タイトル | Fragment screening for a protein-protein interaction inhibitor to WDR5. |
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ジャーナル・号・ページ | Struct Dyn., Vol. 6, Page 064701-064701, Year 2019 |
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掲載日 | 2019年6月24日 (構造データの登録日) |
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著者 | Dennis, M.L. / Morrow, B.J. / Dolezal, O. / Cuzzupe, A.N. / Stupple, A.E. / Newman, J. / Bentley, J. / Hattarki, M. / Nuttall, S.D. / Foitzik, R.C. ...Dennis, M.L. / Morrow, B.J. / Dolezal, O. / Cuzzupe, A.N. / Stupple, A.E. / Newman, J. / Bentley, J. / Hattarki, M. / Nuttall, S.D. / Foitzik, R.C. / Street, I.P. / Stupple, P.A. / Monahan, B.J. / Peat, T.S. |
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リンク | Struct Dyn. / PubMed:31768400 |
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手法 | X線回折 |
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解像度 | 1.5 - 2.45 Å |
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構造データ | PDB-6pg3: WDR5delta23 bound to (2-butyl-1H-imidazol-4-yl)methanol 手法: X-RAY DIFFRACTION / 解像度: 2.04 Å PDB-6pg4: WDR5delta32 bound to (2-methyl-1H-imidazol-4-yl)methanol 手法: X-RAY DIFFRACTION / 解像度: 1.6 Å PDB-6pg5: WDR5delta32 bound to benzyl (4-(5-(hydroxymethyl)-1H-imidazol-2-yl)butyl)carbamate 手法: X-RAY DIFFRACTION / 解像度: 1.99 Å PDB-6pg6: WDR5delta23 bound to N-(4-(5-(hydroxymethyl)-1H-imidazol-2-yl)butyl)acetamide 手法: X-RAY DIFFRACTION / 解像度: 1.68 Å PDB-6pg7: WDR5delta32 bound to (2-(3-methoxy-3-phenylpropyl)-1H-imidazol-4-yl)methanol 手法: X-RAY DIFFRACTION / 解像度: 2.45 Å PDB-6pg8: WDR5delta23 bound to (2-(3-phenylpropyl)-1H-imidazol-4-yl)methanol 手法: X-RAY DIFFRACTION / 解像度: 1.67 Å PDB-6pg9: WDR5delta23 bound to N-(4-(5-(hydroxymethyl)-1H-imidazol-2-yl)butyl)benzamide 手法: X-RAY DIFFRACTION / 解像度: 1.75 Å PDB-6pga: WDR5delta32 bound to methyl (4-(4-(hydroxymethyl)-1H-imidazol-2-yl)butyl)carbamate 手法: X-RAY DIFFRACTION / 解像度: 2.45 Å PDB-6pgb: WDR5delta32 bound to N-(4-(5-(hydroxymethyl)-1H-imidazol-2-yl)butyl)-2-phenylacetamide 手法: X-RAY DIFFRACTION / 解像度: 1.73 Å PDB-6pgc: WDR5delta32 bound to methyl benzyl(4-(4-(hydroxymethyl)-1H-imidazol-2-yl)butyl)carbamate 手法: X-RAY DIFFRACTION / 解像度: 1.81 Å PDB-6pgd: WDR5delta32 bound to peptidomimetic 手法: X-RAY DIFFRACTION / 解像度: 1.5 Å PDB-6pge: WDR5delta32 bound to ethyl 3-(4-(hydroxymethyl)-1H-imidazol-2-yl)propanoate 手法: X-RAY DIFFRACTION / 解像度: 1.76 Å PDB-6pgf: WDR5delta32 bound to N-(4-(4-(hydroxymethyl)-1H-imidazol-2-yl)butyl)acrylamide 手法: X-RAY DIFFRACTION / 解像度: 1.54 Å |
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化合物 | ChemComp-OHV: benzyl {4-[5-(hydroxymethyl)-1H-imidazol-2-yl]butyl}carbamate
ChemComp-OH7: N-{4-[4-(hydroxymethyl)-1H-imidazol-2-yl]butyl}acetamide
ChemComp-OH4: {2-[(3S)-3-methoxy-3-phenylpropyl]-1H-imidazol-4-yl}methanol
ChemComp-OGY: [2-(3-phenylpropyl)-1H-imidazol-4-yl]methanol
ChemComp-OH1: N-{4-[4-(hydroxymethyl)-1H-imidazol-2-yl]butyl}benzamide
ChemComp-OGM: methyl {4-[5-(hydroxymethyl)-1H-imidazol-2-yl]butyl}carbamate
ChemComp-OJG: N-{4-[5-(hydroxymethyl)-1H-imidazol-2-yl]butyl}-2-phenylacetamide
ChemComp-OJJ: methyl benzyl{4-[4-(hydroxymethyl)-1H-imidazol-2-yl]butyl}carbamate
ChemComp-OK4: N-acetyl-L-alanyl-5-[5-(hydroxymethyl)-1H-imidazol-2-yl]-L-norvalyl-L-valinamide
ChemComp-OJM: ethyl 3-[4-(hydroxymethyl)-1H-imidazol-2-yl]propanoate
ChemComp-OJP: N-{4-[4-(hydroxymethyl)-1H-imidazol-2-yl]butyl}prop-2-enamide
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由来 | - homo sapiens (ヒト)
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キーワード | PROTEIN BINDING/Inhibitor / Inhibitor / Scaffolding Protein (足場タンパク質) / B-propellor / Chromatin regulator / PROTEIN BINDING (タンパク質) / PROTEIN BINDING-Inhibitor complex |
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