4Y30
Crystal structure of human protein arginine methyltransferase PRMT6 bound to SAH and EPZ020411
Summary for 4Y30
Entry DOI | 10.2210/pdb4y30/pdb |
Related | 4Y2H |
Descriptor | Protein arginine N-methyltransferase 6, S-ADENOSYL-L-HOMOCYSTEINE, N,N'-dimethyl-N-({3-[4-({trans-3-[2-(tetrahydro-2H-pyran-4-yl)ethoxy]cyclobutyl}oxy)phenyl]-1H-pyrazol-4-yl}methyl)ethane-1,2-diamine, ... (6 entities in total) |
Functional Keywords | transferase |
Biological source | Homo sapiens (Human) |
Cellular location | Nucleus : Q96LA8 |
Total number of polymer chains | 2 |
Total formula weight | 81004.27 |
Authors | Swinger, K.K.,Boriack-Sjodin, P.A. (deposition date: 2015-02-10, release date: 2015-04-22, Last modification date: 2024-02-28) |
Primary citation | Mitchell, L.H.,Drew, A.E.,Ribich, S.A.,Rioux, N.,Swinger, K.K.,Jacques, S.L.,Lingaraj, T.,Boriack-Sjodin, P.A.,Waters, N.J.,Wigle, T.J.,Moradei, O.,Jin, L.,Riera, T.,Porter-Scott, M.,Moyer, M.P.,Smith, J.J.,Chesworth, R.,Copeland, R.A. Aryl Pyrazoles as Potent Inhibitors of Arginine Methyltransferases: Identification of the First PRMT6 Tool Compound. Acs Med.Chem.Lett., 6:655-659, 2015 Cited by PubMed: 26101569DOI: 10.1021/acsmedchemlett.5b00071 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (2.1 Å) |
Structure validation
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