GapMind for catabolism of small carbon sources

 

L-fucose catabolism in Amantichitinum ursilacus IGB-41

Best path

fucP, fucU, fucI, fucK, fucA, tpi, fucO

Rules

Overview: Fucose degradation in GapMind is based on the MetaCyc pathway via L-fuculose (link) or the oxidative pathway via 2,4-diketo-3-deoxy-L-fuconate (KDF) hydrolase (PMC6336799).

23 steps (19 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
fucP L-fucose:H+ symporter FucP WG78_RS19555
fucU L-fucose mutarotase FucU WG78_RS08805
fucI L-fucose isomerase FucI
fucK L-fuculose kinase FucK
fucA L-fuculose-phosphate aldolase FucA WG78_RS16620
tpi triose-phosphate isomerase WG78_RS15400 WG78_RS03140
fucO L-lactaldehyde reductase WG78_RS06220 WG78_RS03390
Alternative steps:
aldA lactaldehyde dehydrogenase WG78_RS14820 WG78_RS16670
BPHYT_RS34240 ABC transporter for L-fucose, permease component WG78_RS19935 WG78_RS08790
BPHYT_RS34245 ABC transporter for L-fucose, ATPase component WG78_RS15685 WG78_RS19930
BPHYT_RS34250 ABC transporter for L-fucose, substrate-binding component WG78_RS21610
fdh L-fucose 1-dehydrogenase WG78_RS08365
fucD L-fuconate dehydratase WG78_RS01020
fucDH 2-keto-3-deoxy-L-fuconate 4-dehydrogenase WG78_RS19235 WG78_RS04575
fuconolactonase L-fucono-1,5-lactonase WG78_RS08800
HSERO_RS05250 ABC transporter for L-fucose, ATPase component WG78_RS19010 WG78_RS19930
HSERO_RS05255 ABC transporter for L-fucose, permease component WG78_RS19935 WG78_RS15675
HSERO_RS05260 ABC transporter for L-fucose, substrate-binding component
KDF-hydrolase 2,4-diketo-3-deoxy-L-fuconate hydrolase WG78_RS08825 WG78_RS02700
SM_b21103 ABC transporter for L-fucose, substrate-binding component
SM_b21104 ABC transporter for L-fucose, permease component 1 WG78_RS20145 WG78_RS09985
SM_b21105 ABC transporter for L-fucose, permease component 2 WG78_RS06135 WG78_RS09980
SM_b21106 ABC transporter for L-fucose, ATPase component WG78_RS08570 WG78_RS07490

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