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. Author manuscript; available in PMC: 2012 Apr 3.
Published in final edited form as: J Comput Aided Mol Des. 2011 Apr 3;25(4):329–338. doi: 10.1007/s10822-011-9423-3

Table 1.

Percentages of sequence identity between the aligned sequences of the hP2Y12R and the available structural templates.

hP2Y12R bRHO, % tADRB1, % hADRB2, % hA2AAR, % hCXCR4, % hDRD3, %
overall 15.9 17.5 17.6 15.5 21.9 18.2
TMs 18.8 23.2 20.8 19.3 25.6 23.2
TM1 16.7 13.3 10.0 6.7 23.3 23.3
TM2 20.0 16.7 16.7 6.7 20.0 10.0
TM3 18.2 33.3 33.3 27.3 33.3 30.4
TM4 12.0 24.0 16.0 24.0 26.0 16.0
TM5 21.2 21.2 18.2 15.2 18.2 24.2
TM6 25.0 28.1 25.0 18.8 21.9 28.1
TM7 16.7 25.0 25.0 25.0 29.0 33.3
EL3-TM7 10.3 15.4 15.4 20.5 27.5 23.1

hP2Y12R = human P2Y12 receptor; bRHO = bovine rhodopsin; tADRB1 = turkey β1 adrenergic receptor; hADRB2 = human β2 adrenergic receptor; hA2AAR = human A2A adenosine receptor; hCXCR4 = human C-X-C chemokine type 4 receptor; hDRD3 = human dopamine type 3 receptor. The residues considered for the TM segments: from 1.30 to 1.59 for TM1; from 2.38 to 2.67 for TM2; from 3.33 to 3.55 for TM3; from 4.39 to 4.63 for TM4; from 5.36 to 5.68 for TM5; from 6.29 to 6.60 for TM6; from 7.32 to 7.55 for TM7; from 6.61 to 7.55 for EL3-TM7.