permease | ||
NEADBANL_00167 | 1e-125 | XK27_06785 | V | ABC transporter, ATP-binding protein | ||
NEADBANL_00168 | 2.6e-239 | 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 | ||
NEADBANL_00169 | 1.2e-168 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NEADBANL_00170 | 0.0 | clpE | O | AAA domain (Cdc48 subfamily) | ||
NEADBANL_00171 | 1.2e-109 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
NEADBANL_00172 | 3.7e-233 | cycA | E | Amino acid permease | ||
NEADBANL_00173 | 7e-248 | yifK | E | Amino acid permease | ||
NEADBANL_00174 | 4.9e-135 | S | PFAM Archaeal ATPase | |||
NEADBANL_00175 | 2.5e-26 | V | HNH endonuclease | |||
NEADBANL_00176 | 1.3e-122 | V | HNH endonuclease | |||
NEADBANL_00178 | 1.3e-139 | puuD | S | peptidase C26 | ||
NEADBANL_00179 | 1e-230 | steT_1 | E | amino acid | ||
NEADBANL_00180 | 6.5e-190 | asnA | 6.3.1.1 | F | aspartate--ammonia ligase | |
NEADBANL_00181 | 3.9e-206 | 4.2.1.126 | S | Bacterial protein of unknown function (DUF871) | ||
NEADBANL_00184 | 2e-188 | 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 | |
NEADBANL_00185 | 1.9e-250 | purA | 6.3.4.4 | F | Plays an important role in the de novo pathway of purine nucleotide biosynthesis. Catalyzes the first committed step in the biosynthesis of AMP from IMP | |
NEADBANL_00186 | 3.1e-245 | purB | 4.3.2.2 | F | Belongs to the lyase 1 family. Adenylosuccinate lyase subfamily | |
NEADBANL_00187 | 1.2e-28 | S | Protein conserved in bacteria | |||
NEADBANL_00188 | 3.9e-57 | |||||
NEADBANL_00189 | 7.7e-88 | |||||
NEADBANL_00190 | 1.9e-264 | yheS_2 | S | ATPases associated with a variety of cellular activities | ||
NEADBANL_00191 | 8.3e-185 | XK27_05540 | S | DUF218 domain | ||
NEADBANL_00192 | 1.1e-110 | |||||
NEADBANL_00193 | 2.5e-107 | |||||
NEADBANL_00194 | 5.6e-118 | yicL | EG | EamA-like transporter family | ||
NEADBANL_00195 | 1.6e-166 | EG | EamA-like transporter family | |||
NEADBANL_00196 | 8.6e-165 | EG | EamA-like transporter family | |||
NEADBANL_00197 | 3.5e-37 | |||||
NEADBANL_00199 | 2.2e-162 | |||||
NEADBANL_00201 | 1.6e-82 | M | NlpC/P60 family | |||
NEADBANL_00202 | 1.3e-133 | cobQ | S | glutamine amidotransferase | ||
NEADBANL_00204 | 4.3e-68 | L | RelB antitoxin | |||
NEADBANL_00205 | 6.5e-44 | yefM | 2.3.1.15 | D | Antitoxin component of a toxin-antitoxin (TA) module | |
NEADBANL_00206 | 5.9e-47 | yoeB | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | ||
NEADBANL_00207 | 2.9e-143 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00208 | 4.3e-20 | |||||
NEADBANL_00209 | 3e-73 | |||||
NEADBANL_00210 | 9.6e-152 | thiD | 2.5.1.3, 2.7.1.49, 2.7.4.7, 4.1.99.17 | H | Phosphomethylpyrimidine kinase | |
NEADBANL_00211 | 3.5e-293 | 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 | |
NEADBANL_00212 | 6.3e-145 | ptp2 | 3.1.3.48 | T | Tyrosine phosphatase family | |
NEADBANL_00213 | 4.1e-178 | yvdE | K | helix_turn _helix lactose operon repressor | ||
NEADBANL_00214 | 3.7e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NEADBANL_00215 | 4.8e-78 | S | PAS domain | |||
NEADBANL_00216 | 0.0 | malL | 3.2.1.10, 3.2.1.20 | GH13,GH31 | G | Alpha amylase, catalytic domain |
NEADBANL_00217 | 0.0 | nplT | 3.2.1.133, 3.2.1.135, 3.2.1.54 | GH13 | G | Belongs to the glycosyl hydrolase 13 family |
NEADBANL_00218 | 0.0 | map2 | 2.4.1.8 | GH65 | G | hydrolase, family 65, central catalytic |
NEADBANL_00219 | 1.4e-116 | pgmB | 2.4.1.64, 3.1.3.12, 3.2.1.28, 5.4.2.6 | GH37,GH65 | S | beta-phosphoglucomutase |
NEADBANL_00220 | 4.7e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_00221 | 2.5e-212 | malE | G | Bacterial extracellular solute-binding protein | ||
NEADBANL_00222 | 3.3e-250 | malF | P | Binding-protein-dependent transport system inner membrane component | ||
NEADBANL_00223 | 3.3e-147 | malG | P | ABC transporter permease | ||
NEADBANL_00225 | 2.5e-39 | S | COG NOG15344 non supervised orthologous group | |||
NEADBANL_00227 | 1.7e-125 | NU | StbA protein | |||
NEADBANL_00228 | 1.9e-57 | NU | StbA protein | |||
NEADBANL_00229 | 8e-42 | |||||
NEADBANL_00230 | 1.1e-161 | repA | S | Replication initiator protein A | ||
NEADBANL_00231 | 4e-47 | |||||
NEADBANL_00232 | 4.2e-43 | S | Bacterial epsilon antitoxin | |||
NEADBANL_00233 | 3e-149 | 2.7.1.176 | S | Zeta toxin | ||
NEADBANL_00234 | 1.3e-39 | |||||
NEADBANL_00235 | 2.9e-29 | |||||
NEADBANL_00236 | 2e-23 | traA | L | MobA/MobL family | ||
NEADBANL_00237 | 0.0 | L | MobA MobL family protein | |||
NEADBANL_00238 | 1.2e-24 | L | MobA MobL family protein | |||
NEADBANL_00239 | 4.4e-25 | 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 | ||
NEADBANL_00240 | 2.4e-125 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
NEADBANL_00241 | 7e-159 | S | cog cog1373 | |||
NEADBANL_00242 | 1.1e-80 | tnpR1 | L | Resolvase, N terminal domain | ||
NEADBANL_00243 | 9.2e-61 | K | helix_turn_helix multiple antibiotic resistance protein | |||
NEADBANL_00244 | 1.2e-18 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
NEADBANL_00245 | 3.4e-103 | M | Forms passive diffusion pores that allow small molecular weight hydrophilic materials across the outer membrane | |||
NEADBANL_00246 | 3.2e-225 | L | Transposase | |||
NEADBANL_00247 | 8.7e-187 | manL | 2.7.1.191 | G | PTS system sorbose subfamily IIB component | |
NEADBANL_00248 | 1.7e-129 | manY | G | PTS system | ||
NEADBANL_00249 | 1e-173 | manN | G | system, mannose fructose sorbose family IID component | ||
NEADBANL_00250 | 4.9e-63 | manO | S | Domain of unknown function (DUF956) | ||
NEADBANL_00251 | 1.8e-159 | K | Transcriptional regulator | |||
NEADBANL_00252 | 2.8e-85 | maa | S | transferase hexapeptide repeat | ||
NEADBANL_00253 | 2e-242 | cycA | E | Amino acid permease | ||
NEADBANL_00254 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
NEADBANL_00255 | 0.0 | glmS | 2.6.1.16 | M | Catalyzes the first step in hexosamine metabolism, converting fructose-6P into glucosamine-6P using glutamine as a nitrogen source | |
NEADBANL_00256 | 0.0 | mtlR | K | Mga helix-turn-helix domain | ||
NEADBANL_00257 | 0.0 | mtlA | 2.7.1.197 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NEADBANL_00258 | 2.1e-79 | mtlF | 2.7.1.197 | G | catalyzes the phosphorylation of incoming sugar substrates concomitant with their translocation across the cell membrane | |
NEADBANL_00259 | 1.8e-220 | mtlD | 1.1.1.17 | C | mannitol-1-phosphate 5-dehydrogenase activity | |
NEADBANL_00260 | 1.8e-133 | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | ||
NEADBANL_00261 | 1.6e-32 | |||||
NEADBANL_00262 | 9.4e-71 | apfA | 2.7.7.72, 3.6.1.61 | F | Nudix hydrolase | |
NEADBANL_00263 | 2.3e-156 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00265 | 1.9e-297 | V | ABC transporter transmembrane region | |||
NEADBANL_00266 | 0.0 | pckA | 4.1.1.49 | H | Phosphoenolpyruvate carboxykinase | |
NEADBANL_00267 | 0.0 | S | TerB-C domain | |||
NEADBANL_00268 | 2.7e-252 | P | P-loop Domain of unknown function (DUF2791) | |||
NEADBANL_00269 | 0.0 | lhr | L | DEAD DEAH box helicase | ||
NEADBANL_00270 | 1.9e-59 | |||||
NEADBANL_00271 | 4.4e-141 | nfrA | 1.5.1.38, 1.5.1.39 | C | nitroreductase | |
NEADBANL_00272 | 2.9e-200 | amtB | P | ammonium transporter | ||
NEADBANL_00274 | 1e-61 | psiE | S | Phosphate-starvation-inducible E | ||
NEADBANL_00275 | 3.8e-113 | yncA | 2.3.1.79 | S | Maltose acetyltransferase | |
NEADBANL_00276 | 1.5e-70 | S | Iron-sulphur cluster biosynthesis | |||
NEADBANL_00278 | 4.6e-31 | |||||
NEADBANL_00279 | 3.6e-173 | pphA | 3.1.3.16 | T | Calcineurin-like phosphoesterase | |
NEADBANL_00280 | 1.6e-12 | |||||
NEADBANL_00281 | 2.1e-37 | celB | 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 | ||
NEADBANL_00282 | 5.3e-64 | celB | 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 | ||
NEADBANL_00283 | 3.9e-74 | M | LysM domain protein | |||
NEADBANL_00284 | 2.7e-194 | D | nuclear chromosome segregation | |||
NEADBANL_00285 | 6.4e-110 | G | Phosphoglycerate mutase family | |||
NEADBANL_00286 | 3.3e-109 | G | Histidine phosphatase superfamily (branch 1) | |||
NEADBANL_00287 | 4.2e-113 | VY92_08690 | 5.3.1.32 | G | Antibiotic biosynthesis monooxygenase | |
NEADBANL_00288 | 1.2e-114 | glpQ1 | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NEADBANL_00289 | 2.9e-179 | msmR | K | helix_turn _helix lactose operon repressor | ||
NEADBANL_00290 | 1.4e-237 | msmE | G | Bacterial extracellular solute-binding protein | ||
NEADBANL_00291 | 1.2e-163 | msmF | P | ABC-type sugar transport systems, permease components | ||
NEADBANL_00292 | 2.2e-154 | msmG | G | Binding-protein-dependent transport system inner membrane component | ||
NEADBANL_00293 | 1.5e-244 | sacA | 3.2.1.26 | GH32 | G | Glycosyl hydrolases family 32 |
NEADBANL_00294 | 2.5e-211 | msmX | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_00295 | 1.1e-272 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
NEADBANL_00296 | 1.5e-230 | XK27_04775 | S | PAS domain | ||
NEADBANL_00297 | 2.1e-103 | S | Iron-sulfur cluster assembly protein | |||
NEADBANL_00298 | 8.7e-141 | 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 | |
NEADBANL_00299 | 0.0 | nrdD | 1.1.98.6 | F | Ribonucleoside-triphosphate reductase | |
NEADBANL_00300 | 5.6e-255 | yxbA | 6.3.1.12 | S | ATP-grasp enzyme | |
NEADBANL_00301 | 0.0 | asnB | 6.3.5.4 | E | Asparagine synthase | |
NEADBANL_00302 | 3.4e-274 | S | Calcineurin-like phosphoesterase | |||
NEADBANL_00303 | 1.5e-83 | |||||
NEADBANL_00304 | 3.3e-106 | tag | 3.2.2.20 | L | glycosylase | |
NEADBANL_00305 | 2.2e-148 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
NEADBANL_00306 | 2.3e-118 | phnE | 3.6.1.63 | P | Binding-protein-dependent transport system inner membrane component | |
NEADBANL_00307 | 4.1e-136 | phnC | 3.6.3.28 | P | Part of the ABC transporter complex PhnCDE involved in phosphonates import. Responsible for energy coupling to the transport system | |
NEADBANL_00308 | 4.1e-151 | phnD | P | Phosphonate ABC transporter | ||
NEADBANL_00309 | 5.2e-84 | uspA | T | universal stress protein | ||
NEADBANL_00310 | 1.3e-148 | ptp3 | 3.1.3.48 | T | Tyrosine phosphatase family | |
NEADBANL_00311 | 2.3e-87 | 2.7.1.200, 2.7.1.202, 2.7.1.204 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | ||
NEADBANL_00312 | 3.6e-90 | ntd | 2.4.2.6 | F | Nucleoside | |
NEADBANL_00313 | 2.3e-08 | |||||
NEADBANL_00314 | 2.4e-275 | S | Archaea bacterial proteins of unknown function | |||
NEADBANL_00315 | 4.1e-217 | nagA | 3.5.1.25 | G | Belongs to the metallo-dependent hydrolases superfamily. NagA family | |
NEADBANL_00316 | 0.0 | G | Belongs to the glycosyl hydrolase 31 family | |||
NEADBANL_00317 | 1.6e-146 | I | alpha/beta hydrolase fold | |||
NEADBANL_00318 | 1.7e-129 | yibF | S | overlaps another CDS with the same product name | ||
NEADBANL_00319 | 4.1e-201 | yibE | S | overlaps another CDS with the same product name | ||
NEADBANL_00320 | 2.1e-108 | |||||
NEADBANL_00321 | 2.6e-205 | ddl | 6.3.2.4 | F | Belongs to the D-alanine--D-alanine ligase family | |
NEADBANL_00322 | 5.8e-225 | S | Cysteine-rich secretory protein family | |||
NEADBANL_00323 | 3.1e-133 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NEADBANL_00324 | 1.1e-257 | glnPH2 | P | ABC transporter permease | ||
NEADBANL_00325 | 2.8e-135 | |||||
NEADBANL_00326 | 8.4e-125 | luxT | K | Bacterial regulatory proteins, tetR family | ||
NEADBANL_00327 | 2.6e-183 | 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) | |
NEADBANL_00328 | 1e-53 | |||||
NEADBANL_00329 | 7.3e-126 | S | Alpha/beta hydrolase family | |||
NEADBANL_00330 | 1.3e-156 | epsV | 2.7.8.12 | S | glycosyl transferase family 2 | |
NEADBANL_00331 | 4.4e-140 | ypuA | S | Protein of unknown function (DUF1002) | ||
NEADBANL_00332 | 9.7e-146 | rnhA | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NEADBANL_00333 | 7.7e-182 | S | Alpha/beta hydrolase of unknown function (DUF915) | |||
NEADBANL_00334 | 3.5e-282 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NEADBANL_00335 | 4.2e-86 | |||||
NEADBANL_00336 | 1e-133 | cobB | K | SIR2 family | ||
NEADBANL_00337 | 3.2e-92 | ogt | 2.1.1.63 | L | 6-O-methylguanine DNA methyltransferase, DNA binding domain | |
NEADBANL_00338 | 1.8e-123 | terC | P | Integral membrane protein TerC family | ||
NEADBANL_00339 | 5.8e-64 | yeaO | S | Protein of unknown function, DUF488 | ||
NEADBANL_00340 | 4e-121 | mpg | 3.2.2.21 | L | Belongs to the DNA glycosylase MPG family | |
NEADBANL_00341 | 1.3e-290 | glnP | P | ABC transporter permease | ||
NEADBANL_00342 | 1.7e-134 | glnQ | E | ABC transporter, ATP-binding protein | ||
NEADBANL_00343 | 9.8e-137 | S | Protein of unknown function (DUF805) | |||
NEADBANL_00344 | 1.5e-155 | L | HNH nucleases | |||
NEADBANL_00345 | 1.4e-121 | yfbR | S | HD containing hydrolase-like enzyme | ||
NEADBANL_00346 | 6.2e-178 | G | Glycosyl hydrolases family 8 | |||
NEADBANL_00347 | 1e-216 | ydaM | M | Glycosyl transferase | ||
NEADBANL_00349 | 6.9e-116 | |||||
NEADBANL_00350 | 1.2e-17 | |||||
NEADBANL_00351 | 1.9e-309 | glpQ | 3.1.4.46 | C | Membrane domain of glycerophosphoryl diester phosphodiesterase | |
NEADBANL_00352 | 2.7e-70 | S | Iron-sulphur cluster biosynthesis | |||
NEADBANL_00353 | 3.9e-196 | ybiR | P | Citrate transporter | ||
NEADBANL_00354 | 2.7e-97 | lemA | S | LemA family | ||
NEADBANL_00355 | 2.6e-158 | htpX | O | Belongs to the peptidase M48B family | ||
NEADBANL_00356 | 7.9e-174 | K | helix_turn_helix, arabinose operon control protein | |||
NEADBANL_00357 | 4.8e-249 | cbiO1 | S | ABC transporter, ATP-binding protein | ||
NEADBANL_00358 | 9.6e-78 | P | Cobalt transport protein | |||
NEADBANL_00359 | 1.8e-175 | pepI | 3.4.11.5, 3.5.1.101 | E | Releases the N-terminal proline from various substrates | |
NEADBANL_00360 | 5.9e-92 | G | Peptidase_C39 like family | |||
NEADBANL_00361 | 4.4e-163 | M | NlpC/P60 family | |||
NEADBANL_00362 | 4.6e-33 | G | Peptidase_C39 like family | |||
NEADBANL_00363 | 5.2e-81 | rlmH | 2.1.1.177 | J | Specifically methylates the pseudouridine at position 1915 (m3Psi1915) in 23S rRNA | |
NEADBANL_00364 | 3.3e-151 | htrA | 3.4.21.107 | O | serine protease | |
NEADBANL_00365 | 1.4e-147 | vicX | 3.1.26.11 | S | domain protein | |
NEADBANL_00366 | 3.4e-149 | yycI | S | YycH protein | ||
NEADBANL_00367 | 3.3e-258 | yycH | S | YycH protein | ||
NEADBANL_00368 | 1.1e-304 | vicK | 2.7.13.3 | T | Histidine kinase | |
NEADBANL_00369 | 8.2e-131 | K | response regulator | |||
NEADBANL_00370 | 2e-247 | lysA | 4.1.1.19, 4.1.1.20 | E | Specifically catalyzes the decarboxylation of meso- diaminopimelate (meso-DAP) to L-lysine | |
NEADBANL_00371 | 1.3e-259 | lysC | 2.7.2.4 | E | Belongs to the aspartokinase family | |
NEADBANL_00372 | 3.4e-191 | 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 | |
NEADBANL_00373 | 4e-126 | yjeM | E | Amino Acid | ||
NEADBANL_00374 | 1.3e-22 | yjeM | E | Amino Acid | ||
NEADBANL_00375 | 3.7e-105 | engB | D | Necessary for normal cell division and for the maintenance of normal septation | ||
NEADBANL_00376 | 2e-233 | 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 | ||
NEADBANL_00377 | 4e-216 | tig | D | Involved in protein export. Acts as a chaperone by maintaining the newly synthesized protein in an open conformation. Functions as a peptidyl-prolyl cis-trans isomerase | ||
NEADBANL_00378 | 1.5e-225 | tuf | J | This protein promotes the GTP-dependent binding of aminoacyl-tRNA to the A-site of ribosomes during protein biosynthesis | ||
NEADBANL_00379 | 8.3e-151 | |||||
NEADBANL_00380 | 0.0 | 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 | ||
NEADBANL_00381 | 4.6e-42 | rpsO | J | Forms an intersubunit bridge (bridge B4) with the 23S rRNA of the 50S subunit in the ribosome | ||
NEADBANL_00382 | 6.7e-35 | rpsT | J | Binds directly to 16S ribosomal RNA | ||
NEADBANL_00383 | 2.8e-174 | holA | 2.7.7.7 | L | DNA polymerase III delta subunit | |
NEADBANL_00384 | 0.0 | comEC | S | Competence protein ComEC | ||
NEADBANL_00385 | 1.6e-78 | comEA | L | Competence protein ComEA | ||
NEADBANL_00386 | 4.3e-189 | ylbL | T | Belongs to the peptidase S16 family | ||
NEADBANL_00387 | 7.3e-83 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NEADBANL_00388 | 4.5e-97 | rsmD | 2.1.1.171 | L | RNA methyltransferase, RsmD family | |
NEADBANL_00389 | 5.1e-54 | ylbG | S | Uncharacterized protein conserved in bacteria (DUF2129) | ||
NEADBANL_00390 | 5.4e-212 | ftsW | D | Belongs to the SEDS family | ||
NEADBANL_00391 | 0.0 | typA | T | GTP-binding protein TypA | ||
NEADBANL_00392 | 4e-101 | def | 3.5.1.31, 3.5.1.88 | J | Removes the formyl group from the N-terminal Met of newly synthesized proteins. Requires at least a dipeptide for an efficient rate of reaction. N-terminal L-methionine is a prerequisite for activity but the enzyme has broad specificity at other positions | |
NEADBANL_00393 | 4.6e-32 | ykzG | S | Belongs to the UPF0356 family | ||
NEADBANL_00394 | 0.0 | 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 | ||
NEADBANL_00395 | 6.1e-182 | ytlR | 2.7.1.91 | I | Diacylglycerol kinase catalytic domain | |
NEADBANL_00396 | 4.1e-295 | L | Nuclease-related domain | |||
NEADBANL_00397 | 0.0 | recD2 | 3.1.11.5 | L | DNA-dependent ATPase and ATP-dependent 5'-3' DNA helicase. Has no activity on blunt DNA or DNA with 3'-overhangs, requires at least 10 bases of 5'-ssDNA for helicase activity | |
