GapMind for catabolism of small carbon sources

 

Protein WP_159441877.1 in Williamsia sterculiae CPCC 203464

Annotation: NCBI__GCF_900156495.1:WP_159441877.1

Length: 460 amino acids

Source: GCF_900156495.1 in NCBI

Candidate for 39 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine catabolism bgtB med Basic amino acid uptake transporter, BgtAB (characterized) 35% 92% 255.4 Glutamine ABC transporter permease and substrate binding protein protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity 30% 234.2
L-asparagine catabolism bgtA med Basic amino acid uptake transporter, BgtAB (characterized) 35% 92% 255.4 BgtB aka GLNH aka SLL1270, component of Arginine/lysine/histidine/glutamine porter 34% 246.5
L-aspartate catabolism bgtA med Basic amino acid uptake transporter, BgtAB (characterized) 35% 92% 255.4 BgtB aka GLNH aka SLL1270, component of Arginine/lysine/histidine/glutamine porter 34% 246.5
L-histidine catabolism bgtB med Basic amino acid uptake transporter, BgtAB (characterized) 35% 92% 255.4 Glutamine ABC transporter permease and substrate binding protein protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity 30% 234.2
L-lysine catabolism bgtB med Basic amino acid uptake transporter, BgtAB (characterized) 35% 92% 255.4 Glutamine ABC transporter permease and substrate binding protein protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity 30% 234.2
L-asparagine catabolism glnP lo Glutamine ABC transporter permease and substrate binding protein protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) 30% 65% 234.2 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-glutamate catabolism glnP lo Glutamine ABC transporter permease and substrate binding protein protein, component of Glutamine transporter, GlnQP. Takes up glutamine, asparagine and glutamate which compete for each other for binding both substrate and the transmembrane protein constituent of the system (Fulyani et al. 2015). Tandem substrate binding domains (SBDs) differ in substrate specificity and affinity, allowing cells to efficiently accumulate different amino acids via a single ABC transporter. Analysis revealed the roles of individual residues in determining the substrate affinity (characterized) 30% 65% 234.2 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-histidine catabolism Ac3H11_2554 lo ABC transporter for L-Histidine, permease component 1 (characterized) 37% 92% 142.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-histidine catabolism BPHYT_RS24010 lo Polar amino acid ABC transporter, inner membrane subunit (characterized, see rationale) 35% 87% 128.3 Basic amino acid uptake transporter, BgtAB 35% 255.4
D-glucosamine (chitosamine) catabolism AO353_21715 lo ABC transporter for D-Glucosamine, permease component 2 (characterized) 36% 93% 124.4 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-arginine catabolism artM lo L-Arginine ABC transporter, permease component 1 (characterized) 36% 87% 122.5 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-lysine catabolism hisQ lo Amino acid ABC transporter, membrane protein (characterized, see rationale) 34% 94% 120.6 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-citrulline catabolism AO353_03045 lo ABC transporter for L-Arginine and L-Citrulline, permease component 1 (characterized) 35% 87% 119.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-lysine catabolism hisM lo ABC transporter for L-Lysine, permease component 2 (characterized) 34% 97% 119.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-histidine catabolism aapM lo ABC transporter for L-Glutamine, L-Histidine, and other L-amino acids, permease component 2 (characterized) 32% 59% 116.3 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-histidine catabolism hisM lo Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter membrane protein, 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) 32% 95% 115.9 Basic amino acid uptake transporter, BgtAB 35% 255.4
D-glucosamine (chitosamine) catabolism AO353_21720 lo ABC transporter for D-Glucosamine, permease component 1 (characterized) 33% 91% 114.4 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-arginine catabolism artQ lo Arginine ABC transporter permease protein ArtQ (characterized) 32% 94% 113.2 Basic amino acid uptake transporter, BgtAB 35% 255.4
