| 251l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.4 |
58.1 |
X-RAY DIFFRACTION |
GOOD
|
| 252d |
CRYSTAL STRUCTURE OF THE B-DNA DECAMER D(CGCAATTGCG)2; SEQUENCE-DEPENDENT CROSSED HELIX PACKING |
12.4 |
41.5 |
X-RAY DIFFRACTION |
GOOD
|
| 252l |
GENERATING LIGAND BINDING SITES IN T4 LYSOZYME USING DEFICIENCY-CREATING SUBSTITUTIONS |
17.6 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 253d |
CRYSTAL STRUCTURE OF THE B-DNA NONAMER D(GCGTACGCG) WITH A NOVEL D[G*(G.C)] BASE-TRIPLET INVOLVING THE MINOR GROOVE |
11.7 |
40.1 |
X-RAY DIFFRACTION |
GOOD
|
| 253l |
LYSOZYME |
17.6 |
57.4 |
X-RAY DIFFRACTION |
GOOD
|
| 254d |
ALTERNATING AND NON-ALTERNATING DG-DC HEXANUCLEOTIDES CRYSTALLIZE AS CANONICAL A-DNA |
10.0 |
32.1 |
X-RAY DIFFRACTION |
GOOD
|
| 254l |
LYSOZYME |
17.6 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 255d |
CRYSTAL STRUCTURE OF AN RNA DOUBLE HELIX INCORPORATING A TRACK OF NON-WATSON-CRICK BASE PAIRS |
13.7 |
42.8 |
X-RAY DIFFRACTION |
GOOD
|
| 255l |
HYDROLASE |
17.6 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 256b |
;IMPROVEMENT OF THE 2.5 ANGSTROMS RESOLUTION MODEL OF CYTOCHROME B562 BY REDETERMINING THE PRIMARY STRUCTURE AND USING MOLECULAR GRAPHICS
; |
20.4 |
63.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 256d |
ALTERNATING AND NON-ALTERNATING DG-DC HEXANUCLEOTIDES CRYSTALLIZE AS CANONICAL A-DNA |
10.0 |
32.1 |
X-RAY DIFFRACTION |
GOOD
|
| 256l |
BACTERIOPHAGE T4 LYSOZYME |
17.6 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 257d |
ALTERNATING AND NON-ALTERNATING DG-DC HEXANUCLEOTIDES CRYSTALLIZE AS CANONICAL A-DNA |
9.8 |
32.1 |
X-RAY DIFFRACTION |
GOOD
|
| 257l |
AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME |
17.4 |
58.7 |
X-RAY DIFFRACTION |
GOOD
|
| 258d |
FACTORS AFFECTING SEQUENCE SELECTIVITY ON NOGALAMYCIN INTERCALATION: THE CRYSTAL STRUCTURE OF D(TGTACA)-NOGALAMYCIN |
15.1 |
49.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 258l |
AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME |
17.4 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 259d |
RNA HYDRATION: A DETAILED LOOK |
11.0 |
35.9 |
X-RAY DIFFRACTION |
GOOD
|
| 259l |
AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME |
17.4 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 25bv |
Crystal structure of P450cam mutant-F87R |
28.9 |
86.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 25c8 |
CATALYTIC ANTIBODY 5C8, FAB-HAPTEN COMPLEX |
25.6 |
78.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 25hf |
SFX crystal structure of insulin aspart |
14.8 |
48.0 |
X-RAY DIFFRACTION |
GOOD
|
| 25hk |
Crystal structure of a TctC solute binding protein from Vibrio sp. C42, no ligand |
27.5 |
94.6 |
X-RAY DIFFRACTION |
GOOD
|
| 25hl |
SFX crystal structure of insulin detemir |
24.6 |
85.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 25hn |
Cryo-EM structure of native Rubisco from Nitrosospira multiformis |
47.7 |
144.2 |
ELECTRON MICROSCOPY |
GOOD
|
| 25ih |
Cryo-EM structure of human Nav1.6 in complex with Cn2 |
41.3 |
139.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 25ii |
Cryo-EM structure of human Nav1.6 in complex with Iota-Conotoxin RXIA |
40.8 |
138.6 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 25ij |
