Molecule Information
General Information of the Molecule (ID: Mol01029)
Name |
Outer membrane porin C (OMPC)
,Escherichia coli
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Synonyms |
Outer membrane protein 1B; Outer membrane protein C; Porin OmpC; meoA; par; b2215; JW2203
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Molecule Type |
Protein
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Gene Name |
ompC
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Gene ID | |||||
Sequence |
MKVKVLSLLVPALLVAGAANAAEVYNKDGNKLDLYGKVDGLHYFSDNKDVDGDQTYMRLG
FKGETQVTDQLTGYGQWEYQIQGNSAENENNSWTRVAFAGLKFQDVGSFDYGRNYGVVYD VTSWTDVLPEFGGDTYGSDNFMQQRGNGFATYRNTDFFGLVDGLNFAVQYQGKNGNPSGE GFTSGVTNNGRDALRQNGDGVGGSITYDYEGFGIGGAISSSKRTDAQNTAAYIGNGDRAE TYTGGLKYDANNIYLAAQYTQTYNATRVGSLGWANKAQNFEAVAQYQFDFGLRPSLAYLQ SKGKNLGRGYDDEDILKYVDVGATYYFNKNMSTYVDYKINLLDDNQFTRDAGINTDNIVA LGLVYQF Click to Show/Hide
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Function |
Forms pores that allow passive diffusion of small molecules across the outer membrane.; FUNCTION: (Microbial infection) Supports colicin E5 entry in the absence of its major receptor OmpF.
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Uniprot ID | |||||
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Type(s) of Resistant Mechanism of This Molecule
Drug Resistance Data Categorized by Drug
Approved Drug(s)
3 drug(s) in total
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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Disease Class: Bacterial infection | [1], [2], [3] | |||
Resistant Disease | Bacterial infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Cefazolin | |||
Molecule Alteration | Expression | Down-regulation |
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Experimental Note | Discovered Using In-vivo Testing Model | |||
In Vitro Model | Escherichia coli 1422 | 562 | ||
Escherichia coli 1437 | 562 | |||
Escherichia coli B1343 | 562 | |||
Escherichia coli B1350 | 562 | |||
Escherichia coli B1421 | 562 | |||
Escherichia coli pop1010 | 562 | |||
Experiment for Drug Resistance |
Disk diffusion test assay | |||
Mechanism Description | Permeability of the outer membrane to lowmolecular-weight hydrophilic molecules is due to the presence of porin protein molecules such as OmpF and OmpC, which form pores in the outer membrane that allow small molecules to diffuse rapidly into the periplasmic space.The case of cephaloridine and cefazolin is remarkable because mutants lacking the OmpF or the OmpC proteins individually were as susceptible to cefaloridine and cefazolin as was the wild type, but mutants lacking both proteins were resistant to these Beta-lactams. |
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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Disease Class: Bacterial infection | [1], [2], [3] | |||
Resistant Disease | Bacterial infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Cephaloridine | |||
Molecule Alteration | Expression | Down-regulation |
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Experimental Note | Discovered Using In-vivo Testing Model | |||
In Vitro Model | Escherichia coli 1422 | 562 | ||
Escherichia coli 1437 | 562 | |||
Escherichia coli B1343 | 562 | |||
Escherichia coli B1350 | 562 | |||
Escherichia coli B1421 | 562 | |||
Escherichia coli pop1010 | 562 | |||
Experiment for Drug Resistance |
Disk diffusion test assay | |||
Mechanism Description | Permeability of the outer membrane to lowmolecular-weight hydrophilic molecules is due to the presence of porin protein molecules such as OmpF and OmpC, which form pores in the outer membrane that allow small molecules to diffuse rapidly into the periplasmic space.The case of cephaloridine and cefazolin is remarkable because mutants lacking the OmpF or the OmpC proteins individually were as susceptible to cefaloridine and cefazolin as was the wild type, but mutants lacking both proteins were resistant to these Beta-lactams. |
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
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Disease Class: Escherichia coli infection | [4] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Triclosan | |||
Molecule Alteration | Expression | Up-regulation |
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Experimental Note | Discovered Using In-vivo Testing Model | |||
In Vitro Model | E. coli IFN4 | 562 | ||
Experiment for Molecule Alteration |
Microarray hybridization assay | |||
Experiment for Drug Resistance |
MIC assay | |||
Mechanism Description | Concerning up-regulated porins and transporters (ompF, ompC, ykgG, ydjXYZ), they can either provide an efflux mechanism to export triclosan from the cells or accelerate the import of triclosan into the cytoplasm before the cell membrane is destabilized, thereby contributing to increasing the MICs of triclosan. |
References
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