GapMind for Amino acid biosynthesis

 

Protein WP_012991725.1 in Thermocrinis albus DSM 14484

Annotation: NCBI__GCF_000025605.1:WP_012991725.1

Length: 658 amino acids

Source: GCF_000025605.1 in NCBI

Candidate for 6 steps in Amino acid biosynthesis

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-isoleucine biosynthesis leuC med 3-isopropylmalate dehydratase large subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized) 41% 100% 303.5 aconitate hydratase; EC 4.2.1.3 37% 394.0
L-leucine biosynthesis leuC med 3-isopropylmalate dehydratase large subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized) 41% 100% 303.5 aconitate hydratase; EC 4.2.1.3 37% 394.0
L-lysine biosynthesis lysT med Homoaconitase large subunit; HACN; Homoaconitate hydratase; EC 4.2.1.36 (characterized) 40% 99% 282 aconitate hydratase; EC 4.2.1.3 37% 394.0
L-isoleucine biosynthesis leuD lo 3-isopropylmalate dehydratase small subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized) 37% 92% 98.6 aconitate hydratase; EC 4.2.1.3 37% 394.0
L-leucine biosynthesis leuD lo 3-isopropylmalate dehydratase small subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized) 37% 92% 98.6 aconitate hydratase; EC 4.2.1.3 37% 394.0
L-lysine biosynthesis lysU lo Methanogen homoaconitase small subunit; HACN; Homoaconitate hydratase; EC 4.2.1.114 (characterized) 35% 94% 90.9 aconitate hydratase; EC 4.2.1.3 37% 394.0

Sequence Analysis Tools

View WP_012991725.1 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

MAKGTVAYKILQQHLVSGRLVPGEEIAIKIDQTLTQDATGTMAYLQLEAMGIDRVKTELS
VSYIDHNMLQTDYKNPDDHKYLMTVAKRYGIYLSKPGNGICHQVHLERFAKPGKTLLGSD
SHTPTAGGIGMLAIGAGGLDVAAAMAGEPFYMKMPKIVGVHLKGKLPPWVTAKDIILELL
RRLTVKGGLGKIFEYFGEGIRELSVPERATITNMGAELGATTSIFPSDDITRAYLRAQGR
EEDWIELLPDPDAQYDEVIELDLSSLEPLIACPHSPDNVVPVREVEGIKVDQVVIGSCTN
SSFVDLTRAAKLLEGRKVHPDVVFAVAPGSKQALELITQNGALLSFLKAGARILETACGP
CIGMGFAPPSGGVSVRSFNRNFEGRSGTPDAKVYLASPEVCVACAIAGEIIDPRKLAQKE
KITWVKVEMPERFPYGDEAIIEPLPEEEAKKVEIYRGPNIKPLPQFDPLPETLEAEVSLI
VGDNITTDHIMPAGAKILPLRSNIYAISEYVYHYVDPEFVARAKKIRDEKKKFSVIIGGE
NYGQGSSREHAALAPRFLGVRVVIAKSFARIHHANLVNFGILPLEFVDKEDYNKFSLGDE
IYIPELYESLNSGKELVVINKTTGHEILCRYNLTPKQVSVLMAGGLLNWIKNKQGVKV

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