TY - JOUR
T1 - Classification Model for the Second Extracellular Loop of Class A GPCRs
AU - Nicoli, Alessandro
AU - Dunkel, Andreas
AU - Giorgino, Toni
AU - De Graaf, Chris
AU - Di Pizio, Antonella
N1 - Publisher Copyright:
© 2022 The Authors. Published by American Chemical Society.
PY - 2022/2/14
Y1 - 2022/2/14
N2 - The extracellular loop 2 (ECL2) is the longest and the most diverse loop among class A G protein-coupled receptors (GPCRs). It connects the transmembrane (TM) helices 4 and 5 and contains a highly conserved cysteine through which it is bridged with TM3. In this paper, experimental ECL2 structures were analyzed based on their sequences, shapes, and intramolecular contacts. To take into account the flexibility, we incorporated into our analyses information from the molecular dynamics trajectories available on the GPCRmd website. Despite the high sequence variability, shapes of the analyzed structures, defined by the backbone volume overlaps, can be clustered into seven main groups. Conformational differences within the clusters can be then identified by intramolecular interactions with other GPCR structural domains. Overall, our work provides a reorganization of the structural information of the ECL2 of class A GPCR subfamilies, highlighting differences and similarities on sequence and conformation levels.
AB - The extracellular loop 2 (ECL2) is the longest and the most diverse loop among class A G protein-coupled receptors (GPCRs). It connects the transmembrane (TM) helices 4 and 5 and contains a highly conserved cysteine through which it is bridged with TM3. In this paper, experimental ECL2 structures were analyzed based on their sequences, shapes, and intramolecular contacts. To take into account the flexibility, we incorporated into our analyses information from the molecular dynamics trajectories available on the GPCRmd website. Despite the high sequence variability, shapes of the analyzed structures, defined by the backbone volume overlaps, can be clustered into seven main groups. Conformational differences within the clusters can be then identified by intramolecular interactions with other GPCR structural domains. Overall, our work provides a reorganization of the structural information of the ECL2 of class A GPCR subfamilies, highlighting differences and similarities on sequence and conformation levels.
UR - http://www.scopus.com/inward/record.url?scp=85124266009&partnerID=8YFLogxK
U2 - 10.1021/acs.jcim.1c01056
DO - 10.1021/acs.jcim.1c01056
M3 - Article
C2 - 35113559
AN - SCOPUS:85124266009
SN - 1549-9596
VL - 62
SP - 511
EP - 522
JO - Journal of Chemical Information and Modeling
JF - Journal of Chemical Information and Modeling
IS - 3
ER -