Align D-serine/D-alanine/glycine transporter (characterized, see rationale)
to candidate 14258 b0112 aromatic amino acid transporter (NCBI)
Query= uniprot:A0A0C4YRF7 (472 letters) >FitnessBrowser__Keio:14258 Length = 457 Score = 424 bits (1090), Expect = e-123 Identities = 205/455 (45%), Positives = 303/455 (66%), Gaps = 8/455 (1%) Query: 10 EERVHEEKDLHRGLKDRHIQMIAIGGAIGVGLFLGAGRAIAIAGPGLMLSYAIGGVAIFF 69 E + H E+ L RGLK+RHIQ+IA+GGAIG GLFLG+ I AGPG++L YAI G F Sbjct: 3 EGQQHGEQ-LKRGLKNRHIQLIALGGAIGTGLFLGSASVIQSAGPGIILGYAIAGFIAFL 61 Query: 70 IMRALGELLLYRPVSGSFATYAEEFVGPFAGFATGWSYWFMWVVTGMAEITAVAVYVHYW 129 IMR LGE+++ PV+GSF+ +A ++ G FAGFA+GW+YW ++V+ MAE+TAV Y+ +W Sbjct: 62 IMRQLGEMVVEEPVAGSFSHFAYKYWGSFAGFASGWNYWVLYVLVAMAELTAVGKYIQFW 121 Query: 130 FPDVPQWIPALATLAVLYLVNCVAVAVFGELEFWFALIKVVTIVAMIVIGLAIIFFGVTP 189 +P++P W+ A V+ +N V VFGE+EFWFA+IKV+ +VAMI+ G ++F G Sbjct: 122 YPEIPTWVSAAVFFVVINAINLTNVKVFGEMEFWFAIIKVIAVVAMIIFGGWLLFSGNG- 180 Query: 190 LGPTASFSNLWTHGGFMPFGTLGVVLTLQIVMFAYQGVELIGVTAGEAQNPEKVLPHATN 249 GP A+ SNLW GGF+P G G+V+ + I+MF++ G+EL+G+TA EA NPE+ +P ATN Sbjct: 181 -GPQATVSNLWDQGGFLPHGFTGLVMMMAIIMFSFGGLELVGITAAEADNPEQSIPKATN 239 Query: 250 GVVWRILIFYVGALIIMMALVPWNELKPGVSPFVYVFERIGVPGAAAIVNLVVITAAASS 309 V++RILIFY+G+L ++++L+PW + SPFV +F +G A +N+VV+TAA S Sbjct: 240 QVIYRILIFYIGSLAVLLSLMPWTRVTADTSPFVLIFHELGDTFVANALNIVVLTAALSV 299 Query: 310 CNSGIFSTGRMLYTLAQFGQAPRAFGRVSSKHVPSIAITFSAALMGIGVLLNYIVPEQVF 369 NS ++ RML+ LAQ G AP+A V + VP I SA + + VL+NY+ PE F Sbjct: 300 YNSCVYCNSRMLFGLAQQGNAPKALASVDKRGVPVNTILVSALVTALCVLINYLAPESAF 359 Query: 370 VWVTSISLVGSLWTWSIIMIAHLGYRKAIAAGRVKAVAFRMPGA--PYANWLVVAFMIAV 427 + ++ + + W++I +AH+ +R+ A + + V R P P NW+ + FM AV Sbjct: 360 GLLMALVVSALVINWAMISLAHMKFRR---AKQEQGVVTRFPALLYPLGNWICLLFMAAV 416 Query: 428 AVLLSLDPGTRVALYVAPVWFALLGIGYRFTKSRA 462 V++ + PG +++Y+ PVW +LGIGY F + A Sbjct: 417 LVIMLMTPGMAISVYLIPVWLIVLGIGYLFKEKTA 451 Lambda K H 0.328 0.142 0.445 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: 696 Number of extensions: 35 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: 472 Length of database: 457 Length adjustment: 33 Effective length of query: 439 Effective length of database: 424 Effective search space: 186136 Effective search space used: 186136 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