Align L-alanine and D-alanine permease (characterized)
to candidate GFF4342 PS417_22235 aromatic amino acid transporter
Query= reanno::pseudo5_N2C3_1:AO356_17670 (473 letters) >FitnessBrowser__WCS417:GFF4342 Length = 473 Score = 394 bits (1013), Expect = e-114 Identities = 197/451 (43%), Positives = 283/451 (62%), Gaps = 12/451 (2%) Query: 13 AQGGPLKRELGERHIRLMALGACIGVGLFLGSAKAIEMAGPAIMLSYIIGGLAILVIMRA 72 + G LKR L RHI+L+ALG IG GLFLGSA ++ AGP+++L Y I G +IMR Sbjct: 6 SSSGELKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPSMILGYAICGFIAFMIMRQ 65 Query: 73 LGEMAVHNPVAGSFSRYAQDYLGPLAGFLTGWNYWFLWLVTCVAEITAVAVYMGIWFPDV 132 LGEM V PVAGSFS +A Y G AGFL+GWN W L+++ ++E+TAV Y+ W+P++ Sbjct: 66 LGEMIVEEPVAGSFSHFAHKYWGGFAGFLSGWNCWILYILVGMSELTAVGKYVHYWWPEI 125 Query: 133 PRWIWALAALVSMGSINLIAVKAFGEFEFWFALIKIVTIIAMVIGGVGIIAFGFGNDGVA 192 P W+ A A V + INL VK FGE EFWFA+IK+V I+ M+ G ++ G G G Sbjct: 126 PTWVSAAAFFVLINLINLANVKVFGEAEFWFAIIKVVAIVGMIALGSYLLVSGTG--GPQ 183 Query: 193 LGISNLWAHGGFMPNGVSGVLMSLQMVMFAYLGVEMIGLTAGEAKNPQKTIPNAIGSVFW 252 ++NLW HGGF P+GV G++M++ ++MF++ G+EM+G TA EA P+ IP AI V + Sbjct: 184 ASVTNLWEHGGFFPHGVGGLVMAMAIIMFSFGGLEMLGFTAAEADKPRTVIPKAINQVIY 243 Query: 253 RILLFYVGALFVILSIYPWNEI---------GTQGSPFVMTFERLGIKTAAGIINFVVIT 303 RIL+FY+GAL V+LS+ PW+ + GSPFV F LG TAA I+NFVV+T Sbjct: 244 RILIFYIGALVVLLSLTPWDSLLATLNASGDAYSGSPFVQVFSMLGSDTAAHILNFVVLT 303 Query: 304 AALSSCNGGIFSTGRMLYSLAQNGQAPAGFAKTSTNGVPRRALLLSIAALLLGVLLNYLV 363 AALS N G + RML +A+ G AP AK GVP R++L S A L+ VL+NYL+ Sbjct: 304 AALSVYNSGTYCNSRMLLGMAEQGDAPKALAKIDKRGVPVRSILASAAITLVAVLMNYLI 363 Query: 364 PEKVFVWVTSIATFGAIWTWVMILLAQLKFRKSLSASERAALKYRMWLYPVSSYLALAFL 423 P+ + S+ + W MI + KFR+ ++ + + L +W YP +Y+ LAF+ Sbjct: 364 PQHALELLMSLVVATLVINWAMISFSHFKFRQHMNRTGQVPLFKALW-YPYGNYVCLAFV 422 Query: 424 VLVVGLMAYFPDTRVALYVGPAFLVLLTVLF 454 V ++ +M P +V+++ P +++ + V + Sbjct: 423 VFILVIMLMIPGIQVSVFAIPVWVMFMAVCY 453 Lambda K H 0.328 0.142 0.444 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: 629 Number of extensions: 30 Number of successful extensions: 3 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: 473 Length of database: 473 Length adjustment: 33 Effective length of query: 440 Effective length of database: 440 Effective search space: 193600 Effective search space used: 193600 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 (21.7 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