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3LCD

Inhibitor Bound to A DFG-In structure of the Kinase Domain of CSF-1R

Summary for 3LCD
Entry DOI10.2210/pdb3lcd/pdb
DescriptorMacrophage colony-stimulating factor 1 receptor, SULFATE ION, N~3~-(2,6-dichlorobenzyl)-5-(4-{[(2R)-2-(pyrrolidin-1-ylmethyl)pyrrolidin-1-yl]carbonyl}phenyl)pyrazine-2,3-diamine, ... (4 entities in total)
Functional Keywordskinase cfms csf-1r csf tyrosine-kinase colony stimulating factor 1 receptor, atp-binding, disulfide bond, glycoprotein, immunoglobulin domain, kinase, membrane, nucleotide-binding, phosphoprotein, proto-oncogene, receptor, transferase, transmembrane, tyrosine-protein kinase
Biological sourceHomo sapiens (human)
More
Cellular locationCell membrane; Single-pass type I membrane protein: P07333
Total number of polymer chains1
Total formula weight38051.35
Authors
Kamtekar, S.,Day, J.E.,Reitz, B.A.,Mathis, K.J.,Meyers, M.J. (deposition date: 2010-01-10, release date: 2010-03-02, Last modification date: 2017-07-26)
Primary citationMeyers, M.J.,Pelc, M.,Kamtekar, S.,Day, J.,Poda, G.I.,Hall, M.K.,Michener, M.L.,Reitz, B.A.,Mathis, K.J.,Pierce, B.S.,Parikh, M.D.,Mischke, D.A.,Long, S.A.,Parlow, J.J.,Anderson, D.R.,Thorarensen, A.
Structure-based drug design enables conversion of a DFG-in binding CSF-1R kinase inhibitor to a DFG-out binding mode
Bioorg.Med.Chem.Lett., 20:1543-1547, 2010
Cited by
PubMed: 20137931
DOI: 10.1016/j.bmcl.2010.01.078
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

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数据于2024-04-24公开中

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