Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_084933726.1 HA51_RS07045 L-fucose:H+ symporter permease
Query= uniprot:A0A1I2JXG1 (442 letters) >NCBI__GCF_002095475.1:WP_084933726.1 Length = 441 Score = 204 bits (519), Expect = 5e-57 Identities = 121/401 (30%), Positives = 216/401 (53%), Gaps = 10/401 (2%) Query: 31 VLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVARLG 90 +L+ +F +WG LNDILI K+VF L+ + LVQ F+G YFL+++PA L++ + Sbjct: 23 LLSCLFPLWGCAASLNDILITQFKSVFALSDFASALVQSAFYGGYFLIAIPASLVIRKAT 82 Query: 91 YKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGPEK 150 YK I+ GL + VG F+PA+ M Y FL A+F +A G++ L+ AAN Y +++G Sbjct: 83 YKLAILMGLVLYIVGCVLFYPASHMATYTMFLAAIFAIAIGLSFLETAANTYSSMIGHRD 142 Query: 151 SASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQEAQTVQG 210 A+ RL ++Q +G + G L+ Q+A ++ + A+R+ + Sbjct: 143 HATLRLNISQTFYPIGALMGIVLGKYLVFQDGDSLHTQMAGMNAEQAHAFRLTMLEHTLE 202 Query: 211 PYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLVSPLRH----PHVLFGVLAIFF 266 PY L +VL ++ + R P ++ + S+ SL R+ H G++A F Sbjct: 203 PYKYLVMVLVVVMLLFLFTRYPRCKPESSEKSLP--SLGETFRYLAGNRHFKRGIVAQFL 260 Query: 267 YVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRKLL 326 YVG +VA+ SF + +G +E+ A+N++ Y ++ IG+F+ + L+ + K+L Sbjct: 261 YVGMQVAVWSFTIRLAL--TLGATNERHASNFMIYSFICFFIGKFVANFLMTRFRAEKVL 318 Query: 327 AIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERM-GPMTGEASSLL 385 +++ + + + M A+Y+ V + + + TI++ + + T A + + Sbjct: 319 IVYSVLGVITLAWVMFVPNFTAVYAAVFVSVLFGPCWATIYAGTLATVDNKYTEVAGAFI 378 Query: 386 IMAIVGGAIVPFVQGLFADHIG-VQHAFFLPLLCYAYIVFY 425 +M+IVG A +P +QG +DH+G +Q AF + LLC+A++ FY Sbjct: 379 VMSIVGAAFIPAIQGFVSDHLGSMQLAFGVSLLCFAWVGFY 419 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: 462 Number of extensions: 28 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: 441 Length adjustment: 32 Effective length of query: 410 Effective length of database: 409 Effective search space: 167690 Effective search space used: 167690 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 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