GapMind for catabolism of small carbon sources


glycerol catabolism in Burkholderia phytofirmans PsJN

Best path

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

Also see fitness data for the top candidates


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 (18 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
glpS glycerol ABC transporter, ATPase component 1 (GlpS) BPHYT_RS33300 BPHYT_RS27955
glpT glycerol ABC transporter, ATPase component 2 (GlpT) BPHYT_RS33295 BPHYT_RS27960
glpP glycerol ABC transporter, permease component 1 (GlpP) BPHYT_RS33290 BPHYT_RS27975
glpQ glycerol ABC transporter, permease component 2 (GlpQ) BPHYT_RS33285 BPHYT_RS27970
glpV glycerol ABC transporter, substrate-binding component GlpV BPHYT_RS33275
glpK glycerol kinase BPHYT_RS16495
glpD glycerol 3-phosphate dehydrogenase (monomeric) BPHYT_RS16490
tpi triose-phosphate isomerase BPHYT_RS06610 BPHYT_RS16270
Alternative steps:
aqp-3 glycerol porter aqp-3 BPHYT_RS19040
dhaD glycerol dehydrogenase BPHYT_RS20205 BPHYT_RS16040
dhaK dihydroxyacetone:PEP phosphotransferase, subunit K BPHYT_RS27945 BPHYT_RS32475
dhaK' dihydroxyacetone kinase, ATP dependent (monomeric) BPHYT_RS32475 BPHYT_RS27945
dhaL dihydroxyacetone:PEP phosphotransferase, subunit L BPHYT_RS27950 BPHYT_RS32475
dhaM dihydroxyacetone:PEP phosphotransferase, subunit M
fps1 glycerol uptake/efflux facilitator protein
glpA glycerol 3-phosphate dehydrogenase subunit A BPHYT_RS16490
glpB glycerol 3-phosphate dehydrogenase subunit B
glpC glycerol 3-phosphate dehydrogenase subunit C
glpF glycerol facilitator glpF BPHYT_RS16500 BPHYT_RS19040
glpF' glycerol facilitator-aquaporin BPHYT_RS16500
glpO glycerol 3-phosphate oxidase BPHYT_RS16490 BPHYT_RS28480
PLT5 glycerol:H+ symporter PLT5
stl1 glycerol:H+ symporter Stl1p
TIPa glycerol facilitator TIPa BPHYT_RS19040
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.



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 (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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 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