GapMind for Amino acid biosynthesis

 

Protein WP_013530453.1 in Mesorhizobium ciceri biovar biserrulae WSM1271

Annotation: NCBI__GCF_000185905.1:WP_013530453.1

Length: 386 amino acids

Source: GCF_000185905.1 in NCBI

Candidate for 3 steps in Amino acid biosynthesis

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine biosynthesis argE med acetylornithine deacetylase (EC 3.5.1.16) (characterized) 39% 99% 279.6 Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase; EC 3.5.1.18 30% 137.5
L-arginine biosynthesis argE hi argE: acetylornithine deacetylase (ArgE) (EC 3.5.1.16) (TIGR01892) 100% 384.7 Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase; EC 3.5.1.18 30% 137.5
L-proline biosynthesis argE med acetylornithine deacetylase (EC 3.5.1.16) (characterized) 39% 99% 279.6 Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase; EC 3.5.1.18 30% 137.5
L-proline biosynthesis argE hi argE: acetylornithine deacetylase (ArgE) (EC 3.5.1.16) (TIGR01892) 100% 384.7 Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase; EC 3.5.1.18 30% 137.5
L-lysine biosynthesis dapE lo Succinyl-diaminopimelate desuccinylase; SDAP desuccinylase; EC 3.5.1.18; N-succinyl-LL-2,6-diaminoheptanedioate amidohydrolase (uncharacterized) 30% 99% 139 acetylornithine deacetylase (EC 3.5.1.16) 39% 279.6

Sequence Analysis Tools

View WP_013530453.1 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

MDSTQILEKLLAFPTVSRDSNLALVNYVADLLDAHGTASQIIHSEDGHKANLFATIGPTD
ASGIMLSGHTDVVPVDGQAWTLPPFEMTNRDGKLYGRGAADMKGFVACALAACLKAAKMT
LKTPLHLALSYDEEIGCIGVRSLVDMLQAAPHRPLLCIVGEPTDMQVATGHKGKLAARAL
CKGREGHSALAPLALNAIHLGCDFVAALRREQDRLVRDGARDGDYDISYTTVHVGKINAG
VALNIVPNLCQVDFEIRNVAADDPHEILDRLRKEAAHIASEASTIAPEAAIDIDITNTYP
GLDTPASSQAVAFVKSLTGANNTIKMAFGTEGGLFSRDLGTPTVVCGPGSMAQGHKPDEF
VSVEQMRRCDDMLEKLLKRLADQQLP

This GapMind analysis is from Jul 25 2024. The underlying query database was built on Jul 25 2024.

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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