GapMind for Amino acid biosynthesis


Protein 199805 in Shewanella oneidensis MR-1

Annotation: FitnessBrowser__MR1:199805

Length: 405 amino acids

Source: MR1 in FitnessBrowser

Candidate for 10 steps in Amino acid biosynthesis

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine biosynthesis argD'B hi Succinylornithine transaminase (EC (characterized) 65% 100% 538.5
L-arginine biosynthesis argD'B hi astC: succinylornithine transaminase family (EC (TIGR03246) 99% 693
L-arginine biosynthesis argD hi succinylornithine transaminase (EC (characterized) 65% 98% 532.7
L-proline biosynthesis argD hi succinylornithine transaminase (EC (characterized) 65% 98% 532.7
L-lysine biosynthesis dapC hi Acetylornithine/succinyldiaminopimelate aminotransferase; ACOAT; DapATase; Succinyldiaminopimelate transferase; EC; EC (characterized) 62% 100% 526.2
L-proline biosynthesis OAT lo Ornithine aminotransferase 1; OAT 1; EC; Ornithine--oxo-acid aminotransferase 1 (uncharacterized) 38% 95% 260.8 Succinylornithine transaminase (EC 65% 538.5
L-lysine biosynthesis lysJ lo [amino group carrier protein]-gamma-(L-lysyl)-L-glutamate aminotransferase (EC (characterized) 39% 94% 252.3 Succinylornithine transaminase (EC 65% 538.5
L-arginine biosynthesis lysJ lo [amino group carrier protein]-C-terminal-L-glutamyl-γ-L-lysine aminotransferase (EC; EC (characterized) 39% 99% 245.4 Succinylornithine transaminase (EC 65% 538.5
L-proline biosynthesis lysJ lo [amino group carrier protein]-C-terminal-L-glutamyl-γ-L-lysine aminotransferase (EC; EC (characterized) 39% 99% 245.4 Succinylornithine transaminase (EC 65% 538.5
L-lysine biosynthesis lysN lo 2-aminoadipate transaminase; 2-aminoadipate aminotransferase; L-2AA aminotransferase; EC (characterized) 33% 97% 203.4 Succinylornithine transaminase (EC 65% 538.5
glycine biosynthesis agx1 lo Alanine--glyoxylate aminotransferase 2 homolog 1, mitochondrial; Beta-alanine-pyruvate aminotransferase 1; EC (characterized) 32% 80% 179.5 Succinylornithine transaminase (EC 65% 538.5

Sequence Analysis Tools

View 199805 at FitnessBrowser

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...



This GapMind analysis is from Apr 09 2024. The underlying query database was built on Apr 09 2024.



Related tools

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