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Membrane Binding by Prothrombin Mediates Its Constrained Presentation to Prothrombinase for Cleavage

The Journal of biological chemistry, 2013-09, Vol.288 (39), p.27789-27800

2013

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Occlusion of anion-binding exosite 2 in meizothrombin explains its impaired ability to activate factor V

The Journal of biological chemistry, 2019-02, Vol.294 (7), p.2422-2435

2019

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The Fragment 1 Region of Prothrombin Facilitates the Favored Binding of Fragment 12 to Zymogen and Enforces Zymogen-like Character in the Proteinase

The Journal of biological chemistry, 2016-05, Vol.291 (21), p.11114-11123

2016

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Meizothrombin Is an Unexpectedly Zymogen-like Variant of Thrombin

The Journal of biological chemistry, 2012-08, Vol.287 (36), p.30414-30425

2012

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Domain 5 of cleaved high molecular weight kininogen inhibits endothelial cell migration through Akt

Thrombosis and haemostasis, 2005-09, Vol.94 (3), p.606-614

2005

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Regulated Cleavage of Prothrombin by Prothrombinase: REPOSITIONING A CLEAVAGE SITE REVEALS THE UNIQUE KINETIC BEHAVIOR OF THE ACTION OF PROTHROMBINASE ON ITS COMPOUND SUBSTRATE

The Journal of biological chemistry, 2010-01, Vol.285 (1), p.328-338

2010

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High-molecular-weight kininogen fragments stimulate the secretion of cytokines and chemokines through uPAR, Mac-1, and gC1qR in monocytes

Arteriosclerosis, thrombosis, and vascular biology, 2006-10, Vol.26 (10), p.2260-2266

2006

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Regulated Cleavage of Prothrombin by Prothrombinase

The Journal of biological chemistry, 2010-01, Vol.285 (1), p.328-338

2010

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A Single Cleavage Reaction in the Proteolytic Activation of Factor V to the Cofactor Is Rate-Limiting in a Step That Is Selectively Dependent on Anion Binding Exosite 2 of Thrombin

Blood, 2017-12, Vol.130, p.3649-3649

2017

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Human Factor XII Binding to the Glycoprotein Ib-IX-V Complex Inhibits Thrombin-induced Platelet Aggregation

The Journal of biological chemistry, 2000-07, Vol.275 (30), p.22756-22763

2000

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JNJ-64179375 Inhibits Exosite I-Mediated Thrombin Activity While Preserving Exosite II and Active Site Function in Vitro

Blood, 2018-11, Vol.132 (Supplement 1), p.24-24

2018

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Antithrombotic activity of kininogen is mediated by inhibitory effects of domain 3 during arterial injury in vivo

American journal of physiology. Heart and circulatory physiology, 2007-06, Vol.292 (6), p.H2959-H2965

2007

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Inhibition of tumor angiogenesis in vivo by a monoclonal antibody targeted to domain 5 of high molecular weight kininogen

Blood, 2004-10, Vol.104 (7), p.2065-2072

2004

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Human Kininogens Regulate Thrombin Binding to Platelets Through the Glycoprotein Ib-IX-V Complex

Blood, 1997-08, Vol.90 (4), p.1508-1515

1997

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Potent Affinity Labeling Peptide Inhibitors of Calpain

Chemistry letters, 1990-02, Vol.19 (2), p.191-194

1990

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Effects of Substrate Geometry on Active Site Engagement Govern the Preferential Action of Prothrombinase on One of the Two Cleavage Sites in Prothrombin

Blood, 2008-11, Vol.112 (11), p.2022-2022

2008

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Human Platelets and Endothelial Cells Differentially Regulate the Pathway for Prothrombin Cleavage by Prothrombinase

Blood, 2007-11, Vol.110 (11), p.269-269

2007

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Antithrombotic activity of kininogen is mediated by inhibitory effects of domain 3 during arterial injury in vivo

American journal of physiology. Heart and circulatory physiology, 2007, Vol.61 (6)

2007

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High Molecular Weight Kininogen Fragments Stimulate the Secretion of Interleukin 1β through the Urokinase-Type Plasminogen Activator Receptor (uPAR) and CD11b/CD18 (Mac-1) in Human Blood Mononuclear Cells

Blood, 2004-11, Vol.104 (11), p.3800-3800

2004

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Human kininogens regulate thrombin binding to platelets through the glycoprotein Ib-IX-V complex

Blood, 1997-08, Vol.90 (4), p.1508-1515

1997

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Contiguous binding and inhibitory sites on kininogens required for the inhibition of platelet calpain

The Journal of biological chemistry, 1993-12, Vol.268 (35), p.26546-26551

1993

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Membrane Expression of Platelet Calpain

Blood, 1990-03, Vol.75 (6), p.1273-1281

1990

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Inhibition of the conversion of pre-interleukins-1α and 1β to mature cytokines by p-benzoquinone, a metabolite of benzene

Chemico-biological interactions, 1995-12, Vol.98 (3), p.211-222

1995

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Thrombin-induced Platelet Aggregation Is Inhibited by the Heptapeptide LeuAla of Domain 3 in the Heavy Chain of High Molecular Weight Kininogen

The Journal of biological chemistry, 1996-05, Vol.271 (19), p.11228

1996

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Thrombin-induced Platelet Aggregation Is Inhibited by the Heptapeptide Leu271-Ala277 of Domain 3 in the Heavy Chain of High Molecular Weight Kininogen (∗)

The Journal of biological chemistry, 1996-05, Vol.271 (19), p.11228-11235

1996

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Membrane Binding by Prothrombin Mediates Its Constrained Presentation to Prothrombinase for Cleavage

Occlusion of anion-binding exosite 2 in meizothrombin explains its impaired ability to activate factor V

The Fragment 1 Region of Prothrombin Facilitates the Favored Binding of Fragment 12 to Zymogen and Enforces Zymogen-like Character in the Proteinase

Meizothrombin Is an Unexpectedly Zymogen-like Variant of Thrombin

Domain 5 of cleaved high molecular weight kininogen inhibits endothelial cell migration through Akt

Regulated Cleavage of Prothrombin by Prothrombinase: REPOSITIONING A CLEAVAGE SITE REVEALS THE UNIQUE KINETIC BEHAVIOR OF THE ACTION OF PROTHROMBINASE ON ITS COMPOUND SUBSTRATE

High-molecular-weight kininogen fragments stimulate the secretion of cytokines and chemokines through uPAR, Mac-1, and gC1qR in monocytes

Regulated Cleavage of Prothrombin by Prothrombinase

A Single Cleavage Reaction in the Proteolytic Activation of Factor V to the Cofactor Is Rate-Limiting in a Step That Is Selectively Dependent on Anion Binding Exosite 2 of Thrombin

Human Factor XII Binding to the Glycoprotein Ib-IX-V Complex Inhibits Thrombin-induced Platelet Aggregation

JNJ-64179375 Inhibits Exosite I-Mediated Thrombin Activity While Preserving Exosite II and Active Site Function in Vitro

Antithrombotic activity of kininogen is mediated by inhibitory effects of domain 3 during arterial injury in vivo

Inhibition of tumor angiogenesis in vivo by a monoclonal antibody targeted to domain 5 of high molecular weight kininogen

Human Kininogens Regulate Thrombin Binding to Platelets Through the Glycoprotein Ib-IX-V Complex

Potent Affinity Labeling Peptide Inhibitors of Calpain

Effects of Substrate Geometry on Active Site Engagement Govern the Preferential Action of Prothrombinase on One of the Two Cleavage Sites in Prothrombin

Human Platelets and Endothelial Cells Differentially Regulate the Pathway for Prothrombin Cleavage by Prothrombinase

Antithrombotic activity of kininogen is mediated by inhibitory effects of domain 3 during arterial injury in vivo

High Molecular Weight Kininogen Fragments Stimulate the Secretion of Interleukin 1β through the Urokinase-Type Plasminogen Activator Receptor (uPAR) and CD11b/CD18 (Mac-1) in Human Blood Mononuclear Cells

Human kininogens regulate thrombin binding to platelets through the glycoprotein Ib-IX-V complex

Contiguous binding and inhibitory sites on kininogens required for the inhibition of platelet calpain

Membrane Expression of Platelet Calpain

Inhibition of the conversion of pre-interleukins-1α and 1β to mature cytokines by p-benzoquinone, a metabolite of benzene

Thrombin-induced Platelet Aggregation Is Inhibited by the Heptapeptide LeuAla of Domain 3 in the Heavy Chain of High Molecular Weight Kininogen

Thrombin-induced Platelet Aggregation Is Inhibited by the Heptapeptide Leu271-Ala277 of Domain 3 in the Heavy Chain of High Molecular Weight Kininogen (∗)

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