Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate 202604 SO3503 glucose/galactose transporter (NCBI ptt file)
Query= uniprot:A0A1I2JXG1 (442 letters) >lcl|FitnessBrowser__MR1:202604 SO3503 glucose/galactose transporter (NCBI ptt file) Length = 435 Score = 194 bits (492), Expect = 6e-54 Identities = 139/428 (32%), Positives = 224/428 (52%), Gaps = 29/428 (6%) Query: 27 MAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNYAEAMLVQFTFFGAYFLMSLPAGLLV 86 + M ++ ++FF+ GF T LN L+P+LK + +LN +A L+ F+F+ A +LP+ ++ Sbjct: 13 LPMAIVAALFFILGFATWLNGSLMPYLKQILQLNPFQASLILFSFYIAVTFTALPSAWVI 72 Query: 87 ARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAFLGALFVLATGITVLQVAANAYVALL 146 ++GYK G+ G+ V + F PAA + FL A V+ G T+LQ A N YV L Sbjct: 73 RKVGYKNGMALGMGVMMIAGLLFIPAAKTQVFALFLFAQLVMGAGQTLLQTAVNPYVVRL 132 Query: 147 GPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSAAVLSA--EQIAKLSPAEQVAYRVQE 204 GPE+SA++R+++ LN +AP L+ SA +L + ++I Q+ + Sbjct: 133 GPEESAAARVSVMGILNKGAGVIAP-----LVFSALILDSFKDRIGTTLTQVQID---EM 184 Query: 205 AQTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQASVKQHSLV-SPLRHPHVLFGVLA 263 A + PYLG+A+ + +LA+ V LP L+ + E A S + + L HP++ GVLA Sbjct: 185 ANGLVLPYLGMAVFIGILALAVKKSPLPELSNEDEVADHTDKSQIKAALSHPNLALGVLA 244 Query: 264 IFFYVGGEV----AIGSFLVNYLSMPDIGNMSEQAAANWVAYYWLG-AMIGRFIGSALLA 318 +F YV EV IG+F ++ L + G M+ V Y LG +I R I Sbjct: 245 LFVYVAVEVIAGDTIGTFALS-LGIDHYGVMTSYTMVCMVLGYILGILLIPRVISQPTAL 303 Query: 319 KLSPRKLLAIFAAI------NMALVLTTMMTKGTVA----MYSVVSIGLFNSIMFPTIFS 368 +S L + I + A+ ++ G VA + + +GL N+I++P ++ Sbjct: 304 MISAILGLLLTLGILFGDNNSYAIANLLLVPFGGVALPDTLLLIAFLGLANAIVWPAVWP 363 Query: 369 LGIERMGPMTGEASSLLIMAIVGGAIVPFVQGLF--ADHIGVQHAFFLPLLCYAYIVFYG 426 L + MG +T S+LLIM I GGA P GL A +G Q + + L CY +I+FY Sbjct: 364 LALSGMGKLTSTGSALLIMGIAGGAFGPVSWGLMSSATDMGQQGGYMVMLPCYLFILFYA 423 Query: 427 LYGSRIKS 434 + G +++S Sbjct: 424 VKGHKMRS 431 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: 502 Number of extensions: 28 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: 435 Length adjustment: 32 Effective length of query: 410 Effective length of database: 403 Effective search space: 165230 Effective search space used: 165230 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