| 8pga |
Crystal structure of the metallo-beta-lactamase VIM1 with 2818 |
17.1 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgb |
Crystal structure of the metallo-beta-lactamase VIM1 with 2850 |
17.2 |
60.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pgc |
Crystal structure of the metallo-beta-lactamase VIM1 with 2868 |
17.2 |
49.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pge |
Crystal structure of the metallo-beta-lactamase VIM1 with 2936 |
17.4 |
56.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgf |
Crystal structure of the metallo-beta-lactamase VIM1 with 2941 |
17.2 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgg |
Crystal structure of the metallo-beta-lactamase VIM1 with 2954 |
17.1 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgh |
Crystal structure of the metallo-beta-lactamase VIM1 with 2955 |
17.2 |
54.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pgi |
Crystal structure of the metallo-beta-lactamase VIM1 with 2984 |
17.2 |
52.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgj |
Crystal structure of the metallo-beta-lactamase VIM1 with 2985 |
17.1 |
52.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgk |
Crystal structure of the metallo-beta-lactamase VIM1 with 3016 |
17.2 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgl |
Crystal structure of the metallo-beta-lactamase VIM1 with 3027 |
17.0 |
55.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgm |
Crystal structure of the metallo-beta-lactamase VIM1 with 3062 |
17.2 |
53.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgn |
Crystal structure of the metallo-beta-lactamase VIM1 with 3169 |
17.2 |
49.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pgo |
Crystal structure of the metallo-beta-lactamase VIM1 with 3183 |
17.2 |
59.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgp |
Crystal structure of the metallo-beta-lactamase VIM1 with 3193 |
17.1 |
49.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pgq |
Crystal structure of the metallo-beta-lactamase VIM1 with 3225 |
17.2 |
53.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgr |
Crystal structure of the metallo-beta-lactamase VIM1 with 3270 |
17.2 |
53.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgs |
Crystal structure of the metallo-beta-lactamase VIM1 with 3380 |
17.2 |
53.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgt |
Crystal structure of the metallo-beta-lactamase VIM1 with 3393 |
17.2 |
53.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgu |
Crystal structure of the metallo-beta-lactamase VIM1 with 3394 |
17.2 |
64.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pgv |
Crystal structure of the metallo-beta-lactamase VIM1 with 3396 |
17.2 |
49.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pgw |
Crystal structure of the metallo-beta-lactamase VIM1 with 3460 |
17.2 |
55.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgx |
Crystal structure of the metallo-beta-lactamase VIM1 with 3461 |
17.2 |
54.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgy |
Crystal structure of the metallo-beta-lactamase VIM1 with 3462 |
17.2 |
56.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8pgz |
Crystal structure of the metallo-beta-lactamase VIM1 with 3528 |
17.2 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph0 |
Crystal structure of the metallo-beta-lactamase VIM1 with 3637 |
17.2 |
55.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph1 |
Crystal structure of the metallo-beta-lactamase VIM1 with 3708 |
17.2 |
53.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph2 |
Crystal structure of the metallo-beta-lactamase VIM1 with 3746 |
17.2 |
49.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8ph3 |
Crystal structure of the metallo-beta-lactamase VIM1 with 3747 |
17.2 |
56.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph4 |
Co-Crystal structure of the SARS-CoV2 main protease Nsp5 with an Uracil-carrying X77-like inhibitor |
26.5 |
82.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8ph5 |
X-ray structure of the adduct formed upon reaction of Lysozyme with [Ru2Cl(DPhF)2(O2CCH3)2] in condition B |
15.7 |
52.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph6 |
X-ray structure of the adduct formed upon reaction of Lysozyme with K2[Ru2(DPhF)(CO3)3] in condition B |
16.0 |
54.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph7 |
X-ray structure of the adduct formed upon reaction of Lysozyme with [Ru2Cl(DPhF)(O2CCH3)3] in condition A |
15.6 |
51.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph8 |
X-ray structure of the adduct formed upon reaction of Lysozyme with [Ru2Cl(DPhF)2(O2CCH3)2] in condition A |
15.7 |
52.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8ph9 |
E. coli RNA polymerase paused at ops site (non-complementary scaffold) |
48.2 |
155.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pha |
O(S)-methyltransferase from Pleurotus sapidus |
44.4 |
150.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8phb |
Crystal structure of apo Cami1 |
30.9 |
97.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8phd |
Structure of Human Cdc123 bound to domain 3 of eIF2 gamma and ATP |
34.1 |
107.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8phe |
ACAD9-WT in complex with ECSIT-CTER |
32.1 |
109.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phf |
Cryo-EM structure of human ACAD9-S191A |
31.9 |
109.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phh |
Cryo-EM structure of Atkinsonella Hypoxylon Virus-like particles. |
36.0 |
120.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phi |
Crystal structure of prefusion-stabilized RSV F Variant DS-Cav1 in complex with Lonafarnib |
30.7 |
126.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8phj |
cA4-bound Cami1 in complex with 70S ribosome |
84.7 |
217.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8phk |
fully recruited RfaH bound to E. coli transcription complex paused at ops site |
48.9 |
158.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phl |
Human carbonic anhydrase II containing 4-fluorophenylalanine |
18.6 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8phm |
Oxalate-bound cobalt(II) human carbonic anhydrase II |
18.6 |
59.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8phn |
Receiver domain from hybrid Histidine Kinase 3 from Chaetomium thermophilum |
14.7 |
47.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8pho |
Portal from the Borrelia bacteriophage BB1 procapsid |
30.5 |
117.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8php |
Portal from the Borrelia bacteriophage BB1 procapsid with bound scaffold protein |
33.9 |
128.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8phq |
Top cap of the Borrelia bacteriophage BB1 procapsid, fivefold-symmetrized outer shell |
— |
292.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|