GapMind for catabolism of small carbon sources

 

Protein WP_015329941.1 in Fibrella aestuarina BUZ 2

Annotation: NCBI__GCF_000331105.1:WP_015329941.1

Length: 241 amino acids

Source: GCF_000331105.1 in NCBI

Candidate for 46 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-proline catabolism opuBA med BilEA aka OpuBA protein, component of A proline/glycine betaine uptake system. Also reported to be a bile exclusion system that exports oxgall and other bile compounds, BilEA/EB or OpuBA/BB (required for normal virulence) (characterized) 49% 72% 214.9 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-histidine catabolism hutV med ABC transporter for L-Histidine, ATPase component (characterized) 44% 81% 174.9 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-proline catabolism hutV med HutV aka HISV aka R02702 aka SMC00670, component of Uptake system for hisitidine, proline, proline-betaine and glycine-betaine (characterized) 40% 81% 162.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
putrescine catabolism potA lo PotG aka B0855, component of Putrescine porter (characterized) 43% 63% 178.3 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-proline catabolism proV lo glycine betaine/l-proline transport atp-binding protein prov (characterized) 43% 55% 176.8 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism malK1 lo MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) 41% 65% 168.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
trehalose catabolism thuK lo MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) 41% 65% 168.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-mannitol catabolism mtlK lo SmoK aka POLK, component of Hexitol (glucitol; mannitol) porter (characterized) 40% 70% 166.8 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism malK_Bb lo ABC-type maltose transport, ATP binding protein (characterized, see rationale) 39% 67% 162.5 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
N-acetyl-D-glucosamine catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 40% 71% 161.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-fucose catabolism SM_b21106 lo ABC transporter for L-Fucose, ATPase component (characterized) 39% 64% 161.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 40% 71% 161.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-sorbitol (glucitol) catabolism mtlK lo ABC transporter for D-Sorbitol, ATPase component (characterized) 38% 63% 160.6 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
lactose catabolism lacK lo ABC transporter for Lactose, ATPase component (characterized) 41% 65% 158.3 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
sucrose catabolism thuK lo ABC transporter (characterized, see rationale) 39% 61% 157.9 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-cellobiose catabolism SMc04256 lo ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 40% 61% 156.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism musK lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 40% 63% 156.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-cellobiose catabolism msiK lo MsiK protein, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized) 39% 63% 155.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism malK lo ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized) 38% 63% 155.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-glucosamine (chitosamine) catabolism SM_b21216 lo ABC transporter for D-Glucosamine, ATPase component (characterized) 39% 65% 153.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 38% 68% 151.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-arabinose catabolism xacK lo Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale) 40% 62% 151 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-arabinose catabolism xacJ lo Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) 40% 61% 148.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism malK_Aa lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 39% 61% 148.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-maltose catabolism malK_Sm lo MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) 38% 65% 147.5 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
trehalose catabolism malK lo MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) 38% 65% 147.5 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-arginine catabolism artP lo Arginine transport ATP-binding protein ArtM (characterized) 38% 98% 146.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-alanine catabolism Pf6N2E2_5405 lo ABC transporter for D-Alanine, ATPase component (characterized) 37% 93% 145.6 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
xylitol catabolism Dshi_0546 lo ABC transporter for Xylitol, ATPase component (characterized) 36% 69% 144.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-asparagine catabolism bztD lo BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 36% 90% 143.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-aspartate catabolism bztD lo BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 36% 90% 143.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-glutamate catabolism gltL lo BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 36% 90% 143.7 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-asparagine catabolism aapP lo AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 35% 92% 142.1 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-aspartate catabolism aapP lo AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 35% 92% 142.1 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-glutamate catabolism aapP lo AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 35% 92% 142.1 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-histidine catabolism aapP lo AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 35% 92% 142.1 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-leucine catabolism aapP lo AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 35% 92% 142.1 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-proline catabolism aapP lo AapP, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 35% 92% 142.1 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-asparagine catabolism peb1C lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 35% 97% 140.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-aspartate catabolism peb1C lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 35% 97% 140.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-citrulline catabolism PS417_17605 lo ATP-binding cassette domain-containing protein; SubName: Full=Amino acid transporter; SubName: Full=Histidine ABC transporter ATP-binding protein; SubName: Full=Histidine transport system ATP-binding protein (characterized, see rationale) 35% 91% 139.8 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-glucosamine (chitosamine) catabolism AO353_21725 lo ABC transporter for D-Glucosamine, putative ATPase component (characterized) 34% 94% 134.4 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-tryptophan catabolism ecfA1 lo Energy-coupling factor transporter ATP-binding protein EcfA1; Short=ECF transporter A component EcfA; EC 7.-.-.- (characterized, see rationale) 33% 79% 120.9 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
L-tryptophan catabolism ecfA2 lo Energy-coupling factor transporter ATP-binding protein EcfA2; Short=ECF transporter A component EcfA2; EC 7.-.-.- (characterized, see rationale) 35% 76% 118.6 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-cellobiose catabolism TM0027 lo TM0027, component of β-glucoside porter (Conners et al., 2005). Binds cellobiose, laminaribiose (Nanavati et al. 2006). Regulated by cellobiose-responsive repressor BglR (characterized) 32% 87% 110.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8
D-cellobiose catabolism cbtD lo CbtD, component of Cellobiose and cellooligosaccharide porter (characterized) 32% 65% 108.2 Glycine betaine/carnitine/choline transport ATP-binding protein OpuCA 52% 248.8

Sequence Analysis Tools

View WP_015329941.1 at NCBI

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

Find the best match in UniProt

Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

Find homologs in fast.genomics

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Sequence

MATPAIVLSQVTKRYHQQPVVDSVSLTIAAGETLVLLGTSGSGKTTTLKMMNRLIDADEG
TIAINGTDVRQQSPHELRRGIGYVIQEAGLFPHYTVADNIALVPRLLDWPPDRIAQRTHE
LLTMLHLPESLLTRFPDQLSGGQRQRVGLARALAADPPIILMDEPFGALDPLTRADIRRE
FRELDALQRKTIVLVTHDVREAFALADRVALMDAGRIVQLGEPNVLRDSPATPFVRRFVD
A

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.

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About GapMind

Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.

A candidate for a step is "high confidence" if either:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

Otherwise, a candidate is "medium confidence" if either:

Other blast hits with at least 50% coverage are "low confidence."

Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:

GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).

For more information, see:

If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know

by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory