Align alpha-ketoglutarate permease (MHS family) (characterized)
to candidate 18139 b4111 proline/glycine betaine transporter (NCBI)
Query= reanno::pseudo5_N2C3_1:AO356_17790 (439 letters) >lcl|FitnessBrowser__Keio:18139 b4111 proline/glycine betaine transporter (NCBI) Length = 500 Score = 228 bits (580), Expect = 4e-64 Identities = 133/425 (31%), Positives = 220/425 (51%), Gaps = 28/425 (6%) Query: 26 KSIFSGSVGNMVEWYDWYVYAAFSLYFAKVFFPKGDTTAQLLNTAAIFAVGFLMRPIGGW 85 K+I + S+GN +EW+D+ VY + KVFFP D + Q++ A F+V FL+RP+GG Sbjct: 25 KAITAASLGNAMEWFDFGVYGFVAYALGKVFFPGADPSVQMVAALATFSVPFLIRPLGGL 84 Query: 86 LMGLYADRAGRKRALMASVYLMCFGSLIIALSPSYETIGVGAPILLVFARLLQGLSVGGE 145 G+ D+ GR++ L ++ +M + I L PSY+TIG+ APILL+ ++ QG SVGGE Sbjct: 85 FFGMLGDKYGRQKILAITIVIMSISTFCIGLIPSYDTIGIWAPILLLICKMAQGFSVGGE 144 Query: 146 YGTSATYLSEMATKERRGFFSSFQYVTLISGQLIALGVLIVLQQFLTTEQLYAWGWRIPF 205 Y ++ +++E + +RGF S+ I+G ++ GV++++ + WGWRIPF Sbjct: 145 YTGASIFVAEYSPDRKRGFMGSWLDFGSIAGFVLGAGVVVLISTIVGEANFLDWGWRIPF 204 Query: 206 AIGALCAVVALYLRRGMEETESFTK-------------KEKSKESAMRTLLRHPKELMTV 252 I ++ LYLR +EET +F + ++ K S ++ + L+T Sbjct: 205 FIALPLGIIGLYLRHALEETPAFQQHVDKLEQGDREGLQDGPKVSFKEIATKYWRSLLTC 264 Query: 253 VGLTMGGTLAFYTYTTYMQKYLVNTVGMSISDSTTISAATLFLFMCLQPVIGGLSDKIGR 312 +GL + + +Y TYM YL + + S I A + + +QPV+G LSD+ GR Sbjct: 265 IGLVIATNVTYYMLLTYMPSYLSHNLHYSEDHGVLIIIAIMIGMLFVQPVMGLLSDRFGR 324 Query: 313 RPILIAFGILGTLFTVPILTTLHTIQTWWGAFFLIMAAL----IIVSGYTSINAVVKAEL 368 RP ++ + + +P +++ LI A L +I++ +T + A + Sbjct: 325 RPFVLLGSVALFVLAIPAFILINS-----NVIGLIFAGLLMLAVILNCFTGVMASTLPAM 379 Query: 369 FPTEIRALGVGLPYALTVSIFGGTAEYIALWFKSIG---METGYYWYVTACIAVSLLVYI 425 FPT IR + + ++V + G T +A W M YY V A V L+ + Sbjct: 380 FPTHIRYSALAAAFNISVLVAGLTPT-LAAWLVESSQNLMMPAYYLMVVA--VVGLITGV 436 Query: 426 TMKDT 430 TMK+T Sbjct: 437 TMKET 441 Lambda K H 0.326 0.138 0.416 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: 556 Number of extensions: 26 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: 439 Length of database: 500 Length adjustment: 33 Effective length of query: 406 Effective length of database: 467 Effective search space: 189602 Effective search space used: 189602 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: 40 (21.7 bits) S2: 51 (24.3 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 paper from 2022 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