| 23on |
Crystal Structure Analysis of Bovine Carbonic Anhydrase II to 4-2-methyl-1,3-oxazol-5-ylbenzenesulfonamide |
24.3 |
78.4 |
X-RAY DIFFRACTION |
GOOD
|
| 23pg |
Cryo-EM structure of human ABCB7 in complex with CoPP:GSH/ADPVO4 |
39.9 |
131.9 |
ELECTRON MICROSCOPY |
GOOD
|
| 23ph |
Cryo-EM structures of the human ABCB7 in the apo state |
42.8 |
138.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 23pi |
Cryo-EM structure of the human ABCB7 in occluded state |
37.5 |
126.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 23qh |
Structure of importin alpha bound to the Psittacine Adenovirus B Fiber 1 protein nuclear localization signal |
28.3 |
98.9 |
X-RAY DIFFRACTION |
GOOD
|
| 23ri |
l-alanoyl-d-glutamate peptidase bacteriophage RB49 comlpex with Zn2+ |
15.5 |
51.9 |
SOLUTION NMR |
REASONABLE
|
| 23sf |
Cryo-EM structure of icosahedrally averaged bacteriophage RAN69 capsid |
58.4 |
205.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 23sg |
The composite Cryo-EM structure of bacteriophage RAN69 pre-ejectosome-portal complex |
72.5 |
217.3 |
ELECTRON MICROSCOPY |
GOOD
|
| 23sh |
The composite Cryo-EM structure of the tail region of bacteriophage RAN69 |
87.4 |
234.1 |
ELECTRON MICROSCOPY |
GOOD
|
| 23si |
Hen Egg-White Lysozyme (HEWL) complexed with Trans-Ferulic Acid |
15.3 |
51.2 |
X-RAY DIFFRACTION |
GOOD
|
| 23sp |
TamA complex with TamB DUF490 in lipid nanodisc |
40.7 |
148.0 |
ELECTRON MICROSCOPY |
GOOD
|
| 23sq |
TamA complex with TamB DUF490 in detergent micelles. |
40.5 |
145.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 23tz |
Crystal structure of cleaved DL-endopeptidase CwlO from Bacillus subtilis |
14.5 |
46.2 |
X-RAY DIFFRACTION |
GOOD
|
| 23vj |
Crystal structure of the MafR protein from Enterococcus faecalis |
36.7 |
121.3 |
X-RAY DIFFRACTION |
GOOD
|
| 23vk |
Crystal structure of full-length of APS kinase from Entamoeba histolytica |
49.0 |
165.1 |
X-RAY DIFFRACTION |
GOOD
|
| 23vl |
Crystal structure of AS-like domain of APS kinase from Entamoeba histolytica |
21.2 |
71.9 |
X-RAY DIFFRACTION |
GOOD
|
| 23vy |
Crystal structure of the mouse RORalpha ligand binding domain in fusion with an NRIP1 LXXLL peptide |
25.8 |
81.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 23wj |
Subtomogram average of Apoferrtin (11x11) using CRYO ARM 300II |
53.5 |
133.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 23xk |
Cryo-EM structure of human sodium/proton antiporter NHE1 in complex with Cariporide in an outward-open conformation |
31.5 |
102.4 |
ELECTRON MICROSCOPY |
GOOD
|
| 23xm |
Cryo-EM structure of human sodium/proton antiporter NHE1 in complex with Eniporide in an outward-open conformation |
31.3 |
101.8 |
ELECTRON MICROSCOPY |
GOOD
|
| 23xo |
Cryo-EM structure of human sodium/proton antiporter NHE1 in complex with Rimeporide in an outward-open conformation |
31.3 |
101.7 |
ELECTRON MICROSCOPY |
GOOD
|
| 240d |
EFFECT OF END BASE STEPS ON DNA FORM: CRYSTAL STRUCTURE OF THE A-DNA DECAMER D(CCGGGCCCGG) |
12.5 |
42.0 |
X-RAY DIFFRACTION |
GOOD
|
| 240l |
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
|
| 241d |
EXTENSION OF THE FOUR-STRANDED INTERCALATED CYTOSINE MOTIF BY ADENINE.ADENINE BASE PAIRING IN THE CRYSTAL STRUCTURE OF D(CCCAAT) |
11.9 |
