Align Serine/threonine transporter SstT; Na(+)/serine-threonine symporter (characterized)
to candidate BWI76_RS24715 BWI76_RS24715 serine/threonine transporter SstT
Query= SwissProt::P0AGE4 (414 letters) >lcl|FitnessBrowser__Koxy:BWI76_RS24715 BWI76_RS24715 serine/threonine transporter SstT Length = 415 Score = 701 bits (1809), Expect = 0.0 Identities = 358/406 (88%), Positives = 389/406 (95%) Query: 9 LFRRLAHGSLVKQILVGLVLGILLAWISKPAAEAVGLLGTLFVGALKAVAPILVLMLVMA 68 L RRLA GSLVKQIL+GLVLG+LLA +SKPAA AVGLLGTLFVGALKAVAP+LVLMLVMA Sbjct: 10 LLRRLAQGSLVKQILIGLVLGVLLATVSKPAAVAVGLLGTLFVGALKAVAPVLVLMLVMA 69 Query: 69 SIANHQHGQKTNIRPILFLYLLGTFSAALAAVVFSFAFPSTLHLSSSAGDISPPSGIVEV 128 SIANHQ GQKT+IRPILFLYLLGTF+AAL AVVFSF FPSTLHL+++A I+PPSGIVEV Sbjct: 70 SIANHQQGQKTSIRPILFLYLLGTFAAALTAVVFSFIFPSTLHLNAAAESITPPSGIVEV 129 Query: 129 MRGLVMSMVSNPIDALLKGNYIGILVWAIGLGFALRHGNETTKNLVNDMSNAVTFMVKLV 188 +RGL+MSMVSNPIDALL NYIGILVWA+GLGFALRHGNETTKNL+ND+S+AVTF+VK+V Sbjct: 130 LRGLLMSMVSNPIDALLNANYIGILVWAVGLGFALRHGNETTKNLINDVSHAVTFIVKVV 189 Query: 189 IRFAPIGIFGLVSSTLATTGFSTLWGYAQLLVVLVGCMLLVALVVNPLLVWWKIRRNPFP 248 IRFAP+GIFGLV+STLATTGF TLWGYAQLL+VLVGCMLLVALV+NPLLV+WKIRRNP+P Sbjct: 190 IRFAPLGIFGLVASTLATTGFETLWGYAQLLLVLVGCMLLVALVINPLLVFWKIRRNPYP 249 Query: 249 LVLLCLRESGVYAFFTRSSAANIPVNMALCEKLNLDRDTYSVSIPLGATINMAGAAITIT 308 LVLLCLRESGVYAFFTRSSAANIPVNMAL EKLNLDRDTYSVSIPLGATINMAGAAITIT Sbjct: 250 LVLLCLRESGVYAFFTRSSAANIPVNMALSEKLNLDRDTYSVSIPLGATINMAGAAITIT 309 Query: 309 VLTLAAVNTLGIPVDLPTALLLSVVASLCACGASGVAGGSLLLIPLACNMFGISNDIAMQ 368 VLTLAAV+TL +PVDLPTALLLSVVASLCACGASGVAGGSLLLIPLACNMFGI ND+AMQ Sbjct: 310 VLTLAAVHTLNVPVDLPTALLLSVVASLCACGASGVAGGSLLLIPLACNMFGIPNDVAMQ 369 Query: 369 VVAVGFIIGVLQDSCETALNSSTDVLFTAAACQAEDDRLANSALRN 414 VVAVGFIIGVLQDSCETALNSSTDVLFTAAAC AED+++A +ALRN Sbjct: 370 VVAVGFIIGVLQDSCETALNSSTDVLFTAAACIAEDEQIAKNALRN 415 Lambda K H 0.325 0.138 0.405 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: 545 Number of extensions: 16 Number of successful extensions: 1 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: 414 Length of database: 415 Length adjustment: 31 Effective length of query: 383 Effective length of database: 384 Effective search space: 147072 Effective search space used: 147072 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 (21.6 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 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