PDB ID: 3UDV
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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ACT | Acetate ion | PoSSuM | |||
J1C | 5'-S-[1-(2-{[(2-amino-7,7-dimethyl-4-oxo-3,4,7,8-tetrahydropteridin-6-yl)carbonyl]amino}ethyl)piperidin-4-yl]-5'-thioadenosine | PoSSuM |
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Download interaction data: 3UDV
Structure summary
Code : | 3UDV PDBj RCSB PDB PDBe | ||||||||||||
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Header : | TRANSFERASE/TRANSFERASE INHIBITOR | ||||||||||||
Title : | Crystal structure of E. coli HPPK in complex with bisubstrate analogue inhibitor J1C | ||||||||||||
Release Data : | 2012-01-04 | ||||||||||||
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Authors : | Shaw, G., Shi, G., Ji, X. | ||||||||||||
Keywords : | Alpha Beta, Kinase, ATP Binding, Pyrophosphoryl Transfer, TRANSFERASE-TRANSFERASE INHIBITOR complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 1.8800 Å ) | ||||||||||||
Citation : |
Bisubstrate analogue inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase: New design with improved properties.
Shi, G.,Shaw, G.,Liang, Y.H.
et al.
PubMed: 22169600 Bisubstrate analogue inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase: synthesis and biochemical and crystallographic studies.
Shi, G.,Blaszczyk, J.,Ji, X.
et al.
PubMed: 11311059 |
Reaction
Chain : | A | ||||||||
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UniProt : | P26281 (HPPK_ECOLI) | ||||||||
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