Align Inositol transport system sugar-binding protein (characterized)
to candidate WP_046158460.1 VL52_RS18725 ribose ABC transporter substrate-binding protein RbsB
Query= reanno::WCS417:GFF2331 (309 letters) >NCBI__GCF_000971335.1:WP_046158460.1 Length = 311 Score = 163 bits (413), Expect = 4e-45 Identities = 88/284 (30%), Positives = 163/284 (57%), Gaps = 7/284 (2%) Query: 17 ASGVASAADLKIGVSMSAFDDTFLTYLREDMDKQAKSYPKGDGVQLQFEDARADVVKQLS 76 AS A+ + +G+++S ++ F LR+ +AK GV L DA+ D KQ + Sbjct: 33 ASAAAADGKVTVGLAVSTLNNPFFVELRDGAAAEAKK----QGVNLITVDAQDDPAKQQA 88 Query: 77 QVENFISQKVDAIIVNPVDTASTANIIKAATAAKIPLVFVNRRPDSQTLAPGVAAVTSDD 136 VE+ I +KV I++NP D+++ AN++K AT+ I +V ++R + ++ A + SD+ Sbjct: 89 SVEDLIQKKVSVILINPTDSSAVANVVKEATSKGIKVVSLDRSVNGAEVS---AHIASDN 145 Query: 137 VEAGKLQMQYIAEKLGGKGNIVILLGDLANNSTTNRTKGVKEVLTKYPGIKIEQEQTGIW 196 + G + +Y+ +KLGGKG IV L G +++ R +G +V+ K G+K+ +Q + Sbjct: 146 IAGGVMAGKYLLDKLGGKGRIVELEGIAGSSAARERGEGFHQVVDKKEGVKLLAKQPADF 205 Query: 197 LRDRGMTLVNDWLTQGRDFQAVLSNNDEMAIGAAMALKSAGKKGVLIAGVDGTPDGLNAI 256 R +G++++ + + +D Q V ++NDEMA+GA A+++AG K V + G D TPD + A+ Sbjct: 206 DRAKGLSVMENIIQGNKDIQGVFAHNDEMALGAVKAIQAAGLKNVAVVGFDATPDAVAAV 265 Query: 257 TKGDMTVSAFQDAKGQADKSVETARKMAKNEPIEQNVVIPFQLI 300 G ++ + Q V+ A+K+A + +++ + +P L+ Sbjct: 266 KAGALSATVQQQPALIGQYGVQAAKKLADGQKVDKFIPVPLNLV 309 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: 235 Number of extensions: 14 Number of successful extensions: 3 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: 311 Length adjustment: 27 Effective length of query: 282 Effective length of database: 284 Effective search space: 80088 Effective search space used: 80088 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