Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_008482148.1 B3C1_RS00390 sugar MFS transporter
Query= SwissProt::P11551 (438 letters) >NCBI__GCF_000299915.1:WP_008482148.1 Length = 424 Score = 232 bits (591), Expect = 2e-65 Identities = 146/418 (34%), Positives = 217/418 (51%), Gaps = 9/418 (2%) Query: 20 QSRSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPI 79 + + Y + LFF+ LNDIL+P + F+L QA LIQ F+ YF++ Sbjct: 15 EHQGYTFALTSMTFLFFMMGFITCLNDILIPHLKNVFSLNYTQAMLIQFCFFGAYFVVSY 74 Query: 80 PAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAAN 139 PAG L ++L YK ++ L + A+G LF AA Y LFL LFI+A+G+ L+ A N Sbjct: 75 PAGALARRLGYKWALVISLVVSAIGCLLFITAASYRVYELFLGALFILASGVTTLQVAVN 134 Query: 140 PFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSA 199 P+VTVLG + RL L Q FNS G +A FG LIL +S EQ++A Sbjct: 135 PYVTVLGKPETASARLTLNQAFNSLGTTLAPTFGAMLILGAATAD----FTGLSQEQVTA 190 Query: 200 YKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRH 259 + S +V+ PY+++ + L++A ++ K P ++ +++ A Q S S + RH Sbjct: 191 LRLSEADAVKFPYLLLASTFLVLAAVLAYLKLPDMREQDNAAAAQASQGGS---AWQYRH 247 Query: 260 WRWAVLAQFCYVGAQTACWSYLIRYAVE-EIPGMTAGFAANYLTGTMVCFFIGRFTGTWL 318 L F YVGA+ + S L+ + E I G+ AA+Y++ +GRF G+ + Sbjct: 248 LVLGALGLFVYVGAEVSIGSLLVNFLGEANIAGLAEADAAHYVSYYWGGAMVGRFIGSAV 307 Query: 319 ISRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQ 378 + + KVLA AL A+ L + G + + A+ F SI +PTIFSL +K LG Sbjct: 308 MRQVGAGKVLAFNALAAVLLLAAAVLGNGALAMWAVLAVGLFNSIMFPTIFSLAVKGLGH 367 Query: 379 DTKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIFARFRSQTA 436 T GS + M I+GG IV ++G +D G I A +P LC+ I + SQTA Sbjct: 368 HTAQGSGILCMAIVGGAIVPLLVGVAADNLG-IQLAFALPILCYLYIAFYGLKGSQTA 424 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: 435 Number of extensions: 32 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: 438 Length of database: 424 Length adjustment: 32 Effective length of query: 406 Effective length of database: 392 Effective search space: 159152 Effective search space used: 159152 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