Structure of PDB 3qfr Chain A Binding Site BS01
Receptor Information
>3qfr Chain A (length=604) Species:
9606
(Homo sapiens) [
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SSFVEKMKKTGRNIIVFYGSQTGTAEEFANRLSKDAHRYGMRGMSADPEE
YDLADLSSLPEIDNALVVFCMATYGEGDPTDNAQDFYDWLQETDVDLSGV
KFAVFGLGNKTYEHFNAMGKYVDKRLEQLGAQRIFELGLGDDDGNLEEDF
ITWREQFWPAVCEHFGVEATGEESSIRQYELVVHTDIDAAKVYMGEMGRL
KSYENQKPPFDAKNPFLAAVTTNRKLNQGTERHLMHLELDISDSKIRYES
GDHVAVYPANDSALVNQLGKILGADLDVVMSLNNLDEESNKKHPFPCPTS
YRTALTYYLDITNPPRTNVLYELAQYASEPSEQELLRKMASSSGEGKELY
LSWVVEARRHILAILQDCPSLRPPIDHLCELLPRLQAHYYSIASSSKVHP
NSVHICAVVVEYETKAGRINKGVATNWLRAKEPALVPMFVRKSQFRLPFK
ATTPVIMVGPGTGVAPFIGFIQERAWLRQQGKEVGETLLYYGCRRSDEDY
LYREELAQFHRDGALTQLNVAFSREQSHKVYVQHLLKQDREHLWKLIEGG
AHIYVCGDARNMARDVQNTFYDIVAELGAMEHAQAVDYIKKLMTKGRYSL
DVWS
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
3qfr Chain A Residue 752 [
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Receptor-Ligand Complex Structure
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PDB
3qfr
Structural basis for human NADPH-cytochrome P450 oxidoreductase deficiency.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
H322 R427 H457 Y458 Y459 S460 A476 V479 Y481 G491 V492 A493 T494 W679
Binding residue
(residue number reindexed from 1)
H253 R358 H388 Y389 Y390 S391 A407 V410 Y412 G422 V423 A424 T425 W603
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
Y459 S460 C632 D677 W679
Catalytic site (residue number reindexed from 1)
Y390 S391 C556 D601 W603
Enzyme Commision number
1.6.2.4
: NADPH--hemoprotein reductase.
Gene Ontology
Molecular Function
GO:0003958
NADPH-hemoprotein reductase activity
GO:0005515
protein binding
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0050660
flavin adenine dinucleotide binding
GO:0050661
NADP binding
Biological Process
GO:0006805
xenobiotic metabolic process
GO:0009725
response to hormone
GO:0022900
electron transport chain
GO:0032770
positive regulation of monooxygenase activity
GO:0090346
cellular organofluorine metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005829
cytosol
GO:0016020
membrane
GO:0043231
intracellular membrane-bounded organelle
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3qfr
,
PDBe:3qfr
,
PDBj:3qfr
PDBsum
3qfr
PubMed
21808038
UniProt
P16435
|NCPR_HUMAN NADPH--cytochrome P450 reductase (Gene Name=POR)
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