| 221p |
THREE-DIMENSIONAL STRUCTURES OF H-RAS P21 MUTANTS: MOLECULAR BASIS FOR THEIR INABILITY TO FUNCTION AS SIGNAL SWITCH MOLECULES |
16.4 |
48.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 222d |
INFLUENCE OF COUNTER-IONS ON THE CRYSTAL STRUCTURES OF DNA DECAMERS: BINDING OF [CO(NH3)6]3+ AND BA2+ TO A-DNA |
12.7 |
44.1 |
X-RAY DIFFRACTION |
GOOD
|
| 222l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.6 |
60.3 |
X-RAY DIFFRACTION |
GOOD
|
| 223d |
;DIRECT OBSERVATION OF TWO BASE-PAIRING MODES OF A CYTOSINE-THYMINE ANALOGUE WITH GUANINE IN A DNA Z-FORM DUPLEX: SIGNIFICANCE FOR BASE ANALOGUE MUTAGENESIS
; |
9.4 |
31.0 |
X-RAY DIFFRACTION |
GOOD
|
| 223l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.5 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 224d |
;DNA-DRUG REFINEMENT: A COMPARISON OF THE PROGRAMS NUCLSQ, PROLSQ, SHELXL93 AND X-PLOR, USING THE LOW TEMPERATURE D(TGATCA)-NOGALAMYCIN STRUCTURE
; |
10.6 |
34.6 |
X-RAY DIFFRACTION |
GOOD
|
| 224l |
;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 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 225d |
A TETRAMERIC DNA STRUCTURE WITH PROTONATED CYTOSINE:CYTOSINE BASE PAIRS |
12.1 |
42.4 |
SOLUTION NMR |
GOOD
|
| 225l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 226d |
SOLUTION CONFORMATION OF A BIZELESIN A-TRACT DUPLEX ADDUCT, NMR, 1 STRUCTURE |
12.7 |
41.6 |
SOLUTION NMR |
GOOD
|
| 226l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.4 |
60.2 |
X-RAY DIFFRACTION |
GOOD
|
| 227d |
;A CRYSTALLOGRAPHIC AND SPECTROSCOPIC STUDY OF THE COMPLEX BETWEEN D(CGCGAATTCGCG)2 AND 2,5-BIS(4-GUANYLPHENYL)FURAN, AN ANALOGUE OF BERENIL. STRUCTURAL ORIGINS OF ENHANCED DNA-BINDING AFFINITY
; |
13.8 |
46.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 227l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.5 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 228l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.5 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 229d |
DNA ANALOG OF YEAST TRANSFER RNA PHE ANTICODON DOMAIN WITH MODIFIED BASES 5-METHYL CYTOSINE AND 1-METHYL GUANINE |
12.3 |
43.1 |
SOLUTION NMR |
GOOD
|
| 229l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.4 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 22ae |
The costructure of MitM and mitomycin F with SAH |
25.9 |
89.1 |
X-RAY DIFFRACTION |
GOOD
|
| 22aj |
GDP human alpha1A/beta3 S239C microtubule |
30.2 |
101.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 22ak |
GDP human alpha1A/beta3 microtubule |
30.2 |
101.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 22ao |
Crystal structure of Bacillus cereus GmaR in the apo form |
26.6 |
82.4 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22ap |
Crystal structure of Bacillus cereus GmaR in complex with UDP-GlcNAc and Mg2+ |
21.6 |
83.3 |
X-RAY DIFFRACTION |
GOOD
|
| 22aq |
The costructure of MitM and dehydromitomycin B with SAH |
25.9 |
90.1 |
X-RAY DIFFRACTION |
GOOD
|
| 22as |
The costructure of MitM and trans-1-hydroxy-7-methoxy-2-dimethylaminomitosene with SAH |
26.0 |
91.5 |
X-RAY DIFFRACTION |
GOOD
|
| 22ay |
KCNQ2 homotetramer in apo state |
34.7 |
112.8 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 22az |
ICA-1103811 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 1 |
34.3 |
109.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 22ba |
ICA-1103811 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 2 |
34.2 |
109.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bc |
ICA-1103811 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 3 |
34.2 |
108.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bd |
ICA-1103811 bound KCNQ2/3 heteromer with 2:2 stoichiometry |
34.4 |
111.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 22be |
XEN1101 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 1 |
34.4 |
111.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bf |
XEN1101 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 2 |
34.2 |
110.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bg |
XEN1101 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 3 |
34.0 |
108.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bh |
XEN1101 bound KCNQ2/3 heteromer with 3:1 stoichiometry, state 4 |
34.0 |
108.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bi |
XEN1101 bound KCNQ2/3 heteromer with 2:2 stoichiometry |
34.4 |
111.0 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 22bj |
KCNQ2/3 heterotetramer with 3:1 stoichiometry |
34.5 |
110.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 22bk |
KCNQ2/3 heterotetramer with 2:2 stoichiometry |
34.6 |
111.6 |
ELECTRON MICROSCOPY |
GOOD
|
| 22dr |
Crystal structure of SARS-CoV-2 3CL protease in complex with compound 7c |
26.3 |
83.5 |
X-RAY DIFFRACTION |
GOOD
|
| 22em |
Gi bound kappa-opioid receptor in complex with beta01 |
34.9 |
121.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 22es |
Gi bound kappa-opioid receptor in complex with difelikefalin |
38.0 |
125.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 22ey |
Crystal structure of thioredoxin gluthathione reductase from Schistosoma japonicum SjTGR-WT |
34.2 |
107.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22fc |
Crystal structure of thioredoxin gluthathione reductase from Schistosoma japonicum with the U597C mutation SjTGR-U597C |
34.1 |
107.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22fd |
Crystal structure of thioredoxin gluthathione reductase from Schistosoma japonicum with the U597C mutation in complex with NADPH |
33.9 |
105.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22fe |
Crystal structure of thioredoxin gluthathione reductase from Schistosoma japonicum with the U597C mutation in complex with GSH |
34.3 |
107.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22ff |
;Crystal structure of thioredoxin gluthathione reductase from Schistosoma japonicum with the U597C mutation in complex with auranofin
; |
34.0 |
106.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22fg |
Crystal structure of the oxidized state of TRP14 from Schistosoma japonicum |
15.0 |
47.6 |
X-RAY DIFFRACTION |
GOOD
|
| 22fh |
Crystal structure of the reduced state of TRP14 from Schistosoma japonicum |
21.3 |
68.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 22fj |
Crystal structure of the oxidized state of Trx1 from Schistosoma japonicum |
29.1 |
87.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22fk |
Crystal structure of the reduced state of Trx1 from Schistosoma japonicum |
29.2 |
87.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 22fn |
Cryo-EM structure of AsCas12a in complex with crDNA and RNA target |
37.5 |
121.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 22fx |
Cryo-EM structure of mouse heavy-chain apoferritin at 1.24 A on CRYO ARM 200 II |
19.2 |
72.3 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 22ga |
Crystal structure of sorghum sulfotransferase LGS1 reveals sulfation-assisted BC-ring formation in strigolactone biosynthesis |
30.0 |
97.5 |
X-RAY DIFFRACTION |
GOOD
|