Required Buried α-Helical Structure in the Bilirubin UDP-Glucuronosyltransferase, UGT1A1, Contains a Nonreplaceable Phenylalanine

Author:

Ciotti Marco1,Cho Jeong W.1,George John1,Owens Ida S.1

Affiliation:

1. Human Genetics Branch, National Institute of Child Health and Human Development, National Institutes of Health, and Laboratory of Molecular Immunology, National Heart, Lung and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892

Publisher

American Chemical Society (ACS)

Subject

Biochemistry

Reference29 articles.

1. Roy Chowdhury, J., Wolkoff, A. W., Roy Chowdhury, N., and Arias, I. M. (1995) inThe Metabolic Basis of Inherited Disease(Scriver, C. R., Beaudet, A. L., Sly, W. S., and Valle, D., Eds.) 7th ed., Vol. II, pp 2161−2208, McGraw-Hill Book Co., New York.

2. Identification of a genetic alteration in the code for bilirubin UDP-glucuronosyltransferase in the UGT1 gene complex of a Crigler-Najjar type I patient.

3. Cloning of two human liver bilirubin UDP-glucuronosyltransferase cDNAs with expression in COS-1 cells.

4. A novel complex locus UGT1 encodes human bilirubin, phenol, and other UDP-glucuronosyltransferase isozymes with identical carboxyl termini.

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