GapMind for catabolism of small carbon sources

 

Protein WP_068336976.1 in Photobacterium jeanii R-40508

Annotation: NCBI__GCF_001650345.1:WP_068336976.1

Length: 622 amino acids

Source: GCF_001650345.1 in NCBI

Candidate for 11 steps in catabolism of small carbon sources

Pathway Step Score Similar to Id. Cov. Bits Other hit Other id. Other bits
D-fructose catabolism fruII-C lo Sugar phosphotransferase system IIC component, component of Fructose-specific Enzyme I-HPr-Enzyme IIABC complex, all encoded within a single operon with genes in the order: ptsC (IIC), ptsA (IIA), ptsH (HPr), ptsI (Enzyme I) and ptsB (IIB) (characterized) 39% 96% 237.7 Fructose-like permease IIC component 2; PTS system fructose-like EIIC component 2 45% 303.9
sucrose catabolism fruII-C lo Sugar phosphotransferase system IIC component, component of Fructose-specific Enzyme I-HPr-Enzyme IIABC complex, all encoded within a single operon with genes in the order: ptsC (IIC), ptsA (IIA), ptsH (HPr), ptsI (Enzyme I) and ptsB (IIB) (characterized) 39% 96% 237.7 Fructose-like permease IIC component 2; PTS system fructose-like EIIC component 2 45% 303.9
D-fructose catabolism fruA lo protein-Npi-phosphohistidine-D-fructose phosphotransferase (subunit 2/2) (EC 2.7.1.202) (characterized) 33% 98% 226.1 Fructose-like permease IIC component 2; PTS system fructose-like EIIC component 2 45% 303.9
sucrose catabolism fruA lo protein-Npi-phosphohistidine-D-fructose phosphotransferase (subunit 2/2) (EC 2.7.1.202) (characterized) 33% 98% 226.1 Fructose-like permease IIC component 2; PTS system fructose-like EIIC component 2 45% 303.9
D-fructose catabolism fruII-A lo PTS system fructose-specific EIIA component; EIIA-Fru; Fructose-specific phosphotransferase enzyme IIA component (characterized) 36% 99% 89 protein-Npi-phosphohistidine-D-mannose phosphotransferase (EC 2.7.1.191) 37% 276.6
sucrose catabolism fruII-A lo PTS system fructose-specific EIIA component; EIIA-Fru; Fructose-specific phosphotransferase enzyme IIA component (characterized) 36% 99% 89 protein-Npi-phosphohistidine-D-mannose phosphotransferase (EC 2.7.1.191) 37% 276.6
D-ribose catabolism fru2-IIA lo PTS system, fructose-specific, IIA component, component of D-allose/D-ribose transporting Enzyme II complex (Fru2; IIA/IIB/IIC) (Patron et al. 2017). This system is similar to Frz of E. coli (TC#4.A.2.1.9) which is involved in environmental sensing, host adaptation and virulence (characterized) 30% 100% 81.3 protein-Npi-phosphohistidine-D-mannose phosphotransferase (EC 2.7.1.191) 37% 276.6
D-fructose catabolism fruD lo protein-Npi-phosphohistidine-D-fructose phosphotransferase (subunit 1/2) (EC 2.7.1.202) (characterized) 31% 96% 78.2 protein-Npi-phosphohistidine-D-mannose phosphotransferase (EC 2.7.1.191) 37% 276.6
sucrose catabolism fruD lo protein-Npi-phosphohistidine-D-fructose phosphotransferase (subunit 1/2) (EC 2.7.1.202) (characterized) 31% 96% 78.2 protein-Npi-phosphohistidine-D-mannose phosphotransferase (EC 2.7.1.191) 37% 276.6
D-fructose catabolism fruII-B lo Phosphotransferase system IIB component, component of Fructose-specific Enzyme I-HPr-Enzyme IIABC complex, all encoded within a single operon with genes in the order: ptsC (IIC), ptsA (IIA), ptsH (HPr), ptsI (Enzyme I) and ptsB (IIB) (characterized) 42% 64% 75.1
sucrose catabolism fruII-B lo Phosphotransferase system IIB component, component of Fructose-specific Enzyme I-HPr-Enzyme IIABC complex, all encoded within a single operon with genes in the order: ptsC (IIC), ptsA (IIA), ptsH (HPr), ptsI (Enzyme I) and ptsB (IIB) (characterized) 42% 64% 75.1

Sequence Analysis Tools

View WP_068336976.1 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

MDITDLIESEIICLDLKATNKEDVLAELTDLLDAAGKLVDKTQFLADVWKREEIGNTGFE
EGIAIPHAKSGAVAKPAVAVGISRSGIDYGAEDGELSDVFFMLASPDGQDHHHIEVLAQL
STKLIEESFITKLKGAESVEEALELLTDIEPTQFGHTAFDVPEFIAEPLSPFKQRLAHIK
EHLLFGTSHMIPFIVAGGVLLSLSVMISGHGGVPETGMLADIAEMGIAGLTLFTAVLGGY
IAYSIADKPGLAPGMIGSWVAVNHYHTGFLGAIVVGFFAGFVVQMLKKITLPDSMSSLGS
IFIYPLVGTFATCGAVMWLIGNPIASAMLMLNEWLTGMAGSGKVLLGSILGAMTAFDMGG
PINKVATLFAQTQVNTQPWLMGGVGIAICTPPLGLALATFLSPKKFKRDEREAGKAAGIM
GMIGISEGAIPFAAADPARVLPAIVAGGIVGNVTGFMFHVLNHAPWGGWIVLPVVDGKLG
YLIGTLLGALTTALIVIALKKTVNEDEDHALASGHYSSVEGEGEADILAVTSCPSGVAHT
FLAAKSLEKAACALGVKIKVETQGANGIINRITERDIAKAKLVIFAHDVAIKAPERFTNI
ATIDVSTKDAMLNAAALIQSKR

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