| 8sfk |
Crystal structure of the engineered SsoPox variant IVE2 |
19.8 |
60.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8sfl |
WT CRISPR-Cas12a with a 15bp R-loop |
39.1 |
132.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sfm |
Crystal structure of the engineered SsoPox variant IVB10 in alternate state |
19.4 |
59.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8sfn |
WT CRISPR-Cas12a with a 16bp R-loop and nontarget strand in the RuvC active site. |
37.6 |
124.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8sfo |
WT CRISPR-Cas12a with a 20bp R-loop and nontarget strand in the RuvC active site. |
37.8 |
132.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sfp |
WT CRISPR-Cas12a with the target strand in the RuvC active site. |
37.5 |
124.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sfq |
WT CRISPR-Cas12a post nontarget strand-cleavage with the the RuvC active site exposed. |
37.9 |
131.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sfr |
WT CRISPR-Cas12a post nontarget strand cleavage. |
38.5 |
134.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8sfs |
High Affinity nanobodies against GFP |
31.6 |
106.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8sft |
Crystal structure of TuUGT202A2 (Tetur22g00270) in complex with kaempferol |
— |
— |
X-RAY DIFFRACTION |
—
|
| 8sfu |
Crystal structure of TuUGT202A2 (Tetur22g00270) in complex with naringin |
31.0 |
96.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8sfv |
High affinity nanobodies to GFP |
22.3 |
72.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8sfw |
Crystal structure of TuUGT202A2 (Tetur22g00270) in complex with quercetin |
22.2 |
69.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8sfx |
High Affinity nanobodies against GFP |
32.7 |
102.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8sfy |
Crystal structure of TuUGT202A2 (Tetur22g00270) in complex with UDP-glucose |
22.6 |
71.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8sfz |
High Affinity nanobodies against GFP |
35.6 |
115.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8sg0 |
Crystal Structure of GDP-manose 3,5 epimerase de Myrciaria dubia in complex with substrate, product and NAD |
28.4 |
96.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8sg1 |
Cryo-EM structure of CMKLR1 signaling complex |
37.7 |
122.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sg2 |
BIVALENT INTERACTIONS OF PIN1 WITH THE C-TERMINAL TAIL OF PKC |
17.6 |
61.7 |
SOLUTION NMR |
REASONABLE
|
| 8sg3 |
High Affinity nanobodies against GFP |
22.0 |
71.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8sg4 |
E1435Q Ycf1 mutant in dephosphorylated state |
42.3 |
145.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sg5 |
Cytochrome P450 (CYP) 3A5 crystallized with clotrimazole |
53.6 |
166.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8sg6 |
SARS-CoV-2 Main Protease (Mpro) H163A Mutant Reduced with 20mM TCEP |
27.1 |
84.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8sg7 |
Adeno-Associated Virus Bat origin capsid protein basic regions in complex with importin-alpha 2 |
28.1 |
98.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8sg8 |
CCT G beta 5 complex closed state 1 |
65.3 |
163.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sg9 |
CCT G beta 5 complex closed state 3 |
65.8 |
162.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8sga |
Crystal structure of 770E11, a monoclonal antibody isolated from a human Epstein-Barr virus seropositive donor |
25.1 |
79.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8sgb |
Crystal Structure of CD1d-lipid complexed with Beta-2-Microglobulin, TCR Alpha-Chain and TCR Beta-Chain |
39.6 |
142.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgc |
CCT G beta 5 complex closed state 2 |
65.3 |
164.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8sgd |
Crystal Structure of CDC3(G) - CDC10(Delta 1-10) heterocomplex from Saccharomyces cerevisiae |
36.6 |
124.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8sge |
KLHDC2 Kelch Domain with ligand KDRLKZ-1 |
29.6 |
97.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgf |
KLHDC2 Kelch Domain with KLHDC2 c-terminal peptide bound |
29.4 |
100.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgg |
;Crystal structure of Cy137D09, a monoclonal antibody isolated from macaques immunized with an Epstein-Barr virus glycoprotein 350 (gp350) nanoparticle vaccine
; |
31.1 |
98.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgh |
Cryo-EM structure of Karyopherin-beta2 bound to HNRNPH2 PY-NLS |
35.4 |
111.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sgi |
Cryo-EM structure of human NCX1 in complex with SEA0400 |
41.9 |
141.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sgj |
Cryo-EM structure of human NCX1 in apo inactivated state |
41.9 |
141.5 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8sgk |
CryoEM structure of Deinococcus radiodurans BphP photosensory module in Pr state |
33.3 |
100.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8sgl |
CCT G beta 5 complex closed state 15 |
65.2 |
163.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sgm |
Crystal Structure of CD1d-lipid complexed with Beta-2-Microglobulin, TCR Alpha-Chain and TCR Beta-Chain |
39.0 |
129.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgn |
;Crystal structure of Epstein-Barr virus glycoprotein 350 (gp350) in complex with Cy651H02, a monoclonal antibody isolated from macaques immunized with a gp350 nanoparticle vaccine
; |
36.2 |
129.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgo |
Human GABAA receptor alpha1-beta2-gamma2 subtype in complex with GABA plus pregnenolone sulfate |
43.5 |
141.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sgp |
human liver mitochondrial Medium-chain specific acyl-CoA dehydrogenase |
35.2 |
108.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8sgq |
CCT G beta 5 complex intermediate state |
70.4 |
218.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sgr |
human liver mitochondrial Isovaleryl-CoA dehydrogenase |
34.9 |
105.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8sgs |
human liver mitochondrial Short-chain specific acyl-CoA dehydrogenase |
34.8 |
106.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8sgt |
Cryo-EM structure of human NCX1 in Ca2+ bound, activated state (group II in the presence of 0.5 mM Ca2+) |
46.5 |
154.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8sgu |
Crystal structure of the SARS-CoV-2 receptor binding domain |
19.9 |
74.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8sgv |
human liver mitochondrial Catalase |
37.0 |
114.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8sgw |
Pendrin in complex with chloride |
35.8 |
111.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8sgx |
Leishmania tarentolae propionyl-CoA carboxylase (alpha-4-beta-6) |
63.7 |
209.9 |
ELECTRON MICROSCOPY |
GOOD
|