BMRB Entry 18415
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                PDB ID: 
                
                
                Entry in NMR Restraints Grid
                Validation report in NRG-CING
            Chem Shift validation:  AVS_anomalous, AVS_full, LACS, SPARTA
BMRB Entry DOI: doi:10.13018/BMR18415
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Title: Solution structure of human C-type lectin domain family 4 member D
Deposition date: 2012-04-23 Original release date: 2012-05-22
Authors: Harris, R.; Gaudette, J.; Bandaranayake, A.; Banu, R.; Bonanno, J.; Calarese, D.; Celikgil, A.; Chamala, S.; Chan, M.; Chaparro, R.; Evans, B.; Garforth, S.; Gizzi, A.; Hillerich, B.; Kar, A.; Lafleur, J.; Lim, S.; Love, J.; Matikainen, B.; Patel, H.; Seidel, R.; Smith, B.; Stead, M.; Girvin, M.; Almo, S.
Citation: Harris, R.; Gaudette, J.; Bandaranayake, A.; Banu, R.; Bonanno, J.; Calarese, D.; Celikgil, A.; Chamala, S.; Chan, M.; Chaparro, R.; Evans, B.; Garforth, S.; Gizzi, A.; Hillerich, B.; Kar, A.; Lafleur, J.; Lim, S.; Love, J.; Matikainen, B.; Patel, H.; Seidel, R.; Smith, B.; Stead, M.; Girvin, M.; Almo, S.. "Solution structure of human C-type lectin domain family 4 member D" To be published ., .-..
Assembly members:
C-type_lectin, polymer, 156 residues,   18610.879 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):
C-type_lectin: MVCPIDWRAFQSNCYFPLTD
NKTWAESERNCSGMGAHLMT
ISTEAEQNFIIQFLDRRLSY
FLGLRDENAKGQWRWVDQTP
FNPRRVFWHKNEPDNSQGEN
CVVLVYNQDKWAWNDVPCNF
EASRICKIPGTTLNAENLYF
QSHHHHHHWSHPQFEK
- assigned_chemical_shifts
| Data type | Count | 
| 13C chemical shifts | 673 | 
| 15N chemical shifts | 169 | 
| 1H chemical shifts | 1047 | 
Additional metadata:
Assembly:
| Entity Assembly ID | Entity Name | Entity ID | 
|---|---|---|
| 1 | human C-type lectin domain family 4 member D | 1 | 
Entities:
Entity 1, human C-type lectin domain family 4 member D 156 residues - 18610.879 Da.
expressed sequence start-stop 84-215 (156 aa incl tag) N-term cloning artifact MV- C-term cloning artifact -AENLYFQSHHHHHHWSHPQFEK Only residues 1-142 included in structure calculations
| 1 | MET | VAL | CYS | PRO | ILE | ASP | TRP | ARG | ALA | PHE | ||||
| 2 | GLN | SER | ASN | CYS | TYR | PHE | PRO | LEU | THR | ASP | ||||
| 3 | ASN | LYS | THR | TRP | ALA | GLU | SER | GLU | ARG | ASN | ||||
| 4 | CYS | SER | GLY | MET | GLY | ALA | HIS | LEU | MET | THR | ||||
| 5 | ILE | SER | THR | GLU | ALA | GLU | GLN | ASN | PHE | ILE | ||||
| 6 | ILE | GLN | PHE | LEU | ASP | ARG | ARG | LEU | SER | TYR | ||||
| 7 | PHE | LEU | GLY | LEU | ARG | ASP | GLU | ASN | ALA | LYS | ||||
| 8 | GLY | GLN | TRP | ARG | TRP | VAL | ASP | GLN | THR | PRO | ||||
| 9 | PHE | ASN | PRO | ARG | ARG | VAL | PHE | TRP | HIS | LYS | ||||
| 10 | ASN | GLU | PRO | ASP | ASN | SER | GLN | GLY | GLU | ASN | ||||
| 11 | CYS | VAL | VAL | LEU | VAL | TYR | ASN | GLN | ASP | LYS | ||||
| 12 | TRP | ALA | TRP | ASN | ASP | VAL | PRO | CYS | ASN | PHE | ||||
| 13 | GLU | ALA | SER | ARG | ILE | CYS | LYS | ILE | PRO | GLY | ||||
| 14 | THR | THR | LEU | ASN | ALA | GLU | ASN | LEU | TYR | PHE | ||||
| 15 | GLN | SER | HIS | HIS | HIS | HIS | HIS | HIS | TRP | SER | ||||
| 16 | HIS | PRO | GLN | PHE | GLU | LYS | 
Samples:
sample_1: C-type lectin, [U-13C; U-15N], 1 mM; sodium acetate 10 mM; EDTA 0.1 mM; H2O 90%; D2O 10%
sample_2: C-type lectin, [U-13C; U-15N], 1 mM; sodium acetate 10 mM; EDTA 0.1 mM; D2O 100%
sample_conditions_1: ionic strength: 10 mM; pH: 4.5; pressure: 1 atm; temperature: 303 K
Experiments:
| Name | Sample | Sample state | Sample conditions | 
|---|---|---|---|
| 15N HSQC | sample_1 | isotropic | sample_conditions_1 | 
| 15N NOESY-HSQC | sample_1 | isotropic | sample_conditions_1 | 
| 13C CT-HSQC | sample_2 | isotropic | sample_conditions_1 | 
| aromatic 13C CT-HSQC | sample_2 | isotropic | sample_conditions_1 | 
| 13C NOESY-HSQC | sample_2 | isotropic | sample_conditions_1 | 
| 13C aromatic NOESY-HSQC | sample_2 | isotropic | sample_conditions_1 | 
| HNCO | sample_1 | isotropic | sample_conditions_1 | 
| HNCACO | sample_1 | isotropic | sample_conditions_1 | 
| HNCA | sample_1 | isotropic | sample_conditions_1 | 
| HNCOCA | sample_1 | isotropic | sample_conditions_1 | 
| HNCACB | sample_1 | isotropic | sample_conditions_1 | 
| CBCACONH | sample_1 | isotropic | sample_conditions_1 | 
Software:
CCPN v2.1.5, CCPN - chemical shift assignment, peak picking
CNS v1.21, Brunger, Adams, Clore, Gros, Nilges and Read - refinement, structure solution
ARIA v2.3, Linge, O, . - structure solution
NMRPipe v5.4, Delaglio, Grzesiek, Vuister, Zhu, Pfeifer and Bax - processing
VNMRJ v2.2D, Varian - collection
TOPSPIN, Bruker Biospin - collection
MDDNMR v2.0, (MDDNMR) Orekhov, Jaravine, Kazimierczuk - collection, processing
MDDGUI v1.0, (MDDGUI) Lemak, Gutmanas, Chitayat, Karra, Fares, Sunnerhagen, Arrowsmith - collection, processing
NMR spectrometers:
- Varian Inova 600 MHz
- Bruker Avance 800 MHz
Related Database Links:
| PDB | |
| GB | AAH32313 AAL37713 AAM75389 AAQ63173 AAS59161 | 
| REF | NP_525126 XP_001134875 XP_003265492 XP_003808712 XP_004052704 | 
| SP | Q8WXI8 | 
Download simulated HSQC data in one of the following formats:
            
CSV: Backbone
            or all simulated shifts
            
SPARKY: Backbone
            or all simulated shifts
    
