GapMind for Amino acid biosynthesis

 

Protein BPHYT_RS27000 in Burkholderia phytofirmans PsJN

Annotation: FitnessBrowser__BFirm:BPHYT_RS27000

Length: 392 amino acids

Source: BFirm in FitnessBrowser

Candidate for 7 steps in Amino acid biosynthesis

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-phenylalanine biosynthesis ptransferase lo aspartate transaminase (EC 2.6.1.1); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized) 33% 98% 219.9 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1
L-tyrosine biosynthesis ptransferase lo aspartate transaminase (EC 2.6.1.1); glutamate-prephenate aminotransferase (EC 2.6.1.79) (characterized) 33% 98% 219.9 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1
L-lysine biosynthesis lysN lo 2-aminoadipate:2-oxoglutarate aminotransferase (EC 2.6.1.39) (characterized) 34% 93% 209.9 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1
L-lysine biosynthesis dapX lo Probable N-acetyl-LL-diaminopimelate aminotransferase; Putative aminotransferase A; EC 2.6.1.- (characterized) 34% 90% 203.8 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1
L-lysine biosynthesis DAPtransferase lo LL-diaminopimelate aminotransferase (EC 2.6.1.83) (characterized) 32% 94% 190.3 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1
L-methionine biosynthesis metC lo kynurenine-oxoglutarate transaminase (EC 2.6.1.7); cysteine-S-conjugate beta-lyase (EC 4.4.1.13) (characterized) 31% 90% 164.9 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1
L-histidine biosynthesis hisC lo Histidinol-phosphate aminotransferase; EC 2.6.1.9; Imidazole acetol-phosphate transaminase (uncharacterized) 31% 59% 90.1 arginine-pyruvate transaminase (EC 2.6.1.84) 51% 382.1

Sequence Analysis Tools

View BPHYT_RS27000 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

MKYSNLVERLQGRRTSAWEIHRVAQQAEARGEDVIVLSVGDPDFATPAPIVERAIEALRG
GDTHYSAVSGREPVRAAIAAEHTRMTGCAASAANVILTAGAQNGVFAASLCLLEAGDEVI
VPEPMYLTYEACVRAAGATLVTVPVDAARAFHVDCDALEAAVTSRTKAIFFATPCNPTGV
VMQRADLERIARLACRHDLWVLSDEVYAELTFEREHVSIAALPGMAERTVTLGSLSKSHA
MAGWRVGWAIGPTELIEHMGRLALAMLYGLPGFIQQAALTAVQHKARIAAEMREIYRRRR
DVVFERLHRVPGLRCLLPEAGMFMMVDVSGTGLDTVDFTWQLFRARGVSLLDASAFGETA
NGFVRLGFVVDEARLIDACERIAAFVGGLLGR

This GapMind analysis is from Aug 03 2021. The underlying query database was built on Aug 03 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