Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR17994
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Citation: Huang, Xi; Fanucci, Gail. "Backbone 1H, 13C, and 15N Chemical Shift Assignment for HIV-1 protease Variants" Biomol. NMR Assignments ., .-..
Assembly members:
HIV-1_PR_Homodimer_Bmut5, polymer, 99 residues, 21115.04 Da.
Natural source: Common Name: HIV-1 Taxonomy ID: 11676 Superkingdom: Viruses Kingdom: not available Genus/species: Lentivirus HIV-1
Experimental source: Production method: chemical synthesis Host organism: Escherichia coli
Entity Sequences (FASTA):
HIV-1_PR_Homodimer_Bmut5: PQITLWKRPLVTIKVGGQLK
EALLNTGADDTVIEDMNLPG
KWKPKMIGGIGGFIKVKQYD
QIIIEIAGHKAIGTVLVGPT
PVNIIGRNLLTQIGATLNF
Data type | Count |
13C chemical shifts | 177 |
15N chemical shifts | 88 |
1H chemical shifts | 88 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | HIV-1 Protease Bmut5, chain 1 | 1 |
2 | HIV-1 Protease Bmut5, chain 2 | 1 |
Entity 1, HIV-1 Protease Bmut5, chain 1 99 residues - 21115.04 Da.
1 | PRO | GLN | ILE | THR | LEU | TRP | LYS | ARG | PRO | LEU | ||||
2 | VAL | THR | ILE | LYS | VAL | GLY | GLY | GLN | LEU | LYS | ||||
3 | GLU | ALA | LEU | LEU | ASN | THR | GLY | ALA | ASP | ASP | ||||
4 | THR | VAL | ILE | GLU | ASP | MET | ASN | LEU | PRO | GLY | ||||
5 | LYS | TRP | LYS | PRO | LYS | MET | ILE | GLY | GLY | ILE | ||||
6 | GLY | GLY | PHE | ILE | LYS | VAL | LYS | GLN | TYR | ASP | ||||
7 | GLN | ILE | ILE | ILE | GLU | ILE | ALA | GLY | HIS | LYS | ||||
8 | ALA | ILE | GLY | THR | VAL | LEU | VAL | GLY | PRO | THR | ||||
9 | PRO | VAL | ASN | ILE | ILE | GLY | ARG | ASN | LEU | LEU | ||||
10 | THR | GLN | ILE | GLY | ALA | THR | LEU | ASN | PHE |
sample_1: HIV-1 PR Homodimer Bmut5, [U-100% 13C; U-100% 15N], 0.1 mM
sample_conditions_1: ionic strength: 2 mM; pH: 5.0; pressure: 1 atm; temperature: 293 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
3D HNCA | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
3D HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_1 | isotropic | sample_conditions_1 |
xwinnmr, Bruker Biospin - collection
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - data analysis
SPARKY, Goddard - peak picking, processing
Download HSQC peak lists in one of the following formats:
CSV: Backbone
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SPARKY: Backbone
or all simulated peaks