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Subunit asymmetry in the three-dimensional structure of a human CuZnSOD mutant found in familial amyotrophic lateral sclerosis.
Hart, P J; Liu, H; Pellegrini, M; Nersissian, A M; Gralla, E B; Valentine, J S; Eisenberg, D.
Affiliation
  • Hart PJ; UCLA-DOE Laboratory of Structural Biology and Molecular Medicine, University of California, Los Angeles 90095, USA.
Protein Sci ; 7(3): 545-55, 1998 Mar.
Article in En | MEDLINE | ID: mdl-9541385
ABSTRACT
The X-ray crystal structure of a human copper/zinc superoxide dismutase mutant (G37R CuZnSOD) found in some patients with the inherited form of Lou Gehrig's disease (FALS) has been determined to 1.9 angstroms resolution. The two SOD subunits have distinct environments in the crystal and are different in structure at their copper binding sites. One subunit (subunit[intact]) shows a four-coordinate ligand geometry of the copper ion, whereas the other subunit (subunit[broken]) shows a three-coordinate geometry of the copper ion. Also, subunit(intact) displays higher atomic displacement parameters for backbone atoms ((B) = 30 +/- 10 angstroms2) than subunit(broken) ((B) = 24 +/- 11 angstroms2). This structure is the first CuZnSOD to show large differences between the two subunits. Factors that may contribute to these differences are discussed and a possible link of a looser structure to FALS is suggested.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Superoxide Dismutase / Amyotrophic Lateral Sclerosis Type of study: Prognostic_studies Limits: Humans Language: En Journal: Protein Sci Journal subject: BIOQUIMICA Year: 1998 Document type: Article Affiliation country: Estados Unidos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Superoxide Dismutase / Amyotrophic Lateral Sclerosis Type of study: Prognostic_studies Limits: Humans Language: En Journal: Protein Sci Journal subject: BIOQUIMICA Year: 1998 Document type: Article Affiliation country: Estados Unidos