| 159l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
63.1 |
X-RAY DIFFRACTION |
GOOD
|
| 15c8 |
CATALYTIC ANTIBODY 5C8, FREE FAB |
25.6 |
78.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 160d |
HIGH RESOLUTION CRYSTAL STRUCTURE OF THE A-DNA DECAMER D(CCCGGCCGGG): NOVEL INTERMOLECULAR BASE-PAIRED G*(G.C) TRIPLETS |
12.1 |
41.8 |
X-RAY DIFFRACTION |
GOOD
|
| 160l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.5 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 161d |
A SINGLE 2'-HYDROXYL GROUP CONVERTS B-DNA TO A-DNA: CRYSTAL STRUCTURE OF THE DNA-RNA CHIMERIC DECAMER DUPLEX D(CCGGC)R(G)D(CCGG) WITH A NOVEL INTERMOLECULAR G.C BASE-PAIRED QUADRUPLET |
12.3 |
43.2 |
X-RAY DIFFRACTION |
GOOD
|
| 161l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 162l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 163l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 164l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 165d |
THE STRUCTURE OF A MISPAIRED RNA DOUBLE HELIX AT 1.6 ANGSTROMS RESOLUTION AND IMPLICATIONS FOR THE PREDICTION OF RNA SECONDARY STRUCTURE |
12.7 |
48.7 |
X-RAY DIFFRACTION |
GOOD
|
| 165l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.5 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 166d |
DRUG-DNA MINOR GROOVE RECOGNITION: CRYSTAL STRUCTURE OF GAMMA-OXAPENTAMIDINE COMPLEXED WITH D(CGCGAATTCGCG)2 |
13.7 |
46.4 |
X-RAY DIFFRACTION |
GOOD
|
| 166l |
CONTROL OF ENZYME ACTIVITY BY AN ENGINEERED DISULFIDE BOND |
17.4 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 167d |
THE CRYSTAL STRUCTURE OF C-C-A-T-T-A-A-T-G-G: IMPLICATIONS FOR BENDING OF B-DNA AT T-A STEPS |
12.4 |
41.1 |
X-RAY DIFFRACTION |
GOOD
|
| 167l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
24.0 |
76.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 168d |
STABILIZING EFFECTS OF THE RNA 2'-SUBSTITUENT: CRYSTAL STRUCTURE OF AN OLIGODEOXYNUCLEOTIDE DUPLEX CONTAINING 2'-O-METHYLATED ADENOSINES |
12.0 |
40.9 |
X-RAY DIFFRACTION |
GOOD
|
| 168l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
35.3 |
102.9 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 169d |
THE SOLUTION STRUCTURE OF THE R(GCG)D(TATACCC):D(GGGTATACGC) OKAZAKI FRAGMENT CONTAINS TWO DISTINCT DUPLEX MORPHOLOGIES CONNECTED BY A JUNCTION |
12.2 |
39.9 |
SOLUTION NMR |
REASONABLE
|
| 169l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
35.0 |
101.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 16gs |
GLUTATHIONE S-TRANSFERASE P1-1 APO FORM 3 |
22.0 |
64.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 16pk |
PHOSPHOGLYCERATE KINASE FROM TRYPANOSOMA BRUCEI BISUBSTRATE ANALOG |
23.8 |
73.7 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 16vp |
CONSERVED CORE OF THE HERPES SIMPLEX VIRUS TRANSCRIPTIONAL REGULATORY PROTEIN VP16 |
23.7 |
86.9 |
X-RAY DIFFRACTION |
GOOD
|
| 170d |
SOLUTION STRUCTURE OF A DNA DODECAMER CONTAINING THE ANTI-NEOPLASTIC AGENT ARABINOSYLCYTOSINE: COMBINED USE OF NMR, RESTRAINED MOLECULAR DYNAMICS AND FULL RELAXATION MATRIX REFINEMENT |
14.3 |
47.9 |
SOLUTION NMR |
REASONABLE
|
| 170l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
17.4 |
56.4 |
X-RAY DIFFRACTION |
REASONABLE
|
| 171d |
SOLUTION STRUCTURE OF A DNA DODECAMER CONTAINING THE ANTI-NEOPLASTIC AGENT ARABINOSYLCYTOSINE: COMBINED USE OF NMR, RESTRAINED MOLECULAR DYNAMICS AND FULL RELAXATION MATRIX REFINEMENT |
14.0 |
47.0 |
SOLUTION NMR |
GOOD
|
| 171l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