NEADBANL_00398 | 2.7e-104 | S | Repeat protein | |||
NEADBANL_00399 | 1.5e-126 | pgm6 | 5.4.2.11, 5.4.2.12 | G | Phosphoglycerate mutase family | |
NEADBANL_00400 | 4.6e-221 | 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 | |
NEADBANL_00401 | 2.2e-57 | XK27_04120 | S | Putative amino acid metabolism | ||
NEADBANL_00402 | 3.2e-217 | iscS | 2.8.1.7 | E | Aminotransferase class V | |
NEADBANL_00403 | 1.2e-126 | mtnN | 3.2.2.9 | E | Catalyzes the irreversible cleavage of the glycosidic bond in both 5'-methylthioadenosine (MTA) and S- adenosylhomocysteine (SAH AdoHcy) to adenine and the corresponding thioribose, 5'-methylthioribose and S-ribosylhomocysteine, respectively | |
NEADBANL_00404 | 2.1e-38 | |||||
NEADBANL_00405 | 9.8e-103 | nudF | 3.6.1.13 | L | ADP-ribose pyrophosphatase | |
NEADBANL_00406 | 3.6e-31 | cspA | K | 'Cold-shock' DNA-binding domain | ||
NEADBANL_00407 | 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) | |
NEADBANL_00408 | 2.8e-74 | gpsB | D | DivIVA domain protein | ||
NEADBANL_00409 | 6.7e-150 | ylmH | S | S4 domain protein | ||
NEADBANL_00410 | 1.7e-45 | yggT | S | YGGT family | ||
NEADBANL_00411 | 7.3e-74 | 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 | ||
NEADBANL_00412 | 1.8e-219 | 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 | ||
NEADBANL_00413 | 2.6e-247 | 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 | ||
NEADBANL_00414 | 4.1e-153 | divIB | D | Cell division protein that may be involved in stabilizing or promoting the assembly of the division complex | ||
NEADBANL_00415 | 4.4e-208 | 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) |
NEADBANL_00416 | 7.3e-261 | murD | 6.3.2.9 | M | Cell wall formation. Catalyzes the addition of glutamate to the nucleotide precursor UDP-N-acetylmuramoyl-L-alanine (UMA) | |
NEADBANL_00417 | 1.1e-175 | mraY | 2.7.8.13 | M | First step of the lipid cycle reactions in the biosynthesis of the cell wall peptidoglycan | |
NEADBANL_00418 | 0.0 | ftsI | 3.4.16.4 | M | Penicillin-binding Protein | |
NEADBANL_00419 | 4.1e-54 | ftsL | D | Cell division protein FtsL | ||
NEADBANL_00420 | 3.8e-176 | rsmH | 2.1.1.199 | J | Specifically methylates the N4 position of cytidine in position 1402 (C1402) of 16S rRNA | |
NEADBANL_00421 | 6.3e-78 | mraZ | K | Belongs to the MraZ family | ||
NEADBANL_00422 | 6.4e-54 | S | Protein of unknown function (DUF3397) | |||
NEADBANL_00424 | 3.5e-94 | mreD | ||||
NEADBANL_00425 | 8.8e-148 | mreC | M | Involved in formation and maintenance of cell shape | ||
NEADBANL_00426 | 2.4e-176 | mreB | D | cell shape determining protein MreB | ||
NEADBANL_00427 | 2.9e-103 | radC | L | DNA repair protein | ||
NEADBANL_00428 | 2e-126 | S | Haloacid dehalogenase-like hydrolase | |||
NEADBANL_00429 | 1.5e-239 | folC | 6.3.2.12, 6.3.2.17 | H | Belongs to the folylpolyglutamate synthase family | |
NEADBANL_00430 | 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 | |
NEADBANL_00431 | 6e-42 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00432 | 1.2e-61 | S | Phage derived protein Gp49-like (DUF891) | |||
NEADBANL_00433 | 4.9e-15 | 1.3.5.4 | C | FAD binding domain | ||
NEADBANL_00434 | 8.6e-31 | K | Helix-turn-helix domain | |||
NEADBANL_00435 | 1.4e-110 | K | Helix-turn-helix domain | |||
NEADBANL_00436 | 4.3e-156 | |||||
NEADBANL_00437 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
NEADBANL_00438 | 6e-08 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NEADBANL_00439 | 2.9e-44 | |||||
NEADBANL_00440 | 9.8e-94 | S | Protein of unknown function (DUF3990) | |||
NEADBANL_00441 | 1.2e-171 | yfdH | 2.4.2.53 | GT2 | M | Glycosyltransferase, group 2 family protein |
NEADBANL_00442 | 2.1e-65 | 2.4.1.83 | GT2 | S | GtrA-like protein | |
NEADBANL_00443 | 2.8e-149 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NEADBANL_00444 | 2.2e-120 | rsuA | 5.4.99.19, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NEADBANL_00445 | 1.3e-184 | 3.6.4.12 | K | Putative ATP-dependent DNA helicase recG C-terminal | ||
NEADBANL_00446 | 3e-145 | |||||
NEADBANL_00447 | 1.1e-134 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00448 | 4.3e-112 | |||||
NEADBANL_00452 | 4e-35 | |||||
NEADBANL_00453 | 5.7e-33 | gepA | S | Protein of unknown function (DUF4065) | ||
NEADBANL_00454 | 5.3e-63 | |||||
NEADBANL_00455 | 5.4e-83 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00457 | 3.9e-226 | 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 | |
NEADBANL_00458 | 1.7e-215 | iscS2 | 2.8.1.7 | E | Aminotransferase class V | |
NEADBANL_00459 | 6.2e-294 | 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 | ||
NEADBANL_00460 | 1.4e-110 | 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 | ||
NEADBANL_00461 | 9.9e-85 | yueI | S | Protein of unknown function (DUF1694) | ||
NEADBANL_00462 | 7.4e-239 | rarA | L | recombination factor protein RarA | ||
NEADBANL_00463 | 2.4e-38 | |||||
NEADBANL_00464 | 9.8e-77 | usp6 | T | universal stress protein | ||
NEADBANL_00465 | 0.0 | pulA | 3.2.1.41 | CBM48,GH13 | G | belongs to the glycosyl hydrolase 13 family |
NEADBANL_00466 | 7.8e-112 | L | Transposase | |||
NEADBANL_00467 | 1.2e-216 | rodA | D | Belongs to the SEDS family | ||
NEADBANL_00468 | 1.5e-33 | S | Protein of unknown function (DUF2969) | |||
NEADBANL_00469 | 2e-51 | yidD | S | Could be involved in insertion of integral membrane proteins into the membrane | ||
NEADBANL_00470 | 2.5e-178 | mbl | D | Cell shape determining protein MreB Mrl | ||
NEADBANL_00471 | 4.1e-31 | ywzB | S | Protein of unknown function (DUF1146) | ||
NEADBANL_00472 | 7.6e-71 | atpC | C | Produces ATP from ADP in the presence of a proton gradient across the membrane | ||
NEADBANL_00473 | 8.1e-255 | 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 | |
NEADBANL_00474 | 1.7e-168 | 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 | ||
NEADBANL_00475 | 2.2e-279 | atpA | 3.6.3.14 | C | Produces ATP from ADP in the presence of a proton gradient across the membrane. The alpha chain is a regulatory subunit | |
NEADBANL_00476 | 3.7e-91 | 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 | ||
NEADBANL_00477 | 6.6e-50 | atpF | C | Component of the F(0) channel, it forms part of the peripheral stalk, linking F(1) to F(0) | ||
NEADBANL_00478 | 6.6e-29 | atpE | C | F(1)F(0) ATP synthase produces ATP from ADP in the presence of a proton or sodium gradient. F-type ATPases consist of two structural domains, F(1) containing the extramembraneous catalytic core and F(0) containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP synthesis in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation | ||
NEADBANL_00479 | 5.1e-125 | atpB | C | it plays a direct role in the translocation of protons across the membrane | ||
NEADBANL_00480 | 6.8e-113 | upp | 2.4.2.9 | F | Catalyzes the conversion of uracil and 5-phospho-alpha- D-ribose 1-diphosphate (PRPP) to UMP and diphosphate | |
NEADBANL_00481 | 1.4e-189 | 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 | |
NEADBANL_00482 | 1.1e-155 | 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 | |
NEADBANL_00483 | 3.1e-182 | prfA | J | Peptide chain release factor 1 directs the termination of translation in response to the peptide chain termination codons UAG and UAA | ||
NEADBANL_00484 | 1.3e-113 | tdk | 2.7.1.21 | F | thymidine kinase | |
NEADBANL_00485 | 5.8e-263 | murF | 6.3.2.10, 6.3.2.13 | M | Domain of unknown function (DUF1727) | |
NEADBANL_00486 | 1.3e-141 | sip | L | Belongs to the 'phage' integrase family | ||
NEADBANL_00488 | 4.6e-15 | S | Helix-turn-helix domain | |||
NEADBANL_00489 | 1.2e-07 | |||||
NEADBANL_00490 | 6.6e-23 | |||||
NEADBANL_00493 | 5.4e-08 | arpU | S | Phage transcriptional regulator, ArpU family | ||
NEADBANL_00496 | 5.6e-194 | ampC | V | Beta-lactamase | ||
NEADBANL_00497 | 3.4e-218 | EGP | Major facilitator Superfamily | |||
NEADBANL_00498 | 2.1e-260 | pgi | 5.3.1.9 | G | Belongs to the GPI family | |
NEADBANL_00499 | 3.2e-104 | vanZ | V | VanZ like family | ||
NEADBANL_00500 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
NEADBANL_00501 | 2.7e-266 | yclK | 2.7.13.3, 4.6.1.1 | T | Histidine kinase | |
NEADBANL_00502 | 7.5e-132 | K | Transcriptional regulatory protein, C terminal | |||
NEADBANL_00503 | 5e-66 | S | SdpI/YhfL protein family | |||
NEADBANL_00504 | 2.5e-191 | manA | 5.3.1.8 | G | mannose-6-phosphate isomerase | |
NEADBANL_00505 | 1.7e-223 | patB | 4.4.1.8 | E | Aminotransferase, class I | |
NEADBANL_00506 | 1.8e-79 | M | Protein of unknown function (DUF3737) | |||
NEADBANL_00507 | 4.1e-16 | M | Protein of unknown function (DUF3737) | |||
NEADBANL_00508 | 6.5e-138 | sip | L | Belongs to the 'phage' integrase family | ||
NEADBANL_00509 | 1.3e-16 | K | sequence-specific DNA binding | |||
NEADBANL_00510 | 2.6e-12 | S | Helix-turn-helix domain | |||
NEADBANL_00511 | 2.6e-30 | |||||
NEADBANL_00515 | 1.6e-33 | |||||
NEADBANL_00517 | 9.1e-14 | |||||
NEADBANL_00519 | 3.7e-221 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NEADBANL_00520 | 1.3e-187 | ytxK | 2.1.1.72 | L | N-6 DNA Methylase | |
NEADBANL_00521 | 6e-21 | |||||
NEADBANL_00522 | 1.5e-76 | comGF | U | Putative Competence protein ComGF | ||
NEADBANL_00523 | 2.3e-41 | |||||
NEADBANL_00524 | 7.4e-71 | |||||
NEADBANL_00525 | 3.1e-43 | comGC | U | competence protein ComGC | ||
NEADBANL_00526 | 1.3e-171 | comGB | NU | type II secretion system | ||
NEADBANL_00527 | 1.7e-179 | comGA | NU | Type II IV secretion system protein | ||
NEADBANL_00528 | 8.9e-133 | yebC | K | Transcriptional regulatory protein | ||
NEADBANL_00529 | 6.4e-93 | S | VanZ like family | |||
NEADBANL_00530 | 3.2e-110 | ylbE | GM | NAD(P)H-binding | ||
NEADBANL_00531 | 9.8e-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 | ||
NEADBANL_00533 | 9.7e-305 | E | Amino acid permease | |||
NEADBANL_00534 | 1.3e-176 | D | Alpha beta | |||
NEADBANL_00535 | 1.7e-303 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
NEADBANL_00536 | 0.0 | bglP | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NEADBANL_00537 | 1.4e-142 | licT | K | CAT RNA binding domain | ||
NEADBANL_00538 | 7.5e-211 | glxK | 2.7.1.165 | G | Belongs to the glycerate kinase type-1 family | |
NEADBANL_00539 | 3.1e-83 | ptpA | 3.1.3.48 | T | Belongs to the low molecular weight phosphotyrosine protein phosphatase family | |
NEADBANL_00540 | 9.4e-119 | |||||
NEADBANL_00541 | 1.1e-74 | K | Penicillinase repressor | |||
NEADBANL_00542 | 1.4e-147 | S | hydrolase | |||
NEADBANL_00543 | 5.3e-256 | glmM | 5.4.2.10 | G | Catalyzes the conversion of glucosamine-6-phosphate to glucosamine-1-phosphate | |
NEADBANL_00544 | 2.2e-171 | ybbR | S | YbbR-like protein | ||
NEADBANL_00545 | 6.4e-151 | 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 | |
NEADBANL_00546 | 5.8e-205 | potD | P | ABC transporter | ||
NEADBANL_00547 | 2.1e-127 | potC | P | ABC transporter permease | ||
NEADBANL_00548 | 5.4e-131 | potB | P | ABC transporter permease | ||
NEADBANL_00549 | 4.1e-206 | 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 | |
NEADBANL_00550 | 1.8e-164 | murB | 1.3.1.98 | M | Cell wall formation | |
NEADBANL_00551 | 5.8e-97 | dnaQ | 2.7.7.7 | L | DNA polymerase III | |
NEADBANL_00552 | 1.4e-86 | ydiB | 2.7.1.221, 5.1.1.1 | O | Hydrolase, P-loop family | |
NEADBANL_00553 | 6.3e-182 | pta | 2.3.1.8, 3.6.3.21 | C | phosphate acetyltransferase | |
NEADBANL_00554 | 9.7e-137 | 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 | |
NEADBANL_00555 | 1.8e-156 | ycsE | S | Sucrose-6F-phosphate phosphohydrolase | ||
NEADBANL_00556 | 1.2e-94 | |||||
NEADBANL_00557 | 1.7e-142 | 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) | |
NEADBANL_00558 | 1e-226 | pgk | 2.7.2.3, 5.3.1.1 | F | Belongs to the phosphoglycerate kinase family | |
NEADBANL_00559 | 6.5e-190 | gap | 1.2.1.12 | G | Belongs to the glyceraldehyde-3-phosphate dehydrogenase family | |
NEADBANL_00560 | 1.5e-189 | cggR | K | Putative sugar-binding domain | ||
NEADBANL_00562 | 1.1e-289 | |||||
NEADBANL_00563 | 1.3e-273 | ycaM | E | amino acid | ||
NEADBANL_00564 | 2.4e-139 | S | Cysteine-rich secretory protein family | |||
NEADBANL_00565 | 1.4e-77 | K | MerR HTH family regulatory protein | |||
NEADBANL_00566 | 6.4e-263 | lmrB | EGP | Major facilitator Superfamily | ||
NEADBANL_00567 | 2.2e-94 | S | Domain of unknown function (DUF4811) | |||
NEADBANL_00568 | 5.6e-130 | ybbM | S | Uncharacterised protein family (UPF0014) | ||
NEADBANL_00569 | 4.9e-111 | ybbL | S | ABC transporter, ATP-binding protein | ||
NEADBANL_00570 | 0.0 | S | SH3-like domain | |||
NEADBANL_00571 | 2.3e-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 | |
NEADBANL_00572 | 2.1e-171 | whiA | K | May be required for sporulation | ||
NEADBANL_00573 | 1.1e-195 | ybhK | S | Required for morphogenesis under gluconeogenic growth conditions | ||
NEADBANL_00574 | 6.2e-165 | rapZ | S | Displays ATPase and GTPase activities | ||
NEADBANL_00575 | 4.1e-90 | S | Short repeat of unknown function (DUF308) | |||
NEADBANL_00576 | 0.0 | uvrA | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrA is an ATPase and a DNA-binding protein. A damage recognition complex composed of 2 UvrA and 2 UvrB subunits scans DNA for abnormalities. When the presence of a lesion has been verified by UvrB, the UvrA molecules dissociate | ||
NEADBANL_00577 | 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 | ||
NEADBANL_00578 | 0.0 | pgm | 5.4.2.2, 5.4.2.8 | G | Phosphoglucomutase phosphomannomutase, alpha beta alpha domain | |
NEADBANL_00579 | 3.9e-181 | trxB | 1.8.1.9 | C | Belongs to the class-II pyridine nucleotide-disulfide oxidoreductase family | |
NEADBANL_00580 | 3.9e-187 | gpsA | 1.1.1.94 | I | Glycerol-3-phosphate dehydrogenase | |
NEADBANL_00581 | 4.9e-159 | lgt | 2.1.1.199 | M | Transfers the N-acyl diglyceride group on what will become the N-terminal cysteine of membrane lipoproteins | |
NEADBANL_00582 | 5.8e-180 | 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 | ||
NEADBANL_00583 | 5.1e-17 | |||||
NEADBANL_00584 | 5.9e-188 | prfB | J | Peptide chain release factor 2 directs the termination of translation in response to the peptide chain termination codons UGA and UAA | ||
NEADBANL_00585 | 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 | ||
NEADBANL_00586 | 1.6e-94 | hpf | J | Required for dimerization of active 70S ribosomes into 100S ribosomes in stationary phase | ||
NEADBANL_00587 | 3.1e-135 | comFC | S | Competence protein | ||
NEADBANL_00588 | 3.6e-246 | comFA | L | Helicase C-terminal domain protein | ||
NEADBANL_00589 | 1.9e-118 | yvyE | 3.4.13.9 | S | YigZ family | |
NEADBANL_00590 | 1.3e-210 | tagO | 2.7.8.33, 2.7.8.35 | M | transferase | |
NEADBANL_00591 | 4.3e-220 | rny | S | Endoribonuclease that initiates mRNA decay | ||
NEADBANL_00592 | 8.5e-196 | 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 | ||
NEADBANL_00593 | 1.1e-95 | pgsA | 2.7.8.41, 2.7.8.5 | I | Belongs to the CDP-alcohol phosphatidyltransferase class-I family | |
NEADBANL_00594 | 5.2e-97 | ymfM | S | Helix-turn-helix domain | ||
NEADBANL_00595 | 1.4e-133 | IQ | Enoyl-(Acyl carrier protein) reductase | |||
NEADBANL_00596 | 2.1e-235 | S | Peptidase M16 | |||
NEADBANL_00597 | 1.7e-221 | 2.7.1.26, 2.7.7.2 | S | Peptidase M16 inactive domain protein | ||
NEADBANL_00598 | 0.0 | ftsK | D | Belongs to the FtsK SpoIIIE SftA family | ||
NEADBANL_00599 | 1.7e-69 | WQ51_03320 | S | Protein of unknown function (DUF1149) | ||
NEADBANL_00600 | 4.2e-106 | trmL | 2.1.1.207 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family. TrmL subfamily | |
NEADBANL_00601 | 2.6e-214 | yubA | S | AI-2E family transporter | ||
NEADBANL_00602 | 2.2e-66 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
NEADBANL_00603 | 8.2e-201 | pgl | 3.1.1.31 | G | Lactonase, 7-bladed beta-propeller | |
NEADBANL_00604 | 2.5e-92 | S | SNARE associated Golgi protein | |||
NEADBANL_00605 | 0.0 | mycA | 4.2.1.53 | S | Myosin-crossreactive antigen | |
NEADBANL_00606 | 6.4e-173 | rluD | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NEADBANL_00607 | 3.8e-153 | 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 | |
NEADBANL_00608 | 1.2e-114 | yjbM | 2.7.6.5 | S | RelA SpoT domain protein | |
NEADBANL_00609 | 3.6e-111 | yjbK | S | CYTH | ||
NEADBANL_00610 | 3.5e-114 | yjbH | Q | Thioredoxin | ||
NEADBANL_00611 | 5.8e-160 | coiA | 3.6.4.12 | S | Competence protein | |
NEADBANL_00612 | 7.2e-138 | mecA | NOT | Enables the recognition and targeting of unfolded and aggregated proteins to the ClpC protease or to other proteins involved in proteolysis | ||
NEADBANL_00613 | 6.1e-67 | 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 | |
NEADBANL_00614 | 0.0 | ptsI | 2.7.3.9 | G | General (non sugar-specific) component of the phosphoenolpyruvate-dependent sugar phosphotransferase system (sugar PTS). This major carbohydrate active-transport system catalyzes the phosphorylation of incoming sugar substrates concomitantly with their translocation across the cell membrane. Enzyme I transfers the phosphoryl group from phosphoenolpyruvate (PEP) to the phosphoryl carrier protein (HPr) | |
NEADBANL_00615 | 8.5e-41 | ptsH | G | phosphocarrier protein HPR | ||
NEADBANL_00616 | 5.3e-26 | |||||
NEADBANL_00617 | 0.0 | clpE | O | Belongs to the ClpA ClpB family | ||
NEADBANL_00618 | 2.3e-44 | XK27_09445 | S | Domain of unknown function (DUF1827) | ||
NEADBANL_00619 | 9.4e-305 | 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 | ||
NEADBANL_00620 | 1.1e-140 | hlyX | S | Transporter associated domain | ||
NEADBANL_00621 | 1.6e-74 | |||||
NEADBANL_00622 | 1.6e-85 | |||||
NEADBANL_00623 | 8.6e-145 | recX | 2.4.1.337 | GT4 | S | Regulatory protein RecX |
NEADBANL_00624 | 3e-262 | rumA | 2.1.1.190, 2.1.1.35 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NEADBANL_00625 | 1.5e-177 | D | Alpha beta | |||
NEADBANL_00626 | 9.4e-46 | |||||
NEADBANL_00627 | 4.2e-217 | mvaS | 2.3.3.10 | I | Hydroxymethylglutaryl-CoA synthase | |
NEADBANL_00628 | 1.2e-214 | mvaA | 1.1.1.34, 1.1.1.88, 2.3.1.9 | C | Belongs to the HMG-CoA reductase family | |
NEADBANL_00629 | 2.3e-215 | atoB | 1.1.1.88, 2.3.1.9 | I | Belongs to the thiolase family | |
NEADBANL_00630 | 7.3e-169 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NEADBANL_00631 | 3.6e-163 | yihY | S | Belongs to the UPF0761 family | ||
NEADBANL_00632 | 6.5e-164 | map | 3.4.11.18 | E | Methionine Aminopeptidase | |
NEADBANL_00633 | 4.1e-80 | fld | C | Flavodoxin | ||
NEADBANL_00634 | 3.1e-87 | gtcA | S | Teichoic acid glycosylation protein | ||
NEADBANL_00635 | 2e-216 | mnaA | 5.1.3.14 | G | Belongs to the UDP-N-acetylglucosamine 2-epimerase family | |
NEADBANL_00637 | 8e-249 | celB | 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 | ||
NEADBANL_00638 | 2.8e-211 | yfmL | 3.6.4.13 | L | DEAD DEAH box helicase | |
NEADBANL_00639 | 4.7e-131 | M | Glycosyl hydrolases family 25 | |||
NEADBANL_00640 | 2.8e-230 | potE | E | amino acid | ||
NEADBANL_00641 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
NEADBANL_00642 | 5.9e-89 | L | PFAM transposase, IS4 family protein | |||
NEADBANL_00643 | 0.0 | 1.3.5.4 | C | FAD binding domain | ||
NEADBANL_00644 | 8.9e-104 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NEADBANL_00645 | 2.3e-251 | yhdP | S | Transporter associated domain | ||
NEADBANL_00646 | 2.3e-119 | C | nitroreductase | |||
NEADBANL_00647 | 2.1e-39 | |||||
NEADBANL_00648 | 2.9e-87 | pts23A | G | phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 1 | ||
NEADBANL_00649 | 7e-81 | |||||
NEADBANL_00650 | 4.1e-147 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NEADBANL_00651 | 0.0 | glvC | 2.7.1.199, 2.7.1.208, 2.7.1.211 | G | phosphotransferase system, EIIB | |
NEADBANL_00652 | 1.2e-141 | S | hydrolase | |||
NEADBANL_00653 | 2.1e-157 | rssA | S | Phospholipase, patatin family | ||
NEADBANL_00654 | 0.0 | xfp | 4.1.2.22, 4.1.2.9 | G | Phosphoketolase | |
NEADBANL_00655 | 1.6e-137 | glcR | K | DeoR C terminal sensor domain | ||
NEADBANL_00656 | 1.9e-59 | S | Enterocin A Immunity | |||
NEADBANL_00657 | 1.2e-154 | S | hydrolase | |||
NEADBANL_00658 | 2.8e-134 | ydhQ | K | UbiC transcription regulator-associated domain protein | ||
NEADBANL_00659 | 2.8e-176 | rihB | 3.2.2.1 | F | Nucleoside | |
NEADBANL_00660 | 0.0 | kup | P | Transport of potassium into the cell | ||
NEADBANL_00661 | 2.6e-126 | rpiA | 2.7.1.12, 2.7.1.15, 5.3.1.6 | G | Catalyzes the reversible conversion of ribose-5- phosphate to ribulose 5-phosphate | |
NEADBANL_00662 | 5.9e-166 | 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 | |
NEADBANL_00663 | 1.7e-161 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
NEADBANL_00664 | 1e-235 | G | Bacterial extracellular solute-binding protein | |||
NEADBANL_00665 | 6.3e-212 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NEADBANL_00666 | 2.1e-85 | |||||
NEADBANL_00667 | 8e-38 | |||||
NEADBANL_00668 | 1.8e-110 | K | WHG domain | |||
NEADBANL_00669 | 2.4e-95 | nqr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
NEADBANL_00670 | 2e-97 | azr | 1.5.1.36 | S | NADPH-dependent FMN reductase | |
NEADBANL_00671 | 6e-151 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
NEADBANL_00672 | 2.5e-180 | 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 | |
NEADBANL_00673 | 3e-53 | cvpA | S | Colicin V production protein | ||
NEADBANL_00674 | 1.3e-111 | rsmG | 2.1.1.170 | J | Specifically methylates the N7 position of a guanine in 16S rRNA | |
NEADBANL_00675 | 8e-146 | noc | K | Belongs to the ParB family | ||
NEADBANL_00676 | 3.4e-138 | soj | D | Sporulation initiation inhibitor | ||
NEADBANL_00677 | 1.7e-154 | spo0J | K | Belongs to the ParB family | ||
NEADBANL_00678 | 9.6e-45 | yyzM | S | Bacterial protein of unknown function (DUF951) | ||
NEADBANL_00679 | 3.6e-202 | ychF | J | ATPase that binds to both the 70S ribosome and the 50S ribosomal subunit in a nucleotide-independent manner | ||
NEADBANL_00680 | 1.6e-135 | XK27_01040 | S | Protein of unknown function (DUF1129) | ||
NEADBANL_00681 | 7.4e-303 | V | ABC transporter, ATP-binding protein | |||
NEADBANL_00682 | 0.0 | V | ABC transporter | |||
NEADBANL_00684 | 9.6e-121 | K | response regulator | |||
NEADBANL_00685 | 4.6e-208 | hpk31 | 2.7.13.3 | T | His Kinase A (phospho-acceptor) domain | |
NEADBANL_00686 | 4.6e-304 | 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 | |
NEADBANL_00687 | 8e-145 | racD | 5.1.1.13 | M | Belongs to the aspartate glutamate racemases family | |
NEADBANL_00688 | 4e-53 | S | Enterocin A Immunity | |||
NEADBANL_00689 | 2.2e-33 | |||||
NEADBANL_00690 | 1.2e-25 | |||||
NEADBANL_00691 | 1e-24 | |||||
NEADBANL_00692 | 2.5e-272 | glcD2 | 1.1.3.15 | C | FAD linked oxidases, C-terminal domain | |
NEADBANL_00693 | 0.0 | malZ | 3.2.1.20 | GH31 | G | Belongs to the glycosyl hydrolase 31 family |
NEADBANL_00694 | 6e-255 | S | Archaea bacterial proteins of unknown function | |||
NEADBANL_00695 | 1.2e-16 | |||||
NEADBANL_00696 | 2.6e-138 | 2.7.13.3 | T | GHKL domain | ||
NEADBANL_00697 | 1.2e-127 | K | LytTr DNA-binding domain | |||
NEADBANL_00698 | 6.5e-238 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NEADBANL_00699 | 5.1e-139 | comA | V | ABC-type bacteriocin lantibiotic exporters, contain an N-terminal double-glycine peptidase domain | ||
NEADBANL_00700 | 2.4e-107 | M | Transport protein ComB | |||
NEADBANL_00701 | 2.2e-129 | blpT | ||||
NEADBANL_00705 | 8.8e-29 | cysE_1 | 2.3.1.30 | E | Bacterial transferase hexapeptide (six repeats) | |
NEADBANL_00706 | 3.1e-246 | cps1C | S | Membrane protein involved in the export of O-antigen and teichoic acid | ||
NEADBANL_00707 | 8.6e-204 | glf | 5.4.99.9 | M | UDP-galactopyranose mutase | |
NEADBANL_00708 | 7.1e-28 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
NEADBANL_00709 | 1e-12 | MA20_43635 | M | Capsular polysaccharide synthesis protein | ||
NEADBANL_00711 | 8.4e-49 | cps1D | M | Domain of unknown function (DUF4422) | ||
NEADBANL_00712 | 6.1e-189 | M | Glycosyl transferases group 1 | |||
NEADBANL_00713 | 9e-43 | GT2 | M | transferase activity, transferring glycosyl groups | ||
NEADBANL_00714 | 3.4e-149 | M | Glycosyl transferases group 1 | |||
NEADBANL_00715 | 2.3e-172 | M | Glycosyl transferases group 1 | |||
NEADBANL_00716 | 3.2e-113 | rfbP | M | Bacterial sugar transferase | ||
NEADBANL_00717 | 2.2e-145 | ywqE | 3.1.3.48 | GM | PHP domain protein | |
NEADBANL_00718 | 2.7e-119 | ywqD | 2.7.10.1 | D | Capsular exopolysaccharide family | |
NEADBANL_00719 | 7.6e-147 | epsB | M | biosynthesis protein | ||
NEADBANL_00720 | 1.4e-176 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NEADBANL_00721 | 1.3e-47 | yoeB | S | YoeB-like toxin of bacterial type II toxin-antitoxin system | ||
NEADBANL_00722 | 1.3e-41 | relB | L | RelB antitoxin | ||
NEADBANL_00724 | 1.4e-221 | hflX | S | GTPase that associates with the 50S ribosomal subunit and may have a role during protein synthesis or ribosome biogenesis | ||
NEADBANL_00725 | 3.3e-173 | S | Cysteine-rich secretory protein family | |||
NEADBANL_00727 | 3.5e-41 | |||||
NEADBANL_00728 | 2.6e-118 | M | NlpC/P60 family | |||
NEADBANL_00729 | 1.4e-136 | M | NlpC P60 family protein | |||
NEADBANL_00730 | 1e-80 | M | NlpC/P60 family | |||
NEADBANL_00731 | 4.6e-94 | gmk2 | 2.7.4.8 | F | Guanylate kinase homologues. | |
NEADBANL_00732 | 2.3e-42 | |||||
NEADBANL_00733 | 1.4e-278 | S | O-antigen ligase like membrane protein | |||
NEADBANL_00734 | 3.7e-111 | |||||
NEADBANL_00735 | 1.9e-77 | nrdI | F | NrdI Flavodoxin like | ||
NEADBANL_00736 | 7.8e-174 | nrdF | 1.17.4.1 | F | Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides | |
NEADBANL_00737 | 4.3e-76 | |||||
NEADBANL_00738 | 4.5e-111 | yvpB | S | Peptidase_C39 like family | ||
NEADBANL_00739 | 7.3e-83 | S | Threonine/Serine exporter, ThrE | |||
NEADBANL_00740 | 4.8e-137 | thrE | S | Putative threonine/serine exporter | ||
NEADBANL_00741 | 1.4e-289 | S | ABC transporter | |||
NEADBANL_00742 | 2.5e-62 | |||||
NEADBANL_00743 | 8.4e-102 | rimL | J | Acetyltransferase (GNAT) domain | ||
NEADBANL_00744 | 5.3e-98 | |||||
NEADBANL_00745 | 6.5e-125 | S | Protein of unknown function (DUF554) | |||
NEADBANL_00746 | 4.4e-209 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NEADBANL_00747 | 0.0 | pepF | E | oligoendopeptidase F | ||
NEADBANL_00748 | 2.9e-31 | |||||
NEADBANL_00749 | 1.3e-69 | doc | S | Prophage maintenance system killer protein | ||
NEADBANL_00750 | 1.5e-136 | S | CAAX amino terminal protease | |||
NEADBANL_00751 | 5.3e-26 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00752 | 2.6e-11 | |||||
NEADBANL_00753 | 1.2e-213 | 2.1.1.14 | E | methionine synthase, vitamin-B12 independent | ||
NEADBANL_00754 | 6.1e-90 | luxS | 4.4.1.21 | H | Involved in the synthesis of autoinducer 2 (AI-2) which is secreted by bacteria and is used to communicate both the cell density and the metabolic potential of the environment. The regulation of gene expression in response to changes in cell density is called quorum sensing. Catalyzes the transformation of S-ribosylhomocysteine (RHC) to homocysteine (HC) and 4,5- dihydroxy-2,3-pentadione (DPD) | |
NEADBANL_00755 | 1.7e-263 | lctP | C | L-lactate permease | ||
NEADBANL_00756 | 3.2e-128 | znuB | U | ABC 3 transport family | ||
NEADBANL_00757 | 1.6e-117 | fhuC | P | ABC transporter | ||
NEADBANL_00758 | 9.2e-148 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NEADBANL_00759 | 5.4e-41 | K | helix_turn_helix, Arsenical Resistance Operon Repressor | |||
NEADBANL_00760 | 0.0 | fruA | 2.7.1.202, 2.7.1.204 | GT | Phosphotransferase System | |
NEADBANL_00761 | 4.2e-43 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
NEADBANL_00762 | 1.2e-109 | pfkB | 2.7.1.11, 2.7.1.56 | H | Belongs to the carbohydrate kinase PfkB family. LacC subfamily | |
NEADBANL_00763 | 1.8e-136 | fruR | K | DeoR C terminal sensor domain | ||
NEADBANL_00764 | 2.7e-219 | natB | CP | ABC-2 family transporter protein | ||
NEADBANL_00765 | 9.2e-164 | natA | S | ABC transporter, ATP-binding protein | ||
NEADBANL_00766 | 4.9e-29 | |||||
NEADBANL_00767 | 3.6e-08 | |||||
NEADBANL_00768 | 4.4e-68 | |||||
NEADBANL_00769 | 1.3e-13 | |||||
NEADBANL_00770 | 8.2e-31 | yozG | K | Transcriptional regulator | ||
NEADBANL_00771 | 3.1e-82 | |||||
NEADBANL_00772 | 1.5e-95 | V | ABC transporter | |||
NEADBANL_00773 | 3e-123 | S | domain protein | |||
NEADBANL_00774 | 1.8e-43 | yyaR | K | Acetyltransferase (GNAT) domain | ||
NEADBANL_00775 | 3.5e-48 | yyaR | K | Acetyltransferase (GNAT) domain | ||
NEADBANL_00776 | 1.1e-72 | 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 | ||
NEADBANL_00777 | 8.1e-28 | rpmI | J | Belongs to the bacterial ribosomal protein bL35 family | ||
NEADBANL_00778 | 3e-57 | 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 | ||
NEADBANL_00779 | 3.3e-154 | add | 3.5.4.4 | F | Catalyzes the hydrolytic deamination of adenine to hypoxanthine. Plays an important role in the purine salvage pathway and in nitrogen catabolism | |
NEADBANL_00780 | 5.5e-84 | yqeG | S | HAD phosphatase, family IIIA | ||
NEADBANL_00781 | 8e-202 | yqeH | S | Ribosome biogenesis GTPase YqeH | ||
NEADBANL_00782 | 2.5e-118 | nadD | 2.7.7.18, 3.6.1.55 | H | Catalyzes the reversible adenylation of nicotinate mononucleotide (NaMN) to nicotinic acid adenine dinucleotide (NaAD) | |
NEADBANL_00783 | 1.9e-109 | nadD | 2.7.6.3, 2.7.7.18 | H | Hydrolase, HD family | |
NEADBANL_00784 | 5.3e-59 | 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 | ||
NEADBANL_00785 | 1.2e-216 | ylbM | S | Belongs to the UPF0348 family | ||
NEADBANL_00786 | 5.5e-98 | yceD | S | Uncharacterized ACR, COG1399 | ||
NEADBANL_00787 | 2.7e-126 | K | response regulator | |||
NEADBANL_00788 | 1.3e-277 | arlS | 2.7.13.3 | T | Histidine kinase | |
NEADBANL_00789 | 1.6e-99 | S | CAAX protease self-immunity | |||
NEADBANL_00790 | 1.6e-224 | S | SLAP domain | |||
NEADBANL_00791 | 2.5e-86 | S | Aminoacyl-tRNA editing domain | |||
NEADBANL_00792 | 2.9e-163 | 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 | ||
NEADBANL_00793 | 2.9e-44 | acyP | 3.6.1.7 | C | Belongs to the acylphosphatase family | |
NEADBANL_00794 | 2.3e-139 | spoU | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NEADBANL_00795 | 3.6e-63 | yodB | K | Transcriptional regulator, HxlR family | ||
NEADBANL_00797 | 5.1e-111 | papP | P | ABC transporter, permease protein | ||
NEADBANL_00798 | 3.1e-116 | P | ABC transporter permease | |||
NEADBANL_00799 | 9.7e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NEADBANL_00800 | 2.9e-162 | cjaA | ET | ABC transporter substrate-binding protein | ||
NEADBANL_00801 | 2.7e-199 | pheS | 6.1.1.20 | J | Belongs to the class-II aminoacyl-tRNA synthetase family. Phe-tRNA synthetase alpha subunit type 1 subfamily | |
NEADBANL_00802 | 0.0 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NEADBANL_00803 | 4.9e-63 | 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 | ||
NEADBANL_00804 | 1.6e-168 | ldh | 1.1.1.27 | C | lactate/malate dehydrogenase, alpha/beta C-terminal domain | |
NEADBANL_00805 | 1.6e-157 | metQ1 | P | Belongs to the nlpA lipoprotein family | ||
NEADBANL_00806 | 5.7e-25 | |||||
NEADBANL_00807 | 0.0 | mco | Q | Multicopper oxidase | ||
NEADBANL_00808 | 1.2e-151 | S | Sucrose-6F-phosphate phosphohydrolase | |||
NEADBANL_00809 | 0.0 | oppA | E | ABC transporter | ||
NEADBANL_00810 | 1.8e-231 | Q | Imidazolonepropionase and related amidohydrolases | |||
NEADBANL_00811 | 3.8e-248 | 3.5.1.47 | S | Peptidase dimerisation domain | ||
NEADBANL_00812 | 1.6e-138 | S | Protein of unknown function (DUF3100) | |||
NEADBANL_00813 | 4.4e-83 | S | An automated process has identified a potential problem with this gene model | |||
NEADBANL_00814 | 2.9e-47 | S | Uncharacterized protein conserved in bacteria (DUF2263) | |||
NEADBANL_00815 | 2.2e-113 | S | SLAP domain | |||
NEADBANL_00816 | 1.9e-88 | |||||
NEADBANL_00817 | 1.1e-08 | isdH | M | Iron Transport-associated domain | ||
NEADBANL_00818 | 1e-109 | M | Iron Transport-associated domain | |||
NEADBANL_00819 | 6.7e-159 | isdE | P | Periplasmic binding protein | ||
NEADBANL_00820 | 2.5e-148 | isdF | U | Belongs to the binding-protein-dependent transport system permease family. FecCD subfamily | ||
NEADBANL_00821 | 4.7e-140 | fhuC | 3.6.3.34 | HP | abc transporter atp-binding protein | |
NEADBANL_00822 | 6.7e-44 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
NEADBANL_00823 | 1.2e-51 | S | Bacterial toxin of type II toxin-antitoxin system, YafQ | |||
NEADBANL_00824 | 1.3e-38 | S | RelB antitoxin | |||
NEADBANL_00825 | 5.2e-170 | 2.7.1.59 | G | BadF/BadG/BcrA/BcrD ATPase family | ||
NEADBANL_00826 | 0.0 | S | membrane | |||
NEADBANL_00827 | 0.0 | pbp2b | 3.4.16.4 | M | Penicillin-binding Protein | |
NEADBANL_00828 | 1.2e-20 | rpmG | J | Belongs to the bacterial ribosomal protein bL33 family | ||
NEADBANL_00829 | 2.1e-97 | ygfA | 6.3.3.2 | H | Belongs to the 5-formyltetrahydrofolate cyclo-ligase family | |
NEADBANL_00830 | 3.1e-119 | gluP | 3.4.21.105 | S | Rhomboid family | |
NEADBANL_00831 | 9.7e-36 | yqgQ | S | Bacterial protein of unknown function (DUF910) | ||
NEADBANL_00832 | 1.5e-65 | yqhL | P | Rhodanese-like protein | ||
NEADBANL_00833 | 1.2e-169 | 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) | |
NEADBANL_00834 | 7.6e-225 | ynbB | 4.4.1.1 | P | aluminum resistance | |
NEADBANL_00835 | 2e-263 | glnA | 6.3.1.2 | E | glutamine synthetase | |
NEADBANL_00836 | 5.1e-170 | |||||
NEADBANL_00837 | 6e-148 | |||||
NEADBANL_00838 | 9.1e-59 | L | An automated process has identified a potential problem with this gene model | |||
NEADBANL_00839 | 3.6e-25 | L | An automated process has identified a potential problem with this gene model | |||
NEADBANL_00840 | 1.3e-252 | E | Amino acid permease | |||
NEADBANL_00841 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
NEADBANL_00842 | 9.8e-109 | yisY | 1.11.1.10 | S | Alpha/beta hydrolase family | |
NEADBANL_00843 | 8.7e-107 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NEADBANL_00844 | 6.1e-111 | crt | 4.2.1.17 | I | Enoyl-CoA hydratase/isomerase | |
NEADBANL_00845 | 1.1e-07 | arbV | 2.3.1.51 | I | Acyl-transferase | |
NEADBANL_00846 | 3.1e-115 | arbV | 2.3.1.51 | I | Acyl-transferase | |
NEADBANL_00847 | 4.3e-71 | arbx | M | Glycosyl transferase family 8 | ||
NEADBANL_00848 | 1.3e-75 | arbx | M | Glycosyl transferase family 8 | ||
NEADBANL_00849 | 4.5e-185 | arbY | M | Glycosyl transferase family 8 | ||
NEADBANL_00850 | 3.9e-181 | arbY | M | Glycosyl transferase family 8 | ||
