Protein WP_025168401.1 in Streptococcus oralis 7747
Annotation: NCBI__GCF_000382825.1:WP_025168401.1
Length: 727 amino acids
Source: GCF_000382825.1 in NCBI
Candidate for 29 steps in catabolism of small carbon sources
Pathway | Step | Score | Similar to | Id. | Cov. | Bits | Other hit | Other id. | Other bits |
D-maltose catabolism | malEIICBA | hi | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) (characterized) | 70% | 100% | 1020.4 | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 | 36% | 394.0 |
D-maltose catabolism | malEIICB | hi | The Maltose group translocator, MalT of 470 aas and 10 TMSs. Takes up extracellular maltose, releasing maltose-phosphate into the cytoplasm (characterized) | 63% | 100% | 695.7 | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 | 36% | 394.0 |
N-acetyl-D-glucosamine catabolism | nagEIIA | med | Putative phosphotransferase enzyme IIA component YpqE (characterized, see rationale) | 50% | 88% | 147.1 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | nagEIIA | med | Putative phosphotransferase enzyme IIA component YpqE (characterized, see rationale) | 50% | 88% | 147.1 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-maltose catabolism | malEIIA | med | Putative phosphotransferase enzyme IIA component YpqE (characterized, see rationale) | 50% | 88% | 147.1 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
trehalose catabolism | treEIIA | med | Putative phosphotransferase enzyme IIA component YpqE (characterized, see rationale) | 50% | 88% | 147.1 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-cellobiose catabolism | ptsG-crr | lo | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized) | 36% | 96% | 394 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucose catabolism | ptsG-crr | lo | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized) | 36% | 96% | 394 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
lactose catabolism | ptsG-crr | lo | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized) | 36% | 96% | 394 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-maltose catabolism | ptsG-crr | lo | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized) | 36% | 96% | 394 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
sucrose catabolism | ptsG-crr | lo | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized) | 36% | 96% | 394 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
trehalose catabolism | ptsG-crr | lo | PTS system glucose-specific EIICBA component; EIICBA-Glc; EII-Glc; EIICBA-Glc 1; EC 2.7.1.199 (characterized) | 36% | 96% | 394 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | gamP | lo | Putative PTS system glucosamine-specific EIICBA component; EC 2.7.1.193 (characterized) | 35% | 100% | 372.9 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
N-acetyl-D-glucosamine catabolism | nagEcba | lo | protein-Npi-phosphohistidine-N-acetyl-D-glucosamine phosphotransferase (EC 2.7.1.193) (characterized) | 34% | 92% | 295.8 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | nagEcba | lo | protein-Npi-phosphohistidine-N-acetyl-D-glucosamine phosphotransferase (EC 2.7.1.193) (characterized) | 34% | 92% | 295.8 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
N-acetyl-D-glucosamine catabolism | nagEcb | lo | N-acetylglucosamine-specific PTS system, IIBC components (nagE) (characterized) | 30% | 81% | 191 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | nagEcb | lo | N-acetylglucosamine-specific PTS system, IIBC components (nagE) (characterized) | 30% | 81% | 191 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-cellobiose catabolism | crr | lo | glucose-specific phosphotransferase enzyme IIA component; EC 2.7.1.- (characterized) | 35% | 97% | 116.7 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucose catabolism | crr | lo | glucose-specific phosphotransferase enzyme IIA component; EC 2.7.1.- (characterized) | 35% | 97% | 116.7 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
lactose catabolism | crr | lo | glucose-specific phosphotransferase enzyme IIA component; EC 2.7.1.- (characterized) | 35% | 97% | 116.7 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-maltose catabolism | crr | lo | glucose-specific phosphotransferase enzyme IIA component; EC 2.7.1.- (characterized) | 35% | 97% | 116.7 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
sucrose catabolism | crr | lo | glucose-specific phosphotransferase enzyme IIA component; EC 2.7.1.- (characterized) | 35% | 97% | 116.7 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
trehalose catabolism | crr | lo | glucose-specific phosphotransferase enzyme IIA component; EC 2.7.1.- (characterized) | 35% | 97% | 116.7 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
N-acetyl-D-glucosamine catabolism | nagPcb | lo | PTS system N-acetylglucosamine-specific EIICB component; EIICB-Nag; EC 2.7.1.- (characterized) | 32% | 50% | 112.1 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | nagPcb | lo | PTS system N-acetylglucosamine-specific EIICB component; EIICB-Nag; EC 2.7.1.- (characterized) | 32% | 50% | 112.1 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
N-acetyl-D-glucosamine catabolism | crr | lo | Putative PTS system sugar phosphotransferase component IIA (characterized, see rationale) | 36% | 93% | 82.4 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | crr | lo | Putative PTS system sugar phosphotransferase component IIA (characterized, see rationale) | 36% | 93% | 82.4 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
N-acetyl-D-glucosamine catabolism | ptsB | lo | IIB aka PtsB, component of N-Acetylglucosamine (NAG) porter (PtsBC1C2)(also may facilitate xylose transport) (characterized) | 40% | 93% | 61.6 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
D-glucosamine (chitosamine) catabolism | ptsB | lo | IIB aka PtsB, component of N-Acetylglucosamine (NAG) porter (PtsBC1C2)(also may facilitate xylose transport) (characterized) | 40% | 93% | 61.6 | The maltose/maltotriose porter, MalT (31% identical to 4.A.1.1.9) | 70% | 1020.4 |
Sequence Analysis Tools
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Find functional residues: SitesBLAST
Search for conserved domains
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Predict transmenbrane helices: Phobius
Predict protein localization: PSORTb
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Sequence
MKATFKNVLSFEFWQKFGKALMVVIAVMPAAGLMISIGKSIVMIDPNLAPLVITGGILEQ
IGWGVIGNLHILFALAIGGSWAKERAGGAFAAGLAFILINRITGTIFGVTSDMLKNPEAM
VTTLFGGSIKVADYFISVLEAPALNMGVFVGIISGFVGATAYNKYYNYRKLPDALSFFNG
KRFVPFVVILRSAIAAIVLAAFWPVVQTGINSFGIWIANSQETAPILAPFLYGTLERLLL
PFGLHHMLTIPMNYTALGGTYEILTGAAKGTQVFGQDPLWLAWVTDLVNLKGTDASHYQQ
LLDTVHPARFKVGQMIGSFGILMGVIVAIYRNVDADKKHQYKGMMIATALATFLTGVTEP
IEYMFMFIATPLYLVYALVQGAAFAMADIVHLRMHSFGSIEFLTRTPLAINAGIGMDIVN
FIWVTVLFAVIMYFIANFMIKKFNYATPGRNGNYETAEGASEDAASGETKVAAASQAVNI
INLLGGRANIVDVDACMTRLRVTVKDADRVGTEEQWKAEGAMGLVMKGQGVQAIYGPKAD
VLKSDIQDILDSGEVIPETLPSQMTEVQKNTVHFKGVTEEVYSVADGQVIALEQVKDPVF
AQKMMGDGFAVEPANGNIVSPVTGTVSSIFPTKHALGLVTESGLEVLVHIGLDTVSLEGK
PFTVHVSEGQKVAAGDLLVTADLDAIRAAGRETSTVVVFTNGDVLKSVKLEQTGSLAAKT
AVAKVEL
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:
- 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