Align Serine/threonine transporter SstT; Na(+)/serine-threonine symporter (characterized)
to candidate PP_2443 PP_2443 Serine/threonine transporter SstT
Query= SwissProt::P0AGE4 (414 letters) >FitnessBrowser__Putida:PP_2443 Length = 403 Score = 548 bits (1411), Expect = e-160 Identities = 280/396 (70%), Positives = 333/396 (84%) Query: 11 RRLAHGSLVKQILVGLVLGILLAWISKPAAEAVGLLGTLFVGALKAVAPILVLMLVMASI 70 R L SLV QI++GL+ GI LA ++ A + LG +FV ALKAVAP+LV +LVMAS+ Sbjct: 6 RILNRTSLVTQIVIGLLAGIALALLAPAIARDLAFLGKVFVSALKAVAPVLVFILVMASV 65 Query: 71 ANHQHGQKTNIRPILFLYLLGTFSAALAAVVFSFAFPSTLHLSSSAGDISPPSGIVEVMR 130 ANH+HGQ+T+IRPIL+LYLLGTF+AA+ AV S FPS L LS+S +S P GI EV++ Sbjct: 66 ANHRHGQETHIRPILWLYLLGTFAAAVVAVFASMLFPSHLALSTSEATLSAPGGIAEVLQ 125 Query: 131 GLVMSMVSNPIDALLKGNYIGILVWAIGLGFALRHGNETTKNLVNDMSNAVTFMVKLVIR 190 L+++ V NP++ALL N+IG+L WAIGLG ALRH ETT+ +V D+SN VT +V++VIR Sbjct: 126 NLLLNAVDNPVNALLNANFIGVLTWAIGLGVALRHAGETTRTVVEDLSNGVTLIVRVVIR 185 Query: 191 FAPIGIFGLVSSTLATTGFSTLWGYAQLLVVLVGCMLLVALVVNPLLVWWKIRRNPFPLV 250 FAP+GIFGLVSSTLA +G L GY LL VL+GCML VALV+NPL+V+WKIRRNP+PL Sbjct: 186 FAPLGIFGLVSSTLAQSGLDALLGYLHLLAVLIGCMLFVALVMNPLIVFWKIRRNPYPLT 245 Query: 251 LLCLRESGVYAFFTRSSAANIPVNMALCEKLNLDRDTYSVSIPLGATINMAGAAITITVL 310 LLCLRESG+ AFFTRSSAANIPVN+AL E+L L DTYSVSIPLGATINMAGAAITITVL Sbjct: 246 LLCLRESGITAFFTRSSAANIPVNLALSERLGLHEDTYSVSIPLGATINMAGAAITITVL 305 Query: 311 TLAAVNTLGIPVDLPTALLLSVVASLCACGASGVAGGSLLLIPLACNMFGISNDIAMQVV 370 TLAAV+TLGI VDLPTA+LLSVVA++CACGASGVAGGSLLLIPLAC++FGI ++IAMQVV Sbjct: 306 TLAAVHTLGIQVDLPTAVLLSVVAAVCACGASGVAGGSLLLIPLACSLFGIPSEIAMQVV 365 Query: 371 AVGFIIGVLQDSCETALNSSTDVLFTAAACQAEDDR 406 AVGFIIGVLQDS ETALNSSTDVLFTAAACQA++ R Sbjct: 366 AVGFIIGVLQDSAETALNSSTDVLFTAAACQAQEQR 401 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: 428 Number of extensions: 11 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: 403 Length adjustment: 31 Effective length of query: 383 Effective length of database: 372 Effective search space: 142476 Effective search space used: 142476 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:
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