Structure of PDB 5dqr Chain D Binding Site BS03

Receptor Information
>5dqr Chain D (length=411) Species: 3702 (Arabidopsis thaliana) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
EDWREKSRPIPPGGTYPAKDHCSQCGLCDTYYIAHVKEACAFLGDGMSRI
ESLEPVVHGRGRKADSLQDTYFGVHQEQLYARKLKPVEGAQWTGIVTTIA
IEMLKSNMVEAVVCVQSDPEDRLSPRPVLARTPEEVLAARGVKPTLSPNL
NTLELIEASGVKRLLFCGVGCQVQALRSVEQHLNLEKLYVLGTNCVDNGT
RDGLDKFLKAASKEPETVLHYEFMQDYKVQLKHLDGHIEEVPYFSLPAND
LVDVIAPSCYSCFDYTNALADLVIGYMGVPKYSGLNMTDHPQYITVRNER
GKEMLSLVENLLEITPTISSGDRRPFVTETVKADDAPAPLFVGNIIAFIL
NLVGPKGLEFARYSLDYHTIRNYLYVNRKWGKQRANTHMPSYAKKIVEMY
NKNGQIDKMLS
Ligand information
Ligand IDFAD
InChIInChI=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
InChIKeyVWWQXMAJTJZDQX-UYBVJOGSSA-N
SMILES
SoftwareSMILES
CACTVS 3.341Cc1cc2N=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 1.5.0Cc1cc2c(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 1.5.0Cc1cc2c(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 3.341Cc1cc2N=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 10.04O=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
FormulaC27 H33 N9 O15 P2
NameFLAVIN-ADENINE DINUCLEOTIDE
ChEMBLCHEMBL1232653
DrugBankDB03147
ZINCZINC000008215434
PDB chain5dqr Chain D Residue 503 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
[Spin on] [Spin off] [Reset]
[High quality] [Low quality]
[White background] [Black background]
PDB5dqr Crystal Structure and Catalytic Mechanism of 7-Hydroxymethyl Chlorophyll a Reductase
Resolution2.7 Å
Binding residue
(original residue number in PDB)		Q131 W132 G134 I135 V136 T137 V155 A179 G181 V182 K183 S187 T233 N234 C235 E262 Y305 I314 G315 Y316 M317 Q332
Binding residue
(residue number reindexed from 1)		Q91 W92 G94 I95 V96 T97 V115 A139 G141 V142 K143 S147 T193 N194 C195 E222 Y265 I274 G275 Y276 M277 Q292
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) D237 E262 Q332 H417
Catalytic site (residue number reindexed from 1) D197 E222 Q292 H368
Enzyme Commision number 1.17.7.2: 7-hydroxymethyl chlorophyll a reductase.
Gene Ontology
Molecular Function
GO:0003824 catalytic activity
GO:0016491 oxidoreductase activity
GO:0046872 metal ion binding
GO:0051536 iron-sulfur cluster binding
GO:0090415 7-hydroxymethyl chlorophyll a reductase activity
Biological Process
GO:0015994 chlorophyll metabolic process
GO:0033354 chlorophyll cycle
Cellular Component
GO:0005576 extracellular region
GO:0009507 chloroplast

View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB RCSB:5dqr, PDBe:5dqr, PDBj:5dqr
PDBsum5dqr
PubMed27072131
UniProtQ8GS60|HCAR_ARATH 7-hydroxymethyl chlorophyll a reductase, chloroplastic (Gene Name=HCAR)

[Back to BioLiP]