4lkq: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
Line 1: | Line 1: | ||
{{STRUCTURE_4lkq| PDB=4lkq | SCENE= }} | |||
===Crystal structure of PDE10A2 with fragment ZT017=== | |||
{{ABSTRACT_PUBMED_24375910}} | |||
==Function== | |||
[[http://www.uniprot.org/uniprot/PDE10_HUMAN PDE10_HUMAN]] Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. Can hydrolyze both cAMP and cGMP, but has higher affinity for cAMP and is more efficient with cAMP as substrate.<ref>PMID:17389385</ref> | |||
==About this Structure== | |||
[[4lkq]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4LKQ OCA]. | |||
==Reference== | |||
<ref group="xtra">PMID:024375910</ref><references group="xtra"/><references/> | |||
[[Category: Badger, J.]] | |||
[[Category: Chie-Leon, B.]] | |||
[[Category: Logan, C.]] | |||
[[Category: Nienaber, V.]] | |||
[[Category: Sridhar, V.]] | |||
[[Category: Fragment screening]] | |||
[[Category: Hydrolase]] | |||
[[Category: Hydrolase-hydrolase inhibitor complex]] |
Revision as of 21:14, 3 March 2014
Crystal structure of PDE10A2 with fragment ZT017Crystal structure of PDE10A2 with fragment ZT017
Template:ABSTRACT PUBMED 24375910
FunctionFunction
[PDE10_HUMAN] Plays a role in signal transduction by regulating the intracellular concentration of cyclic nucleotides. Can hydrolyze both cAMP and cGMP, but has higher affinity for cAMP and is more efficient with cAMP as substrate.[1]
About this StructureAbout this Structure
4lkq is a 2 chain structure. Full crystallographic information is available from OCA.
ReferenceReference
- ↑ Recht MI, Sridhar V, Badger J, Bounaud PY, Logan C, Chie-Leon B, Nienaber V, Torres FE. Identification and Optimization of PDE10A Inhibitors Using Fragment-Based Screening by Nanocalorimetry and X-ray Crystallography. J Biomol Screen. 2013 Dec 27. PMID:24375910 doi:http://dx.doi.org/10.1177/1087057113516493