Structure of PDB 5nuc Chain A Binding Site BS02
Receptor Information
>5nuc Chain A (length=135) Species:
1280
(Staphylococcus aureus) [
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LHKEPATLIKAIDGDTCKLMYKGQPMTFRLLLVDTPETKHPKKGVEKYGP
EASAFTKKMVENAKKIEVEFDKGQRTDKYGRGLAYIYADGKMVNEALVRQ
GLAKVAYVYKPNNTHEQHLRKSEAQAKKEKLNIWS
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
5nuc Chain A Residue 151 [
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Receptor-Ligand Complex Structure
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PDB
5nuc
Mobile unnatural amino acid side chains in the core of staphylococcal nuclease.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
R35 D83 K84 Y85 R87 L89 Y113 Y115
Binding residue
(residue number reindexed from 1)
R29 D77 K78 Y79 R81 L83 Y107 Y109
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)
D15 R29 D34 T35 E37 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:5nuc
,
PDBe:5nuc
,
PDBj:5nuc
PDBsum
5nuc
PubMed
8762134
UniProt
P00644
|NUC_STAAU Thermonuclease (Gene Name=nuc)
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