Structure of PDB 1gos Chain B Binding Site BS01
Receptor Information
>1gos Chain B (length=493) Species:
9606
(Homo sapiens) [
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KCDVVVVGGGISGMAAAKLLHDSGLNVVVLEARDRVGGRTYTLRNQKVKY
VDLGGSYVGPTQNRILRLAKELGLETYKVNEVERLIHHVKGKSYPFRGPF
PPVWNPITYLDHNNFWRTMDDMGREIPSDAPWKAPLAEEWDNMTMKELLD
KLCWTESAKQLATLFVNLCVTAETHEVSALWFLWYVKQCGGTTRIISTTN
GGQERKFVGGSGQVSERIMDLLGDRVKLERPVIYIDQTRENVLVETLNHE
MYEAKYVISAIPPTLGMKIHFNPPLPMMRNQMITRVPLGSVIKCIVYYKE
PFWRKKDYCGTMIIDGEEAPVAYTLDDTKPEGNYAAIMGFILAHKARKLA
RLTKEERLKKLCELYAKVLGSLEALEPVHYEEKNWCEEQYSGGCYTTYFP
PGILTQYGRVLRQPVDRIYFAGTETATHWSGYMEGAVEAGERAAREILHA
MGKIPEDEIWQSEPESVDVPAQPITTTFLERHLPSVPGLLRLI
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
1gos Chain B Residue 600 [
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Receptor-Ligand Complex Structure
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PDB
1gos
Structure of Human Monoamine Oxidase B, a Drug Target for the Treatment of Neurological Disorders
Resolution
3.0 Å
Binding residue
(original residue number in PDB)
V10 S15 E34 A35 G41 R42 G57 G58 S59 Y60 P234 V235 W388 Y393 C397 Y398 T426 G434 Y435 M436 A439
Binding residue
(residue number reindexed from 1)
V7 S12 E31 A32 G38 R39 G54 G55 S56 Y57 P231 V232 W385 Y390 C394 Y395 T423 G431 Y432 M433 A436
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G62 R197 K296
Catalytic site (residue number reindexed from 1)
G59 R194 K293
Enzyme Commision number
1.4.3.21
: primary-amine oxidase.
1.4.3.4
: monoamine oxidase.
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008131
primary methylamine oxidase activity
GO:0009055
electron transfer activity
GO:0016491
oxidoreductase activity
GO:0042802
identical protein binding
GO:0050660
flavin adenine dinucleotide binding
GO:0052595
aliphatic amine oxidase activity
GO:0097621
monoamine oxidase activity
Biological Process
GO:0009410
response to xenobiotic stimulus
GO:0009636
response to toxic substance
GO:0010044
response to aluminum ion
GO:0010269
response to selenium ion
GO:0014063
negative regulation of serotonin secretion
GO:0019607
phenylethylamine catabolic process
GO:0021762
substantia nigra development
GO:0032496
response to lipopolysaccharide
GO:0042420
dopamine catabolic process
GO:0045471
response to ethanol
GO:0045964
positive regulation of dopamine metabolic process
GO:0048545
response to steroid hormone
GO:0050665
hydrogen peroxide biosynthetic process
GO:0051412
response to corticosterone
Cellular Component
GO:0005739
mitochondrion
GO:0005740
mitochondrial envelope
GO:0005741
mitochondrial outer membrane
GO:0030425
dendrite
GO:0043025
neuronal cell body
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1gos
,
PDBe:1gos
,
PDBj:1gos
PDBsum
1gos
PubMed
11753429
UniProt
P27338
|AOFB_HUMAN Amine oxidase [flavin-containing] B (Gene Name=MAOB)
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