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EC Number
Crystallization
Reference
complexed with H261, crystals grow in two different crystal forms with the same monoclinic sopace group, P2(1), unit cell parameters a : 43.0A, b : 75.7A, c : 42.9A
complexes of pepstatin A and a statine-containing human renin inhibitor with endothiapepsin; X-ray crystallographic analysis
crystal structure of enzyme bound to inhibitor Pd130328, inhibitor binding structure and analysis
in complex with gem-diol inhibitor PD-135,040, hanging-drop vapour-diffusion method, space group P2(1), unit-cell parameters a : 53.20, b : 73.25, c : 46.00
of inhibition of endothiapepsin by cyclohexyl renin inhibitors; X-ray crystallographic analysis
of the complex between endothiapepsin and an oligopeptide inhibitor
sitting drop vapor diffusion method, using 0.1 M NH4Ac, 0.1 M acetate buffer, pH 4.6, and 26% (w/v) PEG 4000
space group P2(1), in complex with H189 unit cell parameters a : 42.48, b : 75.78, c : 42.99, in complex with CP-80,794 unit cell parameters a : 42.55, b : 74.62, c : 44.43, in complex with CP-129,541 unit cell parameters a : 42.47, b : 74.31, c : 42.81, in complex with PD-130,328 unit cell parameters a : 43.88, b : 75.44, c : 43.23, in complex with H256 unit cell parameters a : 43.88, b : 75.44, c : 43.23
structure studied by neutron crystallography, crystals are monocliic, P2(1), unit cell dimensions a : 43.1 A, b : 75.7 A, c : 42.9 A, endothiapepsin-H261 complex
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