GapMind for catabolism of small carbon sources

 

Protein WP_106713881.1 in Phyllobacterium brassicacearum STM 196

Annotation: NCBI__GCF_003010955.1:WP_106713881.1

Length: 512 amino acids

Source: GCF_003010955.1 in NCBI

Candidate for 14 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-galactose catabolism ytfR hi galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) (characterized) 46% 98% 421.4 Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved 45% 406.4
L-arabinose catabolism araVsh med ABC transporter related (characterized, see rationale) 42% 100% 429.5 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
L-fucose catabolism HSERO_RS05250 med Ribose import ATP-binding protein RbsA; EC 7.5.2.7 (characterized, see rationale) 44% 94% 419.1 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
myo-inositol catabolism iatA med Inositol transport ATP-binding protein IatA, component of The myoinositol (high affinity)/ D-ribose (low affinity) transporter IatP/IatA/IbpA. The structure of IbpA with myoinositol bound has been solved (characterized) 45% 97% 406.4 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
D-ribose catabolism rbsA med ribose transport, ATP-binding protein RbsA; EC 3.6.3.17 (characterized) 43% 99% 404.4 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
D-xylose catabolism xylG med Monosaccharide-transporting ATPase, component of Glucose porter. Also bind xylose (Boucher and Noll 2011). Induced by glucose (Frock et al. 2012). Directly regulated by glucose-responsive regulator GluR (characterized) 41% 99% 402.5 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
myo-inositol catabolism PS417_11890 med m-Inositol ABC transporter, ATPase component (itaA) (characterized) 42% 96% 397.5 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
D-fructose catabolism fruK med Fructose import ATP-binding protein FruK; EC 7.5.2.- (characterized) 40% 99% 396 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
sucrose catabolism fruK med Fructose import ATP-binding protein FruK; EC 7.5.2.- (characterized) 40% 99% 396 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
D-xylose catabolism xylK_Tm med Ribose import ATP-binding protein RbsA 1; EC 7.5.2.7 (characterized, see rationale) 42% 95% 377.9 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
D-galactose catabolism BPHYT_RS16930 med Arabinose import ATP-binding protein AraG; EC 7.5.2.12 (characterized, see rationale) 41% 95% 368.6 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
L-arabinose catabolism araG med L-arabinose ABC transporter, ATP-binding protein AraG; EC 3.6.3.17 (characterized) 42% 99% 364.8 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
L-fucose catabolism BPHYT_RS34245 lo ABC transporter related; Flags: Precursor (characterized, see rationale) 34% 95% 300.8 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4
L-rhamnose catabolism BPHYT_RS34245 lo ABC transporter related; Flags: Precursor (characterized, see rationale) 34% 95% 300.8 galactofuranose ABC transporter putative ATP binding subunit (EC 7.5.2.9) 46% 421.4

Sequence Analysis Tools

View WP_106713881.1 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

Fitness BLAST: loading...

Sequence

MNDDILLSMTGIDKRFAGIPALSGASFAVGRGEVHALIGQNGAGKSTLIKVLTGYYRRDA
GDVAFDGKPFEVFSPQLAQASGISTIYQEINLVPYRSITENICLGREARHYGLLDWKRMH
KEAETLLRRFNVRVDVDRPLMEFNTATQQMVAIARAIGFSAKLVVMDEPTSSLDDREVTV
LFDVIRQLKQEGVSVVFVSHKLDELYEVCDRVTIMRDGRTVKTAAMTEIDKIGLVSSMLG
RTINRAEGHATAFSDRDEKKIGKVLLSAQNLSINRTVQDVSFDVRSGEIAGFAGLLGAGR
TETARLVFGIDRPRAGIMHYDGQQFDPRSPADAIAAGMGFCTEDRKSEGIVPEMSVAENM
MLALMPKVSKSGVIDEKAQRKIVERFIRQLDIKCSGPDQKVRELSGGNQQKVLLGRWLAM
NPTLLILDEPTRGIDVGAKGEIQSLIKSLADRGLAVLMISSELEEVIEGADRVFVLREGI
TVAEFDRNQATEDVLMSAMAHGNAPRIVEAAS

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