3TZM: Tgf-Beta Receptor Type 1 In Complex With Sb431542

Citation:
Abstract
Transforming growth factor-beta (TGFbeta) receptor kinase inhibitors have a great therapeutic potential. SB431542 is one of the mainly used kinase inhibitors of the TGFbeta/Activin pathway receptors, but needs improvement of its EC(50) (EC(50)=1 muM) to be translated to clinical use. A key feature of SB431542 is that it specifically targets receptors from the TGFbeta/Activin pathway but not the closely related receptors from the bone morphogenic proteins (BMP) pathway. To understand the mechanisms of this selectivity, we solved the crystal structure of the TGFbeta type I receptor (TbetaRI) kinase domain in complex with SB431542. We mutated TbetaRI residues coordinating SB431542 to their counterparts in activin-receptor like kinase 2 (ALK2), a BMP receptor kinase, and tested the kinase activity of mutated TbetaRI. We discovered that a Ser280Thr mutation yielded a TbetaRI variant that was resistant to SB431542 inhibition. Furthermore, the corresponding Thr283Ser mutation in ALK2 yielded a BMP receptor sensitive to SB431542. This demonstrated that Ser280 is the key determinant of selectivity for SB431542. This work provides a framework for optimising the SB431542 scaffold to more potent and selective inhibitors of the TGFbeta/Activin pathway.
PDB ID: 3TZMDownload
MMDB ID: 99840
PDB Deposition Date: 2011/9/27
Updated in MMDB: 2012/05
Experimental Method:
x-ray diffraction
Resolution: 1.7  Å
Source Organism:
Similar Structures:
Biological Unit for 3TZM: monomeric; determined by author and by software (PISA)
Molecular Components in 3TZM
Label Count Molecule
Protein (1 molecule)
1
Tgf-beta Receptor Type-1(Gene symbol: TGFBR1)
Molecule annotation
Chemical (1 molecule)
1
1
* Click molecule labels to explore molecular sequence information.

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