SandboxPKA: Difference between revisions

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- The '''catalytic loop''' is composed by β6 and β7, whereas β8 and β9 strands flank the DGF motif, where the aspartic/glutamic residue is critical for recognizing one of the ATP-bound Mg++ ions
- The '''catalytic loop''' is composed by β6 and β7, whereas β8 and β9 strands flank the DGF motif, where the aspartic/glutamic residue is critical for recognizing one of the ATP-bound Mg++ ions


- The '''<scene name='Dasatinib/Mact/1'>Activation Loop Movement</scene>''' contains Tyr412 responsible for activation of the kinase activity.  
- The '''<scene name='Dasatinib/Mact/1'>Activation Loop Movement</scene>''' involves Tyr412 responsible for activation of the kinase activity.  


- The unactivated, autoinhibited conformation (in which the Asp-810-Phe-811-Gly-812 (DFG) triad at the beginning of the A-loop is in the “DFG-out” conformation) can <scene name='Dasatinib/Mdfg/3'>move</scene> when ATP Tyr412 is phosphorlated, rising an active conformation. <Ref>PMID: 19164557</Ref>
- In the unactivated, autoinhibited conformation, the Asp-810-Phe-811-Gly-812 (DFG) triad at the beginning of the A-loop is in the “DFG-out” conformation. The DFG motif can <scene name='Dasatinib/Mdfg/3'>move</scene> when ATP Tyr412 is phosphorylated, thus promoting the change towards the active conformation. <Ref>PMID: 19164557</Ref>


- The '''myristoyl group''' complements activation loop in turning on and off c-Abl protein. It has been shown to be a key regulator of this kinase.   
- The '''myristoyl group''' complements activation loop in turning on and off c-Abl protein. It has been shown to be a key regulator of this kinase.