| 8inp |
A reversible glycosyltransferase of tectorigenin - Bc7OUGT |
23.2 |
73.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8inq |
Crystal Structure of SARS-CoV-2 Main Protease (Mpro) G15S Mutant |
22.5 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8inr |
Cryo-EM structure of the alpha-MSH-bound human melanocortin receptor 5 (MC5R)-Gs complex |
33.5 |
109.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8int |
Crystal Structure of SARS-CoV-2 Main Protease (Mpro) K90R Mutant |
22.5 |
73.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8inu |
Crystal Structure of SARS-CoV-2 Main Protease (Mpro) G15S Mutant in Complex with Inhibitor nirmatrelvir |
22.5 |
76.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8inv |
Crystal structure of UGT74AN3-UDP-BUF |
22.2 |
68.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8inw |
Crystal Structure of SARS-CoV-2 Main Protease (Mpro) K90R Mutant in Complex with Inhibitor nirmatrelvir |
22.5 |
81.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8inx |
Crystal Structure of SARS-CoV-2 Main Protease (Mpro) G15S Mutant in Complex with Inhibitor ensitrelvir |
22.6 |
79.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8iny |
Crystal Structure of SARS-CoV-2 Main Protease (Mpro) K90R Mutant in Complex with Inhibitor ensitrelvir |
22.5 |
80.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8inz |
Cryo-EM structure of human HCN3 channel in apo state |
41.1 |
127.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io0 |
Cryo-EM structure of human HCN3 channel with cAMP |
41.6 |
129.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io2 |
The Rubisco assembly intermidate of Arabidopsis thaliana Rubisco accumulation factor 1 (AtRaf1) and Rubisco large subunit (RbcL) |
57.7 |
191.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io3 |
Cryo-EM structure of human HCN3 channel with cilobradine |
39.8 |
116.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io4 |
Herg1a-herg1b open state |
41.3 |
123.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io5 |
Herg1a-herg1b closed state 2 |
42.1 |
120.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io6 |
Cryo-EM structure of phosphoketolase from Bifidobacterium longum in octameric assembly |
61.7 |
203.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io7 |
Cryo-EM structure of phosphoketolase from Bifidobacterium longum in dimeric assembly |
33.9 |
103.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io8 |
Cryo-EM structure of cyanobacteria phosphoketolase complexed with AMPPNPin dimeric assembly |
33.8 |
102.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8io9 |
Cryo-EM structure of cyanobacteria phosphoketolase complexed with AMPPNP in dodecameric assembly |
71.0 |
246.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8ioa |
Cryo-EM structure of cyanobacteria phosphoketolase |
33.9 |
103.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iob |
Herg1a-herg1b closed state 1 |
42.1 |
124.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ioc |
Cryo-EM structure of the gamma-MSH-bound human melanocortin receptor 3 (MC3R)-Gs complex |
34.5 |
115.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iod |
Cryo-EM structure of the PG-901-bound human melanocortin receptor 5 (MC5R)-Gs complex |
33.9 |
114.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ioe |
Cryo-EM structure of cyanobacteria phosphoketolase in dodecameric assembly |
71.6 |
249.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8iof |
Crystal structure of N-methyl-Cis-4-hydroxy-D-proline dehydratase in Clostridium sp. FS41 |
45.9 |
138.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8iog |
Cryo-EM structure of porcine bc1 complex in isolated state |
57.8 |
189.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ioi |
Crystal Structure of PadR- family transcriptional regulator Rv1176c from Mycobacterium tuberculosis H37Rv. |
23.0 |
75.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8ioj |
The Rubisco assembly intermidiate of Rubisco large subunit (RbcL) and Arabidopsis thaliana Rubisco accumulation factor 1 (AtRaf1) |
52.3 |
171.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8iok |
Crystal structure of AtHPPD-CLJ507 complex |
21.6 |
73.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8iol |
The complex of Rubisco large subunit (RbcL) |
45.3 |
137.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iom |
Crystal structure of the carboxy-terminal channel-forming domain of Colicin Ib |
18.4 |
71.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8ioo |
Crystal structure of Deinococcus radiodurans RecJ-like protein in complex with Mg2+ |
36.4 |
129.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8ios |
Structure of the SARS-CoV-2 XBB.1 spike glycoprotein (closed-1 state) |
50.2 |
159.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iot |
Structure of the SARS-CoV-2 XBB.1 spike glycoprotein (closed-2 state) |
50.8 |
153.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iou |
Structure of SARS-CoV-2 XBB.1 spike glycoprotein in complex with ACE2 (1-up state) |
62.9 |
205.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8iov |
Structure of SARS-CoV-2 XBB.1 spike RBD in complex with ACE2 |
32.2 |
110.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iow |
Cryo-EM structure of the sarilumab Fab/IL-6R complex |
28.9 |
96.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8iox |
Escherichia coli OpgD mutant-D388N |
81.5 |
284.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8ioy |
Structure of ATP7B C983S/C985S/D1027A mutant with AMP-PNP |
35.5 |
126.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ioz |
Crystal structure of transaminase |
28.3 |
88.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8ip0 |
Cryo-EM structure of type I-B Cascade bound to a PAM-containing dsDNA target at 3.6 angstrom resolution |
56.8 |
199.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ip1 |
Escherichia coli OpgD mutant-D388N with beta-1,2-glucan |
34.1 |
113.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8ip2 |
Escherichia coli OpgG mutant-D361N with beta-1,2-glucan |
24.6 |
84.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8ip3 |
Cryo-EM structure of hMRS2-Mg |
41.7 |
137.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ip4 |
Cryo-EM structure of hMRS-highEDTA |
41.8 |
138.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ip5 |
Cryo-EM structure of hMRS2-lowEDTA |
41.8 |
140.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ip6 |
Cryo-EM structure of hMRS2-rest |
42.7 |
140.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ip8 |
Wheat 80S ribosome stalled on AUG-Stop boron dependently |
91.0 |
234.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8ip9 |
Wheat 40S ribosome in complex with a tRNAi |
72.6 |
251.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ipa |
Wheat 80S ribosome stalled on AUG-Stop boron dependently with cycloheximide |
90.3 |
232.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|