PDB 编号 标题 Rg (Å) Dmax (Å) 实验方法 质量评级
8geq E. eligens beta-glucuronidase bound to ceritinib-glucuronide 25.4 90.7 X-RAY DIFFRACTION GOOD
8ger E. eligens beta-glucuronidase bound to norquetiapine-glucuronide 25.0 78.2 X-RAY DIFFRACTION EXCELLENT
8ges R. hominis 2 beta-glucuronidase bound to UNC10201652-glucuronide 53.5 194.6 X-RAY DIFFRACTION GOOD
8get R. hominis 2 beta-glucuronidase bound to norquetiapine-glucuronide 53.4 194.4 X-RAY DIFFRACTION GOOD
8geu ;Crystal structure of human cellular retinol binding protein 1 in complex with methyl({3-[1-(4-methylphenyl)cyclopentyl]-1,2,4-oxadiazol-5-yl}methyl)[(1-methylpyrazol-4-yl)methyl]amine ; 15.8 49.0 X-RAY DIFFRACTION GOOD
8gev ;Crystal structure of human cellular retinol binding protein 1 in complex with 1-{[3-(diphenylmethyl)-1,2,4-oxadiazol-5-yl]methyl}-4-(methoxymethyl)piperidine ; 15.7 47.8 X-RAY DIFFRACTION EXCELLENT
8gew H-FABP crystal soaked in a bromo palmitic acid solution 15.4 49.5 X-RAY DIFFRACTION GOOD
8gex Crystal structure of the ferric enterobactin transporter (XusB) from Bacteroides thetaiotaomicron 49.9 159.5 X-RAY DIFFRACTION GOOD
8gey ;Crystal structure of human cellular retinol binding protein 1 in complex with 4-(hydroxymethyl)-1-[(4-methoxy-5,6,7,8-tetrahydronaphthalen-1-yl)sulfonyl]piperidin-4-ol ; 15.8 48.9 X-RAY DIFFRACTION GOOD
8gez Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with LV8036 inhibitor 28.0 86.7 X-RAY DIFFRACTION EXCELLENT
8gf0 Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with LV8044 inhibitor 28.1 87.0 X-RAY DIFFRACTION EXCELLENT
8gf1 Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with LV8060 inhibitor 28.1 86.1 X-RAY DIFFRACTION EXCELLENT
8gf2 Crystal structure of SARS-CoV-2 receptor binding domain in complex with antibodies eCR3022.20 and CC12.3 54.4 193.3 X-RAY DIFFRACTION GOOD
8gf3 Crystallographic structure from BlMan5_7 20.3 59.5 X-RAY DIFFRACTION EXCELLENT
8gf4 Crystal structure of Domain Related to Iron (DRI) in complex with heme 24.9 77.2 X-RAY DIFFRACTION EXCELLENT
8gf5 McrD binds asymmetrically to methyl-coenzyme M reductase improving active site accessibility during assembly 39.1 126.1 ELECTRON MICROSCOPY GOOD
8gf6 Apo-apo MCR assembly intermediate 39.1 124.7 ELECTRON MICROSCOPY GOOD
8gf7 Cryo-EM structure of serine 87 O-GlcNAc-modified alpha-synuclein fibrils 35.8 122.8 ELECTRON MICROSCOPY GOOD
8gf8 Cryo-EM structure of human TRPV1 in cNW11 nanodisc and soybean lipids 47.2 144.3 ELECTRON MICROSCOPY GOOD
8gf9 Cryo-EM structure of human TRPV1 in cNW11 nanodisc and POPC:POPE:POPG lipids 43.3 130.8 ELECTRON MICROSCOPY GOOD
8gfa Cryo-EM structure of human TRPV1 in complex with the analgesic drug SB-366791 43.5 131.6 ELECTRON MICROSCOPY GOOD
8gfb Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Fv16b inhibitor 28.0 86.1 X-RAY DIFFRACTION EXCELLENT
8gfc Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Fv17b inhibitor 28.1 86.2 X-RAY DIFFRACTION EXCELLENT
8gfd Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z3252 inhibitor 28.1 86.7 X-RAY DIFFRACTION EXCELLENT
8gfe Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z3261 inhibitor 28.1 86.2 X-RAY DIFFRACTION EXCELLENT
8gff Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7146 inhibitor 28.1 87.1 X-RAY DIFFRACTION EXCELLENT
