GapMind for catabolism of small carbon sources

 

Protein WP_086511720.1 in Halomonas desiderata SP1

Annotation: NCBI__GCF_002151265.1:WP_086511720.1

Length: 255 amino acids

Source: GCF_002151265.1 in NCBI

Candidate for 11 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
4-hydroxybenzoate catabolism badH hi BadH (characterized) 60% 100% 308.9 2-hydroxy-4-isopropenyl-cyclohexan-1-carboxyl-CoA dehydrogenase 54% 263.8
phenylacetate catabolism badH hi BadH (characterized) 60% 100% 308.9 2-hydroxy-4-isopropenyl-cyclohexan-1-carboxyl-CoA dehydrogenase 54% 263.8
L-phenylalanine catabolism badH hi BadH (characterized) 60% 100% 308.9 2-hydroxy-4-isopropenyl-cyclohexan-1-carboxyl-CoA dehydrogenase 54% 263.8
xylitol catabolism xdhA lo D-xylulose reductase (EC 1.1.1.9) (characterized) 31% 97% 141 BadH 60% 308.9
D-xylose catabolism xdhA lo D-xylulose reductase (EC 1.1.1.9) (characterized) 31% 97% 141 BadH 60% 308.9
L-rhamnose catabolism LRA1 lo NAD(P)+-dependent L-rhamnose 1-dehydrogenase (EC 1.1.1.378; EC 1.1.1.173) (characterized) 39% 97% 137.9 BadH 60% 308.9
L-rhamnose catabolism LRA5 lo 2-dehydro-3-deoxy-L-rhamnonate dehydrogenase (NAD(+)); 2-keto-3-deoxy-L-rhamnonate dehydrogenase; KDRDH; L-KDR dehydrogenase; L-KDR 4-dehydrogenase; EC 1.1.1.401 (characterized) 32% 95% 132.5 BadH 60% 308.9
L-fucose catabolism fucDH lo Short-chain dehydrogenase/reductase SDR (characterized, see rationale) 33% 97% 128.6 BadH 60% 308.9
D-xylose catabolism DKDP-dehydrog lo SDR family oxidoreductase (characterized, see rationale) 31% 96% 125.6 BadH 60% 308.9
D-sorbitol (glucitol) catabolism srlD lo sorbitol-6-phosphate dehydrogenase (characterized) 31% 99% 111.7 BadH 60% 308.9
L-isoleucine catabolism ivdG lo 3-hydroxy-2-methylbutyryl-CoA dehydrogenase subunit (EC 1.1.1.178) (characterized) 31% 99% 102.1 BadH 60% 308.9

Sequence Analysis Tools

View WP_086511720.1 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

MRGLEDKTVIVTGGGGGIGRAVCRRFAAEGSKVAVLDRDLDAARRTVEVIAEAGGQARAY
GADITDYAAIVDTVERIEAELGVPRVLVNNAGFDRFMPFLKTEPALWESLIAVNLTGALN
MHHVVLPRMIEAGGGKVINVASDAARVGSSGEAVYAACKAGLLGLSKTLARELATKGVTL
NVVCPGPTDTALLQGFAETSRDPEKLLEAFRNAVPMRRIGQPEDYPGIIALLASDDADFI
TGQVISVSGGLTMAG

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