| 9arj |
CryoEM structure of BoNT-NTNH-OrfX2 complex from Clostridium botulinum E1, major class |
59.8 |
208.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9ark |
CryoEM structure of BoNT-NTNH-OrfX2 complex from Clostridium botulinum E1, minor class |
53.3 |
190.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9arl |
CryoEM structure of BoNT-NTNH-OrfX2 complex from Clostridium botulinum strain A1-ST7B, major class |
60.0 |
209.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9arn |
Structure and interactions of HIV-1 gp41 CHR-NHR reverse hairpin constructs reveal molecular determinants of antiviral activity |
22.7 |
81.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9aro |
Crystal structure of AF9 YEATS domain in complex with acetylated at K1007 MOZ |
34.4 |
114.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9arp |
Structure and interactions of HIV-1 gp41 CHR-NHR reverse hairpin constructs reveal molecular determinants of antiviral activity |
37.3 |
135.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9arq |
Crystal structure of SARS-CoV-2 main protease (authentic protein) in complex with an inhibitor TKB-245 |
22.5 |
75.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9arr |
Crystal structure of AF9 YEATS domain in complex with dicrotonylated at K1007 and K1014 MOZ |
29.8 |
108.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9ars |
Crystal structure of SARS-CoV-2 main protease E166V mutant in complex with an inhibitor TKB-245 |
26.5 |
82.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9art |
Crystal structure of SARS-CoV-2 main protease A191T mutant in complex with an inhibitor 5h |
26.4 |
83.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9aru |
COVA2-15 fragment antigen binding in complex with SARS-CoV-2 6P-mut7 S protein |
55.9 |
188.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9arv |
CryoEM structure of AMETA-A3 |
56.9 |
176.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9arw |
Structure of the guideless DtCmr Type III CRISPR complex |
45.2 |
153.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9arx |
;Local refinement of 5-HT2AR bound to 5-HT in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
20.0 |
66.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ary |
;Global reconstruction 5-HT2AR bound to 5-HT in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
36.9 |
120.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9arz |
;Local refinement of 5-HT2AR bound to 2-bromo-LSD in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
19.9 |
65.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as0 |
;Global reconstruction of 5-HT2AR bound to 2-bromo-LSD in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
36.5 |
117.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as1 |
Local refinement of 5-HT2AR bound to DMT in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM) |
19.8 |
64.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as2 |
;Global reconstruction of 5-HT2AR bound to DMT in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
35.9 |
115.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9as3 |
Local refinement of 5-HT2AR bound to LSD in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM) |
19.9 |
64.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as4 |
;Global reconstruction of 5-HT2AR bound to LSD in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
36.3 |
117.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as5 |
;Local refinement of 5-HT2AR bound to Mescaline in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
20.0 |
65.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as6 |
;Global reconstruction of 5-HT2AR bound to mescaline in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
36.8 |
119.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as7 |
Local refinement of 5-HT2AR bound to psilocin in complex with a mini-Gq and scFv16 obtained by cryo-electron microscopy (cryoEM) |
20.2 |
66.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9as8 |
;Global reconstruction of 5-HT2AR bound to psilocin in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
36.7 |
120.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9as9 |
;Local refinement of 5-HT2AR bound to RS130-180 in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
20.3 |
64.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9asa |
;Global reconstruction of 5-HT2AR bound to RS130-180 in complex with a mini-Gq protein and scFv16 obtained by cryo-electron microscopy (cryoEM)
; |
36.7 |
119.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asb |
Structure of human calcium-sensing receptor in complex with chimeric Gq (miniGisq) protein in nanodiscs |
74.3 |
215.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9asc |
;Cryo-EM Structure of the Glycosyltransferase ArnC from Salmonella enterica in the UDP-bound State Determined on Talos Arctica microscope
; |
36.2 |
106.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asd |
VIR-7229 Fab fragment bound the SARS-CoV-2 BA.2.86 spike trimer (local refinement of the BA 2.86 RBD/VIR-7229 VHVL) |
24.6 |
83.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asf |
Crystal structure of HLA-A*03:01 in complex with a wild-type PIK3CA peptide analogue (Trp-6 Bta) |
24.0 |
74.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9asg |
Crystal structure of HLA-A*03:01 in complex with a mutant PIK3CA peptide analogue (Trp-6 Bta) |
24.1 |
74.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9ash |
Cryo-EM structure of the active Lactococcus lactis Csm bound to target in post-cleavage stage |
55.0 |
197.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asi |
Cryo-EM structure of the active Lactococcus lactis Csm bound to target in pre-cleavage stage |
54.8 |
186.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asj |
Human DNA polymerase theta helicase domain in complex with AMP-PNP, dimer form |
41.0 |
139.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ask |
Human DNA polymerase theta helicase domain dimer, apo-form |
40.9 |
140.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asl |
Human DNA polymerase theta helicase domain tetramer, apo-form |
51.0 |
151.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asm |
Human Drosha and DGCR8 in complex with Pri-let-7f1 |
45.6 |
177.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9asn |
Human Drosha and DGCR8 in complex with Pri-miR-98 |
46.2 |
183.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9aso |
Human Drosha and DGCR8 in complex with Pri-let-7a2 |
38.6 |
142.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9asp |
Human Drosha and DGCR8 in complex with Pri-let-7a1 |
46.5 |
179.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asq |
Human Drosha, DGCR8 and SRSF3 in complex with Pri-let-7f1 |
46.5 |
178.8 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9ass |
Crystal Structure of Neutrophil Elastase Inhibited by Eap4 from S. aureus |
20.8 |
68.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9ast |
Cryo-EM structure of XCR1 signaling complex |
37.9 |
124.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9asv |
Crystal structure of SARS-CoV-2 3CL protease in complex with a benzyl 2-pyrrolidone inhibitor |
26.5 |
81.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9asw |
Crystal structure of SARS-CoV-2 3CL protease in complex with a m-fluorobenzyl 2-pyrrolidone inhibitor |
26.5 |
81.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9asx |
BIFUNCTIONAL INHIBITION OF NEUTROPHIL ELASTASE AND CATHEPSIN G by Eap3 of S. aureus |
29.1 |
101.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9asy |
Crystal structure of SARS-CoV-2 3CL protease in complex with a m-chlorobenzyl 2-pyrrolidone inhibitor |
26.6 |
80.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9asz |
Crystal structure of SARS-CoV-2 3CL protease in complex with a phenylethyl 2-pyrrolidone inhibitor |
26.5 |
82.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9at0 |
Crystal structure of SARS-CoV-2 3CL protease in complex with a methylcyclohexyl 2-pyrrolidone inhibitor (S-enantiomer) |
26.5 |
82.1 |
X-RAY DIFFRACTION |
EXCELLENT
|