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. Author manuscript; available in PMC: 2024 Apr 1.
Published in final edited form as: Thromb Haemost. 2022 Dec 6;123(4):380–392. doi: 10.1055/a-1993-4193

Fig. 6. PONDR Analysis of Fbg αC (233–425), actin, and α2-antiplasmin and fibronectin for order-disorder characteristics.

Fig. 6

Intrinsic disorder propensity (ID propensity) of the amino acid sequences of (A) Fbg αC (233–425) (B) actin (C) α2-antiplasmin (1–225) and (D) Fibronectin (1–225) were calculated with the PONDR VLXT algorithm (www.pondr.com). The amino acid sequences of the proteins were accessed from the UniProt database (Uniprot ID for actin (P68135), α2-antiplasmin (P08697), and Fibronectin (P02751)). ID propensity value equal to or greater than 0.5 indicated disorder. The major and other potential reactive glutamines are labeled in the graph. For α2-antiplasmin and fibronectin only 225 amino acid residues from the N-terminus were used for plotting since the major reactive Qs are located in the said region.