2DN3
1.25A resolution crystal structure of human hemoglobin in the carbonmonoxy form
2DN3 の概要
エントリーDOI | 10.2210/pdb2dn3/pdb |
関連するPDBエントリー | 2DN1 2DN2 |
分子名称 | Hemoglobin alpha subunit, Hemoglobin beta subunit, PROTOPORPHYRIN IX CONTAINING FE, ... (5 entities in total) |
機能のキーワード | human hemoglobin, high resolution crystal structure, oxygen transport, oxygen storage-transport complex, oxygen storage/transport |
由来する生物種 | Homo sapiens (human) 詳細 |
タンパク質・核酸の鎖数 | 2 |
化学式量合計 | 32329.54 |
構造登録者 | Park, S.-Y.,Yokoyama, T.,Shibayama, N.,Shiro, Y.,Tame, J.R. (登録日: 2006-04-25, 公開日: 2006-05-09, 最終更新日: 2024-03-13) |
主引用文献 | Park, S.-Y.,Yokoyama, T.,Shibayama, N.,Shiro, Y.,Tame, J.R. 1.25 a resolution crystal structures of human haemoglobin in the oxy, deoxy and carbonmonoxy forms. J.Mol.Biol., 360:690-701, 2006 Cited by PubMed Abstract: The most recent refinement of the crystallographic structure of oxyhaemoglobin (oxyHb) was completed in 1983, and differences between this real-space refined model and later R state models have been interpreted as evidence of crystallisation artefacts, or numerous sub-states. We have refined models of deoxy, oxy and carbonmonoxy Hb to 1.25 A resolution each, and compare them with other Hb structures. It is shown that the older structures reflect the software used in refinement, and many differences with newer structures are unlikely to be physiologically relevant. The improved accuracy of our models clarifies the disagreement between NMR and X-ray studies of oxyHb, the NMR experiments suggesting a hydrogen bond to exist between the distal histidine and oxygen ligand of both the alpha and beta-subunits. The high-resolution crystal structure also reveals a hydrogen bond in both subunit types, but with subtly different geometry which may explain the very different behaviour when this residue is mutated to glycine in alpha or beta globin. We also propose a new set of relatively fixed residues to act as a frame of reference; this set contains a similar number of atoms to the well-known "BGH" frame yet shows a much smaller rmsd value between R and T state models of HbA. PubMed: 16765986DOI: 10.1016/j.jmb.2006.05.036 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.25 Å) |
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