Align D-serine transporter DsdX (characterized)
to candidate Ga0059261_1667 Ga0059261_1667 gluconate permease GntT (TC 2.A.8.1.4)
Query= SwissProt::P08555 (445 letters) >FitnessBrowser__Korea:Ga0059261_1667 Length = 447 Score = 289 bits (740), Expect = 1e-82 Identities = 166/452 (36%), Positives = 264/452 (58%), Gaps = 12/452 (2%) Query: 1 MHSQIWVVSTLLISIVLIVLTIVKFKFHPFLALLLASFFVGTMMGMGPLDMVNAI-ESGI 59 M ++++V L S+ ++ I + K +PF+ALL+ S +G G+ PLD + I E+G+ Sbjct: 1 MSREVFLVLLGLASVGGLIFLIARLKLNPFIALLVTSLALGASAGL-PLDKLLVIYEAGV 59 Query: 60 GGTLGFLAAVIGLGTILGKMMEVSGAAERIGLTLQRCRWLS---VDVIMVLVGLICGITL 116 G LG +A V+GLGT++GK+M SG AERI T+ W V M+ + G+ + Sbjct: 60 GNALGHIALVVGLGTMMGKLMAESGGAERIAQTM--IGWFGPARVHWAMMAAAFLVGLPV 117 Query: 117 FVEVGVVLLIPLAFSIAKKTNTSLLKLAIPLCTALMAVHCVVPPHPAALYVANKLGADIG 176 F EVG VLL+P+ F++A +T TS+LK+ +P+ L VH ++PPHPAAL ADIG Sbjct: 118 FFEVGFVLLMPIVFTVAMRTGTSILKVGLPMVAGLSVVHGLIPPHPAALLAVGAYKADIG 177 Query: 177 SVIVYGLLVGLMASLIGGPLFLKFLGQRLPF---KPVPTEFADLKVRDEKTLPSLGATLF 233 ++Y L+VG+ + + GP+F + + + P+ + KV D + LP G T+ Sbjct: 178 LTVLYALIVGIPTAALAGPIFATLIDRHVTVDGVNPMAEALTERKV-DSRELPGFGITVA 236 Query: 234 TILLPIALMLVKTIAELNMARESGLYILVEFIGNPITAMFIAVFVAYYVLGIRQHMSMGT 293 TILLP+ALML+ + A+L AR S + + F G+P+TA+ + +++ G + + Sbjct: 237 TILLPVALMLIGSWADLFAARGSLVNDAIRFSGHPVTALLAGLLLSFVTFGSARGFDRES 296 Query: 294 MLTHTENGFGSIANILLIIGAGGAFNAILKSSSLADTLAVILSNMHMHPILLAWLVALIL 353 + E+ A I LI+GAG F IL + ++ ++ + ++ + ++LAWLVA ++ Sbjct: 297 IGRFLEDCLAPTALITLIVGAGAGFGKILMEAGISTSVVGMAQSVEVPLLVLAWLVAAMM 356 Query: 354 HAAVGSATVAMMGATAIVAPMLPLYPDISPEIIAIAIGSGAIGCTIVTDSLFWLVKQYCG 413 A GSATVAM A IVAP + +SPE++ +A G+G++ + V D FWLVK Y G Sbjct: 357 RIATGSATVAMATAAGIVAP-VAAGSGVSPELLVLATGAGSLILSHVNDGGFWLVKTYFG 415 Query: 414 ATLNETFKYYTTATFIASVVALAGTFLLSFII 445 TL++TFK +T + S+VAL T LS ++ Sbjct: 416 LTLSQTFKTWTVCETLISIVALLLTLALSAVL 447 Lambda K H 0.329 0.143 0.418 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: 562 Number of extensions: 37 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: 447 Length adjustment: 32 Effective length of query: 413 Effective length of database: 415 Effective search space: 171395 Effective search space used: 171395 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