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MAGI2

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

MAGI2
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Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 also known as membrane-associated guanylate kinase inverted 2 (MAGI-2) and atrophin-1-interacting protein 1 (AIP-1) is an enzyme that in humans is encoded by the MAGI2 gene.[5][6][7]

Quick Facts Available structures, PDB ...
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Function

The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral-pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family.[7]

Interactions

MAGI2 has been shown to interact with ATN1[8] and PTEN (gene).

References

Further reading

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