CATH Classification
Level | CATH Code | Description |
---|---|---|
3 | Alpha Beta | |
3.40 | 3-Layer(aba) Sandwich | |
3.40.630 | Aminopeptidase | |
3.40.630.30 | Gcn5-related N-acetyltransferase (GNAT) |
Domain Context
CATH Clusters
Superfamily | 3.40.630.30 |
Functional Family |
Enzyme Information
2.7.1.190 |
Aminoglycoside 2''-phosphotransferase.
based on mapping to UniProt Q7ATH7
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 Q7ATH7
|
UniProtKB Entries (1)
Q7ATH7 |
AACA_STAWA
Staphylococcus warneri
Bifunctional AAC/APH
|
PDB Structure
PDB | 4QC6 |
External Links | |
Method | X-RAY DIFFRACTION |
Organism | |
Primary Citation |
Structure of the bifunctional aminoglycoside-resistance enzyme AAC(6')-Ie-APH(2'')-Ia revealed by crystallographic and small-angle X-ray scattering analysis.
Acta Crystallogr.,Sect.D
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