BMRB Entry 30004

Title:
Solution Structure of TAZ2-p53TAD
Deposition date:
2016-01-20
Original release date:
2016-03-14
Authors:
Krois, A.; Ferreon, J.; Martinez-Yamout, M.; Dyson, H.; Wright, P.
Citation:

Citation: Krois, A.; Ferreon, J.; Martinez-Yamout, M.; Dyson, H.; Wright, P.. "Recognition of the disordered p53 transactivation domain by the transcriptional adapter zinc finger domains of CREB-binding protein"  Proc. Natl. Acad. Sci. U. S. A. 113, E1853-E1862 (2016).
PubMed: 26976603

Assembly members:

Assembly members:
CREB-binding protein,Cellular tumor antigen p53 fusion protein, polymer, 158 residues, 17711.236 Da.
ZINC ION, non-polymer, 65.409 Da.

Natural source:

Natural source:   Common Name: Mouse   Taxonomy ID: 10090   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Mus musculus

Experimental source:

Experimental source:   Production method: recombinant technology   Host organism: Escherichia coli

Entity Sequences (FASTA):

Data sets:
Data typeCount
13C chemical shifts509
15N chemical shifts153
1H chemical shifts1073

Additional metadata:

  • Assembly
  • Samples and Experiments
  • Software
  • Spectrometers
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Assembly:

Entity Assembly IDEntity NameEntity ID
1entity_11
2entity ZN, 12
3entity ZN, 22
4entity ZN, 32

Entities:

Entity 1, entity_1 158 residues - 17711.236 Da.

1   SERPROGLNGLUSERARGARGLEUSERILE
2   GLNARGCYSILEGLNSERLEUVALHISALA
3   CYSGLNCYSARGASNALAASNCYSSERLEU
4   PROSERCYSGLNLYSMETLYSARGVALVAL
5   GLNHISTHRLYSGLYCYSLYSARGLYSTHR
6   ASNGLYGLYCYSPROVALCYSLYSGLNLEU
7   ILEALALEUCYSCYSTYRHISALALYSHIS
8   CYSGLNGLUASNLYSCYSPROVALPROPHE
9   CYSLEUASNILELYSHISLYSLEUARGGLN
10   GLNGLNGLYSERGLYSERGLYSERGLUGLU
11   PROGLNSERASPPROSERVALGLUPROPRO
12   LEUSERGLNGLUTHRPHESERASPLEUTRP
13   LYSLEULEUPROGLUASNASNVALLEUSER
14   PROLEUPROSERGLNALAMETASPASPLEU
15   METLEUSERPROASPASPILEGLUGLNTRP
16   PHETHRGLUASPPROGLYPROASP

Entity 2, entity ZN, 1 - Zn - 65.409 Da.

1   ZN

Download HSQC peak lists in one of the following formats:
CSV: Backbone or all simulated peaks
SPARKY: Backbone or all simulated peaks