PDB 编号 标题 Rg (Å) Dmax (Å) 实验方法 质量评级
8rzf RNase W from Sulfolobus acidocaldarius 26.0 84.0 X-RAY DIFFRACTION GOOD
8rzg ZgGH129 from Zobellia galactanivorans soaked with the product of the reaction ADG (3,6-anhydro-D-galactose). 48.0 160.9 X-RAY DIFFRACTION GOOD
8rzh ZgGH129 from Zobellia galactanivorans in complex with the inhibitor AD-DGJ (3,6-anhydro-D-1-deoxygalactonojirimycin). 47.9 160.6 X-RAY DIFFRACTION GOOD
8rzi ;ZgGH129 from Zobellia galactanivorans soaked with 1,2-diF-ADG (3,6-Anhydro-2-deoxy-2-fluoro-a-D-galactopyranosyl fluoride) resulting in a trapped glycosyl-enzyme intermediate. ; 47.9 160.5 X-RAY DIFFRACTION GOOD
8rzj ZgGH129 from Zobellia galactanivorans in complex with the inhibitor ADG-IF (3,6-anhydro-D-galacto-isofagomine). 47.8 158.3 X-RAY DIFFRACTION GOOD
8rzk ;The Michaelis complex of ZgGH129 D486N from Zobellia galactanivorans with neo-b/k-oligo-carrageenan tetrasaccharide (beta-kappa neo-oligo-carrageenan DP4). ; 47.5 160.4 X-RAY DIFFRACTION GOOD
8rzl Sulfolobus acidocaldarius threads (0406) filament. 48.0 196.0 ELECTRON MICROSCOPY REASONABLE
8rzu Structure of human SETD2 L1609P mutant in complex with SAM and H3K36M peptide 20.6 71.6 X-RAY DIFFRACTION GOOD
8rzv Structure of UP1 S4ES6E phosphomimetic mutant in complex with human telomeric repeat DNA 21.1 66.3 X-RAY DIFFRACTION EXCELLENT
8rzw A fragment-based inhibitor of SHP2 38.3 129.5 X-RAY DIFFRACTION GOOD
8rzx Solution structure of a parallel stranded G-quadruplex formed in ORAI1 promoter 12.3 41.5 SOLUTION NMR REASONABLE
8rzy A fragment-based inhibitor of SHP2 38.2 129.5 X-RAY DIFFRACTION GOOD
8rzz Crystal structure of Renilla luciferase RLuc8-GFP BRET complex at pH 9.0 (space group P32) 54.2 190.2 X-RAY DIFFRACTION GOOD
8s00 CpKRS complexed with lysine and an inhibitor 32.8 104.8 X-RAY DIFFRACTION GOOD
8s01 A fragment-based inhibitor of SHP2 39.0 132.7 X-RAY DIFFRACTION GOOD
8s02 BzdNO-benzoyl-CoA complex 38.3 123.6 X-RAY DIFFRACTION GOOD
8s03 NMR solution structure of the CysD2 domain of MUC2 14.8 39.6 SOLUTION NMR REASONABLE
8s04 A fragment-based inhibitor of SHP2 38.2 128.0 X-RAY DIFFRACTION GOOD
8s05 ArnAB complex an archaeal ortholog of the Sec23/24 core motif 31.7 100.7 X-RAY DIFFRACTION EXCELLENT
8s06 A fragment-based inhibitor of SHP2 38.4 130.2 X-RAY DIFFRACTION GOOD
8s07 A fragment-based inhibitor of SHP2 38.2 129.7 X-RAY DIFFRACTION GOOD
8s09 H. sapiens MCM2-7 double hexamer bound to double stranded DNA 72.5 255.3 ELECTRON MICROSCOPY REASONABLE
8s0a H. sapiens MCM2-7 hexamer bound to double stranded DNA 50.2 156.8 ELECTRON MICROSCOPY GOOD
