5BYB
Crystal structure of the catalytic domain of human diphosphoinositol pentakisphosphate kinase 2 (PPIP5K2) in complex with ADP and 1,5-(PA)2-IP4
Summary for 5BYB
Entry DOI | 10.2210/pdb5byb/pdb |
Related | 5BYA |
Descriptor | Inositol hexakisphosphate and diphosphoinositol-pentakisphosphate kinase 2, ADENOSINE-5'-DIPHOSPHATE, {[(1R,3S,4S,5R,6S)-2,4,5,6-tetrakis(phosphonooxy)cyclohexane-1,3-diyl]bis[oxy(2-oxoethane-2,1-diyl)]}bis(phosphonic acid), ... (7 entities in total) |
Functional Keywords | methylenebisphosphonate, phosphonoacetate, non-hydrolyzable, pyrophosphate mimics, transferase |
Biological source | Homo sapiens (Human) |
Cellular location | Cytoplasm, cytosol : O43314 |
Total number of polymer chains | 1 |
Total formula weight | 39238.52 |
Authors | Wang, H.,Shears, S.B. (deposition date: 2015-06-10, release date: 2015-07-22, Last modification date: 2023-09-27) |
Primary citation | Riley, A.M.,Wang, H.,Shears, S.B.,L Potter, B.V. Synthetic tools for studying the chemical biology of InsP8. Chem.Commun.(Camb.), 51:12605-12608, 2015 Cited by PubMed Abstract: To synthesise stabilised mimics of InsP8, the most phosphorylated inositol phosphate signalling molecule in Nature, we replaced its two diphosphate (PP) groups with either phosphonoacetate (PA) or methylenebisphosphonate (PCP) groups. Utility of the PA and PCP analogues was verified by structural and biochemical analyses of their interactions with enzymes of InsP8 metabolism. PubMed: 26153667DOI: 10.1039/c5cc05017k PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.3 Å) |
Structure validation
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