Structure of PDB 3hej Chain B Binding Site BS01
Receptor Information
>3hej Chain B (length=135) Species:
1280
(Staphylococcus aureus) [
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ATSTKKLHKEPATLIKAIDGDTVKLMYKGQPMTFRLLLVDTPEFNEKYGP
EASAFRKKMVENAKKIEVEFDKGQRTDKYGRGLAYIYADGKMVNEALVRQ
GLAKVAYVYKGNNTHEQLLRKAEAQAKKEKLNIWS
Ligand information
Ligand ID
THP
InChI
InChI=1S/C10H16N2O11P2/c1-5-3-12(10(14)11-9(5)13)8-2-6(23-25(18,19)20)7(22-8)4-21-24(15,16)17/h3,6-8H,2,4H2,1H3,(H,11,13,14)(H2,15,16,17)(H2,18,19,20)/t6-,7+,8+/m0/s1
InChIKey
CSNCBOPUCJOHLS-XLPZGREQSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC1=CN([CH]2C[CH](O[P](O)(O)=O)[CH](CO[P](O)(O)=O)O2)C(=O)NC1=O
ACDLabs 10.04
O=C1NC(=O)N(C=C1C)C2OC(C(OP(=O)(O)O)C2)COP(=O)(O)O
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)C2CC(C(O2)COP(=O)(O)O)OP(=O)(O)O
CACTVS 3.341
CC1=CN([C@H]2C[C@H](O[P](O)(O)=O)[C@@H](CO[P](O)(O)=O)O2)C(=O)NC1=O
OpenEye OEToolkits 1.5.0
CC1=CN(C(=O)NC1=O)[C@H]2C[C@@H]([C@H](O2)COP(=O)(O)O)OP(=O)(O)O
Formula
C10 H16 N2 O11 P2
Name
THYMIDINE-3',5'-DIPHOSPHATE
ChEMBL
CHEMBL1235491
DrugBank
DB04205
ZINC
ZINC000011422512
PDB chain
3hej Chain B Residue 150 [
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Receptor-Ligand Complex Structure
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PDB
3hej
Domain swapping promoted by a single mutation that introduces an ionizable group into the hydrophobic core of a protein
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
R35 K84 Y85 R87 L89 Y113
Binding residue
(residue number reindexed from 1)
R35 K78 Y79 R81 L83 Y107
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
D21 R35 D40 T41 E43 R87
Catalytic site (residue number reindexed from 1)
D21 R35 D40 T41 E43 R81
Enzyme Commision number
3.1.31.1
: micrococcal nuclease.
Gene Ontology
Molecular Function
GO:0003676
nucleic acid binding
GO:0004518
nuclease activity
View graph for
Molecular Function
External links
PDB
RCSB:3hej
,
PDBe:3hej
,
PDBj:3hej
PDBsum
3hej
PubMed
UniProt
P00644
|NUC_STAAU Thermonuclease (Gene Name=nuc)
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