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-Structure paper
Title | Structural basis for enzymatic evolution from a dedicated ADP-ribosyl cyclase to a multifunctional NAD hydrolase |
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Journal, issue, pages | J. Biol. Chem., Vol. 284, Page 27637-27645, Year 2009 |
Publish date | Jul 12, 2009 (structure data deposition date) |
Authors | Liu, Q. / Graeff, R. / Kriksunov, I.A. / Jiang, H. / Zhang, B. / Oppenheimer, N. / Lin, H. / Potter, B.V.L. / Lee, H.C. / Hao, Q. |
External links | J. Biol. Chem. / PubMed:19640846 |
Methods | X-ray diffraction |
Resolution | 1.75 - 2.18 Å |
Structure data | PDB-3i9j: PDB-3i9k: PDB-3i9l: PDB-3i9m: PDB-3i9n: |
Chemicals | ChemComp-NFD: ChemComp-AVV: ChemComp-NCA: ChemComp-HOH: ChemComp-NAD: ChemComp-N1C: ChemComp-AVU: ChemComp-AVW: |
Source |
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Keywords | HYDROLASE / Homodimer / enzyme-analog-nicotinamide complex / ADP-ribosyl cyclase / Disulfide bond / Fertilization / NAD / protein substrate NAD complex / enzyme-product analog complex / Enzyme-analog complex / covalent reaction intermediate / Alpha helices rich domain and alpha/beta domain / Alternative splicing / Diabetes mellitus / Glycoprotein / Membrane / Polymorphism / Receptor / Signal-anchor / Transmembrane |