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PDB ID: 2rui
Entry in NMR Restraints Grid
Validation report in NRG-CING
Chem Shift validation: AVS_full
BMRB Entry DOI: doi:10.13018/BMR11570
MolProbity Validation Chart
NMR-STAR file interactive viewer.
NMR-STAR v3 text file.
XML gzip file.
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Citation: Chan, Albert; Yi, Sung Wook; Jung, Michael; Clubb, Robert. "Structure of the Bacillus anthracis Sortase-Substrate Complex Reveals Important Roles of the N-terminus Tail in Transpeptidation Reaction" J. Biol. Chem. ., .-..
Assembly members:
BaSrtA, polymer, 158 residues, 17110.521 Da.
Boc-LPAT*, polymer, 5 residues, 402.551 Da.
Natural source: Common Name: Bacillus anthracis Taxonomy ID: 1392 Superkingdom: Bacteria Kingdom: not available Genus/species: Bacillus anthracis
Experimental source: Production method: recombinant technology Host organism: Escherichia coli Vector: pET15b
Entity Sequences (FASTA):
BaSrtA: GSHMDASKIDQPDLAEVANA
SLDKKQVIGRISIPSVSLEL
PVLKSSTEKNLLSGAATVKE
NQVMGKGNYALAGHNMSKKG
VLFSDIASLKKGDKIYLYDN
ENEYEYAVTGVSEVTPDKWE
VVEDHGKDEITLITCVSVKD
NSKRYVVAGDLVGTKAKK
Boc-LPAT*: XLPAX
Data type | Count |
13C chemical shifts | 642 |
15N chemical shifts | 152 |
1H chemical shifts | 1004 |
Entity Assembly ID | Entity Name | Entity ID |
---|---|---|
1 | entity_1 | 1 |
2 | entity_2 | 2 |
Entity 1, entity_1 158 residues - 17110.521 Da.
First four residues represent a non-native tag left over from cleaving off the 6xHis tag using Thrombin
1 | GLY | SER | HIS | MET | ASP | ALA | SER | LYS | ILE | ASP | ||||
2 | GLN | PRO | ASP | LEU | ALA | GLU | VAL | ALA | ASN | ALA | ||||
3 | SER | LEU | ASP | LYS | LYS | GLN | VAL | ILE | GLY | ARG | ||||
4 | ILE | SER | ILE | PRO | SER | VAL | SER | LEU | GLU | LEU | ||||
5 | PRO | VAL | LEU | LYS | SER | SER | THR | GLU | LYS | ASN | ||||
6 | LEU | LEU | SER | GLY | ALA | ALA | THR | VAL | LYS | GLU | ||||
7 | ASN | GLN | VAL | MET | GLY | LYS | GLY | ASN | TYR | ALA | ||||
8 | LEU | ALA | GLY | HIS | ASN | MET | SER | LYS | LYS | GLY | ||||
9 | VAL | LEU | PHE | SER | ASP | ILE | ALA | SER | LEU | LYS | ||||
10 | LYS | GLY | ASP | LYS | ILE | TYR | LEU | TYR | ASP | ASN | ||||
11 | GLU | ASN | GLU | TYR | GLU | TYR | ALA | VAL | THR | GLY | ||||
12 | VAL | SER | GLU | VAL | THR | PRO | ASP | LYS | TRP | GLU | ||||
13 | VAL | VAL | GLU | ASP | HIS | GLY | LYS | ASP | GLU | ILE | ||||
14 | THR | LEU | ILE | THR | CYS | VAL | SER | VAL | LYS | ASP | ||||
15 | ASN | SER | LYS | ARG | TYR | VAL | VAL | ALA | GLY | ASP | ||||
16 | LEU | VAL | GLY | THR | LYS | ALA | LYS | LYS |
Entity 2, entity_2 5 residues - 402.551 Da.
1 | BOC | LEU | PRO | ALA | B27 |
BMRB | 16811 26510 |
PDB | 2KW8 2RUI |
DBJ | BAL16456 BAR78533 GAE96182 GAO57723 GAO63420 |
EMBL | CJA38300 CJJ39486 CKE38654 CKE81514 CKE96545 |
GB | AAP24701 AAS39688 AAT29792 AAT52982 AAU19641 |
REF | NP_843215 WP_001041406 WP_001041710 WP_001041711 WP_001041715 |
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