GapMind for catabolism of small carbon sources

 

Protein WP_038206091.1 in Xenophilus azovorans DSM 13620

Annotation: NCBI__GCF_000745855.1:WP_038206091.1

Length: 295 amino acids

Source: GCF_000745855.1 in NCBI

Candidate for 12 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-galacturonate catabolism uxuL hi Senescence marker protein-30 family protein (characterized, see rationale) 69% 100% 426.4 L-arabinolactonase (EC 3.1.1.15) 36% 167.5
D-glucuronate catabolism uxuL hi Senescence marker protein-30 family protein (characterized, see rationale) 69% 100% 426.4 L-arabinolactonase (EC 3.1.1.15) 36% 167.5
D-galactose catabolism galactonolactonase hi galactaro-1,5-lactonase (characterized) 63% 100% 370.2 2-deoxy-ribono-1,5-lactonase 37% 162.2
lactose catabolism galactonolactonase hi galactaro-1,5-lactonase (characterized) 63% 100% 370.2 2-deoxy-ribono-1,5-lactonase 37% 162.2
L-arabinose catabolism xacC lo L-arabinolactonase (EC 3.1.1.15) (characterized) 36% 100% 167.5 galactaro-1,5-lactonase 63% 370.2
D-xylose catabolism xylC lo Xylonolactonase (EC 3.1.1.68) (characterized) 37% 92% 153.7 galactaro-1,5-lactonase 63% 370.2
D-cellobiose catabolism gnl lo gluconolactonase (EC 3.1.1.17) (characterized) 36% 98% 145.6 galactaro-1,5-lactonase 63% 370.2
D-glucose catabolism gnl lo gluconolactonase (EC 3.1.1.17) (characterized) 36% 98% 145.6 galactaro-1,5-lactonase 63% 370.2
lactose catabolism gnl lo gluconolactonase (EC 3.1.1.17) (characterized) 36% 98% 145.6 galactaro-1,5-lactonase 63% 370.2
D-maltose catabolism gnl lo gluconolactonase (EC 3.1.1.17) (characterized) 36% 98% 145.6 galactaro-1,5-lactonase 63% 370.2
sucrose catabolism gnl lo gluconolactonase (EC 3.1.1.17) (characterized) 36% 98% 145.6 galactaro-1,5-lactonase 63% 370.2
trehalose catabolism gnl lo gluconolactonase (EC 3.1.1.17) (characterized) 36% 98% 145.6 galactaro-1,5-lactonase 63% 370.2

Sequence Analysis Tools

View WP_038206091.1 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

MTAELVLDARNGTGESPVWHAAEQALYWVDIPARAIHRWSPADGHRQWTTGEMPACIAAR
AGRPGQWVAGMESGIFALQLGDDGRAAATPLATVAHAAPAMRFNDGRCDRQGRLWAGTMC
LDMAAAVRAGAWYRFGAGDDALPPRLTGFIVPNGLAFSPDGRTMYLSDSHPEVQAVWAFD
YDTDSGTPANRRLFVDMAPLPGRPDGAAVDVDGCYWICGNDAGLVHRFTPQGRLDRSLAL
PVKKPAMCAFGGPRLDTLYVTSIRPGGDLSGQPLAGGVFALDPGTQGIAEPAFAG

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