GapMind for catabolism of small carbon sources

 

Finding step AO353_21715 for D-glucosamine (chitosamine) catabolism in Pseudomonas fluorescens FW300-N2E2

5 candidates for AO353_21715: glucosaminate ABC transporter, permease component 1

Score Gene Description Similar to Id. Cov. Bits Other hit Other id. Other bits
hi Pf6N2E2_2052 amino acid ABC transporter, permease protein ABC transporter for D-Glucosamine Hydrochloride, permease component 2 (characterized) 100% 100% 422.5 Glutamine transport system permease protein GlnP aka B0810, component of Three component ABC L-glutamine porter. The basal ATPase activity (ATP hydrolysis in the absence of substrate) is mainly caused by the docking of the closed-unliganded state of GlnH onto the transporter domain of GlnPQ. Unlike glutamine, arginine binds both GlnH domains, but does not trigger their closing. Comparison of the ATPase activity in nanodiscs with glutamine transport in proteoliposomes suggested that the stoichiometry of ATP per substrate is close to two 39% 161.4
med Pf6N2E2_4281 Amino acid ABC transporter, permease protein ABC transporter for D-glucosamine, permease component 1 (characterized) 40% 91% 138.7 Arginine transport system permease protein ArtQ 36% 150.2
lo Pf6N2E2_3920 Cystine ABC transporter, permease protein ABC transporter for D-Glucosamine, permease component 2 (characterized) 37% 92% 133.7 L-cystine transport system permease protein YecS 75% 327.4
lo Pf6N2E2_3857 Arginine ABC transporter, permease protein ArtQ ABC transporter for D-glucosamine, permease component 1 (characterized) 38% 93% 132.9 ABC transporter for L-Lysine, permease component 1 95% 436.8
lo Pf6N2E2_3404 Multi antimicrobial extrusion protein (Na(+)/drug antiporter), MATE family of MDR efflux pumps ABC transporter for D-Glucosamine Hydrochloride, permease component 2 (characterized) 35% 100% 132.1 L-cystine transport system permease protein YecS 37% 133.3

Confidence: high confidence medium confidence low confidence
transporter – transporters and PTS systems are shaded because predicting their specificity is particularly challenging.

Also see fitness data for the candidates

Definition of step AO353_21715

Or cluster all characterized AO353_21715 proteins

This GapMind analysis is from Sep 17 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 against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer. 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. 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 the paper from 2019 on GapMind for amino acid biosynthesis, or view the source code.

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