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Crystal structure of Smad8_9-MH1 bound to the GGCGC site.
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Structural highlights
Disease[SMAD9_HUMAN] Heritable pulmonary arterial hypertension. The disease may be caused by mutations affecting the gene represented in this entry. Function[SMAD9_HUMAN] Transcriptional modulator activated by BMP (bone morphogenetic proteins) type 1 receptor kinase. SMAD9 is a receptor-regulated SMAD (R-SMAD). Contents | ||||||||||||||||||||
This page was last modified 06:27, 7 October 2020.