| 9ip2 |
Cryo-EM structure of the RNA-dependent RNA polymerase complex from Marburg virus |
38.3 |
118.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ip3 |
Cryo-EM structure of the RNA-dependent RNA polymerase complex in a compact conformation from Ebola virus |
37.0 |
113.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9ip4 |
Cryo-EM structure of the RNA-dependent RNA polymerase complex from Marburg virus |
38.4 |
119.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ip5 |
;Hemichannel sub-structure of Cx36/GJD2 gap junction intercellular channel (FN conformation) in brain polar lipid nanodiscs, treated with a 14-fold molar excess of carbenoxolone
; |
33.3 |
96.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9ip6 |
The complex of rice immune receptor RGA5-HMA8 with rice blast effector protein AVR1-CO39 |
23.8 |
73.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9ip7 |
Local refinement structure of sEGFR and 528 Fv (from HL-type bispecific diabody Ex3) complex |
37.2 |
116.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ip8 |
;Poly-alanine model for HL-type bispecific diabody Ex3 composed of 528 and OKT3 Fvs in ternary complex with sEGFR and CD3gamma-epsilon (closed conformation)
; |
46.7 |
160.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ip9 |
;Poly-alanine model for HL-type bispecific diabody Ex3 composed of 528 and OKT3 Fvs in ternary complex with sEGFR and CD3gamma-epsilon (middle conformation)
; |
46.0 |
152.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipa |
;Poly-alanine model for HL-type bispecific diabody Ex3 composed of 528 and OKT3 Fvs in ternary complex with sEGFR and CD3gamma-epsilon (open conformation)
; |
46.3 |
150.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipb |
Local refinement structure of sEGFR and 528 Fv (from LH-type bispecific diabody Ex3) complex |
37.7 |
117.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipc |
;Poly-alanine model for LH-type bispecific diabody Ex3 composed of 528 and OKT3 Fvs in ternary complex with sEGFR and CD3gamma-epsilon (closed conformation)
; |
49.5 |
161.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipd |
;Poly-alanine model for LH-type bispecific diabody Ex3 composed of 528 and OKT3 Fvs in ternary complex with sEGFR and CD3gamma-epsilon (middle conformation)
; |
49.1 |
153.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipe |
;Poly-alanine model for LH-type bispecific diabody Ex3 composed of 528 and OKT3 Fvs in ternary complex with sEGFR and CD3gamma-epsilon (open conformation)
; |
49.5 |
147.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipl |
A tetrapyrrole binding domain variant of CoaR in closed conformation at 2.28 angstrom resolution |
22.9 |
72.0 |
X-RAY DIFFRACTION |
GOOD
|
| 9ipm |
;Hemichannel sub-structure of Cx36/GJD2 gap junction intercellular channel (FN conformation) in soybean polar lipid nanodiscs, treated with a 20-fold molar excess of carbenoxolone
; |
33.3 |
97.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9ipn |
;Hemichannel sub-structure of Cx36/GJD2 gap junction intercellular channel (FN conformation) in soybean polar lipid nanodiscs, treated with a 10-fold molar excess of carbenoxolone and incubated shortly
; |
32.8 |
96.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9ipo |
;Hemichannel sub-structure of Cx36/GJD2 gap junction intercellular channel (FN conformation) in soybean polar lipid nanodiscs, treated with a 10-fold molar excess of carbenoxolone
; |
32.7 |
96.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9ipp |
Crystal structure of MERS main protease in complex with carmofur |
26.5 |
80.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9ipr |
Crystal structure of CTB10-M1 |
39.6 |
130.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9ipt |
Crystal structure of a TetR family regulator AmvR from Acinetobacter baumannii with spermidine bound |
25.4 |
79.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9ipu |
cryo-EM structure of the RNF168(1-193)/UbcH5c-Ub ubiquitylation module bound to H1.0-K63-Ub3 modified chromatosome |
45.5 |
159.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 9ipv |
Structure of JR14a-C3aR-Gi-scFv16 complex |
36.8 |
117.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 9ipw |
Crystal structure of VHL-EloB-EloC in complex with a fragment compound 7HC_5(D3) |
41.6 |
128.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9ipy |
Structure of JR14a-bound human C3aR |
30.6 |
106.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9iq3 |
AkaM,SnoaL-lile Protein |
24.9 |
72.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9iq4 |
Crystal structure of African swine fever virus methyltransferase EP424R in complex with S-Adenosylhomocysteine |
32.7 |
104.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9iq5 |
CatM, SnoaL-like protein |
19.9 |
64.5 |
X-RAY DIFFRACTION |
GOOD
|
| 9iq7 |
SacM-homologous of AkaM |
20.0 |
64.9 |
X-RAY DIFFRACTION |
GOOD
|
| 9iq8 |
Ankyrin-like protein, AnkB |
28.7 |
93.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9iqa |
structure of the oleate hydratase V206L-mutant from Staphylococcus aureus |
41.1 |
135.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqb |
Crystal structure of beta-glucosidase from Acetivibrio thermocellus |
63.8 |
191.1 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqc |
Monooxygenase dependent on riboflavin with dCMP and FAD |
18.8 |
58.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9iqd |
Apo-MicM,homologous of AkaM, SnoaL-like protein |
26.2 |
80.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 9iqe |
;Cryo-EM structure of MsRv1273c/72c from Mycobacterium smegmatis in the ADP-bound IFasym-3 (peptidisc) state (ATP 37degrees C treated)
; |
38.4 |
133.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 9iqf |
;Cryo-EM structure of MsRv1273c/72c from Mycobacterium smegmatis in the ADP-bound IFasym-3 (peptidisc) state (ADP 4degrees C treated)
; |
38.5 |
135.5 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 9iqg |
Cryo-EM structure of MsRv1273c/72c from Mycobacterium smegmatis in the ATP|ADP+Vi-bound Occ (Vi) state |
37.9 |
134.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 9iqh |
Crystal structure of sulfhydrylase |
28.5 |
94.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqi |
Structure of oleate hydratase mutant - V135A/L212V from Staphylococcus aureus in the complex with FAD |
41.1 |
135.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqj |
Structure of oleate hydratase mutant L151V from Staphylococcus aureus in the complex with linoleic acid |
41.1 |
135.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqk |
SacM in complex with LC3 |
19.6 |
60.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9iql |
SacM in complex with L6S |
19.7 |
59.2 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqm |
CatM-L6S, a SnoaL-like protein in complex with substrate mimic L6S |
15.3 |
48.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqn |
CatM-W86A-L6R, a SnoaL-like protein in complex with substrate mimic L6R |
15.1 |
49.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 9iqo |
Cryo-EM structure of the Rubisco from thermophilic purple bacterial Rubisco |
47.0 |
136.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 9iqp |
Crystal structure of the Wuhan SARS-CoV-2 Spike RBD (319-541) complexed with 1p1B10 nanobody |
24.0 |
85.7 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqq |
Crystal structure of PKM2 in complex with a natural activator |
40.5 |
131.8 |
X-RAY DIFFRACTION |
GOOD
|
| 9iqr |
Cryo-EM structure of MT3-alpha2AAR |
24.8 |
84.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 9iqs |
Cryo-EM structure of MT3-Muscarinic acetylcholine receptor 4 |
24.6 |
81.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 9iqt |
structure of niacin-HCA2-Gi |
37.7 |
125.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 9iqu |
phage HY126 dCMP hydroxylase-AfhB with sustrate dCMP |
18.5 |
66.9 |
X-RAY DIFFRACTION |
GOOD
|