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| {{STRUCTURE_2ic2| PDB=2ic2 | SCENE= }} | | {{STRUCTURE_2ic2| PDB=2ic2 | SCENE= }} |
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| '''Crystal Structure of the First FNIII Domain of Ihog'''
| | ===Crystal Structure of the First FNIII Domain of Ihog=== |
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| ==Overview==
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| Hedgehog (Hh) signaling molecules mediate key tissue-patterning events during animal development, and inappropriate activation of Hh signaling in adults has been associated with human cancers. Recently, a conserved family of type I integral membrane proteins required for normal response to the Hh signal was discovered. One member of this family, Ihog (interference hedgehog), functions upstream or at the level of Patched (Ptc), but how Ihog participates in Hh signaling remains unclear. Here, we show that heparin binding induces Ihog dimerization and is required to mediate high-affinity interactions between Ihog and Hh. We also present crystal structures of a Hh-binding fragment of Ihog, both alone and complexed with Hh. Heparin is not well ordered in these structures, but a basic cleft in the first FNIII domain of Ihog (IhogFn1) is shown by mutagenesis to mediate heparin binding. These results establish that Hh directly binds Ihog and provide the first demonstration of a specific role for heparin in Hh responsiveness.
| | The line below this paragraph, {{ABSTRACT_PUBMED_17077139}}, adds the Publication Abstract to the page |
| | (as it appears on PubMed at http://www.pubmed.gov), where 17077139 is the PubMed ID number. |
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| | {{ABSTRACT_PUBMED_17077139}} |
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| ==About this Structure== | | ==About this Structure== |
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| [[Category: Hedgehog]] | | [[Category: Hedgehog]] |
| [[Category: Ihog]] | | [[Category: Ihog]] |
| ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 07:18:58 2008'' | | |
| | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Jul 27 17:21:27 2008'' |
