Structure of PDB 2ia5 Chain H Binding Site BS01
Receptor Information
>2ia5 Chain H (length=301) Species:
10665
(Tequatrovirus T4) [
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MKKIILTIGCPGSGKSTWAREFIAKNPGFYNINRDDYRQSIMAHEERDEY
KYTKKKEGIVTGMQFDTAKSILYGGDSVKGVIISDTNLNPERRLAWETFA
KEYGWKVEHKVFDVPWTELVKRNSKRGTKAVPIDVLRSMYKSMREYLGLP
VYNGTPGKPKAVIFDVDGTLAKMNGRGPYDLEKCDTDVINPMVVELSKMY
ALMGYQIVVVSGRESGTKEDPTKYYRMTRKWVEDIAGVPLVMQCQREQGD
TRKDDVVKEEIFWKHIAPHFDVKLAIDDRTQVVEMWRRIGVECWQVASGD
F
Ligand information
Ligand ID
MG
InChI
InChI=1S/Mg/q+2
InChIKey
JLVVSXFLKOJNIY-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mg+2]
CACTVS 3.341
[Mg++]
Formula
Mg
Name
MAGNESIUM ION
ChEMBL
DrugBank
DB01378
ZINC
PDB chain
2ia5 Chain H Residue 906 [
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Receptor-Ligand Complex Structure
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PDB
2ia5
Structure-function analysis of the 3' phosphatase component of T4 polynucleotide kinase/phosphatase.
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
D165 D167
Binding residue
(residue number reindexed from 1)
D165 D167
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K15 D35 R126 D165
Catalytic site (residue number reindexed from 1)
K15 D35 R126 D165
Enzyme Commision number
2.7.1.78
: polynucleotide 5'-hydroxyl-kinase.
3.1.3.34
: deoxynucleotide 3'-phosphatase.
Gene Ontology
Molecular Function
GO:0005524
ATP binding
GO:0016301
kinase activity
GO:0016787
hydrolase activity
GO:0046404
ATP-dependent polydeoxyribonucleotide 5'-hydroxyl-kinase activity
GO:0047846
deoxynucleotide 3'-phosphatase activity
GO:0051734
ATP-dependent polynucleotide 5'-hydroxyl-kinase activity
Biological Process
GO:0006281
DNA repair
GO:0016310
phosphorylation
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:2ia5
,
PDBe:2ia5
,
PDBj:2ia5
PDBsum
2ia5
PubMed
17493655
UniProt
P06855
|KIPN_BPT4 Polynucleotide kinase (Gene Name=pseT)
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