Structure of PDB 4fvt Chain A Binding Site BS02
Receptor Information
>4fvt Chain A (length=274) Species:
9606
(Homo sapiens) [
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KLSLQDVAELIRARACQRVVVMVGAGISTPSGIPDFRSPGSGLYSNLQQY
DLPYPEAIFELPFFFHNPKPFFTLAKELYPGNYKPNVTHYFLRLLHDKGL
LLRLYTQNIDGLERVSGIPASKLVEAHGTFASATCTVCQRPFPGEDIRAD
VMADRVPRCPVCTGVVKPDIVFFGEPLPQRFLLHVVDFPMADLLLILGTS
LEVEPFASLTEAVRSSVPRLLINRDLVGPLAWHPRSRDVAQLGDVVHGVE
SLVELLGWTEEMRDLVQRETGKLD
Ligand information
Ligand ID
CNA
InChI
InChI=1S/C22H29N7O13P2/c23-19-14-21(26-8-25-19)29(9-27-14)22-18(33)17(32)13(41-22)7-40-44(37,38)42-43(35,36)39-6-11-4-12(16(31)15(11)30)28-3-1-2-10(5-28)20(24)34/h1-3,5,8-9,11-13,15-18,22,30-33H,4,6-7H2,(H5-,23,24,25,26,34,35,36,37,38)/p+1/t11-,12-,13-,15-,16+,17-,18-,22-/m1/s1
InChIKey
DGPLSUKWXXSBCU-VGXGLJSLSA-O
SMILES
Software
SMILES
ACDLabs 12.01
O=C(N)c1ccc[n+](c1)C2CC(C(O)C2O)COP(=O)(O)OP(=O)(O)OCC5OC(n4cnc3c(ncnc34)N)C(O)C5O
OpenEye OEToolkits 1.7.6
c1cc(c[n+](c1)[C@@H]2C[C@@H]([C@H]([C@H]2O)O)COP(=O)(O)OP(=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)C(=O)N
CACTVS 3.370
NC(=O)c1ccc[n+](c1)[CH]2C[CH](CO[P](O)(=O)O[P](O)(=O)OC[CH]3O[CH]([CH](O)[CH]3O)n4cnc5c(N)ncnc45)[CH](O)[CH]2O
OpenEye OEToolkits 1.7.6
c1cc(c[n+](c1)C2CC(C(C2O)O)COP(=O)(O)OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)C(=O)N
CACTVS 3.370
NC(=O)c1ccc[n+](c1)[C@@H]2C[C@H](CO[P](O)(=O)O[P](O)(=O)OC[C@H]3O[C@H]([C@H](O)[C@@H]3O)n4cnc5c(N)ncnc45)[C@@H](O)[C@H]2O
Formula
C22 H30 N7 O13 P2
Name
CARBA-NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL5220997
DrugBank
DB02498
ZINC
ZINC000024666703
PDB chain
4fvt Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
4fvt
Synthesis of Carba-NAD and the Structures of Its Ternary Complexes with SIRT3 and SIRT5.
Resolution
2.47 Å
Binding residue
(original residue number in PDB)
G145 A146 G147 T150 P155 D156 F157 N229 I230 D231 H248 T320 S321 V324 N344 R345 V366
Binding residue
(residue number reindexed from 1)
G24 A25 G26 T29 P34 D35 F36 N108 I109 D110 H127 T199 S200 V203 N223 R224 V245
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
P155 D156 F157 R158 N229 D231 H248
Catalytic site (residue number reindexed from 1)
P34 D35 F36 R37 N108 D110 H127
Enzyme Commision number
2.3.1.286
: protein acetyllysine N-acetyltransferase.
Gene Ontology
Molecular Function
GO:0017136
NAD-dependent histone deacetylase activity
GO:0051287
NAD binding
GO:0070403
NAD+ binding
View graph for
Molecular Function
External links
PDB
RCSB:4fvt
,
PDBe:4fvt
,
PDBj:4fvt
PDBsum
4fvt
PubMed
22849721
UniProt
Q9NTG7
|SIR3_HUMAN NAD-dependent protein deacetylase sirtuin-3, mitochondrial (Gene Name=SIRT3)
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