GapMind for catabolism of small carbon sources

 

L-valine catabolism in Flammeovirga pacifica WPAGA1

Best path

Bap2, bkdA, bkdB, bkdC, lpd, acdH, ech, bch, mmsB, mmsA, pccA, pccB, epi, mcm-large, mcm-small

Rules

Overview: Valine degradation in GapMind is based on MetaCyc pathway L-valine degradation I (link). The other pathways do not produce any fixed carbon and are not included.

47 steps (25 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
Bap2 L-valine permease Bap2
bkdA branched-chain alpha-ketoacid dehydrogenase, E1 component alpha subunit NH26_RS14285
bkdB branched-chain alpha-ketoacid dehydrogenase, E1 component beta subunit NH26_RS16575 NH26_RS04255
bkdC branched-chain alpha-ketoacid dehydrogenase, E2 component NH26_RS10650 NH26_RS18295
lpd branched-chain alpha-ketoacid dehydrogenase, E3 component NH26_RS15205 NH26_RS05325
acdH isobutyryl-CoA dehydrogenase NH26_RS05485 NH26_RS11310
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase NH26_RS03310 NH26_RS17105
bch 3-hydroxyisobutyryl-CoA hydrolase NH26_RS03310
mmsB 3-hydroxyisobutyrate dehydrogenase
mmsA methylmalonate-semialdehyde dehydrogenase NH26_RS05385 NH26_RS24650
pccA propionyl-CoA carboxylase, alpha subunit NH26_RS03725 NH26_RS18360
pccB propionyl-CoA carboxylase, beta subunit NH26_RS04540 NH26_RS19460
epi methylmalonyl-CoA epimerase NH26_RS04545
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit NH26_RS04515 NH26_RS18430
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit NH26_RS04515 NH26_RS01715
Alternative steps:
acn (2R,3S)-2-methylcitrate dehydratase NH26_RS22365
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
bcaP L-valine uptake transporter BcaP/CitA
brnQ L-valine:cation symporter BrnQ/BraZ/BraB
dddA 3-hydroxypropionate dehydrogenase
hpcD 3-hydroxypropionyl-CoA dehydratase NH26_RS03310 NH26_RS17105
iolA malonate semialdehyde dehydrogenase (CoA-acylating) NH26_RS05385 NH26_RS24650
livF L-valine ABC transporter, ATPase component 1 (LivF/BraG) NH26_RS03480 NH26_RS01915
livG L-valine ABC transporter, ATPase component 2 (LivG/BraF) NH26_RS03480 NH26_RS16900
livH L-valine ABC transporter, permease component 1 (LivH/BraD)
livJ L-valine ABC transporter, substrate-binding component (LivJ/LivK/BraC/BraC3)
livM L-valine ABC transporter, permease component 2 (LivM/BraE)
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components NH26_RS18430 NH26_RS04515
natA L-valine ABC transporter, ATPase component 1 (NatA) NH26_RS03480
natB L-valine ABC transporter, substrate-binding component NatB
natC L-valine ABC transporter, permease component 1 (NatC)
natD L-valine ABC transporter, permease component 2 (NatD)
natE L-valine ABC transporter, ATPase component 2 (NatE) NH26_RS03480 NH26_RS17495
ofo branched-chain alpha-ketoacid:ferredoxin oxidoreductase, fused
ofoA branched-chain alpha-ketoacid:ferredoxin oxidoreductase, alpha subunit OfoA
ofoB branched-chain alpha-ketoacid:ferredoxin oxidoreductase, beta subunit OfoB
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit NH26_RS03725 NH26_RS18360
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pco propanyl-CoA oxidase NH26_RS01945 NH26_RS13030
phtJ L-valine uptake permease PhtJ
prpB 2-methylisocitrate lyase NH26_RS05090
prpC 2-methylcitrate synthase NH26_RS03425
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase
vorA branched-chain alpha-ketoacid:ferredoxin oxidoreductase, alpha subunit VorA
vorB branched-chain alpha-ketoacid:ferredoxin oxidoreductase, beta subunit VorB
vorC branched-chain alpha-ketoacid:ferredoxin oxidoreductase, gamma subunit VorC

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 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