Align D-serine transporter DsdX; D-serine-specific permease (characterized)
to candidate BPHYT_RS13375 BPHYT_RS13375 permease
Query= SwissProt::A0A0H2VAP9 (445 letters) >FitnessBrowser__BFirm:BPHYT_RS13375 Length = 456 Score = 304 bits (779), Expect = 3e-87 Identities = 171/448 (38%), Positives = 259/448 (57%), Gaps = 19/448 (4%) Query: 12 LISIVLIVLTIVKFKFHPFLALLLASFFVGTMMGMGPLDMVNAIESGIGGTLGFLAAVIG 71 LI+I+ +V+ I +FK +PF+ L++ S + +GM ++ + E+G+GGTLG +A V+G Sbjct: 14 LIAIIALVVLIARFKMNPFITLMVVSVALALAVGMPATSILKSFETGVGGTLGHIAIVVG 73 Query: 72 LGTILGKMMEVSGAAERIGLTL------QRCRWLSADVIMVLVGLICGITLFVEVGVVLL 125 LGT+LGKMM SG AERI TL + W M+ + + G+ +F EVG VLL Sbjct: 74 LGTMLGKMMAESGGAERIARTLIDLFGPKNVHWA-----MMCIAFLVGLPVFFEVGFVLL 128 Query: 126 IPLAFSIAKKTNTSLLKLAIPLCTALMAVHCVVPPHPAALYVANKLGADIGSVIVYGLLV 185 IP+AF++A++T TS++++ IP+ L VH ++PPHPAAL ADIG I Y L+V Sbjct: 129 IPIAFNVAQRTGTSMIRVGIPMVAGLSVVHGLIPPHPAALLAVTAYNADIGHTIFYALIV 188 Query: 186 GLMASLIGGPLFLKFLGQRLPF---KPVPTEFADLKV-RDEKTLPSLGATLFTVLLPIAL 241 G+ + I GPLF K + + + P+ +F + R + LP G TL TVLLP+ L Sbjct: 189 GIPTAAIAGPLFSKLIARFVVLDGVNPMAQQFIEQDAKRSHQELPGFGITLLTVLLPVLL 248 Query: 242 MLVKTIAELNMARESGLYTLLEFIGNPITATFIAVFVAYYVLGIRQHMSMGTMLTHTENG 301 MLV + A+L + +S +L IG+P A +AV +++ G + + +L T Sbjct: 249 MLVGSWADLIVPAKSTANNVLRLIGHPDMALLLAVLLSFITFGKARGFNRDQILKFTNEC 308 Query: 302 FGSIANILLIIGAGGAFNAILKSSSLADTLAVILSNMHMHPILLAWLVALILHAAVGSAT 361 A+I L++GAG F IL S + + + + H+ ++LAWLVA ++ A GSAT Sbjct: 309 LAPTASITLVVGAGAGFGRILIDSGASKAIVDVATGAHVPLLILAWLVAALIRVATGSAT 368 Query: 362 VAMMGATAIVAPMLPLYPD----ISPEIIAIAIGSGAIGCTIVTDSLFWLVKQYCGATLN 417 VAM A I+AP+ + PE++ +A G+G++ + V D FWLVK+Y G T+ Sbjct: 369 VAMATAAGIIAPIAAAAASTVGGVRPELLVLATGAGSLILSHVNDGGFWLVKEYFGMTVP 428 Query: 418 ETFKYYTTATFIASVIALAGTFLLSFII 445 +TFK +T I SV AL T LS +I Sbjct: 429 QTFKTWTVCETIISVTALLLTLGLSTVI 456 Lambda K H 0.328 0.142 0.417 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: 533 Number of extensions: 34 Number of successful extensions: 5 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: 445 Length of database: 456 Length adjustment: 33 Effective length of query: 412 Effective length of database: 423 Effective search space: 174276 Effective search space used: 174276 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: 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