Align Rhizopine-binding protein (characterized, see rationale)
to candidate BPHYT_RS11220 BPHYT_RS11220 LacI family transcriptional regulator
Query= uniprot:A0A0N9WNI6 (308 letters) >FitnessBrowser__BFirm:BPHYT_RS11220 Length = 320 Score = 109 bits (273), Expect = 7e-29 Identities = 90/306 (29%), Positives = 138/306 (45%), Gaps = 19/306 (6%) Query: 8 ASLALSLMLASGAALADLRIGVSMSQFDDTWLTYLRESMDKQAKSMPDGVKLQFEDAR-- 65 A+L LS A A ++ + M + + + K P L + Sbjct: 20 AALPLSSAYAQSAPAHKPKVALVMKSLANEFFLTMETGAKDYQKHNPSQFDLITNGIKDE 79 Query: 66 SDVVKQLSQVESFISQKVDAIVVNPVDTAATRKITEAAVKAGIPLVYVNRRPD------- 118 +D Q+ VE I KVDAIV+ P D+ A + + AV AGI +V ++ R D Sbjct: 80 TDTANQIRIVEQMIVSKVDAIVLAPADSKALVPVVKKAVDAGIIVVNIDNRLDPEVLKSK 139 Query: 119 DLKLPKGVITVASNDLEAGQMQMQYLAEKMKGKGDIVILLGDLANNSTTNRTKGVKEVLA 178 DL +P V ++ + Q YLA+K+K ++ I+ G + RT G K+ + Sbjct: 140 DLNVP----FVGPDNRKGAQKVGDYLAKKLKAGDEVGIIEGVSTTTNAQQRTAGFKDAMQ 195 Query: 179 KYPGIKIDQEQTGTWSRDKGMTLVNDWLTQGRKFDAIVSNNDEMAIGAAMALKQAGVEKG 238 K G K+ Q+G W DKG + + L + A+++ ND MAIGA A++ AG ++G Sbjct: 196 KV-GAKVVSVQSGEWEIDKGNAVASAMLNEYPNLKALLAGNDNMAIGAVSAVRAAG-KQG 253 Query: 239 SVLIAGVDGTPDGLRAVKKGDLAVSVFQDANGQAVDSIDAAVKM----AKNEPVEQAVWV 294 VL+ G D +K G + + Q A QAV ID A+K K + V Sbjct: 254 KVLVVGYDNINAIKPMLKDGRVLATADQYAAKQAVFGIDTALKALSGHKKQAELSGVVET 313 Query: 295 PYRLIT 300 P L+T Sbjct: 314 PCDLVT 319 Lambda K H 0.315 0.130 0.360 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: 221 Number of extensions: 20 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: 308 Length of database: 320 Length adjustment: 27 Effective length of query: 281 Effective length of database: 293 Effective search space: 82333 Effective search space used: 82333 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: 41 (21.5 bits) S2: 48 (23.1 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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