8okd
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Human pseudouridine synthase 3 and tRNA-Gln
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Structural highlights
DiseasePUS3_HUMAN Severe growth deficiency-strabismus-extensive dermal melanocytosis-intellectual disability syndrome. The disease is caused by variants affecting the gene represented in this entry. FunctionPUS3_HUMAN Formation of pseudouridine at position 39 in the anticodon stem and loop of transfer RNAs.[1] References
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This page was last modified 08:41, 14 July 2024.