7X9Y
Cryo-EM structure of the apo CCR3-Gi complex
Summary for 7X9Y
| Entry DOI | 10.2210/pdb7x9y/pdb |
| EMDB information | 33085 |
| Descriptor | Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (5 entities in total) |
| Functional Keywords | gpcr, ccr3, chemokine receptor, membrne protein, membrane protein |
| Biological source | Homo sapiens (human) More |
| Total number of polymer chains | 5 |
| Total formula weight | 152898.78 |
| Authors | |
| Primary citation | Shao, Z.,Tan, Y.,Shen, Q.,Hou, L.,Yao, B.,Qin, J.,Xu, P.,Mao, C.,Chen, L.N.,Zhang, H.,Shen, D.D.,Zhang, C.,Li, W.,Du, X.,Li, F.,Chen, Z.H.,Jiang, Y.,Xu, H.E.,Ying, S.,Ma, H.,Zhang, Y.,Shen, H. Molecular insights into ligand recognition and activation of chemokine receptors CCR2 and CCR3. Cell Discov, 8:44-44, 2022 Cited by PubMed Abstract: Chemokine receptors are a family of G-protein-coupled receptors with key roles in leukocyte migration and inflammatory responses. Here, we present cryo-electron microscopy structures of two human CC chemokine receptor-G-protein complexes: CCR2 bound to its endogenous ligand CCL2, and CCR3 in the apo state. The structure of the CCL2-CCR2-G-protein complex reveals that CCL2 inserts deeply into the extracellular half of the transmembrane domain, and forms substantial interactions with the receptor through the most N-terminal glutamine. Extensive hydrophobic and polar interactions are present between both two chemokine receptors and the Gα-protein, contributing to the constitutive activity of these receptors. Notably, complemented with functional experiments, the interactions around intracellular loop 2 of the receptors are found to be conserved and play a more critical role in G-protein activation than those around intracellular loop 3. Together, our findings provide structural insights into chemokine recognition and receptor activation, shedding lights on drug design targeting chemokine receptors. PubMed: 35570218DOI: 10.1038/s41421-022-00403-4 PDB entries with the same primary citation |
| Experimental method | ELECTRON MICROSCOPY (3.1 Å) |
Structure validation
Download full validation report






