GapMind for catabolism of small carbon sources

 

D-mannose catabolism in Verminephrobacter eiseniae EF01-2

Best path

frcA, frcB, frcC, man-isomerase, scrK

Rules

Overview: Mannose utilization in GapMind is based on MetaCyc pathways D-mannose degradation I via a PTS system (link), pathway II via mannose kinase (link), or conversion to fructose by mannose isomerase.

32 steps (18 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
frcA mannose ABC transporter, ATPase component FrcA VEIS_RS02620 VEIS_RS07200
frcB mannose ABC transporter, substrate-binding component FrcB VEIS_RS02640 VEIS_RS02630
frcC mannose ABC transporter, permease component FrcC VEIS_RS02625 VEIS_RS05350
man-isomerase D-mannose isomerase VEIS_RS27015
scrK fructokinase VEIS_RS02650 VEIS_RS16575
Alternative steps:
glcP mannose:H+ symporter
glcS mannose ABC transporter, substrate-binding component GlcS
glcT mannose ABC transporter, permease component 1 (GlcT)
glcU mannose ABC transporter, permease component 2 (GlcU) VEIS_RS22010 VEIS_RS04890
glcV mannose ABC transporter, ATPase component GlcV VEIS_RS06050 VEIS_RS21870
gluP mannose:Na+ symporter
HSERO_RS03635 mannose ABC transporter, substrate-binding component VEIS_RS02630 VEIS_RS09920
HSERO_RS03640 mannose ABC transporter, ATPase component VEIS_RS00315 VEIS_RS05355
HSERO_RS03645 mannose ABC transporter, permease component VEIS_RS10005 VEIS_RS16580
manA mannose-6-phosphate isomerase
manMFS mannose transporter, MFS superfamily
mannokinase D-mannose kinase
manP mannose PTS system, EII-CBA components
manX mannose PTS system, EII-AB component ManX/ManL
manY mannose PTS system, EII-C component ManY/ManM
manZ mannose PTS system, EII-D component ManZ/ManN
MST1 mannose:H+ symporter
STP6 mannose:H+ symporter
TM1746 mannose ABC transporter, substrate-binding component
TM1747 mannose ABC transporter, permease component 1 VEIS_RS22220 VEIS_RS09800
TM1748 mannose ABC transporter, permease component 2 VEIS_RS22225 VEIS_RS06345
TM1749 mannose ABC transporter, ATPase component 1 VEIS_RS24080 VEIS_RS09110
TM1750 mannose ABC transporter, ATPase component 2 VEIS_RS09105 VEIS_RS24075
TT_C0211 mannose ABC transporter, ATPase component MalK1 VEIS_RS06050 VEIS_RS21870
TT_C0326 mannose ABC transporter, permease component 2 VEIS_RS17325 VEIS_RS09195
TT_C0327 mannose ABC transporter, permease component 1 VEIS_RS17320
TT_C0328 mannose ABC transporter, substrate-binding component VEIS_RS17315

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.

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 (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