Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate BWI76_RS23685 BWI76_RS23685 MFS transporter
Query= uniprot:A0A1I2JXG1 (442 letters) >FitnessBrowser__Koxy:BWI76_RS23685 Length = 444 Score = 234 bits (597), Expect = 4e-66 Identities = 137/401 (34%), Positives = 216/401 (53%), Gaps = 8/401 (1%) Query: 35 IFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVARLGYKKG 94 +F +WG LNDILI K F L + LVQ FF YF ++LPA L+ R YK Sbjct: 39 LFALWGMAGNLNDILIAQFKKGFDLTDTQTALVQSIFFLGYFFVALPAAALIKRYSYKAA 98 Query: 95 IVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGPEKSASS 154 I+ GL + +G F PAA + Y AFL L V+A G++ L+ +AN Y +LLGP +S++ Sbjct: 99 IIIGLCLYALGCFLFVPAAQIMTYGAFLACLGVIACGLSFLETSANTYSSLLGPIQSSTQ 158 Query: 155 RLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQEAQTVQGPYLG 214 R+ +Q NSLG G +++ S EQ+ + A A R Q V GPYL Sbjct: 159 RINFSQIFNSLGVISGVLIGQVMVFGENDPSHEQLLAMPAAAADAARHQMVGQVVGPYLI 218 Query: 215 LAIVLFLLAVFVYLFRLPALT-EKTEQASVKQHSLVSPLRH----PHVLFGVLAIFFYVG 269 + VL +LA+ + P+ ++Q + S+ S L+ P G+L+ F YVG Sbjct: 219 IGSVLVVLALVFVFIKFPSCKGTPSQQQQIPTESMGSTLKRLFAIPRFRLGILSQFLYVG 278 Query: 270 GEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRKLLAIF 329 +V + SF + ++ + G SE +A W+ + +G+ + + L+ +L+P LL F Sbjct: 279 AQVGVWSFTIRFVQLVQQGT-SEHSATYWLLASLVIYAVGKTVATWLMNRLNPALLLGTF 337 Query: 330 AAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPMTGEASSLLIMAI 389 A L+L + + +A+Y+++ + + +PT F L I+ MG T A S+++M+I Sbjct: 338 ALAATVLLLIAVFSSSMLAVYALILVSFCMAPCWPTNFGLVIKGMGKDTQTAGSIVVMSI 397 Query: 390 VGGAIVPFVQGLFADHIG--VQHAFFLPLLCYAYIVFYGLY 428 +GGA++P V G+ +D G +Q AF PLLC+ Y+ FYG + Sbjct: 398 IGGAVIPLVMGIISDMNGGNMQIAFIAPLLCFVYVAFYGFW 438 Lambda K H 0.327 0.140 0.414 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: 457 Number of extensions: 26 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: 442 Length of database: 444 Length adjustment: 32 Effective length of query: 410 Effective length of database: 412 Effective search space: 168920 Effective search space used: 168920 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.1 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 40 (21.7 bits) S2: 51 (24.3 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