Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate 353142 BT3616 fucose permease (NCBI ptt file)
Query= SwissProt::P11551 (438 letters) >FitnessBrowser__Btheta:353142 Length = 418 Score = 275 bits (704), Expect = 1e-78 Identities = 159/405 (39%), Positives = 227/405 (56%), Gaps = 3/405 (0%) Query: 20 QSRSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPI 79 + +Y IP AL+ SLFFLWA+++NL ++ Q + L F+A ++A++ YFI PI Sbjct: 2 KKNTYTIPLALVFSLFFLWAISSNLLPTMIRQLMKTCELNTFEASFTETAYWLAYFIFPI 61 Query: 80 PAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAAN 139 P + MK+ SYKAGII GL L A+G LF+PAA + Y +L FIIA G+ LETAAN Sbjct: 62 PIAMFMKRYSYKAGIIFGLLLAAVGGLLFFPAAMLKEYWAYLCIFFIIATGMCFLETAAN 121 Query: 140 PFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSA 199 P+VTVLG + RLNLAQ+FN GA IA +F LILS H +++ L P A Sbjct: 122 PYVTVLGAPETAPRRLNLAQSFNGLGAFIAAMFLSKLILSGT-HYTRETLPVDYPGGWQA 180 Query: 200 YKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRH 259 Y +++ PY+I+ ++L +A++ + +K P + + A + + H Sbjct: 181 YIQLETDAMKLPYLILALLLLAIAVVFVFSKLPKIGDEGAEPASGKKEKLIDFDVLKRSH 240 Query: 260 WRWAVLAQFCYVGAQTACWSYLIRYAVEEIPGMTAGFAANYLTGTMVCFFIGRFTGTWLI 319 RW V+AQF Y G QTA S + Y G+ A + M+ F +GR+ GT L+ Sbjct: 241 LRWGVIAQFFYNGGQTAINSLFLVYCC-TYAGLPEDTATTFFGLYMLAFLLGRWIGTGLM 299 Query: 320 SRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQD 379 +F P +L YAL+ + LC + GG +GL A+ S FMSI YPT FSL +K LG Sbjct: 300 VKFRPQGMLLVYALMNILLCGVVMLWGGMIGLYAMLAISFFMSIMYPTQFSLALKGLGNQ 359 Query: 380 TKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNI-PTAELIPALCFA 423 TK GS+F+VM I+G + + + +I A IP +CFA Sbjct: 360 TKSGSAFLVMAIVGNACLPQLTAYFMHVNEHIYYVAYGIPMICFA 404 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: 489 Number of extensions: 18 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: 438 Length of database: 418 Length adjustment: 32 Effective length of query: 406 Effective length of database: 386 Effective search space: 156716 Effective search space used: 156716 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 Apr 09 2024. 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