Display Settings:

Format

Send to:

Choose Destination

    Biochemistry. 1998 Apr 7;37(14):4767-72.

    Structural evidence for the presence of a secondary calcium binding site in human alpha-lactalbumin.

    Chandra N, Brew K, Acharya KR.

    Department of Biology and Biochemistry, University of Bath, Claverton Down, Bath BA2 7AY, U.K.

    The high-resolution X-ray crystal structure of human alpha-lactalbumin (at 1.8 A) in the presence of an elevated level of calcium reveals a new secondary calcium binding site, 7.9 A away from the primary calcium binding site known in all alpha-lactalbumin structures so far. The new calcium binding site is different from the zinc and sulfate binding sites [Ren, J., et al. (1993) J. Biol. Chem. 268, 19292-19298] but shares common features with the manganese binding site as described by Gerkin [Gerkin, T. A. (1984) Biochemistry 23, 4688-4697]. The proximity of the manganese and calcium binding region and the location of the functional site on one side of the charged surface of the alpha-lactalbumin molecule suggest that these binding sites might play a role in the formation of the lactose synthase complex.

    PMID: 9537992 [PubMed - indexed for MEDLINE]

    Supplemental Content

    Click here to read Click here to read Click here to read Click here to read Click here to read

    Structures reported by this article