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PDBsum entry 4ay5
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Transferase/peptide
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PDB id
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4ay5
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PDB id:
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| Name: |
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Transferase/peptide
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Title:
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Human o-glcnac transferase (ogt) in complex with udp and glycopeptide
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Structure:
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Udp-n-acetylglucosamine--peptide n-acetylglucosaminyl transferase 110 kda subunit. Chain: a, b, c, d. Fragment: tpr (truncated) and catalytic domain, residues 313-1031. Synonym: o-glcnac transferase subunit p110, o-linked n-acetyl glucosamine transferase 110 kda subunit, ogt. Engineered: yes. Gtab1tide. Chain: i, j, k, l.
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Expressed in: escherichia coli. Expression_system_taxid: 511693. Expression_system_variant: arcticexpress (ril). Synthetic: yes. Synthetic construct. Organism_taxid: 32630
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Resolution:
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3.15Å
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R-factor:
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0.174
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R-free:
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0.204
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Authors:
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M.Schimpl,X.Zheng,D.E.Blair,A.W.Schuettelkopf,I.Navratilova, T.Aristotelous,A.T.Ferenbach,M.A.Macnaughtan,V.S.Borodkin,D.M.F.Van Aalten
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Key ref:
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M.Schimpl
et al.
(2012).
O-GlcNAc transferase invokes nucleotide sugar pyrophosphate participation in catalysis.
Nat Chem Biol,
8,
969-974.
PubMed id:
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Date:
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18-Jun-12
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Release date:
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24-Oct-12
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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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Chains A, B, C, D:
E.C.2.4.1.255
- protein O-GlcNAc transferase.
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Reaction:
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1.
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L-seryl-[protein] + UDP-N-acetyl-alpha-D-glucosamine = 3-O-(N-acetyl- beta-D-glucosaminyl)-L-seryl-[protein] + UDP + H+
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2.
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L-threonyl-[protein] + UDP-N-acetyl-alpha-D-glucosamine = 3-O- (N-acetyl-beta-D-glucosaminyl)-L-threonyl-[protein] + UDP + H+
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L-seryl-[protein]
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+
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UDP-N-acetyl-alpha-D-glucosamine
Bound ligand (Het Group name = )
matches with 47.06% similarity
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=
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3-O-(N-acetyl- beta-D-glucosaminyl)-L-seryl-[protein]
Bound ligand (Het Group name = )
corresponds exactly
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+
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UDP
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+
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H(+)
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L-threonyl-[protein]
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+
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UDP-N-acetyl-alpha-D-glucosamine
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=
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3-O- (N-acetyl-beta-D-glucosaminyl)-L-threonyl-[protein]
Bound ligand (Het Group name = )
corresponds exactly
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+
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UDP
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+
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H(+)
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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Nat Chem Biol
8:969-974
(2012)
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PubMed id:
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O-GlcNAc transferase invokes nucleotide sugar pyrophosphate participation in catalysis.
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M.Schimpl,
X.Zheng,
V.S.Borodkin,
D.E.Blair,
A.T.Ferenbach,
A.W.Schüttelkopf,
I.Navratilova,
T.Aristotelous,
O.Albarbarawi,
D.A.Robinson,
M.A.Macnaughtan,
D.M.van Aalten.
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ABSTRACT
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');
}
}
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