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PDBsum entry 4x60
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Transferase/transferase inhibitor
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PDB id
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4x60
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PDB id:
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| Name: |
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Transferase/transferase inhibitor
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Title:
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Crystal structure of prmt5:mep50 with epz015666 and sinefungin
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Structure:
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Protein arginine n-methyltransferase 5. Chain: a. Synonym: 72 kda icln-binding protein,histone-arginine n- methyltransferase prmt5,jak-binding protein 1,shk1 kinase-binding protein 1 homolog,skb1hs. Engineered: yes. Methylosome protein 50. Chain: b. Synonym: mep-50,androgen receptor cofactor p44,wd repeat-containing
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Gene: prmt5, hrmt1l5, ibp72, jbp1, skb1. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108. Expression_system_cell_line: sf9. Gene: wdr77, mep50, wd45, hkmt1069, nbla10071.
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Resolution:
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2.35Å
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R-factor:
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0.205
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R-free:
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0.254
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Authors:
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P.A.Boriack-Sjodin
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Key ref:
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E.Chan-Penebre
et al.
(2015).
A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models.
Nat Chem Biol,
11,
432-437.
PubMed id:
DOI:
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Date:
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06-Dec-14
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Release date:
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22-Apr-15
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PROCHECK
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Headers
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References
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Enzyme class:
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Chain A:
E.C.2.1.1.320
- type Ii protein arginine methyltransferase.
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Reaction:
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L-arginyl-[protein] + 2 S-adenosyl-L-methionine = N(omega),N(omega)'-dimethyl-L-arginyl-[protein] + 2 S-adenosyl-L- homocysteine + 2 H+
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L-arginyl-[protein]
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+
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2
×
S-adenosyl-L-methionine
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=
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N(omega),N(omega)'-dimethyl-L-arginyl-[protein]
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+
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2
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S-adenosyl-L- homocysteine
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+
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2
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H(+)
Bound ligand (Het Group name = )
matches with 51.43% similarity
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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DOI no:
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Nat Chem Biol
11:432-437
(2015)
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PubMed id:
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A selective inhibitor of PRMT5 with in vivo and in vitro potency in MCL models.
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E.Chan-Penebre,
K.G.Kuplast,
C.R.Majer,
P.A.Boriack-Sjodin,
T.J.Wigle,
L.D.Johnston,
N.Rioux,
M.J.Munchhof,
L.Jin,
S.L.Jacques,
K.A.West,
T.Lingaraj,
K.Stickland,
S.A.Ribich,
A.Raimondi,
M.P.Scott,
N.J.Waters,
R.M.Pollock,
J.J.Smith,
O.Barbash,
M.Pappalardi,
T.F.Ho,
K.Nurse,
K.P.Oza,
K.T.Gallagher,
R.Kruger,
M.P.Moyer,
R.A.Copeland,
R.Chesworth,
K.W.Duncan.
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ABSTRACT
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');
}
}
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