GapMind for catabolism of small carbon sources

 

Protein WP_057508082.1 in Stenotrophomonas chelatiphaga DSM 21508

Annotation: NCBI__GCF_001431535.1:WP_057508082.1

Length: 238 amino acids

Source: GCF_001431535.1 in NCBI

Candidate for 16 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-lysine catabolism hisP med Amino-acid ABC transporter, ATP-binding protein (characterized, see rationale) 42% 78% 153.7 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-histidine catabolism Ac3H11_2560 med ABC transporter for L-Histidine, ATPase component (characterized) 42% 76% 142.5 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-histidine catabolism PA5503 lo Methionine import ATP-binding protein MetN 2, component of L-Histidine uptake porter, MetIQN (characterized) 38% 72% 154.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-glutamate catabolism gltL lo GluA aka CGL1950, component of Glutamate porter (characterized) 39% 89% 150.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-arginine catabolism artP lo Probable ATP-binding component of ABC transporter, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) 39% 84% 145.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-histidine catabolism hisP lo Probable ATP-binding component of ABC transporter, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) 39% 84% 145.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-asparagine catabolism bgtA lo ATPase (characterized, see rationale) 39% 78% 139 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
L-aspartate catabolism bgtA lo ATPase (characterized, see rationale) 39% 78% 139 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
D-cellobiose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 36% 62% 130.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
D-glucose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 36% 62% 130.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
lactose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 36% 62% 130.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
D-maltose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 36% 62% 130.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
sucrose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 36% 62% 130.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
trehalose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 36% 62% 130.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
N-acetyl-D-glucosamine catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 35% 60% 127.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 35% 60% 127.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 217.6

Sequence Analysis Tools

View WP_057508082.1 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

Fitness BLAST: loading...

Sequence

MLEMRAVAKVFRTEQVETHALRSLDLLVNEGEFVAVTGPSGSGKTTFLNIAGLLETFTSG
TYLLDGQDVSTLGDDARSRLRNQKIGFIFQGFNLIPDLNLFDNVDVPLRYRGMSAAERRE
RIEKALSQVGLGSRMKHYPSELSGGQQQRAAIARALAGSPRLLLADEPTGNLDSTMARGV
MELLEEINAAGTTIVMVTHDPELAARAQRNVHIVDGQVTDLLREPVLATARRIAAVNE

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