Structure of PDB 1gyl Chain A Binding Site BS01

Receptor Information
>1gyl Chain A (length=352) Species: 3562 (Spinacia oleracea) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
MEITNVNEYEAIAKQKLPKMVYDFYASGAEDQWTLAENRNAFSRILFRPR
ILIDVTNIDMTTTILGFKISMPIMIAPTAMQKMAHPEGEYATARAASAAG
TIMTLSSWATSSVEEVASTGPGIRFFQLYVYKDRNVVAQLVRRAERAGFK
AIALTVDTPRLGRREADIKNRFVLPPFLTLKNFEGIDLGKGLSSYVAGQI
DRSLSWKDVAWLQTITSLPILVKGVITAEDARLAVQHGAAGIIVSNHGAR
QLDYVPATIMALEEVVKAAQGRIPVFLDGGVRRGTDVFKALALGAAGVFI
GRPVVFSLAAEGEAGVKKVLQMMRDEFELTMALSGCRSLKEISRSHIAAD
WD
Ligand information
Ligand IDFMN
InChIInChI=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
InChIKeyFVTCRASFADXXNN-SCRDCRAPSA-N
SMILES
SoftwareSMILES
OpenEye OEToolkits 1.7.6Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)CC(C(C(COP(=O)(O)O)O)O)O
OpenEye OEToolkits 1.7.6Cc1cc2c(cc1C)N(C3=NC(=O)NC(=O)C3=N2)C[C@@H]([C@@H]([C@@H](COP(=O)(O)O)O)O)O
ACDLabs 12.01N=2C(=O)NC(=O)C3=Nc1cc(C)c(C)cc1N(C=23)CC(O)C(O)C(O)COP(=O)(O)O
CACTVS 3.385Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[CH](O)[CH](O)[CH](O)CO[P](O)(O)=O)c2cc1C
CACTVS 3.385Cc1cc2N=C3C(=O)NC(=O)N=C3N(C[C@H](O)[C@H](O)[C@H](O)CO[P](O)(O)=O)c2cc1C
FormulaC17 H21 N4 O9 P
NameFLAVIN MONONUCLEOTIDE;
RIBOFLAVIN MONOPHOSPHATE
ChEMBLCHEMBL1201794
DrugBankDB03247
ZINCZINC000003831425
PDB chain1gyl Chain A Residue 370 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
Global viewLocal viewStructure summary

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PDB1gyl Involvement of Tyr24 and Trp108 in substrate binding and substrate specificity of glycolate oxidase.
Resolution3.0 Å
Binding residue
(original residue number in PDB)
F24 A76 P77 A79 S106 Q127 Y129 T155 K230 H254 R257 D285 G286 R289 G308 R309
Binding residue
(residue number reindexed from 1)
F24 A76 P77 A79 S106 Q127 Y129 T155 K223 H247 R250 D278 G279 R282 G301 R302
Annotation score1
Enzymatic activity
Catalytic site (original residue number in PDB) S106 Y129 T155 D157 K230 H254
Catalytic site (residue number reindexed from 1) S106 Y129 T155 D157 K223 H247
Enzyme Commision number 1.1.3.15: (S)-2-hydroxy-acid oxidase.
Gene Ontology
Molecular Function
GO:0003973 (S)-2-hydroxy-acid oxidase activity
GO:0010181 FMN binding
GO:0016491 oxidoreductase activity
Biological Process
GO:0009853 photorespiration
GO:0009854 oxidative photosynthetic carbon pathway
GO:0051707 response to other organism
Cellular Component
GO:0005777 peroxisome

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:1gyl, PDBe:1gyl, PDBj:1gyl
PDBsum1gyl
PubMed7705356
UniProtP05414|GOX_SPIOL Glycolate oxidase

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