Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate WP_091372717.1 BLU33_RS11695 L-fucose:H+ symporter permease
Query= uniprot:A0A1I2JXG1 (442 letters) >NCBI__GCF_900105165.1:WP_091372717.1 Length = 444 Score = 246 bits (627), Expect = 1e-69 Identities = 135/411 (32%), Positives = 222/411 (54%), Gaps = 4/411 (0%) Query: 27 MAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLV 86 ++ ++T +F +WG +NDILI F+L+ +A L+Q F+ YF +++P+GL++ Sbjct: 21 LSFSLVTMLFLIWGIPNNMNDILIKQFMKSFELSRTQAGLIQSAFYMGYFFLAVPSGLIM 80 Query: 87 ARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALL 146 + YK G++AGL + +G FWPAA Y FL ALFV+A+G+T L+ AN ++ L Sbjct: 81 KKYSYKVGLIAGLLLFALGCCLFWPAAVAGKYGLFLFALFVIASGLTFLETGANIFIVEL 140 Query: 147 GPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSAEQIAKLS-PAEQVAYRVQEA 205 G +SA RL +QA N +G L G + ILS +I + E Y QE Sbjct: 141 GESQSAERRLNFSQAFNPIGAVLGVLIGTIFILSGIEHDPLKITAMKLSGEYQHYLQQET 200 Query: 206 QTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLVSPLRHPHVLFGVLAIF 265 V PYL LA L ++F+ + P ++ ++ + + + L++PH GV++ F Sbjct: 201 MRVVTPYLVLAAFAVLWSIFLMFTKFPKGRDELKEENAVKANSRELLKYPHFYKGVISQF 260 Query: 266 FYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLGAMIGRFIGSALLAKLSPRKL 325 FY G + SF + Y+ D E+ A ++ + +GRF + ++ +SP KL Sbjct: 261 FYCGAQTCTWSFFIQYVQ--DFTGQPEKIAGYFLTGTLVAFGVGRFSATYIMRYVSPGKL 318 Query: 326 LAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNSIMFPTIFSLGIERMGPMTGEASSLL 385 + I+ +N+ LV ++ G + ++++ F S+M+PT F+L I +G S++ Sbjct: 319 MGIYGFVNVGLVAIAILIPGFIGVWAIFFTSFFMSLMYPTNFALSIRNLGNNAKIGGSIM 378 Query: 386 IMAIVGGAIVPFVQGLFADHI-GVQHAFFLPLLCYAYIVFYGLYGSRIKSD 435 +MAIVGGA P V GL A+ + A +PL+CY YI +Y L GS+I + Sbjct: 379 VMAIVGGAFFPPVMGLIAESTKSMAIAMVIPLICYLYIAYYALRGSKIPGE 429 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: 495 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 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