8e22 | pdb_00008e22
From Proteopedia
VPS37A_21-148
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Structural highlights
DiseaseVP37A_HUMAN Autosomal recessive spastic paraplegia type 53. The disease is caused by variants affecting the gene represented in this entry. FunctionVP37A_HUMAN Component of the ESCRT-I complex, a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into multivesicular bodies. May be involved in cell growth and differentiation.[1] References
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This page was last modified 05:26, 9 August 2023.