Molecule Information
General Information of the Molecule (ID: Mol04418)
| Name |
Membrane-associated protein TcaA (tcaA)
,Homo sapiens
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| Molecule Type |
Protein
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| Gene Name |
tcaA
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| Sequence |
MKSCPKCGQQAQDDVQICTQCGHKFDSRQALYRKSTDEDIQTNNIKMRKMVPWAIGFFIL
ILIIILFFLLRNFNSPEAQTKILVNAIENNDKQKVATLLSTKDNKVDSEEAKVYINYIK D EVGLKQFVSDLKNTVHKLNKSKTSVASYIQTRSGQNILRVSKNGTRYIFFDNMSFTAP TK QPIVKPKEKTKYEFKSGGKKKMVIAEANKVTPIGNFILGTYRIPAMKSTENGDFAGY LKF DFRQSNSETVDVTEDFEEANITVTLKGDTKLNDSSKKVTINDREMAFSSSKTYGPY PQNK DITISASGKAKGKTFTTQTKTIKASDLKYNTEITLNFDSEDIEDYVEKKEKEENS LKNKL IEFFAGYSLANNAAFNQSDFDFVSSYIKKGSSFYDDVKKRVSKGSLMMISSPQI IDAEKH GDKITATVRLINENGKQVDKEYELEQGSQDRLQLIKTSEK Click to Show/Hide
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| Function |
Plays a major role in decreasing resistance to glycopeptideantibiotics. {ECO:0000250}.
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| Uniprot ID | |||||
| Click to Show/Hide the Complete Species Lineage | |||||
Type(s) of Resistant Mechanism of This Molecule
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
| Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Staphylococcus aureus infection [ICD-11: 1B54.0] | [1] | |||
| Resistant Disease | Staphylococcus aureus infection [ICD-11: 1B54.0] | |||
| Resistant Drug | Oxacillin | |||
| Molecule Alteration | Expression | . |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| Experiment for Molecule Alteration |
qPCR | |||
| Experiment for Drug Resistance |
E-test assay | |||
| Mechanism Description | The MIC of penicillin plus clavulanate decreased from 3 mg/L to 0.064 mg/L and that of oxacillin decreased from 16 to 0.5 mg/L when?tcaA?was knocked out in the LAC strain. Compared with wild-type MRSA isolates, when?tcaA?was deleted, all selected strains were more susceptible to beta-lactams. Susceptibility to ceftobiprole was restored in the ceftobiprole-resistant strain when?tcaA?was deleted.?tcaA?knockout caused "log-like" abnormal division of MRSA, and?tcaA?deficiency mediated low expression of?mecA, ponA, and?murA2. tcaA is a potential resistance breaker target for beta-lactams, including ceftobiprole, in MRSA. | |||
| Drug Sensitivity Data Categorized by Their Corresponding Mechanisms | ||||
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| Disease Class: Staphylococcus aureus infection [ICD-11: 1B54.0] | [1] | |||
| Sensitive Disease | Staphylococcus aureus infection [ICD-11: 1B54.0] | |||
| Sensitive Drug | Oxacillin | |||
| Molecule Alteration | Expression | . |
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| Experimental Note | Revealed Based on the Cell Line Data | |||
| Experiment for Molecule Alteration |
qPCR | |||
| Experiment for Drug Resistance |
E-test assay | |||
| Mechanism Description | The MIC of penicillin plus clavulanate decreased from 3 mg/L to 0.064 mg/L and that of oxacillin decreased from 16 to 0.5 mg/L when?tcaA?was knocked out in the LAC strain. Compared with wild-type MRSA isolates, when?tcaA?was deleted, all selected strains were more susceptible to beta-lactams. Susceptibility to ceftobiprole was restored in the ceftobiprole-resistant strain when?tcaA?was deleted.?tcaA?knockout caused "log-like" abnormal division of MRSA, and?tcaA?deficiency mediated low expression of?mecA, ponA, and?murA2. tcaA is a potential resistance breaker target for beta-lactams, including ceftobiprole, in MRSA. | |||
References
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