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3SYC

Crystal structure of the G protein-gated inward rectifier K+ channel GIRK2 (Kir3.2) D228N mutant

Summary for 3SYC
Entry DOI10.2210/pdb3syc/pdb
Related3SYA 3SYO 3SYP 3SYQ
DescriptorG protein-activated inward rectifier potassium channel 2, POTASSIUM ION (2 entities in total)
Functional Keywordsion channel, potassium channel, inward rectification, sodium binding, pip2 binding, g protein binding, metal transport
Biological sourceMus musculus (mouse)
Cellular locationMembrane; Multi-pass membrane protein: P48542
Total number of polymer chains1
Total formula weight39295.56
Authors
Whorton, M.R.,MacKinnon, R. (deposition date: 2011-07-16, release date: 2011-10-12, Last modification date: 2024-10-30)
Primary citationWhorton, M.R.,Mackinnon, R.
Crystal Structure of the Mammalian GIRK2 K(+) Channel and Gating Regulation by G Proteins, PIP(2), and Sodium.
Cell(Cambridge,Mass.), 147:199-208, 2011
Cited by
PubMed Abstract: G protein-gated K(+) channels (Kir3.1-Kir3.4) control electrical excitability in many different cells. Among their functions relevant to human physiology and disease, they regulate the heart rate and govern a wide range of neuronal activities. Here, we present the first crystal structures of a G protein-gated K(+) channel. By comparing the wild-type structure to that of a constitutively active mutant, we identify a global conformational change through which G proteins could open a G loop gate in the cytoplasmic domain. The structures of both channels in the absence and presence of PIP(2) suggest that G proteins open only the G loop gate in the absence of PIP(2), but in the presence of PIP(2) the G loop gate and a second inner helix gate become coupled, so that both gates open. We also identify a strategically located Na(+) ion-binding site, which would allow intracellular Na(+) to modulate GIRK channel activity. These data provide a structural basis for understanding multiligand regulation of GIRK channel gating.
PubMed: 21962516
DOI: 10.1016/j.cell.2011.07.046
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (3.41 Å)
Structure validation

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数据于2024-11-06公开中

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