| 8g8j |
Crystal structure of human DNA polymerase eta incorporating ITP across dT |
24.4 |
84.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8k |
Crystal structure of Rv1916 (residues 233-398) |
16.9 |
55.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8n |
CTLA4 Fab with peptide |
50.9 |
157.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8o |
The crystal structure of JAK2 in complex with Compound 31 |
30.5 |
104.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8p |
F420-2/GTP(GDP) complex of F420-gamma glutamyl ligase (CofE) from Archaeoglobus fulgidus |
19.7 |
65.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8q |
Monopartite p52 NLS in complex with Importin alpha 2 |
28.1 |
98.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8r |
RelB NLS in complex with Importin alpha 2 |
28.1 |
98.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8g8s |
bipartite p52 NLS in complex with Importin alpha 2 |
27.9 |
98.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8g8v |
GTP Cyclohydrolase-IB with sodium |
25.8 |
81.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8g8w |
Molecular mechanism of nucleotide inhibition of human uncoupling protein 1 |
51.8 |
187.7 |
ELECTRON MICROSCOPY |
SUSPICIOUS
|
| 8g8x |
X-ray co-crystal structure of compound 27 in with complex JAK2 |
30.5 |
105.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8g8y |
Hepatitis B virus capsid bound to importin alpha1 |
50.9 |
168.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g8z |
Cryo-EM structure of 3DVA component 1 of Escherichia coli que-PEC (paused elongation complex) RNA Polymerase plus preQ1 ligand |
48.5 |
154.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g90 |
LaM domain of human LARP1 in complex with Sp phosphorothioate isomer of AAAAA(SRA) RNA |
13.8 |
43.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8g91 |
LaM domain of human LARP1 in complex with Rp phosphorothioate isomer of AAAAA(SRA) RNA |
14.1 |
44.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8g92 |
Structure of inhibitor 16d-bound SPNS2 |
22.7 |
73.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8g93 |
Crystal structures of 17-beta-hydroxysteroid dehydrogenase 13 |
24.9 |
85.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8g94 |
Structure of CD69-bound S1PR1 coupled to heterotrimeric Gi |
38.1 |
124.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g95 |
Adenylation domain structure from NRPS-like Delta-Poly-L-Ornithine synthetase |
29.6 |
88.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8g96 |
Adenylation domain structure from NRPS-like Delta-Poly-L-Ornithine synthetase (L-Ornithine bound) |
29.7 |
89.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8g97 |
Adenylation domain structure from NRPS-like Delta-Poly-L-Ornithine synthetase (D-Ornithine bound) |
29.4 |
88.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8g98 |
Adenylation domain structure from NRPS-like Delta-Poly-L-Ornithine synthetase (L-Lysine bound) |
29.3 |
88.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8g99 |
Partial auto-inhibitory complex of Xenopus laevis DNA polymerase alpha-primase |
40.8 |
125.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8g9a |
Crystal structure of a resurrected ancestor (AncRNase) of the pancreatic-type RNases 2 and 3 sub-families |
30.6 |
97.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9b |
Human IMPDH2 mutant - L245P, treated with GTP, ATP, IMP, and NAD+; compressed filament segment reconstruction |
50.1 |
157.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9c |
;Diphosphoinositol polyphosphate phosphohydrolase 1 (DIPP1/NUDT3) in complex with 5- difluoromethylenebisphosphonate inositol pentakisphosphate (5-PCF2P-IP5), an analogue of 5-InsP7
; |
15.1 |
47.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9d |
;Diphosphoinositol polyphosphate phosphohydrolase 1 (DIPP1/NUDT3) in complex with 5- phosphonodifluoroacetamide inositol pentakisphosphate (5-PCF2Am-InsP5), an analogue of 5-InsP7
; |
15.2 |
47.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9e |
;Crystal structure of the catalytic domain of human diphosphoinositol pentakisphosphate kinase 2 (PPIP5K2) in complex with AMP-PNP and 5-(PCF2P)-IP5, an analog of 5-IP7
; |
21.5 |
75.8 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9f |
Complete auto-inhibitory complex of Xenopus laevis DNA polymerase alpha-primase |
46.8 |
153.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8g9j |
Geometrically programmable nanomaterial construction using regularized protein building blocks |
18.4 |
60.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9k |
Geometrically programmable nanomaterial construction using regularized protein building blocks |
26.9 |
87.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9l |
DNA initiation subcomplex of Xenopus laevis DNA polymerase alpha-primase |
35.4 |
111.4 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8g9m |
Acinetobacter_baumannii short-chain dehydrogenase |
17.9 |
64.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8g9n |
Partial DNA elongation subcomplex of Xenopus laevis DNA polymerase alpha-primase |
31.8 |
101.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9o |
Complete DNA elongation subcomplex of Xenopus laevis DNA polymerase alpha-primase |
41.6 |
142.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9p |
Tricomplex of RMC-4998, KRAS G12C, and CypA |
28.6 |
87.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8g9q |
Tricomplex of Compound-1, KRAS G12C, and CypA |
22.7 |
74.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8g9r |
Cardiac amyloid fibrils extracted from a wild-type ATTR amyloidosis patient |
26.8 |
87.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9s |
Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications |
57.3 |
182.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9t |
Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications |
55.3 |
204.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8g9u |
Exploiting Activation and Inactivation Mechanisms in Type I-C CRISPR-Cas3 for Genome Editing Applications |
57.2 |
204.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9v |
Crystal structures of 17-beta-hydroxysteroid dehydrogenase 13 |
43.6 |
136.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8g9w |
Cryo-EM structure of vFP49.02 Fab in complex with HIV-1 Env BG505 DS-SOSIP.664 (conformation 1) |
44.6 |
138.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9x |
Cryo-EM structure of vFP49.02 Fab in complex with HIV-1 Env BG505 DS-SOSIP.664 (conformation 2) |
44.7 |
138.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9y |
Cryo-EM structure of vFP49.02 Fab in complex with HIV-1 Env BG505 DS-SOSIP.664 (conformation 3) |
45.2 |
143.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8g9z |
High-resolution crystal structure of the human selenomethionine-derived SepSecS-tRNASec complex |
50.6 |
169.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8ga0 |
CLC-ec1 E202Y at pH 4.5 100mM Cl Turn |
29.7 |
100.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ga1 |
CLC-ec1 R230C/L249C/C85A at pH 4.5 100mM Cl Swap |
29.0 |
99.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ga2 |
Bromodomain of CBP liganded with inhibitor iCBP5 |
25.6 |
77.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8ga3 |
CLC-ec1 R230C/L249C/C85A at pH 4.5 100mM Cl Turn |
29.4 |
98.5 |
ELECTRON MICROSCOPY |
REASONABLE
|