GapMind for Amino acid biosynthesis

 

Protein WP_037570303.1 in Streptacidiphilus oryzae TH49

Annotation: NCBI__GCF_000744815.1:WP_037570303.1

Length: 661 amino acids

Source: GCF_000744815.1 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 lo 3-isopropylmalate dehydratase large subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized) 37% 99% 257.3 aconitate hydratase; EC 4.2.1.3 34% 325.1
L-leucine biosynthesis leuC lo 3-isopropylmalate dehydratase large subunit 1; EC 4.2.1.33; Alpha-IPM isomerase 1; IPMI 1; Isopropylmalate isomerase 1 (uncharacterized) 37% 99% 257.3 aconitate hydratase; EC 4.2.1.3 34% 325.1
L-lysine biosynthesis lysT lo Homoaconitase large subunit; HACN; Homoaconitate hydratase; EC 4.2.1.36 (characterized) 34% 99% 203 aconitate hydratase; EC 4.2.1.3 34% 325.1
L-lysine biosynthesis lysU lo Methanogen homoaconitase small subunit; HACN; Homoaconitate hydratase; EC 4.2.1.114 (characterized) 35% 94% 86.3 aconitate hydratase; EC 4.2.1.3 34% 325.1
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% 78% 85.5 aconitate hydratase; EC 4.2.1.3 34% 325.1
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% 78% 85.5 aconitate hydratase; EC 4.2.1.3 34% 325.1

Sequence Analysis Tools

View WP_037570303.1 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

MTAEQEARSAQNGSLAYRLIADHLVEGRMTAGEEIALRVDQTLTQDATGTLVMQELEALG
LDRAQTEVSVQYVDHNLLQADERNAEDHAFLRSAAHRYGLWYSKPGNGVSHPVHMQRFGV
PGRSLAGSDSHTCAAGALGMLAVGVGGLEVALAIAGQPLHLVMPRIRGIRLTGQLPPWVS
AKDVILELLRRHGVKGGVGWILEYHGPGLDHLSAMDRHVIANMGAELGATASVFPSDRVT
RDFLRAQGRGEDFAMLTAGPDARYDETEEIDLSTLEPLIARPSSPGDVVPVGEVEGEEIA
QSVIGSSANPGLRDFAVAAGIVAGRQTAPGVSLDVNPTSRELLQDLARSGAVLDLIAAGA
RLHQAGCLGCIGMGQAPAAGRNSLRTFPRNFPGRSGTEEDAVWLCSPETAAVSALTGRIT
DPRRWAEENKAEYPRFTEPDRYTVNLTSLEEPPPHQRAVDTELERGPNISALPELEPLPD
RLALRVLLKAGDDVSTDEISPAGAKALPYRSNLPKLAEFTLTRIDPDYPERAAASREDGG
HAIVAGENWGQGSSREHAAICPRLLGLHAVLAKSFARIHWQNLVNFGVLPLEFEDVADYD
RLDRDDELILDDLHQSLAEDAPPVILATGADGTEYRLRHRLSTRQRAVVRAGGIIPSLAR
S

This GapMind analysis is from Jul 26 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