| 184d |
SELF-ASSOCIATION OF A DNA LOOP CREATES A QUADRUPLEX: CRYSTAL STRUCTURE OF D(GCATGCT) AT 1.8 ANGSTROMS RESOLUTION |
8.2 |
29.9 |
X-RAY DIFFRACTION |
GOOD
|
| 184l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.5 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 185d |
;SEQUENCE SPECIFICITY OF QUINOXALINE ANTIBIOTICS. 1. SOLUTION STRUCTURE OF A 1:1 COMPLEX BETWEEN TRIOSTIN A AND [D(GACGTC)]2 AND COMPARISON WITH THE SOLUTION STRUCTURE OF THE [N-MECYS3, N-MECYS7]TANDEM-[D(GATATC)]2 COMPLEX
; |
10.0 |
34.4 |
SOLUTION NMR |
GOOD
|
| 185l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.5 |
58.6 |
X-RAY DIFFRACTION |
GOOD
|
| 186d |
SOLUTION STRUCTURE OF THE TETRAHYMENA TELOMERIC REPEAT D(T2G4)4 G-TETRAPLEX |
10.7 |
38.8 |
SOLUTION NMR |
GOOD
|
| 186l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.5 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 187d |
HYDRATION PATTERNS AND INTERMOLECULAR INTERACTIONS IN A-DNA CRYSTAL STRUCTURES. IMPLICATIONS FOR DNA RECOGNITION |
10.7 |
35.9 |
X-RAY DIFFRACTION |
GOOD
|
| 187l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.5 |
58.8 |
X-RAY DIFFRACTION |
GOOD
|
| 188d |
HYDRATION PATTERNS AND INTERMOLECULAR INTERACTIONS IN A-DNA CRYSTAL STRUCTURES. IMPLICATIONS FOR DNA RECOGNITION |
10.6 |
35.6 |
X-RAY DIFFRACTION |
GOOD
|
| 188l |
SPECIFICITY OF LIGAND BINDING IN A BURIED NON-POLAR CAVITY OF T4 LYSOZYME: LINKAGE OF DYNAMICS AND STRUCTURAL PLASTICITY |
17.4 |
57.9 |
X-RAY DIFFRACTION |
GOOD
|
| 189d |
HYDRATION PATTERNS AND INTERMOLECULAR INTERACTIONS IN A-DNA CRYSTAL STRUCTURES. IMPLICATIONS FOR DNA RECOGNITION |
10.5 |
35.9 |
X-RAY DIFFRACTION |
GOOD
|
| 189l |
ENHANCEMENT OF PROTEIN STABILITY BY THE COMBINATION OF POINT MUTATIONS IN T4 LYSOZYME IS ADDITIVE |
17.8 |
58.9 |
X-RAY DIFFRACTION |
GOOD
|
| 18gs |
GLUTATHIONE S-TRANSFERASE P1-1 COMPLEXED WITH 1-(S-GLUTATHIONYL)-2,4-DINITROBENZENE |
21.9 |
64.6 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 190d |
Crystal structure of a four-stranded intercalated DNA: d(C4) |
12.5 |
40.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 190l |
A HELIX INITIATION SIGNAL IN T4 LYSOZYME IDENTIFIED BY POLYALANINE MUTAGENESIS |
17.3 |
56.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1914 |
SIGNAL RECOGNITION PARTICLE ALU RNA BINDING HETERODIMER, SRP9/14 |
17.8 |
66.3 |
X-RAY DIFFRACTION |
GOOD
|
| 191d |
CRYSTAL STRUCTURE OF INTERCALATED FOUR-STRANDED D(C3T) |
10.2 |
35.3 |
X-RAY DIFFRACTION |
GOOD
|
| 191l |
A HELIX INITIATION SIGNAL IN T4 LYSOZYME IDENTIFIED BY POLYALANINE MUTAGENESIS |
17.3 |
57.5 |
X-RAY DIFFRACTION |
GOOD
|
| 192d |
RECOMBINATION-LIKE STRUCTURE OF D(CCGCGG) |
10.5 |
36.5 |
X-RAY DIFFRACTION |
GOOD
|
| 192l |
A HELIX INITIATION SIGNAL IN T4 LYSOZYME IDENTIFIED BY POLYALANINE MUTAGENESIS |
17.2 |
61.2 |
X-RAY DIFFRACTION |
GOOD
|
| 193d |
SOLUTION STRUCTURE OF A QUINOMYCIN BISINTERCALATOR-DNA COMPLEX |
11.9 |
40.3 |
SOLUTION NMR |
GOOD
|
| 193l |
THE 1.33 A STRUCTURE OF TETRAGONAL HEN EGG WHITE LYSOZYME |
15.1 |
51.5 |
X-RAY DIFFRACTION |
GOOD
|
| 194d |
X-RAY STRUCTURES OF THE B-DNA DODECAMER D(CGCGTTAACGCG) WITH AN INVERTED CENTRAL TETRANUCLEOTIDE AND ITS NETROPSIN COMPLEX |
13.8 |
47.4 |
X-RAY DIFFRACTION |
GOOD
|
| 194l |
THE 1.40 A STRUCTURE OF SPACEHAB-01 HEN EGG WHITE LYSOZYME |
15.2 |
51.4 |
X-RAY DIFFRACTION |
GOOD
|
| 195d |
X-RAY STRUCTURES OF THE B-DNA DODECAMER D(CGCGTTAACGCG) WITH AN INVERTED CENTRAL TETRANUCLEOTIDE AND ITS NETROPSIN COMPLEX |
13.6 |
47.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 195l |
;THERMODYNAMIC AND STRUCTURAL COMPENSATION IN "SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME
; |
17.4 |
59.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 196d |
CRYSTAL STRUCTURE OF C-T-C-T-C-G-A-G-A-G: IMPLICATIONS FOR THE STRUCTURE OF THE HOLLIDAY JUNCTION |
12.2 |
47.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 196l |
;THERMODYNAMIC AND STRUCTURAL COMPENSATION IN "SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME
; |
17.4 |
59.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 197d |
ORTHORHOMBIC CRYSTAL STRUCTURE OF THE A-DNA OCTAMER D(GTACGTAC). COMPARISON WITH THE TETRAGONAL STRUCTURE |
10.7 |
41.1 |
X-RAY DIFFRACTION |
REASONABLE
|
| 197l |
;THERMODYNAMIC AND STRUCTURAL COMPENSATION IN "SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME
; |
17.4 |
58.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 198d |
A TRIGONAL FORM OF THE IDARUBICIN-D(CGATCG) COMPLEX: CRYSTAL AND MOLECULAR STRUCTURE AT 2.0 ANGSTROMS RESOLUTION |
16.3 |
55.9 |
X-RAY DIFFRACTION |
GOOD
|
| 198l |
;THERMODYNAMIC AND STRUCTURAL COMPENSATION IN "SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME
; |
17.4 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 199d |
Solution structure of the monoalkylated mitomycin c-DNA complex |
10.8 |
36.0 |
SOLUTION NMR |
GOOD
|
| 199l |
;THERMODYNAMIC AND STRUCTURAL COMPENSATION IN "SIZE-SWITCH" CORE-REPACKING VARIANTS OF T4 LYSOZYME
; |
17.4 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 19gs |
Glutathione s-transferase p1-1 |
21.9 |
65.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 19hc |
NINE-HAEM CYTOCHROME C FROM DESULFOVIBRIO DESULFURICANS ATCC 27774 |
27.9 |
85.2 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a00 |
HEMOGLOBIN (VAL BETA1 MET, TRP BETA37 TYR) MUTANT |
24.8 |
74.5 |
X-RAY DIFFRACTION |
GOOD
|
| 1a01 |
HEMOGLOBIN (VAL BETA1 MET, TRP BETA37 ALA) MUTANT |
24.9 |
70.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1a02 |
STRUCTURE OF THE DNA BINDING DOMAINS OF NFAT, FOS AND JUN BOUND TO DNA |
26.9 |
93.4 |
X-RAY DIFFRACTION |
GOOD
|
| 1a03 |
;THE THREE-DIMENSIONAL STRUCTURE OF CA2+-BOUND CALCYCLIN: IMPLICATIONS FOR CA2+-SIGNAL TRANSDUCTION BY S100 PROTEINS, NMR, 20 STRUCTURES
; |
17.5 |
58.7 |
SOLUTION NMR |
REASONABLE
|
| 1a04 |
THE STRUCTURE OF THE NITRATE/NITRITE RESPONSE REGULATOR PROTEIN NARL IN THE MONOCLINIC C2 CRYSTAL FORM |
26.3 |
89.7 |
X-RAY DIFFRACTION |
GOOD
|
| 1a05 |
CRYSTAL STRUCTURE OF THE COMPLEX OF 3-ISOPROPYLMALATE DEHYDROGENASE FROM THIOBACILLUS FERROOXIDANS WITH 3-ISOPROPYLMALATE |
27.2 |
90.0 |
X-RAY DIFFRACTION |
GOOD
|
| 1a06 |
CALMODULIN-DEPENDENT PROTEIN KINASE FROM RAT |
21.2 |
67.5 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 1a07 |
C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-MALONYL TYR-GLU-(N,N-DIPENTYL AMINE) |
19.6 |
64.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a08 |
C-SRC (SH2 DOMAIN) COMPLEXED WITH ACE-DIFLUORO PHOSPHOTYR-GLU-(N,N-DIPENTYL AMINE) |
19.7 |
65.9 |
X-RAY DIFFRACTION |
GOOD
|
| 1a09 |
C-src (SH2 domain) complexed with ace-formyl phosphotyr-glu-(n,n-dipentyl amine) |
19.7 |
64.1 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0a |
PHOSPHATE SYSTEM POSITIVE REGULATORY PROTEIN PHO4/DNA COMPLEX |
20.3 |
68.2 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0b |
HISTIDINE-CONTAINING PHOSPHOTRANSFER DOMAIN OF ARCB FROM ESCHERICHIA COLI |
15.6 |
55.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 1a0c |
XYLOSE ISOMERASE FROM THERMOANAEROBACTERIUM THERMOSULFURIGENES |
34.4 |
103.3 |
X-RAY DIFFRACTION |
GOOD
|
| 1a0d |
XYLOSE ISOMERASE FROM BACILLUS STEAROTHERMOPHILUS |
34.5 |
102.7 |
X-RAY DIFFRACTION |
GOOD
|