Cryo-EM structure of human Nav1.6 in complex with delta-paraponeritoxin-Pc1a |
40.7 |
136.5 |
ELECTRON MICROSCOPY |
GOOD
|
| 25ik |
Cryo-EM structure of MasR(FL)-Gq |
36.8 |
118.7 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 25il |
Cryo-EM structure of MasR(del2-25)-Gq |
36.7 |
119.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 25nv |
A complex of PTH1R/Gs bound to a PTHrP analogue with five beta-amino acids |
41.5 |
158.4 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 25nx |
A complex of PTH1R/Gs bound to a PTHrP analogue with three beta-amino acids |
41.2 |
154.9 |
ELECTRON MICROSCOPY |
REASONABLE
|
| 25pt |
Crystal structure of TsaBGL |
41.5 |
123.5 |
X-RAY DIFFRACTION |
GOOD
|
| 25pv |
Structure of the anthrax protective antigen in complex with a potent neutralizing antibody |
34.3 |
117.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 25sj |
An NMR solution model of duplex RNA r(GGUCGACC)2 |
10.7 |
34.9 |
SOLUTION NMR |
GOOD
|
| 25sm |
An NMR solution model of 3-CN-3-deazaguanosine modified duplex RNA |
10.6 |
34.1 |
SOLUTION NMR |
GOOD
|
| 25vx |
Crystal Structure of MYST histone acetyltransferase KAT6A in complex with inhibitor Compound 9 |
20.9 |
76.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 25wn |
Crystal structure of Candida albicans Eukaryotic translation initiation factor 5A |
20.3 |
78.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 25yr |
High-resolution crystal structure of Arp2/3 complex inhibitor Arpin |
23.2 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 25yv |
Crystal structure of SchOMT2 from Schisandra chinensis |
29.9 |
102.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 260d |
;CRYSTAL STRUCTURE OF THE SELF-COMPLEMENTARY 5'-PURINE START DECAMER D(GCACGCGTGC) IN THE A-DNA CONFORMATION-PART II
; |
11.4 |
36.4 |
X-RAY DIFFRACTION |
GOOD
|
| 260l |
AN ADAPTABLE METAL-BINDING SITE ENGINEERED INTO T4 LYSOZYME |
17.5 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 261d |
CRYSTAL STRUCTURE OF THE DNA DECAMER D(CGCAATTGCG) COMPLEXED WITH THE MINOR GROOVE BINDING DRUG NETROPSIN |
12.1 |
43.7 |
X-RAY DIFFRACTION |
GOOD
|
| 261l |
STRUCTURAL CHARACTERISATION OF AN ENGINEERED TANDEM REPEAT CONTRASTS THE IMPORTANCE OF CONTEXT AND SEQUENCE IN PROTEIN FOLDING |
18.3 |
61.6 |
X-RAY DIFFRACTION |
GOOD
|
| 262l |
STRUCTURAL CHARACTERISATION OF AN ENGINEERED TANDEM REPEAT CONTRASTS THE IMPORTANCE OF CONTEXT AND SEQUENCE IN PROTEIN FOLDING |
31.6 |
94.2 |
X-RAY DIFFRACTION |
GOOD
|
| 263d |
ISOHELICITY AND PHASING IN DRUG-DNA SEQUENCE RECOGNITION: CRYSTAL STRUCTURE OF A TRIS(BENZIMIDAZOLE)-OLIGONUCLEOTIDE COMPLEX |
13.6 |
46.7 |
X-RAY DIFFRACTION |
GOOD
|
| 264d |
;THREE-DIMENSIONAL CRYSTAL STRUCTURE OF THE A-TRACT DNA DODECAMER D(CGCAAATTTGCG) COMPLEXED WITH THE MINOR-GROOVE-BINDING DRUG HOECHST 33258
; |
13.7 |
47.4 |
X-RAY DIFFRACTION |
GOOD
|
| 265d |
STRUCTURAL STUDIES ON NUCLEIC ACIDS |
13.6 |
47.1 |
X-RAY DIFFRACTION |
GOOD
|
| 266d |
STRUCTURAL STUDIES ON NUCLEIC ACIDS |
13.6 |
46.8 |
X-RAY DIFFRACTION |
GOOD
|
| 267d |
STRUCTURAL STUDIES ON NUCLEIC ACIDS |
13.5 |
46.7 |
X-RAY DIFFRACTION |
GOOD
|
| 268d |
STRUCTURAL STUDIES ON NUCLEIC ACIDS |
13.5 |
46.6 |
X-RAY DIFFRACTION |
GOOD
|