Align D-serine/D-alanine/glycine transporter (characterized)
to candidate N515DRAFT_2630 N515DRAFT_2630 amino acid/polyamine/organocation transporter, APC superfamily
Query= SwissProt::P0AAE0 (470 letters) >FitnessBrowser__Dyella79:N515DRAFT_2630 Length = 454 Score = 387 bits (993), Expect = e-112 Identities = 197/454 (43%), Positives = 286/454 (62%), Gaps = 12/454 (2%) Query: 18 SLRRNLTNRHIQLIAIGGAIGTGLFMGSGKTISLAGPSIIFVYMIIGFMLFFVMRAMGEL 77 SL+R L RHI+L+A+G AIG GLF+GS I LAGP+I+ Y++ G +F +MRA+GE+ Sbjct: 6 SLQRGLQERHIRLMALGSAIGVGLFLGSANAIRLAGPAILLSYLLGGVAIFIIMRALGEM 65 Query: 78 LLSNLEYKSFSDFASDLLGPWAGYFTGWTYWFCWVVTGMADVVAITAYAQFWFPDLSDWV 137 + N SFS +A D LGP GY TGW YWF W++T +A++ A+ Y WFPD+ W+ Sbjct: 66 AVQNPVAGSFSRYAQDYLGPLPGYLTGWNYWFMWLMTCIAEITAVGVYMGVWFPDVPQWI 125 Query: 138 ASLAVIVLLLTLNLATVKMFGEMEFWFAMIKIVAIVSLIVVGLVMVAMHFQSPTGVEASF 197 +LA +V + +NLA VK +GE EFWFAMIK+V IV +IV G M+ + GV Sbjct: 126 WALAALVTMGAVNLAAVKAYGEFEFWFAMIKVVTIVLMIVGGGAMIVFGLGN-QGVPTGI 184 Query: 198 AHLWNDGGWFPKGLSGFFAGFQIAVFAFVGIELVGTTAAETKDPEKSLPRAINSIPIRII 257 ++LW GG+ P G G Q+ +FA++G+E++G TA E +P+KS+P AINS+ RI+ Sbjct: 185 SNLWTHGGFMPNGAKGMLMALQMVMFAYLGVEMIGLTAGEADNPKKSIPDAINSVFWRIL 244 Query: 258 MFYVFALIVIMSVTPWSSVVPEKSPFVELFVLVGLPAAASVINFVVLTSAASSANSGVFS 317 +FYV AL VIMS+ PW+ + SPFV F +G+ +AA +INFVVLT+A SS N G++S Sbjct: 245 IFYVGALFVIMSIYPWNELGTHGSPFVMTFERLGIKSAAGIINFVVLTAALSSCNGGIYS 304 Query: 318 TSRMLFGLAQEGVAPKAFAKLSKRAVPAKGLTFSCICLLGGVVMLYVNPSVIGAFTMITT 377 T RMLF LAQ+G AP+ FA S +P + + S + LL GV++ Y+ P+ + F +T+ Sbjct: 305 TGRMLFNLAQQGQAPRTFAVTSPSGIPNRAVLVSLVALLFGVLLNYLVPAKV--FVWVTS 362 Query: 378 VSAILFMFVWTIILCSYLVYRK-----QRPHLHEKSIYKMPLGKLMCWVCMAFFVFVVVL 432 + ++ W I+L + + YR+ QR L +++MP ++ +AF V VV L Sbjct: 363 AATFGAIWTWGIVLITQMKYRRGLSEAQRSQL----VFRMPFFPYASYLALAFLVLVVGL 418 Query: 433 LTLEDDTRQALLVTPLWFIALGLGWLFIGKKRAA 466 + DTR AL+V PLW + L + + G R A Sbjct: 419 MGYFPDTRVALIVGPLWLVLLTVLYYVFGLGRRA 452 Lambda K H 0.329 0.141 0.440 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: 658 Number of extensions: 37 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: 470 Length of database: 454 Length adjustment: 33 Effective length of query: 437 Effective length of database: 421 Effective search space: 183977 Effective search space used: 183977 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