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4AKT

PatG macrocyclase in complex with peptide

Summary for 4AKT
Entry DOI10.2210/pdb4akt/pdb
Related4AKS
DescriptorTHIAZOLINE OXIDASE/SUBTILISIN-LIKE PROTEASE, SUBSTRATE ANALOGUE (3 entities in total)
Functional Keywordshydrolase-peptide complex, hydrolase, patellamide, hydrolase/peptide
Biological sourcePROCHLORON DIDEMNI
More
Total number of polymer chains3
Total formula weight78218.09
Authors
Primary citationKoehnke, J.,Bent, A.,Houssen, W.E.,Zollman, D.,Morawitz, F.,Shirran, S.,Vendome, J.,Nneoyiegbe, A.F.,Trembleau, L.,Botting, C.H.,Smith, M.C.,Jaspars, M.,Naismith, J.H.
The Mechanism of Patellamide Macrocyclization Revealed by the Characterization of the Patg Macrocyclase Domain.
Nat.Struct.Mol.Biol., 19:767-, 2012
Cited by
PubMed Abstract: Peptide macrocycles are found in many biologically active natural products. Their versatility, resistance to proteolysis and ability to traverse membranes has made them desirable molecules. Although technologies exist to synthesize such compounds, the full extent of diversity found among natural macrocycles has yet to be achieved synthetically. Cyanobactins are ribosomal peptide macrocycles encompassing an extraordinarily diverse range of ring sizes, amino acids and chemical modifications. We report the structure, biochemical characterization and initial engineering of the PatG macrocyclase domain of Prochloron sp. from the patellamide pathway that catalyzes the macrocyclization of linear peptides. The enzyme contains insertions in the subtilisin fold to allow it to recognize a three-residue signature, bind substrate in a preorganized and unusual conformation, shield an acyl-enzyme intermediate from water and catalyze peptide bond formation. The ability to macrocyclize a broad range of nonactivated substrates has wide biotechnology applications.
PubMed: 22796963
DOI: 10.1038/NSMB.2340
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.63 Å)
Structure validation

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