8gfg Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7912 inhibitor 28.1 87.2 X-RAY DIFFRACTION EXCELLENT
8gfh ;Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7285 inhibitor soaked at 10 mM concentration ; 28.1 84.2 X-RAY DIFFRACTION EXCELLENT
8gfi ;Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Z7285 inhibitor soaked at 3 mM concentration ; 28.1 87.2 X-RAY DIFFRACTION EXCELLENT
8gfj ;Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni dose-response soaking with 1 mM concentration Z7285 inhibitor (no inhibitor binding observed) ; 28.1 87.3 X-RAY DIFFRACTION EXCELLENT
8gfk Room temperature X-ray structure of truncated SARS-CoV-2 main protease C145A mutant, residues 1-304 22.7 79.8 X-RAY DIFFRACTION GOOD
8gfl ;Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with 4-Nitrophenyl N,N' diacetyl-beta-D-chitobioside inhibitor ; 28.0 85.5 X-RAY DIFFRACTION EXCELLENT
8gfm Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with zanamivir amine inhibitor 28.1 86.2 X-RAY DIFFRACTION EXCELLENT
8gfn Room temperature X-ray structure of truncated SARS-CoV-2 main protease C145A mutant, residues 1-304, in complex with BBH1 26.7 82.7 X-RAY DIFFRACTION EXCELLENT
8gfo Room temperature X-ray structure of truncated SARS-CoV-2 main protease C145A mutant, residues 1-304, in complex with GC373 22.7 78.8 X-RAY DIFFRACTION GOOD
8gfp ;Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with N-acetyl-2,3-dehydro-2-deoxyneuraminic acid inhibitor ; 28.2 87.6 X-RAY DIFFRACTION EXCELLENT
8gfq Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with Fv32r inhibitor 28.0 86.0 X-RAY DIFFRACTION EXCELLENT
8gfr Room temperature X-ray structure of truncated SARS-CoV-2 main protease C145A mutant, residues 1-304, in complex with NBH2 22.7 78.2 X-RAY DIFFRACTION GOOD
8gfs Crystal structure of soluble lytic transglycosylase Cj0843 of Campylobacter jejuni in complex with siastatin B inhibitor 28.1 87.2 X-RAY DIFFRACTION EXCELLENT
8gft Hsp90 provides platform for CRaf dephosphorylation by PP5 46.9 170.4 ELECTRON MICROSCOPY GOOD
8gfu ;Room temperature X-ray structure of truncated SARS-CoV-2 main protease C145A mutant, residues 1-304, in complex with nirmatrelvir (NMV) ; 22.6 79.8 X-RAY DIFFRACTION GOOD
8gfv CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #1 of 20) 34.5 115.7 ELECTRON MICROSCOPY GOOD
8gfw CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #2 of 20) 34.6 115.1 ELECTRON MICROSCOPY GOOD
8gfx CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #3 of 20) 34.7 115.3 ELECTRON MICROSCOPY GOOD
8gfy CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #4 of 20) 34.6 115.9 ELECTRON MICROSCOPY GOOD
8gfz CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #5 of 20) 34.7 115.2 ELECTRON MICROSCOPY GOOD
8gg0 CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #6 of 20) 34.8 116.0 ELECTRON MICROSCOPY GOOD
8gg1 CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #7 of 20) 34.8 116.8 ELECTRON MICROSCOPY GOOD
8gg2 CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #8 of 20) 34.9 117.9 ELECTRON MICROSCOPY GOOD
8gg3 CryoEM structure of beta-2-adrenergic receptor in complex with GTP-bound Gs heterotrimer (transition intermediate #9 of 20) 34.9 115.5 ELECTRON MICROSCOPY GOOD