GapMind for catabolism of small carbon sources

 

N-acetyl-D-glucosamine catabolism in Bacillus coahuilensis m4-4

Best path

nagEIIA, nagPcb, nagA, nagB

Rules

Overview: N-acetylglucosamine utilization in GapMind is based on MetaCyc pathways N-acetylglucosamine degradation I (link) and pathway II (link). These pathways differ in whether uptake and phosphorylation are performed by a PTS system or performed separately by a transporter and a kinase.

21 steps (15 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
nagEIIA N-acetylglucosamine phosphotransferase system, EII-A component (PtsG/YpqE/GamP) M44_RS03225 M44_RS06300
nagPcb N-acetylglucosamine phosphotransferase system, EII-CB component NagP M44_RS18445 M44_RS03225
nagA N-acetylglucosamine 6-phosphate deacetylase M44_RS15315
nagB glucosamine 6-phosphate deaminase (isomerizing) M44_RS16860 M44_RS01075
Alternative steps:
crr N-acetylglucosamine phosphotransferase system, EII-A component Crr M44_RS06300 M44_RS03225
nag3 N-acetylglucosamine transporter nag3/nag4
nagEcb N-acetylglucosamine phosphotransferase system, EII-CB components M44_RS18445 M44_RS03225
nagEcba N-acetylglucosamine phosphotransferase system, EII-CBA components M44_RS18445 M44_RS03225
nagF N-acetylglucosamine phosphotransferase system, E-I, Hpr, and EII-A components (NagF) M44_RS05530
nagK N-acetylglucosamine kinase M44_RS10615
nagP N-acetylglucosamine transporter NagP
ngcE N-acetylglucosamine ABC transporter, substrate-binding component (NgcE)
ngcF N-acetylglucosamine ABC transporter, permease component 1 (NgcF) M44_RS14310
ngcG N-acetylglucosamine ABC transporter, permease component 2 (NgcG)
ngt1 N-acetylglucosamine:H+ symporter Ngt1
ptsB N-acetylglucosamine-specific phosphotransferase system, EII-B component PtsB M44_RS03225 M44_RS18445
ptsC N-acetylglucosamine phosphotransferase system, EII-C component PtsC M44_RS18445 M44_RS03225
SMc02869 N-acetylglucosamine ABC transporter, ATPase component M44_RS04595 M44_RS02045
SMc02871 N-acetylglucosamine ABC transporter, permease component 2 M44_RS14315
SMc02872 N-acetylglucosamine ABC transporter, permease component 1 M44_RS16325
SMc02873 N-acetylglucosamine ABC transporter, substrate-binding component

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