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Crystal structure of human Gle1 CTD-Nup42 GBM-DDX19B(AMPPNP) complexCrystal structure of human Gle1 CTD-Nup42 GBM-DDX19B(AMPPNP) complex
Structural highlights
DiseaseGLE1_HUMAN Lethal arthrogryposis - anterior horn cell disease;Lethal congenital contracture syndrome type 1. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. FunctionGLE1_HUMAN Required for the export of mRNAs containing poly(A) tails from the nucleus into the cytoplasm. May be involved in the terminal step of the mRNA transport through the nuclear pore complex (NPC).[1] [2] [3] See AlsoReferences
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