GapMind for catabolism of small carbon sources

 

Protein BWI76_RS03135 in Klebsiella michiganensis M5al

Annotation: FitnessBrowser__Koxy:BWI76_RS03135

Length: 290 amino acids

Source: Koxy in FitnessBrowser

Candidate for 18 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
N-acetyl-D-glucosamine catabolism ngcF lo NgcF, component of N-Acetylglucosamine/N,N'-diacetyl chitobiose porter (NgcK (C) not identified) (characterized) 32% 93% 141.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-glucosamine (chitosamine) catabolism ngcF lo NgcF, component of N-Acetylglucosamine/N,N'-diacetyl chitobiose porter (NgcK (C) not identified) (characterized) 32% 93% 141.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-cellobiose catabolism aglF' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-glucose catabolism aglF' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
lactose catabolism aglF' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-maltose catabolism aglF lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-maltose catabolism aglF' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
sucrose catabolism aglF lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
sucrose catabolism aglF' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
trehalose catabolism aglF lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
trehalose catabolism aglF' lo Inner membrane ABC transporter permease protein (characterized, see rationale) 31% 79% 133.7 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-glucosamine (chitosamine) catabolism SM_b21220 lo ABC transporter for D-Glucosamine, permease component 2 (characterized) 31% 93% 123.6 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-cellobiose catabolism cebF lo CBP protein aka CebF, component of The cellobiose/cellotriose (and possibly higher cellooligosaccharides), CebEFGMsiK [MsiK functions to energize several ABC transporters including those for maltose/maltotriose and trehalose] (characterized) 30% 94% 122.5 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
N-acetyl-D-glucosamine catabolism SMc02872 lo ABC transporter for N-Acetyl-D-glucosamine, permease protein 1 (characterized) 30% 92% 121.3 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-glucosamine (chitosamine) catabolism SMc02872 lo ABC transporter for N-Acetyl-D-glucosamine, permease protein 1 (characterized) 30% 92% 121.3 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
lactose catabolism lacF lo LacF, component of Lactose porter (characterized) 31% 83% 119 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-cellobiose catabolism msdC1 lo Binding-protein-dependent transport systems inner membrane component (characterized, see rationale) 30% 95% 113.6 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5
D-sorbitol (glucitol) catabolism mtlF lo ABC transporter for D-Sorbitol, permease component 2 (characterized) 31% 91% 105.1 ABC-type glycerol 3-phosphate transporter (EC 7.6.2.10) 32% 164.5

Sequence Analysis Tools

View BWI76_RS03135 at FitnessBrowser

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

Find the best match in UniProt

Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

Find homologs in fast.genomics

Fitness BLAST: loading...

Sequence

MRKTWLPWLILSPSLLFLLLFTWFPLGRSVYDSLFDTRMVSDGGQYVGLENFSRLFADSV
FWQSLVNNLLYILLTVVPGVTLALLLAVALTENHRVNRWLRTAFFFPMIIPMVSAAALWL
FIFMPGLGLLDHYLAKLFGPMNNNWLGRSNSALLALALIGVWKFAGYYMLFFLAGLQSIP
ASTREAAIMEGATRTQVFFKVTLPLLRPTLSFVITTALIYSITQIDHVAVMTRGGPDNAT
TVLLYYIQNLAWDTHDLGKASAATFLTLAGLFAFSLINLKLLEKGAHYER

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