Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

8SMK

hPAD4 bound to Activating Fab hA362

Summary for 8SMK
Entry DOI10.2210/pdb8smk/pdb
EMDB information40589
DescriptorProtein-arginine deiminase type-4, Activating Fab 362 heavy chain, Activating Fab 362 light chain, ... (4 entities in total)
Functional Keywordscomplex, enzyme, inflammation, calcium binding, immune system
Biological sourceHomo sapiens (human)
More
Total number of polymer chains6
Total formula weight251662.95
Authors
Maker, A.,Verba, K.A. (deposition date: 2023-04-26, release date: 2024-03-06, Last modification date: 2024-11-06)
Primary citationZhou, X.,Kong, S.,Maker, A.,Remesh, S.G.,Leung, K.K.,Verba, K.A.,Wells, J.A.
Antibody discovery identifies regulatory mechanisms of protein arginine deiminase 4.
Nat.Chem.Biol., 20:742-750, 2024
Cited by
PubMed Abstract: Unlocking the potential of protein arginine deiminase 4 (PAD4) as a drug target for rheumatoid arthritis requires a deeper understanding of its regulation. In this study, we use unbiased antibody selections to identify functional antibodies capable of either activating or inhibiting PAD4 activity. Through cryogenic-electron microscopy, we characterized the structures of these antibodies in complex with PAD4 and revealed insights into their mechanisms of action. Rather than steric occlusion of the substrate-binding catalytic pocket, the antibodies modulate PAD4 activity through interactions with allosteric binding sites adjacent to the catalytic pocket. These binding events lead to either alteration of the active site conformation or the enzyme oligomeric state, resulting in modulation of PAD4 activity. Our study uses antibody engineering to reveal new mechanisms for enzyme regulation and highlights the potential of using PAD4 agonist and antagonist antibodies for studying PAD4-dependency in disease models and future therapeutic development.
PubMed: 38308046
DOI: 10.1038/s41589-023-01535-8
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (3.5 Å)
Structure validation

247536

PDB entries from 2026-01-14

PDB statisticsPDBj update infoContact PDBjnumon