| 9j7l |
Structure of AAV8 capsid in complex with receptor |
39.0 |
121.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9j7m |
Cryo-EM structure of TauT |
25.4 |
86.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j7n |
Cryo-EM structure of TauT |
25.4 |
85.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j7o |
Cryo-EM structure of TauT |
25.6 |
85.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j7p |
Crystal structure of S. aureus MccB mutant S323A |
21.7 |
70.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9j7q |
Crystal structure of S. aureus MccB with PLP |
22.5 |
76.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9j7r |
Crystal structure of S. aureus MccB mutant K196A |
28.7 |
95.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9j7s |
;Crystal structure of 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase (DAHP synthase) from Providencia alcalifaciens complexed with Phe
; |
37.6 |
121.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j7t |
De Novo Designed Cell-Penetrating Peptide Self-Assembly Featuring Distinctive Tertiary Structure |
25.8 |
76.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9j7u |
H176A mutant of human G6PC1 in complex with G6P |
23.2 |
80.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j7v |
Human G6PC1 in apo state |
23.8 |
88.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j7w |
Channel Rhodospin from Klebsormidium nitens (KnChR) |
25.5 |
84.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j7x |
Crystal structure of quintuple mutant C terminal fragment of Clostridium perfringens enterotoxin (C-CPEm19) |
15.2 |
48.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9j7y |
the complex structure of MPXV M1R and nanobody M1R-01 |
20.6 |
72.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j82 |
Cryo-EM structure of wild type Aquifex aeolicus RseP in complex with Fab |
37.4 |
124.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j83 |
Cryo-EM structure of Aquifex aeolicus RseP E18Q mutant in complex with Fab |
37.3 |
121.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j84 |
Structureal mechanism of human TRPM3 ion channel inhibition |
48.1 |
140.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j85 |
The complex structure of okaE with a-ketoglutarate |
34.5 |
112.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9j87 |
Structure of Receptor |
36.9 |
117.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j88 |
Structures and mechanisms of serine protease inhibitors of Trichinella spiralis and Trichinella pseudospiralis |
27.1 |
87.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9j89 |
zbp1 nucleic acid complex |
32.9 |
118.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j8a |
Structure of antibody BA8 in complex with sulfated peptide from CCR5 |
25.8 |
88.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j8b |
Human Glycine Transporter 1 in the Apo State with an Inward-Facing Conformation |
25.9 |
84.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8c |
Human Glycine Transporter 1 in the Sarcosine-Bound State with an Occluded Conformation |
25.6 |
85.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8d |
Human Glycine Transporter 1 in the Iclepertin-Bound State with an Inward-Facing Conformation |
25.4 |
86.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8e |
;Structural insights into BirA from Haemophilus influenzae, a bifunctional protein as a biotin protein ligase and a transcriptional repressor
; |
27.9 |
85.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j8f |
;Structural insights into BirA from Haemophilus influenzae, a bifunctional protein as a biotin protein ligase and a transcriptional repressor
; |
28.6 |
86.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j8g |
mouse zbp1 hybrid complex |
13.0 |
40.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9j8i |
Mutant of a deep sea bacterial PET hydrolase MtCut |
40.7 |
132.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9j8k |
Crystal structure of the GluA2 ligand binding core (S1S2J) in complex with fluorophore-ligand conjugate |
20.4 |
65.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9j8l |
apo form of GMPK |
23.5 |
69.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j8m |
Cryo-EM structure of BAF-Lamin A/C IgF-nucleosome complex (High mobility complex) |
51.3 |
179.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9j8n |
Cryo-EM structure of BAF-Lamin A/C IgF-nucleosome complex (Low mobility complex) |
71.3 |
233.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8o |
Cryo-EM structure of BAF-Lamin A/C IgF-H1-nucleosome complex |
63.8 |
203.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8p |
Cryo-EM structure of human TUT1 complexed with U6 snRNA |
37.3 |
116.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9j8q |
MprF from Pseudomonas aeruginosa in GDN micelle, C2 symmetry |
42.1 |
136.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8r |
MprF from Pseudomonas aeruginosa in GDN micelle, C1 symmetry |
42.1 |
129.5 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9j8s |
MprF from Pseudomonas aeruginosa in nanodisc, C2 symmetry |
41.3 |
130.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8t |
Crystal structure of SARS-CoV-2 main protease in complex with Mp-4L2 |
22.5 |
78.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9j8u |
Crystal structure of SARS-CoV-2 main protease in complex with Mp-4D7 |
22.4 |
75.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9j8v |
TSWV L protein in complex with ribavirin 5-triphosphate |
37.3 |
111.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9j8w |
Cryo-EM structure of NCP-UV-DDB complex containing CPD |
44.0 |
140.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j8z |
Cryo-EM structure of human HCAR1-Gi complex without ligand (apo state) |
37.9 |
124.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j90 |
Crystal structure of Pseudomonas aeruginosa SuhB complexed with Gallic acid in orthorhombic space group |
24.2 |
84.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9j91 |
Structures and mechanisms of serine protease inhibitors of Trichinella spiralis and Trichinella pseudospiralis |
21.9 |
72.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9j92 |
Native GluA1/GluA4-CNIH3 complex in resting state |
48.2 |
159.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j93 |
Native GluA1/GluA4 ATD dimer binding with 1D8 and 11B8 |
42.8 |
151.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j94 |
Native GluA1/GluA4-CNIH3 complex in active state |
47.8 |
150.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j95 |
Native GluA1/GluA4-CNIH3 complex in desensitized state |
48.5 |
151.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j97 |
Closed structure of human XPR1 |
36.2 |
118.6 |
ELECTRON MICROSCOPY |
GOOD
|