5zzd
From Proteopedia
(Difference between revisions)
Line 1: | Line 1: | ||
- | '''Unreleased structure''' | ||
- | + | ==Crystal structure of a protein from Aspergillus flavus== | |
- | + | <StructureSection load='5zzd' size='340' side='right'caption='[[5zzd]], [[Resolution|resolution]] 1.85Å' scene=''> | |
- | + | == Structural highlights == | |
- | + | <table><tr><td colspan='2'>[[5zzd]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5ZZD OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5ZZD FirstGlance]. <br> | |
- | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene></td></tr> | |
- | [[Category: | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5zzd FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5zzd OCA], [http://pdbe.org/5zzd PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5zzd RCSB], [http://www.ebi.ac.uk/pdbsum/5zzd PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5zzd ProSAT]</span></td></tr> |
- | [[Category: Chang, Z | + | </table> |
- | [[Category: Liu, W | + | == Function == |
- | [[Category: | + | [[http://www.uniprot.org/uniprot/LEPI_ASPFN LEPI_ASPFN]] O-methyltransferase; part of the gene cluster 23 that mediates the biosynthesis of a family of 2-pyridones known as leporins (PubMed:20447271, PubMed:26051490). The hybrid PKS-NRPS synthetase lepA and the enoyl reductase lepG are responsible for fusion of phenylalanine with a hexaketide and subsequent release of the stable tetramic acid precursor, pre-leporin C (PubMed:26051490). Because lepA lacks a designated enoylreductase (ER) domain, the required activity is provided the enoyl reductase lepG (PubMed:26051490). It is possible that the dehydrogenase lepF also participates in production of pre-leporin C (PubMed:26051490). Cytochrome P450 monooxygenase lepH is then required for the ring expansion step to yield leporin C (PubMed:26051490). Leporin C is then presumably further oxidized by the N-hydroxylase lepD to form leporin B (PubMed:26051490). LepI may possess a function in biosynthesis upstream of lepA (PubMed:26051490). Leporin B is further oxidized in the presence of ferric ion to give the leporin B trimer-iron chelate, but whether or not this reaction is catalyzed by an enzyme in the pathway or by ferric ion is not determined yet (PubMed:26051490).<ref>PMID:26051490</ref> <ref>PMID:20447271</ref> |
- | [[Category: | + | == References == |
+ | <references/> | ||
+ | __TOC__ | ||
+ | </StructureSection> | ||
+ | [[Category: Large Structures]] | ||
+ | [[Category: Chang, Z Y]] | ||
+ | [[Category: Chen, C C]] | ||
+ | [[Category: Guo, R T]] | ||
+ | [[Category: Liu, W D]] | ||
+ | [[Category: Sam]] | ||
+ | [[Category: Substrate binding]] | ||
+ | [[Category: Transferase]] |
Revision as of 22:40, 5 June 2019
Crystal structure of a protein from Aspergillus flavus
|
Categories: Large Structures | Chang, Z Y | Chen, C C | Guo, R T | Liu, W D | Sam | Substrate binding | Transferase