2KHT
NMR Structure of human alpha defensin HNP-1
2KHT の概要
エントリーDOI | 10.2210/pdb2kht/pdb |
NMR情報 | BMRB: 16254 |
分子名称 | Neutrophil defensin 1 (1 entity in total) |
機能のキーワード | microcrystalline protein, human alpha defensin, defensin, secreted, antibiotic, antiviral defense, fungicide, phosphoprotein, antimicrobial protein |
由来する生物種 | Homo sapiens (human) |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 3452.11 |
構造登録者 | Zhang, Y.,Li, S.,Doherty, T.F.,Lubkowski, J.,Lu, W.,Li, J.,Barinka, C.,Hong, M. (登録日: 2009-04-11, 公開日: 2010-02-09, 最終更新日: 2024-05-01) |
主引用文献 | Zhang, Y.,Doherty, T.,Li, J.,Lu, W.,Barinka, C.,Lubkowski, J.,Hong, M. Resonance assignment and three-dimensional structure determination of a human alpha-defensin, HNP-1, by solid-state NMR. J.Mol.Biol., 397:408-422, 2010 Cited by PubMed Abstract: Human alpha-defensins [human neutrophil peptides (HNPs)] are immune defense mini-proteins that act by disrupting microbial cell membranes. Elucidating the three-dimensional (3D) structures of HNPs in lipid membranes is important for understanding their mechanisms of action. Using solid-state NMR (SSNMR), we have determined the 3D structure of HNP-1 in a microcrystalline state outside the lipid membrane, which provides benchmarks for structure determination and comparison with the membrane-bound state. From a suite of two-dimensional and 3D magic-angle spinning experiments, (13)C and (15)N chemical shifts that yielded torsion angle constraints were obtained, while inter-residue distances were obtained to restrain the 3D fold. Together, these constraints led to the first high-resolution SSNMR structure of a human defensin. The SSNMR structure has close similarity to the crystal structures of the HNP family, with the exception of the loop region between the first and second beta-strands. The difference, which is partially validated by direct torsion angle measurements of selected loop residues, suggests possible conformational variation and flexibility of this segment of the protein, which may regulate HNP interaction with the phospholipid membrane of microbial cells. PubMed: 20097206DOI: 10.1016/j.jmb.2010.01.030 主引用文献が同じPDBエントリー |
実験手法 | SOLID-STATE NMR |
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