GapMind for Amino acid biosynthesis

 

L-isoleucine biosynthesis in Cereibacter sphaeroides ATCC 17029

Best path

cimA, leuC, leuD, leuB, ilvI, ilvH, ilvC, ilvD, ilvE

Rules

Overview: Isoleucine biosynthesis in GapMind is based on MetaCyc pathways L-isoleucine biosynthesis I (from threonine) (link), II via citramalate (link), or IV from propanoate (link). These pathways share a common intermediate, 2-oxobutanoate, but vary in how the 2-oxobutanoate is formed. Pathway IV is included because propanoate is a common fermentative end product and need not be a nutrient requirement, but it is not always clear if it could be the main pathway to isoleucine. Pathway III (link), via glutamate mutase, is not included because the first step (glutamate mutase, EC 5.4.99.1) has not been linked to sequence and because no organism has been demonstrated to rely on this pathway to form oxobutanoate. MetaCyc L-isoleucine biosynthesis V describes biosynthesis from 2-methylbutanoate, which is a fermentation end product in the rumen; this is an an unusual precursor so we did not include it.

13 steps (11 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
cimA (R)-citramalate synthase RSPH17029_RS06990 RSPH17029_RS05125
leuC 3-isopropylmalate dehydratase / citramalate isomerase, large subunit RSPH17029_RS12730
leuD 3-isopropylmalate dehydaratase / citramalate isomerase, small subunit RSPH17029_RS12720 RSPH17029_RS02300
leuB 3-methylmalate dehydrogenase / 3-isopropylmalate dehydrogenase RSPH17029_RS12705 RSPH17029_RS15290
ilvI acetolactate/acetohydroxybutanoate synthase catalytic subunit RSPH17029_RS06560 RSPH17029_RS19665
ilvH acetolactate/acetohydroxybutanoate synthase regulatory subunit RSPH17029_RS06555
ilvC 2-hydroxy-3-ketol-acid reductoisomerase RSPH17029_RS02605
ilvD dihydroxy-acid dehydratase RSPH17029_RS19210 RSPH17029_RS09155
ilvE isoleucine transaminase RSPH17029_RS14130 RSPH17029_RS14500 with RSPH17029_RS14495
Alternative steps:
ilvA threonine deaminase RSPH17029_RS14480 RSPH17029_RS04715
ofoa 2-oxobutanoate:ferredoxin oxidoreductase, alpha subunit
ofob 2-oxobutanoate:ferredoxin oxidoreductase, beta subunit
prpE propionyl-CoA synthetase RSPH17029_RS01250 RSPH17029_RS11250

Confidence: high confidence medium confidence low confidence
? – known gap: despite the lack of a good candidate for this step, this organism (or a related organism) performs the pathway

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