BMRB Entry 16907
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full
BMRB Entry DOI: doi:10.13018/BMR16907
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Title: The hemagglutinin fusion peptide (H1 subtype) at pH 7.4 PubMed: 20534508
Deposition date: 2010-04-29 Original release date: 2010-07-28
Authors: Lorieau, Justin; Louis, John; Bax, Ad
Citation: Lorieau, Justin; Louis, John; Bax, Ad. "The complete influenza hemagglutinin fusion domain adopts a tight helical hairpin arrangement at the lipid:water interface." Proc. Natl. Acad. Sci. U.S.A. 107, 11341-11346 (2010).
Assembly members:
HAfp, polymer, 30 residues, Formula weight is not available
Natural source: Common Name: Influenza virus type A Taxonomy ID: 11320 Superkingdom: Viruses Kingdom: not available Genus/species: Influenzavirus A Influenza virus type A
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
HAfp: GLFGAIAGFIEGGWTGMIDG
WYGSGKKKKD
- assigned_chemical_shifts
- heteronucl_NOEs
- heteronucl_T1_relaxation
- heteronucl_T2_relaxation
- H_exch_rates
Data type | Count |
13C chemical shifts | 76 |
15N chemical shifts | 23 |
1H chemical shifts | 147 |
heteronuclear NOE values | 43 |
H exchange rates | 22 |
T1 relaxation values | 43 |
T2 relaxation values | 43 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | HAfp | 1 |
Entities:
Entity 1, HAfp 30 residues - Formula weight is not available
1 | GLY | LEU | PHE | GLY | ALA | ILE | ALA | GLY | PHE | ILE | |
2 | GLU | GLY | GLY | TRP | THR | GLY | MET | ILE | ASP | GLY | |
3 | TRP | TYR | GLY | SER | GLY | LYS | LYS | LYS | LYS | ASP |
Samples:
HAfp_H2O_1: HAfp, [U-13C; U-15N; U-2H], 0.6 0.8 mM; D2O, [U-2H], 7%; TRIS, [U-99% 2H], 25 mM; DPC, [U-99% 2H], 130 180 mM
HAfp_D2O_1: HAfp, [U-13C; U-15N], 0.6 0.8 mM; TRIS, [U-99% 2H], 25 mM; DPC, [U-99% 2H], 130 180 mM
HAfp_H2O_2: HAfp, [U-13C; U-15N], 0.6 0.8 mM; D2O, [U-2H], 7%; TRIS, [U-99% 2H], 25 mM; DPC, [U-99% 2H], 130 180 mM
HAfp_H2O_3: HAfp, [U-15N], 0.6 0.8 mM; D2O, [U-2H], 7%; TRIS, [U-99% 2H], 25 mM; DPC, [U-99% 2H], 130 180 mM
HAfp_D2O_2: HAfp, [U-15N], 0.6 0.8 mM; TRIS, [U-99% 2H], 25 mM; DPC, [U-99% 2H], 130 180 mM
pH_7.4: ionic strength: 0 M; pH: 7.4; pressure: 1 atm; temperature: 305 K
pH_4.0: ionic strength: 0 M; pH: 4.0; pressure: 1 atm; temperature: 305 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | HAfp_H2O_1 | isotropic | pH_7.4 |
2D 1H-13C HSQC | HAfp_D2O_1 | isotropic | pH_7.4 |
2D 1H-1H NOESY | HAfp_D2O_1 | isotropic | pH_7.4 |
3D HNCO | HAfp_H2O_1 | isotropic | pH_7.4 |
3D HNCA | HAfp_H2O_1 | isotropic | pH_7.4 |
3D HN(CO)CA | HAfp_H2O_1 | isotropic | pH_7.4 |
3D 1H-15N NOESY | HAfp_H2O_1 | isotropic | pH_7.4 |
2D 1H-15N HSQC | HAfp_H2O_1 | isotropic | pH_4.0 |
2D 1H-13C HSQC | HAfp_H2O_1 | isotropic | pH_4.0 |
3D HN(CO)CA | HAfp_H2O_1 | isotropic | pH_4.0 |
Software:
SPARKY v3.113, Goddard - chemical shift assignment, data analysis, peak picking
NMRPipe v5.0, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - data analysis, peak picking, processing
NMRDraw v5.0, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - data analysis, peak picking
ModelFree v4.2, Palmer - data analysis
PSVS v1.4, Bhattacharya and Montelione - data analysis
TALOS v1.2009.0721.18, Cornilescu, Delaglio and Bax - data analysis
X-PLOR NIH v2.24, Schwieters, Kuszewski, Tjandra and Clore - refinement, structure solution
NMR spectrometers:
- Bruker Avance 900 MHz
- Bruker Avance 750 MHz
- Bruker Avance 600 MHz
- Bruker Avance 500 MHz
Related Database Links:
BMRB | 26507 |
PDB | |
DBJ | BAA00718 BAA00722 BAA01280 BAA02765 BAA02766 |
EMBL | CAA24272 CAA35094 CAA42444 CAA82950 CAA86560 |
GB | AAA16879 AAA16880 AAA19934 AAA43171 AAA43172 |
PIR | HMIV HMIV17 HMIV5 HMIVN1 HMIVSA |
PRF | 0707273A |
REF | NP_040980 YP_163736 |
SP | A3DRP0 A4GBX7 A4GCH5 A4GCI6 A4GCJ7 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts