CATH Classification
Level | CATH Code | Description |
---|---|---|
3 | Alpha Beta | |
3.30 | 2-Layer Sandwich | |
3.30.200 | Phosphorylase Kinase; domain 1 | |
3.30.200.20 | Phosphorylase Kinase; domain 1 |
Domain Context
CATH Clusters
Superfamily | Phosphorylase Kinase; domain 1 |
Functional Family |
Enzyme Information
2.7.1.190 |
Aminoglycoside 2''-phosphotransferase.
based on mapping to UniProt P0A0C1
GTP + gentamicin = GDP + gentamicin 2''-phosphate.
-!- This bacterial enzyme phosphorylates many 4,6-disubstituted aminoglycoside antibiotics that have a hydroxyl group at position 2'', including kanamycin A, kanamycin B, tobramycin, dibekacin, arbekacin, amikacin, gentamicin C, sisomicin and netilmicin. -!- In most, but not all, cases the phosphorylation confers resistance against the antibiotic. -!- Some forms of the enzyme use ATP as a phosphate donor in appreciable amount. -!- The enzyme is often found as a bifunctional enzyme that also catalyzes 6'-aminoglycoside N-acetyltransferase activity. -!- The bifunctional enzyme is the most clinically important aminoglycoside-modifying enzyme in Gram-positive bacteria, responsible for high-level resistance in both Enterococci and Staphylococci.
|
2.3.1.- |
Transferring groups other than amino-acyl groups.
based on mapping to UniProt P0A0C1
|
UniProtKB Entries (1)
P0A0C1 |
AACA_STAAU
Staphylococcus aureus
Bifunctional AAC/APH
|
PDB Structure
PDB | 5IQE |
External Links | |
Method | X-RAY DIFFRACTION |
Organism | |
Primary Citation |
Antibiotic Binding Drives Catalytic Activation of Aminoglycoside Kinase APH(2)-Ia.
Structure
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