Align Inositol transport system sugar-binding protein (characterized)
to candidate WP_156804529.1 B3C1_RS10875 substrate-binding domain-containing protein
Query= reanno::WCS417:GFF2331 (309 letters) >NCBI__GCF_000299915.1:WP_156804529.1 Length = 309 Score = 128 bits (321), Expect = 2e-34 Identities = 87/266 (32%), Positives = 139/266 (52%), Gaps = 18/266 (6%) Query: 10 LALSMLLASGVA----SAADLKIGVSMSAFDDTFLTYLREDMDKQAKSYPKGDGVQLQFE 65 + L L A+G+ SA + +G S + + + +DM +AKS G+ L+F Sbjct: 2 MTLKTLFAAGLMALSHSALAITVGFSQVGSESGWRSSFSQDMKDEAKSR----GIDLKFA 57 Query: 66 DARADVVKQLSQVENFISQKVDAIIVNPVDTASTANIIKAATAAKIPLVFVNRRPDSQTL 125 D + Q+ V +FI+Q VDAII+ PV ++K A A+IP+V ++R + Sbjct: 58 DGQQKQENQIRAVRSFIAQGVDAIIIAPVVETGWTPVLKEAKRARIPVVILDRNIKA--- 114 Query: 126 APG--VAAVTSDDVEAGKLQMQYIAEKLGGKGNIVILLGDLANNSTTNRTKGVKEVLTKY 183 A G V + SD E G+ +++ +K G+ NIV L G + + +R KG EV+ Y Sbjct: 115 AEGLYVTRIASDFTEEGRKAARWLMDKTKGQCNIVELQGTVGATAAIDRAKGFNEVIGAY 174 Query: 184 PGIKIEQEQTGIWLRDRGMTLVNDWL--TQGRDFQAVLSNNDEMAIGAAMALKSAG---K 238 P KI + QT + R +G ++ +L + A+ S+NDEMA+GA A+K AG Sbjct: 175 PQAKIVRSQTAEFTRAKGKEVMESFLKAEDPQSLCALWSHNDEMALGAIQAIKEAGLKPG 234 Query: 239 KGVLIAGVDGTPDGLNAITKGDMTVS 264 K +L+ VDG PD A+ +GD ++ Sbjct: 235 KDLLVVSVDGVPDYFKAMAEGDANIT 260 Lambda K H 0.314 0.131 0.357 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 205 Number of extensions: 16 Number of successful extensions: 4 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 309 Length of database: 309 Length adjustment: 27 Effective length of query: 282 Effective length of database: 282 Effective search space: 79524 Effective search space used: 79524 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (22.0 bits) S2: 48 (23.1 bits)
This GapMind analysis is from Sep 24 2021. The underlying query database was built on Sep 17 2021.
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:
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