GapMind for catabolism of small carbon sources

 

Protein WP_028583721.1 in Desulfobulbus mediterraneus DSM 13871

Annotation: NCBI__GCF_000429965.1:WP_028583721.1

Length: 409 amino acids

Source: GCF_000429965.1 in NCBI

Candidate for 23 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-proline catabolism proV hi Glycine betaine/proline betaine transport system ATP-binding protein ProV (characterized) 57% 99% 443.7 OtaA, component of The salt-induced glycine betaine OtaABC transporter 49% 375.9
L-proline catabolism opuBA med BusAA, component of Uptake system for glycine-betaine (high affinity) and proline (low affinity) (OpuAA-OpuABC) or BusAA-ABC of Lactococcus lactis). BusAA, the ATPase subunit, has a C-terminal tandem cystathionine β-synthase (CBS) domain which is the cytoplasmic K+ sensor for osmotic stress (osmotic strength)while the BusABC subunit has the membrane and receptor domains fused to each other (Biemans-Oldehinkel et al., 2006; Mahmood et al., 2006; Gul et al. 2012). An N-terminal amphipathic α-helix of OpuA is necessary for high activity but is not critical for biogenesis or the ionic regulation of transport (characterized) 45% 95% 334.3 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
L-histidine catabolism hutV med ABC transporter for L-Histidine, ATPase component (characterized) 57% 95% 302.4 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
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) 57% 96% 298.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
L-histidine catabolism Ac3H11_2560 med ABC transporter for L-Histidine, ATPase component (characterized) 41% 76% 151 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
putrescine catabolism potA lo PotG aka B0855, component of Putrescine porter (characterized) 42% 59% 176.8 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
L-arabinose catabolism xacJ lo Xylose/arabinose import ATP-binding protein XacJ; EC 7.5.2.13 (characterized, see rationale) 40% 60% 169.1 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
D-cellobiose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 40% 64% 167.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
D-glucose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 40% 64% 167.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
lactose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 40% 64% 167.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
D-maltose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 40% 64% 167.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
sucrose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 40% 64% 167.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
trehalose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 40% 64% 167.9 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
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) 37% 65% 166 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
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) 37% 65% 166 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
N-acetyl-D-glucosamine catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 36% 65% 153.3 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 36% 65% 153.3 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
D-maltose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 36% 67% 149.1 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
sucrose catabolism thuK lo ThuK aka RB0314 aka SMB20328, component of Trehalose/maltose/sucrose porter (trehalose inducible) (characterized) 36% 67% 149.1 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
D-maltose catabolism musK lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 37% 57% 144.4 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
trehalose catabolism treV lo TreV, component of Trehalose porter (characterized) 31% 76% 142.5 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
xylitol catabolism HSERO_RS17020 lo ABC-type sugar transport system, ATPase component protein (characterized, see rationale) 34% 56% 142.1 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4
L-tryptophan catabolism ecfA1 lo Energy-coupling factor transporter ATP-binding protein EcfA1; Short=ECF transporter A component EcfA; EC 7.-.-.- (characterized, see rationale) 36% 89% 140.2 Glycine betaine/choline transport system ATP-binding protein OusV 59% 451.4

Sequence Analysis Tools

View WP_028583721.1 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

MDIITVKNLYKVFGADPAKGLALVKAGNSKEEIYEQTGLTVGVQDASFTVAKGEIFVVMG
LSGSGKSTLVRMLNRLIEPTAGEVWVDGDNVLTMNRDQLVKFRRSKTSMVFQSFALMPHL
NVLDNVCFGLELDGMPRPQREERGMDALKQVGLEGWEKAAPGELSGGMQQRVGLARGLAM
DPDILLMDEAFSALDPLIRSEMQDELLKLQDRHERTIVFISHDLDEALRIGDRIAIMEGG
RVVQVGSPEEILQNPADDYVRAFFRGVDPTGVISAGDIVRDNQPKVIWHTPEGSPRATLE
LLNNQDREFGYVVGSDRKFYGVVSTDSLRDLLEAKNGKGNIEQAFLEAATPVQEGECLQD
ILPQVASHLWPIPVVDENNLYQGVVSKNRFLRTLYRAGNDNGNGNDLDQ

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