NEADBANL_00851 | 1.7e-167 | arbZ | I | Phosphate acyltransferases | ||
NEADBANL_00852 | 1.4e-36 | S | Cytochrome B5 | |||
NEADBANL_00853 | 1.2e-257 | L | Putative transposase DNA-binding domain | |||
NEADBANL_00854 | 6e-114 | L | Resolvase, N-terminal | |||
NEADBANL_00855 | 3.9e-165 | S | Protein of unknown function (DUF2974) | |||
NEADBANL_00856 | 4.7e-109 | glnP | P | ABC transporter permease | ||
NEADBANL_00857 | 9.7e-91 | gluC | P | ABC transporter permease | ||
NEADBANL_00858 | 2.4e-150 | glnH | ET | ABC transporter substrate-binding protein | ||
NEADBANL_00859 | 1.9e-135 | glnQ | 3.6.3.21 | E | ABC transporter, ATP-binding protein | |
NEADBANL_00860 | 3.6e-114 | udk | 2.7.1.48 | F | Zeta toxin | |
NEADBANL_00861 | 3.3e-253 | G | MFS/sugar transport protein | |||
NEADBANL_00862 | 3.5e-100 | S | ABC-type cobalt transport system, permease component | |||
NEADBANL_00863 | 0.0 | V | ABC transporter transmembrane region | |||
NEADBANL_00864 | 2.9e-310 | XK27_09600 | V | ABC transporter, ATP-binding protein | ||
NEADBANL_00865 | 1.4e-80 | K | Transcriptional regulator, MarR family | |||
NEADBANL_00866 | 7.1e-147 | glnH | ET | ABC transporter | ||
NEADBANL_00867 | 4.9e-130 | yfeJ | 6.3.5.2 | F | glutamine amidotransferase | |
NEADBANL_00868 | 9.9e-115 | steT | E | amino acid | ||
NEADBANL_00869 | 1e-93 | steT | E | amino acid | ||
NEADBANL_00870 | 2.3e-240 | steT | E | amino acid | ||
NEADBANL_00871 | 6.1e-151 | |||||
NEADBANL_00872 | 5.9e-174 | S | Aldo keto reductase | |||
NEADBANL_00873 | 1.1e-310 | ybiT | S | ABC transporter, ATP-binding protein | ||
NEADBANL_00874 | 6e-210 | pepA | E | M42 glutamyl aminopeptidase | ||
NEADBANL_00875 | 1.2e-103 | |||||
NEADBANL_00876 | 3.7e-137 | |||||
NEADBANL_00877 | 1.1e-217 | mdtG | EGP | Major facilitator Superfamily | ||
NEADBANL_00878 | 9.2e-262 | emrY | EGP | Major facilitator Superfamily | ||
NEADBANL_00879 | 4.7e-91 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NEADBANL_00880 | 2.9e-238 | pyrP | F | Permease | ||
NEADBANL_00881 | 2.2e-290 | K | Putative DNA-binding domain | |||
NEADBANL_00882 | 9.3e-35 | |||||
NEADBANL_00883 | 7.8e-157 | S | reductase | |||
NEADBANL_00884 | 3.4e-60 | 6.3.2.4 | 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 | ||
NEADBANL_00885 | 3.1e-61 | exuT | G | Major Facilitator Superfamily | ||
NEADBANL_00886 | 7.4e-20 | F | ATP-grasp domain | |||
NEADBANL_00887 | 4.1e-07 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NEADBANL_00888 | 1.5e-09 | yjjG | 3.1.3.102, 3.1.3.104, 3.8.1.2 | S | HAD hydrolase, TIGR02254 family | |
NEADBANL_00889 | 9.4e-11 | S | DNA polymerase beta domain protein region | |||
NEADBANL_00890 | 1.6e-227 | L | COG3547 Transposase and inactivated derivatives | |||
NEADBANL_00891 | 3.5e-299 | oppA2 | E | ABC transporter, substratebinding protein | ||
NEADBANL_00892 | 1.1e-179 | |||||
NEADBANL_00893 | 5e-125 | gntR1 | K | UTRA | ||
NEADBANL_00894 | 1.5e-70 | tagD | 2.7.7.15, 2.7.7.39 | IM | Glycerol-3-phosphate cytidylyltransferase | |
NEADBANL_00895 | 7.3e-135 | tagA | 2.4.1.187 | GT26 | F | Catalyzes the conversion of GlcNAc-PP-undecaprenol into ManNAc-GlcNAc-PP-undecaprenol, the first committed lipid intermediate in the de novo synthesis of teichoic acid |
NEADBANL_00896 | 2.9e-204 | csaB | M | Glycosyl transferases group 1 | ||
NEADBANL_00897 | 2.7e-285 | pncB | 6.3.4.21 | F | Catalyzes the synthesis of beta-nicotinate D- ribonucleotide from nicotinate and 5-phospho-D-ribose 1-phosphate at the expense of ATP | |
NEADBANL_00898 | 1.2e-152 | nadE | 6.3.1.5 | F | Catalyzes the ATP-dependent amidation of deamido-NAD to form NAD. Uses ammonia as a nitrogen source | |
NEADBANL_00899 | 0.0 | pacL | 3.6.3.8 | P | P-type ATPase | |
NEADBANL_00900 | 3.5e-224 | M | CDP-Glycerol:Poly(glycerophosphate) glycerophosphotransferase | |||
NEADBANL_00901 | 4.9e-260 | epsU | S | Polysaccharide biosynthesis protein | ||
NEADBANL_00902 | 3.5e-134 | M | Glycosyltransferase sugar-binding region containing DXD motif | |||
NEADBANL_00903 | 5.7e-85 | ydcK | S | Belongs to the SprT family | ||
NEADBANL_00905 | 1.2e-85 | acmC | 3.2.1.17, 3.2.1.96 | NU | mannosyl-glycoprotein | |
NEADBANL_00906 | 0.0 | pcrA | 3.6.4.12 | L | ATP-dependent DNA helicase | |
NEADBANL_00907 | 0.0 | ligA | 6.5.1.2 | L | DNA ligase that catalyzes the formation of phosphodiester linkages between 5'-phosphoryl and 3'-hydroxyl groups in double-stranded DNA using NAD as a coenzyme and as the energy source for the reaction. It is essential for DNA replication and repair of damaged DNA | |
NEADBANL_00908 | 5.8e-203 | camS | S | sex pheromone | ||
NEADBANL_00909 | 1.5e-49 | 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) | |
NEADBANL_00910 | 3.4e-269 | 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) | |
NEADBANL_00911 | 4.1e-275 | 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) | |
NEADBANL_00912 | 7.2e-172 | yegS | 2.7.1.107 | G | Lipid kinase | |
NEADBANL_00913 | 6.9e-106 | ybhL | S | Belongs to the BI1 family | ||
NEADBANL_00914 | 5.9e-50 | |||||
NEADBANL_00915 | 8.3e-117 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
NEADBANL_00916 | 2e-226 | nhaC | C | Na H antiporter NhaC | ||
NEADBANL_00917 | 6.3e-201 | pbpX | V | Beta-lactamase | ||
NEADBANL_00918 | 8.4e-254 | rumA | 2.1.1.190 | J | Belongs to the class I-like SAM-binding methyltransferase superfamily. RNA M5U methyltransferase family | |
NEADBANL_00919 | 1.1e-94 | MA20_25245 | K | Acetyltransferase (GNAT) domain | ||
NEADBANL_00924 | 8.5e-260 | emrY | EGP | Major facilitator Superfamily | ||
NEADBANL_00925 | 2e-91 | yxdD | K | Bacterial regulatory proteins, tetR family | ||
NEADBANL_00926 | 0.0 | 4.2.1.53 | S | Myosin-crossreactive antigen | ||
NEADBANL_00927 | 1.4e-84 | L | the current gene model (or a revised gene model) may contain a | |||
NEADBANL_00928 | 1.7e-62 | V | Abi-like protein | |||
NEADBANL_00929 | 0.0 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
NEADBANL_00930 | 4.9e-69 | S | HicB_like antitoxin of bacterial toxin-antitoxin system | |||
NEADBANL_00931 | 2e-42 | S | RelB antitoxin | |||
NEADBANL_00932 | 1.1e-52 | |||||
NEADBANL_00933 | 2.9e-61 | |||||
NEADBANL_00934 | 4.1e-51 | |||||
NEADBANL_00935 | 8.8e-73 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
NEADBANL_00936 | 3.1e-17 | pac | 3.5.1.24 | M | Linear amide C-N hydrolases, choloylglycine hydrolase family | |
NEADBANL_00938 | 6.5e-107 | 3.2.2.20 | K | acetyltransferase | ||
NEADBANL_00939 | 3.9e-93 | hpt | 2.4.2.8 | F | Belongs to the purine pyrimidine phosphoribosyltransferase family | |
NEADBANL_00940 | 1.9e-23 | |||||
NEADBANL_00941 | 1.8e-153 | |||||
NEADBANL_00942 | 2.3e-267 | aglB | 3.2.1.122, 3.2.1.86 | GH4,GT4 | G | Family 4 glycosyl hydrolase C-terminal domain |
NEADBANL_00943 | 1.8e-136 | glvR | K | Helix-turn-helix domain, rpiR family | ||
NEADBANL_00944 | 4.2e-186 | ansA | 3.5.1.1 | EJ | L-asparaginase, type I | |
NEADBANL_00945 | 7.7e-09 | |||||
NEADBANL_00946 | 3.6e-42 | |||||
NEADBANL_00947 | 1.9e-65 | 2.7.1.191 | G | PTS system fructose IIA component | ||
NEADBANL_00948 | 0.0 | 3.6.3.8 | P | P-type ATPase | ||
NEADBANL_00949 | 1.9e-124 | |||||
NEADBANL_00950 | 1.2e-241 | S | response to antibiotic | |||
NEADBANL_00951 | 1.4e-126 | pgm3 | G | Phosphoglycerate mutase family | ||
NEADBANL_00952 | 2.1e-117 | XK27_08875 | O | PFAM peptidase M10A and M12B, matrixin and adamalysin | ||
NEADBANL_00953 | 0.0 | helD | 3.6.4.12 | L | DNA helicase | |
NEADBANL_00954 | 3.2e-110 | glnP | P | ABC transporter permease | ||
NEADBANL_00955 | 7.1e-107 | glnQ | 3.6.3.21 | E | ABC transporter | |
NEADBANL_00956 | 7.3e-144 | aatB | ET | ABC transporter substrate-binding protein | ||
NEADBANL_00957 | 1.8e-62 | yjcF | S | Acetyltransferase (GNAT) domain | ||
NEADBANL_00958 | 5.2e-73 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_00960 | 6.8e-108 | 2.7.7.73, 2.7.7.80 | H | ThiF family | ||
NEADBANL_00962 | 1.5e-16 | S | Putative adhesin | |||
NEADBANL_00963 | 7.2e-82 | E | GDSL-like Lipase/Acylhydrolase | |||
NEADBANL_00964 | 2.3e-170 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NEADBANL_00965 | 4.4e-103 | efp | J | Involved in peptide bond synthesis. Stimulates efficient translation and peptide-bond synthesis on native or reconstituted 70S ribosomes in vitro. Probably functions indirectly by altering the affinity of the ribosome for aminoacyl-tRNA, thus increasing their reactivity as acceptors for peptidyl transferase | ||
NEADBANL_00966 | 1.5e-101 | S | Peptidase propeptide and YPEB domain | |||
NEADBANL_00967 | 3.8e-61 | ypaA | S | Protein of unknown function (DUF1304) | ||
NEADBANL_00968 | 1.5e-308 | oppA3 | E | ABC transporter, substratebinding protein | ||
NEADBANL_00969 | 1.4e-239 | V | ABC transporter transmembrane region | |||
NEADBANL_00970 | 8.5e-65 | yybA | 2.3.1.57 | K | Transcriptional regulator | |
NEADBANL_00971 | 4.7e-83 | paiA | 2.3.1.57 | K | Acetyltransferase (GNAT) domain | |
NEADBANL_00972 | 2.5e-72 | S | Peptidase propeptide and YPEB domain | |||
NEADBANL_00973 | 3.4e-76 | S | Peptidase propeptide and YPEB domain | |||
NEADBANL_00974 | 7.4e-186 | T | GHKL domain | |||
NEADBANL_00975 | 7e-130 | T | Transcriptional regulatory protein, C terminal | |||
NEADBANL_00976 | 2.1e-179 | pip | 3.4.11.5 | E | Releases the N-terminal proline from various substrates | |
NEADBANL_00977 | 5.6e-281 | V | ABC transporter transmembrane region | |||
NEADBANL_00978 | 1.1e-138 | S | PAS domain | |||
NEADBANL_00979 | 1.3e-34 | |||||
NEADBANL_00980 | 1.9e-158 | bglG2 | K | CAT RNA binding domain | ||
NEADBANL_00981 | 0.0 | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | ||
NEADBANL_00982 | 1.1e-294 | arbB | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NEADBANL_00983 | 7.6e-140 | pnuC | H | nicotinamide mononucleotide transporter | ||
NEADBANL_00984 | 1.1e-72 | S | Protein of unknown function (DUF3290) | |||
NEADBANL_00985 | 3e-116 | yviA | S | Protein of unknown function (DUF421) | ||
NEADBANL_00986 | 2.4e-158 | K | NAD-dependent lysine deacetylase and desuccinylase that specifically removes acetyl and succinyl groups on target proteins. Modulates the activities of several proteins which are inactive in their acylated form | |||
NEADBANL_00987 | 6.1e-182 | dnaQ | 2.7.7.7 | L | EXOIII | |
NEADBANL_00988 | 1.9e-158 | endA | F | DNA RNA non-specific endonuclease | ||
NEADBANL_00989 | 2.7e-282 | pipD | E | Dipeptidase | ||
NEADBANL_00990 | 1.9e-203 | malK | P | ATPases associated with a variety of cellular activities | ||
NEADBANL_00991 | 1.6e-157 | gtsB | P | ABC-type sugar transport systems, permease components | ||
NEADBANL_00992 | 6.1e-146 | gtsC | P | Binding-protein-dependent transport system inner membrane component | ||
NEADBANL_00993 | 2.4e-258 | YSH1 | S | Zn-dependent metallo-hydrolase RNA specificity domain | ||
NEADBANL_00994 | 2.5e-239 | G | Bacterial extracellular solute-binding protein | |||
NEADBANL_00995 | 1.8e-154 | corA | P | CorA-like Mg2+ transporter protein | ||
NEADBANL_00996 | 2e-148 | 3.5.2.6 | V | Beta-lactamase enzyme family | ||
NEADBANL_00997 | 6.6e-99 | yobS | K | Bacterial regulatory proteins, tetR family | ||
NEADBANL_00998 | 0.0 | ydgH | S | MMPL family | ||
NEADBANL_00999 | 2e-162 | |||||
NEADBANL_01000 | 3.6e-171 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
NEADBANL_01001 | 6.6e-262 | gabD | 1.2.1.16, 1.2.1.20, 1.2.1.79 | C | Belongs to the aldehyde dehydrogenase family | |
NEADBANL_01002 | 5.4e-89 | F | Nucleoside 2-deoxyribosyltransferase | |||
NEADBANL_01003 | 1.3e-148 | hipB | K | Helix-turn-helix | ||
NEADBANL_01004 | 1.9e-152 | I | alpha/beta hydrolase fold | |||
NEADBANL_01005 | 2.6e-109 | yjbF | S | SNARE associated Golgi protein | ||
NEADBANL_01006 | 7.5e-100 | J | Acetyltransferase (GNAT) domain | |||
NEADBANL_01007 | 2.1e-249 | 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) | |
NEADBANL_01008 | 4.4e-12 | UW | LPXTG-motif cell wall anchor domain protein | |||
NEADBANL_01009 | 3.3e-45 | UW | LPXTG-motif cell wall anchor domain protein | |||
NEADBANL_01010 | 0.0 | UW | LPXTG-motif cell wall anchor domain protein | |||
NEADBANL_01011 | 0.0 | pepN | 3.4.11.2 | E | aminopeptidase | |
NEADBANL_01012 | 1.8e-241 | dtpT | U | amino acid peptide transporter | ||
NEADBANL_01013 | 1.7e-70 | XK27_02470 | K | LytTr DNA-binding domain | ||
NEADBANL_01014 | 1e-91 | liaI | S | membrane | ||
NEADBANL_01015 | 6.9e-191 | S | Putative peptidoglycan binding domain | |||
NEADBANL_01016 | 2.5e-157 | 2.7.7.12 | C | Domain of unknown function (DUF4931) | ||
NEADBANL_01017 | 7.6e-120 | |||||
NEADBANL_01018 | 3.4e-143 | S | Belongs to the UPF0246 family | |||
NEADBANL_01019 | 4.9e-142 | aroD | S | Alpha/beta hydrolase family | ||
NEADBANL_01020 | 5.5e-112 | G | phosphoglycerate mutase | |||
NEADBANL_01021 | 3.1e-95 | ygfC | K | Bacterial regulatory proteins, tetR family | ||
NEADBANL_01022 | 4.7e-175 | hrtB | V | ABC transporter permease | ||
NEADBANL_01023 | 1.5e-102 | devA | 3.6.3.25 | V | ABC transporter, ATP-binding protein | |
NEADBANL_01024 | 8.2e-276 | pipD | E | Dipeptidase | ||
NEADBANL_01025 | 1.4e-180 | lacX | 5.1.3.3 | G | Aldose 1-epimerase | |
NEADBANL_01026 | 1.4e-74 | C | Aldo keto reductase | |||
NEADBANL_01027 | 3.7e-44 | S | aldo-keto reductase (NADP) activity | |||
NEADBANL_01028 | 1.9e-63 | M | LysM domain protein | |||
NEADBANL_01029 | 2.5e-152 | xerD | L | Phage integrase, N-terminal SAM-like domain | ||
NEADBANL_01030 | 7.9e-67 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NEADBANL_01031 | 9.2e-65 | crcB | U | Important for reducing fluoride concentration in the cell, thus reducing its toxicity | ||
NEADBANL_01032 | 1.7e-14 | dapD | 2.3.1.117, 2.3.1.89 | E | Catalyzes the transfer of an acetyl group from acetyl- CoA to tetrahydrodipicolinate | |
NEADBANL_01033 | 1.1e-220 | hipO | 3.5.1.47 | E | Catalyzes the conversion of N-acetyl-diaminopimelate to diaminopimelate and acetate | |
NEADBANL_01034 | 2.8e-176 | dapA | 4.3.3.7 | E | Catalyzes the condensation of (S)-aspartate-beta- semialdehyde (S)-ASA and pyruvate to 4-hydroxy- tetrahydrodipicolinate (HTPA) | |
NEADBANL_01035 | 3.5e-143 | dapB | 1.17.1.8 | E | Catalyzes the conversion of 4-hydroxy- tetrahydrodipicolinate (HTPA) to tetrahydrodipicolinate | |
NEADBANL_01036 | 3.8e-218 | aspC | 2.6.1.1 | E | Aminotransferase | |
NEADBANL_01037 | 1e-198 | asd | 1.2.1.11 | E | Catalyzes the NADPH-dependent formation of L-aspartate- semialdehyde (L-ASA) by the reductive dephosphorylation of L- aspartyl-4-phosphate | |
NEADBANL_01038 | 3.8e-196 | pbpX1 | V | Beta-lactamase | ||
NEADBANL_01039 | 5.1e-298 | I | Protein of unknown function (DUF2974) | |||
NEADBANL_01040 | 4e-38 | C | FMN_bind | |||
NEADBANL_01041 | 2.3e-82 | |||||
NEADBANL_01042 | 1.3e-176 | iunH | 3.2.2.1 | F | inosine-uridine preferring nucleoside hydrolase | |
NEADBANL_01043 | 2.4e-89 | alkD | L | DNA alkylation repair enzyme | ||
NEADBANL_01044 | 2.4e-294 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NEADBANL_01045 | 1.4e-127 | K | UTRA domain | |||
NEADBANL_01046 | 1.6e-55 | celA1 | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NEADBANL_01047 | 8.7e-60 | chbA | 2.7.1.196, 2.7.1.205 | G | PTS system, Lactose Cellobiose specific IIA subunit | |
NEADBANL_01048 | 2.8e-85 | |||||
NEADBANL_01049 | 7.4e-250 | celD | 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 | ||
NEADBANL_01050 | 3.2e-71 | S | Domain of unknown function (DUF3284) | |||
NEADBANL_01051 | 3.5e-301 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family | |
NEADBANL_01052 | 1.2e-118 | gmuR | K | UTRA | ||
NEADBANL_01053 | 4.4e-142 | pts23C | 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 | ||
NEADBANL_01054 | 2.2e-72 | pts23C | 2.7.1.207 | 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 | |
NEADBANL_01055 | 7e-272 | bglA3 | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NEADBANL_01056 | 4.1e-137 | ypbG | 2.7.1.2 | GK | ROK family | |
NEADBANL_01057 | 1.2e-85 | C | nitroreductase | |||
NEADBANL_01058 | 1.1e-86 | S | Domain of unknown function (DUF4767) | |||
NEADBANL_01059 | 1.5e-244 | 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 | |
NEADBANL_01060 | 1.1e-147 | yitS | S | Uncharacterised protein, DegV family COG1307 | ||
NEADBANL_01061 | 2.2e-102 | 3.6.1.27 | I | Acid phosphatase homologues | ||
NEADBANL_01062 | 1.6e-190 | cbh | 3.5.1.24 | M | Linear amide C-N hydrolase, choloylglycine hydrolase family protein | |
NEADBANL_01064 | 1.5e-178 | MA20_14895 | S | Conserved hypothetical protein 698 | ||
NEADBANL_01065 | 1.2e-85 | dps | P | Belongs to the Dps family | ||
NEADBANL_01066 | 1.1e-14 | K | Acetyltransferase (GNAT) domain | |||
NEADBANL_01067 | 1.6e-18 | 1.3.5.4 | C | FAD dependent oxidoreductase | ||
NEADBANL_01068 | 2e-106 | yihX | 3.1.3.10, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | |
NEADBANL_01069 | 3.8e-70 | S | Putative adhesin | |||
NEADBANL_01070 | 1.7e-78 | yjaB | 2.3.1.181 | K | Acetyltransferase (GNAT) domain | |
NEADBANL_01071 | 4.6e-236 | mepA | V | MATE efflux family protein | ||
NEADBANL_01072 | 5e-102 | S | SLAP domain | |||
NEADBANL_01073 | 1.6e-50 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NEADBANL_01074 | 1.1e-25 | |||||
NEADBANL_01075 | 4.7e-77 | K | DNA-templated transcription, initiation | |||
