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Crystal structure of Trypanosoma cruzi CYP51 bound to the inhibitor (R)-N-(3-(1H-indol-3-yl)-1-oxo-1-(pyridin-4-ylamino)propan-2-yl)-3,3'- difluoro-(1,1'-biphenyl)-4-carboxamide
Descriptor:	(R)-N-(3-(1H-indol-3-yl)-1-oxo-1-(pyridin-4-ylamino)propan-2-yl)-3,3'-difluoro-(1,1'-biphenyl)-4-carboxamide, PROTOPORPHYRIN IX CONTAINING FE, STEROL 14-ALPHA DEMETHYLASE
Authors:	Choi, J.Y, Calvet, C.M, Vierira, D.F, Gunatilleke, S.S, Cameron, M.D, McKerrow, J.H, Podust, L.M, Roush, W.R.
Deposit date:	2013-07-16
Release date:	2014-01-22
Last modified:	2023-12-20
Method:	X-RAY DIFFRACTION (3.1 Å)
Cite:	R-Configuration of 4-Aminopyridyl-Based Inhibitors of Cyp51 Confers Superior Efficacy Against Trypanosoma Cruzi Acs Med.Chem.Lett., 5, 2014

Crystal structure of BbKI, a Kunitz-type kallikrein inhibitor
Descriptor:	1,2-ETHANEDIOL, Kunitz-type serine protease inhibitor BbKI
Authors:	Navarro, M.V.A.S, Garratt, R.C.
Deposit date:	2006-04-12
Release date:	2007-03-13
Last modified:	2024-02-14
Method:	X-RAY DIFFRACTION (1.87 Å)
Cite:	The Crystal Structure of BbKI, a kunitz-type kallikrein inhibitor devoid of disulfide bridges To be Published, 2006