PDB 编号 标题 Rg (Å) Dmax (Å) 实验方法 质量评级
8pbm Mutant R1789Q of the dihydroorotase domain of human CAD protein bound to the substrate dihydroorotate 20.0 61.2 X-RAY DIFFRACTION GOOD
8pbn Mutant R1789Q of the dihydroorotase domain of human CAD protein bound to the inhibitor fluoorotate 20.0 61.0 X-RAY DIFFRACTION GOOD
8pbo Deep interactome learning for generative drug design 26.2 84.4 X-RAY DIFFRACTION GOOD
8pbp Mutant R1785C of the dihydroorotase domain of human CAD protein bound to the substrate carbamoyl aspartate 19.9 60.7 X-RAY DIFFRACTION GOOD
8pbq Mutant R1810Q of the dihydroorotase domain of human CAD protein bound to the substrates 19.7 59.6 X-RAY DIFFRACTION EXCELLENT
8pbr Mutant R1475Q of the dihydroorotase domain of human CAD protein in apo form 20.0 62.1 X-RAY DIFFRACTION GOOD
8pbs Mutant K1482M of the dihydroorotase domain of human CAD protein in apo form 19.7 62.3 X-RAY DIFFRACTION REASONABLE
8pbt Mutant K1482M of the dihydroorotase domain of human CAD protein bound to the substrate dihydroorotate 20.0 61.7 X-RAY DIFFRACTION GOOD
8pbu Mutant K1482M of the dihydroorotase domain of human CAD protein bound to the inhibitor fluoorotate 19.9 60.3 X-RAY DIFFRACTION GOOD
8pbv Solution NMR structure of D. melanogaster TotA 14.7 48.6 SOLUTION NMR GOOD
8pbw Histidine-containing phosphotransfer protein from Chaetomium thermophilum 30.8 98.5 X-RAY DIFFRACTION GOOD
8pbx Single particle cryo-EM of the P140-P110 heterodimer of Mycoplasma genitalium at 3.3 Angstrom resolution. 39.8 127.0 ELECTRON MICROSCOPY GOOD
8pby ;Single particle cryo-EM of the P140-P110 heterodimer with an alternative conformation in the P140 stalk of Mycoplasma genitalium at a resolution of 3.7 Angstrom. ; 40.0 126.4 ELECTRON MICROSCOPY GOOD
8pbz Sub-tomogram average of the Nap adhesion complex from the human pathogen Mycoplasma genitalium at 11 Angstrom. 58.8 214.5 ELECTRON MICROSCOPY GOOD
8pc0 Sub-tomogram average of the open conformation of the Nap adhesion complex from the human pathogen Mycoplasma genitalium. 41.0 128.1 ELECTRON MICROSCOPY GOOD
8pc1 Sub-tomogram average of the closed conformation of the Nap adhesion complex from the human pathogen Mycoplasma genitalium. 40.2 127.6 ELECTRON MICROSCOPY GOOD
8pc2 SelDeg51 in complex with FKBP51FK1 domain and pVHL:EloB:EloC 33.5 104.8 X-RAY DIFFRACTION GOOD
8pc3 Crystal structure of Paradendryphiella salina PL7C alginate lyase in complex with pentamannuronic acid 17.8 57.5 X-RAY DIFFRACTION GOOD
8pc4 MEMBRANE TARGET COMPLEX 1 28.4 91.6 X-RAY DIFFRACTION GOOD
8pc5 H3K36me3 nucleosome-LEDGF/p75 PWWP domain complex 41.7 133.3 ELECTRON MICROSCOPY GOOD
8pc6 H3K36me3 nucleosome-LEDGF/p75 PWWP domain complex - pose 2 42.4 134.6 ELECTRON MICROSCOPY GOOD
8pc7 ;STRUCTURE OF ESTER-HYDROLASE EH3 FROM THE METAGENOME OF MARINE SEDIMENTS AT MILAZZO HARBOR (SICILY, ITALY) COMPLEXED WITH A DERIVATIVE OF BIPYRIDINE PHOSPHONATE ; 39.2 126.2 X-RAY DIFFRACTION GOOD
8pc8 Crystal structure of Paradendryphiella salina PL7C alginate lyase soaked with hexamannuronic acid 17.9 60.6 X-RAY DIFFRACTION GOOD
8pc9 Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 0 ms - native. 18.4 60.4 X-RAY DIFFRACTION REASONABLE
8pca Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 50 ms 18.4 61.6 X-RAY DIFFRACTION GOOD
8pcb Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 80 ms 18.4 67.8 X-RAY DIFFRACTION GOOD
8pcc Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 100 ms 18.5 68.1 X-RAY DIFFRACTION REASONABLE
8pcd Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 150 ms 18.4 62.0 X-RAY DIFFRACTION GOOD
8pce Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 250 ms 18.4 64.8 X-RAY DIFFRACTION GOOD
8pcf Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 500 ms 18.4 67.9 X-RAY DIFFRACTION REASONABLE
8pcg Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 2000 ms 18.4 60.3 X-RAY DIFFRACTION GOOD
8pch ;CRYSTAL STRUCTURE OF PORCINE CATHEPSIN H DETERMINED AT 2.1 ANGSTROM RESOLUTION: LOCATION OF THE MINI-CHAIN C-TERMINAL CARBOXYL GROUP DEFINES CATHEPSIN H AMINOPEPTIDASE FUNCTION ; 17.7 59.2 X-RAY DIFFRACTION GOOD
8pci Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 5000 ms 18.4 60.1 X-RAY DIFFRACTION GOOD
8pcj Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid, 10000 ms 18.4 59.9 X-RAY DIFFRACTION GOOD
8pck ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 0 ms ; 18.4 61.0 X-RAY DIFFRACTION GOOD
8pcl ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 50 ms ; 18.5 61.1 X-RAY DIFFRACTION GOOD
8pcm ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 80 ms ; 18.5 62.5 X-RAY DIFFRACTION REASONABLE
8pcn ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 100 ms ; 18.5 62.1 X-RAY DIFFRACTION GOOD
8pco ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 150 ms ; 18.5 61.1 X-RAY DIFFRACTION GOOD
8pcp ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 250 ms ; 18.5 61.5 X-RAY DIFFRACTION GOOD
8pcq ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 500 ms ; 18.4 61.7 X-RAY DIFFRACTION GOOD
8pcr ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 750 ms ; 18.5 63.1 X-RAY DIFFRACTION REASONABLE
8pcs ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 1250 ms ; 18.5 60.6 X-RAY DIFFRACTION GOOD
8pct ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 2500 ms ; 18.5 61.1 X-RAY DIFFRACTION GOOD
8pcu ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 5000 ms ; 18.5 60.1 X-RAY DIFFRACTION GOOD
8pcv ;Structure of serine-beta-lactamase CTX-M-14 following the time-resolved active site binding of boric acid and subsequent glycerol-boric acid-ester formation, 10000 ms ; 18.5 60.0 X-RAY DIFFRACTION GOOD
8pcw ;Structure of Csm6' from Streptococcus thermophilus ; 34.2 113.6 X-RAY DIFFRACTION GOOD
8pcx Crystal structure of Paradendryphiella salina PL7C alginate lyase soaked with tetramannuronic acid 18.0 57.2 X-RAY DIFFRACTION GOOD
8pcz Ligand-free SpSLC9C1 in lipid nanodiscs, dimer 41.9 134.0 ELECTRON MICROSCOPY GOOD
8pd0 cryo-EM structure of Doa10 in MSP1E3D1 38.5 129.2 ELECTRON MICROSCOPY GOOD