BMRB Entry 16902
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR16902
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Title: Backbone 1H, 15N, 13C and ile, leu, val sidechain CH3 Chemical Shift assignments for Aagglutinin-like ALS1 N-terminal domain PubMed: 20556550
Deposition date: 2010-04-27 Original release date: 2010-07-26
Authors: Yan, Robert; Cota, Ernesto
Citation: Yan, Robert; Simpson, Peter; Matthews, Stephen; Cota, Ernesto. "Backbone 1H, 15N, 13C and Ile, Leu, Val methyl chemical shift assignments for the 33.5 kDa N-terminal domain of Candida albicans ALS1." Biomol. NMR Assignments 4, 187-190 (2010).
Assembly members:
ALS1, polymer, 312 residues, 33556.0 Da.
Natural source: Common Name: Ascomycetes Taxonomy ID: 5476 Superkingdom: Eukaryota Kingdom: Fungi Genus/species: Candida albicans
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 941 |
15N chemical shifts | 291 |
1H chemical shifts | 547 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | ALS1 | 1 |
Entities:
Entity 1, ALS1 312 residues - 33556.0 Da.
Residues 18-329 of ALS1. This is the adhesion domain from full length protein
1 | LYS | THR | ILE | THR | GLY | VAL | PHE | ASP | SER | PHE | ||||
2 | ASN | SER | LEU | THR | TRP | SER | ASN | ALA | ALA | ASN | ||||
3 | TYR | ALA | PHE | LYS | GLY | PRO | GLY | TYR | PRO | THR | ||||
4 | TRP | ASN | ALA | VAL | LEU | GLY | TRP | SER | LEU | ASP | ||||
5 | GLY | THR | SER | ALA | ASN | PRO | GLY | ASP | THR | PHE | ||||
6 | THR | LEU | ASN | MET | PRO | CYS | VAL | PHE | LYS | TYR | ||||
7 | THR | THR | SER | GLN | THR | SER | VAL | ASP | LEU | THR | ||||
8 | ALA | ASP | GLY | VAL | LYS | TYR | ALA | THR | CYS | GLN | ||||
9 | PHE | TYR | SER | GLY | GLU | GLU | PHE | THR | THR | PHE | ||||
10 | SER | THR | LEU | THR | CYS | THR | VAL | ASN | ASP | ALA | ||||
11 | LEU | LYS | SER | SER | ILE | LYS | ALA | PHE | GLY | THR | ||||
12 | VAL | THR | LEU | PRO | ILE | ALA | PHE | ASN | VAL | GLY | ||||
13 | GLY | THR | GLY | SER | SER | THR | ASP | LEU | GLU | ASP | ||||
14 | SER | LYS | CYS | PHE | THR | ALA | GLY | THR | ASN | THR | ||||
15 | VAL | THR | PHE | ASN | ASP | GLY | ASP | LYS | ASP | ILE | ||||
16 | SER | ILE | ASP | VAL | GLU | PHE | GLU | LYS | SER | THR | ||||
17 | VAL | ASP | PRO | SER | GLY | TYR | LEU | TYR | ALA | SER | ||||
18 | ARG | VAL | MET | PRO | SER | LEU | ASN | LYS | VAL | THR | ||||
19 | THR | LEU | PHE | VAL | ALA | PRO | GLN | CYS | GLU | ASN | ||||
20 | GLY | TYR | THR | SER | GLY | THR | MET | GLY | PHE | SER | ||||
21 | SER | SER | ASN | GLY | ASP | VAL | ALA | ILE | ASP | CYS | ||||
22 | SER | ASN | ILE | HIS | ILE | GLY | ILE | THR | LYS | GLY | ||||
23 | LEU | ASN | ASP | TRP | ASN | TYR | PRO | VAL | SER | SER | ||||
24 | GLU | SER | PHE | SER | TYR | THR | LYS | THR | CYS | THR | ||||
25 | SER | ASN | GLY | ILE | GLN | ILE | LYS | TYR | GLN | ASN | ||||
26 | VAL | PRO | ALA | GLY | TYR | ARG | PRO | PHE | ILE | ASP | ||||
27 | ALA | TYR | ILE | SER | ALA | THR | ASP | VAL | ASN | GLN | ||||
28 | TYR | THR | LEU | ALA | TYR | THR | ASN | ASP | TYR | THR | ||||
29 | CYS | ALA | GLY | SER | ARG | SER | GLN | SER | LYS | PRO | ||||
30 | PHE | THR | LEU | ARG | TRP | THR | GLY | TYR | LYS | ASN | ||||
31 | SER | ASP | ALA | GLY | SER | ASN | GLY | ILE | VAL | ILE | ||||
32 | VAL | ALA |
Samples:
sample_1: ALS1, [U-100% 13C; U-100% 15N; U-80% 2H], 500 uM; H2O 90%; D2O 10%; Sodium Phosphate 50 mM; Sodium Chloride 50 mM
sample_conditions_1: ionic strength: 0.1 M; pH: 6.0; pressure: 1 atm; temperature: 308 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D TROSY 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HNCACB | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HN(CO)CACB | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HNCO | sample_1 | isotropic | sample_conditions_1 |
3D TROSY HN(CA)CO | sample_1 | isotropic | sample_conditions_1 |
3D TROSY 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D SIMULTANEOUS 1H-15N/13C NOESY | sample_1 | isotropic | sample_conditions_1 |
3D TROSY H(CCCO)NH TOCSY | sample_1 | isotropic | sample_conditions_1 |
3D TROSY (H)C(CCO)NH TOCSY | sample_1 | isotropic | sample_conditions_1 |
Software:
NMRView, Johnson, One Moon Scientific - data analysis
TOPSPIN, Bruker Biospin - collection
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
NMR spectrometers:
- Bruker Avance 800 MHz
- Bruker DRX 500 MHz
Related Database Links:
GB | AAC41649 AFD62903 AFD63116 AFD63117 AFD63118 |
REF | XP_718010 XP_718077 |
SP | P46590 Q5A8T4 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts