Finding step sacP for sucrose catabolism in Phaeobacter inhibens BS107
No candidates for sacP: sucrose phosphotransferase enzyme EII-BC
GapMind classifies a step as low confidence even if it does not find any candidates. You can still try to find candidates by using Curated BLAST (which searches the 6-frame translation) or by text search of the annotations (which may indicate weak homology, under 30% identity or 50% coverage, that GapMind does not consider). See the links below.
Definition of step sacP
- Curated sequence P27219: protein-Npi-phosphohistidine-sucrose phosphotransferase (EC 2.7.1.211). Enzyme IIscr (EC 2.7.1.211)
- Curated sequence P51184: protein-Npi-phosphohistidine-sucrose phosphotransferase (EC 2.7.1.211). Enzyme IIscr (EC 2.7.1.211)
- Curated sequence P15400: Negative regulator of SacY activity; PTS system sac EIIBC component; EC 2.7.1.-. Sucrose porter and regulatory sensor, IIBC (SacX) (43% identical to 4.A.1.2.1) (Tortosa and Le Coq 1995). The IIA domains of PtsA, GamP, PtsG and GmuA can all phosphorylate the IIB domain in the SacX sensor
- Curated sequence P05306: Sucrose porter, IIBC (SacP) (55% identical to 4.A.1.2.1)
- Curated sequence P08470: Sucrose porter (ScrA)
- Comment: This is PTS-II-BC system (TIGR01996). TIGRFam describes it as relying on the glucose II-A protein (crr). But in B. subtilis, many different II-A proteins can phosphorylate the II-B domains (PMID:30038046). So, treat it as a single-component system. Since the II-A component is not specific, describe it as a 1-component system.
Or cluster all characterized sacP proteins
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:
- ublast finds a hit to a characterized protein at above 40% identity and 80% coverage, and bits >= other bits+10.
- (Hits to curated proteins without experimental data as to their function are never considered high confidence.)
- HMMer finds a hit with 80% coverage of the model, and either other identity < 40 or other coverage < 0.75.
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:
- ublast finds a hit at above 40% identity and 70% coverage (ignoring otherBits).
- ublast finds a hit at above 30% identity and 80% coverage, and bits >= other bits.
- HMMer finds a hit (regardless of coverage or other bits).
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:
- our ignorance of proteins' functions,
- omissions in the gene models,
- frame-shift errors in the genome sequence, or
- the organism lacks the pathway.
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