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4X2G

Selection of fragments for kinase inhibitor design: decoration is key

Summary for 4X2G
Entry DOI10.2210/pdb4x2g/pdb
Related4X2F
DescriptorTGF-beta receptor type-1, 4-[(4-aminophenyl)amino]pyrido[2,3-d]pyrimidin-5(6H)-one, SULFATE ION, ... (5 entities in total)
Functional Keywordstransferase, protein kinase, inhibitor complex, transferase-transferase inhibitor complex, transferase/transferase inhibitor
Biological sourceHomo sapiens (Human)
Cellular locationCell membrane; Single-pass type I membrane protein: P36897
Total number of polymer chains1
Total formula weight35353.61
Authors
Czodrowski, P.,Hoelzemann, G.,Barnickel, G.,Greiner, H.,Musil, D. (deposition date: 2014-11-26, release date: 2015-08-12, Last modification date: 2024-02-28)
Primary citationCzodrowski, P.,Holzemann, G.,Barnickel, G.,Greiner, H.,Musil, D.
Selection of fragments for kinase inhibitor design: decoration is key.
J.Med.Chem., 58:457-465, 2015
Cited by
PubMed: 25437144
DOI: 10.1021/jm501597j
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.51 Å)
Structure validation

220472

数据于2024-05-29公开中

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