BMRB Entry 15576
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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_anomalous, AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR15576
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Title: Ubiquitin-like domain of NFATC2IP. Northeast Structural Genomics Consortium Target hr5627.
Deposition date: 2007-11-30 Original release date: 2007-12-11
Authors: Doherty, Ryan; Dhe-Paganon, Sirano; Fares, Christophe; Lemak, Alex; Butler, Chris; Srisailam, Sampath; Karra, Murthy; Yee, Adelinda; Edwards, Aled; Weigelt, Johan; Arrowsmith, Cheryl
Citation: Doherty, Ryan; Dhe-Paganon, Sirano; Fares, Christophe; Lemak, Alex; Butler, Chris; Srisailam, Sampath; Karra, Murthy; Yee, Adelinda; Weigelt, Johan; Edwards, Aled; Arrowsmith, Cheryl. "Solution structure of Ubiquitin-like domain of NFATC2IP." The BMRB entry is the only known published source for the data..
Assembly members:
NFATC2IP, polymer, 97 residues, 8739.932 Da.
Natural source: Common Name: Human Taxonomy ID: 9606 Superkingdom: Eukaryota Kingdom: Metazoa Genus/species: Homo sapiens
Experimental source: Production method: recombinant technology Host organism: Escherichia coli
Entity Sequences (FASTA):
NFATC2IP: MGSSHHHHHHSSGLVPRGST
ETSQQLQLRVQGKEKHQTLE
VSLSRDSPLKTLMSHYEEAM
GLSGRKLSFFFDGTKLSGRE
LPADLGMESGDLIEVWG
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 312 |
15N chemical shifts | 71 |
1H chemical shifts | 512 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | NFATC2IP | 1 |
Entities:
Entity 1, NFATC2IP 97 residues - 8739.932 Da.
Residues 1-19 represent a non-native affinity tag.
1 | MET | GLY | SER | SER | HIS | HIS | HIS | HIS | HIS | HIS | ||||
2 | SER | SER | GLY | LEU | VAL | PRO | ARG | GLY | SER | THR | ||||
3 | GLU | THR | SER | GLN | GLN | LEU | GLN | LEU | ARG | VAL | ||||
4 | GLN | GLY | LYS | GLU | LYS | HIS | GLN | THR | LEU | GLU | ||||
5 | VAL | SER | LEU | SER | ARG | ASP | SER | PRO | LEU | LYS | ||||
6 | THR | LEU | MET | SER | HIS | TYR | GLU | GLU | ALA | MET | ||||
7 | GLY | LEU | SER | GLY | ARG | LYS | LEU | SER | PHE | PHE | ||||
8 | PHE | ASP | GLY | THR | LYS | LEU | SER | GLY | ARG | GLU | ||||
9 | LEU | PRO | ALA | ASP | LEU | GLY | MET | GLU | SER | GLY | ||||
10 | ASP | LEU | ILE | GLU | VAL | TRP | GLY |
Samples:
H2O_CN_phage: NFATC2IP, [U-13C; U-15N], 0.9 mM; NaCl 500 mM; Tris-HCl 50 mM; Benzamidine 1 mM; NaN3 0.01%; ZnSO4 0.01 mM; Pf1 co-solvent Protease free Phage 12 mg/ml; D2O, [U-100% 2H], 10%; H2O 90%
H2O_NH: NFATC2IP, [U-15N], 0.9 mM; NaCl 500 mM; Tris-HCl 50 mM; Benzamidine 1 mM; NaN3 0.01%; ZnSO4 0.01 mM; D2O, [U-100% 2H], 10%; H2O 90%
D2O_CN: NFATC2IP, [U-13C; U-15N], 0.9 mM; NaCl 500 mM; Tris-HCl 50 mM; Benzamidine 1 mM; NaN3 0.01%; ZnSO4 0.01 mM; D2O, [U-100% 2H], 100%
H2O_CN: NFATC2IP, [U-13C; U-15N], 0.9 mM; NaCl 500 mM; Tris-HCl 50 mM; Benzamidine 1 mM; NaN3 0.01%; ZnSO4 0.01 mM; D2O, [U-100% 2H], 10%; H2O 90%
sample_conditions_1: ionic strength: 500 mM; pH: 8; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | H2O_NH | isotropic | sample_conditions_1 |
2D 1H-13C Constant Time HSQC | D2O_CN | isotropic | sample_conditions_1 |
3D HNCO | H2O_CN | isotropic | sample_conditions_1 |
3D HNCA | H2O_CN | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | H2O_CN | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | H2O_CN | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | H2O_CN | isotropic | sample_conditions_1 |
3D 1H-13C Aromatic NOESY | H2O_CN | isotropic | sample_conditions_1 |
3D (H)CCH-TOCSY | D2O_CN | isotropic | sample_conditions_1 |
3D H(C)CH-TOCSY | D2O_CN | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | H2O_CN | isotropic | sample_conditions_1 |
2D 1H-15N IPAP HSQC | H2O_CN | isotropic | sample_conditions_1 |
2D 1H-15N IPAP HSQC | H2O_CN_phage | anisotropic | sample_conditions_1 |
3D 1H-15N NOESY | H2O_CN | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | D2O_CN | isotropic | sample_conditions_1 |
Software:
CNS v1.1, Brunger, Adams, Clore, Gros, Nilges and Read - refinement, structure solution
NMRPipe, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
TALOS, Cornilescu, Delaglio and Bax - data analysis
SPARKY, Goddard - peak picking
TOPSPIN, Bruker Biospin - collection
PSVS, Bhattacharya and Montelione - refinement
WhatIF, Vriend - refinement
NMR spectrometers:
- Bruker Avance 500 MHz
- Bruker Avance 600 MHz
- Bruker Avance 800 MHz
Related Database Links:
PIR | Q8NCF5 |
REF | NP_116204 NP_116204 XP_001102777 XP_001146533 XP_002802482 XP_002826318 |
PDB | |
DBJ | BAB17279 BAB55189 BAC11189 BAH12551 BAH14223 |
GB | AAH18311 AAH21551 AAH68007 AAH80628 AAI01742 |
SP | Q8NCF5 Q9GLZ9 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts