BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
Member of WWPDB

BMRB Entry 19311

Title: Chemical shifts and structural restraints for Saccharomyces cerevisiae Est3 protein   PubMed: 24344315

Deposition date: 2013-06-21 Original release date: 2013-12-16

Authors: Rao, Timsi; Armstrong, Geoffrey; Wuttke, Deborah

Citation: Rao, Timsi; Lubin, Johnathan; Armstrong, Geoffrey; Tucey, Timothy; Lundblad, Victoria; Wuttke, Deborah. "Structure of Est3 reveals a bimodal surface with differential roles in telomere replication."  Proc. Natl. Acad. Sci. U.S.A. 111, 214-218 (2014).

Assembly members:
entity, polymer, 170 residues, 19297.996 Da.

Natural source:   Common Name: baker   Taxonomy ID: 4932   Superkingdom: not available   Kingdom: not available   Genus/species: Eukaryota Fungi

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

Entity Sequences (FASTA):
entity: STDSVFLQPWIKALIEDNSE HDQYHPSGHVIPSLTKQDLA LPHMSPTILTNPCHFAKITK FYNVCDYKVYASIRDSSHQI LVEFSQECVSNFERTHNCRI TSETTNCLMIIGDADLVYVT NSRAMSHFKISLSNISSKEI VPVLNVNQATIFDIDQVGSL STFPFVYKYL

Data sets:
Data typeCount
13C chemical shifts568
15N chemical shifts151
1H chemical shifts352

Additional metadata:

  • Assembly
  • Samples and Experiments
  • Software
  • Spectrometers
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Related Database Links:

PDB 2M9V
DBJ GAA24105
GB AHY75987 AJR36748 AJR36943 AJR37282 AJR37668
REF NP_012256
SP Q03096
TPG DAA08536

Download simulated HSQC data in one of the following formats:
CSV: Backbone or all simulated shifts
SPARKY: Backbone or all simulated shifts