PDB ID Title official curves Structure unit Experimental Method
9r1x PLK1 SURFACE ENTROPY REDUCTION (SER) MUTANT IN COMPLEX WITH INHIBITOR BI 2536 1 1 X-RAY DIFFRACTION
9r1y PLK1 SURFACE ENTROPY REDUCTION (SER) MUTANT IN COMPLEX WITH INHIBITOR GSK461364 1 1 X-RAY DIFFRACTION
9r1z Keap1 - inhibitor complex - 3 1 1 X-RAY DIFFRACTION
9r21 Cryo-EM structure of the flotillin-associated rhodopsin PsFAR in detergent micelle 1 1 ELECTRON MICROSCOPY
9r22 Cryo-EM structure of the light-driven proton pump PsPR in detergent micelle 1 1 ELECTRON MICROSCOPY
9r23 Cryo-EM structure of the double mutant H84V/E120G of the flotillin-associated rhodopsin PsFAR in detergent micelle 1 1 ELECTRON MICROSCOPY
9r25 Sorafenib in complex with p38alpha (MAPK14) 1 1 X-RAY DIFFRACTION
9r27 Regorafenib in complex with p38alpha (MAPK14) 1 1 X-RAY DIFFRACTION
9r2b De novo-designed alpha-helical barrel 2 2 X-RAY DIFFRACTION
9r2c CpKRS in complex with inhibitor DDD01038762 1 1 X-RAY DIFFRACTION
9r2e Structure of ARGX-121 Fab fragment in complex with the Fc fragment of IgA1 1 1 X-RAY DIFFRACTION
9r2f Tau filaments seeded by AD homogenate using 0N3R C322A 1 1 ELECTRON MICROSCOPY
9r2g Cytochrome bd II oxidase qOR-2 type from Mycobacterium smegmatis 1 1 ELECTRON MICROSCOPY
9r2h Tau filaments seeded by AD homogenate using 0N3R C322S 1 1 ELECTRON MICROSCOPY
9r2i Cryo-EM structure of the complex CDK16:CCNY:14-3-3 1 1 ELECTRON MICROSCOPY
9r2j Crystal structure of human MAO B in complex with (E)-3-(4-nitrophenyl)-1-(3-(trifluoromethyl)phenyl)prop-2-en-1-one (chalcone inhibitor, 4a) 1 1 X-RAY DIFFRACTION
9r2k De novo designed N30 protein fold 1 1 X-RAY DIFFRACTION
9r2l De novo designed N37 protein fold 8 8 X-RAY DIFFRACTION
9r2m p53 bound to nucleosome at position SHL+5.9 (non-crosslinked sample, composite map) 1 1 ELECTRON MICROSCOPY
9r2n Cryo-EM structure of the complex CCNY:14-3-3 1 1 ELECTRON MICROSCOPY
9r2o De novo designed N5 protein fold 2 2 X-RAY DIFFRACTION
9r2p p53 bound to nucleosome at position SHL+5.9 (crosslinked sample) 1 1 ELECTRON MICROSCOPY
9r2q p53 bound to nucleosome at position SHL-5.7 (non-crosslinked sample) 1 1 ELECTRON MICROSCOPY
9r2r De novo designed M7 protein fold 4 4 X-RAY DIFFRACTION
9r2s Structure of the S.aureus ClpP degradation chamber in the context of the MecA/ClpC/CLpC complex 1 1 ELECTRON MICROSCOPY
9r2v De novo designed M16 protein fold 8 8 X-RAY DIFFRACTION
9r2z RptR transcriptional repressor 1 1 X-RAY DIFFRACTION
9r30 Three dimensional structure of human carbonic anhydrase IX in complex with sulfonamide 2 2 X-RAY DIFFRACTION
9r31 Three dimensional structure of human carbonic anhydrase XII in complex with sulfonamide 2 2 X-RAY DIFFRACTION
9r32 CRYSTAL STRUCTURE OF LYSYL-TRNA SYNTHETASE FROM Cryptosporidium parvum COMPLEXED WITH L-LYSINE AND INHIBITOR DDD01887015 2 2 X-RAY DIFFRACTION
9r33 Improved crystallization and diffraction quality of Mycobacterium tuberculosis OmamC/Rv1363c upon heat treatment 2 2 X-RAY DIFFRACTION
9r34 Norovirus NS3 hexamer in complex with ATP-gamma-S 1 1 ELECTRON MICROSCOPY
9r35 Crystal structure of the Pseudomonas putida Xre-RES toxin-antitoxin complex bound to promoter DNA 4 4 X-RAY DIFFRACTION
9r3a Structure of Stalled Beta-Galactosidase 70S Ribosome Nascent Chain 1 1 ELECTRON MICROSCOPY
9r3b Recombinant human Butyrylcholinesterase in complex with N-([(3R)-1-benzylpiperidin-3-yl]methyl)-N-(2-methoxyethyl)naphthalene-2-sulfonamide 1 1 X-RAY DIFFRACTION
9r3c Recombinant human butyrylcholinesterase in complex with N-([(3S)-1-benzylpiperidin-3-yl]methyl)-N-(2-methoxyethyl)naphthalene-2-sulfonamide 1 1 X-RAY DIFFRACTION
9r3d Cryo-EM structure of the human pre-Bact-OTS complex (whole map) 1 1 ELECTRON MICROSCOPY
9r3e Human FAM118B(34-334) 2 protomers 1 1 ELECTRON MICROSCOPY
9r3f CRYSTAL STRUCTURE OF LYSYL-TRNA SYNTHETASE FROM Cryptosporidium parvum COMPLEXED WITH L-LYSINE AND INHIBITOR DDD01932549 1 1 X-RAY DIFFRACTION
9r3g CRYSTAL STRUCTURE OF LYSYL-TRNA SYNTHETASE FROM Cryptosporidium parvum / Plasmodium falciparum chimera COMPLEXED WITH L-LYSINE AND INHIBITOR DDD02174286 1 1 X-RAY DIFFRACTION
9r3h Structure of liver pyruvate kinase in complex with fluorescent probe 4b 2 2 X-RAY DIFFRACTION
9r3i Structure of liver pyruvate kinase in complex with fluorescent probe 4c 1 1 X-RAY DIFFRACTION
9r3j Crystal structure of human MAO B in complex with (E)-3-(benzo[d][1,3]dioxol-5-yl)-1-(3-(trifluoromethyl)phenyl)prop-2-en-1-one (chalcone inhibitor, 4e) 1 1 X-RAY DIFFRACTION
9r3k Crystal structure of human MAO B in complex with ((E)-3-(3-nitrophenyl)-1-(3-(trifluoromethyl)phenyl)prop-2-en-1-one (4b) 1 1 X-RAY DIFFRACTION
9r3l Structure of liver pyruvate kinase in complex with fluorescent probe 4d 2 2 X-RAY DIFFRACTION
9r3m Structure of liver pyruvate kinase in complex with fluorescent probe 8a 2 2 X-RAY DIFFRACTION
9r3n The structure of Aspergillus fumigatus phosphoglucose isomerase in complex with fragments 1 1 X-RAY DIFFRACTION
9r3o Structure of liver pyruvate kinase in complex with fluorescent probe 4a 2 2 X-RAY DIFFRACTION
9r3p Hemoglobin Glb2-1 of Lotus japonicus (cyano-ferric form) 2 2 X-RAY DIFFRACTION
9r3q The structure of Aspergillus fumigatus phosphoglucose isomerase in complex with an inhibitor 1 1 X-RAY DIFFRACTION