6IDH
Antibody 64M-5 Fab in ligand-free form
Summary for 6IDH
Entry DOI | 10.2210/pdb6idh/pdb |
Descriptor | Anti-(6-4) photoproduct antibody 64M-5 Fab (light chain), Anti-(6-4) photoproduct antibody 64M-5 Fab (heavy chain) (3 entities in total) |
Functional Keywords | dna (6-4) photoproduct, immunoglobulin, fab, immune system |
Biological source | Mus musculus More |
Total number of polymer chains | 2 |
Total formula weight | 47822.21 |
Authors | Yokoyama, H.,Mizutani, R.,Noguchi, S.,Hayashida, N. (deposition date: 2018-09-10, release date: 2019-02-13, Last modification date: 2024-10-09) |
Primary citation | Yokoyama, H.,Mizutani, R.,Noguchi, S.,Hayashida, N. Structures of the antibody 64M-5 Fab and its complex with dT(6-4)T indicate induced-fit and high-affinity mechanisms. Acta Crystallogr.,Sect.F, 75:80-88, 2019 Cited by PubMed Abstract: DNA photoproducts with (6-4) pyrimidine-pyrimidone adducts produced by ultraviolet light are mutagenic and carcinogenic. The crystal structures of the anti-(6-4) photoproduct antibody 64M-5 Fab and of its complex with dT(6-4)T were determined at 2.5 and 2.0 Å resolution, respectively. A comparison between the dT(6-4)T-liganded and unliganded structures indicates that the side chain of His93L is greatly rotated and shifted on binding to dT(6-4)T, leading to the formation of an electrostatic interaction with the phosphate moiety of dT(6-4)T, which shows a remarkable induced fit. Based on a comparison of the dT(6-4)T-liganded structures of the 64M-5 and 64M-2 Fabs, the electrostatic interaction between the side chain of His93L in 64M-5 and the phosphate moiety of dT(6-4)T is lost for Leu93L in 64M-2, while Arg90L in 64M-5 instead of Gln90L in 64M-2 stabilizes the conformation of complementarity-determining region (CDR) L3. These differences contribute to the higher affinity of 64M-5 for dT(6-4)T compared with that of 64M-2. PubMed: 30713158DOI: 10.1107/S2053230X18017661 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.5 Å) |
Structure validation
Download full validation report