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 34506

Title: Solution NMR Structure of APP TMD   PubMed: 33232115

Deposition date: 2020-03-29 Original release date: 2020-12-04

Authors: Silber, M.; Muhle-Goll, C.

Citation: Silber, M.; Hitzenberger, M.; Zacharias, M.; Muhle-Goll, C.. "Altered Hinge Conformations in APP Transmembrane Helix Mutants May Affect Enzyme-Substrate Interactions of gamma-secretase"  ACS Chem. Neurosci. 11, 4426-4433 (2020).

Assembly members:
entity_1, polymer, 30 residues, 3070.925 Da.

Natural source:   Common Name: Human   Taxonomy ID: 9606   Superkingdom: Eukaryota   Kingdom: Metazoa   Genus/species: Homo sapiens

Experimental source:   Production method: chemical synthesis

Entity Sequences (FASTA):
entity_1: SNKGAIIGLMVGGVVIATVI VITLVMLKKK

Data sets:
Data typeCount
13C chemical shifts110
1H chemical shifts249

Additional metadata:

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

Entity Assembly IDEntity NameEntity ID
1unit_11

Entities:

Entity 1, unit_1 30 residues - 3070.925 Da.

1   SERASNLYSGLYALAILEILEGLYLEUMET
2   VALGLYGLYVALVALILEALATHRVALILE
3   VALILETHRLEUVALMETLEULYSLYSLYS

Samples:

sample_1: APP WT 500 uM

sample_conditions_1: ionic strength: 0 mM; pH: 7.0; pressure: 1 atm; temperature: 298 K

Experiments:

NameSampleSample stateSample conditions
1H-1H-NOESYsample_1isotropicsample_conditions_1

Software:

CNS v1.21, Brunger A. T. et.al. - refinement

ARIA v2.3.2, Linge, O'Donoghue and Nilges - structure calculation

CcpNmr Analysis v2.4.2, Vranken WF, Boucher W, Stevens TJ, Fogh RH, Pajon A, Llinas M, Ulrich EL, Markley JL, Ionides J, Laue ED. - chemical shift assignment, peak picking

NMR spectrometers:

  • Bruker CP TCI 600 MHz