GapMind for catabolism of small carbon sources

 

L-rhamnose catabolism in Mesorhizobium ciceri WSM1271

Best path

rhaP, rhaQ, rhaS, rhaT', rhaM, rhaA, rhaB, rhaD, tpi, aldA

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 (18 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
rhaP L-rhamnose ABC transporter, permease component 1 (RhaP) Mesci_5945 Mesci_2759
rhaQ L-rhamnose ABC transporter, permease component 2 (RhaQ) Mesci_5946 Mesci_3044
rhaS L-rhamnose ABC transporter, substrate-binding component RhaS Mesci_5943 Mesci_1490
rhaT' L-rhamnose ABC transporter, ATPase component RhaT Mesci_5944 Mesci_0295
rhaM L-rhamnose mutarotase Mesci_5947 Mesci_5280
rhaA L-rhamnose isomerase Mesci_5940
rhaB L-rhamnulokinase Mesci_5948 Mesci_1487
rhaD rhamnulose 1-phosphate aldolase Mesci_5941 Mesci_5168
tpi triose-phosphate isomerase Mesci_3956 Mesci_5319
aldA lactaldehyde dehydrogenase Mesci_5941 Mesci_2633
Alternative steps:
BPHYT_RS34240 L-rhamnose ABC transporter, permease component Mesci_0304 Mesci_4405
BPHYT_RS34245 L-rhamnose ABC transporter, ATPase component Mesci_2758 Mesci_6332
BPHYT_RS34250 L-rhamnose ABC transporter, substrate-binding component
Echvi_1617 L-rhamnose transporter
fucO L-lactaldehyde reductase Mesci_2754 Mesci_1841
LRA1 L-rhamnofuranose dehydrogenase Mesci_6219 Mesci_2477
LRA2 L-rhamnono-gamma-lactonase
LRA3 L-rhamnonate dehydratase Mesci_0298 Mesci_1686
LRA4 2-keto-3-deoxy-L-rhamnonate aldolase Mesci_2590 Mesci_4352
LRA5 2-keto-3-deoxy-L-rhamnonate 4-dehydrogenase Mesci_0269 Mesci_0299
LRA6 2,4-diketo-3-deoxyrhamnonate hydrolase Mesci_0703 Mesci_0680
rhaT L-rhamnose:H+ symporter RhaT

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