4V0K
Crystal structure of the CrARL6DN in the GDP bound form
Summary for 4V0K
Entry DOI | 10.2210/pdb4v0k/pdb |
Related | 4V0M 4V0N 4V0O |
Descriptor | ARF-LIKE SMALL GTPASE, GUANOSINE-5'-DIPHOSPHATE, CADMIUM ION, ... (4 entities in total) |
Functional Keywords | hydrolase |
Biological source | CHLAMYDOMONAS REINHARDTII |
Total number of polymer chains | 2 |
Total formula weight | 39623.80 |
Authors | Mourao, A.,Lorentzen, E. (deposition date: 2014-09-17, release date: 2014-11-19, Last modification date: 2024-05-08) |
Primary citation | Mourao, A.,Nager, A.R.,Nachury, M.V.,Lorentzen, E. Structural Basis for Membrane Targeting of the Bbsome by Arl6 Nat.Struct.Mol.Biol., 21:1035-, 2014 Cited by PubMed Abstract: The BBSome is a coat-like ciliary trafficking complex composed of proteins mutated in Bardet-Biedl syndrome (BBS). A critical step in BBSome-mediated sorting is recruitment of the BBSome to membranes by the GTP-bound Arf-like GTPase ARL6. We have determined crystal structures of Chlamydomonas reinhardtii ARL6-GDP, ARL6-GTP and the ARL6-GTP-BBS1 complex. The structures demonstrate how ARL6-GTP binds the BBS1 β-propeller at blades 1 and 7 and explain why GTP- but not GDP-bound ARL6 can recruit the BBSome to membranes. Single point mutations in the ARL6-GTP-BBS1 interface abolish the interaction of ARL6 with the BBSome and prevent the import of BBSomes into cilia. Furthermore, we show that BBS1 with the M390R mutation, responsible for 30% of all reported BBS disease cases, fails to interact with ARL6-GTP, thus providing a molecular rationale for patient pathologies. PubMed: 25402481DOI: 10.1038/NSMB.2920 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.438 Å) |
Structure validation
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