NEADBANL_01076 | 2e-75 | S | SLAP domain | |||
NEADBANL_01077 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NEADBANL_01078 | 1.3e-210 | patA | 2.6.1.1, 2.6.1.57 | E | Aminotransferase | |
NEADBANL_01079 | 6.1e-185 | XK27_10475 | S | Oxidoreductase family, NAD-binding Rossmann fold | ||
NEADBANL_01080 | 2.1e-123 | rpiA | 5.3.1.6 | G | Ribose 5-phosphate isomerase A (phosphoriboisomerase A) | |
NEADBANL_01081 | 1.1e-142 | K | SIS domain | |||
NEADBANL_01082 | 2.3e-228 | slpX | S | SLAP domain | ||
NEADBANL_01083 | 1.3e-22 | 3.6.4.12 | S | transposase or invertase | ||
NEADBANL_01084 | 7.7e-12 | |||||
NEADBANL_01085 | 1.1e-240 | npr | 1.11.1.1 | C | NADH oxidase | |
NEADBANL_01087 | 5.5e-74 | S | Protein of unknown function (DUF3021) | |||
NEADBANL_01088 | 5e-75 | K | LytTr DNA-binding domain | |||
NEADBANL_01089 | 3.5e-91 | |||||
NEADBANL_01090 | 1.4e-161 | V | Abi-like protein | |||
NEADBANL_01091 | 0.0 | thrS | 6.1.1.3 | J | Catalyzes the attachment of threonine to tRNA(Thr) in a two-step reaction L-threonine is first activated by ATP to form Thr-AMP and then transferred to the acceptor end of tRNA(Thr) | |
NEADBANL_01092 | 3.6e-168 | dnaI | L | Primosomal protein DnaI | ||
NEADBANL_01093 | 3e-251 | dnaB | L | Replication initiation and membrane attachment | ||
NEADBANL_01094 | 4.6e-82 | nrdR | K | Negatively regulates transcription of bacterial ribonucleotide reductase nrd genes and operons by binding to NrdR- boxes | ||
NEADBANL_01095 | 3.4e-106 | coaE | 2.7.1.24 | F | Catalyzes the phosphorylation of the 3'-hydroxyl group of dephosphocoenzyme A to form coenzyme A | |
NEADBANL_01096 | 4.2e-155 | fpg | 3.2.2.23, 4.2.99.18 | L | Involved in base excision repair of DNA damaged by oxidation or by mutagenic agents. Acts as DNA glycosylase that recognizes and removes damaged bases. Has a preference for oxidized purines, such as 7,8-dihydro-8-oxoguanine (8-oxoG). Has AP (apurinic apyrimidinic) lyase activity and introduces nicks in the DNA strand. Cleaves the DNA backbone by beta-delta elimination to generate a single-strand break at the site of the removed base with both 3'- and 5'-phosphates | |
NEADBANL_01097 | 0.0 | polA | 2.7.7.7 | L | In addition to polymerase activity, this DNA polymerase exhibits 5'-3' exonuclease activity | |
NEADBANL_01098 | 1.1e-74 | qmcA | O | prohibitin homologues | ||
NEADBANL_01099 | 6e-39 | qmcA | O | prohibitin homologues | ||
NEADBANL_01100 | 8e-51 | L | RelB antitoxin | |||
NEADBANL_01101 | 3.3e-191 | S | Bacteriocin helveticin-J | |||
NEADBANL_01102 | 8.8e-284 | M | Peptidase family M1 domain | |||
NEADBANL_01103 | 2.1e-174 | S | SLAP domain | |||
NEADBANL_01104 | 1.9e-234 | mepA | V | MATE efflux family protein | ||
NEADBANL_01105 | 2.3e-248 | mpl | 6.3.2.4, 6.3.2.45, 6.3.2.8 | M | Belongs to the MurCDEF family | |
NEADBANL_01106 | 1.7e-122 | pheT | 6.1.1.20 | J | Belongs to the phenylalanyl-tRNA synthetase beta subunit family. Type 1 subfamily | |
NEADBANL_01107 | 2.8e-54 | ytpP | 2.7.1.180, 5.3.4.1 | CO | Thioredoxin | |
NEADBANL_01109 | 3.3e-126 | trmB | 2.1.1.297, 2.1.1.33 | J | Catalyzes the formation of N(7)-methylguanine at position 46 (m7G46) in tRNA | |
NEADBANL_01110 | 9.3e-220 | ecsB | U | ABC transporter | ||
NEADBANL_01111 | 2e-135 | ecsA | V | ABC transporter, ATP-binding protein | ||
NEADBANL_01112 | 8.3e-78 | hit | FG | Scavenger mRNA decapping enzyme C-term binding | ||
NEADBANL_01113 | 3.9e-25 | |||||
NEADBANL_01114 | 5.6e-153 | prsA | 5.2.1.8 | M | Plays a major role in protein secretion by helping the post-translocational extracellular folding of several secreted proteins | |
NEADBANL_01115 | 2.5e-69 | eda | 4.1.2.14, 4.1.3.42 | G | KDPG and KHG aldolase | |
NEADBANL_01116 | 8e-274 | |||||
NEADBANL_01117 | 3.3e-17 | S | Domain of unknown function DUF1829 | |||
NEADBANL_01118 | 2.2e-99 | L | Transposase | |||
NEADBANL_01119 | 7.4e-269 | S | Uncharacterised protein family (UPF0236) | |||
NEADBANL_01120 | 5.8e-247 | merA | 1.16.1.1, 1.8.1.7 | C | Belongs to the class-I pyridine nucleotide-disulfide oxidoreductase family | |
NEADBANL_01121 | 2.2e-117 | phoU | P | Plays a role in the regulation of phosphate uptake | ||
NEADBANL_01122 | 7.8e-140 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
NEADBANL_01123 | 6.5e-145 | pstB | 3.6.3.27 | P | Part of the ABC transporter complex PstSACB involved in phosphate import. Responsible for energy coupling to the transport system | |
NEADBANL_01124 | 1.2e-155 | pstA | P | Phosphate transport system permease protein PstA | ||
NEADBANL_01125 | 3.9e-163 | pstC | P | probably responsible for the translocation of the substrate across the membrane | ||
NEADBANL_01126 | 7.3e-158 | pstS | P | Phosphate | ||
NEADBANL_01127 | 3.2e-124 | rplA | J | Binds directly to 23S rRNA. The L1 stalk is quite mobile in the ribosome, and is involved in E site tRNA release | ||
NEADBANL_01128 | 1.2e-68 | rplK | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors | ||
NEADBANL_01129 | 4e-101 | nusG | K | Participates in transcription elongation, termination and antitermination | ||
NEADBANL_01130 | 3.6e-24 | 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 | ||
NEADBANL_01131 | 0.0 | dxs | 2.2.1.7 | H | Catalyzes the acyloin condensation reaction between C atoms 2 and 3 of pyruvate and glyceraldehyde 3-phosphate to yield 1-deoxy-D-xylulose-5-phosphate (DXP) | |
NEADBANL_01132 | 1.5e-288 | gntK | 2.7.1.12, 2.7.1.17 | G | Belongs to the FGGY kinase family | |
NEADBANL_01133 | 1.7e-34 | |||||
NEADBANL_01134 | 4.2e-95 | sigH | K | Belongs to the sigma-70 factor family | ||
NEADBANL_01135 | 1.7e-139 | rlmB | 2.1.1.185 | J | Belongs to the class IV-like SAM-binding methyltransferase superfamily. RNA methyltransferase TrmH family | |
NEADBANL_01136 | 2.3e-75 | 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) | ||
NEADBANL_01137 | 5.2e-278 | cysS | 6.1.1.16, 6.3.1.13 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NEADBANL_01138 | 1.9e-291 | gltX | 6.1.1.17, 6.1.1.24 | J | Catalyzes the attachment of glutamate to tRNA(Glu) in a two-step reaction glutamate is first activated by ATP to form Glu-AMP and then transferred to the acceptor end of tRNA(Glu) | |
NEADBANL_01139 | 2.7e-255 | radA | O | DNA-dependent ATPase involved in processing of recombination intermediates, plays a role in repairing DNA breaks. Stimulates the branch migration of RecA-mediated strand transfer reactions, allowing the 3' invading strand to extend heteroduplex DNA faster. Binds ssDNA in the presence of ADP but not other nucleotides, has ATPase activity that is stimulated by ssDNA and various branched DNA structures, but inhibited by SSB. Does not have RecA's homology-searching function | ||
NEADBANL_01140 | 1.8e-101 | dut | 3.6.1.23, 4.1.1.36, 6.3.2.5 | F | dUTP diphosphatase | |
NEADBANL_01141 | 3.2e-52 | |||||
NEADBANL_01142 | 5.8e-263 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
NEADBANL_01143 | 1.1e-183 | S | AAA domain | |||
NEADBANL_01144 | 1.2e-126 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NEADBANL_01145 | 1.4e-23 | |||||
NEADBANL_01146 | 1.9e-161 | czcD | P | cation diffusion facilitator family transporter | ||
NEADBANL_01147 | 1.7e-125 | gpmB | G | Belongs to the phosphoglycerate mutase family | ||
NEADBANL_01148 | 6e-132 | S | membrane transporter protein | |||
NEADBANL_01149 | 2.5e-118 | 3.1.3.18, 3.8.1.2 | S | Haloacid dehalogenase-like hydrolase | ||
NEADBANL_01150 | 1.4e-104 | thiJ | 2.7.11.1, 3.5.1.124 | S | DJ-1/PfpI family | |
NEADBANL_01151 | 7e-80 | K | Acetyltransferase (GNAT) domain | |||
NEADBANL_01152 | 2.9e-161 | M | Belongs to the glycosyl hydrolase 28 family | |||
NEADBANL_01153 | 1e-66 | rpsI | J | Belongs to the universal ribosomal protein uS9 family | ||
NEADBANL_01154 | 5.9e-79 | rplM | J | This protein is one of the early assembly proteins of the 50S ribosomal subunit, although it is not seen to bind rRNA by itself. It is important during the early stages of 50S assembly | ||
NEADBANL_01155 | 7.8e-151 | truA | 5.4.99.12 | J | Formation of pseudouridine at positions 38, 39 and 40 in the anticodon stem and loop of transfer RNAs | |
NEADBANL_01156 | 2.6e-138 | 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 | ||
NEADBANL_01157 | 7.8e-157 | ecfA | 3.6.3.55 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | |
NEADBANL_01158 | 1.4e-153 | ecfA1 | P | ATP-binding (A) component of a common energy-coupling factor (ECF) ABC-transporter complex. Unlike classic ABC transporters this ECF transporter provides the energy necessary to transport a number of different substrates | ||
NEADBANL_01159 | 1.4e-60 | rplQ | J | Ribosomal protein L17 | ||
NEADBANL_01160 | 1.1e-170 | rpoA | 2.7.7.6 | K | DNA-dependent RNA polymerase catalyzes the transcription of DNA into RNA using the four ribonucleoside triphosphates as substrates | |
NEADBANL_01161 | 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 | ||
NEADBANL_01162 | 4.2e-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 | ||
NEADBANL_01163 | 7.8e-15 | rpmJ | J | Belongs to the bacterial ribosomal protein bL36 family | ||
NEADBANL_01164 | 8.4e-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 | ||
NEADBANL_01165 | 3.5e-120 | adk | 2.7.4.3 | F | Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism | |
NEADBANL_01166 | 3.1e-237 | 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 | ||
NEADBANL_01167 | 2.6e-71 | rplO | J | Binds to the 23S rRNA | ||
NEADBANL_01168 | 2.3e-24 | rpmD | J | Ribosomal protein L30 | ||
NEADBANL_01169 | 4.1e-84 | rpsE | J | Located at the back of the 30S subunit body where it stabilizes the conformation of the head with respect to the body | ||
NEADBANL_01170 | 3.6e-55 | 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 | ||
NEADBANL_01171 | 3.3e-92 | 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 | ||
NEADBANL_01172 | 3.2e-68 | rpsH | J | One of the primary rRNA binding proteins, it binds directly to 16S rRNA central domain where it helps coordinate assembly of the platform of the 30S subunit | ||
NEADBANL_01173 | 8.9e-29 | rpsN | J | Binds 16S rRNA, required for the assembly of 30S particles and may also be responsible for determining the conformation of the 16S rRNA at the A site | ||
NEADBANL_01174 | 5.5e-95 | 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 | ||
NEADBANL_01175 | 3.4e-33 | rplX | J | One of the proteins that surrounds the polypeptide exit tunnel on the outside of the subunit | ||
NEADBANL_01176 | 1.1e-59 | rplN | J | Binds to 23S rRNA. Forms part of two intersubunit bridges in the 70S ribosome | ||
NEADBANL_01177 | 5e-41 | rpsQ | J | One of the primary rRNA binding proteins, it binds specifically to the 5'-end of 16S ribosomal RNA | ||
NEADBANL_01178 | 1.3e-25 | rpmC | J | Belongs to the universal ribosomal protein uL29 family | ||
NEADBANL_01179 | 2.1e-76 | rplP | J | Binds 23S rRNA and is also seen to make contacts with the A and possibly P site tRNAs | ||
NEADBANL_01180 | 2.7e-120 | rpsC | J | Binds the lower part of the 30S subunit head. Binds mRNA in the 70S ribosome, positioning it for translation | ||
NEADBANL_01181 | 4e-54 | 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 | ||
NEADBANL_01182 | 1.1e-46 | rpsS | J | Protein S19 forms a complex with S13 that binds strongly to the 16S ribosomal RNA | ||
NEADBANL_01183 | 7.3e-155 | rplB | J | One of the primary rRNA binding proteins. Required for association of the 30S and 50S subunits to form the 70S ribosome, for tRNA binding and peptide bond formation. It has been suggested to have peptidyltransferase activity | ||
NEADBANL_01184 | 3.1e-47 | rplW | J | One of the early assembly proteins it binds 23S rRNA. One of the proteins that surrounds the polypeptide exit tunnel on the outside of the ribosome. Forms the main docking site for trigger factor binding to the ribosome | ||
NEADBANL_01185 | 2.1e-106 | rplD | J | Forms part of the polypeptide exit tunnel | ||
NEADBANL_01186 | 9e-113 | 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 | ||
NEADBANL_01187 | 4.4e-49 | rpsJ | J | Involved in the binding of tRNA to the ribosomes | ||
NEADBANL_01188 | 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 | ||
NEADBANL_01189 | 7.9e-82 | 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 | ||
NEADBANL_01190 | 7.8e-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 | ||
NEADBANL_01191 | 3.6e-120 | pilD | 3.4.23.43 | NOU | Bacterial Peptidase A24 N-terminal domain | |
NEADBANL_01192 | 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 | |
NEADBANL_01193 | 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 | |
NEADBANL_01194 | 0.0 | clpC | O | Part of a stress-induced multi-chaperone system, it is involved in the recovery of the cell from heat-induced damage, in cooperation with DnaK, DnaJ and GrpE | ||
NEADBANL_01195 | 1.1e-80 | yebR | 1.8.4.14 | T | GAF domain-containing protein | |
NEADBANL_01197 | 1.6e-08 | |||||
NEADBANL_01198 | 1.6e-08 | |||||
NEADBANL_01201 | 6e-296 | lysS | 6.1.1.6 | J | Belongs to the class-II aminoacyl-tRNA synthetase family | |
NEADBANL_01202 | 1.5e-194 | 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 | ||
NEADBANL_01203 | 3.3e-166 | 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 | ||
NEADBANL_01204 | 0.0 | ftsH | O | Acts as a processive, ATP-dependent zinc metallopeptidase for both cytoplasmic and membrane proteins. Plays a role in the quality control of integral membrane proteins | ||
NEADBANL_01205 | 4.5e-241 | tilS | 2.4.2.8, 6.3.4.19 | J | Ligates lysine onto the cytidine present at position 34 of the AUA codon-specific tRNA(Ile) that contains the anticodon CAU, in an ATP-dependent manner. Cytidine is converted to lysidine, thus changing the amino acid specificity of the tRNA from methionine to isoleucine | |
NEADBANL_01206 | 6.3e-63 | yabR | J | S1 RNA binding domain | ||
NEADBANL_01207 | 6.8e-60 | divIC | D | Septum formation initiator | ||
NEADBANL_01208 | 1.6e-33 | yabO | J | S4 domain protein | ||
NEADBANL_01209 | 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 | ||
NEADBANL_01210 | 5.1e-104 | pth | 3.1.1.29 | J | The natural substrate for this enzyme may be peptidyl- tRNAs which drop off the ribosome during protein synthesis | |
NEADBANL_01211 | 4.7e-182 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NEADBANL_01212 | 3.4e-129 | S | (CBS) domain | |||
NEADBANL_01213 | 1e-215 | alr | 5.1.1.1 | E | Catalyzes the interconversion of L-alanine and D- alanine. May also act on other amino acids | |
NEADBANL_01214 | 1.7e-60 | acpS | 2.7.6.3, 2.7.8.7, 5.1.1.1 | I | Transfers the 4'-phosphopantetheine moiety from coenzyme A to a Ser of acyl-carrier-protein | |
NEADBANL_01215 | 1.4e-249 | 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 | |
NEADBANL_01216 | 1.3e-262 | murF | 6.3.2.10, 6.3.2.13 | M | Involved in cell wall formation. Catalyzes the final step in the synthesis of UDP-N-acetylmuramoyl-pentapeptide, the precursor of murein | |
NEADBANL_01217 | 2.5e-39 | rpmE2 | J | Ribosomal protein L31 | ||
NEADBANL_01218 | 0.0 | dexB | 3.2.1.10, 3.2.1.70 | GH13 | G | Alpha amylase, catalytic domain protein |
NEADBANL_01219 | 2.9e-156 | S | Sucrose-6F-phosphate phosphohydrolase | |||
NEADBANL_01220 | 1.9e-297 | ybeC | E | amino acid | ||
NEADBANL_01221 | 1.8e-231 | 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 | |
NEADBANL_01222 | 4.7e-42 | |||||
NEADBANL_01223 | 4e-51 | |||||
NEADBANL_01224 | 2.3e-184 | 5.3.3.2 | C | FMN-dependent dehydrogenase | ||
NEADBANL_01225 | 1.3e-93 | |||||
NEADBANL_01226 | 2.1e-96 | ogt | 2.1.1.63, 3.2.2.20 | L | Involved in the cellular defense against the biological effects of O6-methylguanine (O6-MeG) and O4-methylthymine (O4-MeT) in DNA. Repairs the methylated nucleobase in DNA by stoichiometrically transferring the methyl group to a cysteine residue in the enzyme. This is a suicide reaction the enzyme is irreversibly inactivated | |
NEADBANL_01227 | 1.7e-18 | yjdF | S | Protein of unknown function (DUF2992) | ||
NEADBANL_01228 | 7.9e-57 | ps115 | K | Helix-turn-helix XRE-family like proteins | ||
NEADBANL_01231 | 0.0 | 3.2.1.18 | GH33 | M | Rib/alpha-like repeat | |
NEADBANL_01232 | 1.7e-106 | L | Transposase and inactivated derivatives, IS30 family DNA replication, recombination, and repair | |||
NEADBANL_01234 | 5.1e-303 | guaA | 2.3.1.128, 6.3.5.2 | F | Catalyzes the synthesis of GMP from XMP | |
NEADBANL_01236 | 4.5e-103 | 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 | |
NEADBANL_01237 | 2.8e-222 | pbuX | F | xanthine permease | ||
NEADBANL_01238 | 1.1e-250 | L | Putative transposase DNA-binding domain | |||
NEADBANL_01239 | 6.4e-116 | L | Resolvase, N-terminal | |||
NEADBANL_01240 | 4.6e-154 | msmR | K | AraC-like ligand binding domain | ||
NEADBANL_01241 | 4.4e-285 | pipD | E | Dipeptidase | ||
NEADBANL_01242 | 8.8e-74 | K | acetyltransferase | |||
NEADBANL_01243 | 9.6e-247 | murA | 2.5.1.7 | M | Cell wall formation. Adds enolpyruvyl to UDP-N- acetylglucosamine | |
NEADBANL_01244 | 0.0 | pyrG | 6.3.4.2 | F | Catalyzes the ATP-dependent amination of UTP to CTP with either L-glutamine or ammonia as the source of nitrogen. Regulates intracellular CTP levels through interactions with the four ribonucleotide triphosphates | |
NEADBANL_01245 | 1.7e-46 | 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 | ||
