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Structure paper

TitleStructural Basis for a High Affinity Inhibitor Bound to Protein Kinase Mk2.
Journal, issue, pagesJ. Mol. Biol., Vol. 369, Page 735-, Year 2007
Publish dateDec 9, 2006 (structure data deposition date)
AuthorsHillig, R.C. / Eberspaecher, U. / Monteclaro, F. / Huber, M. / Nguyen, D. / Mengel, A. / Muller-Tiemann, B. / Egner, U.
External linksJ. Mol. Biol. / PubMed:17449059
MethodsX-ray diffraction
Resolution3.1 - 3.31 Å
Structure data

PDB-2jbo:
Protein kinase MK2 in complex with an inhibitor (crystal form-1, soaking)
Method: X-RAY DIFFRACTION / Resolution: 3.1 Å

PDB-2jbp:
Protein kinase MK2 in complex with an inhibitor (crystal form-2, co- crystallization)
Method: X-RAY DIFFRACTION / Resolution: 3.31 Å

Chemicals

ChemComp-PO4:
PHOSPHATE ION

ChemComp-P4O:
2-(2-QUINOLIN-3-YLPYRIDIN-4-YL)-1,5,6,7-TETRAHYDRO-4H-PYRROLO[3,2-C]PYRIDIN-4-ONE

ChemComp-HOH:
WATER

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / SER-THR KINASE / MAPKAP KINASE 2 / PHOSPHORYLATION / MK2 / KINASE / ATP SITE / ATP-BINDING / SERINE/THREONINE-PROTEIN KINASE / SMALL MOLECULE INHIBITOR / NUCLEOTIDE-BINDING / ATP- BINDING / CO-CRYSTALLIZATION

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