GapMind for catabolism of small carbon sources

 

L-valine catabolism in Alkalitalea saponilacus SC/BZ-SP2

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 (26 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 CDL62_RS16610
bkdB branched-chain alpha-ketoacid dehydrogenase, E1 component beta subunit CDL62_RS16610 CDL62_RS02175
bkdC branched-chain alpha-ketoacid dehydrogenase, E2 component CDL62_RS16615 CDL62_RS13425
lpd branched-chain alpha-ketoacid dehydrogenase, E3 component CDL62_RS02380 CDL62_RS02180
acdH isobutyryl-CoA dehydrogenase CDL62_RS00155 CDL62_RS14380
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase CDL62_RS12095
bch 3-hydroxyisobutyryl-CoA hydrolase
mmsB 3-hydroxyisobutyrate dehydrogenase
mmsA methylmalonate-semialdehyde dehydrogenase CDL62_RS06795
pccA propionyl-CoA carboxylase, alpha subunit CDL62_RS16100 CDL62_RS00145
pccB propionyl-CoA carboxylase, beta subunit CDL62_RS18135 CDL62_RS00135
epi methylmalonyl-CoA epimerase CDL62_RS18140
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit CDL62_RS05665
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit CDL62_RS05665
Alternative steps:
acn (2R,3S)-2-methylcitrate dehydratase
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 CDL62_RS12095
iolA malonate semialdehyde dehydrogenase (CoA-acylating) CDL62_RS06795
livF L-valine ABC transporter, ATPase component 1 (LivF/BraG) CDL62_RS06065 CDL62_RS04050
livG L-valine ABC transporter, ATPase component 2 (LivG/BraF) CDL62_RS06065 CDL62_RS04050
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 CDL62_RS05665 CDL62_RS05675
natA L-valine ABC transporter, ATPase component 1 (NatA) CDL62_RS06065
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) CDL62_RS06065 CDL62_RS06690
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 CDL62_RS04925
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit CDL62_RS16100 CDL62_RS00145
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit CDL62_RS18125
pco propanyl-CoA oxidase CDL62_RS00155
phtJ L-valine uptake permease PhtJ
prpB 2-methylisocitrate lyase
prpC 2-methylcitrate synthase CDL62_RS04490 CDL62_RS05565
prpD 2-methylcitrate dehydratase
prpF methylaconitate isomerase
vorA* branched-chain alpha-ketoacid:ferredoxin oxidoreductase, alpha subunit VorA CDL62_RS01470 with CDL62_RS01465
vorB branched-chain alpha-ketoacid:ferredoxin oxidoreductase, beta subunit VorB CDL62_RS01475 CDL62_RS04920
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