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PDBsum entry 3r9a
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Transferase/transport protein
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PDB id
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3r9a
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PDB id:
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| Name: |
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Transferase/transport protein
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Title:
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Human alanine-glyoxylate aminotransferase in complex with the tpr domain of human pex5p
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Structure:
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Serine--pyruvate aminotransferase. Chain: a, c. Synonym: spt, alanine--glyoxylate aminotransferase, agt. Engineered: yes. Peroxisomal targeting signal 1 receptor. Chain: b, d. Fragment: tpr-domain, unp residues 315-639. Synonym: pts1 receptor, pts1r, pts1-bp, peroxin-5, peroxisomal c- terminal targeting signal import receptor, peroxisome receptor 1.
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Source:
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Homo sapiens. Human. Organism_taxid: 9606. Gene: agt1, agxt, spat. Expressed in: escherichia coli. Expression_system_taxid: 562. Gene: pex5, pxr1.
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Resolution:
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2.35Å
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R-factor:
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0.187
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R-free:
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0.239
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Authors:
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K.Fodor,M.Wilmanns
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Key ref:
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K.Fodor
et al.
(2012).
Molecular requirements for peroxisomal targeting of alanine-glyoxylate aminotransferase as an essential determinant in primary hyperoxaluria type 1.
Plos Biol,
10,
e1001309.
PubMed id:
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Date:
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25-Mar-11
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Release date:
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11-May-11
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Supersedes:
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PROCHECK
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Headers
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References
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Enzyme class 2:
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Chains A, C:
E.C.2.6.1.44
- alanine--glyoxylate transaminase.
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Reaction:
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glyoxylate + L-alanine = glycine + pyruvate
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glyoxylate
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+
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L-alanine
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=
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glycine
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+
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pyruvate
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Cofactor:
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Pyridoxal 5'-phosphate
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Pyridoxal 5'-phosphate
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Enzyme class 3:
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Chains A, C:
E.C.2.6.1.51
- serine--pyruvate transaminase.
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Reaction:
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L-serine + pyruvate = 3-hydroxypyruvate + L-alanine
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L-serine
Bound ligand (Het Group name = )
matches with 40.00% similarity
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+
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pyruvate
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=
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3-hydroxypyruvate
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+
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L-alanine
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Cofactor:
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Pyridoxal 5'-phosphate
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Pyridoxal 5'-phosphate
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Note, where more than one E.C. class is given (as above), each may
correspond to a different protein domain or, in the case of polyprotein
precursors, to a different mature protein.
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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Plos Biol
10:e1001309
(2012)
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PubMed id:
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Molecular requirements for peroxisomal targeting of alanine-glyoxylate aminotransferase as an essential determinant in primary hyperoxaluria type 1.
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K.Fodor,
J.Wolf,
R.Erdmann,
W.Schliebs,
M.Wilmanns.
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ABSTRACT
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');
}
}
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