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3L17

Discovery of (thienopyrimidin-2-yl)aminopyrimidines as Potent, Selective, and Orally Available Pan-PI3-Kinase and Dual Pan-PI3-Kinase/mTOR Inhibitors for the Treatment of Cancer

Entity
Entity IDChain IDDescriptionTypeChain lengthFormula weightNumber of moleculesDB Name (Accession)Biological sourceDescriptive keywords
1APhosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit gamma isoformpolymer966110727.11UniProt (P48736)
Pfam (PF00794)
Pfam (PF00792)
Pfam (PF00613)
Pfam (PF00454)
In PDB
Homo sapiens (human)PI3-kinase p110 subunit gamma, PtdIns-3-kinase subunit p110, PI3Kgamma, PI3K, p120-PI3K
2A4-methyl-5-(6-{[4-(methylsulfonyl)piperazin-1-yl]methyl}-4-morpholin-4-ylthieno[3,2-d]pyrimidin-2-yl)pyrimidin-2-aminenon-polymer504.61Chemie (JZY)
Sequence modifications
A: 144 - 1102 (UniProt: P48736)
PDBExternal DatabaseDetails
Met 143-expression tag
His 1103-expression tag
His 1104-expression tag
His 1105-expression tag
His 1106-expression tag
His 1107-expression tag
His 1108-expression tag
Sequence viewer
Contents of the asymmetric unit
PolymersNumber of chains1
Total formula weight110727.1
Non-Polymers*Number of molecules1
Total formula weight504.6
All*Total formula weight111231.7
*Water molecules are not included.

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PDB entries from 2024-05-01

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