BMRB Entry 31071

Name: Backbone modifications in the inter-helix loop of designed miniprotein oPPalpha: Pro10DPro11 turn
Published: 2023-03-28

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PDB ID: 8g0x
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR31071
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Nicholas Rego and David Koes
3Dmol.js: molecular visualization with WebGL
Bioinformatics (2015) 31 (8): 1322-1324 doi:10.1093/bioinformatics/btu829

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Title:

Backbone modifications in the inter-helix loop of designed miniprotein oPPalpha: Pro10DPro11 turn

Deposition date:

2023-02-01

Original release date:

2023-03-28

Authors:

Harmon, T.; Horne, W.

Citation:

Citation: Harmon, T.; Horne, W.. "Protein Backbone Alteration in Non-Hairpin beta-Turns: Impacts on Tertiary Folded Structure and Folded Stability" Chembiochem 24, e202300113-e202300113 (2023).
PubMed: 36920327

Assembly members:

Assembly members:
entity_1, polymer, 36 residues, 3756.386 Da.

Natural source:

Natural source: Common Name: Streptococcus mutans Taxonomy ID: 1309 Superkingdom: Bacteria Kingdom: not available Genus/species: Streptococcus mutans

Experimental source:

Experimental source: Production method: chemical synthesis

Entity Sequences (FASTA):

Entity Sequences (FASTA):
entity_1: XPPKKPKKPGPXATPEKLAA YEKELAAYEKELAAYX

Data sets:

assigned_chemical_shifts
- assigned_chemical_shifts_1

Data type	Count
1H chemical shifts	251

Additional metadata:

Assembly
Samples and Experiments
Software
Spectrometers
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Assembly:

Entity Assembly ID	Entity Name	Entity ID
1	unit_1	1

Entities:

Entity 1, unit_1 36 residues - 3756.386 Da.

1

ACE

PRO

LYS

PRO

LYS

PRO

GLY

2

PRO

DPR

ALA

THR

PRO

GLU

LYS

LEU

ALA

3

TYR

GLU

LYS

GLU

LEU

ALA

TYR

GLU

LYS

4

GLU

LEU

ALA

TYR

NH2

Samples:

sample_1: Designed miniprotein oPPalpha: Pro10DPro11 turn 2.5 mM; DSS 0.2 mM; sodium phosphate 8.2 mM; potassium phosphate 1.8 mM; sodium chloride 137 mM; potassium chloride 2.7 mM

sample_conditions_1: ionic strength: 163 mM; pH: 7.4 pH*; pressure: 1 atm; temperature: 278 K

Experiments:

Name	Sample	Sample state	Sample conditions
2D 1H-1H TOCSY	sample_1	isotropic	sample_conditions_1
2D 1H-1H COSY	sample_1	isotropic	sample_conditions_1
2D 1H-1H NOESY	sample_1	isotropic	sample_conditions_1

Software:

TopSpin, Bruker Biospin - processing

NMRFAM-SPARKY, Lee, Tonelli, Markley - data analysis

ARIA, Linge, O'Donoghue and Nilges - refinement, structure calculation

NMR spectrometers:

Bruker AVANCE III 700 MHz