General Information of the Molecule (ID: Mol00827)
Name
Beta-lactamase (BLA) ,Pseudomonas aeruginosa
Synonyms
blaOxa-50c; blaOXA-50b; blaOXA-50g; IPC1494_23315; IPC152_19190; IPC1595_21065; IPC57_19425; IPC607_22635; EC 3.5.2.6; OXA-50 family oxacillin-hydrolyzing class D beta-lactamase OXA-488; Oxacillinase
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Molecule Type
Protein
Gene Name
blaOxa-50c
Sequence
MRPLLFSALLLLSGHAQASEWNDSRAVDKLFGAAGVKGTFVLYDVQRQRYVGHDRERAET
RFVPASTYKVANSLIGLSTGAVRSADEVLPYGGKPQRFKAWEHDMSLRDAIKASNVPVYQ
ELARRIGLERMRANVSRLGYGNAEIGQVVDNFWLVGPLKISAMEQTRFLLRLAQGELPFP
APVQSTVRAMTLLESGPGWELHGKTGWCFDCTPELGWWVGWVKRNERLYGFALNIDMPGG
EADIGKRVELGKASLKALGILP
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Uniprot ID
Q6JTT6_PSEAI
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Kingdom: N.A.
Phylum: Proteobacteria
Class: Gammaproteobacteria
Order: Pseudomonadales
Family: Pseudomonadaceae
Genus: Pseudomonas
Species: Pseudomonas aeruginosa
Type(s) of Resistant Mechanism of This Molecule
  DISM: Drug Inactivation by Structure Modification
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
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Ampicillin
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Drug Resistance Data Categorized by Their Corresponding Mechanisms
       Drug Inactivation by Structure Modification (DISM) Click to Show/Hide
Disease Class: Pseudomonas aeruginosa infection [1]
Resistant Disease Pseudomonas aeruginosa infection [ICD-11: 1A00-1C4Z]
Resistant Drug Ampicillin
Molecule Alteration Expression
Inherence
Experimental Note Identified from the Human Clinical Data
In Vitro Model Pseudomonas aeruginosa PAO1 208964
Experiment for
Molecule Alteration
DNA sequencing and protein assay
Experiment for
Drug Resistance
Disk diffusion assay
Mechanism Description P. aeruginosa harbors two naturally encoded Beta-lactamase genes, one of which encodes an inducible cephalosporinase and the other of which encodes a constitutively expressed oxacillinase. OXA-50 is a kind of oxacillinase which lead to drug resistance.
References
Ref 1 Biochemical characterization of the naturally occurring oxacillinase OXA-50 of Pseudomonas aeruginosa. Antimicrob Agents Chemother. 2004 Jun;48(6):2043-8. doi: 10.1128/AAC.48.6.2043-2048.2004.

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