| 8rj2 |
Crystal structure of carbonic anhydrase II with N-butyl-4-chloro-2-(cyclohexylsulfanyl)-5-sulfamoylbenzamide |
18.5 |
57.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8rj3 |
Human RAD52 open ring conformation |
35.9 |
105.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rj4 |
E. coli adenylate kinase in complex with two ADP molecules and Mg2+ as a result of enzymatic AP4A hydrolysis |
36.3 |
127.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8rj5 |
P1-15 T-cell Receptor bound to HLA A*2402-NF9 pMHC complex |
44.7 |
151.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8rj6 |
E. coli adenylate kinase in complex with ATP and AMP and Mg2+ as a result of enzymatic AP4A hydrolysis. |
26.1 |
89.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8rj7 |
The crystal structure of the SARS-CoV-2 receptor binding domain in complex with the neutralizing nanobody 1.29 |
38.8 |
128.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8rj8 |
CytK nanopore mutant |
40.2 |
119.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8rj9 |
E. coli adenylate kinase Asp84Ala variant in complex with two ADP molecules as a result of enzymatic AP4A hydrolysis. |
25.9 |
81.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8rja |
;Crystal structure of the F420-reducing formylmethanofuran dehydrogenase complex from the ethanotroph Candidatus Ethanoperedens thermophilum
; |
56.6 |
196.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjb |
Structure of the rabbit 80S ribosome stalled on a 2-TMD rhodopsin intermediate in complex with Sec61-RAMP4 |
78.5 |
204.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rjc |
Structure of the rabbit 80S ribosome stalled on a 2-TMD rhodopsin intermediate in complex with Sec61-TRAP, open conformation 1 |
80.5 |
207.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rjd |
Structure of the rabbit 80S ribosome stalled on a 2-TMD rhodopsin intermediate in complex with Sec61-TRAP, open conformation 2 |
80.5 |
207.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rjf |
TadA/CpaF with ADP |
46.0 |
144.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rjh |
HLA A*2402-NF9_6F pMHC complex |
61.6 |
188.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8rji |
HLA A*2402-NF9_5R pMHC complex |
45.3 |
155.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjj |
HCV E1/E2 homodimer complex |
34.9 |
112.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rjk |
Pseudoatomic model of a second-order Sierpinski triangle formed by the citrate synthase from Synechococcus elongatus |
— |
467.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rjl |
Structure of a first order Sierpinski triangle formed by the H369R mutant of the citrate synthase from Synechococcus elongatus |
72.0 |
201.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8rjm |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in its Pfr state (I0a).
; |
41.0 |
142.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjn |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in its Pfr state (I0b).
; |
40.8 |
142.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8rjo |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I1 intermediate state.
; |
40.9 |
143.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8rjp |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I2 intermediate state.
; |
41.0 |
143.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjq |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I3 intermediate state.
; |
41.0 |
143.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8rjr |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I4 intermediate state.
; |
40.7 |
142.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjs |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I5 intermediate state.
; |
40.7 |
142.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjt |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I6 intermediate state.
; |
41.0 |
144.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8rju |
;Serial femtosecond X-ray structure of a fluorescence optimized bathy phytochrome PAiRFP2 derived from wild-type Agp2 in I7 intermediate state.
; |
40.8 |
143.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjv |
Crystal structure of SARS-CoV-2 main protease (MPro) in complex with the covalent inhibitor GUE-3778 (compound 12 in publication) |
22.4 |
83.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8rjw |
Human RAD52 open ring - ssDNA complex |
37.0 |
110.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rjx |
Solution structure of osmoregulator OsmY from E. coli. |
35.3 |
87.5 |
SOLUTION NMR |
REASONABLE
|
| 8rjy |
Crystal structure of SARS-CoV-2 main protease (MPro) in complex with the covalent inhibitor GUE-3899 (compound 58 in publication) |
22.6 |
80.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8rjz |
;Crystal structure of SARS-CoV-2 main protease (MPro) in complex with the non-covalent inhibitor GUE-3801 (compound 80 in publication)
; |
26.5 |
81.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8rk0 |
HCV E1/E2 homodimer complex, ectodomain |
31.2 |
100.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rk1 |
Crystal structure of FutA bound to Fe(III) solved by neutron diffraction |
20.7 |
66.3 |
NEUTRON DIFFRACTION |
GOOD
|
| 8rk2 |
Human Replication protein A (RPA; trimeric core) - ssDNA complex |
26.8 |
91.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8rk3 |
Bacteriophage JBD30 baseplate - composite structure |
— |
322.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rk4 |
Receptor binding protein of bacteriophage JBD30 computed with C3 symmetry |
36.7 |
124.8 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8rk5 |
Tail fibres of bacteriophage JBD30 |
44.3 |
142.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8rk6 |
Baseplate core of bacteriophage JBD30 computed in C3 symmetry |
57.7 |
190.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rk7 |
Baseplate of bacteriophage JBD30 computed in C3 symmetry |
57.7 |
190.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rk8 |
Tail of bacteriophage JBD30 computed in C6 symmetry |
29.1 |
108.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8rk9 |
Stopper protein of bacteriophage JBD30 computed in C6 symmetry |
18.3 |
61.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rka |
Connector complex of empty bacteriophage JBD30 particle computed in C12 symmetry |
44.4 |
161.5 |
ELECTRON MICROSCOPY |
SUSPICIOUS
|
| 8rkb |
Connector complex of bacteriophage JBD30 computed in C12 symmetry |
44.5 |
171.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8rkc |
Capsid of bacteriophage JBD30 decorated with minor capsid protein trimers computed in I4 symmetry |
57.6 |
200.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rkd |
TadA/CpaF with AMPPNP |
46.6 |
146.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8rke |
Crystal structure of the complete N-terminal region of human ZP2 (hZP2-N1N2N3) |
36.0 |
111.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8rkf |
Crystal structure of the ZP-N1 and ZP-N2 domains of human ZP2 (hZP2-N1N2) |
25.9 |
81.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8rkg |
Crystal structure of tetrameric collagenase-cleaved Xenopus ZP2-N2N3 (cleaved xZP2-N2N3) |
47.5 |
161.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8rkh |
Crystal structure of the ZP-N2 and ZP-N3 domains of mouse ZP2 (mZP2-N2N3) |
32.6 |
126.8 |
X-RAY DIFFRACTION |
REASONABLE
|