7ZI0
Structure of human Smoothened in complex with cholesterol and SAG
Summary for 7ZI0
Entry DOI | 10.2210/pdb7zi0/pdb |
Descriptor | Smoothened homolog,Soluble cytochrome b562, 3-chloro-N-[trans-4-(methylamino)cyclohexyl]-N-{[3-(pyridin-4-yl)phenyl]methyl}-1-benzothiophene-2-carboxamide, CHOLESTEROL, ... (6 entities in total) |
Functional Keywords | class f g protein coupled receptor, hedgehog signalling, oncoprotein, drug target, signal transduction, morphogen, cholesterol, membrane protein |
Biological source | Homo sapiens (human) More |
Total number of polymer chains | 2 |
Total formula weight | 143945.09 |
Authors | Byrne, E.F.X.,Woolley, R.E.,Ansell, B.,Sansom, M.S.P.,Newstead, S.,Siebold, C. (deposition date: 2022-04-07, release date: 2022-06-15, Last modification date: 2024-10-23) |
Primary citation | Kinnebrew, M.,Woolley, R.E.,Ansell, T.B.,Byrne, E.F.X.,Frigui, S.,Luchetti, G.,Sircar, R.,Nachtergaele, S.,Mydock-McGrane, L.,Krishnan, K.,Newstead, S.,Sansom, M.S.P.,Covey, D.F.,Siebold, C.,Rohatgi, R. Patched 1 regulates Smoothened by controlling sterol binding to its extracellular cysteine-rich domain. Sci Adv, 8:eabm5563-eabm5563, 2022 Cited by PubMed Abstract: Smoothened (SMO) transduces the Hedgehog (Hh) signal across the plasma membrane in response to accessible cholesterol. Cholesterol binds SMO at two sites: one in the extracellular cysteine-rich domain (CRD) and a second in the transmembrane domain (TMD). How these two sterol-binding sites mediate SMO activation in response to the ligand Sonic Hedgehog (SHH) remains unknown. We find that mutations in the CRD (but not the TMD) reduce the fold increase in SMO activity triggered by SHH. SHH also promotes the photocrosslinking of a sterol analog to the CRD in intact cells. In contrast, sterol binding to the TMD site boosts SMO activity regardless of SHH exposure. Mutational and computational analyses show that these sites are in allosteric communication despite being 45 angstroms apart. Hence, sterols function as both SHH-regulated orthosteric ligands at the CRD and allosteric ligands at the TMD to regulate SMO activity and Hh signaling. PubMed: 35658032DOI: 10.1126/sciadv.abm5563 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (3 Å) |
Structure validation
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