O-linked-N-acetylglucosamine on extracellular protein domains mediates epithelial cell-matrix interactions. (Q44729096)

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18 January 2020

title

O-linked-N-acetylglucosamine on extracellular protein domains mediates epithelial cell-matrix interactions (English)

1 reference

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protein O-GlcNAcylation via threonine

18 January 2020

main subject

extracellular matrix

0 references

1 reference

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0097370

protein O-GlcNAc transferase activity

1 reference

Gene Ontology release 2020-05-02

Gene Ontology ID

GO:0097363

EGF-domain O-GlcNAc transferase Dmel_CG9867

1 reference

GOA release 2020-03-11

author

Tetsuya Okajima

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22158438%20AND%20SRC:MED&resulttype=core&format=json

18 January 2020

Emiko Suzuki

5

1 reference

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18 January 2020

author name string

Yuta Sakaidani

1

1 reference

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18 January 2020

Tomoko Nomura

2

1 reference

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18 January 2020

Aiko Matsuura

3

1 reference

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18 January 2020

Makiko Ito

4

1 reference

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18 January 2020

Kosuke Murakami

6

1 reference

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18 January 2020

Daita Nadano

7

1 reference

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18 January 2020

Tsukasa Matsuda

8

1 reference

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18 January 2020

Koichi Furukawa

9

1 reference

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18 January 2020

language of work or name

English

0 references

publication date

13 December 2011

1 reference

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18 January 2020

published in

Nature Communications

1 reference

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18 January 2020

volume

2

1 reference

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18 January 2020

page(s)

583

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O-linked beta-N-acetylglucosamine (O-GlcNAc): Extensive crosstalk with phosphorylation to regulate signaling and transcription in response to nutrients and stress

18 January 2020

cites work

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O-linked N-acetylglucosamine is present on the extracellular domain of notch receptors

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Rumi is a CAP10 domain glycosyltransferase that modifies Notch and is required for Notch signaling.

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O-GlcNAc modification of the extracellular domain of Notch receptors

21 January 2018

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Molecular requirements for actin-based lamella formation in Drosophila S2 cells

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