Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_084933726.1 HA51_RS07045 L-fucose:H+ symporter permease
Query= SwissProt::P11551 (438 letters) >NCBI__GCF_002095475.1:WP_084933726.1 Length = 441 Score = 261 bits (666), Expect = 4e-74 Identities = 141/408 (34%), Positives = 233/408 (57%), Gaps = 4/408 (0%) Query: 17 DAGQSRSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFI 76 D +++ + F LL LF LW A +LNDIL+ QF+ F L++F + L+QSAFY GYF+ Sbjct: 10 DGYLNKTPLFQFILLSCLFPLWGCAASLNDILITQFKSVFALSDFASALVQSAFYGGYFL 69 Query: 77 IPIPAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLET 136 I IPA ++++K +YK I+ GL LY +G LF+PA+ + YT+FL +F IA GL LET Sbjct: 70 IAIPASLVIRKATYKLAILMGLVLYIVGCVLFYPASHMATYTMFLAAIFAIAIGLSFLET 129 Query: 137 AANPFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQ 196 AAN + +++G RLN++QTF GA++ +V G+ L+ + + M+ EQ Sbjct: 130 AANTYSSMIGHRDHATLRLNISQTFYPIGALMGIVLGKYLVFQD-GDSLHTQMAGMNAEQ 188 Query: 197 LSAYKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLAR 256 A++ +++ PY +V ++++V LL + T++P + ++ S+ S + LA Sbjct: 189 AHAFRLTMLEHTLEPYKYLVMVLVVVMLLFLFTRYPRCKPES-SEKSLPSLGETFRYLAG 247 Query: 257 IRHWRWAVLAQFCYVGAQTACWSYLIRYAVEEIPGMTAGFAANYLTGTMVCFFIGRFTGT 316 RH++ ++AQF YVG Q A WS+ IR A+ + A+N++ + +CFFIG+F Sbjct: 248 NRHFKRGIVAQFLYVGMQVAVWSFTIRLAL-TLGATNERHASNFMIYSFICFFIGKFVAN 306 Query: 317 WLISRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNL 376 +L++RF KVL Y+++ + F + A S + TI++ + + Sbjct: 307 FLMTRFRAEKVLIVYSVLGVITLAWVMFVPNFTAVYAAVFVSVLFGPCWATIYAGTLATV 366 Query: 377 -GQDTKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFA 423 + T+ +FIVM+I+G + + GFVSD G++ A + LCFA Sbjct: 367 DNKYTEVAGAFIVMSIVGAAFIPAIQGFVSDHLGSMQLAFGVSLLCFA 414 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: 474 Number of extensions: 37 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: 441 Length adjustment: 32 Effective length of query: 406 Effective length of database: 409 Effective search space: 166054 Effective search space used: 166054 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