INF2 Is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization. (Q34544252)

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26 December 2019

title

INF2 Is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization (English)

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26 December 2019

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2

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26 December 2019

author name string

Ekta Seth Chhabra

series ordinal

1

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26 December 2019

language of work or name

English

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publication date

3 July 2006

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Journal of Biological Chemistry

26 December 2019

published in

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26 December 2019

volume

281

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26 December 2019

page(s)

26754-26767

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26 December 2019

issue

36

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Stress fibers are generated by two distinct actin assembly mechanisms in motile cells

26 December 2019

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Identification of a carboxyl-terminal diaphanous-related formin homology protein autoregulatory domain

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The mouse Formin mDia1 is a potent actin nucleation factor regulated by autoinhibition

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The basic region of the diaphanous-autoregulatory domain (DAD) is required for autoregulatory interactions with the diaphanous-related formin inhibitory domain

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The mouse formin, FRLalpha, slows actin filament barbed end elongation, competes with capping protein, accelerates polymerization from monomers, and severs filaments

21 January 2018

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The fission yeast cytokinesis formin Cdc12p is a barbed end actin filament capping protein gated by profilin

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Formin is a processive motor that requires profilin to accelerate actin assembly and associated ATP hydrolysis

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Formin Leaky Cap Allows Elongation in the Presence of Tight Capping Proteins

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Profilin-mediated competition between capping protein and formin Cdc12p during cytokinesis in fission yeast

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Binding of phosphate ions to actin.

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21 January 2018

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21 January 2018

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21 January 2018

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Molecular details of formin-mediated actin assembly

21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.M604666200

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:16818491%20AND%20SRC:MED&resulttype=core&format=json

26 December 2019

1 reference