GapMind for catabolism of small carbon sources

 

D-mannose catabolism in Sporolactobacillus vineae SL153

Best path

manX, manY, manZ, manA

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 (19 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
manX mannose PTS system, EII-AB component ManX/ManL RH97_RS02405 RH97_RS10970
manY mannose PTS system, EII-C component ManY/ManM RH97_RS02400 RH97_RS10975
manZ mannose PTS system, EII-D component ManZ/ManN RH97_RS02395 RH97_RS10980
manA mannose-6-phosphate isomerase RH97_RS06085 RH97_RS07565
Alternative steps:
frcA mannose ABC transporter, ATPase component FrcA RH97_RS07960 RH97_RS05715
frcB mannose ABC transporter, substrate-binding component FrcB
frcC mannose ABC transporter, permease component FrcC
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)
glcV mannose ABC transporter, ATPase component GlcV RH97_RS12055 RH97_RS01755
gluP mannose:Na+ symporter
HSERO_RS03635 mannose ABC transporter, substrate-binding component
HSERO_RS03640 mannose ABC transporter, ATPase component RH97_RS07960
HSERO_RS03645 mannose ABC transporter, permease component
man-isomerase D-mannose isomerase RH97_RS09625
manMFS mannose transporter, MFS superfamily
mannokinase D-mannose kinase RH97_RS09765
manP mannose PTS system, EII-CBA components RH97_RS02255 RH97_RS05185
MST1 mannose:H+ symporter
scrK fructokinase RH97_RS06160 RH97_RS12875
STP6 mannose:H+ symporter RH97_RS04785
TM1746 mannose ABC transporter, substrate-binding component RH97_RS06315
TM1747 mannose ABC transporter, permease component 1 RH97_RS06330 RH97_RS11175
TM1748 mannose ABC transporter, permease component 2 RH97_RS06325 RH97_RS11170
TM1749 mannose ABC transporter, ATPase component 1 RH97_RS05360 RH97_RS06320
TM1750 mannose ABC transporter, ATPase component 2 RH97_RS09060 RH97_RS06310
TT_C0211 mannose ABC transporter, ATPase component MalK1 RH97_RS12055 RH97_RS01755
TT_C0326 mannose ABC transporter, permease component 2 RH97_RS11010
TT_C0327 mannose ABC transporter, permease component 1
TT_C0328 mannose ABC transporter, substrate-binding component

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