D-alanine catabolism Pf6N2E2_5404 lo ABC transporter for D-Alanine, permease component 1 (characterized) 36% 56% 112.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-asparagine catabolism natH lo NatH, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized) 33% 57% 112.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-aspartate catabolism natH lo NatH, component of Acidic and neutral amino acid uptake transporter NatFGH/BgtA. BgtA is shared with BgtAB (characterized) 33% 57% 112.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-asparagine catabolism peb1D lo Amino acid ABC transporter, permease protein PEB1 (characterized, see rationale) 35% 85% 109.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-aspartate catabolism peb1D lo Amino acid ABC transporter, permease protein PEB1 (characterized, see rationale) 35% 85% 109.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-asparagine catabolism aapM lo AapM, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 32% 56% 107.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-aspartate catabolism aapM lo AapM, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 32% 56% 107.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-glutamate catabolism aapM lo AapM, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 32% 56% 107.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-leucine catabolism aapM lo AapM, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 32% 56% 107.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-proline catabolism aapM lo AapM, component of General L-amino acid porter; transports basic and acidic amino acids preferentially, but also transports aliphatic amino acids (catalyzes both uptake and efflux) (characterized) 32% 56% 107.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-histidine catabolism BPHYT_RS24005 lo Polar amino acid ABC transporter, inner membrane subunit; Flags: Precursor (characterized, see rationale) 30% 97% 106.7 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-glutamate catabolism gluC lo GluC aka CGL1952, component of Glutamate porter (characterized) 32% 97% 105.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-glutamate catabolism gltJ lo Amino acid ABC transporter membrane protein, component of Amino acid transporter, AatJMQP. Probably transports L-glutamic acid, D-glutamine acid, L-glutamine and N-acetyl L-glutamic acid (Johnson et al. 2008). Very similar to 3.A.1.3.19 of P. putida (characterized) 30% 85% 102.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-citrulline catabolism PS417_17600 lo ABC transporter permease; SubName: Full=Amino acid ABC transporter permease; SubName: Full=Histidine ABC transporter permease HisM; SubName: Full=Histidine transport system permease protein; SubName: Full=Histidine/lysine/arginine/ornithine ABC transporter permease HisM (characterized, see rationale) 34% 92% 101.7 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-glutamate catabolism gluD lo GluD aka CGL1953, component of Glutamate porter (characterized) 31% 85% 100.5 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-arginine catabolism artJ lo Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter periplasmic binding protein, 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) 30% 88% 100.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-histidine catabolism hisJ lo Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter periplasmic binding protein, 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) 30% 88% 100.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-lysine catabolism argT lo Amino acid (Lysine/arginine/ornithine/histidine/octopine) ABC transporter periplasmic binding protein, 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) 30% 88% 100.1 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-citrulline catabolism PS417_17595 lo ABC transporter permease subunit; SubName: Full=Amino acid ABC transporter permease; SubName: Full=Histidine transport system permease protein (characterized, see rationale) 32% 92% 99.8 Basic amino acid uptake transporter, BgtAB 35% 255.4
L-citrulline catabolism AO353_03050 lo ABC transporter for L-Arginine and L-Citrulline, permease component 2 (characterized) 32% 92% 98.6 Basic amino acid uptake transporter, BgtAB 35% 255.4
D-alanine catabolism Pf6N2E2_5403 lo ABC transporter for D-Alanine, permease component 2 (characterized) 30% 54% 79.3 Basic amino acid uptake transporter, BgtAB 35% 255.4

Sequence Analysis Tools

View WP_159441877.1 at NCBI

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

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Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

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Sequence

MGQPTVGAAPQVPTGQPGVLRVGTEGTYSPFTYHDDNGTLTGYDVDIITAVAKKLNLRVE
FVETPFDSIFPALEANRFDIVANQISYTDVRAAKYDLSQSYVQSRGVIVTRSDDDSVHNV
NDLKGKTAAQSLTSNWADVARDAGAQVESVEGFNQAITLLADNRVQTTVNDELTVKNYLA
SSGNKNVKVAAQTPDVSNQVFAMRKNSGLLPAVNQAVSELRADGTLAATYDKYFNAKPIA
PSTWDVVGRNLLPMLGATLKGTIPLTAISFVVGLVIALVIALMRMSANPVASRFARLYIS
IIRGTPLLVQLFFIFFALPELGIVVNPFPSAVVAFSLNVGGYAAEIIRSAIQSLPKGQWE
AASTIGMDYRTTLRRVILPQASRTAVPGLSNTLISLVKDTSLASGIQVAELFRKSQEAAA
PTFQFLALYGVAAVIYWVICLVLSFAQDRLETRLNRFVAR

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