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PDB ID:
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full, LACS
BMRB Entry DOI: doi:10.13018/BMR16648
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
RDF gzip file.
All files associated with the entry
Citation: Mani, Rajeswari; Vorobiev, Sergey; Swapna, G.; Neely, Helen; Janjua, Haleema; Ciccosanti, Colleen; Xiao, Rong; Acton, Thomas; Everett, John; Hunt, John; Montelione, Gaetano. "Solution NMR and X-ray crystal structures of membrane-associated Lipoprotein-17 domain reveal a novel fold." J. Struct. Funct. Genomics 12, 27-32 (2011).
PubMed: 21153711
Assembly members:
UuR17A,_Lipoprotein, polymer, 121 residues, 14356.324 Da.
Natural source: Common Name: Ureaplasma parvum Taxonomy ID: 134821 Superkingdom: Bacteria Kingdom: not available Genus/species: Ureaplasma parvum
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pET 21-23C
Entity Sequences (FASTA):
UuR17A,_Lipoprotein: MLSQANEDFKKIVNNIRLKD
TFDFKLAAFPNQNYDQLLPS
QIYKNYYQGIEIQQHKYQNE
LDIKIINFLYPDGDFGSANK
NGTLKLSLMLTDKKNNQVYY
KLLEVSGFKSNPYLEHHHHH
H
Data type | Count |
13C chemical shifts | 508 |
15N chemical shifts | 120 |
1H chemical shifts | 775 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | UuR17A | 1 |
Entity 1, UuR17A 121 residues - 14356.324 Da.
Last 8 residues LEHHHHHH is a C-terminal tag
1 | MET | LEU | SER | GLN | ALA | ASN | GLU | ASP | PHE | LYS | ||||
2 | LYS | ILE | VAL | ASN | ASN | ILE | ARG | LEU | LYS | ASP | ||||
3 | THR | PHE | ASP | PHE | LYS | LEU | ALA | ALA | PHE | PRO | ||||
4 | ASN | GLN | ASN | TYR | ASP | GLN | LEU | LEU | PRO | SER | ||||
5 | GLN | ILE | TYR | LYS | ASN | TYR | TYR | GLN | GLY | ILE | ||||
6 | GLU | ILE | GLN | GLN | HIS | LYS | TYR | GLN | ASN | GLU | ||||
7 | LEU | ASP | ILE | LYS | ILE | ILE | ASN | PHE | LEU | TYR | ||||
8 | PRO | ASP | GLY | ASP | PHE | GLY | SER | ALA | ASN | LYS | ||||
9 | ASN | GLY | THR | LEU | LYS | LEU | SER | LEU | MET | LEU | ||||
10 | THR | ASP | LYS | LYS | ASN | ASN | GLN | VAL | TYR | TYR | ||||
11 | LYS | LEU | LEU | GLU | VAL | SER | GLY | PHE | LYS | SER | ||||
12 | ASN | PRO | TYR | LEU | GLU | HIS | HIS | HIS | HIS | HIS | ||||
13 | HIS |
sample_1: UuR17A, Lipoprotein, [U-100% 13C; U-100% 15N], 0.91 ± 0.2 mM; NaN3 0.02%; DDT 100 mM; CaCl2 5 mM; NaCl 10 mM; MES 20 mM
sample_2: UuR17A, Lipoprotein, [U-100% 13C; U-100% 15N], 0.91 ± 0.2 mM; NaN3 0.02%; DDT 100 mM; CaCl2 5 mM; NaCl 10 mM; MES 20 mM
sample_3: UuR17A, Lipoprotein, [U-10% 13C; U-99% 15N], 0.7 ± 0.2 mM; NaN3 0.02%; DDT 100 mM; CaCl2 5 mM; NaCl 10 mM; MES 20 mM
sample_conditions_1: ionic strength: 15 mM; pH: 6.5; pressure: 1 atm; temperature: 298 K
Name | Sample | Sample state | Sample conditions |
---|---|---|---|
2D 1H-15N HSQC | sample_1 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_1 | isotropic | sample_conditions_1 |
3D 1H-15N/13C simultaneous NOESY | sample_1 | isotropic | sample_conditions_1 |
3D 1H-13C arom NOESY | sample_1 | isotropic | sample_conditions_1 |
2D 1H-15N HSQC | sample_2 | isotropic | sample_conditions_1 |
2D 1H-13C HSQC | sample_2 | isotropic | sample_conditions_1 |
3D CBCA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HBHA(CO)NH | sample_2 | isotropic | sample_conditions_1 |
3D HNCO | sample_2 | isotropic | sample_conditions_1 |
3D HNCA | sample_2 | isotropic | sample_conditions_1 |
3D HNCACB | sample_2 | isotropic | sample_conditions_1 |
(4,3)D GFT-CBCACACONHN | sample_2 | isotropic | sample_conditions_1 |
(4,3)D GFT-HNNCABCA | sample_2 | isotropic | sample_conditions_1 |
3D CCH-TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D HCCH TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D CCCONH TOCSY | sample_2 | isotropic | sample_conditions_1 |
3D HNHA | sample_3 | isotropic | sample_conditions_1 |
Het NOE sat | sample_3 | isotropic | sample_conditions_1 |
Het NOE no sat | sample_3 | isotropic | sample_conditions_1 |
CNS v2.0.6, Brunger, Adams, Clore, Gros, Nilges and Read - refinement
CYANA v3.0, Guntert, Mumenthaler and Wuthrich - structure solution
AutoStruct v2.2.1, Huang, Tejero, Powers and Montelione - structure solution
PINE v1.0, Bahrami, Markley, Assadi, and Eghbalnia - chemical shift assignment
AutoAssign v2.2.1, Zimmerman, Moseley, Kulikowski and Montelione - chemical shift assignment
PDB | |
DBJ | BAO73398 |
EMBL | CPS23611 |
GB | AAF30450 ACA32833 ACI60006 EDT48851 EDT49831 |
PIR | B82940 |
REF | WP_004026166 WP_004026422 WP_004026736 WP_004027175 WP_004027386 |
SP | Q9PRA0 |
AlphaFold | Q9PRA0 |
Download HSQC peak lists in one of the following formats:
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