Structure of PDB 4rmg Chain A Binding Site BS03
Receptor Information
>4rmg Chain A (length=297) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
HMERLLDELTLEGVARYMQSERCRRVICLVGAGISTSAGIPDFRSPLYDN
LEKYHLPYPEAIFEISYFKKHPEPFFALAKELYPGQFKPTICHYFMRLLK
DKGLLLRCYTQNIDTLERIAGLEQEDLVEAHGTFYTSHCVSASCRHEYPL
SWMKEKIFSEVTPKCEDCQSLVKPDIVFFGESLPARFFSCMQSDFLKVDL
LLVMGTSLQVQPFASLISKAPLSTPRLLINKEKAGQSDGMIMGLGGGMDF
DSKKAYRDVAWLGECDQGCLALAELLGWKKELEDLVRREHASIDAQS
Ligand information
Ligand ID
NAD
InChI
InChI=1S/C21H27N7O14P2/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(32)14(30)11(41-21)6-39-44(36,37)42-43(34,35)38-5-10-13(29)15(31)20(40-10)27-3-1-2-9(4-27)18(23)33/h1-4,7-8,10-11,13-16,20-21,29-32H,5-6H2,(H5-,22,23,24,25,33,34,35,36,37)/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1
InChIKey
BAWFJGJZGIEFAR-NNYOXOHSSA-N
SMILES
Software
SMILES
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[C@@H]2O[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
OpenEye OEToolkits 1.5.0
c1cc(c[n+](c1)C2C(C(C(O2)COP(=O)([O-])OP(=O)(O)OCC3C(C(C(O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
CACTVS 3.341
NC(=O)c1ccc[n+](c1)[CH]2O[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 1.5.0
c1cc(c[n+](c1)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@@](=O)([O-])O[P@@](=O)(O)OC[C@@H]3[C@H]([C@H]([C@@H](O3)n4cnc5c4ncnc5N)O)O)O)O)C(=O)N
Formula
C21 H27 N7 O14 P2
Name
NICOTINAMIDE-ADENINE-DINUCLEOTIDE
ChEMBL
CHEMBL1234613
DrugBank
DB14128
ZINC
PDB chain
4rmg Chain A Residue 403 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
4rmg
Selective Sirt2 inhibition by ligand-induced rearrangement of the active site.
Resolution
1.88 Å
Binding residue
(original residue number in PDB)
G84 A85 G86 T89 P94 D95 F96 Q167 N168 I169 D170 H187 G261 T262 S263 N286 K287 E288 E323 C324
Binding residue
(residue number reindexed from 1)
G31 A32 G33 T36 P41 D42 F43 Q111 N112 I113 D114 H131 G205 T206 S207 N230 K231 E232 E264 C265
Annotation score
4
Enzymatic activity
Catalytic site (original residue number in PDB)
P94 D95 F96 R97 N168 D170 H187
Catalytic site (residue number reindexed from 1)
P41 D42 F43 R44 N112 D114 H131
Enzyme Commision number
2.3.1.-
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:4rmg
,
PDBe:4rmg
,
PDBj:4rmg
PDBsum
4rmg
PubMed
25672491
UniProt
Q8IXJ6
|SIR2_HUMAN NAD-dependent protein deacetylase sirtuin-2 (Gene Name=SIRT2)
[
Back to BioLiP
]