Align Plastidic cationic amino acid transporter, CAT, of 582 aas and 14 TMSs (characterized)
to candidate H281DRAFT_02180 H281DRAFT_02180 amino acid/polyamine/organocation transporter, APC superfamily
Query= TCDB::ALD51314.1 (582 letters) >FitnessBrowser__Burk376:H281DRAFT_02180 Length = 463 Score = 224 bits (570), Expect = 8e-63 Identities = 138/427 (32%), Positives = 233/427 (54%), Gaps = 25/427 (5%) Query: 50 MKRSLRWYDLVGFGVGGMVGAGVFVTSGRASSHCAGPAVVLSYAIAGFCALLSAFCYTEF 109 +K++L DL GVG ++G G+FV +G + AGPA+++S+ IA +A Y EF Sbjct: 22 LKKALGALDLTFLGVGAIIGTGIFVLTGTGAVQ-AGPALMVSFLIAAVACGFAALAYAEF 80 Query: 110 AVDMPVAGGAFSYIRITFGEFLAFLTGANLIIDYVLSNAAVARSFTGYLCTAL---GIES 166 A +PVAG ++Y T GE A++ G +L+++Y L+ +AV+ ++GYL + L G+ Sbjct: 81 ASTIPVAGSIYTYSYATLGELAAWIIGWDLMLEYGLATSAVSVGWSGYLQSLLSGFGVSL 140 Query: 167 KLRITV--NGLPDGFNEIDVVAVLVVLALTVIICYSTRESSVLNMVLTVLHIVFIVFVIV 224 + +T LP ++ A LV++A+T ++ RES+ +N ++ + +V ++ VI Sbjct: 141 PVALTAAPGALPGHETLFNLPAFLVMMAITALLSVGVRESARINNIMVAIKVVVVLLVIA 200 Query: 225 IGFTRGDTKNFTKAGDSNHASGFFPFGASGVFNGAAMVYLSYIGYDAVSTMAEEVKNPVK 284 +G N+ F P G +GVF AA+++ ++IG+D+VS+ AEEVKNP + Sbjct: 201 VGVFHVTPANWHP---------FMPNGWNGVFGAAAVMFFAFIGFDSVSSAAEEVKNPKR 251 Query: 285 DIPVGVSGSVILVTVLYCLMAASMSMLLPY-DMIDPDAPFSGAFMGSDGWRWVSNVIGVG 343 D+P+G+ S+ + VLY +AA ++ ++P + P S A + G +WV+ I +G Sbjct: 252 DLPIGIIASLGVCAVLYVAVAAVVTGIVPSAQFANISHPVSYALQVA-GQKWVAGFIDLG 310 Query: 344 AGFGILTSLLVAMLGQARYMCVIGRSSVVPAWFAKVHPKTSTPVNASAFLGICTAAIALF 403 A G+LT +LV GQ R + + R ++PA ++VHP+ +TP + +GI I Sbjct: 311 AVLGMLTVILVMAYGQTRVIFAMSRDGLLPARLSRVHPRFATPFFTTWLVGIFFGLIGAL 370 Query: 404 TDLQILLNLVSIGTLFVFYMVANAVIYKRYVSVGVTNPW--------PTLSYLFCFSLTS 455 L +L L++IGTL F MV+ AV+ R + + P L+ C L + Sbjct: 371 VPLNVLAELINIGTLAAFSMVSIAVLVLRKTHPELPRAFRCPGVPVVPVLAVASCVFLMA 430 Query: 456 ILFTLLW 462 L + W Sbjct: 431 NLQAVTW 437 Lambda K H 0.326 0.139 0.423 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: 639 Number of extensions: 42 Number of successful extensions: 5 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: 582 Length of database: 463 Length adjustment: 35 Effective length of query: 547 Effective length of database: 428 Effective search space: 234116 Effective search space used: 234116 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: 52 (24.6 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