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Structure paper

TitleCrystal structures of the N-terminal kinase domain of human RSK1 bound to three different ligands: Implications for the design of RSK1 specific inhibitors.
Journal, issue, pagesProtein Sci., Vol. 16, Page 2626-2635, Year 2007
Publish dateAug 28, 2007 (structure data deposition date)
AuthorsIkuta, M. / Kornienko, M. / Byrne, N. / Reid, J.C. / Mizuarai, S. / Kotani, H. / Munshi, S.K.
External linksProtein Sci. / PubMed:17965187
MethodsX-ray diffraction
Resolution2 - 2.1 Å
Structure data

PDB-2z7q:
Crystal structure of the N-terminal kinase domain of human RSK-1 bound to AMP-PCP
Method: X-RAY DIFFRACTION / Resolution: 2 Å

PDB-2z7r:
Crystal Structure of the N-terminal Kinase Domain of Human RSK1 bound to Staurosporine
Method: X-RAY DIFFRACTION / Resolution: 2 Å

PDB-2z7s:
Crystal Structure of the N-terminal Kinase Domain of Human RSK1 bound to Purvalnol A
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

Chemicals

ChemComp-MG:
Unknown entry

ChemComp-ACP:
PHOSPHOMETHYLPHOSPHONIC ACID ADENYLATE ESTER / AMP-PCP, energy-carrying molecule analogue*YM

ChemComp-HOH:
WATER

ChemComp-STU:
STAUROSPORINE / anticancer, antifungal, antibiotic, alkaloid*YM

ChemComp-P01:
2-({6-[(3-CHLOROPHENYL)AMINO]-9-ISOPROPYL-9H-PURIN-2-YL}AMINO)-3-METHYLBUTAN-1-OL / inhibitor*YM

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / protein kinase; cancer; kinase inhibitor / ATP-binding / Magnesium / Metal-binding / Nucleotide-binding / Phosphorylation / Serine/threonine-protein kinase / protein kinase / cancer / kinase inhibitor / Polymorphism

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