PMC:1208879 / 503-1127
Annnotations
craft-sa-dev
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used bioinformatics techniques to characterise a highly conserved peptide at the C-terminus of the PAX6 protein. Yeast two-hybrid library screens were then carried out to identify brain-expressed proteins that interact with the C-terminal peptide and with the entire PAX6 proline-serine-threonine-rich domain. Three novel PAX6-interacting proteins were identified: the post-synaptic density (PSD) protein HOMER3, the dynein subunit DNCL1, and the tripartite motif protein TRIM11. Three C-terminal PAX6 mutations, previously identified in patients with eye malformations, all reduced or abolished the interactions."}
craft-ca-core-ex-dev
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craft-ca-core-dev
{"project":"craft-ca-core-dev","denotations":[{"id":"T82","span":{"begin":278,"end":282},"obj":"PR:000012318"},{"id":"T83","span":{"begin":313,"end":319},"obj":"SO:0000417"},{"id":"T84","span":{"begin":333,"end":337},"obj":"PR:000012318"},{"id":"T85","span":{"begin":380,"end":401},"obj":"GO:0014069"},{"id":"T86","span":{"begin":403,"end":406},"obj":"GO:0014069"},{"id":"T87","span":{"begin":416,"end":422},"obj":"PR:000008680"},{"id":"T88","span":{"begin":428,"end":434},"obj":"GO:0030286"},{"id":"T89","span":{"begin":443,"end":448},"obj":"PR:000002325"},{"id":"T90","span":{"begin":483,"end":489},"obj":"PR:000016642"},{"id":"T91","span":{"begin":508,"end":512},"obj":"PR:000012318"},{"id":"T92","span":{"begin":563,"end":566},"obj":"UBERON:0000970"},{"id":"T79","span":{"begin":110,"end":114},"obj":"PR:000012318"},{"id":"T80","span":{"begin":191,"end":196},"obj":"UBERON:0000955"},{"id":"T81","span":{"begin":197,"end":206},"obj":"GO:0010467"}],"text":"Results\nWe used bioinformatics techniques to characterise a highly conserved peptide at the C-terminus of the PAX6 protein. Yeast two-hybrid library screens were then carried out to identify brain-expressed proteins that interact with the C-terminal peptide and with the entire PAX6 proline-serine-threonine-rich domain. Three novel PAX6-interacting proteins were identified: the post-synaptic density (PSD) protein HOMER3, the dynein subunit DNCL1, and the tripartite motif protein TRIM11. Three C-terminal PAX6 mutations, previously identified in patients with eye malformations, all reduced or abolished the interactions."}