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5DKN

Crystal Structure of Calcium-loaded S100B bound to SBi4225

5DKN の概要
エントリーDOI10.2210/pdb5dkn/pdb
関連するPDBエントリー5DKQ 5DKR
分子名称Protein S100-B, CALCIUM ION, 2,2'-[heptane-1,7-diylbis(oxybenzene-4,1-diyl)]bis(1H-imidazole), ... (4 entities in total)
機能のキーワードmalignant melanoma, calcium binding, covalent inhibitor, metal binding protein-inhibitor complex, metal binding protein/inhibitor
由来する生物種Bos taurus (Bovine)
タンパク質・核酸の鎖数1
化学式量合計11178.65
構造登録者
主引用文献Cavalier, M.C.,Ansari, M.I.,Pierce, A.D.,Wilder, P.T.,McKnight, L.E.,Raman, E.P.,Neau, D.B.,Bezawada, P.,Alasady, M.J.,Charpentier, T.H.,Varney, K.M.,Toth, E.A.,MacKerell, A.D.,Coop, A.,Weber, D.J.
Small Molecule Inhibitors of Ca(2+)-S100B Reveal Two Protein Conformations.
J.Med.Chem., 59:592-608, 2016
Cited by
PubMed Abstract: The drug pentamidine inhibits calcium-dependent complex formation with p53 ((Ca)S100B·p53) in malignant melanoma (MM) and restores p53 tumor suppressor activity in vivo. However, off-target effects associated with this drug were problematic in MM patients. Structure-activity relationship (SAR) studies were therefore completed here with 23 pentamidine analogues, and X-ray structures of (Ca)S100B·inhibitor complexes revealed that the C-terminus of S100B adopts two different conformations, with location of Phe87 and Phe88 being the distinguishing feature and termed the "FF-gate". For symmetric pentamidine analogues ((Ca)S100B·5a, (Ca)S100B·6b) a channel between sites 1 and 2 on S100B was occluded by residue Phe88, but for an asymmetric pentamidine analogue ((Ca)S100B·17), this same channel was open. The (Ca)S100B·17 structure illustrates, for the first time, a pentamidine analog capable of binding the "open" form of the "FF-gate" and provides a means to block all three "hot spots" on (Ca)S100B, which will impact next generation (Ca)S100B·p53 inhibitor design.
PubMed: 26727270
DOI: 10.1021/acs.jmedchem.5b01369
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.528 Å)
構造検証レポート
Validation report summary of 5dkn
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-04に公開中

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