NEADBANL_01246 | 2.6e-68 | S | Domain of unknown function (DUF1934) | |||
NEADBANL_01247 | 2.6e-266 | ywfO | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NEADBANL_01248 | 4.5e-42 | |||||
NEADBANL_01249 | 1.1e-169 | GK | ROK family | |||
NEADBANL_01250 | 1.1e-240 | U | 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 | |||
NEADBANL_01251 | 7.7e-129 | K | Helix-turn-helix domain, rpiR family | |||
NEADBANL_01252 | 3.5e-290 | celA | 3.2.1.86 | GT1 | G | Belongs to the glycosyl hydrolase 1 family |
NEADBANL_01253 | 6.7e-176 | 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) | |
NEADBANL_01254 | 0.0 | S | SLAP domain | |||
NEADBANL_01255 | 5.3e-80 | |||||
NEADBANL_01256 | 2e-173 | 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 | |
NEADBANL_01257 | 1e-148 | purR | 2.4.2.22, 2.4.2.7 | F | pur operon repressor | |
NEADBANL_01258 | 3.5e-39 | veg | S | Biofilm formation stimulator VEG | ||
NEADBANL_01259 | 2.5e-161 | 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 | |
NEADBANL_01260 | 1e-99 | rnmV | 3.1.26.8 | J | Required for correct processing of both the 5' and 3' ends of 5S rRNA precursor. Cleaves both sides of a double-stranded region yielding mature 5S rRNA in one step | |
NEADBANL_01261 | 2.5e-146 | tatD | L | hydrolase, TatD family | ||
NEADBANL_01262 | 0.0 | metG | 6.1.1.10 | J | Is required not only for elongation of protein synthesis but also for the initiation of all mRNA translation through initiator tRNA(fMet) aminoacylation | |
NEADBANL_01263 | 0.0 | mgtA | 3.6.3.2 | P | COG0474 Cation transport ATPase | |
NEADBANL_01264 | 2e-103 | S | TPM domain | |||
NEADBANL_01265 | 5.7e-88 | comEB | 3.5.4.12 | F | MafB19-like deaminase | |
NEADBANL_01266 | 7e-192 | trpS | 6.1.1.2 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NEADBANL_01267 | 1.2e-111 | E | Belongs to the SOS response-associated peptidase family | |||
NEADBANL_01269 | 1.2e-112 | |||||
NEADBANL_01270 | 6.3e-76 | 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 | ||
NEADBANL_01271 | 2.9e-67 | hsp | O | Belongs to the small heat shock protein (HSP20) family | ||
NEADBANL_01272 | 1.4e-256 | pepC | 3.4.22.40 | E | aminopeptidase | |
NEADBANL_01273 | 1.9e-175 | oppF | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_01274 | 7.2e-200 | oppD | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_01275 | 8e-188 | oppC | EP | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NEADBANL_01276 | 1.1e-146 | oppB | P | ABC-type dipeptide oligopeptide nickel transport systems, permease components | ||
NEADBANL_01277 | 1.7e-210 | 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 | |
NEADBANL_01278 | 1.6e-310 | oppA | E | ABC transporter, substratebinding protein | ||
NEADBANL_01279 | 9.3e-300 | oppA | E | ABC transporter, substratebinding protein | ||
NEADBANL_01280 | 2.6e-123 | ypgQ | S | Metal dependent phosphohydrolases with conserved 'HD' motif. | ||
NEADBANL_01281 | 1.4e-258 | pepC | 3.4.22.40 | E | aminopeptidase | |
NEADBANL_01283 | 3.1e-54 | |||||
NEADBANL_01284 | 1.6e-243 | 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) | |
NEADBANL_01285 | 0.0 | XK27_08315 | M | Sulfatase | ||
NEADBANL_01286 | 5.6e-112 | plsY | 2.3.1.15 | 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 | |
NEADBANL_01287 | 1.8e-201 | brpA | K | Cell envelope-like function transcriptional attenuator common domain protein | ||
NEADBANL_01288 | 4.9e-99 | G | Aldose 1-epimerase | |||
NEADBANL_01289 | 5e-133 | gpmA | 5.4.2.11 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NEADBANL_01290 | 7.8e-116 | |||||
NEADBANL_01291 | 4.1e-131 | |||||
NEADBANL_01292 | 1.2e-161 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NEADBANL_01293 | 1e-100 | pcp | 3.4.19.3 | O | Removes 5-oxoproline from various penultimate amino acid residues except L-proline | |
NEADBANL_01294 | 0.0 | yjbQ | P | TrkA C-terminal domain protein | ||
NEADBANL_01295 | 6.3e-191 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
NEADBANL_01296 | 6.6e-213 | NU | Mannosyl-glycoprotein endo-beta-N-acetylglucosaminidase | |||
NEADBANL_01297 | 2.4e-43 | L | transposase activity | |||
NEADBANL_01298 | 1.7e-95 | cadD | P | Cadmium resistance transporter | ||
NEADBANL_01300 | 1e-190 | metN | P | Part of the ABC transporter complex MetNIQ involved in methionine import. Responsible for energy coupling to the transport system | ||
NEADBANL_01301 | 3.8e-159 | metQ2 | P | Belongs to the nlpA lipoprotein family | ||
NEADBANL_01302 | 1.7e-176 | F | DNA/RNA non-specific endonuclease | |||
NEADBANL_01303 | 0.0 | aha1 | P | E1-E2 ATPase | ||
NEADBANL_01304 | 5.9e-91 | folA | 1.5.1.3 | H | Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, and for DNA precursor synthesis | |
NEADBANL_01305 | 4.8e-179 | 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 | |
NEADBANL_01306 | 1.2e-250 | yifK | E | Amino acid permease | ||
NEADBANL_01307 | 6.6e-282 | V | ABC-type multidrug transport system, ATPase and permease components | |||
NEADBANL_01308 | 3.1e-287 | P | ABC transporter | |||
NEADBANL_01309 | 5.1e-37 | |||||
NEADBANL_01311 | 7.5e-123 | S | Glucose-6-phosphate 1-dehydrogenase (EC 1.1.1.49) | |||
NEADBANL_01312 | 1.9e-86 | K | GNAT family | |||
NEADBANL_01313 | 5.4e-203 | XK27_00915 | C | Luciferase-like monooxygenase | ||
NEADBANL_01314 | 6.6e-169 | lmrB | EGP | Major facilitator Superfamily | ||
NEADBANL_01315 | 4.3e-34 | rmaI | K | Transcriptional regulator | ||
NEADBANL_01317 | 1.5e-08 | K | Bacterial regulatory helix-turn-helix protein, lysR family | |||
NEADBANL_01318 | 2.5e-08 | S | Protein of unknown function (DUF3021) | |||
NEADBANL_01319 | 3e-84 | tpx | 1.11.1.15 | O | Thiol-specific peroxidase that catalyzes the reduction of hydrogen peroxide and organic hydroperoxides to water and alcohols, respectively. Plays a role in cell protection against oxidative stress by detoxifying peroxides | |
NEADBANL_01320 | 5.8e-82 | L | Plasmid pRiA4b ORF-3-like protein | |||
NEADBANL_01321 | 1.2e-46 | L | Plasmid pRiA4b ORF-3-like protein | |||
NEADBANL_01322 | 6.3e-57 | L | Plasmid pRiA4b ORF-3-like protein | |||
NEADBANL_01323 | 1.2e-244 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
NEADBANL_01324 | 9.6e-120 | 3.6.1.55 | F | NUDIX domain | ||
NEADBANL_01325 | 7.9e-112 | ltrA | S | Bacterial low temperature requirement A protein (LtrA) | ||
NEADBANL_01326 | 2.8e-112 | S | Protein of unknown function (DUF1211) | |||
NEADBANL_01327 | 3.3e-283 | lsa | S | ABC transporter | ||
NEADBANL_01328 | 3.7e-105 | S | Alpha beta hydrolase | |||
NEADBANL_01329 | 2.1e-157 | K | Transcriptional regulator | |||
NEADBANL_01330 | 2.3e-75 | K | LytTr DNA-binding domain | |||
NEADBANL_01331 | 8.5e-64 | S | Protein of unknown function (DUF3021) | |||
NEADBANL_01332 | 2.1e-143 | IQ | Oxidoreductase, short chain dehydrogenase reductase family protein | |||
NEADBANL_01333 | 7.8e-202 | ribD | 1.1.1.193, 3.5.4.26 | H | Converts 2,5-diamino-6-(ribosylamino)-4(3h)-pyrimidinone 5'-phosphate into 5-amino-6-(ribosylamino)-2,4(1h,3h)- pyrimidinedione 5'-phosphate | |
NEADBANL_01334 | 7.6e-106 | ribE | 2.5.1.9, 3.5.4.25, 4.1.99.12 | H | Riboflavin synthase | |
NEADBANL_01335 | 2.4e-228 | ribBA | 3.5.4.25, 4.1.99.12 | H | Catalyzes the conversion of GTP to 2,5-diamino-6- ribosylamino-4(3H)-pyrimidinone 5'-phosphate (DARP), formate and pyrophosphate | |
NEADBANL_01336 | 1.9e-80 | ribH | 2.5.1.78 | H | Catalyzes the formation of 6,7-dimethyl-8- ribityllumazine by condensation of 5-amino-6-(D- ribitylamino)uracil with 3,4-dihydroxy-2-butanone 4-phosphate. This is the penultimate step in the biosynthesis of riboflavin | |
NEADBANL_01337 | 2.4e-10 | L | Psort location Cytoplasmic, score | |||
NEADBANL_01338 | 1.7e-12 | L | Transposase and inactivated derivatives, IS30 family | |||
NEADBANL_01339 | 1.3e-64 | L | Transposase and inactivated derivatives, IS30 family | |||
NEADBANL_01340 | 6.5e-204 | G | Glycosyl hydrolases family 8 | |||
NEADBANL_01341 | 9.7e-247 | ydaM | M | Glycosyl transferase | ||
NEADBANL_01343 | 3.8e-151 | |||||
NEADBANL_01344 | 0.0 | 3.5.1.28 | UW | LPXTG-motif cell wall anchor domain protein | ||
NEADBANL_01345 | 1.7e-184 | 3.5.1.28 | UW | LPXTG-motif cell wall anchor domain protein | ||
NEADBANL_01346 | 8.4e-64 | L | An automated process has identified a potential problem with this gene model | |||
NEADBANL_01347 | 1.6e-211 | yttB | EGP | Major facilitator Superfamily | ||
NEADBANL_01348 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
NEADBANL_01349 | 0.0 | kup | P | Transport of potassium into the cell | ||
NEADBANL_01350 | 3.3e-74 | |||||
NEADBANL_01351 | 2.7e-67 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NEADBANL_01352 | 1.2e-104 | L | Transposase | |||
NEADBANL_01353 | 7.5e-25 | L | Transposase | |||
NEADBANL_01354 | 1.1e-108 | S | Core-2/I-Branching enzyme | |||
NEADBANL_01355 | 1.2e-155 | galU | 2.7.7.9 | M | UTP-glucose-1-phosphate uridylyltransferase | |
NEADBANL_01356 | 4.1e-15 | sacB | 2.4.1.10, 2.4.1.9, 3.2.1.26 | GH32,GH68 | M | Levansucrase/Invertase |
NEADBANL_01357 | 4e-27 | ptsN | 2.7.1.202 | G | PTS fructose transporter subunit IIA | |
NEADBANL_01358 | 3.4e-184 | frvB | 2.7.1.202 | G | PTS system, Lactose/Cellobiose specific IIB subunit | |
NEADBANL_01359 | 2.1e-128 | malY | 4.4.1.8 | E | Aminotransferase class I and II | |
NEADBANL_01360 | 2.1e-41 | G | Phosphoenolpyruvate-dependent sugar phosphotransferase system, EIIA 2 | |||
NEADBANL_01361 | 1.8e-97 | K | Helix-turn-helix domain, rpiR family | |||
NEADBANL_01362 | 8.2e-112 | nanE | 5.1.3.9 | G | Converts N-acetylmannosamine-6-phosphate (ManNAc-6-P) to N-acetylglucosamine-6-phosphate (GlcNAc-6-P) | |
NEADBANL_01363 | 0.0 | ptsG | 2.7.1.199, 2.7.1.208 | G | phosphotransferase system, EIIB | |
NEADBANL_01364 | 5e-137 | L | Transposase | |||
NEADBANL_01365 | 2.3e-15 | metI | P | ABC transporter permease | ||
NEADBANL_01366 | 2e-266 | fumC | 4.2.1.2 | C | Involved in the TCA cycle. Catalyzes the stereospecific interconversion of fumarate to L-malate | |
NEADBANL_01367 | 6.6e-262 | frdC | 1.3.5.4 | C | FAD binding domain | |
NEADBANL_01368 | 3.1e-170 | ldh | 1.1.1.27 | C | Belongs to the LDH MDH superfamily. LDH family | |
NEADBANL_01369 | 8.8e-256 | pepC | 3.4.22.40 | E | Peptidase C1-like family | |
NEADBANL_01370 | 1.3e-133 | hxlA | 6.2.1.3 | H | Aldolase/RraA | |
NEADBANL_01371 | 4.7e-274 | P | Sodium:sulfate symporter transmembrane region | |||
NEADBANL_01372 | 3.8e-153 | ydjP | I | Alpha/beta hydrolase family | ||
NEADBANL_01373 | 2.2e-196 | citC | 6.2.1.22 | H | Acetylation of prosthetic group (2-(5''-phosphoribosyl)- 3'-dephosphocoenzyme-A) of the gamma subunit of citrate lyase | |
NEADBANL_01374 | 1.2e-43 | citD | C | Covalent carrier of the coenzyme of citrate lyase | ||
NEADBANL_01375 | 8.2e-168 | citE | 4.1.3.25, 4.1.3.34 | G | Belongs to the HpcH HpaI aldolase family | |
NEADBANL_01376 | 5.4e-289 | citF | 2.8.3.10 | H | Citrate (pro-3S)-lyase alpha chain | |
NEADBANL_01377 | 9.3e-72 | yeaL | S | Protein of unknown function (DUF441) | ||
NEADBANL_01378 | 1.8e-22 | |||||
NEADBANL_01379 | 3.6e-146 | cbiQ | P | cobalt transport | ||
NEADBANL_01380 | 0.0 | ykoD | P | ABC transporter, ATP-binding protein | ||
NEADBANL_01381 | 9.6e-95 | S | UPF0397 protein | |||
NEADBANL_01382 | 2.9e-66 | S | Domain of unknown function DUF1828 | |||
NEADBANL_01383 | 1.6e-08 | |||||
NEADBANL_01384 | 8.5e-51 | |||||
NEADBANL_01385 | 2.6e-177 | citR | K | Putative sugar-binding domain | ||
NEADBANL_01386 | 1.9e-250 | yjjP | S | Putative threonine/serine exporter | ||
NEADBANL_01387 | 8.2e-85 | ybaK | S | Belongs to the prolyl-tRNA editing family. YbaK EbsC subfamily | ||
NEADBANL_01388 | 2.5e-175 | prmA | J | Ribosomal protein L11 methyltransferase | ||
NEADBANL_01389 | 2.9e-60 | |||||
NEADBANL_01390 | 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 | |
NEADBANL_01391 | 6e-76 | 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 | ||
NEADBANL_01392 | 6.8e-245 | hisS | 6.1.1.21 | J | histidyl-tRNA synthetase | |
NEADBANL_01393 | 0.0 | aspS | 6.1.1.12 | J | Catalyzes the attachment of L-aspartate to tRNA(Asp) in a two-step reaction L-aspartate is first activated by ATP to form Asp-AMP and then transferred to the acceptor end of tRNA(Asp) | |
NEADBANL_01394 | 2e-222 | patA | 2.6.1.1 | E | Aminotransferase | |
NEADBANL_01395 | 1.8e-215 | 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 | |
NEADBANL_01396 | 1.3e-125 | S | reductase | |||
NEADBANL_01397 | 1.4e-19 | S | reductase | |||
NEADBANL_01398 | 5.2e-150 | yxeH | S | hydrolase | ||
NEADBANL_01399 | 7.6e-82 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NEADBANL_01400 | 8.6e-87 | gyaR | 1.1.1.26, 2.7.1.165 | CH | Belongs to the D-isomer specific 2-hydroxyacid dehydrogenase family | |
NEADBANL_01401 | 4e-243 | yfnA | E | Amino Acid | ||
NEADBANL_01402 | 1.8e-110 | dedA | 3.1.3.1 | S | SNARE associated Golgi protein | |
NEADBANL_01403 | 0.0 | uvrC | L | The UvrABC repair system catalyzes the recognition and processing of DNA lesions. UvrC both incises the 5' and 3' sides of the lesion. The N-terminal half is responsible for the 3' incision and the C-terminal half is responsible for the 5' incision | ||
NEADBANL_01404 | 1.7e-243 | 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 | ||
NEADBANL_01405 | 2.3e-180 | 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 | ||
NEADBANL_01406 | 6.5e-243 | dacA | 3.4.16.4 | M | Belongs to the peptidase S11 family | |
NEADBANL_01407 | 8.1e-154 | 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 | |
NEADBANL_01408 | 1e-98 | M | ErfK YbiS YcfS YnhG | |||
NEADBANL_01409 | 0.0 | argS | 6.1.1.19 | J | Arginyl-tRNA synthetase | |
NEADBANL_01410 | 1.8e-170 | fba | 4.1.2.13, 4.1.2.29 | G | Fructose-1,6-bisphosphate aldolase, class II | |
NEADBANL_01411 | 1.4e-82 | 3.6.1.55 | L | NUDIX domain | ||
NEADBANL_01412 | 2.3e-77 | menA | 2.5.1.74 | H | UbiA prenyltransferase family | |
NEADBANL_01414 | 3.6e-45 | |||||
NEADBANL_01415 | 8.7e-126 | 2.7.13.3 | T | GHKL domain | ||
NEADBANL_01416 | 5.4e-144 | K | LytTr DNA-binding domain | |||
NEADBANL_01417 | 6.3e-111 | |||||
NEADBANL_01419 | 1.4e-94 | |||||
NEADBANL_01421 | 3.2e-71 | yniG | EGP | Major facilitator Superfamily | ||
NEADBANL_01422 | 1e-235 | L | transposase, IS605 OrfB family | |||
NEADBANL_01423 | 4.1e-42 | S | cog cog1373 | |||
NEADBANL_01424 | 3.4e-176 | S | PFAM Archaeal ATPase | |||
NEADBANL_01425 | 1.2e-192 | I | transferase activity, transferring acyl groups other than amino-acyl groups | |||
NEADBANL_01426 | 5.7e-128 | citG | 2.4.2.52, 2.7.7.61 | H | 2-(5''-triphosphoribosyl)-3'-dephosphocoenzyme-A synthase | |
NEADBANL_01427 | 1.6e-140 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NEADBANL_01428 | 3.6e-111 | G | Phosphoglycerate mutase family | |||
NEADBANL_01429 | 0.0 | ppsA | 2.7.9.2 | H | Catalyzes the phosphorylation of pyruvate to phosphoenolpyruvate | |
NEADBANL_01430 | 6.5e-151 | rluA | 5.4.99.23 | J | Responsible for synthesis of pseudouridine from uracil | |
NEADBANL_01431 | 0.0 | pbp2A | 2.4.1.129, 3.4.16.4 | GT51 | M | penicillin-binding protein |
NEADBANL_01432 | 1.6e-55 | yheA | S | Belongs to the UPF0342 family | ||
NEADBANL_01433 | 1.9e-233 | yhaO | L | Ser Thr phosphatase family protein | ||
NEADBANL_01434 | 0.0 | L | AAA domain | |||
NEADBANL_01435 | 2.1e-34 | S | Domain of unknown function (DUF4417) | |||
NEADBANL_01436 | 1.3e-19 | |||||
NEADBANL_01437 | 1.9e-20 | |||||
NEADBANL_01438 | 1.1e-14 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_01439 | 1.7e-27 | E | Zn peptidase | |||
NEADBANL_01440 | 9.5e-47 | apgM | 5.4.2.12 | G | Catalyzes the interconversion of 2-phosphoglycerate and 3-phosphoglycerate | |
NEADBANL_01441 | 4.1e-09 | 2.7.7.47 | S | nucleotidyltransferase activity | ||
NEADBANL_01442 | 1.6e-38 | EGP | Major facilitator Superfamily | |||
NEADBANL_01443 | 5.2e-97 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_01444 | 5.8e-85 | 2.3.1.128 | K | Acetyltransferase (GNAT) domain | ||
NEADBANL_01445 | 5e-69 | O | OsmC-like protein | |||
NEADBANL_01446 | 1.1e-209 | EGP | Major facilitator Superfamily | |||
NEADBANL_01447 | 9.5e-223 | sptS | 2.7.13.3 | T | Histidine kinase | |
NEADBANL_01448 | 1.4e-105 | K | response regulator | |||
NEADBANL_01449 | 1.9e-112 | 2.7.6.5 | T | Region found in RelA / SpoT proteins | ||
NEADBANL_01450 | 1.1e-280 | gtfA | 2.4.1.7 | GH13 | G | Sucrose glucosyltransferase |
NEADBANL_01451 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
NEADBANL_01452 | 2.8e-210 | msmX | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_01453 | 5.2e-153 | msmG | P | Binding-protein-dependent transport system inner membrane component | ||
NEADBANL_01454 | 6.2e-157 | msmF | P | Binding-protein-dependent transport system inner membrane component | ||
NEADBANL_01455 | 3.2e-239 | msmE | G | Bacterial extracellular solute-binding protein | ||
NEADBANL_01456 | 1.6e-174 | scrR | K | Periplasmic binding protein domain | ||
NEADBANL_01457 | 5.5e-36 | |||||
NEADBANL_01458 | 9.8e-199 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
NEADBANL_01459 | 2.2e-287 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
NEADBANL_01460 | 1.3e-221 | 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) | |
