Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

5XLI

Structure of anti-Angiotensin II type2 receptor antibody (D5711-4A03)

Summary for 5XLI
Entry DOI10.2210/pdb5xli/pdb
Related5XJM
DescriptorFabL, FabH (3 entities in total)
Functional Keywordsantigbody, igg, fab, immune system
Biological sourceMus musculus
More
Total number of polymer chains4
Total formula weight93474.09
Authors
Asada, H.,Horita, S.,Iwata, S.,Hirata, K. (deposition date: 2017-05-10, release date: 2018-07-11, Last modification date: 2024-10-16)
Primary citationAsada, H.,Horita, S.,Hirata, K.,Shiroishi, M.,Shiimura, Y.,Iwanari, H.,Hamakubo, T.,Shimamura, T.,Nomura, N.,Kusano-Arai, O.,Uemura, T.,Suno, C.,Kobayashi, T.,Iwata, S.
Crystal structure of the human angiotensin II type 2 receptor bound to an angiotensin II analog.
Nat. Struct. Mol. Biol., 25:570-576, 2018
Cited by
PubMed Abstract: Angiotensin II (AngII) plays a central role in regulating human blood pressure, which is mainly mediated by interactions between AngII and the G-protein-coupled receptors (GPCRs) AngII type 1 receptor (ATR) and AngII type 2 receptor (ATR). We have solved the crystal structure of human ATR binding the peptide ligand [Sar, Ile]AngII and its specific antibody at 3.2-Å resolution. [Sar, Ile]AngII interacts with both the 'core' binding domain, where the small-molecule ligands of ATR and ATR bind, and the 'extended' binding domain, which is equivalent to the allosteric modulator binding site of muscarinic acetylcholine receptor. We generated an antibody fragment to stabilize the extended binding domain that functions as a positive allosteric modulator. We also identified a signature positively charged cluster, which is conserved among peptide-binding receptors, to locate C termini at the bottom of the binding pocket. The reported results should help with designing ligands for angiotensin receptors and possibly to other peptide GPCRs.
PubMed: 29967536
DOI: 10.1038/s41594-018-0079-8
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.696 Å)
Structure validation

226707

건을2024-10-30부터공개중

PDB statisticsPDBj update infoContact PDBjnumon