Structure of PDB 4dgz Chain A Binding Site BS02
Receptor Information
>4dgz Chain A (length=129) Species:
1280
(Staphylococcus aureus) [
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LHKEPATLIKAIDGDTVKLMYKGQPMTFRLLLVDTPEFNEKYGPEASAFT
KKMVENAKKIEVEFDKGQRTDKYGRGLAYAYADGKMVNEALVRQGLAKVA
YVYKGNNTHEQLARKAEAQAKKEKLNIWS
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
4dgz Chain A Residue 202 [
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Receptor-Ligand Complex Structure
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PDB
4dgz
Pressure effects in proteins
Resolution
1.47 Å
Binding residue
(original residue number in PDB)
R35 K84 Y85 R87 L89 Y113 Y115
Binding residue
(residue number reindexed from 1)
R29 K72 Y73 R75 L77 Y101 Y103
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 R75
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:4dgz
,
PDBe:4dgz
,
PDBj:4dgz
PDBsum
4dgz
PubMed
UniProt
P00644
|NUC_STAAU Thermonuclease (Gene Name=nuc)
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