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Structure of human 20S proteasome with bound MPI-5
分子名称:	N-[(1R)-2-([1,1'-biphenyl]-4-yl)-1-boronoethyl]-1-methyl-L-prolinamide, Proteasome subunit alpha type-1, Proteasome subunit alpha type-2, ...
著者	Metcalfe, R.D, Morton, C.J, Liu, B, Xie, S.C, Hanssen, E, Leis, A.P, Tilley, L, Griffin, M.D.W.
登録日	2021-03-05
公開日	2021-09-22
最終更新日	2022-04-13
実験手法	ELECTRON MICROSCOPY (3.4 Å)
主引用文献	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
分子名称:	Probable diphthine synthase, S-ADENOSYL-L-HOMOCYSTEINE, SODIUM ION
著者	Shimizu, K, RIKEN Structural Genomics/Proteomics Initiative (RSGI)
登録日	2006-02-10
公開日	2006-07-18
最終更新日	2023-10-25
実験手法	X-RAY DIFFRACTION (1.65 Å)
主引用文献	Crystal structure of project ID PH0725 from Pyrococcus horikoshii OT3 at 1.65 A resolution To be Published