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20 citations found for Shin, Y.
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In the title compound, C14H14Cl2N2O, the imidazole ring is almost parallel to the benzene ring, the dihedral angle between them being 7.3 (2)°. In the crystal, there is an intermolecular C—Cl
π interaction (Cl
centroid = 3.36 Å and C—Cl
centroid = 89.2°). In addition, a Cl
Cl contact of 3.411 (1) Å and an intermolecular C—H
N hydrogen bond are observed. These interactions contribute to the stabilization of the crystal packing.
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The X-ray structure of the complex of the nuclear transporter importin β with the zinc-finger-type transcription regulator Snail1 is reported.
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A dehydroascorbate reductase (DHAR) from rice (O. sativa L. japonica) was overexpressed, purified and crystallized. The crystals belonged to space group P21 and a complete native data set was obtained to a resolution of 1.9 Å.
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Monodehydroascorbate reductase (OsMDHAR) from O. sativa L. japonica was expressed as the active form using E. coli strain NiCo21 (DE3). X-ray diffraction data were collected to 1.9 Å resolution.
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Crystal structures of three PCNA homologues from Sulfolobus solfataricus have been determined in different oligomeric states. The structural features in different assemblies present a molecular model for clamp-ring forming and opening.
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The FAF1 UBX domain was crystallized. X-ray diffraction data were collected to 3.00 Å resolution and the crystals belonged to space group F4132.
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The title compound, C6H11N2O4PS3, crystallizes with two independent molecules in the asymmetric unit. The dihedral angles between the thiadiazole ring planes and the PS2 planes of the phosphorodithioate group are 86.51 (5) and 56.33 (5)° in the two molecules. In the crystal, weak intermolecular S
S [3.570 (8) Å] interactions and C—H
O and C—H
N hydrogen bonds contribute to the stabilization of the packing.
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The structure of SrB2O4 consists of slightly puckered borate layers with the composition (B2O4)n2n-; the Sr atoms are dodecahedrally coordinated by eight O atoms from neighbouring layers of borate molecules.
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In the title compound {systematic name: 4-chloro-N-[1-(1H-imidazol-1-yl)-2-propoxyethylidene]-2-(trifluoromethyl)aniline}, C15H15ClF3N3O, the dihedral angle between the aniline and imidazole ring planes is 81.80 (4)°. In the crystal structure, weak intermolecular C—H
X (X = N, O or F) hydrogen bonds and C—H
π interactions help to consolidate the packing.
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The title compound, [Ag(NO3)(C20H30S2)]n, was synthesized by the reaction of silver nitrate and 1,4-bis(cyclohexylthiomethyl)benzene (bctmb) in acetonitrile. The coordination polymer exhibits a two-dimensional layer structure. The layers are wave-like and parallel to the crystallographic ac plane; AgI ions are linked by the bctmb ligands and nitrate anions along the crystallographic a and c directions, respectively. In addition, the crystal structure is stabilized by C—H
O hydrogen bonds.
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In the asymmetric unit of the title compound {systematic name: N′-(2,4-dimethylphenyl)-N-[N-(2,4-dimethylphenyl)carboximidoyl]-N-methylmethanimidamide}, C19H23N3, which is a formamidine pesticide, there are two independent and conformationally similar molecules, with the dihedral angle between the mean planes of the 2,4-dimethylbenzene rings in each molecule being 41.63 (6) and 42.09 (5)°. The crystal structure is stabilized by a C—H
N hydrogen bond, as well as weak intermolecular C—H
π and π–π interactions [ring centroid separation = 3.7409 (15) Å], giving one-dimensional chains extending down the b direction.
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The N domain of p97/VCP was crystallized in complex with the UBX domain of FAF1. X-ray diffraction data were collected to 2.60 Å resolution and the crystals belonged to space group C2221.
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The coiled-coil domain of human PIST was crystallized at 293 K and diffracted to a resolution of 4.0 Å. The crystals were found to belong to space group P6222 or P6422, with unit-cell parameters a = b = 85.19, c = 240.09 Å, γ = 120.00°.
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Rab6A'(Q72L), a constitutively active GTP-binding form of Rab6A, was purified and crystallized. The crystals were found to belong to space group P22121, with unit-cell parameters a = 36.84, b = 96.78, c = 109.99 Å. The crystals were obtained at 293 K and diffracted to a resolution of 1.9 Å.
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The microprobe system installed on the nanoprobe/XAFS beamline BL8C at the Pohang Light Source, South Korea, is described.
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In the title compound, C11H18N4O2 (systematic name: 2-dimethylamino-5,6-dimethylpyrimidin-4-yl N,N-dimethylcarbamate), the pyrimidine ring and dimethylamino group are almost in the same plane, making a dihedral angle of 1.6 (1)°. The dihedral angle between the mean plane of the pyrimidine ring and that of the dimethylcarbamate group is 83.42 (5)°. In the crystal structure, intermolecular C—H
O hydrogen bonds contribute to the stabilization of the packing.
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The synthesis and crystal structure of {tris[2-(benzylamino)ethyl]amine-κ4N}silver(I) perchlorate, [Ag(C27H36N4)]ClO4 or [Ag(bz3tren)]ClO4 {bz3tren is tris[2-(benzylamino)ethyl]amine or N,N′,N′′-tribenzyltris(2-aminoethyl)amine} are reported. The Ag atom is coordinated to four N atoms of the tren unit and is located 0.604 (3) Å out of the trigonal plane described by the three secondary amine N atoms, away from the bridgehead N atom. Edge-to-face π–π interactions between the aromatic end groups, and weak interactions between Ag and arene, allow the formation of a pseudo-cage complex.