GapMind for catabolism of small carbon sources

 

propionate catabolism in Pseudomonas fluorescens FW300-N2C3

Best path

putP, prpE, prpC, acnD, prpF, acn, prpB

Also see fitness data for the top candidates

Rules

Overview: Propionate degradation in GapMind is based on MetaCyc pathways for the 2-methylcitrate cycle (link, link) and for propanoyl-CoA degradation (link, link).

24 steps (16 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
putP propionate transporter; proline:Na+ symporter AO356_09010
prpE propionyl-CoA synthetase AO356_18695 AO356_16045
prpC 2-methylcitrate synthase AO356_20870 AO356_19670
acnD 2-methylcitrate dehydratase (2-methyl-trans-aconitate forming) AO356_20875 AO356_02385
prpF methylaconitate isomerase AO356_20880 AO356_28890
acn (2R,3S)-2-methylcitrate dehydratase AO356_20875 AO356_24390
prpB 2-methylisocitrate lyase AO356_20865 AO356_22080
Alternative steps:
dddA 3-hydroxypropionate dehydrogenase AO356_21730 AO356_30225
epi methylmalonyl-CoA epimerase
hpcD 3-hydroxypropionyl-CoA dehydratase AO356_26360 AO356_30355
iolA malonate semialdehyde dehydrogenase (CoA-acylating) AO356_23175 AO356_07950
lctP propionate permease AO356_07550 AO356_22315
mcm-large methylmalonyl-CoA mutase, large (catalytic) subunit
mcm-small methylmalonyl-CoA mutase, small (adenosylcobamide-binding) subunit
mcmA methylmalonyl-CoA mutase, fused catalytic and adenosylcobamide-binding components
mctC propionate:H+ symporter AO356_19665
mctP propionate permease
pccA propionyl-CoA carboxylase, alpha subunit AO356_01595 AO356_02930
pccA1 propionyl-CoA carboxylase, biotin carboxyl carrier subunit AO356_12020 AO356_08195
pccA2 propionyl-CoA carboxylase, biotin carboxylase subunit
pccB propionyl-CoA carboxylase, beta subunit AO356_01585 AO356_02920
pco propanyl-CoA oxidase AO356_10850 AO356_26355
prpD 2-methylcitrate dehydratase
SLC5A8 sodium-coupled monocarboxylate transporter

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 17 2021. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.

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