9az4
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INF2 at the Barbed End of F-Actin
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Structural highlights
DiseaseINF2_HUMAN Autosomal dominant intermediate Charcot-Marie-Tooth disease type E;Genetic steroid-resistant nephrotic syndrome. The disease is caused by variants affecting the gene represented in this entry. The disease is caused by variants affecting the gene represented in this entry. FunctionINF2_HUMAN Severs actin filaments and accelerates their polymerization and depolymerization. Contents | ||||||||||||||||||||
This page was last modified 18:10, 29 May 2024.