Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_084936998.1 HA51_RS22420 L-fucose:H+ symporter permease
Query= SwissProt::P11551 (438 letters) >NCBI__GCF_002095475.1:WP_084936998.1 Length = 408 Score = 297 bits (761), Expect = 4e-85 Identities = 163/402 (40%), Positives = 238/402 (59%), Gaps = 24/402 (5%) Query: 28 FALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLIQSAFYFGYFIIPIPAGILMKK 87 F L+ +LFF+W V+ L D+L FQ+ +T Q+GL+Q A++ YF++ +PAG M + Sbjct: 24 FMLITTLFFMWGVSYGLLDVLNKHFQETLHVTKAQSGLLQGAYFGAYFLVALPAGYFMSR 83 Query: 88 LSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFIIAAGLGCLETAANPFVTVLGP 147 YKAGI+ GL LYA+GA LF PAA + N+ +FL LF++A GLGCLETAANP+ TVLG Sbjct: 84 HGYKAGILVGLALYAIGALLFVPAAMVNNFMMFLFALFVLACGLGCLETAANPYATVLGD 143 Query: 148 ESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQDVLDKMSPEQLSAYKHSLVLS 207 RLNLAQ+FN G + + G +L S + S ++ + + Sbjct: 144 ARGAERRLNLAQSFNGLGQFVGPMIGGTLFFS-----------QASADEAQS-------T 185 Query: 208 VQTPYMIIVAIVLLVALLIMLTKFPALQSDNHSDAKQGSFSASLSRLARIRHWRWAVLAQ 267 V+ Y++I +V+ +ALL T P ++ +A++ + + S L + +H+ V+AQ Sbjct: 186 VKITYVVIACVVIGIALLFKRTALPDIR-----EAEEVNPTHSGQTLWQHKHFVGGVIAQ 240 Query: 268 FCYVGAQTACWSYLIRYAVEEIPGMTAGFAANYLTGTMVCFFIGRFTGTWLISRFAPHKV 327 F YV AQ ++ I YA E G+T AA L+ MVCF +GRF TWL+ R +P + Sbjct: 241 FFYVAAQVGVGAFFINYATEHWQGVTNQSAAYMLSVGMVCFMLGRFFSTWLMGRISPASI 300 Query: 328 LAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSIQYPTIFSLGIKNLGQDTKYGSSFI 387 LAAYALI + LC + G V +IAL FMS +PTIF++G+KNLG TK SSF+ Sbjct: 301 LAAYALINIVLCAVVMLGMGDVSVIALVAIFFFMSTMFPTIFAMGVKNLGPATKQASSFM 360 Query: 388 VMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCFAVIFIFA 429 +M I+GG I+ MG +SD + + A +P +CF V+ +A Sbjct: 361 IMAIVGGAIMPWFMGRISDTS-STALAYGLPLVCFVVVLFYA 401 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: 488 Number of extensions: 15 Number of successful extensions: 2 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: 408 Length adjustment: 32 Effective length of query: 406 Effective length of database: 376 Effective search space: 152656 Effective search space used: 152656 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: 50 (23.9 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