GapMind for catabolism of small carbon sources

 

Protein WP_014450232.1 in Leptospirillum ferrooxidans C2-3

Annotation: NCBI__GCF_000284315.1:WP_014450232.1

Length: 241 amino acids

Source: GCF_000284315.1 in NCBI

Candidate for 26 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
L-arginine catabolism artP lo ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) 38% 85% 138.7 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
L-citrulline catabolism AO353_03040 lo ABC transporter for L-Arginine and L-Citrulline, ATPase component (characterized) 38% 85% 138.7 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
L-asparagine catabolism bgtA lo ATPase (characterized, see rationale) 38% 90% 137.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
L-aspartate catabolism bgtA lo ATPase (characterized, see rationale) 38% 90% 137.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
L-histidine catabolism hisP lo histidine transport ATP-binding protein hisP (characterized) 37% 85% 131 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
L-lysine catabolism hisP lo histidine transport ATP-binding protein hisP (characterized) 37% 85% 131 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-cellobiose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-galactose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-glucose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
lactose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-maltose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-mannose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
sucrose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
trehalose catabolism glcV lo monosaccharide-transporting ATPase (EC 3.6.3.17) (characterized) 37% 60% 130.6 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
L-histidine catabolism Ac3H11_2560 lo ABC transporter for L-Histidine, ATPase component (characterized) 37% 72% 120.9 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-cellobiose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 37% 56% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-glucose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 37% 56% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
lactose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 37% 56% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-maltose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 37% 56% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-maltose catabolism malK1 lo MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) 36% 57% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
sucrose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 37% 56% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
trehalose catabolism gtsD lo GtsD (GLcK), component of Glucose porter, GtsABCD (characterized) 37% 56% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
trehalose catabolism thuK lo MalK; aka Sugar ABC transporter, ATP-binding protein, component of The maltose, maltotriose, mannotetraose (MalE1)/maltose, maltotriose, trehalose (MalE2) porter (Nanavati et al., 2005). For MalG1 (823aas) and MalG2 (833aas), the C-terminal transmembrane domain with 6 putative TMSs is preceded by a single N-terminal TMS and a large (600 residue) hydrophilic region showing sequence similarity to MLP1 and 2 (9.A.14; e-12 & e-7) as well as other proteins (characterized) 36% 57% 119.8 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-maltose catabolism malK lo Maltose/maltodextrin import ATP-binding protein MalK; EC 7.5.2.1 (characterized) 34% 52% 102.4 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
D-cellobiose catabolism cbtF lo CbtF, component of Cellobiose and cellooligosaccharide porter (characterized) 33% 58% 97.1 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7
glycerol catabolism glpS lo ABC transporter for Glycerol, ATPase component 1 (characterized) 31% 56% 94.7 Uncharacterized ABC transporter ATP-binding protein YknY; EC 7.6.2.- 47% 198.7

Sequence Analysis Tools

View WP_014450232.1 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

MAPSGNKPPFGVEARLVNVTKRFQVGEEWVEAISGIDLRVSPGEFLALEGSSGSGKSTLL
HLLGLLDRPTSGEVFLDNSPTSHLSMKDRALFRNLHIGFVFQNFQLISRTTALENVEMPF
LYRKSPNVVSPREAREMAKNLLHRVGLSGRERHYPSQLSGGQQQRVAIARALVASPGLLL
ADEPTGNLDSHSAGAILDLLAELRESVGFTLVLVTHDPGVSSRAGRWVRVKDGLLSGSGG
Q

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