6v6c
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Structure of GCP6 in the native human gamma-tubulin ring complex
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Structural highlights
DiseaseGCP6_HUMAN Autosomal recessive chorioretinopathy-microcephaly syndrome. The disease is caused by mutations affecting the gene represented in this entry. FunctionGCP6_HUMAN Gamma-tubulin complex is necessary for microtubule nucleation at the centrosome.[1] See AlsoReferences | ||||||||||||||
This page was last modified 14:36, 6 March 2024.