8s0b H. sapiens MCM bound to double stranded DNA and ORC6 as part of the MCM-ORC complex 51.2 166.5 ELECTRON MICROSCOPY REASONABLE
8s0c H. sapiens ORC1-5 bound to double stranded DNA as part of the MCM-ORC complex 44.4 147.5 ELECTRON MICROSCOPY GOOD
8s0d H. sapiens MCM bound to double stranded DNA and ORC1-6 67.2 237.0 ELECTRON MICROSCOPY GOOD
8s0e H. sapiens OCCM bound to double stranded DNA 62.4 209.1 ELECTRON MICROSCOPY GOOD
8s0f H. sapiens OC1M bound to double stranded DNA 61.5 204.2 ELECTRON MICROSCOPY REASONABLE
8s0g Crystal structure of Renilla reniformis luciferase-GFP BRET complex 57.6 191.5 X-RAY DIFFRACTION GOOD
8s0h A fragment-based inhibitor of SHP2 38.6 130.8 X-RAY DIFFRACTION GOOD
8s0i A fragment-based inhibitor of SHP2 38.1 129.3 X-RAY DIFFRACTION GOOD
8s0j A fragment-based inhibitor of SHP2 38.4 129.2 X-RAY DIFFRACTION GOOD
8s0k A fragment-based inhibitor of SHP2 38.1 128.1 X-RAY DIFFRACTION GOOD
8s0l Crystal structure of the TMPRSS2 zymogen in complex with the nanobody A07 26.4 95.9 X-RAY DIFFRACTION GOOD
8s0m Crystal structure of the HKU1 receptor binding domain in complex with TMPRSS2 and the nanobody A01 48.9 164.0 X-RAY DIFFRACTION GOOD
8s0n Crystal structure of the TMPRSS2 zymogen in complex with the nanobody A07 34.1 111.5 X-RAY DIFFRACTION GOOD
8s0o A fragment-based inhibitor of SHP2 38.1 129.4 X-RAY DIFFRACTION GOOD
8s0p A fragment-based inhibitor of SHP2 38.0 127.2 X-RAY DIFFRACTION GOOD
8s0q A fragment-based inhibitor of SHP2 38.3 129.9 X-RAY DIFFRACTION GOOD
8s0r Cryo-EM structure of CAK modified by covalent inhibitor SY-1365 27.8 88.4 ELECTRON MICROSCOPY EXCELLENT
8s0s A fragment-based inhibitor of SHP2 38.1 129.4 X-RAY DIFFRACTION GOOD
8s0t Cryo-EM structure of CAK in complex with SY-5609 27.2 85.9 ELECTRON MICROSCOPY EXCELLENT
8s0u Structure of the LytM domain of PrgK from E. faecalis 26.7 83.5 X-RAY DIFFRACTION EXCELLENT
8s0v Crystal structure of Cryptosporidium parvum - Trypanosoma cruzi mutant lysyl tRNA synthetase in complex with inhibitor 32.7 107.0 X-RAY DIFFRACTION GOOD
8s0w ;High pH (8.0) as-isolated MSOX movie series dataset 1 of the copper nitrite reductase (NirK) from Bradyrhizobium japonicum USDA110 [0.35 MGy] ; 22.0 86.1 X-RAY DIFFRACTION GOOD
8s13 apo c-KIT-wt kinase domain 20.4 64.8 X-RAY DIFFRACTION GOOD
8s14 c-KIT kinase domain in complex with sunitinib 20.4 64.1 X-RAY DIFFRACTION GOOD
8s15 c-KIT kinase domain in complex with nintedanib 21.3 69.8 X-RAY DIFFRACTION GOOD
8s16 c-KIT kinase domain in complex with imatinib 27.8 89.6 X-RAY DIFFRACTION GOOD
8s17 c-KIT kinase domain in complex with ponatinib 27.5 98.9 X-RAY DIFFRACTION GOOD