GapMind for catabolism of small carbon sources

 

Protein WP_013421089.1 in Rhodomicrobium vannielii ATCC 17100

Annotation: NCBI__GCF_000166055.1:WP_013421089.1

Length: 278 amino acids

Source: GCF_000166055.1 in NCBI

Candidate for 22 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 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 40% 71% 172.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-glucosamine (chitosamine) catabolism SMc02869 lo N-Acetyl-D-glucosamine ABC transport system, ATPase component (characterized) 40% 71% 172.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-cellobiose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 44% 62% 170.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-glucose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 44% 62% 170.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
lactose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 44% 62% 170.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-maltose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 44% 62% 170.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
sucrose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 44% 62% 170.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
trehalose catabolism gtsD lo Sugar ABC transporter ATP-binding protein (characterized, see rationale) 44% 62% 170.6 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
putrescine catabolism potA lo PotG aka B0855, component of Putrescine porter (characterized) 44% 56% 169.9 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
lactose catabolism lacK lo ABC transporter for Lactose, ATPase component (characterized) 43% 58% 161 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
L-arabinose catabolism xacK lo Xylose/arabinose import ATP-binding protein XacK; EC 7.5.2.13 (characterized, see rationale) 42% 56% 160.2 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
sucrose catabolism thuK lo ABC transporter (characterized, see rationale) 40% 62% 157.5 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-maltose catabolism thuK lo 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% 69% 157.1 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-mannose catabolism TT_C0211 lo 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% 69% 157.1 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
trehalose catabolism thuK lo 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% 69% 157.1 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
xylitol catabolism Dshi_0546 lo ABC transporter for Xylitol, ATPase component (characterized) 40% 64% 157.1 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
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) 38% 65% 156 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-sorbitol (glucitol) catabolism mtlK lo ABC transporter for D-Sorbitol, ATPase component (characterized) 40% 62% 155.2 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-maltose catabolism malK lo Maltose-transporting ATPase (EC 3.6.3.19) (characterized) 39% 65% 154.8 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-maltose catabolism musK lo ABC-type maltose transporter (EC 7.5.2.1) (characterized) 38% 66% 152.9 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
L-fucose catabolism SM_b21106 lo ABC transporter for L-Fucose, ATPase component (characterized) 41% 61% 151.8 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3
D-maltose catabolism malK_Bb lo ABC-type maltose transport, ATP binding protein (characterized, see rationale) 40% 60% 150.2 Aliphatic sulfonates import ATP-binding protein SsuB; EC 7.6.2.- 46% 215.3

Sequence Analysis Tools

View WP_013421089.1 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

MTALANPVTFRLAALELESVGRAFDVAGTKFDALRDVSLTVCEGEFIAFVGASGCGKSTL
LKAIVGLDRGFEGSIRIDGKPVDGPNLDRSIVFQEHRLLPWLTVEANVGAALRRSGLPSS
ERKQRVAEQLDLVGLSSFAKAYPAQLSGGMAQRVAIARALVTRPRFLLLDEPLGALDALT
RLRLQGELARLIRHEGTTALLVTHDVDEAVTLADRIVVMKPHPGRVARILDVPRHAIRDR
SSPAFLRARDEVLGLLGVPGFVEEPDAPRDRPAELQTA

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