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Structure of human 20S proteasome with bound MPI-5
Descriptor:	N-[(1R)-2-([1,1'-biphenyl]-4-yl)-1-boronoethyl]-1-methyl-L-prolinamide, Proteasome subunit alpha type-1, Proteasome subunit alpha type-2, ...
Authors:	Metcalfe, R.D, Morton, C.J, Liu, B, Xie, S.C, Hanssen, E, Leis, A.P, Tilley, L, Griffin, M.D.W.
Deposit date:	2021-03-05
Release date:	2021-09-22
Last modified:	2022-04-13
Method:	ELECTRON MICROSCOPY (3.4 Å)
Cite:	Design of proteasome inhibitors with oral efficacy in vivo against Plasmodium falciparum and selectivity over the human proteasome. Proc.Natl.Acad.Sci.USA, 118, 2021

Crystal structure of project ID PH0725 from Pyrococcus horikoshii OT3 at 1.65 A resolution
Descriptor:	Probable diphthine synthase, S-ADENOSYL-L-HOMOCYSTEINE, SODIUM ION
Authors:	Shimizu, K, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
Deposit date:	2006-02-10
Release date:	2006-07-18
Last modified:	2023-10-25
Method:	X-RAY DIFFRACTION (1.65 Å)
Cite:	Crystal structure of project ID PH0725 from Pyrococcus horikoshii OT3 at 1.65 A resolution To be Published