2riq | pdb_00002riq
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Crystal Structure of the Third Zinc-binding domain of human PARP-1
Overview
Poly(ADP-ribose) polymerase-1 (PARP-1) is a chromatin-associated enzyme with multiple cellular functions, including DNA repair, transcriptional regulation, and cell signaling. PARP-1 has a modular architecture with six independent domains comprising the 113-kDa polypeptide. Two zinc finger domains at the N terminus of PARP-1 bind to DNA and thereby activate the catalytic domain situated at the C terminus of the enzyme. The tight coupling of DNA binding and catalytic activities is critical to the cellular regulation of PARP-1 function; however, the mechanism for coordinating these activities remains an unsolved problem. Here, we demonstrate using spectroscopic and crystallographic analysis that human PARP-1 has a third zinc-binding domain. Biochemical mutagenesis and deletion analysis indicate that this region mediates interdomain contacts important for DNA-dependent enzyme activation. The crystal structure of the third zinc-binding domain reveals a zinc ribbon fold and suggests conserved residues that could form interdomain contacts. The new zinc-binding domain self-associates in the crystal lattice to form a homodimer with a head-totail arrangement. The structure of the homodimer provides a scaffold for assembling the activated state of PARP-1 and suggests a mechanism for coupling the DNA binding and catalytic functions of PARP-1.
About this Structure
2RIQ is a Single protein structure of sequence from Homo sapiens with ZN, EOH and GOL as ligands. Active as NAD(+) ADP-ribosyltransferase, with EC number 2.4.2.30 Known structural/functional Sites: AC1, AC2, AC3, AC4 and AC5. Full crystallographic information is available from OCA.
Reference
A Third Zinc-binding Domain of Human Poly(ADP-ribose) Polymerase-1 Coordinates DNA-dependent Enzyme Activation., Langelier MF, Servent KM, Rogers EE, Pascal JM, J Biol Chem. 2008 Feb 15;283(7):4105-14. Epub 2007 Nov 30. PMID:18055453
Page seeded by OCA on Thu Feb 21 18:47:37 2008
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- Homo sapiens
- NAD(+) ADP-ribosyltransferase
- Single protein
- Langelier, M F.
- Pascal, J M.
- Servent, K M.
- EOH
- GOL
- ZN
- Adp-ribosylation
- Dna damage
- Dna repair
- Dna-binding
- Glycosyltransferase
- Metal-binding
- Nad
- Nucleus
- Phosphorylation
- Polymorphism
- Transferase
- Zinc
- Zinc-finger
- Zn finger
- Zn ribbon
- Zn-binding domain