| 8osj |
Cryo-EM structure of CLOCK-BMAL1 bound to a nucleosomal E-box at position SHL-6.2 (DNA conformation 1) |
42.5 |
142.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 8osk |
Cryo-EM structure of CLOCK-BMAL1 bound to a nucleosomal E-box at position SHL+5.8 (composite map) |
44.7 |
142.1 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 8osl |
;Cryo-EM structure of CLOCK-BMAL1 bound to the native Por enhancer nucleosome (map 2, additional 3D classification and flexible refinement)
; |
48.4 |
157.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8osm |
GTPASE HRAS IN COMPLEX WITH ZN-CYCLEN AT 200 MPA PRESSURE |
16.1 |
48.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8osn |
GTPASE HRAS IN COMPLEX WITH ZN-CYCLEN AT AMBIENT PRESSURE |
16.2 |
48.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8oso |
GTPase HRAS in complex with Zn-cyclen under 500 MPa pressure |
16.1 |
48.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8osp |
GCN5-related N-Acetyltransferase from Lactobacillus curiae |
25.8 |
70.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8osq |
Why does the herpes simplex 1 virus-encoded UL49.5 protein fail to inhibit the TAP-dependent antigen presentation? |
12.7 |
54.0 |
SOLUTION NMR |
REASONABLE
|
| 8ost |
Structure of human terminal uridylyltransferase 4 (TUT4, ZCCHC11) in complex with pre-let7g miRNA and Lin28A |
34.6 |
124.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8osv |
Structural and functional studies of geldanamycin amide synthase ShGdmF |
18.6 |
68.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8osw |
Crystal structure of Rhizobium etli L-asparaginase ReAIV (R4mC-1) |
27.1 |
85.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8osx |
SARS-CoV-2 nsp10-16 methyltransferase in complex with ATP |
23.6 |
77.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8osy |
Trimeric catalytic domain of the E. coli Dihydrolipoamide Acetyltransferase (E2) of the pyruvate dehydrogenase complex |
34.1 |
130.5 |
X-RAY DIFFRACTION |
GOOD
|
| 8osz |
Structural and functional studies of geldanamycin amide synthase ShGdmF |
18.6 |
64.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8ot0 |
SARS-CoV-2 nsp10-16 methyltransferase in complex with MTA and glycine |
23.8 |
76.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8ot1 |
unseeded Abeta(1-40) amyloid fibril (morphology i) |
25.6 |
92.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8ot2 |
Structural and functional studies of geldanamycin amide synthase ShGdmF |
18.4 |
67.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8ot3 |
unseeded Abeta(1-40) amyloid fibril (morphology ii) |
26.0 |
94.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8ot4 |
seeded Abeta(1-40) amyloid fibril (morphology I) |
25.4 |
86.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ot5 |
Crystal structure of the titin domain Fn3-85 |
26.4 |
79.3 |
X-RAY DIFFRACTION |
GOOD
|
| 8ot6 |
CTE typeI tau filament from Guam ALS/PDC |
35.1 |
130.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8ot7 |
Crystal structure of an 8-repeat consensus TPR superhelix with Barium |
26.0 |
88.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 8ot8 |
Alditol oxidase from Actinomycetota bacterium in complex with D-xylulose |
41.8 |
127.2 |
X-RAY DIFFRACTION |
GOOD
|
| 8ot9 |
CTE typeIII tau filament from Guam ALS/PDC |
35.5 |
120.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ota |
High resolution crystal structure of a Leaf-branch compost cutinase quadruple variant |
18.1 |
55.4 |
X-RAY DIFFRACTION |
GOOD
|
| 8otb |
Clostridium perfringens chitinase CP4_3455 |
25.9 |
88.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8otc |
CTE typeII tau filament from Guam ALS/PDC |
35.6 |
149.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8otd |
TMEM106B Fold1-s filament from Guam ALS/PDC |
30.8 |
102.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ote |
TMEM106B Fold I-d filament from Guam ALS/PDC |
62.9 |
198.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8otf |
Ab typeII filament from Guam ALS/PDC |
20.9 |
73.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8otg |
CTE typeI tau filament from Kii ALS/PDC |
35.3 |
127.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8oth |
TypeII tau filament from Kii ALS/PDC |
36.0 |
147.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8oti |
CTE typeIII tau filament |
35.5 |
126.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8otj |
PHF tau filament from Kii ALS/PDC |
36.9 |
146.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8otk |
Structure of ClpC Q11P N-terminal Domain |
15.7 |
50.1 |
X-RAY DIFFRACTION |
GOOD
|
| 8otl |
;structure of InhA from Mycobacterium tuberculosis in complex with 5-(((4-(2-hydroxyphenoxy)benzyl)(octyl)amino)methyl)-2-phenoxyphenol
; |
38.7 |
126.6 |
X-RAY DIFFRACTION |
GOOD
|
| 8otm |
;structure of InhA from mycobacterium tuberculosis in complex with N-((1-(3-hydroxy-4-phenoxybenzyl)-1H-1,2,3-triazol-4-yl)methyl)-2-oxo-2H-chromene-3-carboxamide
; |
29.4 |
89.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8otn |
;structure of InhA from mycobacterium tuberculosis in complex with inhibitor 7-((1-(3-Hydroxy-4-phenoxybenzyl)-1H-1,2,3-triazol-4-yl)methoxy)-4-methyl-2H-chromen-2-one
; |
29.2 |
90.7 |
X-RAY DIFFRACTION |
GOOD
|
| 8oto |
SARS-CoV-2 nsp10-16 methyltransferase in complex with AMP |
23.7 |
75.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8otp |
;Crystal structure of human carbonic anhydrase II with 1-cyclopropyl-6-fluoro-4-oxo-7-(4-(4-sulfamoylbenzoyl)piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid
; |
18.6 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 8otq |
Cryo-EM structure of Strongylocentrotus purpuratus sperm-specific Na+/H+ exchanger SLC9C1 in GDN |
44.1 |
138.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8otr |
SARS-CoV-2 nsp10-16 methyltransferase in complex with SAM analog BDH 33959089 |
23.7 |
77.0 |
X-RAY DIFFRACTION |
GOOD
|
| 8ots |
OCT4 and MYC-MAX co-bound to a nucleosome |
42.2 |
147.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 8ott |
MYC-MAX bound to a nucleosome at SHL+5.8 |
42.2 |
140.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 8otu |
The crystal structure of PET44, a PETase enzyme from Alkalilimnicola ehrlichii |
26.0 |
80.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8otv |
Crystal structure of NUDT14 complexed with novel compound |
22.8 |
67.0 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8otw |
Cryo-EM structure of Strongylocentrotus purpuratus SLC9C1 in presence of cAMP |
38.7 |
121.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 8otx |
Cryo-EM structure of Strongylocentrotus purpuratus sperm-specific Na+/H+ exchanger SLC9C1 in nanodisc |
43.6 |
139.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 8oty |
Crystal structure of the titin domain Fn3-90 |
27.0 |
85.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 8otz |
48-nm repeat of the native axonemal doublet microtubule from bovine sperm |
— |
— |
ELECTRON MICROSCOPY |
—
|