GapMind for catabolism of small carbon sources

 

Protein WP_003468267.1 in Gracilibacillus halophilus YIM-C55.5

Annotation: NCBI__GCF_000359605.1:WP_003468267.1

Length: 358 amino acids

Source: GCF_000359605.1 in NCBI

Candidate for 8 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
xylitol catabolism xdhA hi xylitol 2-dehydrogenase (EC 1.1.1.9) (characterized) 60% 98% 477.2 mannitol 2-dehydrogenase (NADP+) (EC 1.1.1.138) 33% 203.4
D-xylose catabolism xdhA hi xylitol 2-dehydrogenase (EC 1.1.1.9) (characterized) 60% 98% 477.2 mannitol 2-dehydrogenase (NADP+) (EC 1.1.1.138) 33% 203.4
D-sorbitol (glucitol) catabolism sdh lo Sorbitol dehydrogenase; SDH; EC 1.1.1.-; Glucitol dehydrogenase; L-iditol 2-dehydrogenase; EC 1.1.1.14; Polyol dehydrogenase; Xylitol dehydrogenase; EC 1.1.1.9 (uncharacterized) 35% 99% 208 xylitol 2-dehydrogenase (EC 1.1.1.9) 60% 477.2
D-mannitol catabolism mt2d lo mannitol 2-dehydrogenase (NADP+) (EC 1.1.1.138) (characterized) 33% 99% 203.4 xylitol 2-dehydrogenase (EC 1.1.1.9) 60% 477.2
L-threonine catabolism tdh lo L-threonine 3-dehydrogenase (EC 1.1.1.103) (characterized) 35% 99% 190.7 xylitol 2-dehydrogenase (EC 1.1.1.9) 60% 477.2
ethanol catabolism etoh-dh-nad lo L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized) 34% 99% 186.4 xylitol 2-dehydrogenase (EC 1.1.1.9) 60% 477.2
myo-inositol catabolism iolM lo scyllo-inosose 3-dehydrogenase; 2-keto-myo-inositol dehydrogenase; EC 1.1.1.- (characterized) 33% 90% 149.4 xylitol 2-dehydrogenase (EC 1.1.1.9) 60% 477.2
L-rhamnose catabolism LRA5 lo 2-dehydro-3-deoxy-L-rhamnonate dehydrogenase (NAD(+)); 2-keto-3-deoxy-L-rhamnonate dehydrogenase; KDRDH; L-KDR dehydrogenase; EC 1.1.1.401 (characterized) 31% 83% 132.9 xylitol 2-dehydrogenase (EC 1.1.1.9) 60% 477.2

Sequence Analysis Tools

View WP_003468267.1 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

MSQLPETMKAVVCHGPEDYRVEEVNTPTAGPGEIVIKVKACGICGSDLKVYHGADMYWAG
DDPWLKAPVIPGHEFYGEVAELGEGAAETHDLQIGDRITTDQINPCGNCMYCNSGKYWMC
QVHNMYGFQREVAEGAMAEYMKFSPQSKIYKVPEGVNDYEASLLEPMACAVHAVQRATIE
FEDFVVMAGAGTLGLCMIQLIKLKTPKTLVVLDANDRRLELAKKYGADICMNPTKEDVIQ
KVKDLTNGYGCDVYIEATGNPKGVTQGLEMVRKLGRYVEFSVFGKETTTDWSVIGDKKEL
DIRGSHLGPYTYPIAIDLFERGLVSAEGIVTHTFDIDDFPQAIATAQDPEAIKVSIKP

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