Difference between revisions of "Formation of homo-dimer R2"

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(Parameters)
(Parameters with uncertainty)
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==Parameters with uncertainty==
 
==Parameters with uncertainty==
  
The probability distributions, adjusted accordingly in order to reflect the above values, are the following:
+
When deciding how to describe the uncertainty for this parameter we must take into consideration that the values reported in literature correspond to ''in vitro'' testing of different protein-protein interaction and dimerization reactions than ScbR, although they refer to another Streptomyces protein (DnaA). This means that there might be a difference between actual parameter values and the ones reported in literature. These facts influence the quantification of the parameter uncertainty and therefore the shape of the corresponding distributions.
  
 
The most plausible parameter value for the <math>K_{d6}</math> is decided to be <math> 35 nM </math> and the confidence interval <math> 100 </math>. This means that the mode of the PDF is <math>35</math> and the range where 95% of the values are found is between <math>0.1</math> and <math>10^{3} nM </math>.
 
The most plausible parameter value for the <math>K_{d6}</math> is decided to be <math> 35 nM </math> and the confidence interval <math> 100 </math>. This means that the mode of the PDF is <math>35</math> and the range where 95% of the values are found is between <math>0.1</math> and <math>10^{3} nM </math>.

Revision as of 19:46, 15 October 2015

Two ScbR (R) proteins bind together to form an ScbR homo-dimer (R2).

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Chemical equation

2R \rightleftharpoons R_{2}

Rate equation

 r= \frac{k^{-}_{6}}{K_{d6}}\cdot [R]^{2} - k^{-}_{6}\cdot [R_{2}]

Parameters

The parameters of this reaction are the dissociation constant for binding of one ScbR to another (K_{d6}) and the dissociation rate for binding of one ScbR to another (k^{-}_{6}).

Name Value Units Value in previous GBL models Remarks-Reference
K_{d6} 35.3-114 [1] nM N/A Majka et al. published a study on dimerization of the initiator Protein DnaA of Streptomyces and on its mutants, where they report dissociation constants in the range 35.3-114 nM.
Majka et al. 2001[1]

These values agree with Ozbabacan et al. [2] who state that strong protein-protein interactions such as homodimerization have equilibrium dissociation constants  < 10^{-6} M and mostly in the nanomolar range.

k^{-}_{6} 2.12-6.84 [3] [4] min^{-1} N/A According to Northrup et al. the K_{a} of protein-protein bond formations occur in the order of 10^{6} M^{-1}s^{-1}. Therefore, this value is used to calculate the dissociation rate for the ScbR homo-dimer formation. Therefore the range of the k^{-}_{3} values is 2.12-6.84 min^{-1}, calculated as per k^{-}_{6}=K_{d6} \cdot K_{a}.
Northrup et al. 1992[4]

Parameters with uncertainty

When deciding how to describe the uncertainty for this parameter we must take into consideration that the values reported in literature correspond to in vitro testing of different protein-protein interaction and dimerization reactions than ScbR, although they refer to another Streptomyces protein (DnaA). This means that there might be a difference between actual parameter values and the ones reported in literature. These facts influence the quantification of the parameter uncertainty and therefore the shape of the corresponding distributions.

The most plausible parameter value for the K_{d6} is decided to be  35 nM and the confidence interval  100 . This means that the mode of the PDF is 35 and the range where 95% of the values are found is between 0.1 and 10^{3} nM .

In a similar way, the most plausible value for k^{-}_{6} is 10^{-3} min^{-1} and the confidence interval 10. This means that the mode of the PDF is 10^{-3} and the range where 95% of the values are found is between 10^{-4} and 10^{-2} min^{-1}.

The probability distributions for the two parameters, adjusted accordingly in order to reflect the above values, are the following:

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The location and scale parameters of the distributions are:

Parameter μ σ
K_{d6} 5.7331 1.4757
k^{-}_{6} -6.0926 0.9028

References