| 8q8h |
Crystal Structure of Apo beta-D-GalNAcase from Niabella aurantiaca (Structure 2) |
44.0 |
145.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8q8i |
AO75L in complex with a synthetic trisaccharide acceptor. |
20.1 |
64.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8q8j |
Crystal structure of human GPX4-R152H |
16.2 |
47.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8q8k |
KI Polyomavirus LTA NLS bound to importin alpha 2 |
41.1 |
154.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8q8l |
Tau - AD-LIA7 (tau intermediate amyloid) |
33.6 |
113.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8m |
Tau - AD-PHF long crossover |
35.7 |
143.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q8n |
Crystal structure of human GPX4-U46C-I129S-L130S |
16.1 |
48.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8q8o |
PA14_16140 protein: the regulator of an operon involved in the biofilm formation in PA14 P. aeruginosa |
23.2 |
76.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8q8p |
Cryo-EM structure of the magnesium channel CtMrs2 in the closed state |
42.5 |
140.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8q |
Cryo-EM structure of the magnesium channel CtMrs2 in the open state |
45.0 |
145.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8r |
Tau - AD-PHF |
35.5 |
140.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q8s |
Tau - AD-THF |
43.6 |
141.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8u |
Tau - CTE-MIA1 (tau intermediate amyloid) |
32.3 |
117.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8v |
Tau - CTE-MIA3 |
40.0 |
140.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8w |
Tau - CTE-MIA4 (tau intermediate amyloid) |
39.3 |
128.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8x |
Tau - CTE-MIA5 (tau intermediate amyloid) |
41.8 |
126.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q8y |
Tau - CTE-MIA6 (tau intermediate amyloid) |
40.8 |
129.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q8z |
Tau - CTE-MIA7 (tau intermediate amyloid) |
41.6 |
132.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q90 |
Halophilic Lrp transcription factor |
21.5 |
67.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q91 |
Structure of the human 20S U5 snRNP core |
58.1 |
190.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q92 |
P301S Tau Filaments from the Brains of PS19 Transgenic Mouse Line |
33.2 |
119.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q93 |
Crystal structure of the SARS-COV-2 RBD with neutralizing-VHHs Re30H02 and Re21D01 |
25.5 |
87.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8q94 |
Crystal structure of The SARS-COV-2 BA.2.75 RBD with neutralizing-VHHs Re32D03 and Ma3B12 |
26.0 |
83.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q95 |
Crystal structure of the SARS-CoV-2 BA.1 RBD with neutralizing-VHHs Ma16B06 and Ma3F05 |
26.4 |
83.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q96 |
P301S Tau Filaments from the Brains of Tg2541 Transgenic Mouse Line |
25.9 |
82.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q97 |
Tau - CTE-MIA9 (tau intermediate amyloid) |
34.8 |
126.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q98 |
Tau - CTE-MIA8 (tau intermediate amyloid) |
34.1 |
113.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q99 |
Tau - CTE-MIA10 (tau intermediate amyloid) |
32.1 |
105.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9a |
Tau - CTE-MIA11 (tau intermediate amyloid) |
34.4 |
116.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9b |
Tau - CTE-MIA13 (tau intermediate amyloid) |
40.5 |
144.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8q9c |
Tau - CTE-MIA14 (tau intermediate amyloid) |
39.0 |
128.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9d |
Tau - CTE-MIA15 (tau intermediate amyloid) |
35.1 |
115.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9e |
Tau - CTE-MIA18 (tau intermediate amyloid) |
32.7 |
109.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9f |
Tau - CTE-LIA3 (tau intermediate amyloid) |
33.6 |
112.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9g |
Tau - CTE-LIA5 (tau intermediate amyloid) |
37.4 |
134.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9h |
Tau - CTE-LIA4 (tau intermediate amyloid) |
34.6 |
142.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9i |
Tau - CTE-LIA6 (tau intermediate amyloid) |
26.2 |
87.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9j |
Tau - CTE-LIA7 (tau intermediate amyloid) |
37.1 |
119.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9k |
Tau - CTE-LIA13 (tau intermediate amyloid) |
32.7 |
125.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9l |
Tau - CTE-LIA14 (tau intermediate amyloid) |
38.6 |
136.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9m |
Tau - CTE-type I (tau intermediate amyloid) |
35.6 |
128.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9n |
Crystal Structure of the MADS-box/MEF2 Domain of MEF2D bound to dsDNA and MITR deacetylase binding motif mutant L151V. |
20.5 |
62.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q9o |
CTE tau intermediate amyloid (LIA-17) |
38.7 |
156.4 |
ELECTRON MICROSCOPY |
SUSPICIOUS
|
| 8q9p |
Crystal Structure of the MADS-box/MEF2 Domain of MEF2D bound to dsDNA and HDAC5 deacetylase binding motif |
20.3 |
62.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q9q |
Crystal Structure of the MADS-box/MEF2 Domain of MEF2D bound to dsDNA and HDAC7 deacetylase binding motif |
20.1 |
63.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8q9r |
Crystal structure of MADS-box/MEF2D N-terminal domain bound to dsDNA and HDAC9 deacetylase binding motif |
28.3 |
91.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8q9s |
;STRUCTURE OF PROTEIN KINASE CK2 CATALYTIC SUBUNIT (ISOFORM CK2ALPHA'; CSNK2A2 GENE PRODUCT) IN COMPLEX WITH THE INHIBITOR SGC-CK2-1
; |
21.6 |
69.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8q9t |
CryoEM structure of a S. Cerevisiae Ski238 complex bound to RNA |
51.1 |
181.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8q9u |
S-methylthiourocanate hydratase, variant R450A, from Variovorax sp. RA8 in complex with NAD+ |
23.4 |
73.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8q9v |
S-methylthiourocanate hydratase from Variovorax sp. RA8 in complex with NAD+ and imidazolone propionate |
23.4 |
73.1 |
X-RAY DIFFRACTION |
GOOD
|