| 9ka3 |
The cryo-EM structure of Ac-K58D_G51DA53T a-syn fibril. |
27.3 |
97.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ka4 |
The cryo-EM structure of MSA-like fold (P1) formed under the palette stratagy. |
28.9 |
98.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ka5 |
Crystal structure of beta-ketoacyl-ACP synthase FabH C112Q from E. coli |
20.0 |
62.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9ka6 |
Crystal structure of beta-ketoacyl-ACP synthase FabH C112Q in complex with acyl-ACP from E. coli |
27.4 |
107.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9ka7 |
Crystal structure of beta-ketoacyl-ACP synthase FabH C112Q in complex with malonyl-ACP from E. coli |
27.2 |
93.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9ka8 |
Structure of the recombinant structure of the subunit of allophycocyanin (APC) and the formate dehydrogenase (FDH) |
35.2 |
106.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kad |
Solution NMR structure of an RNA duplex containing pure CAG repeats |
14.4 |
53.9 |
SOLUTION NMR |
GOOD
|
| 9kae |
CryoEM structure of LTag bound to SV40 EP half origin DNA |
40.3 |
126.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kaf |
Cryo-EM structure of the SPS3-FBN5 complex in a 2:1 state |
33.4 |
109.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9kag |
Cryo-EM structure of the SPS3-FBN5 complex in a 2:2 state (class 4) |
37.8 |
123.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kah |
Crystal Structure of Chalcone Syntase and Chalcone Isomerase-like Protein Complex from Physcomitrella patens |
45.7 |
144.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kai |
Crystal Structure of Chalcone Isomerase-like Protein from Physcomitrella patens |
18.0 |
55.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9kaj |
Crystal Structure of Chalcone Syntase from Physcomitrella patens complexed with Coenzyme A |
42.5 |
130.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kak |
CryoEM structure of LTag bound to SV40 AT half origin DNA |
40.4 |
127.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kal |
The cryo-EM structure of Ac-E57A_G51DA53T a-syn fibril. |
20.0 |
72.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kan |
Crystal structure of the C. jejuni VapD-VapW toxin-antitoxin complex |
27.2 |
101.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kao |
CTP synthetase of pseudomonas aeruginosa PAO1 |
37.3 |
121.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kap |
Cryo-EM structure of glycopeptide fibril |
15.0 |
48.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kar |
Solution NMR structure of a new lasso peptide streptacidin |
5.1 |
21.2 |
SOLUTION NMR |
GOOD
|
| 9kas |
Crystal structure of anti-sulfonylurea antibody scFv in complex with chlorpropamide |
25.2 |
81.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kat |
Crystal structure of anti-sulfonylurea antibody scFv apo form |
27.1 |
93.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9kau |
Three-dimensional structure of homo-dimer of cystathione beta lyase/PLP/+L-alliin complex from Bacillus cereus(BcPatB) |
28.8 |
92.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9kax |
The outward-open structure of BjSemiSWEET in native cellular membranes determined by in situ solid-state NMR |
16.4 |
55.3 |
SOLID-STATE NMR |
REASONABLE
|
| 9kay |
Bioengineered protein nanocarrier facilitating siRNA escape from lysosomes for targeted RNAi therapy in glioblastoma |
55.1 |
137.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kb0 |
3-hydroxyisobutyrate dehydrogenase |
28.7 |
96.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9kb1 |
The Structure of the Carbohydrate Deacetylase PpOngB from Pseudoalteromonas prydzensis ACAM 620. |
22.9 |
76.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9kb3 |
The structure of the carbohydrate deacetylase inactive mutant PpOngB in complex with GlcNAc1A. |
22.6 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kb4 |
The structure of the PpOngB-citrate |
23.0 |
79.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9kb6 |
Cryo-EM structure of LGR4 |
44.2 |
154.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9kb7 |
Cryo-EM structure of LGR4-RSPO2 complex |
43.5 |
152.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9kb8 |
Cryo-EM structure of LGR4-RSPO2-ZNRF3 complex (1:1:2) |
41.0 |
145.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kb9 |
Cryo-EM structure of LGR4-RSPO2-ZNRF3 complex (2:2:2) |
48.4 |
158.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kba |
The occluded structures of BjSemiSWEET in native cellular membranes determined by in situ solid-state NMR |
16.7 |
62.4 |
SOLID-STATE NMR |
REASONABLE
|
| 9kbb |
3-hydroxyisobutyrate dehydrogenase |
23.9 |
71.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9kbc |
3-hydroxyisobutyrate dehydrogenase |
24.2 |
72.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kbd |
Cryo-EM structure of the CUL1-RBX1-SKP1-FBXO3 SCF ubiquition ligase complex |
52.3 |
170.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kbe |
Crystal structure of mycolic acid transporter MmpL3 from Mycobacterium smegmatis complexed with indolcarboxamide |
31.0 |
100.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9kbf |
Cryo-EM structure of the SKP1-FBXO3 complex |
33.5 |
107.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kbg |
The structure of B19V NS1_2-570/AMPPNP |
50.8 |
151.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kbh |
The structure of B19V NS1_2-570/ssDNA/AMPPNP |
38.4 |
120.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kbi |
The structure of B19V NS1_2-570/dsDNA/AMPPNP |
51.5 |
149.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kbj |
The structure of B19V NS1_200-501/AMPPNP |
50.6 |
148.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9kbk |
Cryo-EM structure of the SPS3-FBN5 complex in a 2:2 state (class 3) |
36.8 |
110.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9kbl |
Crystal structure of T2R-TTL-IKP104 |
55.9 |
183.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9kbn |
Crystal structure of T2R-TTL-IKP104-Colchicine |
55.7 |
184.5 |
X-RAY DIFFRACTION |
SUSPICIOUS
|
| 9kbo |
Crystal structure of human Shiftless (SFL) containing phosphorylation sites Ser249, Thr250, Thr253 and Ser256 |
36.7 |
116.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9kbq |
Crystal structure of PHAb10, a peptidoglycan hydrolase with thermal stability and broad-spectrum |
21.5 |
65.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9kbr |
Crystal structure of the methyltransferase-ribozyme 1 bound to DNA substrate (with 1-methyl-adenosine) |
19.2 |
64.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9kbs |
Crystal structure of PHAb11, another peptidoglycan hydrolase with thermal stability and broad-spectrum |
21.5 |
68.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9kbt |
Crystal structure of PHAB8, a peptidoglycan hydrolase with relatively weak thermal stability and broad-spectrum. |
17.4 |
55.8 |
X-RAY DIFFRACTION |
GOOD
|