Fig. 4From: A thrombophilia family with protein S deficiency due to protein translation disorders caused by a Leu607Ser heterozygous mutation in PROS1Protein S (PROS1) homology modeling and analysis. a Homology modeling of PROS1 has been performed using Swiss-Model. Leu607 is labeled in the alpha helix. b Conserved analysis of amino acid sequences near Leu607 (marked with red) (https://swissmodel.expasy.org/repository/uniprot/P07225?template=1h30.1.A&range=266-673)Back to article page