Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate 353142 BT3616 fucose permease (NCBI ptt file)
Query= uniprot:A0A1I2JXG1 (442 letters) >FitnessBrowser__Btheta:353142 Length = 418 Score = 249 bits (636), Expect = 1e-70 Identities = 145/414 (35%), Positives = 230/414 (55%), Gaps = 9/414 (2%) Query: 25 YPMAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGL 84 Y + + ++ S+FF+W + L +I L +LN EA + ++ AYF+ +P + Sbjct: 6 YTIPLALVFSLFFLWAISSNLLPTMIRQLMKTCELNTFEASFTETAYWLAYFIFPIPIAM 65 Query: 85 LVARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVA 144 + R YK GI+ GL +A VG F+PAA + Y A+L F++ATG+ L+ AAN YV Sbjct: 66 FMKRYSYKAGIIFGLLLAAVGGLLFFPAAMLKEYWAYLCIFFIIATGMCFLETAANPYVT 125 Query: 145 LLGPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLSPAEQVAYRVQE 204 +LG ++A RL LAQ+ N LG F+A F LILS + E + P AY E Sbjct: 126 VLGAPETAPRRLNLAQSFNGLGAFIAAMFLSKLILSGTHYTRETLPVDYPGGWQAYIQLE 185 Query: 205 AQTVQGPYLGLAIVLFLLAVFVYLFRLPAL-TEKTEQASVKQHSLV--SPLRHPHVLFGV 261 ++ PYL LA++L +AV +LP + E E AS K+ L+ L+ H+ +GV Sbjct: 186 TDAMKLPYLILALLLLAIAVVFVFSKLPKIGDEGAEPASGKKEKLIDFDVLKRSHLRWGV 245 Query: 262 LAIFFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLS 321 +A FFY GG+ AI S + Y + E A + Y L ++GR+IG+ L+ K Sbjct: 246 IAQFFYNGGQTAINSLFLVYCC--TYAGLPEDTATTFFGLYMLAFLLGRWIGTGLMVKFR 303 Query: 322 PRKLLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPMTGEA 381 P+ +L ++A +N+ L M+ G + +Y++++I F SIM+PT FSL ++ +G T Sbjct: 304 PQGMLLVYALMNILLCGVVMLWGGMIGLYAMLAISFFMSIMYPTQFSLALKGLGNQTKSG 363 Query: 382 SSLLIMAIVGGAIVPFVQGLFA---DHIGVQHAFFLPLLCYAYIVFYGLYGSRI 432 S+ L+MAIVG A +P + F +HI A+ +P++C+A+ +YG G ++ Sbjct: 364 SAFLVMAIVGNACLPQLTAYFMHVNEHI-YYVAYGIPMICFAFCAYYGWKGYKV 416 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: 489 Number of extensions: 17 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: 418 Length adjustment: 32 Effective length of query: 410 Effective length of database: 386 Effective search space: 158260 Effective search space used: 158260 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 Apr 09 2024. 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