Structure of PDB 4bgk Chain A Binding Site BS02
Receptor Information
>4bgk Chain A (length=385) Species:
9606
(Homo sapiens) [
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MACTIQKAEALDGAHLMQILWYDEEESLYPAVWLRDNCPCSDCYLDSAKA
RKLLVEALDVNIGIKGLIFDRKKVYITWPDEHYSEFQADWLKKRCFSKQA
RAKLQRELFFPECQYWGSELQLPTLDFEDVLRYDEHAYKWLSTLKKVGIV
RLTGASDKPGEVSKLGKRMGFLYLTFYGHTWQVQDKIDANNVAYTTGKLS
FHTDYPALHHPPGVQLLHCIKQTVTGGDSEIVDGFNVCQKLKKNNPQAFQ
ILSSTFVDFTDIGVDYCDFSVQSKHKIIELDDKGQVVRINFNNATRDTIF
DVPVERVQPFYAALKEFVDLMNSKESKFTFKMNPGDVITFDNWRLLHGRR
SYEAGTEISRHLEGAYADWDVVMSRLRILRQRVEN
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
4bgk Chain A Residue 402 [
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Receptor-Ligand Complex Structure
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PDB
4bgk
Targeting Carnitine Biosynthesis: Discovery of New Inhibitors Against Gamma-Butyrobetaine Hydroxylase.
Resolution
2.18 Å
Binding residue
(original residue number in PDB)
H202 D204 H347
Binding residue
(residue number reindexed from 1)
H202 D204 H347
Annotation score
1
Enzymatic activity
Enzyme Commision number
1.14.11.1
: gamma-butyrobetaine dioxygenase.
Gene Ontology
Molecular Function
GO:0005506
iron ion binding
GO:0005515
protein binding
GO:0008270
zinc ion binding
GO:0008336
gamma-butyrobetaine dioxygenase activity
GO:0016491
oxidoreductase activity
GO:0016706
2-oxoglutarate-dependent dioxygenase activity
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
Biological Process
GO:0045329
carnitine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005829
cytosol
GO:0070062
extracellular exosome
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4bgk
,
PDBe:4bgk
,
PDBj:4bgk
PDBsum
4bgk
PubMed
24571165
UniProt
O75936
|BODG_HUMAN Gamma-butyrobetaine dioxygenase (Gene Name=BBOX1)
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