| 9dz8 |
Catalytic domain of Dihydrolipoamide Succinytransferase |
64.7 |
165.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9dza |
Photoactivation in Bacteriophytochrome, high resolution cryo structure in the dark. |
34.6 |
108.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9dzc |
PvRBP2b N-terminal domain stabilised mutant WHT2483 |
28.8 |
99.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9dzd |
PvRBP2b N-terminal domain stabilised mutant WHT2484 |
24.5 |
87.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9dze |
Computationally Designed Bifaceted Protein Nanomaterial pD5-14 |
— |
265.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 9dzf |
Human GC-A bound to ANP and XX16 |
34.0 |
107.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9dzg |
Human GC-A bound to XX16 |
34.3 |
108.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9dzh |
Human GC-A bound to ANP and REGN5308 |
35.2 |
114.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9dzj |
Human GC-A bound to ANP and 2xREGN5308 |
37.1 |
114.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9dzk |
Human GC-A bound to REGN5308 |
35.9 |
112.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9dzm |
Dimeric human OCT2 (POU2F2) POU domain bound to palindromic MORE DNA |
23.7 |
82.3 |
X-RAY DIFFRACTION |
GOOD
|
| 9dzn |
KAT6A MYST domain complexed with a H3K14-CoA bisubstrate inhibitor |
21.4 |
77.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9dzo |
Structure of ALAS bound to succinyl-CoA from S. cerevisiae |
50.3 |
168.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9dzp |
Photoactivation in Bacteriophytochromes, reference (dark) structure for the 100 ps time point |
35.1 |
108.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9dzq |
;CryoEM structure of the human antibodies PIV3HN-05 and PIV3HN-13 in complex with the parainfluenza virus hemagglutinin-neuraminidase protein
; |
36.4 |
114.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9dzr |
The crystal structure of F182AQE CYP199A4 bound to 4-methylthiobenzoic acid |
31.9 |
102.4 |
X-RAY DIFFRACTION |
GOOD
|
| 9dzs |
Acanthamoeba Polyphaga Mimivirus R699 |
24.7 |
82.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9dzv |
Cryo-EM structure of the C. neoformans lipid flippase Apt1-Cdc50 in the E1 state |
46.4 |
164.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9dzw |
De novo calcium channel hexamer, CalC6_3 with DHR extensions |
28.3 |
80.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 9dzx |
MHV spike tail heptapeptide complexed with coatomer alpha-WD40 domain |
19.6 |
63.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9dzy |
Cryo-EM structure of Pre-Chi dynein bound to Lis1 |
64.4 |
220.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9dzz |
Cryo-EM structure of a TatBC complex from Escherichia coli |
32.5 |
93.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e00 |
Cryo-EM structure of human DNMT3A2-DNMT3B3 complex bound to di-nucleosome |
70.6 |
272.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9e01 |
Cryo-EM structure of a TatBC-MdoD complex from Escherichia coli |
31.9 |
92.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e02 |
Cryo-EM structure of a TatBC complex from Nitratifractor salsuginis |
31.8 |
89.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e03 |
Cryo-EM structure of a TatBC complex from Myxococcus xanthus |
37.4 |
120.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e04 |
Cryo-EM structure of TatBC-CueO signal peptide complex from Nitratifractor salsuginis |
32.0 |
87.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e05 |
The consensus model of the cryo-EM structure of human DNMT3A2-DNMT3B3 complex bound to di-nucleosome |
70.1 |
257.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e06 |
Cryo-EM structure of a TatBC complex from Nitratifractor salsuginis in nanodisc |
31.9 |
90.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9e07 |
Cryo-EM structure of a TatAC complex from Nitratifractor salsuginis |
31.7 |
92.8 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e08 |
Cryo-EM structure of MdoD from Escherichia coli |
35.3 |
123.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e09 |
Cryo-EM structure a single nucleosome (2) focus of human DNMT3A2-DNMT3B3 complex bound to di-nucleosome |
42.0 |
132.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9e0a |
Structure of proline utilization A complexed with 1,4-benzenedimethanol |
40.6 |
122.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0b |
Structure of proline utilization A complexed with (2,3-dihydro-1-benzofuran-5-yl)methanol |
40.7 |
119.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0c |
Structure of proline utilization A complexed with 1-benzofuran-5-ylmethanol |
40.5 |
120.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0d |
Structure of proline utilization A complexed with piperonyl alcohol |
40.5 |
120.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0e |
Structure of proline utilization A complexed with (1H-indol-5-yl)methanol |
40.5 |
123.6 |
X-RAY DIFFRACTION |
GOOD
|
| 9e0f |
A focus of DNMT tetramer (1) of the cryo-EM structure of human DNMT3A2-DNMT3B3 complex bound to di-nucleosome |
45.6 |
149.8 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9e0g |
A focus of tetramer (2) of the cryo-EM structure of human DNMT3A2-DNMT3B3 complex bound to di-nucleosome |
45.5 |
147.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0h |
De novo calcium channel heptamer, CalC6_3 with DHR extensions. Off target multimerization state |
31.0 |
87.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0i |
Structure of the HKU5-19s RBD bound to the Bos taurus ACE2 receptor |
31.2 |
102.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0j |
Structure and evolution of Photosystem I in the early-branching cyanobacterium Anthocerotibacter panamensis |
67.2 |
181.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0k |
Cryo-EM structure of human cytoplasmic dynein-1 in the presence of ATP |
48.8 |
187.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0l |
The prefusion conformation of herpes simplex virus type 1 (HSV-1) glycoprotein B (gB) |
46.8 |
176.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0m |
CryoEM structure of holoenzyme of inducible Lysine decarboxylase from Hafnia alvei holoenzyme at 2.19 Angstrom resolution |
64.9 |
234.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0n |
M. smegmatis unmethylated 70S ribosome structure |
85.3 |
293.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e0o |
CryoEM structure of inducible Lysine decarboxylase from Hafnia alvei L-hydrazino-Lysine analog at 2.04 Angstrom resolution |
64.8 |
233.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0p |
M. smegmatis methylated 70S ribosome structure |
85.3 |
294.0 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9e0q |
CryoEM structure of inducible Lysine decarboxylase from Hafnia alvei D-hydrazino-Lysine analog at 2.3 Angstrom resolution |
64.7 |
258.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9e0r |
Cryo-EM structure of a single nucleosome (1) focus of human DNMT3A2-DNMT3B3 complex bound to di-nucleosome |
41.8 |
129.6 |
ELECTRON MICROSCOPY |
GOOD
|