Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_101442931.1 BD749_RS03265 sugar MFS transporter
Query= SwissProt::P11551 (438 letters) >NCBI__GCF_002846395.1:WP_101442931.1 Length = 474 Score = 241 bits (616), Expect = 3e-68 Identities = 159/483 (32%), Positives = 236/483 (48%), Gaps = 83/483 (17%) Query: 4 TSIQTQSYRAVDKDAGQS-RSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQ 62 T I+T + K+ + ++Y P ++ LFF+W +NDIL+P+ Q+ FTL +Q Sbjct: 5 TPIKTDEAASQSKETLRDYKNYTSPLIVVTLLFFMWGFITCMNDILIPKLQEVFTLQLWQ 64 Query: 63 AGLIQSAFY-------FGYFIIPIPAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIM 115 A LIQ+AF+ F YF++ I G ++K+ YK GII GL + ALG LF+PAA Sbjct: 65 AMLIQTAFFGAYFIVSFFYFMLSITKGDPIQKIGYKNGIIIGLIVAALGCVLFYPAAVFH 124 Query: 116 NYTLFLVGLFIIAAGLGCLETAANPFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQS 175 +Y FL+ LFI+A+G+ L+ ANP+V +LGP + R+NL+Q NSFG IA + G Sbjct: 125 SYGFFLMALFILASGITVLQITANPYVAILGPPETSSSRMNLSQALNSFGTTIAPIIGGY 184 Query: 176 LILSNVPHQSQDVLDKMSPEQLSAYKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFPALQ 235 LI V D D SV+ PY+ + A++LL+ALLI + K P L Sbjct: 185 LIFDQVASAEIDTAD----------------SVKLPYLGLAALLLLLALLIKVAKLPRL- 227 Query: 236 SDNHSDAKQGSFSASLSRLA-RIRHWRWAVLAQFCYVGAQTACWSYLIRY-AVEEIPGMT 293 +GS +A + H ++ F YVG + + S LI Y + +I G+T Sbjct: 228 --------EGSGKIETGAVAVKHPHLVLGIICIFMYVGGEVSIGSALINYIKLPQITGLT 279 Query: 294 AGFAANYLTGTMVCFFIGRFTG-------------------------------------- 315 A +YL IGRF G Sbjct: 280 ESEAKHYLAFYWGGAMIGRFFGAVALSTLKRSGKFMVIALIALVTFLTVYALYDLNEALI 339 Query: 316 ----------TWLISRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQY 365 L++RF P++ + +A+ + L LI A G + + A+ F SI + Sbjct: 340 ILGLIALNVVVLLLARFIPNRTVGLFAMAVIGLLLIGVVAEGTLAMWAIIAIGLFNSIMF 399 Query: 366 PTIFSLGIKNLGQDTKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVI 425 PTIF L IK LG+ T GSS +VM I+GG IV P+ G +D G++ + +IP +C+A I Sbjct: 400 PTIFDLAIKGLGRHTSQGSSLLVMAIVGGAIVPPLQGLFADLTGDLQLSFIIPMICYAYI 459 Query: 426 FIF 428 + Sbjct: 460 VYY 462 Lambda K H 0.329 0.140 0.425 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: 456 Number of extensions: 22 Number of successful extensions: 7 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 1 Length of query: 438 Length of database: 474 Length adjustment: 33 Effective length of query: 405 Effective length of database: 441 Effective search space: 178605 Effective search space used: 178605 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 (21.8 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