Align galactose transporter (characterized)
to candidate WP_010536987.1 KCY_RS0109365 sugar porter family MFS transporter
Query= CharProtDB::CH_091029 (574 letters) >NCBI__GCF_000226135.1:WP_010536987.1 Length = 460 Score = 185 bits (469), Expect = 4e-51 Identities = 146/480 (30%), Positives = 227/480 (47%), Gaps = 56/480 (11%) Query: 74 LCLCVAFGGFMFGWDTGTISGFVVQTDFLRRFGMKHKDGTHYLSNVRTGLIVAIFNIGCA 133 +CL A GG +FG+D I G + F + D S GL +++ +GC Sbjct: 12 ICLVSAMGGLLFGYDWVVIGG-------AKPFYELYFDIAD--SPTMQGLAMSVALLGCL 62 Query: 134 FGGIILSKGGDMYGRKKGLSIVVSVYIVGIIIQIA-SINKWYQYFIGRIISGLGVGGIAV 192 G ++ D YGRK L I +++ A S+ W+ + R + G+G+G + Sbjct: 63 IGAMVAGMMADRYGRKPLLLISAFIFLSSAYATGAFSVFSWF--LVARFLGGIGIGIASG 120 Query: 193 LCPMLISEIAPKHLRGTLVSCYQLMITAGIFLGYCTNYGTK--------------SYSNS 238 L PM I+E+AP +RG LVS QL I GI N+ S++ Sbjct: 121 LSPMYIAEVAPTSIRGKLVSLNQLTIVLGILGAQIANWLIAEPIPADFTPADICASWNGQ 180 Query: 239 VQWRVPL-GLCFAWSLFMIGALTLVPESPRYLCEVNKVEDAKRSIAKSNKVSPEDPAVQA 297 + WR G F ++F++ A +PESPR+L K E A ++K + + Sbjct: 181 MGWRWMFWGAAFPAAVFLLLAC-FIPESPRWLAMKGKRERAWNVLSKIGG----NHYAEQ 235 Query: 298 ELDLIMAGIEAEKLAGNASWGELFSTKTKVFQRLL-MGVFVQMFQQLTGNNYFFYYGTVI 356 EL ++ E+ + S G L ++ F+++L +G+ V +FQQ G N F Y I Sbjct: 236 ELQMV------EQTGSSKSEGGLKLLFSRPFRKVLVLGIIVAVFQQWCGTNVIFNYAQEI 289 Query: 357 FKSVG--LDDSFETSIVIGVVNFASTFFSLWTVENLGHRKCLLLGAATMMACMVIYASVG 414 F+S G L D +V GV N TF +++TVE LG R +LLGA + IY +G Sbjct: 290 FQSAGYSLGDVLFNIVVTGVANVIFTFVAIYTVERLGRRVLMLLGAGGLAG---IYLVLG 346 Query: 415 VTRLYPHGKSQPSSKGAGNCMIVFTCFYIFCYATTWAPVAWVITAESFPLRVKSKCMALA 474 + + +G M+V I CYA + P+ WV+ AE FP RV+ MA Sbjct: 347 TCYFF---------QVSGFFMVVLVVLAIACYAMSLGPITWVLLAEIFPNRVRGVAMATC 397 Query: 475 SASNWVWGFLIAFFTPFITSAINFYYGYVFMGCLVAMFFYVFF--FVPETKGLSLEEIQE 532 + + WV F + + P + SA+ YG ++ + + +VFF +PETKG SLE +++ Sbjct: 398 TFALWVGSFTLTYTFPLLNSALG-SYGTFWIYSAICLVGFVFFRRALPETKGKSLETLEK 456 Lambda K H 0.324 0.138 0.433 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: 755 Number of extensions: 59 Number of successful extensions: 8 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: 574 Length of database: 460 Length adjustment: 35 Effective length of query: 539 Effective length of database: 425 Effective search space: 229075 Effective search space used: 229075 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 15 ( 7.0 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (22.0 bits) S2: 52 (24.6 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