| ORF_ID | e_value | Gene_name | EC_number | CAZy | COGs | Description |
|---|---|---|---|---|---|---|
| NKBNNLII_00002 | 6.8e-201 | lctO | C | L-lactate dehydrogenase (FMN-dependent) and related alpha-hydroxy acid dehydrogenases | ||
| NKBNNLII_00003 | 0.0 | poxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
| NKBNNLII_00004 | 8.7e-72 | K | Transcriptional regulator | |||
| NKBNNLII_00005 | 0.0 | spxB | 1.2.3.3, 1.2.5.1 | EH | Belongs to the TPP enzyme family | |
| NKBNNLII_00006 | 8.6e-63 | srlB | 2.7.1.198 | G | PTS system glucitol/sorbitol-specific IIA component | |
| NKBNNLII_00007 | 1.5e-173 | srlE | 2.7.1.198 | G | Sorbitol phosphotransferase enzyme II N-terminus | |
| NKBNNLII_00008 | 2e-100 | srlA | G | PTS system enzyme II sorbitol-specific factor | ||
| NKBNNLII_00009 | 1.1e-86 | gutM | K | Glucitol operon activator protein (GutM) | ||
| NKBNNLII_00010 | 0.0 | srlM | 2.7.1.194, 2.7.1.200, 2.7.1.202 | GKT | Mga helix-turn-helix domain | |
| NKBNNLII_00011 | 3.8e-145 | IQ | NAD dependent epimerase/dehydratase family | |||
| NKBNNLII_00012 | 2.7e-160 | rbsU | U | ribose uptake protein RbsU | ||
| NKBNNLII_00013 | 7.9e-67 | rbsD | 5.4.99.62 | G | Catalyzes the interconversion of beta-pyran and beta- furan forms of D-ribose | |
| NKBNNLII_00014 | 2.3e-162 | 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 | |
| NKBNNLII_00015 | 5.9e-188 | rbsR | K | helix_turn _helix lactose operon repressor | ||
| NKBNNLII_00016 | 0.0 | adhE | 1.1.1.1, 1.2.1.10 | C | belongs to the iron- containing alcohol dehydrogenase family | |
| NKBNNLII_00017 | 2.7e-79 | T | Universal stress protein family | |||
| NKBNNLII_00018 | 2.2e-99 | padR | K | Virulence activator alpha C-term | ||
| NKBNNLII_00019 | 1.7e-104 | padC | Q | Phenolic acid decarboxylase | ||
| NKBNNLII_00020 | 2.9e-145 | tesE | Q | hydratase | ||
| NKBNNLII_00021 | 2.2e-87 | yjaB_1 | K | Acetyltransferase (GNAT) domain | ||
| NKBNNLII_00022 | 1.2e-157 | degV | S | DegV family | ||
| NKBNNLII_00023 | 2.4e-58 | 2.6.1.2, 2.6.1.66 | K | Bacteriophage CI repressor helix-turn-helix domain | ||
| NKBNNLII_00024 | 2.2e-198 | pepC | 3.4.22.40 | E | aminopeptidase | |
| NKBNNLII_00025 | 2e-43 | pepC | 3.4.22.40 | E | aminopeptidase | |
| NKBNNLII_00027 | 1.2e-108 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
| NKBNNLII_00028 | 1.1e-302 | |||||
| NKBNNLII_00030 | 1.2e-159 | S | Bacterial protein of unknown function (DUF916) | |||
| NKBNNLII_00031 | 6.9e-93 | S | Cell surface protein | |||
| NKBNNLII_00032 | 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 | ||
| NKBNNLII_00033 | 4.6e-255 | 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 | ||
| NKBNNLII_00034 | 1.2e-129 | jag | S | R3H domain protein | ||
| NKBNNLII_00035 | 9.3e-239 | Q | Imidazolonepropionase and related amidohydrolases | |||
| NKBNNLII_00036 | 1e-309 | E | ABC transporter, substratebinding protein | |||
