1GP3
| Human IGF2R domain 11 | 分子名称: | CATION-INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR | 著者 | Brown, J, Esnouf, R.M, Jones, M.A, Linnell, J, Harlos, K, Hassan, A.B, Jones, E.Y. | 登録日 | 2001-10-29 | 公開日 | 2002-02-28 | 最終更新日 | 2023-12-13 | 実験手法 | X-RAY DIFFRACTION (1.95 Å) | 主引用文献 | Structure of a Functional Igf2R Fragment Determined from the Anomalous Scattering of Sulfur Embo J., 21, 2002
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5IEI
| X-ray crystallographic structure of a high affinity IGF2 antagonist (Domain11 AB5 RHH) based on human IGF2R domain 11 | 分子名称: | 1,2-ETHANEDIOL, Cation-independent mannose-6-phosphate receptor, GLYCEROL, ... | 著者 | Nicholls, R.D, Williams, C, Strickland, M, Frago, S, Hassan, A.B, Crump, M.P. | 登録日 | 2016-02-25 | 公開日 | 2016-05-18 | 最終更新日 | 2024-10-09 | 実験手法 | X-RAY DIFFRACTION (2.8 Å) | 主引用文献 | Functional evolution of IGF2:IGF2R domain 11 binding generates novel structural interactions and a specific IGF2 antagonist. Proc.Natl.Acad.Sci.USA, 113, 2016
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2CNJ
| NMR studies on the interaction of Insulin-Growth Factor II (IGF-II) with IGF2R domain 11 | 分子名称: | CATION-INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR | 著者 | Williams, C, Prince, S, Zaccheo, O, Hassan, A.B, Crosby, J, Crump, M. | 登録日 | 2006-05-22 | 公開日 | 2007-05-22 | 最終更新日 | 2024-05-15 | 実験手法 | SOLUTION NMR | 主引用文献 | Structural Insights Into the Interaction of Insulin-Like Growth Factor 2 with Igf2R Domain 11. Structure, 15, 2007
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1GP0
| Human IGF2R domain 11 | 分子名称: | CATION-INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR, SULFATE ION | 著者 | Brown, J, Esnouf, R.M, Jones, M.A, Linnell, J, Harlos, K, Hassan, A.B, Jones, E.Y. | 登録日 | 2001-10-29 | 公開日 | 2002-02-28 | 最終更新日 | 2019-04-10 | 実験手法 | X-RAY DIFFRACTION (1.4 Å) | 主引用文献 | Structure of a Functional Igf2R Fragment Determined from the Anomalous Scattering of Sulfur Embo J., 21, 2002
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2L21
| chicken IGF2R domain 11 | 分子名称: | Cation-independent mannose-6-phosphate receptor | 著者 | Williams, C, Hoppe, H, Strickland, M, Frago, S, Ellis, R.Z, Wattana-Amorn, P, Prince, S.N, Zaccheo, O.J, Forbes, B, Jones, E.Y, Rezgui, D.Z, Crump, M.P, Hassan, A.B. | 登録日 | 2010-08-10 | 公開日 | 2012-02-15 | 最終更新日 | 2023-06-14 | 実験手法 | SOLUTION NMR | 主引用文献 | CD loop dependency of the IGF2: M6P/IGF2 receptor binding interaction predates imprinting To be Published
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2L29
| Complex structure of E4 mutant human IGF2R domain 11 bound to IGF-II | 分子名称: | Insulin-like growth factor 2 receptor variant, Insulin-like growth factor II | 著者 | Williams, C, Hoppe, H, Rezgui, D, Strickland, M, Frago, S, Ellis, R.Z, Wattana-Amorn, P, Prince, S.N, Zaccheo, O.J, Forbes, B, Jones, E.Y, Crump, M.P, Hassan, A.B. | 登録日 | 2010-08-13 | 公開日 | 2012-02-15 | 最終更新日 | 2024-10-30 | 実験手法 | SOLUTION NMR | 主引用文献 | An exon splice enhancer primes IGF2:IGF2R binding site structure and function evolution. Science, 338, 2012
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2M68
| NMR solution structure ensemble of 3-4D mutant domain 11 IGF2R in complex with IGF2 (domain 11 structure only) | 分子名称: | Insulin-like growth factor 2 receptor variant | 著者 | Strickland, M, Williams, C, Richards, E, Minnall, L, Crump, M.P, Frago, S, Hughes, J, Garner, L, Hoppe, H, Rezgui, D, Zaccheo, O.J, Prince, S.N, Hassan, A.B, Whittaker, S. | 登録日 | 2013-03-27 | 公開日 | 2014-10-15 | 最終更新日 | 2024-10-30 | 実験手法 | SOLUTION NMR | 主引用文献 | Functional evolution of IGF2:IGF2R domain 11 binding generates novel structural interactions and a specific IGF2 antagonist. Proc.Natl.Acad.Sci.USA, 113, 2016
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2L2A
