PDB ID: 4TMF
Hetero Atom Contents
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JS2 | 5-O-[(R)-{[(S)-[4-(8-amino-6-oxo-1,6-dihydro-9h-purin-9-yl)butoxy](hydroxy)phosphoryl]oxy}(hydroxy)phosphoryl]-alpha-D- ribofuranose | PoSSuM |
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Download interaction data: 4TMF
Structure summary
Code : | 4TMF PDBj RCSB PDB PDBe | ||||||||||||
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Header : | Hydrolase/Hydrolase Inhibitor | ||||||||||||
Title : | Crystal structure of human CD38 in complex with hydrolysed compound JMS713 | ||||||||||||
Release Data : | 2015-05-13 | ||||||||||||
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Authors : | Zhang, H., Swarbrick, J., Potter, B., Hao, Q. | ||||||||||||
Keywords : | CD38, ADP-ribosyl cyclase, cyclic ADP-ribose, X-crystallography, Calcium signaling, inhibitory compound, JMS713, Hydrolase-Hydrolase Inhibitor complex | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.0500 Å ) | ||||||||||||
Citation : |
Cyclic adenosine 5'-diphosphate ribose analogs without a "southern" ribose inhibit ADP-ribosyl cyclase-hydrolase CD38.
Swarbrick, J.M.,Graeff, R.,Zhang, H.
et al.
PubMed: 25226087 |
Reaction
Chain : | A, B | ||||||||||||||||||||||||||||||
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UniProt : | P28907 (CD38_HUMAN) | ||||||||||||||||||||||||||||||
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