PAM amadating monooxigenase wild type and mutant a bifunctional copper carrying protein.

Peptidylglycine alpha-hydroxylating monooxygenase (PHM) locus: 5q14-q21 [§§], and peptidyl-alpha-hydroxyglycine alpha-amidating lyase (PAL), act sequentially. PHM cooperates to mediate all of the vital functions in the body, these peptides bind to three well-characterized vasoactive intestinal peptide-VIP subtypes. PAM is the enzyme producing alpha-amidated bioactive peptides from their inactive glycine-extended precursors for the both forms of PAM, wild type and mutant proregion (AM) gene KO, yielding amidated products, interacting with the cytosolic routing determinants, the posterior pituitary (PP) . PAM proteins that have the noncatalytic exon A region following the monooxygenase domain. PAM is a bifunctional copper- and ascorbate-dependent enzyme, Ceruloplasmin is the major copper-carrying protein in the blood.
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