GapMind for catabolism of small carbon sources

 

L-valine catabolism in Flavobacterium sp. LM5

Best path

Bap2, bkdA, bkdB, bkdC, lpd, acdH, ech, bch, mmsB, mmsA, pccA, pccB, epi, mcmA

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 BXU11_RS10670 BXU11_RS11535
bkdB branched-chain alpha-ketoacid dehydrogenase, E1 component beta subunit BXU11_RS10670 BXU11_RS15630
bkdC branched-chain alpha-ketoacid dehydrogenase, E2 component BXU11_RS09535 BXU11_RS00525
lpd branched-chain alpha-ketoacid dehydrogenase, E3 component BXU11_RS12530 BXU11_RS08250
acdH isobutyryl-CoA dehydrogenase BXU11_RS04315 BXU11_RS10875
ech (S)-3-hydroxybutanoyl-CoA hydro-lyase BXU11_RS02105 BXU11_RS13795
bch 3-hydroxyisobutyryl-CoA hydrolase BXU11_RS02105
mmsB 3-hydroxyisobutyrate dehydrogenase
mmsA methylmalonate-semialdehyde dehydrogenase BXU11_RS01185
pccA propionyl-CoA carboxylase, alpha subunit BXU11_RS09415 BXU11_RS02955
pccB propionyl-CoA carboxylase, beta subunit BXU11_RS09410 BXU11_RS08190
epi methylmalonyl-CoA epimerase BXU11_RS02910
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components BXU11_RS09065
Alternative steps:
acn (2R,3S)-2-methylcitrate dehydratase BXU11_RS10770
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming)
bcaP L-valine uptake transporter BcaP/CitA BXU11_RS10885
brnQ L-valine:cation symporter BrnQ/BraZ/BraB
dddA 3-hydroxypropionate dehydrogenase
hpcD 3-hydroxypropionyl-CoA dehydratase BXU11_RS02105
iolA malonate semialdehyde dehydrogenase (CoA-acylating)
livF L-valine ABC transporter, ATPase component 1 (LivF/BraG) BXU11_RS05265 BXU11_RS06900
livG L-valine ABC transporter, ATPase component 2 (LivG/BraF) BXU11_RS05265 BXU11_RS03565
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)
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit BXU11_RS09065
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit BXU11_RS09065 BXU11_RS11800
natA L-valine ABC transporter, ATPase component 1 (NatA) BXU11_RS05265
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) BXU11_RS05265 BXU11_RS10575
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 BXU11_RS09415 BXU11_RS02955
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pco propanyl-CoA oxidase BXU11_RS00155 BXU11_RS04315
phtJ L-valine uptake permease PhtJ
prpB 2-methylisocitrate lyase BXU11_RS02765
prpC 2-methylcitrate synthase BXU11_RS04785
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