Structure of PDB 6n55 Chain E Binding Site BS01
Receptor Information
>6n55 Chain E (length=214) Species:
9606
(Homo sapiens) [
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GEPFLIGVSGGTASGKSSVCAKIVQLLGQNEVDYRQKQVVILSQDSFYRV
LTSEQKAKALKGQFNFDHPDAFDNELILKTLKEITEGKTVQIPVYDFVSH
SRKEETVTVYPADVVLFEGILAFYSQEVRDLFQMKLFVDTDADTRLSRRV
LRDISERGRDLEQILSQYITFVKPAFEEFCLPTKKYADVIIPRGADNLVA
INLIVQHIQDILNG
Ligand information
Ligand ID
UZ0
InChI
InChI=1S/C9H11N5O5/c10-13-12-6-7(17)4(3-15)19-8(6)14-2-1-5(16)11-9(14)18/h1-2,4,6-8,15,17H,3H2,(H,11,16,18)/t4-,6-,7-,8-/m1/s1
InChIKey
MRUKYOQQKHNMFI-XVFCMESISA-N
SMILES
Software
SMILES
CACTVS 3.385
OC[C@H]1O[C@H]([C@H](N=[N+]=[N-])[C@@H]1O)N2C=CC(=O)NC2=O
OpenEye OEToolkits 2.0.7
C1=CN(C(=O)NC1=O)C2C(C(C(O2)CO)O)N=[N+]=[N-]
OpenEye OEToolkits 2.0.7
C1=CN(C(=O)NC1=O)[C@H]2[C@@H]([C@@H]([C@H](O2)CO)O)N=[N+]=[N-]
CACTVS 3.385
OC[CH]1O[CH]([CH](N=[N+]=[N-])[CH]1O)N2C=CC(=O)NC2=O
ACDLabs 12.01
N1(C=CC(NC1=O)=O)C2OC(C(C2N=[N+]=[N-])O)CO
Formula
C9 H11 N5 O5
Name
2'-azido-2'-deoxyuridine
ChEMBL
DrugBank
ZINC
ZINC000006091560
PDB chain
6n55 Chain E Residue 306 [
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Receptor-Ligand Complex Structure
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PDB
6n55
An optimized chemical-genetic method for cell-specific metabolic labeling of RNA.
Resolution
3.085 Å
Binding residue
(original residue number in PDB)
F83 R174
Binding residue
(residue number reindexed from 1)
F66 R157
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.7.1.48
: uridine/cytidine kinase.
Gene Ontology
Molecular Function
GO:0004849
uridine kinase activity
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0042802
identical protein binding
GO:0043771
cytidine kinase activity
Biological Process
GO:0009224
CMP biosynthetic process
GO:0016310
phosphorylation
GO:0044206
UMP salvage
GO:0044211
CTP salvage
Cellular Component
GO:0005575
cellular_component
GO:0005737
cytoplasm
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:6n55
,
PDBe:6n55
,
PDBj:6n55
PDBsum
6n55
PubMed
32015544
UniProt
Q9BZX2
|UCK2_HUMAN Uridine-cytidine kinase 2 (Gene Name=UCK2)
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