Structure of PDB 6rkf Chain A Binding Site BS01
Receptor Information
>6rkf Chain A (length=335) Species:
9606
(Homo sapiens) [
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MDTARIAVVGAGVVGLSTAVCISKLVPRCSVTIISDKFTPDTTSDVAAGM
LIPHTYPDTPIHTQKQWFRETFNHLFAIANSAEAGDAGVHLVSGWQIFQS
TPTEEVPFWADVVLGFRKMTEAELKKFPQYVFGQAFTTLKYEGPAYLPWL
EKRIKGSGGWTLTRRIEDLWELHPSFDIVVNCSGLGSRQLAGDSKIFPVR
GQVLQVQAPWVEHFIRDGSGLTYIYPGTSHVTLGGTRQKGDWNLSPDAEN
SREILSRCCALEPSLHGACNIREKVGLRPYRPGVRLQTELLARDGQRLPV
VHHYGHGSGGISVHWGTALEAARLVSECVHALRTP
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
6rkf Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6rkf
Structure and kinetic properties of human d-aspartate oxidase, the enzyme-controlling d-aspartate levels in brain.
Resolution
3.219 Å
Binding residue
(original residue number in PDB)
G10 A11 G12 V13 V14 S35 D36 K37 T42 T43 S44 A47 A48 M50 S183 G184 G276 R278 G307 S308 G309 I311 S312
Binding residue
(residue number reindexed from 1)
G10 A11 G12 V13 V14 S35 D36 K37 T42 T43 S44 A47 A48 M50 S183 G184 G276 R278 G307 S308 G309 I311 S312
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M50 S308 S312
Catalytic site (residue number reindexed from 1)
M50 S308 S312
Enzyme Commision number
1.4.3.1
: D-aspartate oxidase.
Gene Ontology
Molecular Function
GO:0003884
D-amino-acid oxidase activity
GO:0005515
protein binding
GO:0008445
D-aspartate oxidase activity
GO:0016491
oxidoreductase activity
GO:0047821
D-glutamate oxidase activity
GO:0071949
FAD binding
Biological Process
GO:0006531
aspartate metabolic process
GO:0006533
aspartate catabolic process
GO:0007320
insemination
GO:0007625
grooming behavior
GO:0010646
regulation of cell communication
GO:0019478
D-amino acid catabolic process
GO:0042445
hormone metabolic process
GO:0046416
D-amino acid metabolic process
GO:0050877
nervous system process
Cellular Component
GO:0005737
cytoplasm
GO:0005777
peroxisome
GO:0005782
peroxisomal matrix
GO:0005829
cytosol
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:6rkf
,
PDBe:6rkf
,
PDBj:6rkf
PDBsum
6rkf
PubMed
31914658
UniProt
Q99489
|OXDD_HUMAN D-aspartate oxidase (Gene Name=DDO)
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