8UO7
Bovine trypsin in complex with deacetylated wild type microviridin J
Summary for 8UO7
Entry DOI | 10.2210/pdb8uo7/pdb |
Related PRD ID | PRD_002533 |
Descriptor | Cationic trypsin, Deacetylated wildtype microviridin J, SULFATE ION, ... (6 entities in total) |
Functional Keywords | hydrolase inhibitor, hydrolase |
Biological source | Bos taurus (cattle) More |
Total number of polymer chains | 2 |
Total formula weight | 25251.35 |
Authors | Chen, W.,Bruner, S.D. (deposition date: 2023-10-19, release date: 2024-02-14, Last modification date: 2024-02-28) |
Primary citation | Patel, K.P.,Chen, W.T.,Delbecq, L.,Bruner, S.D. Alternative Linkage Chemistries in the Chemoenzymatic Synthesis of Microviridin-Based Cyclic Peptides. Org.Lett., 26:1138-1142, 2024 Cited by PubMed Abstract: Engineering biosynthetic pathways to ribosomally synthesized and post-translationally modified peptides (RiPPs) offers several advantages for both and applications. Here we probe the ability of peptide cyclases to generate trimacrocycle microviridin analogs with non-native cross-links. The results demonstrate that diverse chemistries are tolerated by macrocyclases in the ATP-grasp family and allow for the construction of unique cyclic peptide architectures that retain protease inhibition activity. In addition, cocomplex structures of analogs bound to a model protease were determined, illustrating how changes in functional groups maintain peptide conformation and target binding. PubMed: 38306609DOI: 10.1021/acs.orglett.3c04045 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.2 Å) |
Structure validation
Download full validation report