001     139998
005     20210129212737.0
024 7 _ |a 10.1074/jbc.M113.532333
|2 doi
024 7 _ |a 1083-351X
|2 ISSN
024 7 _ |a 0021-9258
|2 ISSN
024 7 _ |a WOS:000329370900007
|2 WOS
037 _ _ |a FZJ-2013-05965
041 _ _ |a English
082 _ _ |a 570
100 1 _ |a Thakur, H. C.
|0 P:(DE-HGF)0
|b 0
245 _ _ |a The centrosomal adaptor TACC3 and the microtubule polymerase chTOG interact via defined C-terminal subdomains in an Aurora-A kinase independent manner
260 _ _ |a Bethesda, Md.
|c 2013
|b Soc.
336 7 _ |a Journal Article
|b journal
|m journal
|0 PUB:(DE-HGF)16
|s 1385650879_8527
|2 PUB:(DE-HGF)
336 7 _ |a Output Types/Journal article
|2 DataCite
336 7 _ |a Journal Article
|0 0
|2 EndNote
336 7 _ |a ARTICLE
|2 BibTeX
336 7 _ |a JOURNAL_ARTICLE
|2 ORCID
336 7 _ |a article
|2 DRIVER
500 _ _ |3 POF3_Assignment on 2016-02-29
520 _ _ |a The cancer-associated, centrosomal adaptor protein TACC3 (Transforming Acidic Coiled-Coil 3) and its direct effector, the microtubule polymerase chTOG (colonic and hepatic tumor overexpressed gene), play a crucial function in centrosome-driven mitotic spindle assembly. It is unclear how TACC3 interacts with chTOG. Here, we show that the C-terminal TACC domain of TACC3 and a C-terminal fragment adjacent to the TOG domains of chTOG mediate the interaction between these two proteins. Interestingly, the TACC domain consists of two functionally distinct subdomains, CC1 (aa 414-530) and CC2 (aa 530-630). Whereas CC1 is responsible for the interaction with chTOG, CC2 performs an intradomain interaction with the central repeat region of TACC3, thereby masking the TACC domain prior to effector binding. Contrary to previous findings, our data clearly demonstrate that Aurora-A kinase does not regulate TACC3-chTOG complex formation, indicating that Aurora-A solely functions as a recruitment factor for the TACC3-chTOG complex to centrosomes and proximal mitotic spindles. We identified with CC1 and CC2 two functionally diverse modules within the TACC domain of TACC3 which mediate and modulate, respectively, TACC3 interaction with chTOG required for spindle assembly and microtubule dynamics during mitotic cell division.
536 _ _ |a 452 - Structural Biology (POF2-452)
|0 G:(DE-HGF)POF2-452
|c POF2-452
|x 0
|f POF II
588 _ _ |a Dataset connected to CrossRef, juser.fz-juelich.de
700 1 _ |a Singh, M.
|0 P:(DE-HGF)0
|b 1
700 1 _ |a Nagel-Steger, L.
|0 P:(DE-HGF)0
|b 2
700 1 _ |a Kremer, J.
|0 P:(DE-HGF)0
|b 3
700 1 _ |a Prumbaum, D.
|0 P:(DE-HGF)0
|b 4
700 1 _ |a Kalawy Fansa, E.
|0 P:(DE-HGF)0
|b 5
700 1 _ |a Ezzahoini, H.
|0 P:(DE-HGF)0
|b 6
700 1 _ |a Nouri, K.
|0 P:(DE-HGF)0
|b 7
700 1 _ |a Gremer, L.
|0 P:(DE-Juel1)145165
|b 8
|u fzj
700 1 _ |a Abts, A.
|0 P:(DE-HGF)0
|b 9
700 1 _ |a Schmitt, L.
|0 P:(DE-HGF)0
|b 10
700 1 _ |a Raunser, S.
|0 P:(DE-HGF)0
|b 11
700 1 _ |a Ahmadian, M. R.
|0 P:(DE-HGF)0
|b 12
700 1 _ |a Piekorz, R. P.
|0 P:(DE-HGF)0
|b 13
|e Corresponding author
773 _ _ |a 10.1074/jbc.M113.532333
|g p. M113.532333
|p -
|0 PERI:(DE-600)1474604-9
|t The @journal of biological chemistry
|v -
|x 1083-351X
856 4 _ |u http://www.jbc.org/content/early/2013/11/22/jbc.M113.532333.abstract
856 4 _ |u https://juser.fz-juelich.de/record/139998/files/FZJ-2013-05965.pdf
|y Restricted
909 C O |o oai:juser.fz-juelich.de:139998
|p VDB
910 1 _ |a Forschungszentrum Jülich GmbH
|0 I:(DE-588b)5008462-8
|k FZJ
|b 8
|6 P:(DE-Juel1)145165
913 2 _ |a DE-HGF
|b Key Technologies
|l BioSoft – Fundamentals for future Technologies in the fields of Soft Matter and Life Sciences
|1 G:(DE-HGF)POF3-550
|0 G:(DE-HGF)POF3-559H
|2 G:(DE-HGF)POF3-500
|v Addenda
|x 0
913 1 _ |a DE-HGF
|b Schlüsseltechnologien
|1 G:(DE-HGF)POF2-450
|0 G:(DE-HGF)POF2-452
|2 G:(DE-HGF)POF2-400
|v Structural Biology
|x 0
|4 G:(DE-HGF)POF
|3 G:(DE-HGF)POF2
|l BioSoft
914 1 _ |y 2013
915 _ _ |a JCR/ISI refereed
|0 StatID:(DE-HGF)0010
|2 StatID
915 _ _ |a JCR
|0 StatID:(DE-HGF)0100
|2 StatID
915 _ _ |a WoS
|0 StatID:(DE-HGF)0110
|2 StatID
|b Science Citation Index
915 _ _ |a WoS
|0 StatID:(DE-HGF)0111
|2 StatID
|b Science Citation Index Expanded
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0150
|2 StatID
|b Web of Science Core Collection
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0199
|2 StatID
|b Thomson Reuters Master Journal List
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0200
|2 StatID
|b SCOPUS
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0300
|2 StatID
|b Medline
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)0310
|2 StatID
|b NCBI Molecular Biology Database
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1030
|2 StatID
|b Current Contents - Life Sciences
915 _ _ |a DBCoverage
|0 StatID:(DE-HGF)1050
|2 StatID
|b BIOSIS Previews
920 _ _ |l yes
920 1 _ |0 I:(DE-Juel1)ICS-6-20110106
|k ICS-6
|l Strukturbiochemie
|x 0
980 _ _ |a journal
980 _ _ |a VDB
980 _ _ |a UNRESTRICTED
980 _ _ |a I:(DE-Juel1)ICS-6-20110106
981 _ _ |a I:(DE-Juel1)IBI-7-20200312


LibraryCollectionCLSMajorCLSMinorLanguageAuthor
Marc 21