38.3 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 241l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.5 |
57.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 242d |
MAD PHASING STRATEGIES EXPLORED WITH A BROMINATED OLIGONUCLEOTIDE CRYSTAL AT 1.65 A RESOLUTION. |
9.4 |
31.1 |
X-RAY DIFFRACTION |
GOOD
|
| 242l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.5 |
57.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 243d |
STRUCTURE OF THE DNA OCTANUCLEOTIDE D(ACGTACGT)2 |
10.6 |
35.8 |
X-RAY DIFFRACTION |
GOOD
|
| 243l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.5 |
58.0 |
X-RAY DIFFRACTION |
GOOD
|
| 244d |
THE HIGH-RESOLUTION CRYSTAL STRUCTURE OF A PARALLEL-STRANDED GUANINE TETRAPLEX |
20.2 |
75.2 |
X-RAY DIFFRACTION |
GOOD
|
| 244l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.4 |
57.8 |
X-RAY DIFFRACTION |
GOOD
|
| 245d |
;DNA-DRUG REFINEMENT: A COMPARISON OF THE PROGRAMS NUCLSQ, PROLSQ, SHELXL93 AND X-PLOR, USING THE LOW TEMPERATURE D(TGATCA)-NOGALAMYCIN STRUCTURE
; |
10.6 |
33.8 |
X-RAY DIFFRACTION |
EXCELLENT
|
| 245l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.5 |
59.1 |
X-RAY DIFFRACTION |
GOOD
|
| 246d |
;STRUCTURE OF THE PURINE-PYRIMIDINE ALTERNATING RNA DOUBLE HELIX, R(GUAUAUA)D(C) , WITH A 3'-TERMINAL DEOXY RESIDUE
; |
10.9 |
35.9 |
X-RAY DIFFRACTION |
GOOD
|
| 246l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.6 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 247d |
CRYSTAL STRUCTURES OF AN A-FORM DUPLEX WITH SINGLE-ADENOSINE BULGES AND A CONFORMATIONAL BASIS FOR SITE SPECIFIC RNA SELF-CLEAVAGE |
12.6 |
42.8 |
X-RAY DIFFRACTION |
GOOD
|
| 247l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.5 |
58.2 |
X-RAY DIFFRACTION |
REASONABLE
|
| 248d |
CRYSTAL STRUCTURES OF AN A-FORM DUPLEX WITH SINGLE-ADENOSINE BULGES AND A CONFORMATIONAL BASIS FOR SITE SPECIFIC RNA SELF-CLEAVAGE |
12.9 |
44.9 |
X-RAY DIFFRACTION |
REASONABLE
|
| 248l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.4 |
58.5 |
X-RAY DIFFRACTION |
GOOD
|
| 249d |
STRUCTURAL COMPARISON BETWEEN THE D(CTAG) SEQUENCE IN OLIGONUCLEOTIDES AND TRP AND MET REPRESSOR-OPERATOR COMPLEXES |
23.4 |
85.0 |
X-RAY DIFFRACTION |
REASONABLE
|
| 249l |
THE RESPONSE OF T4 LYSOZYME TO LARGE-TO-SMALL SUBSTITUTIONS WITHIN THE CORE AND ITS RELATION TO THE HYDROPHOBIC EFFECT |
17.5 |
58.3 |
X-RAY DIFFRACTION |
GOOD
|
| 24ah |
Crystal structure of nuclease MYG1 bound to Mn2+ |
24.9 |
84.5 |
X-RAY DIFFRACTION |
REASONABLE
|
| 24aj |
Crystal structure of nuclease MYG1 bound to Na+ |
24.9 |
82.9 |
X-RAY DIFFRACTION |
GOOD
|
| 24an |
Crystal structure of nuclease MYG1 bound to Mn2+ and AMP |
24.9 |
84.5 |
X-RAY DIFFRACTION |
GOOD
|
| 24ao |
Crystal structure of nuclease MYG1 bound to Mn2+ and GMP |
24.8 |
83.3 |
X-RAY DIFFRACTION |
REASONABLE
|
| 24ap |
Crystal structure of nuclease MYG1 bound to Mn2+ and UMP |
24.8 |
82.6 |
X-RAY DIFFRACTION |
GOOD
|
| 24aq |
Crystal structure of nuclease MYG1 bound to Mn2+ and CMP |
24.8 |
85.0 |
X-RAY DIFFRACTION |
GOOD
|
| 24aw |
Crystal structure of nuclease MYG1 bound to Mn2+ and dCMP |
24.8 |
65.8 |
X-RAY DIFFRACTION |
REASONABLE
|
| 24ay |
Crystal structure of nuclease MYG1 bound to Mn2+ and dTMP |
24.8 |
86.6 |
X-RAY DIFFRACTION |
REASONABLE
|
| 24bd |
Crystal structure of nuclease MYG1(D57A) bound to Mn2+ and AMP |
24.8 |
83.2 |
X-RAY DIFFRACTION |
GOOD
|