GapMind for catabolism of small carbon sources


Finding step SMc04256 for D-cellobiose catabolism in Pseudomonas fluorescens FW300-N1B4

4 candidates for SMc04256: cellobiose ABC transporter, ATPase component

Score Gene Description Similar to Id. Cov. Bits Other hit Other id. Other bits
med Pf1N1B4_593 Glucose ABC transporter, ATP-binding subunit (EC 3.6.3.-) ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 48% 100% 337 ABC transporter for D-Galactose and D-Glucose, ATPase component 96% 734.9
med Pf1N1B4_4847 Various polyols ABC transporter, ATP-binding component ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 45% 99% 318.9 ABC transporter for D-Mannitol, D-Mannose, and D-Mannose, ATPase component 95% 686.8
med Pf1N1B4_5115 Maltose/maltodextrin transport ATP-binding protein MalK (EC ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 45% 99% 295.8 Maltose-transporting ATPase (EC 58% 380.6
lo Pf1N1B4_3974 ABC transporter, ATP-binding protein ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 38% 99% 233 Fe(3+) ions import ATP-binding protein FbpC, component of Hexose-phosphate transporter 47% 273.5

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

GapMind searches the predicted proteins for candidates by using ublast (a fast alternative to protein BLAST) to find similarities to characterized proteins or by using HMMer to find similarities to enzyme models (usually from TIGRFams). For alignments to characterized proteins (from ublast), scores of 44 bits correspond to an expectation value (E) of about 0.001.

Also see fitness data for the candidates

Definition of step SMc04256

Or cluster all characterized SMc04256 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 (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