GapMind for catabolism of small carbon sources

 

L-rhamnose catabolism in Paraburkholderia sp. CCGE1002

Best path

rhaP, rhaQ, rhaS, rhaT', LRA1, LRA2, LRA3, LRA5, LRA6

Rules

Overview: Rhamnose utilization in GapMind is based on MetaCyc pathway I via L-rhamnulose 1-phosphate aldolase (link), pathway II via 2-keto-3-deoxy-L-rhamnonate aldolase (link), and pathway III via 2,4-diketo-3-deoxyrhamnonate hydrolase (link).

22 steps (15 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
rhaP L-rhamnose ABC transporter, permease component 1 (RhaP) BC1002_RS21100 BC1002_RS21095
rhaQ L-rhamnose ABC transporter, permease component 2 (RhaQ) BC1002_RS21095 BC1002_RS12465
rhaS L-rhamnose ABC transporter, substrate-binding component RhaS BC1002_RS21090
rhaT' L-rhamnose ABC transporter, ATPase component RhaT BC1002_RS21105 BC1002_RS23905
LRA1 L-rhamnofuranose dehydrogenase BC1002_RS21125 BC1002_RS08140
LRA2 L-rhamnono-gamma-lactonase
LRA3 L-rhamnonate dehydratase BC1002_RS21130 BC1002_RS30375
LRA5 2-keto-3-deoxy-L-rhamnonate 4-dehydrogenase BC1002_RS21135 BC1002_RS10705
LRA6 2,4-diketo-3-deoxyrhamnonate hydrolase BC1002_RS25600 BC1002_RS20845
Alternative steps:
aldA lactaldehyde dehydrogenase BC1002_RS30590 BC1002_RS16940
BPHYT_RS34240 L-rhamnose ABC transporter, permease component BC1002_RS21100 BC1002_RS21095
BPHYT_RS34245 L-rhamnose ABC transporter, ATPase component BC1002_RS21105 BC1002_RS29635
BPHYT_RS34250 L-rhamnose ABC transporter, substrate-binding component
Echvi_1617 L-rhamnose transporter
fucO L-lactaldehyde reductase BC1002_RS32100 BC1002_RS10265
LRA4 2-keto-3-deoxy-L-rhamnonate aldolase BC1002_RS17870 BC1002_RS18465
rhaA L-rhamnose isomerase
rhaB L-rhamnulokinase
rhaD rhamnulose 1-phosphate aldolase
rhaM L-rhamnose mutarotase BC1002_RS21115
rhaT L-rhamnose:H+ symporter RhaT
tpi triose-phosphate isomerase BC1002_RS04720 BC1002_RS12680

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