7stx
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Cryo-EM structure of human NatB in complex with CoA-Alpha-Synuclein
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Structural highlights
DiseaseNAA20_HUMAN Autosomal recessive non-syndromic intellectual disability. The disease is caused by variants affecting the gene represented in this entry. FunctionNAA20_HUMAN Catalytic subunit of the NatB complex which catalyzes acetylation of the N-terminal methionine residues of peptides beginning with Met-Asp, Met-Glu, Met-Asn and Met-Gln (PubMed:34230638). Proteins with cell cycle functions are overrepresented in the pool of NatB substrates. Required for maintaining the structure and function of actomyosin fibers and for proper cellular migration.[1] [2] See AlsoReferences
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This page was last modified 05:50, 5 July 2023.