Structure of PDB 5gxu Chain A Binding Site BS01
Receptor Information
>5gxu Chain A (length=552) Species:
3702
(Arabidopsis thaliana) [
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KKVTIFFGTQTGTAEGFAKALGEEAKARYEKTRFKIVDLDDYAADDDEYE
EKLKKEDVAFFFLATYGDGEPTDNAARFYKWFTEGNDRGEWLKNLKYGVF
GLGNRQYEHFNKVAKVVDDILVEQGAQRLVQVGLGDDDQCIEDDFTAWRE
ALWPELDTILYTVFDAQHPYKANVAVKRELHTPESDRSCIHLEFDIAGSG
LTYETGDHVGVLCDNLSETVDEALRLLDMSPDTYFSLPFPPCNLRTALTR
YACLLSSPKKSALVALAAHASDPTEAERLKHLASPAGKDEYSKWVVESQR
SLLEVMAEFPSAKPPLGVFFAGVAPRLQPRFYSISSSPKIAETRIHVTCA
LVYEKMPTGRIHKGVCSTWMKNAVPYEKSENCSSAPIFVRQSNFKLPSDS
KVPIIMIGPGTGLAPFRGFLQERLALVESGVELGPSVLFFGCRNRRMDFI
YEEELQRFVESGALAELSVAFSREGPTKEYVQHKMMDKASDIWNMISQGA
YLYVCGDAKGMARDVHRSLHTIAQEQGSMDSTKAEGFVKNLQTSGRYLRD
VW
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
5gxu Chain A Residue 801 [
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Receptor-Ligand Complex Structure
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PDB
5gxu
Structure of the Arabidopsis thaliana NADPH-cytochrome P450 reductase 2 (ATR2) provides insight into its function
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
T111 Q112 T113 T115 A116 T167 Y168 G169 G205 N206 Y209 H211 F212 D239
Binding residue
(residue number reindexed from 1)
T9 Q10 T11 T13 A14 T65 Y66 G67 G103 N104 Y107 H109 F110 D137
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
Y491 S492 C664 D709 W711
Catalytic site (residue number reindexed from 1)
Y332 S333 C505 D550 W552
Enzyme Commision number
1.6.2.4
: NADPH--hemoprotein reductase.
Gene Ontology
Molecular Function
GO:0003958
NADPH-hemoprotein reductase activity
GO:0010181
FMN binding
GO:0016491
oxidoreductase activity
GO:0016651
oxidoreductase activity, acting on NAD(P)H
GO:0050660
flavin adenine dinucleotide binding
GO:0050661
NADP binding
Biological Process
GO:0009698
phenylpropanoid metabolic process
Cellular Component
GO:0005737
cytoplasm
GO:0005783
endoplasmic reticulum
GO:0005789
endoplasmic reticulum membrane
GO:0005886
plasma membrane
GO:0009507
chloroplast
GO:0016020
membrane
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5gxu
,
PDBe:5gxu
,
PDBj:5gxu
PDBsum
5gxu
PubMed
28103421
UniProt
Q9SUM3
|NCPR2_ARATH NADPH--cytochrome P450 reductase 2 (Gene Name=ATR2)
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