Title : Effect of UDP-glucuronosyltransferase 2B15 polymorphism on bisphenol A glucuronidation.

Pub. Date : 2011 Nov

PMID : 21404072






12 Functional Relationships(s)
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1 Effect of UDP-glucuronosyltransferase 2B15 polymorphism on bisphenol A glucuronidation. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
2 Bisphenol A (BPA) is one of a number of potential endocrine-disrupting chemicals, which are metabolized mainly by UDP-glucuronosyltransferase 2B15 (UGT2B15) in humans. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
3 Bisphenol A (BPA) is one of a number of potential endocrine-disrupting chemicals, which are metabolized mainly by UDP-glucuronosyltransferase 2B15 (UGT2B15) in humans. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
4 Bisphenol A (BPA) is one of a number of potential endocrine-disrupting chemicals, which are metabolized mainly by UDP-glucuronosyltransferase 2B15 (UGT2B15) in humans. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
5 Bisphenol A (BPA) is one of a number of potential endocrine-disrupting chemicals, which are metabolized mainly by UDP-glucuronosyltransferase 2B15 (UGT2B15) in humans. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
6 However, the K (m), V (max), and CL (int) values of UGT2B15.3, UGT2B15.4, UGT2B15.6, and UGT2B15.7 having L86S, T352I, and/or K523T substitution(s) for BPA glucuronidation were comparable to those of UGT2B15.1. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
7 However, the K (m), V (max), and CL (int) values of UGT2B15.3, UGT2B15.4, UGT2B15.6, and UGT2B15.7 having L86S, T352I, and/or K523T substitution(s) for BPA glucuronidation were comparable to those of UGT2B15.1. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
8 However, the K (m), V (max), and CL (int) values of UGT2B15.3, UGT2B15.4, UGT2B15.6, and UGT2B15.7 having L86S, T352I, and/or K523T substitution(s) for BPA glucuronidation were comparable to those of UGT2B15.1. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
9 However, the K (m), V (max), and CL (int) values of UGT2B15.3, UGT2B15.4, UGT2B15.6, and UGT2B15.7 having L86S, T352I, and/or K523T substitution(s) for BPA glucuronidation were comparable to those of UGT2B15.1. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
10 However, the K (m), V (max), and CL (int) values of UGT2B15.3, UGT2B15.4, UGT2B15.6, and UGT2B15.7 having L86S, T352I, and/or K523T substitution(s) for BPA glucuronidation were comparable to those of UGT2B15.1. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
11 These findings suggest that D85Y substitution in UGT2B15 decreases enzymatic function and that the polymorphic alleles of UGT2B15 are closely associated with variations in the metabolism and toxicity of BPA. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens
12 These findings suggest that D85Y substitution in UGT2B15 decreases enzymatic function and that the polymorphic alleles of UGT2B15 are closely associated with variations in the metabolism and toxicity of BPA. bisphenol A UDP glucuronosyltransferase family 2 member B15 Homo sapiens