1KBC
PROCARBOXYPEPTIDASE TERNARY COMPLEX
1KBC の概要
エントリーDOI | 10.2210/pdb1kbc/pdb |
分子名称 | NEUTROPHIL COLLAGENASE, CALCIUM ION, ZINC ION, ... (6 entities in total) |
機能のキーワード | hydrolytic enzyme, metalloproteinase, collagenase, matrixin, mmp-8, hnc, inhibitor, hydrolase |
由来する生物種 | Homo sapiens (human) |
細胞内の位置 | Cytoplasmic granule: P22894 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 37742.87 |
構造登録者 | |
主引用文献 | Betz, M.,Huxley, P.,Davies, S.J.,Mushtaq, Y.,Pieper, M.,Tschesche, H.,Bode, W.,Gomis-Ruth, F.X. 1.8-A crystal structure of the catalytic domain of human neutrophil collagenase (matrix metalloproteinase-8) complexed with a peptidomimetic hydroxamate primed-side inhibitor with a distinct selectivity profile. Eur.J.Biochem., 247:356-363, 1997 Cited by PubMed Abstract: Matrix metalloproteinases (MMP) are zinc endopeptidases involved in tissue remodelling. They have been implicated in a series of pathologies, including cancer, arthritis, joint destruction and Alzheimer's disease. Human neutrophil collagenase represents one of the three interstitial collagenases that cleave triple-helical collagen of type I, II and III. Its catalytic domain (residues Phe79-Gly242) has been heterologously expressed in Escherichia coli and crystallized as a non-covalent complex with the hydroxamate inhibitor BB-1909, which has distinct selectivity against different MMP, in a crystal form. The crystal structure, refined to 0.18-nm resolution, shows that BB-1909 is a right-hand-side inhibitor that binds to the S1'-S3' subsites and coordinates to the catalytic Zn2+ in a bidentate manner via the hydroxyl and carbonyl oxygen atoms of the hydroxamate group in a similar manner to batimastat. The collagenase/BB-1909 complex is described in detail and compared with the collagenase/batimastat complex. These studies provide information on MMP specificity and thus may assist the development of more-selective MMP inhibitors. PubMed: 9249047DOI: 10.1111/j.1432-1033.1997.00356.x 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.8 Å) |
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