| 11uc |
Crystal structure of Casein Kinase 2 (CK2) alpha in complex with BMS-595 |
21.1 |
69.8 |
X-RAY DIFFRACTION |
GOOD
|
| 11ue |
Structure of PDGFRb Kinase Domain Bound to JNJ-PDGFRBi-1 |
20.3 |
65.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 11ve |
Cryo-EM structure of substrate engaged p97-Ufd1-NPL4-Faf1 complex (State1) |
56.6 |
186.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 11wx |
Crystal Structure of ribosomal large subunit pseudouridine synthase D from Neisseria gonorrhoea |
32.0 |
101.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 11yc |
The structure of human Vacuolar Protein Sorting 34 catalytic domain bound to RD-II-123 |
26.1 |
83.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 11ye |
Curved structure of mPiezo1 in plasma membrane vesicles |
66.5 |
207.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 11yo |
Single-conformation model re-refinement of 2F/S3-rich PSII intermediate structure at 2.09 Angstrom resolution |
57.8 |
196.3 |
X-RAY DIFFRACTION |
GOOD
|
| 11yv |
;Structure of Bacillus subtilis Nitric Oxide Synthase in complex with 7-((3-(((3-(6-aminopyridin-2-yl)propyl)amino)methyl)phenoxy)methyl)quinolin-2-amine
; |
23.1 |
79.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 11yy |
E.Coli DNA Topoisomerase 3 in complex with an 8mer ssDNA oligo ACTGACTT |
30.1 |
101.9 |
X-RAY DIFFRACTION |
GOOD
|
| 11yz |
Cryo EM Structure of GTP cyclohydrolase 1 (FolE) from Mycobacterium tuberculosis |
44.2 |
118.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 11zc |
Flat structure of mPiezo1 in plasma membrane vesicles |
76.2 |
277.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 11zs |
Cryo EM structure of glutamine synthetase from Brucella melitensis |
55.4 |
165.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 11zv |
;Structure of the Porcine deltacoronavirus (PDCoV) receptor-binding domain bound to the RBD minibinder 11, the PD3 Fab, and the Kappa light chain nanobody (local refinement)
; |
22.1 |
70.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 11zw |
;Structure of the Porcine deltacoronavirus (PDCoV) receptor-binding domain bound to the RBD minibinder 11, the PD3 Fab, and the Kappa light chain nanobody
; |
33.7 |
108.7 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 120l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.6 |
59.8 |
X-RAY DIFFRACTION |
GOOD
|
| 121d |
MOLECULAR STRUCTURE OF THE A-TRACT DNA DODECAMER D(CGCAAATTTGCG) COMPLEXED WITH THE MINOR GROOVE BINDING DRUG NETROPSIN |
13.6 |
46.8 |
X-RAY DIFFRACTION |
GOOD
|
| 121p |
STRUKTUR UND GUANOSINTRIPHOSPHAT-HYDROLYSEMECHANISMUS DES C-TERMINAL VERKUERZTEN MENSCHLICHEN KREBSPROTEINS P21-H-RAS |
16.4 |
48.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 122d |
DNA HELIX STRUCTURE AND REFINEMENT ALGORITHM: COMPARISON OF MODELS FOR D(CCAGGCM==5==CTGG) DERIVED FROM NUCLSQ, TNT, AND X-PLOR |
12.4 |
42.1 |
X-RAY DIFFRACTION |
GOOD
|
| 122l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.5 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 123d |
DNA HELIX STRUCTURE AND REFINEMENT ALGORITHM: COMPARISON OF MODELS FOR D(CCAGGCM==5==CTGG) DERIVED FROM NUCLSQ, TNT, AND X-PLOR |
12.5 |
43.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 123l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.5 |
67.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 124d |
STRUCTURE OF A DNA:RNA HYBRID DUPLEX: WHY RNASE H DOES NOT CLEAVE PURE RNA |
11.0 |
36.0 |
SOLUTION NMR |
GOOD
|
| 125l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.4 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 126d |
CRYSTAL STRUCTURE OF CATGGCCATG AND ITS IMPLICATIONS FOR A-TRACT BENDING MODELS |
12.4 |
42.0 |
X-RAY DIFFRACTION |
GOOD
|
| 126l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.4 |
58.4 |
X-RAY DIFFRACTION |
GOOD
|
| 127d |
;DNA (5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3') COMPLEXED WITH HOECHST 33258
; |
13.6 |
47.4 |
X-RAY DIFFRACTION |
GOOD
|
| 127l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.5 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 128d |
MOLECULAR STRUCTURE OF D(CGC[E6G]AATTCGCG) COMPLEXED WITH HOECHST 33258 |
13.8 |
46.8 |
X-RAY DIFFRACTION |
GOOD
|
| 128l |
;THE ENERGETIC COST AND THE STRUCTURAL CONSEQUENCES OF BURYING A HYDROXYL GROUP WITHIN THE CORE OF A PROTEIN DETERMINED FROM ALA TO SER AND VAL TO THR SUBSTITUTIONS IN T4 LYSOZYME
; |
17.6 |
60.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 129d |
;DNA (5'-D(*CP*GP*CP*GP*AP*AP*TP*TP*CP*GP*CP*G)-3') COMPLEXED WITH HOECHST 33342
; |
13.7 |
47.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 129l |
;STRUCTURES OF RANDOMLY GENERATED MUTANTS OF T4 LYSOZYME SHOW THAT PROTEIN STABILITY CAN BE ENHANCED BY RELAXATION OF STRAIN AND BY IMPROVED HYDROGEN BONDING VIA BOUND SOLVENT
; |
17.5 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 12af |
Crystal Structure of SARS-CoV-2 Mpro with UM-067 |
22.1 |
74.3 |
X-RAY DIFFRACTION |
GOOD
|
| 12ag |
Spermine-blocked open-state cryo-EM structure of human TRPV6 channel in cNW30 nanodiscs |
47.7 |
146.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 12ak |
Q108K:K40L:T51V:T53S:R58W:Y19W:L117E mutant of hCRBPII bound to fluorophore TD-1V-6 |
15.2 |
47.0 |
X-RAY DIFFRACTION |
GOOD
|
| 12as |
ASPARAGINE SYNTHETASE MUTANT C51A, C315A COMPLEXED WITH L-ASPARAGINE AND AMP |
26.7 |
87.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 12ca |
ALTERING THE MOUTH OF A HYDROPHOBIC POCKET. STRUCTURE AND KINETICS OF HUMAN CARBONIC ANHYDRASE II MUTANTS AT RESIDUE VAL-121 |
18.7 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 12ci |
Structure of dopamine-binding aptamer, DGR-1A, in complex with dopamine |
26.4 |
102.8 |
X-RAY DIFFRACTION |
GOOD
|
| 12cj |
Apo structure of dopamine-binding aptamer, DGR-1B |
33.9 |
107.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 12dk |
structure of human KCNQ1-CaM-PIP2 intermediate state |
40.8 |
124.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 12dl |
Native structure of the cytoplasmic lattice (CPL) asymmetric unit from mouse MII eggs |
— |
274.2 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 12e8 |
2E8 FAB FRAGMENT |
36.3 |
113.4 |
X-RAY DIFFRACTION |
GOOD
|
| 12fc |
Crystal structure of unliganded Fab 7118 |
24.9 |
80.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 12fd |
Crystal structure of unliganded Fab 7160 |
38.3 |
128.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 12fe |
Crystal structure of unliganded Fab 399 |
38.6 |
129.9 |
X-RAY DIFFRACTION |
GOOD
|
| 12fh |
Structure of eIF2B bound to a activator |
36.6 |
118.8 |
X-RAY DIFFRACTION |
GOOD
|
| 12fk |
Ancestral Reconstruction of a Homing Endonuclease |
24.5 |
88.1 |
X-RAY DIFFRACTION |
GOOD
|
| 12gb |
High Resolution Structure of Monomorphic AB1-40 Fibrils |
23.9 |
77.8 |
SOLID-STATE NMR |
GOOD
|
| 12gs |
GLUTATHIONE S-TRANSFERASE COMPLEXED WITH S-NONYL-GLUTATHIONE |
21.8 |
64.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 12hh |
Ancestral Reconstruction of a Homing Endonuclease |
24.9 |
95.0 |
X-RAY DIFFRACTION |
GOOD
|
| 12hp |
Crystal structure of the CD7 ectodomain |
34.3 |
108.0 |
X-RAY DIFFRACTION |
GOOD
|