Structure of PDB 4d50 Chain A Binding Site BS02

Receptor Information
>4d50 Chain A (length=290) Species: 9606 (Homo sapiens) [Search protein sequence] [Download receptor structure] [Download structure with residue number starting from 1] [View receptor structure]
GPLGSMVTEQEVDAIGQTLVDPKQPLQARFRALFTLRGLGGPGAIAWISQ
AFDDDSALLKHELAYCLGQMQDARAIPMLVDVLQDTRQEPMVRHEAGEAL
GAIGDPEVLEILKQYSSDPVIEVAETCQLAVRRLEWLQQHGGEPAAGPYL
SVDPAPPAEERDVGRLREALLDESRPLFERYRAMFALRNAGGEEAALALA
EGLHCGSALFRHEVGYVLGQLQHEAAVPQLAAALARCTENPMVRHECAEA
LGAIARPACLAALQAHADDPERVVRESCEVALDMYEHETG
Ligand information
Ligand IDFE
InChIInChI=1S/Fe/q+3
InChIKeyVTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
SoftwareSMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
FormulaFe
NameFE (III) ION
ChEMBL
DrugBankDB13949
ZINC
PDB chain4d50 Chain A Residue 302 [Download ligand structure] [Download structure with residue number starting from 1] [View ligand structure]
Receptor-Ligand Complex Structure
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PDB4d50 Crystal Structure of the Peroxo-Diiron(III) Intermediate of Deoxyhypusine Hydroxylase, an Oxygenase Involved in Hypusination.
Resolution1.7 Å
Binding residue
(original residue number in PDB)
H56 H240 E241
Binding residue
(residue number reindexed from 1)
H61 H245 E246
Annotation score1
Enzymatic activity
Enzyme Commision number 1.14.99.29: deoxyhypusine monooxygenase.
Gene Ontology
Molecular Function
GO:0004497 monooxygenase activity
GO:0005506 iron ion binding
GO:0005515 protein binding
GO:0019135 deoxyhypusine monooxygenase activity
GO:0046872 metal ion binding
Biological Process
GO:0008612 peptidyl-lysine modification to peptidyl-hypusine
Cellular Component
GO:0005575 cellular_component
GO:0005829 cytosol

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Molecular Function

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Biological Process

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Cellular Component
External links
PDB RCSB:4d50, PDBe:4d50, PDBj:4d50
PDBsum4d50
PubMed25865244
UniProtQ9BU89|DOHH_HUMAN Deoxyhypusine hydroxylase (Gene Name=DOHH)

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