| 9kfb |
RABV-G-ecto/NM57-scFv complex |
49.3 |
144.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfc |
Crystal structure of the PIN1 and fragment 40 complex. |
16.4 |
56.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfd |
Truncated Fzo1,GTP-bound |
30.9 |
94.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kfe |
Truncated Fzo1 with modified LB, GTP-bound |
23.2 |
77.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kff |
Truncated Fzo1 with modified LB, transition-like state |
23.5 |
78.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfh |
Crystal structure of the PIN1 and fragment 52 complex |
16.3 |
56.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfi |
Cryo-EM structure of the human relaxin family peptide receptor 3 in complex with relaxin-3 and G protein |
39.0 |
126.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kfj |
Cryo-EM structure of the compound 4-bound human relaxin family peptide receptor 3 (RXFP3)-Gi complex |
37.5 |
122.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kfk |
Cryo-EM structure of the relaxin-3-bound human relaxin family peptide receptor 4 (RXFP4)-Gi complex |
39.1 |
128.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kfl |
KRAS G12V and peptide complex |
37.4 |
134.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfm |
Structure of WDR5 in complex with WIN motif containing EMBOW |
27.4 |
85.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfn |
Structure of WDR5 in complex with mutated EMBOW T3V |
18.8 |
56.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kfo |
Structure of WDR5 in complex with mutated EMBOW |
18.8 |
54.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfp |
Proline engineered disulfide rich peptides |
6.6 |
20.1 |
SOLUTION NMR |
GOOD
|
| 9kfq |
Loop4 engineered disulfide-rich peptides |
8.1 |
27.6 |
SOLUTION NMR |
GOOD
|
| 9kfr |
A multi cyclic peptide binding to TROP2 protein |
7.6 |
24.2 |
SOLUTION NMR |
GOOD
|
| 9kfs |
A multi cyclic peptide binging to 4-1BB protein |
8.1 |
29.7 |
SOLUTION NMR |
GOOD
|
| 9kft |
Cryo-EM structure of the fMLFC-FPR1-Gi complex |
36.6 |
117.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kfu |
Human FGFR3 in complex with inhibitor F1 |
20.6 |
69.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfv |
Crystal structure of the methyltransferase-ribozyme 1 bound to DNA substrate (1-benzyl-adenosine derivative) |
19.0 |
64.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfw |
NMR structure of an agonistic OX40 nanobody |
14.5 |
51.9 |
SOLUTION NMR |
GOOD
|
| 9kfx |
Crystal structure of synthetic PPR-DYW in complex with target RNA |
44.0 |
154.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfy |
Crystal structure of synthetic PPR-DYW in its RNA-free state |
30.1 |
102.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9kfz |
Crystal structure of the PIN1 and fragment 59 complex |
16.3 |
53.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9kg0 |
Alpha-hemolysin heptameric late pre-pore state derived from 10:0 PC/Sphingomyelin liposomes |
39.4 |
112.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kg1 |
Alpha-hemolysin heptameric pre-pore state derived from 10:0 PC liposomes. |
39.1 |
109.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kg2 |
Cryo-EM structure of apo form atABCB19 in lipid nanodisc |
42.4 |
140.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kg3 |
Alpha-hemolysin heptameric pore state derived from egg PC/Cholesterol (3:1 molar ratio) liposomes |
40.1 |
114.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9kg4 |
Solution structure of free hTERT promoter G-quadruplex |
11.0 |
37.8 |
SOLUTION NMR |
GOOD
|
| 9kg5 |
Crystal structure of the CYP154C5 F92A/R114A/T248D/E282A variant from Nocardia farcinica |
29.9 |
92.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kg6 |
Alpha-hemolysin heptameric pore state derived from 10:0 PC liposomes |
39.9 |
117.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kg8 |
Solution structure of the 2:1 berberine- hTERT-G4 complex |
11.7 |
39.3 |
SOLUTION NMR |
GOOD
|
| 9kg9 |
Crystal structure of the PIN1 and fragment 18 complex. |
16.6 |
54.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9kga |
Crystal structure of SpTx1 toxin |
25.9 |
71.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9kgb |
Crystal structure of tolypothrichol synthase |
20.9 |
61.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kgg |
Cryo-EM structure of linear intron of thymidylate synthase (td) gene of bacteriophage T4 |
31.4 |
114.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kgh |
Cryo-EM structure of circular intron of thymidylate synthase (td) gene of bacteriophage T4 |
32.8 |
117.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kgi |
Structural Basis for the Recognition of Blood Group Trisaccharides by Tulane virus |
25.4 |
77.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9kgj |
Discovery of an orally bioavailable reversible covalent SARS-CoV-2 Mpro inhibitor with pan-coronavirus activity |
26.7 |
82.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9kgk |
Structure of the complex of LGR4 with NB18 |
44.4 |
157.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kgl |
Structure of KATP channel in complex with centipede toxin SpTx1 |
72.2 |
233.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kgm |
Complex structure of OsHPPD with MBQ |
28.6 |
87.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kgn |
Discovery of an orally bioavailable reversible covalent SARS-CoV-2 Mpro inhibitor with pan-coronavirus activity |
26.6 |
82.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kgo |
Crystal structure of the PIN1 and fragment 19 complex. |
16.4 |
57.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kgp |
The structure of natural P450BM3-H derived from Bacillus megaterium for catalyzing the steroid DHEA |
31.9 |
101.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kgq |
Discovery of an orally bioavailable reversible covalent SARS-CoV-2 Mpro inhibitor with pan-coronavirus activity |
26.8 |
83.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9kgr |
Discovery of an orally bioavailable reversible covalent SARS-CoV-2 Mpro inhibitor with pan-coronavirus activity |
26.2 |
82.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kgs |
Discovery of an orally bioavailable reversible covalent SARS-CoV-2 Mpro inhibitor with pan-coronavirus activity |
26.5 |
82.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kgt |
;Crystal structure of topoisomerase IV from Klebsiella pneumoniae in complex with DNA and BWC0977, a dual-targeting broad-spectrum novel bacterial topoisomerase inhibitor.
; |
58.4 |
197.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9kgy |
Crystal structure of a de novo designed monomeric mainly-beta protein B10 (orthorhombic) |
25.5 |
77.2 |
X-RAY DIFFRACTION |
EXCELLENT
|