4CLN

STRUCTURE OF A RECOMBINANT CALMODULIN FROM DROSOPHILA MELANOGASTER REFINED AT 2.2-ANGSTROMS RESOLUTION

4CLN の概要

• エントリーDOI: 10.2210/pdb4cln/pdb
• 分子名称: CALMODULIN, CALCIUM ION (3 entities in total)
• 機能のキーワード: calcium binding protein
• 由来する生物種: Drosophila melanogaster (fruit fly)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 16854.64

構造登録者

Taylor, D.A.,Sack, J.S.,Maune, J.F.,Beckingham, K.,Quiocho, F.A. (登録日: 1991-06-24, 公開日: 1992-07-15, 最終更新日: 2024-02-28)

主引用文献

Taylor, D.A.,Sack, J.S.,Maune, J.F.,Beckingham, K.,Quiocho, F.A.
Structure of a recombinant calmodulin from Drosophila melanogaster refined at 2.2-A resolution.
J.Biol.Chem., 266:21375-21380, 1991

PubMed Abstract: The crystal structure of calmodulin (Mr 16,700, 148 residues) from Drosophila melanogaster as expressed in a bacterial system has been determined and refined at 2.2-A resolution. Starting with the structure of mammalian calmodulin, we produced an extensively refitted and refined model with a conventional crystallographic R value of 0.197 for the 5,239 reflections (F greater than or equal to 2 sigma (F)) within the 10.0-2.2-A resolution range. The model includes 1,164 protein atoms, 4 calcium ions, and 78 water molecules and has root mean square deviations from standard values of 0.018 A for bond lengths and 0.043 A for angle distances. The overall structure is similar to mammalian calmodulin, with a seven-turn central helix connecting the two calcium-binding domains. The "dumb-bell" shaped molecule contains seven alpha-helices and four "EF hand" calcium-binding sites. Although the amino acid sequences of mammalian and Drosophila calmodulins differ by only three conservative amino acid changes, the refined model reveals a number of significant differences between the two structures. Superimposition of the structures yields a root mean square deviation of 1.22 A for the 1,120 equivalent atoms. The calcium-binding domains have a root mean square deviation of 0.85 A for the 353 equivalent atoms. There are also differences in the amino terminus, the bend of the central alpha-helix, and the orientations of some of the side chains.

PubMed: 1939171

実験手法

X-RAY DIFFRACTION (2.2 Å)