GapMind for catabolism of small carbon sources

 

Protein WP_010936584.1 in Dehalococcoides mccartyi 195

Annotation: NCBI__GCF_000011905.1:WP_010936584.1

Length: 236 amino acids

Source: GCF_000011905.1 in NCBI

Candidate for 15 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-histidine catabolism PA5503 lo Methionine import ATP-binding protein MetN 2, component of L-Histidine uptake porter, MetIQN (characterized) 35% 66% 140.6 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-arginine catabolism artP lo Probable ATP-binding component of ABC transporter, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) 37% 86% 133.7 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-histidine catabolism hisP lo Probable ATP-binding component of ABC transporter, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) 37% 86% 133.7 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-lysine catabolism hisP lo Probable ATP-binding component of ABC transporter, component of Amino acid transporter, PA5152-PA5155. Probably transports numerous amino acids including lysine, arginine, histidine, D-alanine and D-valine (Johnson et al. 2008). Regulated by ArgR (characterized) 37% 86% 133.7 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-histidine catabolism BPHYT_RS24015 lo ABC transporter related (characterized, see rationale) 39% 83% 130.6 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-asparagine catabolism bztD lo BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 37% 84% 129.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-aspartate catabolism bztD lo BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 37% 84% 129.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-glutamate catabolism gltL lo BztD, component of Glutamate/glutamine/aspartate/asparagine porter (characterized) 37% 84% 129.8 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-citrulline catabolism AO353_03040 lo ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) 33% 89% 124 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-asparagine catabolism peb1C lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 37% 83% 122.9 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-aspartate catabolism peb1C lo PEB1C, component of Uptake system for glutamate and aspartate (characterized) 37% 83% 122.9 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-citrulline catabolism PS417_17605 lo ATP-binding cassette domain-containing protein; SubName: Full=Amino acid transporter; SubName: Full=Histidine ABC transporter ATP-binding protein; SubName: Full=Histidine transport system ATP-binding protein (characterized, see rationale) 35% 81% 121.3 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-asparagine catabolism bgtA lo ATPase (characterized, see rationale) 33% 84% 116.7 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
L-aspartate catabolism bgtA lo ATPase (characterized, see rationale) 33% 84% 116.7 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3
glycerol catabolism glpS lo ABC transporter for Glycerol, ATPase component 1 (characterized) 31% 58% 95.9 Macrolide export ATP-binding/permease protein MacB; EC 7.6.2.- 41% 158.3

Sequence Analysis Tools

View WP_010936584.1 at NCBI

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

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Sequence

MKKSSLEAIHLRRSFRKGVQSIPVLQDINLRVEPGEVVVIRGKSGAGKSVLLWILSGLDN
PDSGKVLFDGRELNTLGNSQRSELRRSRLGIIFQNFNLIGSWNTYENVAIVLRNSALSPL
EKSERIHRILADLGLSDRLQNLPAELSIGQQQRVAIARTLAAKPEIILADEPTGDVDPET
GAEIIEMLLSPVKAGKAGLVVATHGNFPLAVATRVYTLSDGVLIPFEPSTASAAQS

This GapMind analysis is from Apr 09 2024. 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