| 8phr |
Middle part of the Borrelia bacteriophage BB1 procapsid, tenfold-symmetrized outer shell |
82.2 |
276.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phs |
Bottom cap of the Borrelia bacteriophage BB1 procapsid, fivefold-symmetrized outer shell |
— |
275.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pht |
Scaffold rings inside the Borrelia bacteriophage BB1 procapsid |
37.1 |
118.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phu |
Asymmetric structure of the portal-containing cap of the Borrelia bacteriophage BB1 procapsid |
— |
484.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8phv |
Structure of Human selenomethionylated Cdc123 bound to domain 3 of eIF2 gamma |
33.9 |
105.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8phw |
Human OATP1B1 |
32.5 |
106.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8phx |
Receiver Domain of the Hybrid Histidine Kinase Sln1 of Candida albicans |
26.6 |
89.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8phy |
crystal structure of powdery mildews Blumeria graminis f. sp. tritici AVRPM2 (2) |
20.4 |
69.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8phz |
Helical reconstruction of CHIKV nsP3 helical scaffolds |
33.5 |
105.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pi0 |
NMR2 Structure of KRAS G12V (GMPPNP bound) in complex with 5-(1H-indol-2-l)piperazin-2-one |
16.5 |
45.3 |
SOLUTION NMR |
REASONABLE
|
| 8pi1 |
Bicyclic INCYPRO Pseudomonas fluorescens esterase |
53.2 |
180.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pi2 |
Native alpha-1-antitrypsin at 1.5 Angstrom (Cys232Ser) |
22.6 |
81.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pi3 |
Cathepsin S Y132D mutant in complex with NNPI-C10 inhibitor |
17.6 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8pi4 |
Crystal structure of human insulin desB30 precursor with an Alanine-Methionine-Lysine C-peptide in dimer (T2) conformation |
11.4 |
40.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8pi5 |
Crystal structure of human insulin desB30 precursor with an Alanine-Methionine-Lysine C-peptide in hexamer (T3R3) conformation |
14.9 |
55.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pi6 |
;Crystal structure of the monomeric zinc free human insulin A22K, B3E, B26E, B29R, desB30 precursor with a Ser-Glu-Asp-Trp-Trp-Arg C-peptide and a Glu-Glu-Gly-Glu-Pro-Arg N-terminal extension
; |
21.6 |
68.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8pi7 |
DNA binding domain of HNF-1A bound to P2-HNF4A promoter DNA variant (P2 -169C>T) |
26.0 |
86.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8pi8 |
DNA binding domain of HNF-1A bound to P2-HNF4A promoter DNA |
26.0 |
85.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8pi9 |
DNA binding domain of HNF-1A bound to P2-HNF4A promoter DNA variant (P2 -181G>A) |
26.1 |
85.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pia |
DNA binding domain of HNF-1A bound to P2-HNF4A promoter DNA variant (P2 -181G>T) |
25.6 |
81.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8pib |
autoinhibited RfaH bound to E. coli transcription complex paused at ops site (encounter complex) |
48.9 |
159.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8pid |
backtracked E. coli transcription complex paused at ops site and bound to RfaH |
48.9 |
161.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pie |
;Crystal structure of the human nucleoside diphosphate kinase B domain in complex with the product AT-8500 formed by catalysis of compound AT-9010
; |
28.6 |
88.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pif |
Fragment 12 in complex with KLHDC2 |
30.1 |
96.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8pih |
Structure of Api m1 in complex with two nanobodies |
25.6 |
91.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8pii |
VHH Z70 mutant 3 in interaction with PHF6 Tau peptide |
15.2 |
50.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8pij |
Neisseria meningitidis Type IV pilus SB-GATDH variant bound to the C24 nanobody |
25.0 |
64.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8pil |
E. coli transcription complex paused at ops site and bound to RfaH and NusA |
51.1 |
167.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pim |
fully recruited RfaH bound to E. coli transcription complex paused at ops site (not complementary scaffold) |
48.7 |
165.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8pin |
Crystal structure of Ser33 |
41.1 |
127.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8pio |
Crystal structure of Ser33 in complex with PHP (3-phosphohydroxypyruvate) |
41.5 |
132.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8pip |
DNA triplex structure with Polypyridyl Ruthenium Complexes |
25.4 |
89.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8piq |
Crystal Structure of BRD4-BD1 with BI894999 |
16.2 |
53.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8pir |
Crystal structure of Ser33 in complex with 3-PGA (3-phosphoglycerate) |
41.8 |
131.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8pis |
Crystal structure of Ser33 in complex with L-Serine |
51.0 |
162.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8piu |
60-meric complex of dihydrolipoamide acetyltransferase (E2) of the human pyruvate dehydrogenase complex |
99.5 |
246.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8piv |
Homomeric GluA2 flip R/G-unedited Q/R-edited F231A mutant in tandem with TARP gamma-2, desensitized conformation 1 |
46.0 |
139.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8piw |
Crystal structure of Hen Egg White Lysozyme co-crystallized with 10 mM TbXo4-NMet2 |
15.3 |
52.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8pix |
Cryo EM structure of the type 3C polymorph of alpha-synuclein at low pH. |
31.3 |
109.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8piy |
NMR2 Structure of KRAS G12V (GMPPNP bound) in complex with (2E)-3-(1H-indol-2-yl)prop-2-enoic acid |
16.4 |
46.4 |
SOLUTION NMR |
REASONABLE
|
| 8piz |
Neisseria meningitidis Type IV pilus SB-DATDH variant bound to the C24 nanobody |
24.1 |
62.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8pj0 |
;Pseudomonas aeruginosa FabF C164A mutant in complex with N-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)-3-methylbutanamide
; |
38.7 |
123.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8pj1 |
Structure of human 48S translation initiation complex in open codon scanning state (48S-1) |
88.4 |
232.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pj2 |
Structure of human 48S translation initiation complex in AUG recognition state after eIF5-induced GTP hydrolysis by eIF2 (48S-2) |
87.9 |
230.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pj3 |
Structure of human 48S translation initiation complex upon transfer of initiator tRNA to eIF5B (48S-3) |
88.1 |
233.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pj4 |
Structure of human 48S translation initiation complex after eIF5 release (48S-4) |
88.3 |
231.9 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pj5 |
Structure of human 48S translation initiation complex after eIF2 release prior 60S subunit joining (48S-5) |
86.3 |
228.5 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pj6 |
Structure of human 48S translation initiation complex with initiator tRNA, eIF1A and eIF3 (off-pathway) |
86.3 |
228.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8pj7 |
MLLT3 in complex with compound PFI-6 |
17.9 |
63.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8pj8 |
FKBP51FK1 F67E/K60Orn (i, i+7) in complex with SAFit1 |
15.4 |
51.8 |
X-RAY DIFFRACTION |
GOOD
|