Structure of PDB 3g3e Chain D Binding Site BS01
Receptor Information
>3g3e Chain D (length=340) Species:
9606
(Homo sapiens) [
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MRVVVIGAGVIGLSTALCIHERYHSVLQPLDIKVYADRFTPLTTTDVAAG
LWQPYLSDPNNPQEADWSQQTFDYLLSHVHSPNAENLGLFLISGYNLFHE
AIPDPSWKDTVLGFRKLTPRELDMFPDYGYGWFHTSLILEGKNYLQWLTE
RLTERGVKFFQRKVESFEEVAREGADVIVNCTGVWAGALQRDPLLQPGRG
QIMKVDAPWMKHFILTHDPERGIYNSPYIIPGTQTVTLGGIFQLGNWSEL
NNIQDHNTIWEGCCRLEPTLKNARIIGERTGFRPVRPQIRLEREQLRTGP
SNTEVIHNYGHGGYGLTIHWGCALEAAKLFGRILEEKKLS
Ligand information
Ligand ID
FAD
InChI
InChI=1S/C27H33N9O15P2/c1-10-3-12-13(4-11(10)2)35(24-18(32-12)25(42)34-27(43)33-24)5-14(37)19(39)15(38)6-48-52(44,45)51-53(46,47)49-7-16-20(40)21(41)26(50-16)36-9-31-17-22(28)29-8-30-23(17)36/h3-4,8-9,14-16,19-21,26,37-41H,5-7H2,1-2H3,(H,44,45)(H,46,47)(H2,28,29,30)(H,34,42,43)/t14-,15+,16+,19-,20+,21+,26+/m0/s1
InChIKey
VWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P@](O)(=O)O[P@@](O)(=O)OC[C@H]4O[C@H]([C@H](O)[C@@H]4O)n5cnc6c(N)ncnc56)c2cc1C
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)OP(=O)(O)OCC4C(C(C(O4)n5cnc6c5ncnc6N)O)O)O)O)O
OpenEye OEToolkits 1.5.0
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](CO[P@@](=O)(O)O[P@](=O)(O)OC[C@@H]4[C@H]([C@H]([C@@H](O4)n5cnc6c5ncnc6N)O)O)O)O)O
CACTVS 3.341
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(=O)O[P](O)(=O)OC[CH]4O[CH]([CH](O)[CH]4O)n5cnc6c(N)ncnc56)c2cc1C
ACDLabs 10.04
O=C2C3=Nc1cc(c(cc1N(C3=NC(=O)N2)CC(O)C(O)C(O)COP(=O)(O)OP(=O)(O)OCC6OC(n5cnc4c(ncnc45)N)C(O)C6O)C)C
Formula
C27 H33 N9 O15 P2
Name
FLAVIN-ADENINE DINUCLEOTIDE
ChEMBL
CHEMBL1232653
DrugBank
DB03147
ZINC
ZINC000008215434
PDB chain
3g3e Chain D Residue 352 [
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Receptor-Ligand Complex Structure
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PDB
3g3e
Discovery, SAR, and pharmacokinetics of a novel 3-Hydroxyquinolin-2(1H)-one series of potent D-amino acid oxidase (DAAO) inhibitors
Resolution
2.2 Å
Binding residue
(original residue number in PDB)
G7 A8 G9 V10 I11 A36 D37 R38 T44 T45 A48 G50 L51 K163 V164 T182 W185 R283 G312 G313 Y314 G315 L316 T317
Binding residue
(residue number reindexed from 1)
G7 A8 G9 V10 I11 A36 D37 R38 T44 T45 A48 G50 L51 K163 V164 T182 W185 R283 G312 G313 Y314 G315 L316 T317
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
L51 G313 T317
Catalytic site (residue number reindexed from 1)
L51 G313 T317
Enzyme Commision number
1.4.3.3
: D-amino-acid oxidase.
Gene Ontology
Molecular Function
GO:0003884
D-amino-acid oxidase activity
GO:0005515
protein binding
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0071949
FAD binding
Biological Process
GO:0006562
proline catabolic process
GO:0007586
digestion
GO:0019478
D-amino acid catabolic process
GO:0036088
D-serine catabolic process
GO:0042416
dopamine biosynthetic process
GO:0046416
D-amino acid metabolic process
GO:0055130
D-alanine catabolic process
GO:0070178
D-serine metabolic process
GO:0070945
neutrophil-mediated killing of gram-negative bacterium
Cellular Component
GO:0005576
extracellular region
GO:0005737
cytoplasm
GO:0005741
mitochondrial outer membrane
GO:0005777
peroxisome
GO:0005782
peroxisomal matrix
GO:0005829
cytosol
GO:0042995
cell projection
GO:0045202
synapse
GO:0048786
presynaptic active zone
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3g3e
,
PDBe:3g3e
,
PDBj:3g3e
PDBsum
3g3e
PubMed
19438227
UniProt
P14920
|OXDA_HUMAN D-amino-acid oxidase (Gene Name=DAO)
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