NEADBANL_01461 | 0.0 | lacZ | 3.2.1.23 | G | -beta-galactosidase | |
NEADBANL_01462 | 0.0 | lacS | G | Transporter | ||
NEADBANL_01463 | 2.5e-186 | lacR | K | Transcriptional regulator | ||
NEADBANL_01464 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
NEADBANL_01465 | 1.5e-185 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
NEADBANL_01466 | 5.7e-191 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
NEADBANL_01467 | 2e-121 | glpF | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
NEADBANL_01468 | 6.5e-55 | dhaM | 2.7.1.121 | S | PTS system fructose IIA component | |
NEADBANL_01469 | 1.9e-93 | dhaL | 2.7.1.121 | S | Dak2 | |
NEADBANL_01470 | 1.3e-174 | dhaK | 2.7.1.121, 2.7.1.28, 2.7.1.29, 4.6.1.15 | G | Dak1 domain | |
NEADBANL_01471 | 0.0 | O | Belongs to the peptidase S8 family | |||
NEADBANL_01472 | 4.5e-81 | coaA | 2.7.1.33 | F | Pantothenic acid kinase | |
NEADBANL_01473 | 1.4e-75 | S | ECF transporter, substrate-specific component | |||
NEADBANL_01474 | 1.8e-55 | coaD | 2.7.7.3 | H | Reversibly transfers an adenylyl group from ATP to 4'- phosphopantetheine, yielding dephospho-CoA (dPCoA) and pyrophosphate | |
NEADBANL_01475 | 3.1e-143 | gltC_1 | 3.1.3.48 | K | LysR substrate binding domain | |
NEADBANL_01476 | 3.3e-265 | 2.8.3.1 | I | Coenzyme A transferase | ||
NEADBANL_01478 | 4.3e-47 | pspC | KT | PspC domain | ||
NEADBANL_01479 | 1.2e-297 | ytgP | S | Polysaccharide biosynthesis protein | ||
NEADBANL_01480 | 0.0 | leuS | 6.1.1.4 | J | Belongs to the class-I aminoacyl-tRNA synthetase family | |
NEADBANL_01481 | 3.8e-122 | 3.6.1.27 | I | Acid phosphatase homologues | ||
NEADBANL_01482 | 2.8e-168 | K | LysR substrate binding domain | |||
NEADBANL_01483 | 2.1e-91 | 3.6.4.12 | S | PD-(D/E)XK nuclease family transposase | ||
NEADBANL_01484 | 4.1e-231 | ndh | 1.6.99.3 | C | NADH dehydrogenase | |
NEADBANL_01485 | 3e-162 | menA | 2.5.1.74 | H | 1,4-dihydroxy-2-naphthoate | |
NEADBANL_01486 | 1.6e-177 | hepT | 2.5.1.30, 2.5.1.90 | H | Belongs to the FPP GGPP synthase family | |
NEADBANL_01487 | 2.8e-128 | menG | 2.1.1.163, 2.1.1.201 | H | Methyltransferase required for the conversion of demethylmenaquinol (DMKH2) to menaquinol (MKH2) | |
NEADBANL_01488 | 6.4e-270 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydC | ||
NEADBANL_01489 | 0.0 | cydD | CO | ABC transporter, CydDC cysteine exporter (CydDC-E) family, permease ATP-binding protein CydD | ||
NEADBANL_01490 | 3.3e-178 | cydB | 1.10.3.14 | C | Cytochrome d ubiquinol oxidase subunit II | |
NEADBANL_01491 | 2.3e-273 | cydA | 1.10.3.14 | C | ubiquinol oxidase | |
NEADBANL_01492 | 1.7e-143 | ybbH_2 | K | rpiR family | ||
NEADBANL_01493 | 5.2e-195 | S | Bacterial protein of unknown function (DUF871) | |||
NEADBANL_01494 | 1.3e-154 | murQ | 4.2.1.126 | G | Specifically catalyzes the cleavage of the D-lactyl ether substituent of MurNAc 6-phosphate, producing GlcNAc 6- phosphate and D-lactate | |
NEADBANL_01495 | 0.0 | sacX | 2.7.1.208, 2.7.1.211 | G | phosphotransferase system | |
NEADBANL_01496 | 2.2e-260 | qacA | EGP | Major facilitator Superfamily | ||
NEADBANL_01497 | 1.6e-219 | 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 | |
NEADBANL_01500 | 1.3e-111 | psaA | P | Belongs to the bacterial solute-binding protein 9 family | ||
NEADBANL_01510 | 4.8e-49 | |||||
NEADBANL_01511 | 1.8e-284 | V | ABC transporter transmembrane region | |||
NEADBANL_01512 | 2.7e-263 | cls | I | Catalyzes the reversible phosphatidyl group transfer from one phosphatidylglycerol molecule to another to form cardiolipin (CL) (diphosphatidylglycerol) and glycerol | ||
NEADBANL_01513 | 1e-86 | speG | J | Acetyltransferase (GNAT) domain | ||
NEADBANL_01514 | 4.5e-58 | K | Acetyltransferase (GNAT) domain | |||
NEADBANL_01515 | 4.1e-131 | S | Protein of unknown function (DUF2785) | |||
NEADBANL_01516 | 3.7e-11 | S | MazG-like family | |||
NEADBANL_01517 | 1.9e-09 | S | MazG-like family | |||
NEADBANL_01518 | 1.2e-58 | |||||
NEADBANL_01519 | 2.8e-23 | S | Protein of unknown function (DUF3923) | |||
NEADBANL_01520 | 9.2e-111 | 3.1.3.48 | T | Tyrosine phosphatase family | ||
NEADBANL_01521 | 3.1e-114 | glsA | 3.5.1.2 | E | Belongs to the glutaminase family | |
NEADBANL_01522 | 1.3e-07 | |||||
NEADBANL_01523 | 1.6e-196 | |||||
NEADBANL_01524 | 4.5e-94 | rimL | J | Acetyltransferase (GNAT) domain | ||
NEADBANL_01525 | 1.9e-136 | S | Alpha/beta hydrolase family | |||
NEADBANL_01526 | 7.5e-35 | yxaM | EGP | Major facilitator Superfamily | ||
NEADBANL_01527 | 5.4e-37 | |||||
NEADBANL_01528 | 3.6e-45 | yxaM | EGP | Major facilitator Superfamily | ||
NEADBANL_01529 | 1.8e-55 | cdd | 2.4.2.4, 3.5.4.5 | F | Cytidine and deoxycytidylate deaminase zinc-binding region | |
NEADBANL_01530 | 1.7e-120 | fbiB | 6.3.2.12, 6.3.2.17, 6.3.2.31, 6.3.2.34 | S | F420-0:Gamma-glutamyl ligase | |
NEADBANL_01531 | 1.3e-73 | S | AAA domain | |||
NEADBANL_01532 | 2.9e-142 | 2.4.2.3 | F | Phosphorylase superfamily | ||
NEADBANL_01533 | 7.4e-146 | 2.4.2.3 | F | Phosphorylase superfamily | ||
NEADBANL_01534 | 1.2e-149 | aacC | 2.3.1.81 | V | Aminoglycoside 3-N-acetyltransferase | |
NEADBANL_01535 | 1.1e-88 | yagE | E | Amino acid permease | ||
NEADBANL_01536 | 5.6e-34 | yagE | E | Amino acid permease | ||
NEADBANL_01537 | 7.3e-86 | 3.4.21.96 | S | SLAP domain | ||
NEADBANL_01538 | 4.6e-160 | ypjC | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | ||
NEADBANL_01539 | 1.1e-225 | cca | 2.7.7.19, 2.7.7.72 | J | Catalyzes the addition and repair of the essential 3'- terminal CCA sequence in tRNAs without using a nucleic acid template. Adds these three nucleotides in the order of C, C, and A to the tRNA nucleotide-73, using CTP and ATP as substrates and producing inorganic pyrophosphate | |
NEADBANL_01540 | 1.2e-107 | hlyIII | S | protein, hemolysin III | ||
NEADBANL_01541 | 2e-144 | DegV | S | Uncharacterised protein, DegV family COG1307 | ||
NEADBANL_01542 | 7.1e-36 | yozE | S | Belongs to the UPF0346 family | ||
NEADBANL_01543 | 1e-67 | yjcE | P | NhaP-type Na H and K H | ||
NEADBANL_01544 | 1.3e-140 | yjcE | P | Sodium proton antiporter | ||
NEADBANL_01545 | 7.3e-155 | ylqF | S | Required for a late step of 50S ribosomal subunit assembly. Has GTPase activity | ||
NEADBANL_01546 | 4.6e-132 | rnhB | 3.1.26.4 | L | Endonuclease that specifically degrades the RNA of RNA- DNA hybrids | |
NEADBANL_01547 | 2e-152 | dprA | LU | DNA protecting protein DprA | ||
NEADBANL_01548 | 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 | |
NEADBANL_01549 | 2.7e-249 | trmFO | 2.1.1.74 | J | Catalyzes the folate-dependent formation of 5-methyl- uridine at position 54 (M-5-U54) in all tRNAs | |
NEADBANL_01550 | 2.1e-168 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_01551 | 9.9e-85 | dps | P | Belongs to the Dps family | ||
NEADBANL_01552 | 0.0 | pepO | 3.4.24.71 | O | Peptidase family M13 | |
NEADBANL_01553 | 4.5e-121 | mdlB | V | ABC transporter | ||
NEADBANL_01554 | 2.1e-175 | mdlB | V | ABC transporter | ||
NEADBANL_01555 | 0.0 | mdlA | V | ABC transporter | ||
NEADBANL_01556 | 5.5e-30 | yneF | S | Uncharacterised protein family (UPF0154) | ||
NEADBANL_01557 | 3e-38 | ynzC | S | UPF0291 protein | ||
NEADBANL_01558 | 2e-112 | lexA | 3.4.21.88 | K | Represses a number of genes involved in the response to DNA damage (SOS response), including recA and lexA. In the presence of single-stranded DNA, RecA interacts with LexA causing an autocatalytic cleavage which disrupts the DNA-binding part of LexA, leading to derepression of the SOS regulon and eventually DNA repair | |
NEADBANL_01559 | 2e-146 | E | GDSL-like Lipase/Acylhydrolase family | |||
NEADBANL_01560 | 4.9e-122 | ung2 | 3.2.2.27 | L | Uracil-DNA glycosylase | |
NEADBANL_01561 | 1.1e-214 | S | SLAP domain | |||
NEADBANL_01562 | 1.1e-56 | rplS | J | This protein is located at the 30S-50S ribosomal subunit interface and may play a role in the structure and function of the aminoacyl-tRNA binding site | ||
NEADBANL_01563 | 5e-136 | trmD | 2.1.1.228, 4.6.1.12 | J | Belongs to the RNA methyltransferase TrmD family | |
NEADBANL_01564 | 2.2e-93 | 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 | ||
NEADBANL_01565 | 7.6e-45 | rpsP | J | Belongs to the bacterial ribosomal protein bS16 family | ||
NEADBANL_01566 | 5.8e-229 | 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 | |
NEADBANL_01567 | 4.6e-55 | 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 | ||
NEADBANL_01568 | 1.7e-260 | yfnA | E | amino acid | ||
NEADBANL_01569 | 0.0 | V | FtsX-like permease family | |||
NEADBANL_01570 | 2.4e-133 | cysA | V | ABC transporter, ATP-binding protein | ||
NEADBANL_01571 | 2.9e-17 | |||||
NEADBANL_01573 | 3.2e-288 | pipD | E | Dipeptidase | ||
NEADBANL_01574 | 8.7e-163 | 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) | ||
NEADBANL_01575 | 0.0 | smc | D | Required for chromosome condensation and partitioning | ||
NEADBANL_01576 | 1.9e-124 | 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 | |
NEADBANL_01577 | 2.3e-307 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_01578 | 1.3e-218 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_01579 | 1.8e-71 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_01580 | 6.2e-131 | oppC | P | Binding-protein-dependent transport system inner membrane component | ||
NEADBANL_01581 | 7.5e-172 | oppB | P | ABC transporter permease | ||
NEADBANL_01582 | 8.8e-168 | oppF | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_01583 | 1.1e-192 | oppD | P | Belongs to the ABC transporter superfamily | ||
NEADBANL_01584 | 9.8e-36 | acpP | IQ | Carrier of the growing fatty acid chain in fatty acid biosynthesis | ||
NEADBANL_01585 | 9.9e-183 | plsX | 2.3.1.15 | I | Catalyzes the reversible formation of acyl-phosphate (acyl-PO(4)) from acyl- acyl-carrier-protein (acyl-ACP). This enzyme utilizes acyl-ACP as fatty acyl donor, but not acyl-CoA | |
NEADBANL_01586 | 0.0 | recG | 3.6.4.12 | L | Critical role in recombination and DNA repair. Helps process Holliday junction intermediates to mature products by catalyzing branch migration. Has a DNA unwinding activity characteristic of a DNA helicase with a 3'- to 5'- polarity. Unwinds branched duplex DNA (Y-DNA) | |
NEADBANL_01587 | 2.9e-304 | yloV | S | DAK2 domain fusion protein YloV | ||
NEADBANL_01588 | 4e-57 | asp | S | Asp23 family, cell envelope-related function | ||
NEADBANL_01589 | 1.4e-26 | rpmB | J | Belongs to the bacterial ribosomal protein bL28 family | ||
NEADBANL_01590 | 2e-32 | |||||
NEADBANL_01591 | 1.4e-124 | thiN | 2.7.6.2 | H | thiamine pyrophosphokinase | |
NEADBANL_01592 | 1.9e-118 | rpe | 5.1.3.1 | G | Belongs to the ribulose-phosphate 3-epimerase family | |
NEADBANL_01593 | 3.3e-166 | rsgA | 3.1.3.100 | S | One of several proteins that assist in the late maturation steps of the functional core of the 30S ribosomal subunit. Helps release RbfA from mature subunits. May play a role in the assembly of ribosomal proteins into the subunit. Circularly permuted GTPase that catalyzes slow GTP hydrolysis, GTPase activity is stimulated by the 30S ribosomal subunit | |
NEADBANL_01594 | 0.0 | prkC | 2.7.11.1 | KLT | serine threonine protein kinase | |
NEADBANL_01595 | 1.3e-139 | stp | 3.1.3.16 | T | phosphatase | |
NEADBANL_01596 | 3.1e-50 | sun | 2.1.1.176 | J | Specifically methylates the cytosine at position 967 (m5C967) of 16S rRNA | |
NEADBANL_01597 | 2.6e-21 | atl | 3.2.1.96, 3.5.1.28 | GH73 | M | N-acetylmuramoyl-L-alanine amidase |
NEADBANL_01599 | 1.7e-251 | pepT2 | 3.4.11.14, 3.4.11.4 | E | Cleaves the N-terminal amino acid of tripeptides | |
NEADBANL_01600 | 7.3e-191 | yrvN | L | AAA C-terminal domain | ||
NEADBANL_01601 | 1.1e-63 | spxA_2 | 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 | |
NEADBANL_01602 | 5e-284 | treB | G | phosphotransferase system | ||
NEADBANL_01603 | 1.2e-100 | treR | K | UTRA | ||
NEADBANL_01604 | 1.3e-288 | treC | 3.2.1.93 | GH13 | G | Alpha amylase, catalytic domain protein |
NEADBANL_01605 | 1.3e-17 | |||||
NEADBANL_01606 | 4.7e-238 | G | Bacterial extracellular solute-binding protein | |||
NEADBANL_01607 | 1e-60 | pdxH | S | Pyridoxamine 5'-phosphate oxidase | ||
NEADBANL_01608 | 7.7e-238 | XK27_01810 | S | Calcineurin-like phosphoesterase | ||
NEADBANL_01611 | 0.0 | hsdR | 3.1.21.3 | V | Subunit R is required for both nuclease and ATPase activities, but not for modification | |
NEADBANL_01612 | 9.4e-207 | hsdM | 2.1.1.72 | V | type I restriction-modification system | |
NEADBANL_01613 | 3.7e-137 | rpsB | J | Belongs to the universal ribosomal protein uS2 family | ||
NEADBANL_01614 | 8.3e-185 | 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 | ||
NEADBANL_01615 | 1.4e-130 | pyrH | 2.7.4.22 | F | Catalyzes the reversible phosphorylation of UMP to UDP | |
NEADBANL_01616 | 2e-92 | 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 | ||
NEADBANL_01617 | 1.9e-138 | uppS | 2.5.1.31 | H | Catalyzes the condensation of isopentenyl diphosphate (IPP) with allylic pyrophosphates generating different type of terpenoids | |
NEADBANL_01618 | 9.6e-136 | cdsA | 2.7.7.41 | I | Belongs to the CDS family | |
NEADBANL_01619 | 2.8e-195 | rseP | 3.4.21.107, 3.4.21.116 | M | zinc metalloprotease | |
NEADBANL_01620 | 0.0 | proS | 6.1.1.15 | J | Catalyzes the attachment of proline to tRNA(Pro) in a two-step reaction proline is first activated by ATP to form Pro- AMP and then transferred to the acceptor end of tRNA(Pro). As ProRS can inadvertently accommodate and process non-cognate amino acids such as alanine and cysteine, to avoid such errors it has two additional distinct editing activities against alanine. One activity is designated as 'pretransfer' editing and involves the tRNA(Pro)-independent hydrolysis of activated Ala-AMP. The other activity is designated 'posttransfer' editing and involves deacylation of mischarged Ala-tRNA(Pro). The misacylated Cys- tRNA(Pro) is not edited by ProRS | |
NEADBANL_01621 | 0.0 | polC | 2.7.7.7 | L | Required for replicative DNA synthesis. This DNA polymerase also exhibits 3' to 5' exonuclease activity | |
NEADBANL_01622 | 2.5e-83 | rimP | J | Required for maturation of 30S ribosomal subunits | ||
NEADBANL_01623 | 9.9e-198 | nusA | K | Participates in both transcription termination and antitermination | ||
NEADBANL_01624 | 8.8e-47 | ylxR | K | Protein of unknown function (DUF448) | ||
NEADBANL_01625 | 3.2e-47 | rplGA | J | ribosomal protein | ||
NEADBANL_01626 | 0.0 | infB | J | One of the essential components for the initiation of protein synthesis. Protects formylmethionyl-tRNA from spontaneous hydrolysis and promotes its binding to the 30S ribosomal subunits. Also involved in the hydrolysis of GTP during the formation of the 70S ribosomal complex | ||
NEADBANL_01627 | 3e-60 | 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 | ||
NEADBANL_01628 | 3.4e-158 | truB | 5.4.99.25 | J | Responsible for synthesis of pseudouridine from uracil- 55 in the psi GC loop of transfer RNAs | |
NEADBANL_01629 | 1.7e-176 | ribF | 2.7.1.26, 2.7.7.2 | H | Belongs to the ribF family | |
NEADBANL_01630 | 4.5e-194 | hrcA | K | Negative regulator of class I heat shock genes (grpE- dnaK-dnaJ and groELS operons). Prevents heat-shock induction of these operons | ||
NEADBANL_01631 | 8e-68 | 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 | ||
NEADBANL_01632 | 0.0 | dnaK | O | Heat shock 70 kDa protein | ||
NEADBANL_01633 | 5.8e-203 | 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 | ||
NEADBANL_01634 | 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 | ||
NEADBANL_01635 | 2.6e-102 | srtA | 3.4.22.70 | M | sortase family | |
NEADBANL_01636 | 0.0 | recJ | L | Single-stranded-DNA-specific exonuclease RecJ | ||
NEADBANL_01637 | 1.6e-94 | apt | 2.4.2.22, 2.4.2.7 | F | Catalyzes a salvage reaction resulting in the formation of AMP, that is energically less costly than de novo synthesis | |
NEADBANL_01638 | 1.1e-53 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_01639 | 6.9e-77 | oppA | E | ABC transporter substrate-binding protein | ||
NEADBANL_01640 | 1.1e-106 | galR | K | Transcriptional regulator | ||
NEADBANL_01643 | 4.2e-46 | L | COG3547 Transposase and inactivated derivatives | |||
NEADBANL_01644 | 5.9e-43 | |||||
NEADBANL_01645 | 4.2e-286 | lsa | S | ABC transporter | ||
NEADBANL_01646 | 1.3e-73 | clcA | P | chloride | ||
NEADBANL_01647 | 3.2e-118 | 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) | |
NEADBANL_01648 | 1.6e-126 | pyrF | 4.1.1.23 | F | Catalyzes the decarboxylation of orotidine 5'- monophosphate (OMP) to uridine 5'-monophosphate (UMP) | |
NEADBANL_01649 | 2e-166 | pyrD | 1.3.1.14, 1.3.98.1 | F | Belongs to the dihydroorotate dehydrogenase family. Type 1 subfamily | |
NEADBANL_01650 | 2.7e-94 | pyrR | 2.4.2.9 | F | Also displays a weak uracil phosphoribosyltransferase activity which is not physiologically significant | |
NEADBANL_01651 | 1.6e-182 | pyrB | 2.1.3.2 | F | Belongs to the ATCase OTCase family | |
NEADBANL_01652 | 2.6e-244 | pyrC | 3.5.2.3 | F | Belongs to the metallo-dependent hydrolases superfamily. DHOase family. Class I DHOase subfamily | |
NEADBANL_01653 | 2.4e-211 | carA | 6.3.5.5 | F | Carbamoyl-phosphate synthetase glutamine chain | |
NEADBANL_01654 | 0.0 | carB | 6.3.5.5 | F | Carbamoyl-phosphate synthase | |