| NKBNNLII_00037 | 1.8e-105 | yidC | U | Required for the insertion and or proper folding and or complex formation of integral membrane proteins into the membrane. Involved in integration of membrane proteins that insert both dependently and independently of the Sec translocase complex, as well as at least some lipoproteins | ||
| NKBNNLII_00038 | 6.4e-57 | 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 | |
| NKBNNLII_00039 | 9.1e-256 | 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 | ||
| NKBNNLII_00040 | 2e-208 | 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 | |
| NKBNNLII_00041 | 5e-37 | yaaA | S | S4 domain protein YaaA | ||
| NKBNNLII_00042 | 1.9e-206 | 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 | ||
| NKBNNLII_00043 | 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 | |
| NKBNNLII_00044 | 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 | |
| NKBNNLII_00045 | 8.7e-38 | galR | K | Transcriptional regulator | ||
| NKBNNLII_00046 | 4.1e-200 | galM | 5.1.3.3 | G | Catalyzes the interconversion of alpha and beta anomers of maltose | |
| NKBNNLII_00047 | 0.0 | lacS | G | Transporter | ||
| NKBNNLII_00048 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
| NKBNNLII_00049 | 2.9e-184 | lacM | 3.2.1.23, 3.2.1.35, 3.2.1.51, 3.2.1.97 | GH101,GH29 | G | beta-galactosidase |
| NKBNNLII_00050 | 0.0 | lacL | 3.2.1.23 | G | Belongs to the glycosyl hydrolase 2 family | |
| NKBNNLII_00051 | 9.3e-225 | 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) | |
| NKBNNLII_00052 | 3.1e-192 | galE | 5.1.3.2 | M | Belongs to the NAD(P)-dependent epimerase dehydratase family | |
| NKBNNLII_00053 | 1.3e-284 | galT | 2.7.7.12 | G | UDP-glucose--hexose-1-phosphate uridylyltransferase | |
| NKBNNLII_00054 | 2e-183 | galR | K | Transcriptional regulator | ||
| NKBNNLII_00055 | 1.6e-76 | K | Helix-turn-helix XRE-family like proteins | |||
| NKBNNLII_00056 | 7.4e-109 | fic | D | Fic/DOC family | ||
| NKBNNLII_00057 | 1.1e-181 | rhaR | K | helix_turn_helix, arabinose operon control protein | ||
| NKBNNLII_00058 | 8.6e-232 | EGP | Major facilitator Superfamily | |||
| NKBNNLII_00059 | 7.9e-304 | ram2 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | |
| NKBNNLII_00060 | 8.1e-230 | mdtH | P | Sugar (and other) transporter | ||
| NKBNNLII_00061 | 0.0 | 3.2.1.40 | G | Bacterial alpha-L-rhamnosidase 6 hairpin glycosidase domain | ||
| NKBNNLII_00062 | 6.8e-179 | galR | K | Periplasmic binding protein-like domain | ||
| NKBNNLII_00063 | 2.7e-233 | 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 | |||
| NKBNNLII_00064 | 2.2e-68 | S | Domain of unknown function (DUF3284) | |||
| NKBNNLII_00065 | 0.0 | rafA | 3.2.1.22 | G | alpha-galactosidase | |
| NKBNNLII_00066 | 0.0 | lacA | 3.2.1.23 | G | -beta-galactosidase | |
| NKBNNLII_00067 | 1.3e-249 | brnQ | U | Component of the transport system for branched-chain amino acids | ||
| NKBNNLII_00068 | 0.0 | ubiB | S | ABC1 family | ||
| NKBNNLII_00069 | 1.8e-108 | aqpZ | U | Belongs to the MIP aquaporin (TC 1.A.8) family | ||
