Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_025764608.1 X939_RS0117630 L-fucose:H+ symporter permease
Query= uniprot:A0A1I2JXG1 (442 letters) >NCBI__GCF_000566685.1:WP_025764608.1 Length = 433 Score = 212 bits (539), Expect = 2e-59 Identities = 127/409 (31%), Positives = 218/409 (53%), Gaps = 17/409 (4%) Query: 31 VLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLVARLG 90 ++TS+F +WGF + + ++ V +++ A+A LVQ F+G Y M++PA L + + Sbjct: 20 IITSLFALWGFANDITNPMVAAFGTVMEISTAKAALVQLAFYGGYGTMAIPAALFIRKYS 79 Query: 91 YKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALLGPEK 150 YK I+ GL + +GA F+PAA + FLG+L++L G+ L+ AN ++ +G E+ Sbjct: 80 YKSSIILGLTLYAIGALLFYPAAQFEVFGFFLGSLYILTFGLAFLETTANPFILSMGDER 139 Query: 151 SASSRLTLAQALNS----LGTFLAPKFGGLLILSAAVLSAEQI--AKLSPAEQVAYRVQE 204 +A+ RL LAQA N LG F+A KF + + S A ++ LS AE+ R + Sbjct: 140 TATQRLNLAQAFNPIGSLLGMFVASKFILISLDSDKRNEAGELIFTSLSEAEKAIIRTHD 199 Query: 205 AQTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLVSPLRHPHVLFGVLAI 264 ++ PY+ L V+ + V + L ++P +Q+SV S + + GV+A Sbjct: 200 LAVIRNPYVILGFVVVAMLVIIALVKMPERKVDEKQSSVLS-SFSNLWNNGKYKEGVMAQ 258 Query: 265 FFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRK 324 FYV ++ +F++ Y ++G +S+ A N+ + RF+ + ++ ++ R+ Sbjct: 259 LFYVAAQIMCWTFIIQYAE--NLG-ISKAEAQNYNIIAMAIFLSSRFVSTFMMRYVNARQ 315 Query: 325 LLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERM-GPMTGEASS 383 LL FA M ++ G + +Y +++ F S+MFPTI+ + + + T ++ Sbjct: 316 LLMFFALGAMCTTAGVILIDGILGLYMLIATSAFMSLMFPTIYGIALHGLASDDTALGAA 375 Query: 384 LLIMAIVGGAIVPFVQGLFAD------HIGVQHAFFLPLLCYAYIVFYG 426 L+MAIVGGA++P +QGL D GV +F LP LC+ YI YG Sbjct: 376 GLVMAIVGGALMPILQGLIIDMESVGPFSGVNFSFILPFLCFCYIALYG 424 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: 468 Number of extensions: 23 Number of successful extensions: 5 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: 433 Length adjustment: 32 Effective length of query: 410 Effective length of database: 401 Effective search space: 164410 Effective search space used: 164410 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