Align MFS transporter, FHS family, L-fucose permease (characterized, see rationale)
to candidate Ga0059261_2650 Ga0059261_2650 glucose/galactose transporter
Query= uniprot:A0A1I2JXG1 (442 letters) >FitnessBrowser__Korea:Ga0059261_2650 Length = 425 Score = 342 bits (878), Expect = 1e-98 Identities = 187/431 (43%), Positives = 275/431 (63%), Gaps = 17/431 (3%) Query: 2 AFAAPPAPSKTSLPGAARERYTDYPMAMGVLTSIFFMWGFLTCLNDILIPHLKAVFKLNY 61 A A P AP+ S Y A+ +L S+FFMWGF+T +N+ L+PHL++VF L+Y Sbjct: 7 AGAVPAAPAPES-----------YRRALALLASLFFMWGFITVINNTLLPHLRSVFDLDY 55 Query: 62 AEAMLVQFTFFGAYFLMSLPAGLLVARLGYKKGIVAGLAVAGVGAAGFWPAAAMHFYPAF 121 L++ +F AYF+ S+P+ L+ R+GY++ +VAGL V G+AG AA++ Y Sbjct: 56 TRTTLIESVWFIAYFVASIPSARLIERIGYQRSLVAGLLVMAAGSAGMMLAASIPSYGVT 115 Query: 122 LGALFVLATGITVLQVAANAYVALLGPEKSASSRLTLAQALNSLGTFLAPKFGGLLILSA 181 L LFV+A+GIT+LQVAAN YVA++G ++ASSRL L QA+NS GT LAP FG LIL Sbjct: 116 LAMLFVIASGITLLQVAANPYVAVVGRPETASSRLNLVQAMNSAGTMLAPAFGAWLILGR 175 Query: 182 AV-LSAEQIAKLSPAEQVAYRVQEAQTVQGPYLGLAIVLFLLAVFVYLFRLPALTEKTEQ 240 + ++E L+ AE+ A +AQ+V PY +A+ L +LA+ + F LPA+ T + Sbjct: 176 SKGGTSEAGTVLTQAERFA----DAQSVILPYGLVAVALVMLALVIACFPLPAMGAATRR 231 Query: 241 ASVKQHSLVSPLRHPHVLFGVLAIFFYVGGEVAIGSFLVNYLSMPDIGNMSEQAAANWVA 300 + ++ S +H +++FGV AIF Y+ E+ + + VN++S PDI N++ + A +++ Sbjct: 232 LAKEERRNHSLWKHRNLVFGVPAIFIYLIAEIGVANLFVNFVSQPDIANLTHEQAGHYLT 291 Query: 301 YYWLGAMIGRFIGSALLAKLSPRKLLAIFAAINMALVLTTMMTKGTVAMYSVVSIGLFNS 360 + W G M GRF GSAL+ + +LA+FA A++L G AM++++ +G F+S Sbjct: 292 FLWGGMMAGRFAGSALMQRFDAAHVLAVFAIGAFAVMLVATFATGPTAMWALILVGFFHS 351 Query: 361 IMFPTIFSLGIERMGPMTGEASSLLIMAIVGGAIVPFVQGLFADHIGVQHAFFLPLLCYA 420 IMFPTIF+LGI +GP+T E S LLIMAI GGA+V VQG AD G+Q +F L C Sbjct: 352 IMFPTIFTLGIRGLGPLTEEGSGLLIMAIAGGALV-IVQGWLADQWGLQLSFLLTAACEV 410 Query: 421 YIVFYGLYGSR 431 Y++FY L+GSR Sbjct: 411 YVLFYALWGSR 421 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: 459 Number of extensions: 17 Number of successful extensions: 3 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: 425 Length adjustment: 32 Effective length of query: 410 Effective length of database: 393 Effective search space: 161130 Effective search space used: 161130 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