| 9j19 |
The crystal structure of COVID-19 main protease in complex with an inhibitor minocycline |
26.9 |
83.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j1a |
Structure of ConA without ligand |
18.6 |
63.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1b |
Structure of ConA/IMI-Man |
26.1 |
94.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1c |
Structure of ConA/NAP-Man |
30.7 |
89.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j1d |
Structure of ConA/PHE-Man |
25.7 |
88.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1e |
ESTS1 phthalate ester degrading esterase from Sulfobacillus acidophilus at 1.22A |
19.1 |
56.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1f |
Dimeric Structure of ConA/M2P-Man |
32.9 |
104.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j1g |
ESTS1 phthalate ester degrading esterase from Sulfobacillus acidophilus in complex with phthalate |
19.1 |
56.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j1h |
The binary complex structure of F2Y224-FtmOx1 mutant with alpha-ketoglutarate |
25.8 |
86.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1i |
Apo structure of the F2Y224-FtmOx1 mutant with metal Iron |
26.0 |
84.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1j |
Cap region of monocin |
46.1 |
145.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j1k |
Tip region of monocin |
90.9 |
259.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j1l |
Side fiber of monocin |
64.9 |
220.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j1m |
KU13-bond Mycobacterium tuberculosis 70S ribosome |
83.5 |
296.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9j1n |
Mouse Spi-B Ets domain in complex with DNA containing AGAA sequence |
17.8 |
61.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1o |
Mouse Spi-B Ets domain in complex with DNA containing GGAA sequence |
17.9 |
64.3 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1p |
Cryo-EM structure of the g1:Ox-bound human GLP-1R-Gs complex |
42.6 |
155.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9j1q |
Structure of a mutant (PaDa-I) unspecific peroxygenase from Agrocybe aegerita |
19.9 |
61.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1r |
Structure of a triple-helix region of human Collagen type II from Trautec |
21.2 |
87.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j1s |
Human replication protein A: RPA70 subunit N-terminal domain |
14.6 |
45.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1t |
Structure of a triple-helix region of human Collagen type IV from Trautec |
17.9 |
74.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j1u |
Structural basis of the bifunctionality of M. salinexigens ZYF650T glucosylglycerol phosphorylase in glucosylglycerol catabolism |
43.9 |
132.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1v |
ESTS1 phthalate ester degrading esterase from Sulfobacillus acidophilus in complex with Monomethyl phthalate |
19.1 |
56.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j1w |
Endogenous dihydrolipoamide acetyltransferase (E2) core of pyruvate dehydrogenase complex from pig heart |
97.3 |
241.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j1x |
Structure of mutant evolved from PaDa-I, unspecific peroxygenase from Agrocybe aegerita |
19.9 |
62.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1y |
Crystal structure of Nme1Cas9 HNH domain bound to anti-CRISPR AcrIIC1Boe. |
19.4 |
62.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9j1z |
Crystal structure of Nme1Cas9 HNH domain bound to anti-CRISPR AcrIIC1Nme1ST |
24.1 |
79.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9j20 |
Structure of WDR5 in complex with KIF2A |
28.0 |
93.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9j22 |
structure of human urea transport protein slc14A1 with urea |
30.1 |
88.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9j23 |
Structure of a triple-helix region of human Collagen type II from Trautec |
21.9 |
85.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j24 |
Structural basis of the bifunctionality of M. salinexigens ZYF650T glucosylglycerol phosphorylase in glucosylglycerol catabolism |
43.0 |
130.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9j25 |
Structural basis of the bifunctionality of M. salinexigens ZYF650T glucosylglycerol phosphorylase in glucosylglycerol catabolism |
39.4 |
120.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j26 |
Structure of a triple-helix region of human Collagen type IV from Trautec |
25.2 |
100.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j27 |
Fe-SaPolF-L-isoleucine copmplex |
19.5 |
71.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j28 |
Fe2+-SzPolF-2 complex |
26.1 |
88.3 |
X-RAY DIFFRACTION |
GOOD
|
| 9j29 |
Fe/Fe-SzPolF-POIA complex |
25.9 |
88.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9j2a |
Fe/Fe-SzPolF-2 complex |
25.8 |
87.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9j2b |
Fe/Fe-SzPolF-L-isoleucine complex |
26.2 |
87.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9j2c |
Fe-SzPolF-L-isoleucine |
26.4 |
87.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9j2e |
Fe2+/pterin-dependent,apo SnPolE |
29.3 |
89.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j2f |
Structure of photosynthetic LH1-RC complex from the purple bacterium Blastochloris tepida |
47.8 |
126.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j2g |
Crystal structure of Nme1Cas9 HNH domain bound to anti-CRISPR AcrIIC1Vei |
19.6 |
61.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j2k |
Crystal structure of Omega Transaminase TA_2799 from Pseudomonas putida KT2440 |
28.5 |
93.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9j2l |
4,5-DOPA-extradiol-dioxygenase from Mirabilis jalapa |
31.8 |
99.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j2m |
Fe2+/pterin-dependent enzyme,BH4-SnPolE complex |
29.2 |
91.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9j2n |
Cryo-EM structure of the human glucose transporter, GLUT7 in outward-facing open conformation |
24.0 |
78.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9j2p |
Fe2+/pterin-dependent,BH4-L-isoleucine-SnPolE complex |
29.2 |
90.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j2r |
Fe2+/pterin-dependent,SnPolE-L-ile complex,Y157A mutation |
29.4 |
91.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j2w |
Human cGAS catalytic domain bound with XL-3156 |
30.2 |
93.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9j2x |
Human cGAS catalytic domain bound with RU.521 |
29.8 |
93.8 |
X-RAY DIFFRACTION |
EXCELLENT
|