CATH Classification

Domain Context

CATH Clusters

Superfamily 3.40.630.30
Functional Family Phosphotransferase enzyme family protein

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
2.7.1.-
Phosphotransferases with an alcohol group as acceptor.
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.
Smith, C.A., Toth, M., Weiss, T.M., Frase, H., Vakulenko, S.B.
Acta Crystallogr.,Sect.D