6azt

Asparaginyl endopeptidase 1 bound to AAN peptide, a tetrahedral intermediate

spinqualitylabelsall models 6azt, resolution 1.80Å Show:Asymmetric Unit Biological Assembly Drag the structure with the mouse to rotate   Export Animated Image   Print3D Structural highlights 6azt is a 2 chain structure with sequence from Helianthus annuus and Synthetic construct. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance. Method: X-ray diffraction, Resolution 1.8Å Ligands: CE7, GOL, SNN Resources: FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT Function A0A251RPF5_HELAN Publication Abstract from PubMed Constrained, cyclic peptides encoded by plant genes represent a new generation of drug leads. Evolution has repeatedly recruited the Cys-protease asparaginyl endopeptidase (AEP) to perform their head-to-tail ligation. These macrocyclization reactions use the substrates amino terminus instead of water to deacylate, so a peptide bond is formed. How solvent-exposed plant AEPs macrocyclize is poorly understood. Here we present the crystal structure of an active plant AEP from the common sunflower, Helianthus annuus. The active site contained electron density for a tetrahedral intermediate with partial occupancy that predicted a binding mode for peptide macrocyclization. By substituting catalytic residues we could alter the ratio of cyclic to acyclic products. Moreover, we showed AEPs from other species lacking cyclic peptides can perform macrocyclization under favorable pH conditions. This structural characterization of AEP presents a logical framework for engineering superior enzymes that generate macrocyclic peptide drug leads. Structural basis of ribosomal peptide macrocyclization in plants.,Haywood J, Schmidberger JW, James AM, Nonis SG, Sukhoverkov KV, Elias M, Bond CS, Mylne JS Elife. 2018 Jan 31;7. pii: 32955. doi: 10.7554/eLife.32955. PMID:29384475 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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