Title : Mutating a conserved cysteine in GPIHBP1 reduces amounts of GPIHBP1 in capillaries and abolishes LPL binding.

Pub. Date : 2017 Jul

PMID : 28476858






1 Functional Relationships(s)
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1 Mutation of conserved cysteines in proteins of the Ly6 family cause human disease-chylomicronemia in the case of glycosylphosphatidylinositol-anchored HDL binding protein 1 (GPIHBP1) and paroxysmal nocturnal hemoglobinuria in the case of CD59. Cysteine CD59 molecule (CD59 blood group) Homo sapiens