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Structure paper

TitleStructural Basis for Carm1 Inhibition by Indole and Pyrazole Inhibitors
Journal, issue, pagesBiochem. J., Vol. 436, Page 331-, Year 2011
Publish dateDec 10, 2010 (structure data deposition date)
AuthorsSack, J.S. / Thieffine, S. / Bandiera, T. / Fasolini, M. / Duke, G.J. / Jayaraman, L. / Kish, K.F. / Klei, H.E. / Purandare, A.V. / Rosettani, P. ...Sack, J.S. / Thieffine, S. / Bandiera, T. / Fasolini, M. / Duke, G.J. / Jayaraman, L. / Kish, K.F. / Klei, H.E. / Purandare, A.V. / Rosettani, P. / Troiani, S. / Xie, D. / Bertrand, J.A.
External linksBiochem. J. / PubMed:21410432
MethodsX-ray diffraction
Resolution2.1 - 2.4 Å
Structure data

PDB-2y1w:
CRYSTAL STRUCTURE OF COACTIVATOR ASSOCIATED ARGININE METHYLTRANSFERASE 1 (CARM1) IN COMPLEX WITH SINEFUNGIN AND INDOLE INHIBITOR
Method: X-RAY DIFFRACTION / Resolution: 2.1 Å

PDB-2y1x:
CRYSTAL STRUCTURE OF COACTIVATOR ASSOCIATED ARGININE METHYLTRANSFERASE 1 (CARM1) IN COMPLEX WITH SINEFUNGIN AND INDOLE INHIBITOR
Method: X-RAY DIFFRACTION / Resolution: 2.4 Å

Chemicals

ChemComp-SFG:
SINEFUNGIN

ChemComp-849:
2-{4-[3-FLUORO-2-(2-METHOXYPHENYL)-1H-INDOL-5-YL] PIPERIDIN-1-YL}-N-METHYLETHANAMINE

ChemComp-HOH:
WATER

ChemComp-SAH:
S-ADENOSYL-L-HOMOCYSTEINE

ChemComp-845:
N-(3-{5-[5-(1H-INDOL-4-YL)-1,3,4-OXADIAZOL-2-YL]-3-(TRIFLUOROMETHYL)-1H-PYRAZOL-1-YL}BENZYL)-L-ALANINAMIDE

ChemComp-CL:
Unknown entry

Source
  • homo sapiens (human)
KeywordsTRANSFERASE / HISTONE MODIFICATION

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