GapMind for catabolism of small carbon sources

 

L-valine catabolism in Chryseobacterium arthrosphaerae CC-VM-7

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 BBI00_RS13465
bkdA branched-chain alpha-ketoacid dehydrogenase, E1 component alpha subunit BBI00_RS01565 BBI00_RS04340
bkdB branched-chain alpha-ketoacid dehydrogenase, E1 component beta subunit BBI00_RS12485 BBI00_RS01565
bkdC branched-chain alpha-ketoacid dehydrogenase, E2 component BBI00_RS06900 BBI00_RS07000
lpd branched-chain alpha-ketoacid dehydrogenase, E3 component BBI00_RS07265 BBI00_RS09540
acdH isobutyryl-CoA dehydrogenase BBI00_RS01605 BBI00_RS05370
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BBI00_RS21810 BBI00_RS22510
bch 3-hydroxyisobutyryl-CoA hydrolase
mmsB 3-hydroxyisobutyrate dehydrogenase
mmsA methylmalonate-semialdehyde dehydrogenase BBI00_RS10955 BBI00_RS04765
pccA propionyl-CoA carboxylase, alpha subunit BBI00_RS14915
pccB propionyl-CoA carboxylase, beta subunit BBI00_RS19010
epi methylmalonyl-CoA epimerase BBI00_RS19475
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit BBI00_RS21385 BBI00_RS15060
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit BBI00_RS21385 BBI00_RS15060
Alternative steps:
acn (2R,3S)-2-methylcitrate dehydratase BBI00_RS21750
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
bcaP L-valine uptake transporter BcaP/CitA BBI00_RS02720 BBI00_RS08080
brnQ L-valine:cation symporter BrnQ/BraZ/BraB
dddA 3-hydroxypropionate dehydrogenase
hpcD 3-hydroxypropionyl-CoA dehydratase BBI00_RS21810 BBI00_RS06575
iolA malonate semialdehyde dehydrogenase (CoA-acylating) BBI00_RS10955
livF L-valine ABC transporter, ATPase component 1 (LivF/BraG) BBI00_RS11725 BBI00_RS11715
livG L-valine ABC transporter, ATPase component 2 (LivG/BraF) BBI00_RS11725 BBI00_RS09790
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 BBI00_RS15060 BBI00_RS21385
natA L-valine ABC transporter, ATPase component 1 (NatA) BBI00_RS11725 BBI00_RS09790
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) BBI00_RS11725 BBI00_RS01010
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 BBI00_RS14915
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pco propanyl-CoA oxidase BBI00_RS21510 BBI00_RS04080
phtJ L-valine uptake permease PhtJ
prpB 2-methylisocitrate lyase BBI00_RS12685
prpC 2-methylcitrate synthase BBI00_RS18690
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