NZ_CP017297.1|WP_076808668.1|2438559_2439447_+|carbohydrate-ABC-transporter-permease |
gnl|CDD|223472 |
COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].
|
2.68578e-67 |
NZ_CP017297.1|WP_076808671.1|2446027_2447356_+|sugar-ABC-transporter-substrate-binding-protein |
gnl|CDD|270303 |
cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.
|
1.44346e-51 |
NZ_CP017297.1|WP_083713513.1|2437508_2438510_+|sugar-ABC-transporter-permease |
gnl|CDD|224096 |
COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].
|
1.51311e-76 |
NZ_CP017297.1|WP_083713514.1|2444568_2445831_+|multidrug-effflux-MFS-transporter |
gnl|CDD|340878 |
cd17320, MFS_MdfA_MDR_like, Multidrug transporter MdfA and similar multidrug resistance (MDR) transporters of the Major Facilitator Superfamily. This family is composed of bacterial multidrug resistance (MDR) transporters including several proteins from Escherichia coli such as MdfA (also called chloramphenicol resistance pump Cmr), EmrD, MdtM, MdtL, bicyclomycin resistance protein (also called sulfonamide resistance protein), and the uncharacterized inner membrane transport protein YdhC. EmrD is a proton-dependent secondary transporter, first identified as an efflux pump for uncouplers of oxidative phosphorylation. It expels a range of drug molecules and amphipathic compounds across the inner membrane of E. coli. Similarly, MdfA is a secondary multidrug transporter that exports a broad spectrum of structurally and electrically dissimilar toxic compounds. These MDR transporters are drug/H+ antiporters (DHA) belonging to the Major Facilitator Superfamily (MFS) of membrane transport proteins, which are thought to function through a single substrate binding site, alternating-access mechanism involving a rocker-switch type of movement.
|
4.47921e-89 |
NZ_CP017297.1|WP_076808661.1|2427789_2428923_-|aspartate-semialdehyde-dehydrogenase |
gnl|CDD|237845 |
PRK14874, PRK14874, aspartate-semialdehyde dehydrogenase; Provisional.
|
0 |
NZ_CP017297.1|WP_076808658.1|2425911_2426838_-|PRC-barrel-domain-containing-protein |
gnl|CDD|368352 |
pfam05239, PRC, PRC-barrel domain. The PRC-barrel is an all beta barrel domain found in photosystem reaction centre subunit H of the purple bacteria and RNA metabolism proteins of the RimM group. PRC-barrels are approximately 80 residues long, and found widely represented in bacteria, archaea and plants. This domain is also present at the carboxyl terminus of the pan-bacterial protein RimM, which is involved in ribosomal maturation and processing of 16S rRNA. A family of small proteins conserved in all known euryarchaea are composed entirely of a single stand-alone copy of the domain.
|
5.78008e-05 |
NZ_CP017297.1|WP_076808670.1|2442500_2443364_+|sugar-ABC-transporter-permease |
gnl|CDD|224096 |
COG1175, UgpA, ABC-type sugar transport systems, permease components [Carbohydrate transport and metabolism].
|
1.41364e-81 |
NZ_CP017297.1|WP_076808660.1|2426854_2427793_-|TetR/AcrR-family-transcriptional-regulator |
gnl|CDD|224228 |
COG1309, AcrR, Transcriptional regulator [Transcription].
|
4.6687e-15 |
NZ_CP017297.1|WP_076808664.1|2428919_2430287_-|aspartate-kinase |
gnl|CDD|235843 |
PRK06635, PRK06635, aspartate kinase; Reviewed.
|
0 |
NZ_CP017297.1|WP_076811162.1|2443551_2444367_+|carbohydrate-ABC-transporter-permease |
gnl|CDD|223472 |
COG0395, UgpE, ABC-type sugar transport system, permease component [Carbohydrate transport and metabolism].
|
9.02268e-71 |
NZ_CP017297.1|WP_076808675.1|2452045_2452369_+|2Fe-2S-iron-sulfur-cluster-binding-domain-containing-protein |
gnl|CDD|185668 |
PTZ00490, PTZ00490, Ferredoxin superfamily; Provisional.
|
1.02334e-13 |
NZ_CP017297.1|WP_076808673.1|2449601_2450195_-|recombination-protein-RecR |
gnl|CDD|234616 |
PRK00076, recR, recombination protein RecR; Reviewed.
|
3.4932e-110 |
NZ_CP017297.1|WP_076808672.1|2447866_2449582_-|hypothetical-protein |
gnl|CDD|240529 |
cd13124, MATE_SpoVB_like, Stage V sporulation protein B, also known as Stage III sporulation protein F, and related proteins. The integral membrane protein SpoVB has been implicated in the biosynthesis of the peptidoglycan component of the spore cortex in Bacillus subtilis. This model represents a subfamily of the multidrug and toxic compound extrusion (MATE)-like proteins. Proteins from the MATE family are involved in exporting metabolites across the cell membrane and are often responsible for multidrug resistance (MDR).
|
0.002296 |
NZ_CP017297.1|WP_157235892.1|2436006_2437452_+|extracellular-solute-binding-protein |
gnl|CDD|270303 |
cd13585, PBP2_TMBP_like, The periplasmic-binding component of ABC transport systems specific for trehalose/maltose and similar oligosaccharides; possess type 2 periplasmic binding fold. This family includes the periplasmic trehalose/maltose-binding component of an ABC transport system and related proteins from archaea and bacteria. Members of this group belong to the type 2 periplasmic-binding fold superfamily. PBP2 is comprised of two globular subdomains connected by a flexible hinge and bind their ligand in the cleft between these domains in a manner resembling a Venus flytrap. The majority of PBP2 proteins function in the uptake of small soluble substrates in eubacteria and archaea. After binding their specific ligand with high affinity, they can interact with a cognate membrane transport complex comprised of two integral membrane domains and two cytoplasmically located ATPase domains. This interaction triggers the ligand translocation across the cytoplasmic membrane energized by ATP hydrolysis.
|
2.3358e-73 |
NZ_CP017297.1|WP_076808674.1|2450377_2451730_+|glycoside-hydrolase-family-125-protein |
gnl|CDD|377716 |
pfam06824, Glyco_hydro_125, Metal-independent alpha-mannosidase (GH125). This family, which contains bacterial and fungal glycoside hydrolases, is also known as GH125. They function as metal-independent alpha-mannosidases, with specificity for alpha-1,6-linked non-reducing terminal mannose residues. Structurally this family is part of the 6 hairpin glycosidase superfamily.
|
0 |
NZ_CP017297.1|WP_076808677.1|2452477_2453008_+|transcriptional-regulator |
gnl|CDD|227312 |
COG4978, COG4978, Transcriptional regulator, effector-binding domain/component [Transcription / Signal transduction mechanisms].
|
2.32476e-10 |
NZ_CP017297.1|WP_083713511.1|2434607_2435675_-|Cro/Cl-family-transcriptional-regulator |
gnl|CDD|225263 |
COG2390, DeoR, Transcriptional regulator, contains sigma factor-related N-terminal domain [Transcription].
|
6.33547e-42 |
NZ_CP017297.1|WP_076808669.1|2439959_2442092_-|NAD(+)-synthase |
gnl|CDD|235057 |
PRK02628, nadE, NAD synthetase; Reviewed.
|
0 |
NZ_CP017297.1|WP_076808667.1|2432627_2434214_-|mannitol-dehydrogenase-family-protein |
gnl|CDD|223324 |
COG0246, MtlD, Mannitol-1-phosphate/altronate dehydrogenases [Carbohydrate transport and metabolism].
|
3.4633e-166 |