| 8e2g |
Cryo-EM structure of N-terminal arm (aa68-966) of BIRC6 (from local refinement 3) |
26.9 |
82.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8e2h |
Cryo-EM structure of C-terminal arm of BIRC6 (from local refinement 4) |
32.9 |
114.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8e2i |
Cryo-EM structure of BIRC6/Smac |
72.6 |
228.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e2j |
Cryo-EM structure of BIRC6/Smac (from local refinement 1) |
35.8 |
140.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8e2k |
Cryo-EM structure of BIRC6/HtrA2-S306A |
71.4 |
232.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e2l |
Structure of Lates calcarifer Twinkle helicase with ATP and DNA |
49.7 |
167.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e2m |
;Bruton's tyrosine kinase (BTK) with compound 13
; |
20.0 |
63.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8e2n |
Crystal Structure of Nanobody VHH113 Specific for PA14 Cif |
19.7 |
62.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8e2o |
Leveraging the Structure of DNAJA1 to Discover Novel Pancreatic Cancer Therapies |
14.2 |
49.8 |
SOLUTION NMR |
GOOD
|
| 8e2p |
Crystal structure of TadA*8.20 in a complex with ssDNA |
33.3 |
108.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8e2q |
Crystal structure of TadAC-1.17 in a complex with ssDNA |
33.6 |
113.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8e2r |
Crystal structure of TadAC-1.14 |
19.6 |
63.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8e2s |
Crystal structure of TadAC-1.19 |
36.2 |
115.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8e2u |
HMPV F monomer bound to RSV-199 Fab |
38.9 |
135.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e2w |
Structure of CRISPR-Associated DinG |
25.6 |
78.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8e2x |
Purification of Enterovirus A71, strain 4643, WT capsid |
28.9 |
93.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e2y |
Purification of Enterovirus A71, strain 4643, WT capsid |
30.9 |
98.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e2z |
Structures of HLA-B8E76C loaded with long peptides reveal novel features at the N-terminus of the groove |
24.0 |
75.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8e30 |
E. coli 50S ribosome bound to compound streptogramin A analog 3142 |
68.4 |
231.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e31 |
Purification of Enterovirus A71, strain 4643, WT capsid |
31.2 |
102.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e32 |
E. coli 50S ribosome bound to compound streptogramin analogs SA1 and SB1 |
70.1 |
258.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e33 |
E. coli 50S ribosome bound to compound streptogramin analog SAB001 |
68.4 |
231.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e34 |
CryoEM structures of bAE1 captured in multiple states |
35.1 |
116.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e35 |
E. coli 50S ribosome bound to compound SAB002 |
70.6 |
262.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e36 |
E. coli 50S ribosome bound to compound streptogramin A analog 3146 |
68.2 |
231.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e37 |
Structure of Campylobacter concisus wild-type SeMet PglC |
42.4 |
129.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8e38 |
Purification of Enterovirus A71, strain 4643, WT capsid |
31.7 |
99.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e39 |
Purification of Enterovirus A71, strain 4643, WT capsid |
29.6 |
95.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3a |
Purification of Enterovirus A71, strain 4643, WT capsid |
31.5 |
99.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3b |
Purification of Enterovirus A71, strain 4643, WT capsid |
29.7 |
96.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8e3c |
Purification of Enterovirus A71, strain 4643, WT capsid |
30.5 |
99.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3d |
ZBTB7A Zinc Finger Domain Bound to DNA Duplex Containing CAST sequence (#11) |
43.9 |
158.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3e |
ZBTB7A Zinc Finger Domain Bound to DNA Duplex Containing CAST sequence (#10) |
33.6 |
104.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3f |
;Escherichia coli Rho-dependent transcription pre-termination complex containing 18 nt long RNA spacer, Mg-ADP-BeF3, and NusG; TEC part
; |
49.2 |
157.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8e3g |
BMP2/GDF5 heterodimer |
29.1 |
117.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8e3h |
;Escherichia coli Rho-dependent transcription pre-termination complex containing 18 nt long RNA spacer, Mg-ADP-BeF3, and NusG; Rho hexamer part
; |
44.9 |
142.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8e3i |
CRYO-EM STRUCTURE OF the human MPSF IN COMPLEX WITH THE AUUAAA poly(A) signal |
37.6 |
126.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3j |
Co-crystal structure of Chaetomium glucosidase with compound 4 |
38.1 |
122.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3k |
Human PU.1 ETS-Domain (165-270) Bound to d(AATAAGCGGAAGTGGG) |
17.6 |
55.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8e3l |
E. coli 50S ribosome bound to D-linker solithromycin conjugate |
70.1 |
259.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3m |
E. coli 50S ribosome bound to L-linker solithromycin conjugate |
68.5 |
232.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3n |
Crystal structure of pregnane X receptor ligand binding domain complexed with rifamycin S |
20.4 |
64.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3o |
E. coli 50S ribosome bound to solithromycin and VM1 |
68.0 |
229.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8e3p |
Co-crystal structure of Chaetomium glucosidase with compound 5 |
37.9 |
122.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3q |
CRYO-EM STRUCTURE OF the human MPSF |
36.9 |
123.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3r |
Human PU.1 ETS-Domain (165-270) Bound to d(AATAAAAGGAAGTGGG) |
17.6 |
56.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8e3s |
CryoEM structure of yeast Arginyltransferase 1 (ATE1) |
25.9 |
85.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8e3t |
Gallium-reconstituted nitrogenase MoFeP mutant S188A from Azotobacter vinelandii after IDS oxidation |
38.2 |
123.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3u |
Nickel-reconstituted nitrogenase MoFeP mutant S188A from Azotobacter vinelandii after IDS oxidation |
38.2 |
120.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8e3v |
Cobalt-reconstituted nitrogenase MoFeP mutant S188A from Azotobacter vinelandii after IDS oxidation |
38.2 |
117.0 |
X-RAY DIFFRACTION |
GOOD
|