Table 3.

FXI substrate cleavage sequences, separated by physiological process

PathwayFXIa substrateCleavage sequenceReference
Coagulation FIX KLTR145-AET
DFTR180-VVG 
75,76  
FVIII IQIR372-SVA
IEPR740-SFS
EITR1652-TTL
LRNR1740-AQS 
77  
FV KKYR348-SQH
GIQR510-AAD
SSWR1765-LTS 
25,77  
FX NNLTR234-IVG 25,29  
TFPI RIIK86-TTL
GICR107-GYI
GLCR199-ANE 
78  
Platelet activation ADAMTS13 Unknown 79  
KKS FXII SMTR372-VVG 80  
HK SLMK380-RPP
SPFR389-SSR 
81  
Inflammation CFH ENMR341-RPY 82  
β2GPI AFWK336-TDA 83  
Properdin Unknown 84  
Chem163S AFSK158-ALP 85  
HGF DLHR424-HIF
KQLR494-VVN 
86  
PathwayFXIa substrateCleavage sequenceReference
Coagulation FIX KLTR145-AET
DFTR180-VVG 
75,76  
FVIII IQIR372-SVA
IEPR740-SFS
EITR1652-TTL
LRNR1740-AQS 
77  
FV KKYR348-SQH
GIQR510-AAD
SSWR1765-LTS 
25,77  
FX NNLTR234-IVG 25,29  
TFPI RIIK86-TTL
GICR107-GYI
GLCR199-ANE 
78  
Platelet activation ADAMTS13 Unknown 79  
KKS FXII SMTR372-VVG 80  
HK SLMK380-RPP
SPFR389-SSR 
81  
Inflammation CFH ENMR341-RPY 82  
β2GPI AFWK336-TDA 83  
Properdin Unknown 84  
Chem163S AFSK158-ALP 85  
HGF DLHR424-HIF
KQLR494-VVN 
86  

FXIa has a preference for cleaving substrates at peptide bonds between arginine or lysine and alanine, valine, or serine residues. To a lesser extent, FXIa can also cleave between arginine or lysine and threonine or arginine residues.

CFH, complement factor H; Chem163S, prochemerin; HGF, heptaocyte growth factor; KKS, kallikrein-kinin system; TFPI, tissue factor pathway inhibitor.

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