GapMind for Amino acid biosynthesis

 

Protein AO356_18775 in Pseudomonas fluorescens FW300-N2C3

Annotation: FitnessBrowser__pseudo5_N2C3_1:AO356_18775

Length: 413 amino acids

Source: pseudo5_N2C3_1 in FitnessBrowser

Candidate for 6 steps in Amino acid biosynthesis

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
chorismate biosynthesis asp-kinase hi Aspartate kinase; Aspartokinase; EC 2.7.2.4 (characterized) 95% 100% 747.7
chorismate biosynthesis asp-kinase hi aspartate kinase, monofunctional class (EC 2.7.2.4) (TIGR00656) 100% 436.8
L-lysine biosynthesis asp-kinase hi Aspartate kinase; Aspartokinase; EC 2.7.2.4 (characterized) 95% 100% 747.7
L-lysine biosynthesis asp-kinase hi aspartate kinase, monofunctional class (EC 2.7.2.4) (TIGR00656) 100% 436.8
L-methionine biosynthesis asp-kinase hi Aspartate kinase; Aspartokinase; EC 2.7.2.4 (characterized) 95% 100% 747.7
L-methionine biosynthesis asp-kinase hi aspartate kinase, monofunctional class (EC 2.7.2.4) (TIGR00656) 100% 436.8
L-threonine biosynthesis asp-kinase hi Aspartate kinase; Aspartokinase; EC 2.7.2.4 (characterized) 95% 100% 747.7
L-threonine biosynthesis asp-kinase hi aspartate kinase, monofunctional class (EC 2.7.2.4) (TIGR00656) 100% 436.8
L-methionine biosynthesis hom lo homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized) 46% 54% 349.4 Aspartate kinase; Aspartokinase; EC 2.7.2.4 95% 747.7
L-threonine biosynthesis hom lo homoserine dehydrogenase (EC 1.1.1.3); aspartate kinase (EC 2.7.2.4) (characterized) 46% 54% 349.4 Aspartate kinase; Aspartokinase; EC 2.7.2.4 95% 747.7

Sequence Analysis Tools

View AO356_18775 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...

Sequence

MALIVQKFGGTSVGTVERIEQVADKVKKFREAGDDLVVVLSAMSGETNRLIDLAKQISGD
QQPVPRELDVIVSTGEQVTIALLAMALIKRGVPAVSYTGNQVRILTDSAHNKARILQIDD
QKIRGDLKAGRVVVVAGFQGVDEQGNITTLGRGGSDTTGVALAAALKADECQIYTDVDGV
YTTDPRVVPVAQRLDKITFEEMLEMASLGSKVLQIRAVEFAGKYNVPLRVLHSFKEGPGT
LITIDEEESMEQPIISGIAFNRDEAKLTIRGVPDTPGVAFKILGPISAANIEVDMIVQNV
SHDNTTDFTFTVHRNDYQSAEAILKKTAGEIGAREVVGDTKIAKVSIVGVGMRSHAGVAS
RMFESLAKESINIQMISTSEIKVSVVIEEKYLELAVRALHTAFELDAAAQQGE

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