| 28yj |
Molecular basis of ZPD homopolymerization: cryo-EM structure of a native vertebrate egg coat filament |
54.4 |
187.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 28yl |
Crystal structure of the zeamine pathway ketoreductase Zmn13-KR, in complex with NADH |
29.1 |
89.4 |
X-RAY DIFFRACTION |
GOOD
|
| 28ym |
Tobacco Mosaic Virus (TMV) |
62.1 |
173.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 28yn |
VgrG1 from Pseudomonas aeruginosa (PA0091) |
48.3 |
181.8 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 28yo |
Beta-galactosidase from E.Coli |
52.9 |
175.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 28yp |
SpyTag-FtnA from E.Coli |
53.9 |
135.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 28yq |
ALFA-tag-FtnA from E.Coli |
53.9 |
136.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 28yr |
ALFA-tag-FtnA from E.Coli isolated from in vitro translation reaction |
54.0 |
135.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 28zu |
human 48S PIC with Kozak mRNA and eIF1A W70A mutant |
74.6 |
268.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 28zv |
human 48S PIC with mRNA (non-Kozak) |
74.6 |
268.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 28zx |
human 48S PIC with mRNA (Kozak_1) |
86.1 |
230.6 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 28zy |
human 48S PIC with mRNA (Kozak_2) |
86.0 |
230.3 |
ELECTRON MICROSCOPY |
EXCELLENT
|
| 290d |
;CRYSTAL STRUCTURES OF OLIGODEOXYRIBONUCLEOTIDES CONTAINING 6'-ALPHA-METHYL AND 6'-ALPHA-HYDROXY CARBOCYCLIC THYMIDINES
; |
13.9 |
47.4 |
X-RAY DIFFRACTION |
GOOD
|
| 291d |
;CRYSTAL STRUCTURES OF OLIGODEOXYRIBONUCLEOTIDES CONTAINING 6'-ALPHA-METHYL AND 6'-ALPHA-HYDROXY CARBOCYCLIC THYMIDINES
; |
13.8 |
47.6 |
X-RAY DIFFRACTION |
GOOD
|
| 292d |
;INTERACTION BETWEEN THE LEFT-HANDED Z-DNA AND POLYAMINE:THE CRYSTAL STRUCTURE OF THE D(CG)3 AND N-(2-AMINOETHYL)-1,4-DIAMINOBUTANE COMPLEX
; |
9.6 |
32.2 |
X-RAY DIFFRACTION |
GOOD
|
| 293d |
INTERACTION BETWEEN THE LEFT-HANDED Z-DNA AND POLYAMINE-2: THE CRYSTAL STRUCTURE OF THE D(CG)3 AND SPERMIDINE COMPLEX |
9.6 |
31.5 |
X-RAY DIFFRACTION |
GOOD
|
| 294d |
INTERCALATED CYTOSINE MOTIF AND NOVEL ADENINE CLUSTERS IN THE CRYSTAL STRUCTURE OF TETRAHYMENA TELOMERE |
19.6 |
62.8 |
X-RAY DIFFRACTION |
GOOD
|
| 295d |
CRYSTAL AND SOLUTION STRUCTURES OF THE OLIGONUCLEOTIDE D(ATGCGCAT)2: A COMBINED X-RAY AND NMR STUDY |
10.5 |
35.8 |
X-RAY DIFFRACTION |
GOOD
|
| 296d |
SEQUENCE-DEPENDENT EFFECTS IN DRUG-DNA INTERACTION: THE CRYSTAL STRUCTURE OF HOECHST 33258 BOUND TO THE D(CGCAAATTTGCG)2 DUPLEX |
13.8 |
46.6 |
X-RAY DIFFRACTION |
GOOD
|
| 297d |
X-RAY AND SOLUTION STUDIES OF DNA OLIGOMERS AND IMPLICATIONS FOR THE STRUCTURAL BASIS OF A-TRACT-DEPENDENT CURVATURE |
13.5 |
46.0 |
X-RAY DIFFRACTION |
GOOD
|
| 298d |
;TARGETING THE MINOR GROOVE OF DNA: CRYSTAL STRUCTURES OF TWO COMPLEXES BETWEEN FURAN DERIVATIVES OF BERENIL AND THE DNA DODECAMER D(CGCGAATTCGCG)2
; |
13.7 |
46.3 |
X-RAY DIFFRACTION |
GOOD
|
| 299d |
CAPTURING THE STRUCTURE OF A CATALYTIC RNA INTERMEDIATE: THE HAMMERHEAD RIBOZYME |
16.1 |
56.1 |
X-RAY DIFFRACTION |
GOOD
|
| 29aj |
Crystal Structure of the human mARC1 M187K variant |
25.3 |
77.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 29cu |
Crystal Structure of a Cutinase from Saccharopolyspora Dendranthemae |
17.9 |
54.0 |
X-RAY DIFFRACTION |
GOOD
|
| 29hb |
Cryo-EM structure of the ClpE/ClpP degradation complex from E.faecalis |
63.4 |
233.1 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 29hg |
Cryo-EM structure of the CUL1-RBX1-SKP1-FBXO22 SCF ubiquition ligase in complex with NSD2 via UNC10088 |
53.6 |
177.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 29hh |
Cryo-EM structure of the CUL1-RBX1-SKP1-FBXO22 SCF ubiquition ligase in complex with NSD2, UNC10088 and Bach1 |
52.3 |
177.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 29hi |
