Difference between revisions of "Part:BBa K4165047"

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===Usage and Biology===
 
===Usage and Biology===
 
Switch 27 plays a role in mediating HTRA1's function. For HTRA1 to become active, a conformational modification in the linker is necessary, which displaces the associated inhibitor from the active site. The conformational rearrangement can be mediated through the affinity clamp for tau and beta-amyloid binding. These clamps are used for stabilizing the inhibitor away from the active site. These two domains (inhibitor and affinity clamp connected with linker1 beside with amyloid beta binding peptide connected to tau binding peptide by linker 2). Additionally, (H1A) binding peptide bound to the PDZ domain and connected to the affinity clamp on the other side with linker3.
 
Switch 27 plays a role in mediating HTRA1's function. For HTRA1 to become active, a conformational modification in the linker is necessary, which displaces the associated inhibitor from the active site. The conformational rearrangement can be mediated through the affinity clamp for tau and beta-amyloid binding. These clamps are used for stabilizing the inhibitor away from the active site. These two domains (inhibitor and affinity clamp connected with linker1 beside with amyloid beta binding peptide connected to tau binding peptide by linker 2). Additionally, (H1A) binding peptide bound to the PDZ domain and connected to the affinity clamp on the other side with linker3.
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<span class='h3bb'>Sequence and Features</span>
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<partinfo>BBa_K4165047 SequenceAndFeatures</partinfo>
  
 
===Dry lab===
 
===Dry lab===
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                             Figure 1. The 3D structure of switch 27 modeled by TRrosetta.  
 
                             Figure 1. The 3D structure of switch 27 modeled by TRrosetta.  
 
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<span class='h3bb'>Sequence and Features</span>
 
<partinfo>BBa_K4165047 SequenceAndFeatures</partinfo>
 
 
  
 
<!-- Uncomment this to enable Functional Parameter display  
 
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Revision as of 12:45, 10 October 2022


HtrA1 Switch 27

This composite part consists of T7 promoter (BBa_K3633015), lac operator (BBa_K4165062), pGS-21a RBS (BBa_K4165016), 6x His-tag (BBa_K4165020), H1A (BBa_K4165000), GSGS Linker (BBa_K4165065), TD28REV (BBa_K4165006), GGSGGGGG Linker (BBa_K4165019), WWW (BBa_K4165007), GSGS Linker (BBa_K4165065), WAP inhibitor (BBa_K4165008), and T7 terminator (BBa_K731721).

Usage and Biology

Switch 27 plays a role in mediating HTRA1's function. For HTRA1 to become active, a conformational modification in the linker is necessary, which displaces the associated inhibitor from the active site. The conformational rearrangement can be mediated through the affinity clamp for tau and beta-amyloid binding. These clamps are used for stabilizing the inhibitor away from the active site. These two domains (inhibitor and affinity clamp connected with linker1 beside with amyloid beta binding peptide connected to tau binding peptide by linker 2). Additionally, (H1A) binding peptide bound to the PDZ domain and connected to the affinity clamp on the other side with linker3.


Sequence and Features


Assembly Compatibility:
  • 10
    COMPATIBLE WITH RFC[10]
  • 12
    COMPATIBLE WITH RFC[12]
  • 21
    COMPATIBLE WITH RFC[21]
  • 23
    COMPATIBLE WITH RFC[23]
  • 25
    INCOMPATIBLE WITH RFC[25]
    Illegal NgoMIV site found at 526
    Illegal AgeI site found at 262
  • 1000
    COMPATIBLE WITH RFC[1000]

Dry lab

Modeling

we modeled this switch to see the final structure of the switch, the top model which has score 4 out of 6 from TRrosetta.


                            Figure 1. The 3D structure of switch 27 modeled by TRrosetta.