Calculating the isoelectric point of amino acids

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StarryNights

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Given that aspartic acid has the following pkas, how would you calculate the ip? For the COOH group pka is 2.1, for the NH3 group pka is 9.8, and the R group pka is 3.9

I know to average the pkas of carboxyl and amino groups for simple a.acids, but what happens when the R group contributes as well? Kaplan has a 3 paragraph explanation for this, and it might as well be a verbal passage cause I have no clue what they're trying to say. If anyone can help, I'd really appreciate it. Thanks!

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Average the pKa of the functional group that's protonated right after the neutral state and the pKa of the functional group that's protonated right before the neutral state.
 
For neutral amino acids: pKa(N) & pKa(C)
For acidic amino acids: use the two more acidic pKa's
For basic amino acids: use the two more basic pKa's
 
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