Molecule Information
General Information of the Molecule (ID: Mol00782)
Name |
Aminoglycoside 3'-phosphotransferase (A3AP)
,Pasteurella multocida
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Synonyms |
C2800_11465
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Molecule Type |
Protein
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Gene Name |
strA
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Gene ID | |||||
Sequence |
MNRTNIFFGESHSDWLPVRGGESGDFVFRRGDGHAFAKIAPASRRGELAGERDRLIWLKG
RGVACPEVINWQEEQEGACLVITAIPGVPAADLSGADLLKAWPSMGQQLGAVHSLSVDQC PFERRLSRMFGRAVDVVSRNAVNPDFLPDEDKSTPQLDLLARVERELPVRLDQERTDMVV CHGDPCMPNFMVDPKTLQCTGLIDLGRLGTADRYADLALMIANAEENWAAPDEAERAFAV LFNVLGIEAPDRERLAFYLRLDPLTWG Click to Show/Hide
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Uniprot ID | |||||
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Type(s) of Resistant Mechanism of This Molecule
ADTT: Aberration of the Drug's Therapeutic Target
DISM: Drug Inactivation by Structure Modification
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
Streptomycin
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Aberration of the Drug's Therapeutic Target (ADTT) | ||||
Disease Class: Vibrio cholerae infection | [1] | |||
Resistant Disease | Vibrio cholerae infection [ICD-11: 1A00.0] | |||
Resistant Drug | Streptomycin | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli DH5alpha | 668369 | ||
Escherichia coli k-12 strain TOP10 | 83333 | |||
Vibrio cholerae O1 C10488 | 127906 | |||
Vibrio cholerae O1 strain CO943 | 127906 | |||
Vibrio cholerae O139 1811/98 | 45888 | |||
Vibrio cholerae O139 2055 | 45888 | |||
Vibrio cholerae O139 AS207 | 45888 | |||
Vibrio cholerae O139 E712 | 45888 | |||
Vibrio cholerae O139 HkO139-SXTS | 45888 | |||
Vibrio cholerae O139 strain MO10 | 345072 | |||
Experiment for Molecule Alteration |
Sequencing assay | |||
Mechanism Description | Many recent Asian clinical Vibrio cholerae E1 Tor O1 and O139 isolates are resistant to the antibiotics sulfamethoxazole (Su), trimethoprim (Tm), chloramphenicol (Cm), and streptomycin (Sm). The corresponding resistance genes are located on large conjugative elements (SXT constins) that are integrated into prfC on the V. cholerae chromosome. The DNA sequences of the antibiotic resistance genes in the SXT constin in MO10, an O139 isolate. In SXT(MO10), these genes are clustered within a composite transposon-like structure found near the element's 5' end. The genes conferring resistance to Cm (floR), Su (sulII), and Sm (strA and strB) correspond to previously described genes, whereas the gene conferring resistance to Tm, designated dfr18, is novel. | |||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Pasteurella multocida infection | [2] | |||
Resistant Disease | Pasteurella multocida infection [ICD-11: 1B99.0] | |||
Resistant Drug | Streptomycin | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Discovered Using In-vivo Testing Model | |||
In Vitro Model | Escherichia coli ATCC 25922 | 1322345 | ||
Staphylococcus aureus ATCC 29213 | 1280 | |||
Pasteurella multocida 36950 | 1075089 | |||
Experiment for Molecule Alteration |
Whole genome sequence assay; Allelic frequency measurement assay | |||
Experiment for Drug Resistance |
Broth microdilution method assay | |||
Mechanism Description | The analysis of one representative P. multocida isolate identified an 82 kb integrative and conjugative element (ICE) integrated into the chromosomal DNA. This ICE, designated ICEPmu1, harboured 11 resistance genes, which confer resistance to streptomycin/spectinomycin (aadA25), streptomycin (strA and strB), gentamicin (aadB), kanamycin/neomycin (aphA1), tetracycline [tetR-tet(H)], chloramphenicol/florfenicol (floR), sulphonamides (sul2), tilmicosin/clindamycin [erm(42)] or tilmicosin/tulathromycin [msr(E)-mph(E)]. |
References
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