Structure of PDB 5fa6 Chain B Binding Site BS01
Receptor Information
>5fa6 Chain B (length=602) Species:
9606
(Homo sapiens) [
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SSFVEKMKKTGRNIIVFYGSQTGTAEEFANRLSKDAHRYGMRGMSADPEE
YDLADLSSLPEIDNALVVFCMATYGEGDPTDNAQDFYDWLQETDVDLSGV
KFAVFGLGNKTYEHFNAMGKYVDKRLEQLGAQRIFELGLGDDDGNLEEDF
ITWREQFWPAVCEHFGVEATSIRQYELVVHTDIDAAKVYMGEMGRLKSYE
NQKPPFDAKNPFLAAVTTNRKLNQGTERHLMHLELDISDSKIRYESGDHV
AVYPANDSALVNQLGKILGADLDVVMSLNNLDEESNKKHPFPCPTSYRTA
LTYYLDITNPPRTNVLYELAQYASEPSEQELLRKMASSSGEGKELYLSWV
VEARRHILAILQDCPSLRPPIDHLCELLPRLQARYYSIASSSKVHPNSVH
ICAVVVEYETKAGRINKGVATNWLRAKEPARALVPMFVRKSQFRLPFKAT
TPVIMVGPGTGVAPFIGFIQERAWLRQQGKEVGETLLYYGCRRSDEDYLY
REELAQFHRDGALTQLNVAFSREQSHKVYVQHLLKQDREHLWKLIEGGAH
IYVCGDARNMARDVQNTFYDIVAELGAMEHAQAVDYIKKLMTKGRYSLDV
WS
Ligand information
Ligand ID
FMN
InChI
InChI=1S/C17H21N4O9P/c1-7-3-9-10(4-8(7)2)21(15-13(18-9)16(25)20-17(26)19-15)5-11(22)14(24)12(23)6-30-31(27,28)29/h3-4,11-12,14,22-24H,5-6H2,1-2H3,(H,20,25,26)(H2,27,28,29)/t11-,12+,14-/m0/s1
InChIKey
FVTCRASFADXXNN-SCRDCRAPSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)O)O)O)O
OpenEye OEToolkits 1.7.6
Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O
ACDLabs 12.01
N=2C(=O)NC(=O)C3=Nc1cc(C)c(C)cc1N(C=23)CC(O)C(O)C(O)COP(=O)(O)O
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(O)=O)c2cc1C
CACTVS 3.385
Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P](O)(O)=O)c2cc1C
Formula
C17 H21 N4 O9 P
Name
FLAVIN MONONUCLEOTIDE;
RIBOFLAVIN MONOPHOSPHATE
ChEMBL
CHEMBL1201794
DrugBank
DB03247
ZINC
ZINC000003831425
PDB chain
5fa6 Chain B Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
5fa6
Instability of the Human Cytochrome P450 Reductase A287P Variant Is the Major Contributor to Its Antley-Bixler Syndrome-like Phenotype.
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
S89 Q90 T91 T93 A94 T142 Y143 G144 L176 G177 N178 Y181
Binding residue
(residue number reindexed from 1)
S20 Q21 T22 T24 A25 T73 Y74 G75 L107 G108 N109 Y112
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y459 S460 C632 D677 W679
Catalytic site (residue number reindexed from 1)
Y386 S387 C554 D599 W601
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
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5fa6
,
PDBe:5fa6
,
PDBj:5fa6
PDBsum
5fa6
PubMed
27496950
UniProt
P16435
|NCPR_HUMAN NADPH--cytochrome P450 reductase (Gene Name=POR)
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