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CRYSTAL STRUCTURES OF NK1-HEPARIN COMPLEXES REVEAL THE BASIS FOR NK1 ACTIVITY AND ENABLE ENGINEERING OF POTENT AGONISTS OF THE MET RECEPTOR

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Protein Data Bank Japan2024-11-06 更新2026-03-21 收录
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CRYSTAL STRUCTURES OF NK1-HEPARIN COMPLEXES REVEAL THE BASIS FOR NK1 ACTIVITY AND ENABLE ENGINEERING OF POTENT AGONISTS OF THE MET RECEPTOR Descriptor: 2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose, 2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid, 2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid-(1-4)-2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose-(1-4)-2-O-sulfo-alpha-L-idopyranuronic acid, ... Authors: Lietha, D, Chirgadze, D.Y, Mulloy, B, Blundell, T.L, Gherardi, E. Deposit date: 2001-09-20 Release date: 2001-10-02 Last modified: 2024-11-06 Method: X-RAY DIFFRACTION (3 Å) Cite: Crystal Structures of Nk1-Heparin Complexes Reveal the Basis for Nk1 Activity and Enable Engineering of Potent Agonists of the met Receptor Embo J., 20, 2001

本数据集主题为NK1-肝素复合物的晶体结构,其揭示了NK1发挥活性的分子基础,并可用于工程化构建MET受体的强效激动剂。数据集描述的多糖配体序列如下: 1. 2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose) 2. 2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid) 3. 2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid)-(1→4)-2-脱氧-6-O-磺基-2-(磺酰胺基)-α-D-吡喃葡萄糖(2-deoxy-6-O-sulfo-2-(sulfoamino)-alpha-D-glucopyranose)-(1→4)-2-O-磺基-α-L-艾杜吡喃糖醛酸(2-O-sulfo-alpha-L-idopyranuronic acid) …… 作者:Lietha, D、Chirgadze, D.Y、Mulloy, B、Blundell, T.L、Gherardi, E 提交日期:2001年9月20日 发布日期:2001年10月2日 最后修改日期:2024年11月6日 实验方法:X射线衍射(分辨率3埃) 引用文献:《NK1-肝素复合物的晶体结构揭示NK1活性的分子基础并可用于构建MET受体强效激动剂》,发表于《欧洲分子生物学组织期刊(EMBO J.)》,第20卷,2001年。
创建时间:
2001-09-20
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