GapMind for catabolism of small carbon sources

 

D-glucose catabolism in Tatumella morbirosei LMG 23360

Best path

mglA, mglB, mglC, glk

Rules

Overview: In most bacteria, glucose is consumed via glucose 6-phosphate, which is a central metabolic intermediate. It can also be oxidized to 2-ketogluconate in the periplasm before uptake and conversion to gluconate 6-phosphate (link). Periplasmic oxidation to gluconate, uptake, and phosphorylation by gnuK is also a potential path to gluconate-6-phosphate, but is not included in GapMind because it is not known to be the major path for glucose utilization in a prokaryote.

39 steps (25 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
mglA glucose ABC transporter, ATP-binding component (MglA) HA49_RS07345 HA49_RS18545
mglB glucose ABC transporter, substrate-binding component HA49_RS07350
mglC glucose ABC transporter, permease component (MglC) HA49_RS07340 HA49_RS18540
glk glucokinase HA49_RS08260 HA49_RS15320
Alternative steps:
aglE' glucose ABC transporter, substrate-binding component (AglE)
aglF' glucose ABC transporter, permease component 1 (AglF)
aglG' glucose ABC transporter, permease component 2 (AglG)
aglK' glucose ABC transporter, ATPase component (AglK) HA49_RS11785 HA49_RS19415
bglF glucose PTS, enzyme II (BCA components, BglF) HA49_RS10585 HA49_RS06690
crr glucose PTS, enzyme IIA HA49_RS08410 HA49_RS15335
eda 2-keto-3-deoxygluconate 6-phosphate aldolase HA49_RS01090
edd phosphogluconate dehydratase HA49_RS11710 HA49_RS17840
gadh1 gluconate 2-dehydrogenase flavoprotein subunit HA49_RS16140 HA49_RS06575
gadh2 gluconate 2-dehydrogenase cytochrome c subunit HA49_RS16135 HA49_RS01355
gadh3 gluconate 2-dehydrogenase subunit 3 HA49_RS16145 HA49_RS06570
gdh quinoprotein glucose dehydrogenase HA49_RS16290 HA49_RS17695
glcS glucose ABC transporter, substrate-binding component (GlcS)
glcT glucose ABC transporter, permease component 1 (GlcT)
glcU glucose ABC transporter, permease component 2 (GlcU)
glcU' Glucose uptake protein GlcU
glcV glucose ABC transporter, ATPase component (GclV) HA49_RS01440 HA49_RS19415
gnl gluconolactonase HA49_RS11685 HA49_RS04380
gtsA glucose ABC transporter, substrate-binding component (GtsA)
gtsB glucose ABC transporter, permease component 1 (GtsB)
gtsC glucose ABC transporter, permease component 2 (GtsC) HA49_RS11805
gtsD glucose ABC transporter, ATPase component (GtsD) HA49_RS19415 HA49_RS11785
kguD 2-keto-6-phosphogluconate reductase HA49_RS19285 HA49_RS08120
kguK 2-ketogluconokinase
kguT 2-ketogluconate transporter HA49_RS12585 HA49_RS12565
manX glucose PTS, enzyme EIIAB HA49_RS13125
manY glucose PTS, enzyme EIIC HA49_RS13130
manZ glucose PTS, enzyme EIID HA49_RS13135
MFS-glucose glucose transporter, MFS superfamily HA49_RS12775 HA49_RS00475
PAST-A proton-associated sugar transporter A
ptsG glucose PTS, enzyme IICB HA49_RS15335
ptsG-crr glucose PTS, enzyme II (CBA components, PtsG) HA49_RS15335
SemiSWEET Sugar transporter SemiSWEET
SSS-glucose Sodium/glucose cotransporter
SWEET1 bidirectional sugar transporter SWEET1

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