GapMind for catabolism of small carbon sources

 

Protein WP_084703891.1 in Phaeacidiphilus oryzae TH49

Annotation: NCBI__GCF_000744815.1:WP_084703891.1

Length: 389 amino acids

Source: GCF_000744815.1 in NCBI

Candidate for 40 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 SMc02869 med N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 47% 76% 226.9 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-glucosamine (chitosamine) catabolism SMc02869 med N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 47% 76% 226.9 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-cellobiose catabolism gtsD med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-glucose catabolism gtsD med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
lactose catabolism gtsD med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism gtsD med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism thuK med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-mannose catabolism TT_C0211 med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
sucrose catabolism gtsD med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
sucrose catabolism thuK med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
trehalose catabolism gtsD med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
trehalose catabolism thuK med Sugar-binding transport ATP-binding protein aka MalK1 aka TT_C0211, component of The trehalose/maltose/sucrose/palatinose porter (TTC1627-9) plus MalK1 (ABC protein, shared with 3.A.1.1.24) (Silva et al. 2005; Chevance et al., 2006). The receptor (TTC1627) binds disaccharide alpha-glycosides, namely trehalose (alpha-1,1), sucrose (alpha-1,2), maltose (alpha-1,4), palatinose (alpha-1,6) and glucose (characterized) 40% 93% 226.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-mannitol catabolism mtlK med SmoK aka POLK, component of Hexitol (glucitol; mannitol) porter (characterized) 43% 76% 211.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
trehalose catabolism treV med TreV, component of Trehalose porter (characterized) 42% 74% 188.3 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
putrescine catabolism potA lo PotG aka B0855, component of Putrescine porter (characterized) 38% 99% 236.9 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism aglK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 38% 99% 229.2 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
sucrose catabolism aglK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 38% 99% 229.2 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
trehalose catabolism aglK lo ABC transporter for D-Maltose and D-Trehalose, ATPase component (characterized) 38% 99% 229.2 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism malK lo ABC-type maltose transporter (subunit 3/3) (EC 7.5.2.1) (characterized) 38% 97% 225.3 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
lactose catabolism lacK lo LacK, component of Lactose porter (characterized) 38% 98% 223.8 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-xylose catabolism gtsD lo ABC transporter for D-Glucose-6-Phosphate, ATPase component (characterized) 38% 88% 218.8 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-cellobiose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 36% 96% 217.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-glucose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 36% 96% 217.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
lactose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 36% 96% 217.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 36% 96% 217.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
sucrose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 36% 96% 217.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
trehalose catabolism aglK' lo Maltose/maltodextrin import ATP-binding protein; EC 3.6.3.19 (characterized, see rationale) 36% 96% 217.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-galactose catabolism PfGW456L13_1897 lo ABC transporter for D-Galactose and D-Glucose, ATPase component (characterized) 38% 88% 215.7 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism malK_Aa lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 37% 91% 214.9 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
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) 39% 93% 214.2 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-sorbitol (glucitol) catabolism mtlK lo ABC transporter for D-Sorbitol, ATPase component (characterized) 37% 96% 211.8 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
L-fucose catabolism SM_b21106 lo ABC transporter for L-Fucose, ATPase component (characterized) 46% 64% 211.1 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-cellobiose catabolism SMc04256 lo ABC transporter for D-Cellobiose and D-Salicin, ATPase component (characterized) 37% 99% 210.7 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
xylitol catabolism HSERO_RS17020 lo ABC-type sugar transport system, ATPase component protein (characterized, see rationale) 42% 68% 209.1 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism malK_Bb lo ABC-type maltose transport, ATP binding protein (characterized, see rationale) 46% 68% 208.8 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-glucosamine (chitosamine) catabolism SM_b21216 lo ABC transporter for D-Glucosamine, ATPase component (characterized) 36% 99% 203.8 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism musK lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 46% 62% 203 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
xylitol catabolism Dshi_0546 lo ABC transporter for Xylitol, ATPase component (characterized) 37% 91% 201.1 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
trehalose catabolism malK lo MsmK aka SMU.882, component of The raffinose/stachyose transporter, MsmEFGK (MalK (3.A.1.1.27) can probably substitute for MsmK; Webb et al., 2008). This system may also transport melibiose, isomaltotriose and sucrose as well as isomaltosaccharides (characterized) 36% 93% 192.6 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7
D-maltose catabolism malK_Sm lo MalK, component of Maltose/Maltotriose/maltodextrin (up to 7 glucose units) transporters MalXFGK (MsmK (3.A.1.1.28) can probably substitute for MalK; Webb et al., 2008) (characterized) 39% 74% 189.5 Putative 2-aminoethylphosphonate import ATP-binding protein PhnT 50% 329.7

Sequence Analysis Tools

View WP_084703891.1 at NCBI

Find papers: PaperBLAST

Find functional residues: SitesBLAST

Search for conserved domains

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Compare to protein structures

Predict transmenbrane helices: Phobius

Predict protein localization: PSORTb

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Sequence

MNGSATTAAVAAPDAGAAPDAGPAPAARRPGISFEDVTVAYRDQVVLNGFTLDVAAGEVV
ALLGPSGSGKTTALRTVAGFTAPVRGRVGIGGRDVTGLPPHRRGIGMVVQQYALFPHLRV
EQNVAFGLKAHRTPRAQVPGRVAEALEMTGMAGYARRYPRELSGGQQQRVALARALAIRP
EVLLLDEPLSALDAGLRAGMLAELARLHRELPEVSILYVTHDQIEALTLADRIAVLRDAR
LVDCGTPERLYRRPADAFTASFVGRANLLPVTAGQEPDRVVLGAATHRTGAVELRITAQD
GFPAGSPALLCVRPHQLRPATEGGPNLLRGRVSDVQWLGSTHRVQVDLDAGPRVAAELSG
LRVPPAAGEELALGFDPEDGVLLPAEGAS

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