Adenylyl cyclase-associated protein-1/CAP1 as a biological target substrate of gelatinase B/MMP-9. (Q39955195)

15 September 2017

Adenylyl cyclase-associated protein-1/CAP1 as a biological target substrate of gelatinase B/MMP-9. (English)

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15 September 2017

Bénédicte Cauwe

1

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15 September 2017

Erik Martens

2

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15 September 2017

Philippe E Van den Steen

3

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15 September 2017

Paul Proost

4

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15 September 2017

Ilse Van Aelst

5

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15 September 2017

Daniel Blockmans

6

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15 September 2017

Ghislain Opdenakker

7

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15 September 2017

language of work or name

English

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publication date

16 July 2008

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Experimental Cell Research

15 September 2017

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15 September 2017

314

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2739-2749

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15

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How matrix metalloproteinases regulate cell behavior

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A novel rationale for inhibition of gelatinase B in multiple sclerosis: MMP-9 destroys alpha B-crystallin and generates a promiscuous T cell epitope.

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Gelatinase B/matrix metalloproteinase-9 provokes cataract by cleaving lens betaB1 crystallin.

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Purification and identification of 91-kDa neutrophil gelatinase. Release by the activating peptide interleukin-8.

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The hemopexin and O-glycosylated domains tune gelatinase B/MMP-9 bioavailability via inhibition and binding to cargo receptors.

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Analysis of Gelatinases in Complex Biological Fluids and Tissue Extracts

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Cyclase-associated proteins: CAPacity for linking signal transduction and actin polymerization

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A conserved proline-rich region of the Saccharomyces cerevisiae cyclase-associated protein binds SH3 domains and modulates cytoskeletal localization

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CAP2, cyclase-associated protein 2, is a dual compartment protein.

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Cyclase-associated protein 1 (CAP1) promotes cofilin-induced actin dynamics in mammalian nonmuscle cells.

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Angiopathic consequences of saturating the plasma scavenger system for actin

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The Extracellular Actin-Scavenger System and Actin Toxicity

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Gc-globulin: roles in response to injury

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Matrix metalloproteinase-2 degrades the cytoskeletal protein α-actinin in peroxynitrite mediated myocardial injury

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A proteomic approach to identify substrates of matrix metalloproteinase-14 in human plasma.

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7 January 2021

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DOI

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15 September 2017

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