Align L-fucose-proton symporter; 6-deoxy-L-galactose permease; L-fucose permease (characterized)
to candidate WP_008538694.1 HMPREF9454_RS06625 L-fucose:H+ symporter permease
Query= SwissProt::P11551 (438 letters) >NCBI__GCF_000245775.1:WP_008538694.1 Length = 438 Score = 281 bits (718), Expect = 4e-80 Identities = 150/423 (35%), Positives = 253/423 (59%), Gaps = 6/423 (1%) Query: 8 TQSYRAVDKDAGQ-SRSYIIPFALLCSLFFLWAVANNLNDILLPQFQQAFTLTNFQAGLI 66 T+S + + D G +++ I F LL LF LW A +LNDIL+ QF+ FTL++F + L+ Sbjct: 2 TESSKLIQYDDGYLNKTPIFQFVLLSCLFALWGAAASLNDILITQFKSVFTLSDFASALV 61 Query: 67 QSAFYFGYFIIPIPAGILMKKLSYKAGIITGLFLYALGAALFWPAAEIMNYTLFLVGLFI 126 QSAFY GYF+I IPA ++++K +YK I+ GL Y G +LF+PA+ + YT+FLV +F Sbjct: 62 QSAFYGGYFLISIPASVVIRKTTYKLAIMIGLIFYIGGCSLFFPASMMATYTMFLVAIFS 121 Query: 127 IAAGLGCLETAANPFVTVLGPESSGHFRLNLAQTFNSFGAIIAVVFGQSLILSNVPHQSQ 186 IA GLG LETA+N + T+LGP RLN++QTF G+ ++ G+ L+ + Sbjct: 122 IAIGLGFLETASNTYSTMLGPRKYATLRLNISQTFQPIGSASGILLGKYLVFQEGESLAS 181 Query: 187 DVLDKMSPEQLSAYKHSLVLSVQTPYMIIVAIVLLVALLIMLTKFP---ALQSDNHSDAK 243 + +M+P+Q+ ++ ++ PY I++ I++ + +L ++TK+P + N+ + Sbjct: 182 Q-MAQMTPDQIHLFRLQMLQHTLEPYKIMICILVAIFILFLITKYPKCKVKEVANNQNTP 240 Query: 244 QGSFSASLSRLARIRHWRWAVLAQFCYVGAQTACWSYLIRYAVEEIPGMTAGFAANYLTG 303 + + +L L+ ++ ++AQF YVG Q A WS+ IR A++ +P + AA+++ Sbjct: 241 KVTLGETLKYLSGNGLFKKGIVAQFLYVGMQVAVWSFTIRLALDLMPHINERMAADFMVI 300 Query: 304 TMVCFFIGRFTGTWLISRFAPHKVLAAYALIAMALCLISAFAGGHVGLIALTLCSAFMSI 363 + VCFF+G+F +L+++F+ +KVL AY++I L L AF + A S + Sbjct: 301 SFVCFFVGKFIANFLMTKFSVNKVLLAYSIIGCILILYVAFIPNLTAIYAAVAISILLGP 360 Query: 364 QYPTIFSLGIKNLGQD-TKYGSSFIVMTIIGGGIVTPVMGFVSDAAGNIPTAELIPALCF 422 + TI++ +K++ + T+ + IVM+IIGG + V GFVSD G++ + ++ CF Sbjct: 361 CWATIYAETLKSVEKKYTETAGAIIVMSIIGGAFMPAVQGFVSDMVGSMQFSFIVNFFCF 420 Query: 423 AVI 425 A I Sbjct: 421 AYI 423 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: 455 Number of extensions: 23 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: 438 Length adjustment: 32 Effective length of query: 406 Effective length of database: 406 Effective search space: 164836 Effective search space used: 164836 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