Align Serine/threonine transporter SstT; Na(+)/serine-threonine symporter (characterized)
to candidate 5208972 Shew_1458 serine/threonine transporter SstT (RefSeq)
Query= SwissProt::P0AGE4 (414 letters) >lcl|FitnessBrowser__PV4:5208972 Shew_1458 serine/threonine transporter SstT (RefSeq) Length = 407 Score = 533 bits (1372), Expect = e-156 Identities = 272/396 (68%), Positives = 327/396 (82%) Query: 9 LFRRLAHGSLVKQILVGLVLGILLAWISKPAAEAVGLLGTLFVGALKAVAPILVLMLVMA 68 LF +LA GSLV QI++G++ G+ LA S +AE+V LG LFVGALKA+APILV +LV A Sbjct: 7 LFAKLADGSLVLQIILGIIAGVALASFSPSSAESVAFLGDLFVGALKAIAPILVFILVAA 66 Query: 69 SIANHQHGQKTNIRPILFLYLLGTFSAALAAVVFSFAFPSTLHLSSSAGDISPPSGIVEV 128 SIAN + KTN+RPI+ LYL GTF+AA+ AV SF FP++L L S A +PP GI EV Sbjct: 67 SIANQKKNTKTNMRPIIVLYLFGTFAAAITAVTMSFLFPTSLVLVSGAQGATPPEGIGEV 126 Query: 129 MRGLVMSMVSNPIDALLKGNYIGILVWAIGLGFALRHGNETTKNLVNDMSNAVTFMVKLV 188 + L+ +V NP++AL+ GNYIGIL W +GLG AL H +E TK + D+S+ V+ MV+ V Sbjct: 127 LNTLLFKVVDNPVNALMTGNYIGILAWGVGLGIALHHASENTKTVFADVSHGVSQMVRFV 186 Query: 189 IRFAPIGIFGLVSSTLATTGFSTLWGYAQLLVVLVGCMLLVALVVNPLLVWWKIRRNPFP 248 IR APIGIFGLV++T A TGF + GYAQLL VL+G ML++AL++NPL+VW+KIRRNP+P Sbjct: 187 IRLAPIGIFGLVANTFAATGFEAIAGYAQLLAVLLGSMLIIALIINPLIVWFKIRRNPYP 246 Query: 249 LVLLCLRESGVYAFFTRSSAANIPVNMALCEKLNLDRDTYSVSIPLGATINMAGAAITIT 308 LV CLRESGV AFFTRSSAANIPVNMALCEKL+L DT+SVSIPLGATINMAGAAITIT Sbjct: 247 LVFTCLRESGVTAFFTRSSAANIPVNMALCEKLDLHEDTFSVSIPLGATINMAGAAITIT 306 Query: 309 VLTLAAVNTLGIPVDLPTALLLSVVASLCACGASGVAGGSLLLIPLACNMFGISNDIAMQ 368 VLTLAAV+T GI VD+ TA+LLSVVA++ ACGASGVAGGSLLLIPLAC++FGISND+AMQ Sbjct: 307 VLTLAAVHTEGIQVDILTAILLSVVAAVSACGASGVAGGSLLLIPLACSLFGISNDVAMQ 366 Query: 369 VVAVGFIIGVLQDSCETALNSSTDVLFTAAACQAED 404 VVAVGFIIGV+QDS ETALNSSTDVLFTAAAC+A + Sbjct: 367 VVAVGFIIGVIQDSAETALNSSTDVLFTAAACEAAE 402 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: 438 Number of extensions: 14 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: 407 Length adjustment: 31 Effective length of query: 383 Effective length of database: 376 Effective search space: 144008 Effective search space used: 144008 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