Cryo-EM structure of the CUL1-RBX1-SKP1-FBXO22 SCF ubiquition ligase in complex with NSD2 via UNC10415667 |
53.2 |
167.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 29hm |
Crystal structure of Enterovirus D68 3C protease determined via sulfur phasing |
23.4 |
76.5 |
X-RAY DIFFRACTION |
GOOD
|
| 29hn |
Crystal structure of Zika virus NS2B-NS3 protease determined via sulfur phasing |
17.1 |
56.6 |
X-RAY DIFFRACTION |
GOOD
|
| 29iv |
Crystal structure of Borrelia burgdorferi nicotinamidase BBE22 |
17.2 |
57.1 |
X-RAY DIFFRACTION |
GOOD
|
| 29jc |
Crystal structure of Coxsackievirus A16 (G-10) 2A protease determined via sulfur phasing |
21.4 |
71.8 |
X-RAY DIFFRACTION |
GOOD
|
| 29ki |
Spinach Ferredoxin I, Reduced, -400 mV |
13.9 |
48.1 |
X-RAY DIFFRACTION |
GOOD
|
| 29lw |
Crystal structure of PpSB1-LOV protein from Pseudomonas putida in complex with 5-deazaflavin mononucleotide (5dFMN) |
20.3 |
62.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 29lx |
Crystal structure of PpSB1-LOV protein from Pseudomonas putida in covalent complex with 5-deazaflavin mononucleotide (5dFMN) |
20.3 |
62.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 29mo |
Crystal structure of human CLK3 in complex with AZ176 |
22.3 |
74.9 |
X-RAY DIFFRACTION |
GOOD
|
| 29mp |
Crystal structure of human CLK3 in complex with RNAZ88 |
31.8 |
109.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 29mu |
Sesterterpene Synthase from Streptomyces mobaraensis (Sestermobaraene Synthase, SmTS1) in complex with pyrophosphate (PPi) |
42.8 |
126.2 |
X-RAY DIFFRACTION |
GOOD
|
| 29mw |
;Crystal structure of Enterovirus A71 2A protease mutant C110A containing VP1-2A junction in the active site determined via sulfur phasing
; |
15.4 |
47.5 |
X-RAY DIFFRACTION |
GOOD
|
| 29om |
Crystal structure of the staphylococcal efflux pump QacA in the outward open state |
41.3 |
142.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 29on |
Crystal structure of the staphylococcal efflux pump QacA in the inward open state in complex with nanobody 89 |
38.7 |
121.0 |
X-RAY DIFFRACTION |
GOOD
|
| 29os |
AD fold in mouse injected with seeds of AD |
33.8 |
91.2 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 29ou |
CBD fold in mouse injected with seeds of CBD |
28.1 |
96.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 29px |
Crystal structure of the staphylococcal efflux pump QacA in the outward open state bound to ethidium |
31.9 |
99.9 |
X-RAY DIFFRACTION |
GOOD
|
| 29qj |
Respiratory syncytial virus fusion protein N-terminal heptad repeat domain in complex with Double stapled peptide 4/4g |
19.2 |
78.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 29sb |
Solution structure of inhibitor (6-NBT)-bound de novo designed Kemp eliminase KABLE2.5. |
15.7 |
51.5 |
SOLUTION NMR |
GOOD
|
| 29sj |
;Three viral endonucleases bound to the same inhibitor (9-hydroxy-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione derivative). (1a) Influenza virus A/pH1N1 PA subunit endonuclease with magnesium ions.
; |
24.5 |
81.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 29sl |
;Three viral endonucleases bound to the same inhibitor (9-hydroxy-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione derivative). (1b) Influenza virus A/pH1N1 polymerase PA subunit endonuclease with manganese ions.
; |
24.6 |
86.6 |
X-RAY DIFFRACTION |
GOOD
|
| 29ta |
;Three viral endonucleases bound to the same inhibitor (9-hydroxy-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione derivative). (2) La Crosse virus L protein endonuclease with manganese ions.
; |
19.5 |
63.4 |
X-RAY DIFFRACTION |
GOOD
|
| 29tq |
;Three viral endonucleases bound to the same inhibitor (9-hydroxy-3,4-dihydro-2H-pyrazino[1,2-c]pyrimidine-1,8-dione derivative). (3) Lassa virus L protein endonuclease with manganese ions.
; |
19.0 |
51.2 |
X-RAY DIFFRACTION |
REASONABLE
|