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PCMT1
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- Species Reactivity: Human
 - Application: WB
 
 
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For Research Use Only. Not For Clinical Use.
Background
This gene encodes a member of the type II class of protein carboxyl methyltransferase enzymes. The encoded enzyme plays a role in protein repair by recognizing and converting D-aspartyl and L-isoaspartyl residues resulting from spontaneous deamidation back to the normal L-aspartyl form. The encoded protein may play a protective role in the pathogenesis of Alzheimers disease, and single nucleotide polymorphisms in this gene have been associated with spina bifida and premature ovarian failure. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Oct 2011]
                                Protein class
                                        Enzymes, Metabolic proteins, Plasma proteins
Predicted location
                                        Intracellular, Membrane (different isoforms)
Single cell type specificity
                                        Cell type enhanced (Early spermatids, Late spermatids)
Immune cell specificity
                                        Low immune cell specificity
Cell line specificity
                                        Low cell line specificity
Interaction
                                        Monomer.
Molecular function
                                        Methyltransferase, Transferase
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