Conti E, Moser C, Rizzi M, Mattevi A, Lionetti C, Coda A, Ascenzi P, Brunori M, Bolognesi M
Dipartimento di Genetica e Microbiologia, Università di Pavia, Italy.
J Mol Biol. 1993 Oct 5;233(3):498-508. doi: 10.1006/jmbi.1993.1527.
The X-ray crystal structure of the ligand-free ferric form of Aplysia limacina myoglobin (pH 6.0) has been refined at 1.7 A resolution (R = 15.1%), and its cyanide, thiocyanate and imidazole derivatives studied by difference Fourier techniques at atomic resolution. The crystallographic R-factors of the three different derivatives reported are 16.1%, 16.1% and 15.6% at 1.8 A, 2.0 A and 2.0 A resolution, respectively. The present results have been analyzed in parallel with previous crystallographic studies on the molecular structures of the fluoride and azide derivatives of ferric Aplysia limacina myoglobin. Ligand binding to the distal site of the heme pocket results in different networks of hydrogen bonds involving to various degrees the bound ligand, residue Arg(66)E10, the heme propionate III, ordered water molecules and/or protein backbone atoms from the CD region. In particular, Arg(66)E10 stabilizes the bound ligand and compensates for the absence of the hydrogen bond donor residue HisE7, commonly present in oxygen-carrying globins.
海兔肌红蛋白无配体铁形式(pH 6.0)的X射线晶体结构已在1.7埃分辨率下精修(R = 15.1%),并通过差值傅里叶技术在原子分辨率下研究了其氰化物、硫氰酸盐和咪唑衍生物。所报道的三种不同衍生物的晶体学R因子在1.8埃、2.0埃和2.0埃分辨率下分别为16.1%、16.1%和15.6%。已将目前的结果与先前关于海兔肌红蛋白铁形式的氟化物和叠氮化物衍生物分子结构的晶体学研究进行了平行分析。配体与血红素口袋的远端位点结合会导致不同的氢键网络,不同程度地涉及结合的配体、残基Arg(66)E10、血红素丙酸酯III、有序水分子和/或来自CD区域的蛋白质主链原子。特别是,Arg(66)E10稳定了结合的配体,并弥补了通常存在于携氧球蛋白中的氢键供体残基HisE7的缺失。