| 9e0s |
Cryo-EM structure of a the periplasmic insert from Myxococcus TAtC |
25.1 |
80.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0t |
Cryo-EM structure of human cytoplasmic dynein-1 bound to LIS1 in the presence of ATP |
54.1 |
185.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0u |
Cryo-EM structure of human cytoplasmic dynein-1 in the presence of ATP |
48.2 |
183.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0v |
GSDMD bound to a peptide |
19.6 |
61.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0w |
Cryo-EM structure of human cytoplasmic dynein-1 bound to LIS1 in the presence of ATP |
50.7 |
185.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0x |
Cryo-EM structure of Phi dynein |
64.2 |
222.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0y |
Cryo-EM structure of human cytoplasmic dynein-1 in the presence of ATP |
48.3 |
159.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0z |
Dimeric motor domains from phi-like dynein-1 bound to a Lis1 dimer under Nde1-Lis1 condition |
64.4 |
209.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e10 |
Dimeric motor domains from phi dynein-1 under Lis1 condition |
64.5 |
231.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e11 |
Dimeric motor domains from phi-like dynein-1 bound to a Lis1 dimer under Lis1 condition |
64.4 |
209.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e12 |
Full-length human dynein-1 in phi comformation under Lis1 condition |
— |
426.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e13 |
Full-length human dynein-1 in phi-like comformation bound to a Lis1 dimer under Lis1 condition |
— |
430.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e14 |
Full-length human dynein-1 in phi-like comformation bound to a Lis1 dimer under Nde1-Lis1 condition |
— |
430.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e15 |
Alpha-Delta heterodimeric form of soluble hydrogenase I from Pyrococcus furiosus. Data processed and model refined in P1 |
62.4 |
209.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9e17 |
Structure of RyR1 in the primed state in the presence of caffeine (reprocessed/reanalyzed from EMPIAR-10997, 7TZC, EMD-26205) |
— |
269.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e18 |
Structure of RyR1 in the primed state in the presence of pentoxifylline |
— |
270.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e19 |
Structure of RyR1 in the open state in the presence of pentoxifylline |
— |
272.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1a |
Structure of RyR1 in the primed state in the presence of dyphylline |
— |
270.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1b |
Structure of RyR1 in the open state in the presence of dyphylline |
— |
273.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1c |
Structure of RyR1 in the primed state in the presence of IBMX |
— |
270.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1d |
Structure of RyR1 in the primed state in the presence of enprofylline |
— |
271.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1e |
Structure of RyR1 in the primed state in the presence of uracil |
— |
270.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1f |
Structure of RyR1 in the primed state in the presence of allopurinol |
— |
271.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1g |
Structure of RyR1 in the primed state in the presence of oxypurinol |
— |
270.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1h |
Structure of RyR1 in the primed state in the presence of oxopyricid |
— |
270.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1i |
Structure of RyR1 in the open state in the presence of oxopyricid |
— |
273.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e1j |
Alpha-Delta heterodimeric form of soluble hydrogenase I from Pyrococcus furiosus. Data processed and model refined in P21221 |
39.6 |
129.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9e1k |
Discovery of Potent, Highly Selective and Efficacious SMARCA2 Degraders - Compound 11 |
23.7 |
74.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9e1l |
Snf2h bound nucleosome complex - ClassA1 |
45.2 |
142.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1m |
Snf2h bound nucleosome complex - ClassA2 |
45.2 |
148.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1n |
Snf2h bound nucleosome complex-ClassA3 |
45.2 |
148.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1o |
Snf2h bound nucleosome complex - ClassB1 |
45.0 |
148.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1p |
Snf2h bound nucleosome complex - ClassB2 |
45.2 |
149.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1q |
Snf2h bound nucleosome complex - ClassB3 |
45.3 |
147.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1r |
Snf2h bound nucleosome complex - ClassB4 |
45.2 |
147.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1t |
CryoEM structure of LARGE1 bound to UDP-GlcA |
34.1 |
104.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1u |
Snf2h bound nucleosome complex - ClassC1 |
45.4 |
150.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1v |
Snf2h bound nucleosome complex - ClassC2 |
45.4 |
147.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1w |
Snf2h bound nucleosome complex - ClassC3 |
45.4 |
147.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1x |
Snf2h bound nucleosome complex - ClassD1 |
45.2 |
145.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1y |
Empty Nucleosome with 601 widom sequence |
41.3 |
120.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e1z |
[F:Hg2+:T] Mercury base pair with 2-thiothymidine and thymine |
21.1 |
73.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9e20 |
[iU:Hg2+:F] Mercury base pair with 2-thiothymidine and iodouracil |
20.6 |
72.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9e21 |
CryoEM structure of a broadly neutralizing anti-SARS-CoV-2 antibody 52 |
25.4 |
97.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e22 |
Cryo-EM structure of human cytoplasmic dynein-1 bound to LIS1 in the presence of ATP |
50.4 |
164.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e23 |
Cryo-EM structure of Pre-Chi dynein tail |
93.1 |
251.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e24 |
Closed structure of CpaF without nucleotides (Apo dataset) |
44.0 |
136.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e25 |
Compact structure of CpaF without nucleotides (Apo dataset) |
44.4 |
139.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e26 |
Compact structure of CpaF with two ATPs and two ADPs (Under-saturated ATP/ADP dataset) |
44.3 |
139.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9e27 |
Expanded structure of CpaF with two ATPs and four ADPs (Under-saturated ATP/ADP dataset) |
45.0 |
141.6 |
ELECTRON MICROSCOPY |
GOOD
|