Align D-serine/D-alanine/glycine transporter (characterized)
to candidate GFF2849 PS417_14545 amino acid transporter
Query= SwissProt::P0AAE0 (470 letters) >FitnessBrowser__WCS417:GFF2849 Length = 465 Score = 534 bits (1375), Expect = e-156 Identities = 261/442 (59%), Positives = 335/442 (75%) Query: 18 SLRRNLTNRHIQLIAIGGAIGTGLFMGSGKTISLAGPSIIFVYMIIGFMLFFVMRAMGEL 77 +L+R L+NRHIQL+A+GGAIGTGLFMGSGK I+L+G SII +YMIIG ++FVMRAMGEL Sbjct: 13 ALQRTLSNRHIQLMAMGGAIGTGLFMGSGKIIALSGTSIILIYMIIGLFVYFVMRAMGEL 72 Query: 78 LLSNLEYKSFSDFASDLLGPWAGYFTGWTYWFCWVVTGMADVVAITAYAQFWFPDLSDWV 137 LLSNL +KSF+DFA LGP A +F GW+YW W V + D V + + Q+WFP + W+ Sbjct: 73 LLSNLNFKSFADFAGAYLGPRAAFFLGWSYWLSWSVAVIGDAVVVGGFFQYWFPHVPAWM 132 Query: 138 ASLAVIVLLLTLNLATVKMFGEMEFWFAMIKIVAIVSLIVVGLVMVAMHFQSPTGVEASF 197 ++ +++ L LN+ TV++FGE+EFWFA+IK++A+++LI V V++A F SPTGV ASF Sbjct: 133 PAVGMLLTLFALNVLTVRLFGEVEFWFAIIKLIAVLTLIGVSGVLIASSFVSPTGVTASF 192 Query: 198 AHLWNDGGWFPKGLSGFFAGFQIAVFAFVGIELVGTTAAETKDPEKSLPRAINSIPIRII 257 HL + FP GL GFFAGFQ+A+F+F G EL+GT AAET+ PEK+LP+AINSIP+RII Sbjct: 193 THLLDPQAAFPNGLFGFFAGFQMAIFSFAGTELIGTAAAETRAPEKTLPKAINSIPLRII 252 Query: 258 MFYVFALIVIMSVTPWSSVVPEKSPFVELFVLVGLPAAASVINFVVLTSAASSANSGVFS 317 +FYV AL I++VT W V P KSPFVELF++ G PAAA ++NFVVLTSAASSANSGVFS Sbjct: 253 LFYVLALACIIAVTSWQHVSPSKSPFVELFLVAGFPAAAGIVNFVVLTSAASSANSGVFS 312 Query: 318 TSRMLFGLAQEGVAPKAFAKLSKRAVPAKGLTFSCICLLGGVVMLYVNPSVIGAFTMITT 377 SRMLFGLA G AP F +LSK +VP L F+ + +L G+V+L+V P V+ AFT+++T Sbjct: 313 ASRMLFGLADLGDAPGIFRRLSKSSVPFISLAFTTLLMLLGLVLLFVVPEVMTAFTIVST 372 Query: 378 VSAILFMFVWTIILCSYLVYRKQRPHLHEKSIYKMPLGKLMCWVCMAFFVFVVVLLTLED 437 VSAIL +F W+ IL SY+ YRK+RP LH KS+YKMP G LM W +AF FV+ LL L Sbjct: 373 VSAILVIFTWSTILASYIAYRKKRPDLHAKSLYKMPGGVLMAWFSLAFLAFVLGLLALRP 432 Query: 438 DTRQALLVTPLWFIALGLGWLF 459 DTR AL V P WFI L + + F Sbjct: 433 DTRLALCVMPAWFIWLWIAYPF 454 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: 758 Number of extensions: 34 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: 470 Length of database: 465 Length adjustment: 33 Effective length of query: 437 Effective length of database: 432 Effective search space: 188784 Effective search space used: 188784 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