GapMind for catabolism of small carbon sources

 

Protein WP_061533899.1 in Collimonas arenae Ter10

Annotation: NCBI__GCF_001584165.1:WP_061533899.1

Length: 297 amino acids

Source: GCF_001584165.1 in NCBI

Candidate for 27 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-cellobiose catabolism gtsC hi ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
D-glucose catabolism gtsC hi ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
lactose catabolism gtsC hi ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
D-maltose catabolism gtsC hi ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
sucrose catabolism gtsC hi ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
trehalose catabolism gtsC hi ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
D-galactose catabolism PfGW456L13_1896 hi ABC transporter for D-Galactose and D-Glucose, permease component 2 (characterized) 65% 98% 374 ABC transporter for D-Cellobiose and D-Salicin, permease component 1 54% 322.0
D-xylose catabolism gtsC med ABC transporter for D-Glucose-6-Phosphate, permease component 1 (characterized) 66% 97% 383.6 ABC transporter for D-Galactose and D-Glucose, permease component 2 65% 374.0
D-cellobiose catabolism SMc04257 med ABC transporter for D-Cellobiose and D-Salicin, permease component 1 (characterized) 54% 92% 322 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-mannose catabolism TT_C0326 med Sugar transport system permease protein aka TT_C0326, component of The glucose/mannose porter TTC0326-8 plus MalK1 (ABC protein, shared with 3.A.1.1.25) (characterized) 47% 100% 263.5 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
L-arabinose catabolism xacI lo Xylose/arabinose import permease protein XacI (characterized, see rationale) 36% 93% 169.1 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
L-arabinose catabolism araU lo AraU, component of Arabinose, fructose, xylose porter (characterized) 30% 98% 142.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-fructose catabolism araU lo AraU, component of Arabinose, fructose, xylose porter (characterized) 30% 98% 142.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
sucrose catabolism araU lo AraU, component of Arabinose, fructose, xylose porter (characterized) 30% 98% 142.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-xylose catabolism araU lo AraU, component of Arabinose, fructose, xylose porter (characterized) 30% 98% 142.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-maltose catabolism aglG lo ABC transporter for D-Maltose and D-Trehalose, permease component 2 (characterized) 36% 57% 129 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
sucrose catabolism aglG lo ABC transporter for D-Maltose and D-Trehalose, permease component 2 (characterized) 36% 57% 129 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
trehalose catabolism aglG lo ABC transporter for D-Maltose and D-Trehalose, permease component 2 (characterized) 36% 57% 129 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-cellobiose catabolism aglG' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 56% 117.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-glucose catabolism aglG' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 56% 117.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
lactose catabolism aglG' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 56% 117.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-maltose catabolism aglG' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 56% 117.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
sucrose catabolism aglG' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 56% 117.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
trehalose catabolism aglG' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 56% 117.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-cellobiose catabolism cebG lo CBP protein aka CebG, 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) 30% 99% 113.2 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
D-maltose catabolism thuG lo Trehalose/maltose transport system permease protein MalG (characterized) 31% 75% 95.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6
trehalose catabolism thuG lo Trehalose/maltose transport system permease protein MalG (characterized) 31% 75% 95.9 ABC transporter for D-Glucose-6-Phosphate, permease component 1 66% 383.6

Sequence Analysis Tools

View WP_061533899.1 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

MAADSTSNTIYNEGSKLTAGRVVIYALLVLCALYYLAPLYVMLSTSVKTLDEIRSGNLLS
LPMSPTGAAWSKAWSNACTGVDCNGLQPFFWNSIKMAVPAVLISTLIGSLNGYVLAHWRF
RGSEILFTALMVGCFIPFQVVILPMARLLGLVGMANTTPGLVFVHVVYGIAFTTLFFRNY
YVTVPEELVKAARIDGAGFFMTYRKIIFPLSLPIFMVCFIWQFTQIWNDFLFGVVFGGSD
AKPVTVALNNLVNTSTGVTEYNVNMAAAIIAALPTLVVYLLAGKYFVRGLTAGAVKG

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