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Structure paper

TitleIn-plate protein crystallization, in situ ligand soaking and X-ray diffraction.
Journal, issue, pagesActa Crystallogr. ,Sect. D, Vol. 67, Page 747-755, Year 2011
Publish dateMar 4, 2011 (structure data deposition date)
Authorsle Maire, A. / Gelin, M. / Pochet, S. / Hoh, F. / Pirocchi, M. / Guichou, J.F. / Ferrer, J.L. / Labesse, G.
External linksActa Crystallogr. ,Sect. D / PubMed:21904027
MethodsX-ray diffraction
Resolution1.46 - 1.54 Å
Structure data

PDB-3qyu:
Crystal structure of human cyclophilin D at 1.54 A resolution at room temperature
Method: X-RAY DIFFRACTION / Resolution: 1.54 Å

PDB-3qyw:
Crystal structure of ERK2 in complex with an inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.5 Å

PDB-3qyz:
Crystal structure of ERK2 in complex with an inhibitor
Method: X-RAY DIFFRACTION / Resolution: 1.46 Å

Chemicals

ChemComp-HOH:
WATER

ChemComp-6PB:
6-(3-bromophenyl)-7H-purin-2-amine

ChemComp-DMS:
DIMETHYL SULFOXIDE / DMSO, precipitant*YM

ChemComp-SO4:
SULFATE ION

ChemComp-Z8B:
5'-azido-8-bromo-5'-deoxyadenosine

ChemComp-BME:
BETA-MERCAPTOETHANOL

Source
  • homo sapiens (human)
  • rattus norvegicus (Norway rat)
KeywordsISOMERASE / beta barrel / prolyl cis/trans isomerase / mitochondria / TRANSFERASE/TRANSFERASE INHIBITOR / TRANSFERASE / SERINE/THREONINE-PROTEIN KINASE / ATP-BINDING CELL CYCLE / PHOSPHORYLATION / Protein Kinase / TRANSFERASE-TRANSFERASE INHIBITOR complex

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