Structure of PDB 5yak Chain A Binding Site BS03
Receptor Information
>5yak Chain A (length=215) Species:
9606
(Homo sapiens) [
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EHIPFSHNHYPEKEMVKRSQEFYELLNKRRSVRFISNEQVPMEVIDNVIR
TAGTAPSGAHTEPWTFVVVKDPDVKHKIRKIIEEEEEINYMKRMGHRWVT
DLKKLRTNWIKEYLDTAPILILIFKQVHGFAGKKKVHYYNEISVSIACGI
LLAALQNAGLVTVTTAPLNCGPRLRVLLGRPAHEKLLMLLPVGYPSKEAT
VPDLKRKPLDQIMVT
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
5yak Chain F Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
5yak
Redox control of iodotyrosine deiodinase
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
P127 S128 G129 H131 Y212
Binding residue
(residue number reindexed from 1)
P56 S57 G58 H60 Y139
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.21.1.1
: iodotyrosine deiodinase.
Gene Ontology
Molecular Function
GO:0016491
oxidoreductase activity
View graph for
Molecular Function
External links
PDB
RCSB:5yak
,
PDBe:5yak
,
PDBj:5yak
PDBsum
5yak
PubMed
30052294
UniProt
Q6PHW0
|IYD1_HUMAN Iodotyrosine deiodinase 1 (Gene Name=IYD)
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