Align D-serine transporter DsdX; D-serine-specific permease (characterized)
to candidate GFF4613 PS417_23605 permease DsdX
Query= SwissProt::A0A0H2VAP9 (445 letters) >FitnessBrowser__WCS417:GFF4613 Length = 467 Score = 288 bits (737), Expect = 3e-82 Identities = 153/437 (35%), Positives = 254/437 (58%), Gaps = 6/437 (1%) Query: 13 ISIVLIVLTIVKFKFHPFLALLLASFFVGTMMGMGPLDMVNAIESGIGGTLGFLAAVIGL 72 I+I+ +++ I +++ +PF+ + L S + M GM ++ + E+G+G TLG +A V+ L Sbjct: 33 IAIIALIVLIARYRLNPFIVITLVSIGLALMAGMPADTIMGSYEAGVGKTLGHIALVVAL 92 Query: 73 GTILGKMMEVSGAAERIGLTL-QRCRWLSADVIMVLVGLICGITLFVEVGVVLLIPLAFS 131 GT+LGKMM SG AE++ TL R +A MV + + G+ LF EVG VLL+P+AF+ Sbjct: 93 GTMLGKMMAESGGAEQVARTLINRFGERNAHWAMVCIAFLVGLPLFFEVGFVLLVPIAFT 152 Query: 132 IAKKTNTSLLKLAIPLCTALMAVHCVVPPHPAALYVANKLGADIGSVIVYGLLVGLMASL 191 +A++ S+L + +P+ L VH +VPPHPAA+ A +G ++Y +L+G+ ++ Sbjct: 153 VARRVGVSILMVGLPMVAGLSVVHALVPPHPAAMMAVLAYNASVGQTVLYAILIGIPTAI 212 Query: 192 IGGPLFLKFLGQRLPF---KPVPTEFADLKVRDEKTLPSLGATLFTVLLPIALMLVKTIA 248 I GP++ KF+ R+ P+ +F D + R LPS T+ T+LLP+ LM++ A Sbjct: 213 IAGPVYAKFIVPRIHLPAENPLERQFIDREPRTR--LPSFTLTMGTILLPVVLMMIGGWA 270 Query: 249 ELNMARESGLYTLLEFIGNPITATFIAVFVAYYVLGIRQHMSMGTMLTHTENGFGSIANI 308 + + S L FIGN + A +A V+++ LGI Q + ++L T A+I Sbjct: 271 NVISSPGSAFNQFLLFIGNSVIALLVATLVSFWTLGIAQGFNRESILKFTNECLAPTASI 330 Query: 309 LLIIGAGGAFNAILKSSSLADTLAVILSNMHMHPILLAWLVALILHAAVGSATVAMMGAT 368 L++GAGG N IL + + + + + + P+++ WL A ++ A GSATVAM A+ Sbjct: 331 TLLVGAGGGLNRILVDAGVTNEILGLAHAFQLSPLVMGWLFAALMRIATGSATVAMTTAS 390 Query: 369 AIVAPMLPLYPDISPEIIAIAIGSGAIGCTIVTDSLFWLVKQYCGATLNETFKYYTTATF 428 +VAP+ PE++ +A G+G++ + V D FWL+K+Y T+ +TFK +T Sbjct: 391 GVVAPVAMGLGYPHPELLVLATGAGSVIFSHVNDGGFWLIKEYFNMTVIQTFKTWTVLET 450 Query: 429 IASVIALAGTFLLSFII 445 + SV+A T+ LS I+ Sbjct: 451 LISVVAFGLTYGLSCIL 467 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: 549 Number of extensions: 36 Number of successful extensions: 4 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: 467 Length adjustment: 33 Effective length of query: 412 Effective length of database: 434 Effective search space: 178808 Effective search space used: 178808 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