GapMind for catabolism of small carbon sources

 

D-gluconate catabolism in Marinomonas arctica 328

Best path

gntT, gntK, edd, eda

Rules

Overview: In most bacteria, gluconate degradation proceeds via D-gluconate 6-phosphate and either the Entner-Doudoroff pathway or the oxidative pentose phosphate pathway (link). Alternatively, gluconate can be oxidized in the periplasm to 2-ketogluconate before uptake (link).

19 steps (10 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
gntT gluconate:H+ symporter GntT DK187_RS10510 DK187_RS02695
gntK D-gluconate kinase DK187_RS07350
edd phosphogluconate dehydratase DK187_RS13445 DK187_RS19975
eda 2-keto-3-deoxygluconate 6-phosphate aldolase DK187_RS01530 DK187_RS11900
Alternative steps:
gadh1 gluconate 2-dehydrogenase flavoprotein subunit
gadh2 gluconate 2-dehydrogenase cytochrome c subunit
gadh3 gluconate 2-dehydrogenase subunit 3
ght3 gluconate transporter Ght3
gnd 6-phosphogluconate dehydrogenase, decarboxylating DK187_RS00955
gntA gluconate TRAP transporter, small permease component DK187_RS18205 DK187_RS09245
gntB gluconate TRAP transporter, large permease component DK187_RS18210 DK187_RS15800
gntC gluconate TRAP transporter, periplasmic solute-binding component DK187_RS09735 DK187_RS05090
gntEIIA gluconate PTS system, IIA component
gntEIIB gluconate PTS system, IIB component
gntEIIC gluconate PTS system, IIC component
gntEIID gluconate PTS system, IID component
kguD 2-keto-6-phosphogluconate reductase DK187_RS16380 DK187_RS15435
kguK 2-ketogluconokinase DK187_RS16375
kguT 2-ketogluconate transporter

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