GapMind for catabolism of small carbon sources

 

Protein WP_036139849.1 in Lysobacter daejeonensis GH1-9

Annotation: NCBI__GCF_000768355.1:WP_036139849.1

Length: 246 amino acids

Source: GCF_000768355.1 in NCBI

Candidate for 34 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) 39% 73% 161.4 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-lysine catabolism hisP lo Amino-acid ABC transporter, ATP-binding protein (characterized, see rationale) 39% 81% 154.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-glutamate catabolism gltL lo GluA aka CGL1950, component of Glutamate porter (characterized) 38% 91% 149.4 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-histidine catabolism Ac3H11_2560 lo ABC transporter for L-Histidine, ATPase component (characterized) 39% 85% 149.1 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-asparagine catabolism bgtA lo ATPase (characterized, see rationale) 37% 92% 146 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-aspartate catabolism bgtA lo ATPase (characterized, see rationale) 37% 92% 146 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
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) 35% 92% 144.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
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) 35% 92% 144.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-histidine catabolism BPHYT_RS24015 lo ABC transporter related (characterized, see rationale) 33% 97% 138.7 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-alanine catabolism Pf6N2E2_5405 lo ABC transporter for D-Alanine, ATPase component (characterized) 35% 83% 137.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-histidine catabolism aapP lo ABC transporter for L-Glutamine, L-Histidine, and other L-amino acids, ATPase component (characterized) 37% 77% 136.3 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-histidine catabolism bgtA lo BgtA aka SLR1735, component of Arginine/lysine/histidine/glutamine porter (characterized) 34% 84% 136 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
xylitol catabolism HSERO_RS17020 lo ABC-type sugar transport system, ATPase component protein (characterized, see rationale) 36% 56% 133.3 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-arabinose catabolism araV lo AraV, component of Arabinose, fructose, xylose porter (characterized) 34% 61% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-asparagine catabolism aapP lo AapP, 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) 36% 77% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-aspartate catabolism aapP lo AapP, 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) 36% 77% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-cellobiose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 38% 50% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-fructose catabolism araV lo AraV, component of Arabinose, fructose, xylose porter (characterized) 34% 61% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-glucose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 38% 50% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-glutamate catabolism aapP lo AapP, 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) 36% 77% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
lactose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 38% 50% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-leucine catabolism aapP lo AapP, 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) 36% 77% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-maltose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 38% 50% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-proline catabolism aapP lo AapP, 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) 36% 77% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
sucrose catabolism araV lo AraV, component of Arabinose, fructose, xylose porter (characterized) 34% 61% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
sucrose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 38% 50% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
trehalose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 38% 50% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-xylose catabolism araV lo AraV, component of Arabinose, fructose, xylose porter (characterized) 34% 61% 132.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
N-acetyl-D-glucosamine catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 35% 62% 129 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 35% 62% 129 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-proline catabolism proV lo Glycine betaine/proline betaine transport system ATP-binding protein ProV (characterized) 34% 53% 123.2 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
L-proline catabolism HSERO_RS00895 lo ABC-type branched-chain amino acid transport system, ATPase component protein (characterized, see rationale) 30% 96% 104.4 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
glycerol catabolism glpS lo GlpS, component of Glycerol uptake porter, GlpSTPQV (characterized) 31% 54% 100.5 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9
glycerol catabolism glpT lo GlpT, component of Glycerol uptake porter, GlpSTPQV (characterized) 33% 58% 97.4 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 48% 214.9

Sequence Analysis Tools

View WP_036139849.1 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

MLHMQGVTKVFRTELVETHALRSLDLHVREGEFVAVTGPSGSGKTTFLNIAGLLEDFTGG
RYQLDGEDVSGLSDDARSRLRNRKIGFIFQGFNLIPDLNLFDNVDVPLRYRGLPAADRRQ
RIEHALAQVGLGSRMKHYPAELSGGQQQRAAIARALAGQPRLLLADEPTGNLDSQMARGV
MELLEEINAAGTTIVMVTHDPELAARAQRNVHIVDGMATDVSAEPSLVRARQLAAEAEAR
AANPVG

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