| 8w5p |
Cryo-EM structure of Qb-Ab40 |
26.6 |
98.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w5q |
Cryo-EM structure of Qb-Ab45 |
25.5 |
81.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8w5r |
Cryo-EM structure of Qb-Ab53 |
29.4 |
97.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w5s |
Crystal structure of Annexin A7 mutant |
35.1 |
116.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8w5t |
Cryo-EM structure of Qb-Ab57 |
25.5 |
83.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w5u |
Cryo-EM structure of QbN10F-Ab40 |
26.6 |
97.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w5v |
Cryo-EM structure of QbN10K-Ab40 |
27.1 |
100.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w5w |
Cryo-EM structure of Qb-Ab8 |
32.6 |
110.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8w5z |
Crystal structure of tick tyrosylprotein sulfotransferase reveals the activation mechanism of tick anticoagulant protein madanin |
30.2 |
98.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8w68 |
Crystal structure of Q9PR55 at pH 6.0 (use NMR model) |
32.7 |
112.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8w69 |
DegQ-b-casein complex |
37.7 |
122.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w6a |
Crystal structure of TAX1BP1 LIR region in complex with GABARAP |
28.7 |
92.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6b |
crystal structure of TAX1BP1 SKICH domain in complex with RB1CC1 coiled-coil domain |
34.8 |
128.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6c |
CryoEM structure of NaDC1 with Citrate |
33.0 |
106.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w6d |
CryoEM structure of NaDC1 in apo state |
33.2 |
104.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w6e |
De novo design of HBC599 binder |
23.7 |
71.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w6f |
Apo structure of HBC binder |
23.4 |
69.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w6g |
NaDC1 with inhibitor ACA |
33.3 |
106.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w6h |
NaS1 with sulfate - IN/IN state |
31.0 |
96.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8w6i |
Cryo-EM structure of Escherichia coli Str K12 FtsEX complex with ATP-gamma-S in peptidisc |
42.3 |
131.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8w6j |
Cryo-EM structure of Escherichia coli Str K12 FtsE(E163Q)X/EnvC complex with ATP in peptidisc |
46.2 |
172.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8w6k |
in situ room temperature Laue crystallography |
15.2 |
53.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w6l |
Crystal structure of the SLA-2*1001 allele and ASFV antigenic peptide at 2.2A resolution |
24.2 |
75.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w6m |
Native strucutre of ferritin from Ureaplasma diversum |
18.4 |
61.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6n |
NaS1 with sulfate in IN/OUT state |
31.8 |
105.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w6o |
NaS1 in IN/IN state |
31.1 |
96.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8w6p |
Crystal structure of dimeric murine SMPDL3A |
33.1 |
110.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6q |
ferritin from Ureaplasma diversum soaking in Fe2+ solution for 0 min |
18.9 |
69.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w6r |
murine SMPDL3A bound to sulfate |
21.5 |
70.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6s |
Ferritin from Ureaplasma diversum soaking in Fe2+ solution for 2 min |
18.9 |
65.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w6t |
NaS1 in IN/OUT state |
31.8 |
106.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8w6u |
Ferritin from Ureaplasma diversum soaking in Fe2+ solution for 5 min |
18.8 |
68.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6v |
Structural basis of chorismate isomerization by Arabidopsis isochorismate synthase ICS1 |
35.3 |
116.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6w |
Crystal Structure of C-terminal domain of nucleocapsid protein from SARS-CoV-2 in complex with ampicillin |
18.8 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6x |
Neutron structure of [NiFe]-hydrogenase from D. vulgaris Miyazaki F in its oxidized state |
25.6 |
80.0 |
— |
GOOD
|
| 8w6y |
Ferritin from Ureaplasma diversum soaking in Fe2+ solution for 10 min |
18.7 |
65.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8w6z |
;Substrate-bound crystal structure of a P450 enzyme DmlH that catalyze intramolecular phenol coupling in the biosynthesis of cihanmycins
; |
22.2 |
67.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w70 |
Structure of Gemtuzumab Fab |
25.4 |
80.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w71 |
Structural basis of chorismate isomerization by Arabidopsis isochorismate synthase ICS1 |
35.3 |
116.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8w72 |
Crystal structure of a P450 enzyme DmlH that catalyze intramolecular phenol coupling in the biosynthesis of cihanmycins |
22.3 |
67.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w73 |
Fe-O nanocluster of form-I in the 4-fold channel of Ureaplasma diversum ferritin |
18.7 |
64.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8w74 |
Fe-O nanocluster of form-II in the 4-fold channel of Ureaplasma diversum ferritin |
18.8 |
64.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8w75 |
Structure of Drosophila melanogaster L-2-hydroxyglutarate dehydrogenase |
39.0 |
117.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8w76 |
Crystal structure of d(CGTATACG)2 duplex |
12.2 |
39.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8w77 |
Human Consensus Olfactory Receptor OR52c in apo state, OR52c only |
20.3 |
77.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8w78 |
Structure of Drosophila melanogaster L-2-hydroxyglutarate dehydrogenase in complex with FAD and 2-oxoglutarate |
39.2 |
117.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8w79 |
Fe-O nanocluster of form-III in the 4-fold channel of Ureaplasma diversum ferritin |
18.8 |
65.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8w7a |
Cryo-EM structure of ClassIII Lanthipeptide modification enzyme PneKC in the presence of GTP. |
41.6 |
128.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8w7b |
Fe-O nanocluster of form-IV in the 4-fold channel of Ureaplasma diversum ferritin |
18.9 |
61.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8w7c |
Activation of mitochondrial Caseinolytic Protease P (ClpP) induces selective cancer cell lethality |
38.4 |
120.1 |
X-RAY DIFFRACTION |
REASONABLE
|