| 9ktf |
Ni(II)-bound Bacillus subtilis CpfC (HemH) Y13C variant modified with bromobimane |
21.3 |
68.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9ktg |
Cu(II)-bound CpfC (HemH) Y13C variant modified with bromobimane |
21.2 |
68.3 |
X-RAY DIFFRACTION |
GOOD
|
| 9kth |
Zn(II)-bound CpfC (HemH) Y13C variant modified with bromobimane |
21.0 |
68.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9kti |
CryoEM structure of a 2,3-hydroxycinnamic acid 1,2-dioxygenase MhpB in substrate bound form |
48.1 |
144.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ktj |
Solution NMR structures of ATP-binding DNA aptamer in complex with ATP |
15.5 |
50.8 |
SOLUTION NMR |
GOOD
|
| 9ktk |
Crystal structure of human SIRT3 with its activator SKLB-11A |
34.3 |
109.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9ktm |
Alpha-hemolysin heptameric pre-pore state bound to 10:PC lipid chains derived from 10:0 PC liposomes. |
39.1 |
109.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kto |
Alpha-hemolysin heptameric late pre-pore state with bound lipids derived from 10:0 PC/Sphingomyelin liposomes |
39.3 |
109.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ktp |
Fe(II)/2-oxoglutarate-dependent dioxygenase UcsF in complexed with Ni and N-oxalylglycine (NOG) |
29.2 |
94.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9ktq |
Crystal structure of the pathogen-secreted apoplastic GH12 xyloglucan-specific endoglucanase XEG1 |
18.0 |
59.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9kts |
Structure of TauT in the apo state |
24.9 |
84.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ktt |
Structure of TauT in complex with taurine |
24.8 |
83.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ktu |
Structure of TauT in complex with beta-alanine |
24.4 |
83.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ktv |
Structure of TauT in complex with GABA |
24.8 |
82.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ktw |
;Cryo-EM structure of wild type RIG-I with 5'p-RNA
; |
29.0 |
90.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9ktx |
Structure of TauT in complex with Guanidinoethyl sulfonate |
24.8 |
84.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kty |
Cryo-EM structure of the TIA-1 prion-like domain amyloid fibril, WT |
22.6 |
85.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9ktz |
Cryo-EM structure of the TIA-1 prion-like domain amyloid fibril, G355R |
15.9 |
43.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9ku0 |
Crystal structure of CtpA F105R mutant from Helicobacter pylori |
40.5 |
137.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9ku1 |
Cryo-electron microscopy structure of nanofibers formed by reverse azobenzene peptides. |
22.0 |
73.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ku2 |
Structure of taterapox core protease central domain |
17.1 |
52.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9ku3 |
Cryo-EM structure of CtpA S300A/K325A/Q329A mutant from Helicobacter pylori |
52.1 |
157.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ku4 |
;Cryo-EM structure of E373A mutant RIG-I with 5'p-RNA
; |
29.1 |
90.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9ku5 |
;Crystal structure of substrate bound GH5_22 exo-beta-xylosidase from the seaweed-derived thermophile Geobacillus thermodenitrificans OS27
; |
30.4 |
98.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9ku6 |
Crystal structure of the complex of lactoperoxidase with nitric oxide at 1.72 A resolution |
24.8 |
83.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9ku8 |
Solution NMR structure of P1 peptide bound with E. coli LPS |
9.9 |
44.4 |
SOLUTION NMR |
REASONABLE
|
| 9ku9 |
Structure of mpox core protease mutant |
33.6 |
112.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kua |
Crystal structure of GH5_22 exo-beta-xylosidase from the seaweed-derived thermophile Geobacillus thermodenitrificans OS27 |
30.3 |
97.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9kub |
Cryo-EM structure of CtpA from Helicobacter pylori in conformation I |
51.6 |
150.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kuc |
Cryo-EM structure of CtpA from Helicobacter pylori in conformation II |
51.1 |
148.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kud |
Crystal structure of SARS-CoV-2 JN.1 variant RBD complexed with squirrel ACE2 |
41.4 |
133.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9kue |
Crystal structure of the soluble green pigment protein from Tettigonia cantans |
28.1 |
90.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9kuf |
Cryo-EM structure of HsClpP bound to CLPP-2068 |
42.2 |
116.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kug |
Structure of EP67 bound to human C5aR1 in complex with Go |
38.9 |
129.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9kuh |
Co-crystal structure of wild-type OYE2 with 2-(prop-1-en-2-yl)pyridine |
41.7 |
130.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kui |
Crystal Structure of the Kv7.1 C-terminal Domain in Complex with Calmodulin disease mutation F142L |
18.2 |
60.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kuj |
Structure of quinone oxidoreductase from Rouxiella badensis |
30.0 |
98.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9kuk |
Bovine Heart Cytochrome c Oxidase in the Xenon-bound Fully Oxidized State under Aerobic Condition |
— |
— |
X-RAY DIFFRACTION |
—
|
| 9kul |
Bovine Heart Cytochrome c Oxidase in the Xenon-bound Fully Oxidized State under Anaerobic Condition |
— |
— |
X-RAY DIFFRACTION |
—
|
| 9kum |
Bovine Heart Cytochrome c Oxidase in the Xenon-bound Fully Reduced State |
— |
— |
X-RAY DIFFRACTION |
—
|
| 9kun |
Crystal structure of ligand-free trypanosome alternative oxidase |
38.6 |
134.3 |
X-RAY DIFFRACTION |
GOOD
|
| 9kuo |
Crystal Structure of the Kv7.1 C-terminal Domain in Complex with Calmodulin disease mutation Q136P |
25.9 |
84.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kup |
Crystal structure of MCP2201LBD |
20.4 |
63.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kuq |
Crystal structure of a C45 isoprenyl diphosphate synthase, Rv0562 from Mycobacterium tuberculosis |
21.1 |
65.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kur |
Crystal structure of mAb nCoV400Fab with SARS-CoV-2 N-CTD Complex |
35.5 |
110.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9kus |
Cryo-EM structure of C-Methyltransferase from Rhododendron dauricum |
29.9 |
101.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kut |
Structure of JR14a bound to human C3aR in complex with Go |
37.8 |
122.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kuu |
Crystal Structure of the Kv7.1 C-terminal Domain in Complex with Calmodulin disease mutation D130G |
26.1 |
82.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kuv |
Mechanistic insights into the versatile stoichiometry and biased signaling of the apelin receptor-arrestin complex |
36.5 |
124.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9kuw |
Cryo-EM structure of dimeric APJR and two Beta-arrestins complex with small molecules |
44.5 |
138.0 |
ELECTRON MICROSCOPY |
GOOD
|