GapMind for catabolism of small carbon sources

 

glycerol catabolism in Pseudomonas fluorescens FW300-N2E2

Best path

glpS, glpT, glpP, glpQ, glpV, glpK, glpD, tpi

Also see fitness data for the top candidates

Rules

Overview: Glycerol utilization in GapMind is based on MetaCyc pathways glycerol degradation I via glycerol kinase (link), II via dihydroxyacetone kinase (link), or V via dihydroxyacetone:PEP phosphotransferase (link). Two fermentative pathways are not included because they do not lead to carbon incorporation (link, link).

25 steps (14 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
glpS glycerol ABC transporter, ATPase component 1 (GlpS) Pf6N2E2_103 Pf6N2E2_807
glpT glycerol ABC transporter, ATPase component 2 (GlpT) Pf6N2E2_104 Pf6N2E2_1960
glpP glycerol ABC transporter, permease component 1 (GlpP) Pf6N2E2_105
glpQ glycerol ABC transporter, permease component 2 (GlpQ) Pf6N2E2_106 Pf6N2E2_808
glpV glycerol ABC transporter, substrate-binding component GlpV Pf6N2E2_108
glpK glycerol kinase Pf6N2E2_5574
glpD glycerol 3-phosphate dehydrogenase (monomeric) Pf6N2E2_5572
tpi triose-phosphate isomerase Pf6N2E2_3356 Pf6N2E2_4657
Alternative steps:
aqp-3 glycerol porter aqp-3
dhaD glycerol dehydrogenase Pf6N2E2_4819 Pf6N2E2_2802
dhaK dihydroxyacetone:PEP phosphotransferase, subunit K
dhaK' dihydroxyacetone kinase, ATP dependent (monomeric)
dhaL dihydroxyacetone:PEP phosphotransferase, subunit L
dhaM dihydroxyacetone:PEP phosphotransferase, subunit M Pf6N2E2_3339
fps1 glycerol uptake/efflux facilitator protein
glpA glycerol 3-phosphate dehydrogenase subunit A
glpB glycerol 3-phosphate dehydrogenase subunit B
glpC glycerol 3-phosphate dehydrogenase subunit C
glpF glycerol facilitator glpF Pf6N2E2_5575 Pf6N2E2_2686
glpF' glycerol facilitator-aquaporin
glpO glycerol 3-phosphate oxidase Pf6N2E2_5572
PLT5 glycerol:H+ symporter PLT5 Pf6N2E2_883
stl1 glycerol:H+ symporter Stl1p
TIPa glycerol facilitator TIPa Pf6N2E2_2686
YFL054C glycrol facilitator protein

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.

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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