GapMind for catabolism of small carbon sources

 

N-acetyl-D-glucosamine catabolism in Cronobacter condimenti 1330

Best path

nagEcba, 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 (14 with candidates)

Or see definitions of steps

Step Description Best candidate 2nd candidate
nagEcba N-acetylglucosamine phosphotransferase system, EII-CBA components BN137_RS12010 BN137_RS11795
nagA N-acetylglucosamine 6-phosphate deacetylase BN137_RS12020
nagB glucosamine 6-phosphate deaminase (isomerizing) BN137_RS12015 BN137_RS04995
Alternative steps:
crr N-acetylglucosamine phosphotransferase system, EII-A component Crr BN137_RS10310 BN137_RS12010
nag3 N-acetylglucosamine transporter nag3/nag4
nagEcb N-acetylglucosamine phosphotransferase system, EII-CB components BN137_RS12010 BN137_RS11795
nagEIIA N-acetylglucosamine phosphotransferase system, EII-A component (PtsG/YpqE/GamP) BN137_RS12010 BN137_RS18365
nagF N-acetylglucosamine phosphotransferase system, E-I, Hpr, and EII-A components (NagF) BN137_RS10315 BN137_RS18175
nagK N-acetylglucosamine kinase BN137_RS02630 BN137_RS14745
nagP N-acetylglucosamine transporter NagP
nagPcb N-acetylglucosamine phosphotransferase system, EII-CB component NagP BN137_RS12010 BN137_RS11795
ngcE N-acetylglucosamine ABC transporter, substrate-binding component (NgcE)
ngcF N-acetylglucosamine ABC transporter, permease component 1 (NgcF) BN137_RS18075
ngcG N-acetylglucosamine ABC transporter, permease component 2 (NgcG) BN137_RS16135 BN137_RS07340
ngt1 N-acetylglucosamine:H+ symporter Ngt1
ptsB N-acetylglucosamine-specific phosphotransferase system, EII-B component PtsB BN137_RS18365 BN137_RS11795
ptsC N-acetylglucosamine phosphotransferase system, EII-C component PtsC BN137_RS12010 BN137_RS11795
SMc02869 N-acetylglucosamine ABC transporter, ATPase component BN137_RS16695 BN137_RS14585
SMc02871 N-acetylglucosamine ABC transporter, permease component 2
SMc02872 N-acetylglucosamine ABC transporter, permease component 1
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