Structure of PDB 8uaf Chain C Binding Site BS01
Receptor Information
>8uaf Chain C (length=398) Species:
562
(Escherichia coli) [
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SIYQGGNKLNEDDFRSHVYSLCQLDNVGVLLGAGASVGCGGKTMKDVWKS
FKQNYPELLGALIDKYLLVSQIDSDNNLVNVELLIDEATKFLSVAKTRRC
EDEEEEFRKILSSLYKEVTKAALLTGEQFREKNQGKKDAFKYHKELISKL
ISNRQPGQSAPAIFTTNYDLALEWAAEDLGIQLFNGFSGLHTRQFYPQNF
DLAFRNVNHYHAYLYKLHGSLTWYQNDSLTVNEVSASQAYDEYINDIINK
DDFYRGQHLIYPGANKYSHTIGFVYGEMFRRFGEFISKPQTALFINGFGF
GDYHINRIILGALLNPSFHVVIYYPELKEAITKVSKGGGSEAEKAIVTLK
NMAFNQVTVVGGGSKAYFNSFVEHLPYPVLFPRDNIVDELVEAIANLS
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
8uaf Chain C Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
8uaf
E. coli HerA-Sir2 complex (hexamer HerA and dodecamer Sir2)
Resolution
3.18 Å
Binding residue
(original residue number in PDB)
A34 T44 M45 E83 H227 P271 G306 F307 G308 G310 D311 Y376
Binding residue
(residue number reindexed from 1)
A33 T43 M44 E82 H218 P262 G297 F298 G299 G301 D302 Y367
Annotation score
4
External links
PDB
RCSB:8uaf
,
PDBe:8uaf
,
PDBj:8uaf
PDBsum
8uaf
PubMed
38096827
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