GapMind for catabolism of small carbon sources

 

Protein WP_049952773.1 in Halostagnicola larsenii XH-48

Annotation: NCBI__GCF_000517625.1:WP_049952773.1

Length: 471 amino acids

Source: GCF_000517625.1 in NCBI

Candidate for 6 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-lactate catabolism D-LDH med Probable D-lactate dehydrogenase, mitochondrial; DLD; Lactate dehydrogenase D; EC 1.1.2.4 (characterized) 40% 91% 308.1 lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) 34% 238.4
L-threonine catabolism D-LDH med Probable D-lactate dehydrogenase, mitochondrial; DLD; Lactate dehydrogenase D; EC 1.1.2.4 (characterized) 40% 91% 308.1 lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) 34% 238.4
D-lactate catabolism lctD lo lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) (characterized) 34% 90% 238.4 Probable D-lactate dehydrogenase, mitochondrial; DLD; Lactate dehydrogenase D; EC 1.1.2.4 40% 308.1
L-threonine catabolism lctD lo lactate dehydrogenase (NAD+, ferredoxin) (subunit 1/3) (EC 1.3.1.110) (characterized) 34% 90% 238.4 Probable D-lactate dehydrogenase, mitochondrial; DLD; Lactate dehydrogenase D; EC 1.1.2.4 40% 308.1
D-lactate catabolism glcD lo D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized) 34% 88% 228 Probable D-lactate dehydrogenase, mitochondrial; DLD; Lactate dehydrogenase D; EC 1.1.2.4 40% 308.1
L-threonine catabolism glcD lo D-lactate oxidase, FAD-linked subunit (EC 1.1.3.15) (characterized) 34% 88% 228 Probable D-lactate dehydrogenase, mitochondrial; DLD; Lactate dehydrogenase D; EC 1.1.2.4 40% 308.1

Sequence Analysis Tools

View WP_049952773.1 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

MTYDCSFLADLPLEDDQRSFAKSRRETHAADWGTEDSTRAVVPDAVVYPHSTADVSTVLA
AATERGVPVTPYAAGTGLEGGAVPAAAGISLDLTEMDRVVEYRPEDFQIDVEPGILGSTV
NEAAGDDGLFFPPLPSSGDISTIGGMIATDASGMQTVKYGEIADWILRLEAVLADGTVIE
TGSRAVKTSSGYNLTDLLVGSEGTLGVITEATLELAGRPAQVRGGRAIFGALEDATSAVS
DAVRAGVDVAKIEVVDGLSARMANEYFGMDLPDAPMVFLEFHADHGVGEEIEFCRTIFEE
HDVLRFETSRDDEMADLWQARRELAYAVVSYDPDLEPIQPGDVTVPISRYPEIVRTAKRL
GAEHDLLVPCYGHAGDGNLHYTALVDYDDPAHLERCKEVYSRVVDRAIALGGTATGEHGI
GLGKRDYLEDEHGSQAVDAMKAIKRTFDPDGILNPGKIFPEHTDRTEGRSR

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