Align GguB aka ATU2346 aka AGR_C_4262, component of Multiple sugar (arabinose, xylose, galactose, glucose, fucose) putative porter (characterized)
to candidate 3608606 Dshi_1999 inner-membrane translocator (RefSeq)
Query= TCDB::O05177 (398 letters) >lcl|FitnessBrowser__Dino:3608606 Dshi_1999 inner-membrane translocator (RefSeq) Length = 435 Score = 215 bits (548), Expect = 2e-60 Identities = 145/440 (32%), Positives = 225/440 (51%), Gaps = 50/440 (11%) Query: 1 MSSANTTNEESNVISVGSYIRS---NIREYGMLIALVAIMVFFQFYTGGILFRPVNLTNL 57 MS A+ T + S++++ + R GM+ A V + + F T G N+ NL Sbjct: 1 MSDASPTESRLPSRAKRSFLQTLELDTRLLGMIGAFVLVCLVFNLLTDGRFLTARNIFNL 60 Query: 58 ILQNSFIVIMALGMLLVIVAGHIDLSVGSIVAFVGAI-----AAILTVQWGMN------P 106 +Q + IMA GM+ +IV HIDL+VG+++A A AIL +G+ P Sbjct: 61 SIQTVSVAIMATGMVFIIVTRHIDLAVGALLATCSAAMAMTQTAILPQVFGLELGHPAIP 120 Query: 107 FLAALICLVIGGIIGAAQGYWIAYHRIPSFIVTLAGMLVFRGLTLFVLGGKNIGPFPTDF 166 ++A L+ LV G +IGA QGY + Y IP+FIVTL G+LV+R + ++ G+ IGP F Sbjct: 121 WIAMLVGLVTGTVIGAFQGYLVGYLMIPAFIVTLGGLLVWRNVAWYMTNGQTIGPLDPTF 180 Query: 167 QVISTGFLPDIGGIEGL--NTTSMILTVLITVALFYLAWRRRVVNVKHGIDVEPFGFFIV 224 + GGI G T S I+ ++ VA + W R + H V+P + Sbjct: 181 MTL--------GGINGTLGATLSWIVGLVAVVAACWALWSGRKNKIAHDAPVKPVWAELT 232 Query: 225 QNLLISGAILFL-----GYQLSTYR--------------------GLPNVLIVMLVLIAL 259 ++S AIL Y++ T R G+P +++++ + Sbjct: 233 VMGVVSVAILGFVAILNSYEVPTARLRRLFEARGEVMPEGYTEVYGIPYSVLLLIAVAVA 292 Query: 260 YSFVTRRTTIGRRVYAMGGNEKATKLSGINTERLSFLTFVNMGVLAGLAGMIIATRLNSA 319 + + ++T GR ++A GGN A +LSGINT L+ F MG L ++ ++ + RL + Sbjct: 293 MTVIAKKTRFGRYIFATGGNPDAAELSGINTRMLTVKVFALMGALCAISAIVASARLTNH 352 Query: 320 TPKAGVGFELDVIAACFIGGASASGGVGKITGAVIGAFIMGVMNNGMSIVGLGIDFQQMV 379 + G EL VIAA IGG + +GG+G I GA++GA IM + +GM++VG+ Q +V Sbjct: 353 SNDIGTLDELRVIAAAVIGGTALAGGIGTIYGAILGALIMQSLQSGMAMVGVDAPLQNIV 412 Query: 380 KGLVLLAAVFFDV-YNKNKG 398 G VL+AAV D+ Y K G Sbjct: 413 VGTVLVAAVLIDILYRKRMG 432 Lambda K H 0.329 0.145 0.422 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: 536 Number of extensions: 26 Number of successful extensions: 6 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: 398 Length of database: 435 Length adjustment: 31 Effective length of query: 367 Effective length of database: 404 Effective search space: 148268 Effective search space used: 148268 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
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