| NKBNNLII_00070 | 9.2e-220 | 3.1.3.1 | S | associated with various cellular activities | ||
| NKBNNLII_00071 | 6.9e-248 | S | Putative metallopeptidase domain | |||
| NKBNNLII_00072 | 1.5e-49 | |||||
| NKBNNLII_00073 | 1.7e-102 | K | Bacterial regulatory proteins, tetR family | |||
| NKBNNLII_00074 | 3.7e-184 | S | Bacteriophage abortive infection AbiH | |||
| NKBNNLII_00075 | 3.8e-140 | cylB | V | ABC-2 type transporter | ||
| NKBNNLII_00076 | 1.8e-153 | cylA | V | AAA domain, putative AbiEii toxin, Type IV TA system | ||
| NKBNNLII_00077 | 1.1e-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 | |||
| NKBNNLII_00079 | 3.8e-63 | S | Domain of unknown function (DUF4440) | |||
| NKBNNLII_00080 | 1.4e-110 | pgm8 | G | Histidine phosphatase superfamily (branch 1) | ||
| NKBNNLII_00081 | 8.2e-48 | |||||
| NKBNNLII_00082 | 3.2e-37 | |||||
| NKBNNLII_00083 | 2.8e-85 | yvbK | 3.1.3.25 | K | GNAT family | |
| NKBNNLII_00084 | 3.8e-84 | |||||
| NKBNNLII_00086 | 8.4e-116 | lepB | 3.4.21.89 | U | Belongs to the peptidase S26 family | |
| NKBNNLII_00087 | 2.2e-100 | maa | 2.3.1.18, 2.3.1.79 | S | Maltose acetyltransferase | |
| NKBNNLII_00088 | 8e-117 | nth | 4.2.99.18 | L | DNA repair enzyme that has both DNA N-glycosylase activity and AP-lyase activity. The DNA N-glycosylase activity releases various damaged pyrimidines from DNA by cleaving the N- glycosidic bond, leaving an AP (apurinic apyrimidinic) site. The AP-lyase activity cleaves the phosphodiester bond 3' to the AP site by a beta-elimination, leaving a 3'-terminal unsaturated sugar and a product with a terminal 5'-phosphate | |
| NKBNNLII_00090 | 7.5e-121 | macB | V | ABC transporter, ATP-binding protein | ||
| NKBNNLII_00091 | 0.0 | ylbB | V | ABC transporter permease | ||
| NKBNNLII_00092 | 1.7e-235 | dapE | 3.5.1.18 | E | succinyl-diaminopimelate desuccinylase | |
| NKBNNLII_00093 | 9.8e-79 | K | transcriptional regulator, MerR family | |||
| NKBNNLII_00094 | 3.2e-76 | yphH | S | Cupin domain | ||
| NKBNNLII_00095 | 7.3e-55 | yphJ | 4.1.1.44 | S | Carboxymuconolactone decarboxylase family | |
| NKBNNLII_00096 | 1.4e-128 | S | Belongs to the short-chain dehydrogenases reductases (SDR) family | |||
| NKBNNLII_00097 | 4.7e-211 | natB | CP | ABC-2 family transporter protein | ||
| NKBNNLII_00098 | 4e-167 | natA | S | ABC transporter, ATP-binding protein | ||
| NKBNNLII_00100 | 1.5e-52 | |||||
| NKBNNLII_00101 | 1.6e-117 | |||||
| NKBNNLII_00102 | 7.3e-86 | 2.7.7.1, 3.6.1.55 | F | belongs to the nudix hydrolase family | ||
| NKBNNLII_00103 | 2.4e-57 | |||||
| NKBNNLII_00104 | 4.7e-39 | S | Phage gp6-like head-tail connector protein | |||
| NKBNNLII_00107 | 5.4e-273 | S | Caudovirus prohead serine protease | |||
| NKBNNLII_00108 | 6.1e-202 | S | Phage portal protein | |||
| NKBNNLII_00110 | 0.0 | terL | S | overlaps another CDS with the same product name |
Showing 1 to 100 of 2,842 entries
eggNOG-mapper v2 (Database: eggNOG v5.0, Jul. 2018 release)