BMRB Entry 16878
Click here to enlarge.
PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR16878
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
NMR-STAR v2.1 text file (deprecated)
XML gzip file.
RDF gzip file.
All files associated with the entry
Title: NMR Structure of AIRE PHD Finger PubMed: 19446523
Deposition date: 2010-04-18 Original release date: 2010-07-27
Authors: Chakravarty, Suvobrata; Zeng, Lei; ZHOU, MING-MING
Citation: Chakravarty, Suvobrata; Zeng, Lei; Zhou, Ming-Ming. "Structure and site-specific recognition of histone H3 by the PHD finger of human autoimmune regulator." Structure 17, 670-679 (2009).
Assembly members:
AIRE_PHD_finger_1, polymer, 56 residues, 6019.845 Da.
Histone_H3_1-20Cys, polymer, 21 residues, 2293.733 Da.
ZN, non-polymer, 65.409 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):
AIRE_PHD_finger_1: GSKNEDECAVCRDGGELICC
DGCPRAFHLACLSPPLREIP
SGTWRCSSCLQATVQE
Histone_H3_1-20Cys: ARTKQTARKSTGGKAPRKQL
C
- assigned_chemical_shifts
Data type | Count |
13C chemical shifts | 163 |
15N chemical shifts | 47 |
1H chemical shifts | 318 |
Additional metadata:
Assembly:
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | AIRE_PHD_finger_1 | 1 |
2 | Histone_H3_1-20Cys | 2 |
3 | ZINC_1 | 3 |
4 | ZINC_2 | 3 |
Entities:
Entity 1, AIRE_PHD_finger_1 56 residues - 6019.845 Da.
1 | GLY | SER | LYS | ASN | GLU | ASP | GLU | CYS | ALA | VAL | ||||
2 | CYS | ARG | ASP | GLY | GLY | GLU | LEU | ILE | CYS | CYS | ||||
3 | ASP | GLY | CYS | PRO | ARG | ALA | PHE | HIS | LEU | ALA | ||||
4 | CYS | LEU | SER | PRO | PRO | LEU | ARG | GLU | ILE | PRO | ||||
5 | SER | GLY | THR | TRP | ARG | CYS | SER | SER | CYS | LEU | ||||
6 | GLN | ALA | THR | VAL | GLN | GLU |
Entity 2, Histone_H3_1-20Cys 21 residues - 2293.733 Da.
1 | ALA | ARG | THR | LYS | GLN | THR | ALA | ARG | LYS | SER | ||||
2 | THR | GLY | GLY | LYS | ALA | PRO | ARG | LYS | GLN | LEU | ||||
3 | CYS |
Entity 3, ZINC_1 - Zn - 65.409 Da.
1 | ZN |
Samples:
sample_1: AIRE PHD finger 1, [U-100% 15N], 0.5 mM; phosphate buffer 10 mM; NaCl 250 mM; H2O 90%; D2O 10%
sample_conditions_1: ionic strength: 250 mM; pH: 7.0; pressure: 1 atm; temperature: 298 K
Experiments:
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C NOESY | sample_1 | isotropic | sample_conditions_1 |
3D HN(COCA)CB | sample_1 | isotropic | sample_conditions_1 |
3D HN(CO)CA | sample_1 | isotropic | sample_conditions_1 |
2D DQF-COSY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-1H NOESY | sample_1 | isotropic | sample_conditions_1 |
Software:
ARIA v2.2, Linge, O'Donoghue and Nilges - data analysis
CNS v1.0, Brunger, Adams, Clore, Gros, Nilges and Read - structure solution
NMR spectrometers:
- Bruker DRX 800 MHz
Related Database Links:
. | NP_000374 |
PDB | |
DBJ | BAA23988 BAA23989 BAA23990 BAA23991 BAA23992 BAB27616 BAG57022 GAC74844 |
EMBL | CAA08759 CAB10790 CAG04369 CAG11543 CAP39588 CAP53898 CAP72538 |
GB | AAI37269 AAI37271 AIC54015 EAX09441 EAX09442 AAH67493 AAR37358 AAT97343 AAT97344 AAX52110 |
REF | NP_000374 XP_003419041 XP_004062941 XP_006876868 XP_008975805 NP_001281095 XP_001061048 XP_001249529 XP_001712222 XP_002029274 |
SP | O43918 |
BMRB | 11358 16694 |
TPG | DAA24942 DAA45649 |
Download simulated HSQC data in one of the following formats:
CSV: Backbone
or all simulated shifts
SPARKY: Backbone
or all simulated shifts