Structure of the TPR domain of p67phox in complex with Rac.GTP (Q27628646)

1

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S J Smith

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P A Walker

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S J Smerdon

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K Rittinger

Structure of Cdc42 in complex with the GTPase-binding domain of the 'Wiskott-Aldrich syndrome' protein

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language of work or name

English

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publication date

October 2000

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published in

Molecular Cell

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volume

6

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issue

4

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page(s)

899-907

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cites work

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Cryptic Rac-binding and p21(Cdc42Hs/Rac)-activated kinase phosphorylation sites of NADPH oxidase component p67(phox)

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A conserved binding motif defines numerous candidate target proteins for both Cdc42 and Rac GTPases

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Interaction of Rac with p67phox and regulation of phagocytic NADPH oxidase activity

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Rac GTPase interacts with GAPs and target proteins through multiple effector sites.

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Mechanisms of NADPH oxidase activation: translocation of p40phox, Rac1 and Rac2 from the cytosol to the membranes in human neutrophils lacking p47phox or p67phox

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Structure of the complex of Cdc42Hs with a peptide derived from P-21 activated kinase

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Requirement for posttranslational processing of Rac GTP-binding proteins for activation of human neutrophil NADPH oxidase

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The crystal structure of human rac1, a member of the rho-family complexed with a GTP analogue

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Structure of the Rho family GTP-binding protein Cdc42 in complex with the multifunctional regulator RhoGDI

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Tetratricopeptide repeat (TPR) motifs of p67(phox) participate in interaction with the small GTPase Rac and activation of the phagocyte NADPH oxidase

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Identifiers

DOI

0 references

10.1016/S1097-2765(05)00091-2

1 reference

Consolidated OpenCitations Corpus – April 2017

release_ezlcc3s7ybgmxli3vcenzu7koi

Fatcat ID

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release_uarj5dypjrg5pkpce7jicpdham

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1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

11090627

1 reference

Consolidated OpenCitations Corpus – April 2017