17.3 |
57.7 |
X-RAY DIFFRACTION |
GOOD
|
| 172d |
MULTIPLE BINDING MODES OF ANTICANCER DRUG ACTINOMYCIN D: X-RAY, MOLECULAR MODELING, AND SPECTROSCOPIC STUDIES OF D(GAAGCTTC)2-ACTINOMYCIN D COMPLEXES AND ITS HOST DNA |
15.3 |
53.5 |
X-RAY DIFFRACTION |
GOOD
|
| 172l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
18.2 |
60.5 |
X-RAY DIFFRACTION |
GOOD
|
| 173d |
MULTIPLE BINDING MODES OF ANTICANCER DRUG ACTINOMYCIN D: X-RAY, MOLECULAR MODELING, AND SPECTROSCOPIC STUDIES OF D(GAAGCTTC)2-ACTINOMYCIN D COMPLEXES AND ITS HOST DNA |
16.9 |
53.7 |
X-RAY DIFFRACTION |
REASONABLE
|
| 173l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
18.0 |
59.4 |
X-RAY DIFFRACTION |
GOOD
|
| 174l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
22.7 |
73.7 |
X-RAY DIFFRACTION |
GOOD
|
| 175d |
THE DNA SEQUENCE GCGAATGAGC CONTAINING THE HUMAN CENTROMERE CORE SEQUENCE GAAT FORMS A SELF-COMPLEMENTARY DUPLEX WITH SHEARED G:A PAIRS IN SOLUTION |
12.0 |
42.0 |
SOLUTION NMR |
GOOD
|
| 175l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
23.8 |
91.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 176d |
NMR SOLUTION STRUCTURE OF A PEPTIDE NUCLEIC ACID COMPLEXED WITH RNA |
9.1 |
31.9 |
SOLUTION NMR |
GOOD
|
| 176l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
24.2 |
82.2 |
X-RAY DIFFRACTION |
GOOD
|
| 177d |
SOLUTION STRUCTURE AND HYDRATION PATTERNS OF A PYRIMIDINE(DOT)PURINE(DOT)PYRIMIDINE DNA TRIPLEX CONTAINING A NOVEL T(DOT)CG TRIPLE |
10.5 |
32.4 |
SOLUTION NMR |
GOOD
|
| 177l |
Protein flexibility and adaptability seen in 25 crystal forms of T4 LYSOZYME |
17.3 |
57.5 |
X-RAY DIFFRACTION |
GOOD
|
| 178d |
CRYSTAL STRUCTURE OF A DNA DUPLEX CONTAINING 8-HYDROXYDEOXYGUANINE.ADENINE BASE-PAIRS |
13.6 |
46.2 |
X-RAY DIFFRACTION |
GOOD
|
| 178l |
Protein flexibility and adaptability seen in 25 crystal forms of T4 LYSOZYME |
17.9 |
59.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 179d |
SOLUTION STRUCTURE OF THE D(T-C-G-A) DUPLEX AT ACIDIC PH: A PARALLEL-STRANDED HELIX CONTAINING C+.C, G.G AND A.A PAIRS |
6.8 |
22.7 |
SOLUTION NMR |
GOOD
|
| 17gs |
GLUTATHIONE S-TRANSFERASE P1-1 |
22.1 |
65.1 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 17ra |
BRANCHPOINT HELIX FROM YEAST AND BINDING SITE FOR PHAGE GA/MS2 COAT PROTEINS, NMR, 12 STRUCTURES |
13.3 |
51.1 |
SOLUTION NMR |
REASONABLE
|
| 180d |
SEQUENCE-DEPENDENT MICROHETEROGENEITY OF Z-DNA: THE CRYSTAL AND MOLECULAR STRUCTURES OF D(CACGCG).D(CGCGTG) AND D(CGCACG).D(CGTGCG) |
9.4 |
31.5 |
X-RAY DIFFRACTION |
GOOD
|
| 180l |
PROTEIN FLEXIBILITY AND ADAPTABILITY SEEN IN 25 CRYSTAL FORMS OF T4 LYSOZYME |
35.0 |
103.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 181d |
SEQUENCE-DEPENDENT MICROHETEROGENEITY OF Z-DNA: THE CRYSTAL AND MOLECULAR STRUCTURES OF D(CACGCG).D(CGCGTG) AND D(CGCACG).D(CGTGCG) |
9.4 |
31.1 |
X-RAY DIFFRACTION |
GOOD
|
| 181l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.4 |
58.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 182d |
DNA-NOGALAMYCIN INTERACTIONS: THE CRYSTAL STRUCTURE OF D(TGATCA) COMPLEXED WITH NOGALAMYCIN |
10.4 |
33.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 182l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.5 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 183d |
X-RAY STRUCTURE OF A DNA DECAMER CONTAINING 7, 8-DIHYDRO-8-OXOGUANINE |
12.2 |
39.5 |
X-RAY DIFFRACTION |
GOOD
|
| 183l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.4 |
59.9 |
X-RAY DIFFRACTION |
GOOD
|