4UMQ
Structure of MELK in complex with inhibitors
4UMQ の概要
エントリーDOI | 10.2210/pdb4umq/pdb |
関連するPDBエントリー | 4D2T 4D2V 4D2W 4UMP 4UMR 4UMT 4UMU |
分子名称 | MATERNAL EMBRYONIC LEUCINE ZIPPER KINASE, 3-{5-[(3-hydroxy-5-methoxyphenyl)amino]-2-(phenylcarbamoyl)phenoxy}propan-1-aminium (3 entities in total) |
機能のキーワード | transferase, fragment based drug design |
由来する生物種 | HOMO SAPIENS (HUMAN) |
細胞内の位置 | Cell membrane ; Peripheral membrane protein : Q14680 |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 41300.74 |
構造登録者 | Johnson, C.N.,Berdini, V.,Beke, L.,Bonnet, P.,Brehmer, D.,Coyle, J.E.,Day, P.J.,Frederickson, M.,Freyne, E.J.E.,Gilissen, R.A.H.J.,Hamlett, C.C.F.,Howard, S.,Meerpoel, L.,McMenamin, R.,Patel, S.,Rees, D.C.,Sharff, A.,Sommen, F.,Wu, T.,Linders, J.T.M. (登録日: 2014-05-20, 公開日: 2014-10-08, 最終更新日: 2024-05-08) |
主引用文献 | Johnson, C.N.,Berdini, V.,Beke, L.,Bonnet, P.,Brehmer, D.,Coyle, J.E.,Day, P.J.,Frederickson, M.,Freyne, E.J.E.,Gilissen, R.A.H.J.,Hamlett, C.C.F.,Howard, S.,Meerpoel, L.,Mcmenamin, R.,Patel, S.,Rees, D.C.,Sharff, A.,Sommen, F.,Wu, T.,Linders, J.T.M. Fragment-Based Discovery of Type I Inhibitors of Maternal Embryonic Leucine Zipper Kinase Acs Med.Chem.Lett., 6:25-, 2015 Cited by PubMed Abstract: Fragment-based drug design was successfully applied to maternal embryonic leucine zipper kinase (MELK). A low affinity (160 μM) fragment hit was identified, which bound to the hinge region with an atypical binding mode, and this was optimized using structure-based design into a low-nanomolar and cell-penetrant inhibitor, with a good selectivity profile, suitable for use as a chemical probe for elucidation of MELK biology. PubMed: 25589925DOI: 10.1021/ML5001245 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (2.6 Å) |
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