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PDBsum entry 2wpf
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Oxidoreductase
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PDB id
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2wpf
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Contents |
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* Residue conservation analysis
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PDB id:
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| Name: |
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Oxidoreductase
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Title:
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Trypanosoma brucei trypanothione reductase in complex with 3,4- dihydroquinazoline inhibitor (ddd00085762)
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Structure:
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Trypanothione reductase. Chain: a, b, c, d. Engineered: yes
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Source:
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Trypanosoma brucei. Organism_taxid: 185431. Strain: treu927. Expressed in: escherichia coli. Expression_system_taxid: 469008. Expression_system_variant: codonplus ril.
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Resolution:
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1.90Å
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R-factor:
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0.188
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R-free:
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0.247
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Authors:
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M.S.Alphey,S.Patterson,A.H.Fairlamb
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Key ref:
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S.Patterson
et al.
(2011).
Dihydroquinazolines as a novel class of Trypanosoma brucei trypanothione reductase inhibitors: discovery, synthesis, and characterization of their binding mode by protein crystallography.
J Med Chem,
54,
6514-6530.
PubMed id:
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Date:
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06-Aug-09
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Release date:
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13-Oct-10
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PROCHECK
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Headers
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References
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Q389T8
(Q389T8_TRYB2) -
Trypanothione reductase from Trypanosoma brucei brucei (strain 927/4 GUTat10.1)
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Seq: Struc:
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492 a.a.
490 a.a.
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Key: |
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PfamA domain |
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Secondary structure |
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CATH domain |
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Enzyme class:
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E.C.1.8.1.12
- trypanothione-disulfide reductase.
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Reaction:
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trypanothione + NADP+ = trypanothione disulfide + NADPH + H+
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trypanothione
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NADP(+)
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=
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trypanothione disulfide
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+
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NADPH
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+
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H(+)
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Cofactor:
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FAD
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FAD
Bound ligand (Het Group name =
FAD)
corresponds exactly
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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J Med Chem
54:6514-6530
(2011)
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PubMed id:
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Dihydroquinazolines as a novel class of Trypanosoma brucei trypanothione reductase inhibitors: discovery, synthesis, and characterization of their binding mode by protein crystallography.
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S.Patterson,
M.S.Alphey,
D.C.Jones,
E.J.Shanks,
I.P.Street,
J.A.Frearson,
P.G.Wyatt,
I.H.Gilbert,
A.H.Fairlamb.
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ABSTRACT
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');
}
}
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