Difference between revisions of "Part:BBa K5051001"

 
 
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This modification converts PKS1 from the inactive apo-form to the active holo-form, enabling them to participate in downstream reactions. The 4′-PP group acts as a flexible arm that facilitates the transport of acyl or aminoacyl intermediates between the active sites. Without PPTase, PKS1  would be hindered from maximum enzymatic activity (Venkitasubramanian et al., 2006; Xue et al., 2018).  
 
This modification converts PKS1 from the inactive apo-form to the active holo-form, enabling them to participate in downstream reactions. The 4′-PP group acts as a flexible arm that facilitates the transport of acyl or aminoacyl intermediates between the active sites. Without PPTase, PKS1  would be hindered from maximum enzymatic activity (Venkitasubramanian et al., 2006; Xue et al., 2018).  
  
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https://static.igem.wiki/teams/5051/parts/parts2.png
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Fig 1. Structure predicted by ESMFold, coloured by pLDDT (Lin et al., 2023)
  
 
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Latest revision as of 12:55, 2 October 2024


PPTase

PPTase from Aureobasidium pullulans EXF-150 is critical for post-translational modifications (PTMs) of PKS1. The conserved mechanism is that the PPTase transfers a 4'-phosphopantetheinyl (4'-PP) group from Coenzyme A (CoA) to a conserved serine in the acyl carrier (ACP) domains of polyketide synthases (PKS) (Sunbul et al., 2009).

This modification converts PKS1 from the inactive apo-form to the active holo-form, enabling them to participate in downstream reactions. The 4′-PP group acts as a flexible arm that facilitates the transport of acyl or aminoacyl intermediates between the active sites. Without PPTase, PKS1 would be hindered from maximum enzymatic activity (Venkitasubramanian et al., 2006; Xue et al., 2018).

parts2.png Fig 1. Structure predicted by ESMFold, coloured by pLDDT (Lin et al., 2023)

Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    INCOMPATIBLE WITH RFC[12]
    Illegal NheI site found at 924
  • 21
    INCOMPATIBLE WITH RFC[21]
    Illegal BglII site found at 981
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    COMPATIBLE WITH RFC[25]
  • 1000
    COMPATIBLE WITH RFC[1000]