TAP (NXF1) belongs to a multigene family of putative RNA export factors with a conserved modular architecture (Q24290505)

GOA release 2020-03-11

author

Maria do Carmo Fonseca

object named as

M Carmo-Fonseca

6

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Elisa Izaurralde

object named as

E Izaurralde

8

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author name string

A Herold

1

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M Suyama

2

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J P Rodrigues

3

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I C Braun

4

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U Kutay

5

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P Bork

Molecular and Cellular Biology

7

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language of work or name

English

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publication date

December 2000

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published in

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volume

20

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issue

23

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page(s)

8996-9008

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cites work

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RAE1 is a shuttling mRNA export factor that binds to a GLEBS-like NUP98 motif at the nuclear pore complex through multiple domains

19 March 2017

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TAP binds to the constitutive transport element (CTE) through a novel RNA-binding motif that is sufficient to promote CTE-dependent RNA export from the nucleus

19 March 2017

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mRNA binding protein mrnp 41 localizes to both nucleus and cytoplasm

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The structure of the mRNA export factor TAP reveals a cis arrangement of a non-canonical RNP domain and an LRR domain

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Binding of the Mex67p/Mtr2p heterodimer to FXFG, GLFG, and FG repeat nucleoporins is essential for nuclear mRNA export.

19 March 2017

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Nuclear mRNA export requires complex formation between Mex67p and Mtr2p at the nuclear pores.

19 March 2017

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GLE2, a Saccharomyces cerevisiae homologue of the Schizosaccharomyces pombe export factor RAE1, is required for nuclear pore complex structure and function

19 March 2017

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The human RAE1 gene is a functional homologue of Schizosaccharomyces pombe rae1 gene involved in nuclear export of Poly(A)+ RNA

19 March 2017

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TAP, the human homolog of Mex67p, mediates CTE-dependent RNA export from the nucleus

19 March 2017

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REF, an evolutionary conserved family of hnRNP-like proteins, interacts with TAP/Mex67p and participates in mRNA nuclear export.

19 March 2017

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The human Tap protein is a nuclear mRNA export factor that contains novel RNA-binding and nucleocytoplasmic transport sequences

19 March 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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27 September 2017

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PubMed

https://pubmed.ncbi.nlm.nih.gov/11073998

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

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PubMed

https://pubmed.ncbi.nlm.nih.gov/11073998