NEADBANL_01655 | 1.6e-153 | lctP | C | L-lactate permease | ||
NEADBANL_01656 | 1.8e-60 | lctP | C | L-lactate permease | ||
NEADBANL_01657 | 1.8e-148 | glcU | U | sugar transport | ||
NEADBANL_01658 | 6e-45 | |||||
NEADBANL_01659 | 5.2e-80 | msrB | 1.8.4.11, 1.8.4.12 | O | peptide methionine sulfoxide reductase | |
NEADBANL_01660 | 0.0 | pepX | 3.4.14.11 | E | Removes N-terminal dipeptides sequentially from polypeptides having unsubstituted N-termini provided that the penultimate residue is proline | |
NEADBANL_01661 | 1.2e-42 | S | Alpha beta hydrolase | |||
NEADBANL_01662 | 1.9e-37 | |||||
NEADBANL_01663 | 2.6e-52 | |||||
NEADBANL_01664 | 4.6e-154 | S | haloacid dehalogenase-like hydrolase | |||
NEADBANL_01665 | 5.4e-292 | V | ABC-type multidrug transport system, ATPase and permease components | |||
NEADBANL_01666 | 4.4e-278 | V | ABC-type multidrug transport system, ATPase and permease components | |||
NEADBANL_01667 | 1.5e-64 | arsC | 1.20.4.1 | P | Belongs to the ArsC family | |
NEADBANL_01668 | 2.9e-178 | I | Carboxylesterase family | |||
NEADBANL_01670 | 2.1e-206 | M | Glycosyl hydrolases family 25 | |||
NEADBANL_01671 | 2.1e-160 | cinI | S | Serine hydrolase (FSH1) | ||
NEADBANL_01672 | 6.5e-302 | S | Predicted membrane protein (DUF2207) | |||
NEADBANL_01673 | 1.6e-27 | dmpI | 5.3.2.6 | G | Belongs to the 4-oxalocrotonate tautomerase family | |
NEADBANL_01676 | 7e-256 | S | Uncharacterized protein conserved in bacteria (DUF2325) | |||
NEADBANL_01677 | 1.4e-150 | S | Uncharacterised 5xTM membrane BCR, YitT family COG1284 | |||
NEADBANL_01678 | 5.8e-49 | rplU | J | This protein binds to 23S rRNA in the presence of protein L20 | ||
NEADBANL_01679 | 7.8e-48 | rpmA | J | Belongs to the bacterial ribosomal protein bL27 family | ||
NEADBANL_01680 | 1.9e-195 | pepP | 3.4.11.9, 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
NEADBANL_01681 | 4.9e-102 | 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 | ||
NEADBANL_01682 | 3.4e-71 | yqhY | S | Asp23 family, cell envelope-related function | ||
NEADBANL_01683 | 2.1e-64 | 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 | ||
NEADBANL_01684 | 3.4e-144 | folD | 1.5.1.5, 3.5.4.9 | F | Catalyzes the oxidation of 5,10- methylenetetrahydrofolate to 5,10-methenyltetrahydrofolate and then the hydrolysis of 5,10-methenyltetrahydrofolate to 10- formyltetrahydrofolate | |
NEADBANL_01685 | 2.9e-185 | 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 | |
NEADBANL_01686 | 3.2e-34 | 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 | |
NEADBANL_01687 | 2.4e-153 | 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 | |
NEADBANL_01688 | 2.8e-47 | lysM | M | LysM domain | ||
NEADBANL_01689 | 5.1e-176 | |||||
NEADBANL_01690 | 1.4e-210 | mdtG | EGP | Major facilitator Superfamily | ||
NEADBANL_01691 | 4.9e-90 | ymdB | S | Macro domain protein | ||
NEADBANL_01692 | 3.5e-97 | L | Transposase | |||
NEADBANL_01695 | 2e-230 | S | Putative peptidoglycan binding domain | |||
NEADBANL_01696 | 7.5e-95 | S | ECF-type riboflavin transporter, S component | |||
NEADBANL_01697 | 5.1e-100 | pdxK | 2.7.1.35 | H | Phosphomethylpyrimidine kinase | |
NEADBANL_01698 | 9.3e-204 | pbpX1 | V | Beta-lactamase | ||
NEADBANL_01699 | 4.1e-115 | lacA | 2.3.1.79 | S | Transferase hexapeptide repeat | |
NEADBANL_01700 | 4.1e-80 | yvbK | 3.1.3.25 | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | |
NEADBANL_01701 | 1.2e-112 | 3.6.1.27 | I | Acid phosphatase homologues | ||
NEADBANL_01702 | 1.1e-189 | mmuM | 1.5.1.20, 2.1.1.10 | H | homocysteine S-methyltransferase | |
NEADBANL_01703 | 0.0 | uvrA3 | L | excinuclease ABC, A subunit | ||
NEADBANL_01704 | 2.4e-80 | C | Flavodoxin | |||
NEADBANL_01705 | 0.0 | recQ | 3.6.4.12 | L | ATP-dependent DNA helicase RecQ | |
NEADBANL_01706 | 2.3e-245 | ynbB | 4.4.1.1 | P | aluminum resistance | |
NEADBANL_01707 | 0.0 | yaaO | 4.1.1.17, 4.1.1.19 | E | Orn/Lys/Arg decarboxylase, C-terminal domain | |
NEADBANL_01708 | 5e-284 | E | Amino acid permease | |||
NEADBANL_01709 | 1.6e-93 | XK26_02160 | C | Pyridoxamine 5'-phosphate oxidase | ||
NEADBANL_01710 | 1.3e-273 | pepV | 3.5.1.18 | E | dipeptidase PepV | |
NEADBANL_01711 | 4e-80 | mmuP | E | amino acid | ||
NEADBANL_01712 | 6.2e-196 | 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 | |
NEADBANL_01713 | 7e-71 | rimI | 2.3.1.128 | K | Ribosomal-protein-alanine acetyltransferase | |
NEADBANL_01714 | 8.1e-134 | yeaZ | 2.3.1.234 | O | Universal bacterial protein YeaZ | |
NEADBANL_01715 | 5.2e-87 | S | ECF transporter, substrate-specific component | |||
NEADBANL_01716 | 8.4e-139 | fat | 3.1.2.21 | I | Acyl-ACP thioesterase | |
NEADBANL_01717 | 7.9e-157 | rsmI | 2.1.1.198 | H | Catalyzes the 2'-O-methylation of the ribose of cytidine 1402 (C1402) in 16S rRNA | |
NEADBANL_01718 | 1.8e-59 | yabA | L | Involved in initiation control of chromosome replication | ||
NEADBANL_01719 | 4.4e-155 | holB | 2.7.7.7 | L | DNA polymerase III | |
NEADBANL_01720 | 8.9e-53 | yaaQ | S | Cyclic-di-AMP receptor | ||
NEADBANL_01721 | 1.6e-114 | tmk | 2.7.4.9 | F | Phosphorylation of dTMP to form dTDP in both de novo and salvage pathways of dTTP synthesis | |
NEADBANL_01722 | 1.1e-34 | S | Protein of unknown function (DUF2508) | |||
NEADBANL_01723 | 1.6e-108 | 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 | ||
NEADBANL_01724 | 2.8e-41 | yaaK | S | Binds to DNA and alters its conformation. May be involved in regulation of gene expression, nucleoid organization and DNA protection | ||
NEADBANL_01725 | 1.2e-35 | M | lipopolysaccharide 3-alpha-galactosyltransferase activity | |||
NEADBANL_01726 | 4.9e-89 | 2.4.1.58 | GT8 | M | family 8 | |
NEADBANL_01727 | 0.0 | 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 | |
NEADBANL_01728 | 2.2e-90 | tadA | 3.5.4.33 | F | Catalyzes the deamination of adenosine to inosine at the wobble position 34 of tRNA(Arg2) | |
NEADBANL_01729 | 9e-26 | |||||
NEADBANL_01730 | 1.3e-116 | rsmC | 2.1.1.172 | J | Methyltransferase | |
NEADBANL_01731 | 6e-141 | potC | 2.1.1.172, 2.1.1.80, 3.1.1.61 | J | Ion channel | |
NEADBANL_01732 | 1.8e-54 | rplL | J | Forms part of the ribosomal stalk which helps the ribosome interact with GTP-bound translation factors. Is thus essential for accurate translation | ||
NEADBANL_01733 | 7e-84 | rplJ | J | Forms part of the ribosomal stalk, playing a central role in the interaction of the ribosome with GTP-bound translation factors | ||
NEADBANL_01734 | 7.8e-13 | GT2,GT4 | M | family 8 | ||
NEADBANL_01735 | 1e-229 | S | Tetratricopeptide repeat protein | |||
NEADBANL_01736 | 2.3e-41 | hup | L | Histone-like DNA-binding protein which is capable of wrapping DNA to stabilize it, and thus to prevent its denaturation under extreme environmental conditions | ||
NEADBANL_01737 | 1.9e-247 | der | 1.1.1.399, 1.1.1.95 | S | GTPase that plays an essential role in the late steps of ribosome biogenesis | |
NEADBANL_01738 | 5.5e-212 | rpsA | 1.17.7.4 | J | Ribosomal protein S1 | |
NEADBANL_01739 | 2.2e-114 | 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 | |
NEADBANL_01740 | 2.7e-18 | M | Lysin motif | |||
NEADBANL_01741 | 8.7e-114 | 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 | |||
NEADBANL_01742 | 3.1e-130 | rluB | 5.4.99.19, 5.4.99.21, 5.4.99.22 | J | Belongs to the pseudouridine synthase RsuA family | |
NEADBANL_01743 | 4.1e-104 | scpB | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpA that pull DNA away from mid-cell into both cell halves | ||
NEADBANL_01744 | 7.6e-132 | scpA | D | Participates in chromosomal partition during cell division. May act via the formation of a condensin-like complex containing Smc and ScpB that pull DNA away from mid-cell into both cell halves | ||
NEADBANL_01745 | 2.6e-61 | ribT | K | COG0454 Histone acetyltransferase HPA2 and related acetyltransferases | ||
NEADBANL_01746 | 3.1e-167 | xerD | D | recombinase XerD | ||
NEADBANL_01747 | 1.9e-169 | cvfB | S | S1 domain | ||
NEADBANL_01748 | 0.0 | pyk | 2.7.1.40, 2.7.7.4 | G | Belongs to the pyruvate kinase family | |
NEADBANL_01749 | 3.3e-183 | 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 | |
NEADBANL_01750 | 0.0 | dnaE | 2.7.7.7 | L | DNA polymerase | |
NEADBANL_01751 | 2.3e-23 | S | Protein of unknown function (DUF2929) | |||
NEADBANL_01752 | 2.8e-309 | cpdB | 3.1.3.6, 3.1.4.16 | F | Belongs to the 5'-nucleotidase family | |
NEADBANL_01753 | 1.3e-27 | rpmF | J | Belongs to the bacterial ribosomal protein bL32 family | ||
NEADBANL_01754 | 8.6e-28 | yrvD | S | Lipopolysaccharide assembly protein A domain | ||
NEADBANL_01755 | 1.6e-143 | XK27_05435 | 1.1.1.100 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |
NEADBANL_01756 | 5.8e-177 | rnz | 3.1.26.11 | J | Zinc phosphodiesterase, which displays some tRNA 3'- processing endonuclease activity. Probably involved in tRNA maturation, by removing a 3'-trailer from precursor tRNA | |
NEADBANL_01757 | 5.2e-84 | I | Acyltransferase | |||
NEADBANL_01758 | 1.3e-39 | S | Protein of unknown function (DUF2922) | |||
NEADBANL_01759 | 2.3e-28 | |||||
NEADBANL_01760 | 1.1e-95 | ackA | 2.7.2.1 | F | Catalyzes the formation of acetyl phosphate from acetate and ATP. Can also catalyze the reverse reaction | |
NEADBANL_01761 | 1.7e-279 | yjeM | E | Amino Acid | ||
NEADBANL_01762 | 1.9e-81 | S | Fic/DOC family | |||
NEADBANL_01763 | 3.9e-292 | |||||
NEADBANL_01764 | 2.3e-83 | |||||
NEADBANL_01765 | 2.6e-94 | S | Protein of unknown function (DUF805) | |||
NEADBANL_01776 | 4.5e-45 | |||||
NEADBANL_01777 | 3.3e-59 | T | PemK-like, MazF-like toxin of type II toxin-antitoxin system | |||
NEADBANL_01778 | 1.9e-89 | hslV | 3.4.25.2 | O | Protease subunit of a proteasome-like degradation complex believed to be a general protein degrading machinery | |
NEADBANL_01779 | 1.5e-99 | xerC | D | Phage integrase, N-terminal SAM-like domain | ||
NEADBANL_01780 | 4.9e-34 | |||||
NEADBANL_01781 | 8.8e-184 | yumC | 1.18.1.2, 1.19.1.1, 1.8.1.9 | C | Ferredoxin--NADP reductase | |
NEADBANL_01782 | 5.2e-116 | dedA | S | SNARE-like domain protein | ||
NEADBANL_01783 | 3.7e-100 | S | Protein of unknown function (DUF1461) | |||
NEADBANL_01784 | 6.9e-144 | nagD | 2.7.1.25, 3.1.3.41 | G | Catalyzes the dephosphorylation of 2-6 carbon acid sugars in vitro | |
NEADBANL_01785 | 1.7e-105 | yutD | S | Protein of unknown function (DUF1027) | ||
NEADBANL_01786 | 1.2e-274 | yunD | 3.1.3.5 | F | Belongs to the 5'-nucleotidase family | |
NEADBANL_01787 | 4.3e-55 | |||||
NEADBANL_01788 | 2.3e-267 | ugpQ | 3.1.4.46 | C | glycerophosphoryl diester phosphodiesterase | |
NEADBANL_01789 | 4.9e-182 | ccpA | K | catabolite control protein A | ||
NEADBANL_01790 | 9.1e-214 | pepQ | 3.4.13.9 | E | Creatinase/Prolidase N-terminal domain | |
NEADBANL_01791 | 1.3e-36 | |||||
NEADBANL_01792 | 9.5e-10 | WQ51_05790 | S | protein containing a divergent version of the methyl-accepting chemotaxis-like domain | ||
NEADBANL_01793 | 8.6e-148 | ykuT | M | mechanosensitive ion channel | ||
NEADBANL_01794 | 6.6e-18 | |||||
NEADBANL_01795 | 1.4e-153 | K | sequence-specific DNA binding | |||
NEADBANL_01796 | 2.5e-112 | 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 | |
NEADBANL_01797 | 3.9e-145 | murI | 3.6.1.66, 5.1.1.3 | M | Provides the (R)-glutamate required for cell wall biosynthesis | |
NEADBANL_01798 | 1.1e-71 | yslB | S | Protein of unknown function (DUF2507) | ||
NEADBANL_01799 | 9.7e-59 | 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 | ||
NEADBANL_01800 | 3.5e-54 | trxA | O | Belongs to the thioredoxin family | ||
NEADBANL_01801 | 0.0 | mutS2 | L | Endonuclease that is involved in the suppression of homologous recombination and may therefore have a key role in the control of bacterial genetic diversity | ||
NEADBANL_01802 | 1.1e-50 | yrzB | S | Belongs to the UPF0473 family | ||
NEADBANL_01803 | 6.1e-73 | yqgF | J | Could be a nuclease involved in processing of the 5'-end of pre-16S rRNA | ||
NEADBANL_01804 | 2e-42 | yrzL | S | Belongs to the UPF0297 family | ||
NEADBANL_01805 | 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 | |
NEADBANL_01806 | 4.7e-228 | 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 | |
NEADBANL_01807 | 4.7e-182 | nrnA | 3.1.13.3, 3.1.3.7 | S | DHHA1 domain protein | |
NEADBANL_01808 | 2.7e-216 | dinB | 2.7.7.7 | L | Poorly processive, error-prone DNA polymerase involved in untargeted mutagenesis. Copies undamaged DNA at stalled replication forks, which arise in vivo from mismatched or misaligned primer ends. These misaligned primers can be extended by PolIV. Exhibits no 3'-5' exonuclease (proofreading) activity. May be involved in translesional synthesis, in conjunction with the beta clamp from PolIII | |
NEADBANL_01809 | 5.6e-288 | zwf | 1.1.1.363, 1.1.1.49 | G | Catalyzes the oxidation of glucose 6-phosphate to 6- phosphogluconolactone | |
NEADBANL_01810 | 9.6e-41 | yajC | U | Preprotein translocase | ||
NEADBANL_01811 | 6.7e-187 | ruvB | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing | |
NEADBANL_01812 | 2.9e-102 | ruvA | 3.6.4.12 | L | The RuvA-RuvB complex in the presence of ATP renatures cruciform structure in supercoiled DNA with palindromic sequence, indicating that it may promote strand exchange reactions in homologous recombination. RuvAB is a helicase that mediates the Holliday junction migration by localized denaturation and reannealing. RuvA stimulates, in the presence of DNA, the weak ATPase activity of RuvB | |
NEADBANL_01813 | 0.0 | mutL | L | This protein is involved in the repair of mismatches in DNA. It is required for dam-dependent methyl-directed DNA mismatch repair. May act as a molecular matchmaker , a protein that promotes the formation of a stable complex between two or more DNA-binding proteins in an ATP-dependent manner without itself being part of a final effector complex | ||
NEADBANL_01814 | 0.0 | mutS | L | that it carries out the mismatch recognition step. This protein has a weak ATPase activity | ||
NEADBANL_01815 | 2.6e-294 | groL | O | Prevents misfolding and promotes the refolding and proper assembly of unfolded polypeptides generated under stress conditions | ||
NEADBANL_01816 | 1.4e-41 | groS | O | Binds to Cpn60 in the presence of Mg-ATP and suppresses the ATPase activity of the latter | ||
NEADBANL_01817 | 3.5e-75 | |||||
NEADBANL_01818 | 5.4e-178 | M | CHAP domain | |||
NEADBANL_01819 | 0.0 | scrA | 2.7.1.208, 2.7.1.211, 5.3.1.1 | G | phosphotransferase system | |
NEADBANL_01820 | 1.4e-294 | scrB | 3.2.1.26 | GH32 | G | invertase |
NEADBANL_01821 | 7.2e-170 | scrR | K | helix_turn _helix lactose operon repressor | ||
NEADBANL_01822 | 1.1e-142 | L | PFAM RNA-directed DNA polymerase (Reverse transcriptase) | |||
NEADBANL_01823 | 1.9e-116 | V | ABC transporter transmembrane region | |||
NEADBANL_01824 | 1.1e-35 | 2.7.7.73, 2.7.7.80 | H | ThiF family | ||
NEADBANL_01825 | 2.5e-67 | K | Helix-turn-helix XRE-family like proteins | |||
NEADBANL_01826 | 3.8e-111 | rex | K | Modulates transcription in response to changes in cellular NADH NAD( ) redox state | ||
NEADBANL_01827 | 0.0 | uup | S | ABC transporter, ATP-binding protein | ||
NEADBANL_01828 | 1.5e-218 | oxc | 4.1.1.8 | EH | Belongs to the TPP enzyme family | |
NEADBANL_01829 | 8.8e-157 | frc | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
NEADBANL_01830 | 6.9e-96 | yfdE | 2.8.3.16, 2.8.3.19 | C | Involved in the catabolism of oxalate and in the adapatation to low pH via the induction of the oxalate-dependent acid tolerance response (ATR). Catalyzes the transfer of the CoA moiety from formyl-CoA to oxalate | |
NEADBANL_01831 | 4.6e-111 | dnaX | 2.4.99.16, 2.7.7.7 | GH13 | M | domain protein |
NEADBANL_01833 | 1.1e-57 | L | An automated process has identified a potential problem with this gene model | |||
NEADBANL_01834 | 1.2e-113 | K | UTRA | |||
NEADBANL_01835 | 7.6e-164 | S | Oxidoreductase family, NAD-binding Rossmann fold | |||
NEADBANL_01836 | 6e-126 | deoC | 4.1.2.4 | F | Catalyzes a reversible aldol reaction between acetaldehyde and D-glyceraldehyde 3-phosphate to generate 2-deoxy- D-ribose 5-phosphate | |
NEADBANL_01837 | 5.1e-78 | 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 | ||
NEADBANL_01838 | 0.0 | rnr | J | 3'-5' exoribonuclease that releases 5'-nucleoside monophosphates and is involved in maturation of structured RNAs | ||
NEADBANL_01839 | 1.7e-29 | secG | U | Preprotein translocase | ||
NEADBANL_01840 | 0.0 | ltaS | 2.7.8.20 | M | Phosphoglycerol transferase and related proteins, alkaline phosphatase superfamily | |
NEADBANL_01841 | 2.8e-177 | mprF | S | Catalyzes the transfer of a lysyl group from L-lysyl- tRNA(Lys) to membrane-bound phosphatidylglycerol (PG), which produces lysylphosphatidylglycerol (LPG), a major component of the bacterial membrane with a positive net charge. LPG synthesis contributes to bacterial virulence as it is involved in the resistance mechanism against cationic antimicrobial peptides (CAMP) produces by the host's immune system (defensins, cathelicidins) and by the competing microorganisms | ||
NEADBANL_01842 | 1.2e-199 | cpoA | GT4 | M | Glycosyltransferase, group 1 family protein | |
NEADBANL_01843 | 7.9e-224 | mgs | 2.4.1.337 | GT4 | M | Glycosyl transferase 4-like domain |
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)