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Bovine alpha chymotrypsin bound to a cyclic peptide inhibitor, 5b
Descriptor:	(11S)-4,9-dioxo-N-[(2S)-1-oxo-3-phenylpropan-2-yl]-17,22-dioxa-10,30-diazatetracyclo[21.2.2.2~13,16~.1~5,8~]triaconta-1(25),5,7,13,15,23,26,28-octaene-11-carboxamide, Chymotrypsinogen A
Authors:	Chan, H.Y, Bruning, J.B, Abell, A.D.
Deposit date:	2014-04-09
Release date:	2014-07-23
Last modified:	2023-11-08
Method:	X-RAY DIFFRACTION (2.2 Å)
Cite:	Macrocyclic protease inhibitors with reduced peptide character. Angew.Chem.Int.Ed.Engl., 53, 2014

Structure of the DNA binding domain of pSK1 Par partition protein bound to centromere DNA
Descriptor:	DNA (5'-D(TPAPGPTPTPAPGPGPTPAPCPCPTPAPAPCPA)-3'), DNA (5'-D(PTPGPTPTPAPGPGPTPAPCPCPTPAPAPC)-3'), Par
Authors:	Schumacher, M.A.
Deposit date:	2022-05-12
Release date:	2022-08-10
Last modified:	2024-02-14
Method:	X-RAY DIFFRACTION (2.25 Å)
Cite:	Molecular Analysis of pSK1 par: A Novel Plasmid Partitioning System Encoded by Staphylococcal Multiresistance Plasmids. J.Mol.Biol., 434, 2022

Crystal structure of human SENP1 mutant (C603S) in complex with SUMO-1
Descriptor:	SENP1 protein, Small ubiquitin-related modifier 1
Authors:	Xu, Z, Chau, S.F, Lam, K.H, Au, S.W.N.
Deposit date:	2006-02-22
Release date:	2006-10-17
Last modified:	2021-11-10
Method:	X-RAY DIFFRACTION (2.8 Å)
Cite:	Crystal structure of the SENP1 mutant C603S-SUMO complex reveals the hydrolytic mechanism of SUMO-specific protease Biochem.J., 398, 2006