| Mutated Domain 11 of the Cytoplasmic region of the Cation-independent mannose-6-phosphate receptor | 分子名称: | Insulin-like growth factor 2 receptor variant | 著者 | Williams, C, Hoppe, H, Rezgui, D, Strickland, M, Frago, S, Ellis, R.Z, Wattana-Amorn, P, Prince, S.N, Zaccheo, O.J, Forbes, B, Jones, E.Y, Crump, M.P, Hassan, A.B. | 登録日 | 2010-08-13 | 公開日 | 2012-02-15 | 最終更新日 | 2012-12-12 | 実験手法 | SOLUTION NMR | 主引用文献 | An exon splice enhancer primes IGF2:IGF2R binding site structure and function evolution. Science, 338, 2012
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2M6T
| NMR solution structure ensemble of 3-4D mutant domain 11 IGF2R | 分子名称: | Insulin-like growth factor 2 receptor variant | 著者 | Strickland, M, Williams, C, Richards, E, Minnall, L, Crump, M.P, Frago, S, Hughes, J, Garner, L, Hoppe, H, Rezgui, D, Zaccheo, O.J, Prince, S.N, Hassan, A.B, Whittaker, S. | 登録日 | 2013-04-09 | 公開日 | 2014-10-15 | 最終更新日 | 2024-10-16 | 実験手法 | SOLUTION NMR | 主引用文献 | Functional evolution of IGF2:IGF2R domain 11 binding generates novel structural interactions and a specific IGF2 antagonist. Proc.Natl.Acad.Sci.USA, 113, 2016
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2V5P
| COMPLEX STRUCTURE OF HUMAN IGF2R DOMAINS 11-13 BOUND TO IGF-II | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, CATION-INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR, INSULIN-LIKE GROWTH FACTOR II, ... | 著者 | Brown, J, Delaine, C, Zaccheo, O.J, Siebold, C, Gilbert, R.J, van Boxel, G, Denley, A, Wallace, J.C, Hassan, A.B, Forbes, B.E, Jones, E.Y. | 登録日 | 2007-07-06 | 公開日 | 2007-12-11 | 最終更新日 | 2024-10-16 | 実験手法 | X-RAY DIFFRACTION (4.1 Å) | 主引用文献 | Structure and Functional Analysis of the Igf-II/Igf2R Interaction Embo J., 27, 2008
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2V5N
| STRUCTURE OF HUMAN IGF2R DOMAINS 11-12 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, CATION-INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR | 著者 | Brown, J, Delaine, C, Zaccheo, O.J, Siebold, C, Gilbert, R.J, van Boxel, G, Denley, A, Wallace, J.C, Hassan, A.B, Forbes, B.E, Jones, E.Y. | 登録日 | 2007-07-06 | 公開日 | 2007-12-11 | 最終更新日 | 2020-07-29 | 実験手法 | X-RAY DIFFRACTION (3.2 Å) | 主引用文献 | Structure and Functional Analysis of the Igf-II/Igf2R Interaction Embo J., 27, 2008
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2V5O
| STRUCTURE OF HUMAN IGF2R DOMAINS 11-14 | 分子名称: | 2-acetamido-2-deoxy-beta-D-glucopyranose, CATION-INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR, CHLORIDE ION | 著者 | Brown, J, Delaine, C, Zaccheo, O.J, Siebold, C, Gilbert, R.J, van Boxel, G, Denley, A, Wallace, J.C, Hassan, A.B, Forbes, B.E, Jones, E.Y. | 登録日 | 2007-07-06 | 公開日 | 2007-12-11 | 最終更新日 | 2024-10-23 | 実験手法 | X-RAY DIFFRACTION (2.91 Å) | 主引用文献 | Structure and Functional Analysis of the Igf-II/Igf2R Interaction Embo J., 27, 2008
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6DCG
| Discovery of MK-8353: An Orally Bioavailable Dual Mechanism ERK Inhibitor for Oncology | 分子名称: | (3S)-3-(methylsulfanyl)-1-(2-{4-[4-(1-methyl-1H-1,2,4-triazol-3-yl)phenyl]-3,6-dihydropyridin-1(2H)-yl}-2-oxoethyl)-N-(3-{6-[(propan-2-yl)oxy]pyridin-3-yl}-1H-indazol-5-yl)pyrrolidine-3-carboxamide, Mitogen-activated protein kinase 1, SULFATE ION | 著者 | Boga, S.B, Deng, Y, Zhu, L, Nan, Y, Cooper, A, Shipps Jr, G.W, Doll, R, Shih, N, Zhu, H, Sun, R, Wang, T, Paliwal, S, Tsui, H, Gao, X, Yao, X, Desai, J, Wang, J, Alhassan, A.B, Kelly, J, Patel, M, Muppalla, K, Gudipati, S, Zhang, L, Buevich, A, Hesk, D, Carr, D, Dayananth, P, Mei, H, Cox, K, Sherborne, B, Hruza, A.W, Xiao, L, Jin, W, Long, B, Liu, G, Taylor, S.A, Kirschmeier, P, Windsor, W.T, Bishop, R, Samatar, A.A. | 登録日 | 2018-05-06 | 公開日 | 2018-08-08 | 最終更新日 | 2023-10-11 | 実験手法 | X-RAY DIFFRACTION (1.45 Å) | 主引用文献 | MK-8353: Discovery of an Orally Bioavailable Dual Mechanism ERK Inhibitor for Oncology. ACS Med Chem Lett, 9, 2018
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