Align D-serine/D-alanine/glycine transporter (characterized, see rationale)
to candidate Pf1N1B4_3559 Aromatic amino acid transport protein AroP
Query= uniprot:A0A0C4YRF7 (472 letters) >FitnessBrowser__pseudo1_N1B4:Pf1N1B4_3559 Length = 473 Score = 395 bits (1015), Expect = e-114 Identities = 193/454 (42%), Positives = 292/454 (64%), Gaps = 12/454 (2%) Query: 18 DLHRGLKDRHIQMIAIGGAIGVGLFLGAGRAIAIAGPGLMLSYAIGGVAIFFIMRALGEL 77 +L RGLK+RHIQ+IA+GGAIG GLFLG+ + AGP ++L YAI G F IMR LGE+ Sbjct: 10 ELKRGLKNRHIQLIALGGAIGTGLFLGSAGVLKSAGPSMILGYAICGFIAFMIMRQLGEM 69 Query: 78 LLYRPVSGSFATYAEEFVGPFAGFATGWSYWFMWVVTGMAEITAVAVYVHYWFPDVPQWI 137 ++ PV+GSF+ +A ++ G FAGF +GW+ W ++++ GM+E+TAV Y+HYW PD+P W+ Sbjct: 70 IVEEPVAGSFSHFAHKYWGGFAGFLSGWNCWILYILVGMSELTAVGKYIHYWAPDIPTWV 129 Query: 138 PALATLAVLYLVNCVAVAVFGELEFWFALIKVVTIVAMIVIGLAIIFFGVTPLGPTASFS 197 A ++ L+N V VFGE EFWFA+IKVV IV MI +G ++ G GP AS + Sbjct: 130 SAAGFFVLINLINLANVKVFGEAEFWFAIIKVVAIVGMIALGSYLLVSG--DGGPQASVT 187 Query: 198 NLWTHGGFMPFGTLGVVLTLQIVMFAYQGVELIGVTAGEAQNPEKVLPHATNGVVWRILI 257 NLW HGGF P G G+V+ + I+MF++ G+E++G TA EA P+ V+P A N V++RILI Sbjct: 188 NLWEHGGFFPNGVSGLVMAMAIIMFSFGGLEMLGFTAAEADKPKTVIPKAINQVIYRILI 247 Query: 258 FYVGALIIMMALVPWNELKPGV---------SPFVYVFERIGVPGAAAIVNLVVITAAAS 308 FY+GAL+++++L PW+ L + SPFV VF +G AA I+N VV+TAA S Sbjct: 248 FYIGALVVLLSLTPWDSLLTTLNASGDAYSGSPFVQVFSMLGSDTAAHILNFVVLTAALS 307 Query: 309 SCNSGIFSTGRMLYTLAQFGQAPRAFGRVSSKHVPSIAITFSAALMGIGVLLNYIVPEQV 368 NSG + RML +A+ G AP+A ++ + VP +I SAA+ + VLLNY+VP+ Sbjct: 308 VYNSGTYCNSRMLLGMAEQGDAPKALSKIDKRGVPVRSILASAAVTLVAVLLNYLVPQHA 367 Query: 369 FVWVTSISLVGSLWTWSIIMIAHLGYRKAIAAGRVKAVAFRMPGAPYANWLVVAFMIAVA 428 + S+ + + W++I +H +R+ + + + F+ PY N++ +AF++ + Sbjct: 368 LELLMSLVVATLVINWAMISFSHFKFRQHMNKTK-QTPLFKALWYPYGNYVCLAFVVFIL 426 Query: 429 VLLSLDPGTRVALYVAPVWFALLGIGYRFTKSRA 462 ++ L PG ++++Y PVW A + + Y R+ Sbjct: 427 GVMLLIPGIQISVYAIPVWVAFMWVCYGIKNKRS 460 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: 669 Number of extensions: 34 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: 473 Length adjustment: 33 Effective length of query: 439 Effective length of database: 440 Effective search space: 193160 Effective search space used: 193160 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