BMRB

Biological Magnetic Resonance Data Bank


A Repository for Data from NMR Spectroscopy on Proteins, Peptides, Nucleic Acids, and other Biomolecules
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BMRB Entry 16394

Title: NMR Evidence for differential phosphorylation-dependent interactions in WT and deltaF508 CFTR   PubMed: 19927121

Deposition date: 2009-07-03 Original release date: 2009-12-14

Authors: Kanelis, Voula; Hudson, Rhea; Thibodeau, Patrick; Thomas, Philip; Forman-Kay, Julie

Citation: Kanelis, Voula; Hudson, Rhea; Thibodeau, Patrick; Thomas, Philip; Forman-Kay, Julie. "NMR evidence for differential phosphorylation-dependent interactions in WT and DeltaF508 CFTR."  EMBO J. 29, 263-277 (2010).

Assembly members:
deltaF508 CFTR NBD1-RE, polymer, 284 residues, Formula weight is not available

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

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

Entity Sequences (FASTA):
deltaF508 CFTR NBD1-RE: TTGIIMENVTAFWEEGFGEL LEKVQQSNGDRKHSSDENNV SFSHLCLVGNPVLKNINLNI EKGEMLAITGSTGSGKTSLL MLILGELEASEGIIKHSGRV SFCSQFSWIMPGTIKENIIG VSYDEYRYKSVVKACQLQQD ITKFAEQDNTVLGEGGVTLS GGQRARISLARAVYKDADLY LLDSPFGYLDVFTEEQVFES CVCKLMANKTRILVTSKMEH LRKADKILILHQGSSYFYGT FSELQSLRPDFSSKLMGYDT FDQFTEERRSSILTETLRRF SVDD

Data sets:
Data typeCount
15N chemical shifts114
1H chemical shifts114

Additional metadata:

  • Assembly
  • Samples and Experiments
  • Software
  • Spectrometers
  • Hide all

Assembly:

Entity Assembly IDEntity NameEntity ID
1deltaF508 CFTR NBD1-RE1

Entities:

Entity 1, deltaF508 CFTR NBD1-RE 284 residues - Formula weight is not available

1   THRTHRGLYILEILEMETGLUASNVALTHR
2   ALAPHETRPGLUGLUGLYPHEGLYGLULEU
3   LEUGLULYSVALGLNGLNSERASNGLYASP
4   ARGLYSHISSERSERASPGLUASNASNVAL
5   SERPHESERHISLEUCYSLEUVALGLYASN
6   PROVALLEULYSASNILEASNLEUASNILE
7   GLULYSGLYGLUMETLEUALAILETHRGLY
8   SERTHRGLYSERGLYLYSTHRSERLEULEU
9   METLEUILELEUGLYGLULEUGLUALASER
10   GLUGLYILEILELYSHISSERGLYARGVAL
11   SERPHECYSSERGLNPHESERTRPILEMET
12   PROGLYTHRILELYSGLUASNILEILEGLY
13   VALSERTYRASPGLUTYRARGTYRLYSSER
14   VALVALLYSALACYSGLNLEUGLNGLNASP
15   ILETHRLYSPHEALAGLUGLNASPASNTHR
16   VALLEUGLYGLUGLYGLYVALTHRLEUSER
17   GLYGLYGLNARGALAARGILESERLEUALA
18   ARGALAVALTYRLYSASPALAASPLEUTYR
19   LEULEUASPSERPROPHEGLYTYRLEUASP
20   VALPHETHRGLUGLUGLNVALPHEGLUSER
21   CYSVALCYSLYSLEUMETALAASNLYSTHR
22   ARGILELEUVALTHRSERLYSMETGLUHIS
23   LEUARGLYSALAASPLYSILELEUILELEU
24   HISGLNGLYSERSERTYRPHETYRGLYTHR
25   PHESERGLULEUGLNSERLEUARGPROASP
26   PHESERSERLYSLEUMETGLYTYRASPTHR
27   PHEASPGLNPHETHRGLUGLUARGARGSER
28   SERILELEUTHRGLUTHRLEUARGARGPHE
29   SERVALASPASP

Samples:

sample_1: deltaF508 CFTR NBD1-RE, [U-100% 15N], 175 mM; sodium phosphate 20 mM; sodium chloride 150 mM; magnesium chloride 5 mM; ATP 5 mM; DTT 5 mM; H2O 90%; D2O 10%

sample_conditions_1: ionic strength: 170 mM; pH: 7; pressure: 1 atm; temperature: 293 K

Experiments:

NameSampleSample stateSample conditions
2D 1H-15N HSQCsample_1isotropicsample_conditions_1

Software:

NMRDraw, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing

NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing

NMRView, Johnson, One Moon Scientific - chemical shift assignment

NMR spectrometers:

  • Varian INOVA 600 MHz

Related Database Links:

BMRB 16367 16393
PDB

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