Molecule Information
General Information of the Molecule (ID: Mol01002)
Name |
Metallo-beta-lactamase (VIM1)
,Achromobacter denitrificans
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Synonyms |
blaVIM-1; VIM-1 metallo-beta-lactamase
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Molecule Type |
Protein
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Gene Name |
blaVIM-1
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Sequence |
MLKVISSLLVYMTASVMAVASPLAHSGEPSGEYPTVNEIPVGEVRLYQIADGVWSHIATQ
SFDGAVYPSNGLIVRDGDELLLIDTAWGAKNTAALLAEIEKQIGLPVTRAVSTHFHDDRV GGVDVLRAAGVATYASPSTRRLAEAEGNEIPTHSLEGLSSSGDAVRFGPVELFYPGAAHS TDNLVVYVPSANVLYGGCAVHELSSTSAGNVADADLAEWPTSVERIQKHYPEAEVVIPGH GLPGGLDLLQHTANVVKAHKNRSVAE Click to Show/Hide
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Uniprot ID | |||||
Click to Show/Hide the Complete Species Lineage | |||||
Type(s) of Resistant Mechanism of This Molecule
DISM: Drug Inactivation by Structure Modification
Drug Resistance Data Categorized by Drug
Approved Drug(s)
9 drug(s) in total
Ampicillin
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Ampicillin | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Ampicillin | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Aztreonam
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Aztreonam | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Aztreonam | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Cefepime
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Cefepime | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Cefepime | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Cefotaxime
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Cefotaxime | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Cefotaxime | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Ceftazidime
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Ceftazidime | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Ceftazidime | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Meropenem
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Meropenem | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Meropenem | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Mezlocillin
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Mezlocillin | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Mezlocillin | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Piperacillin
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Piperacillin | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Piperacillin | |||
Molecule Alteration | Expression | Acquired |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
Imipenem
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Drug Inactivation by Structure Modification (DISM) | ||||
Disease Class: Achromobacter xylosoxydans infection | [1] | |||
Resistant Disease | Achromobacter xylosoxydans infection [ICD-11: 1A00-1C4Z] | |||
Resistant Drug | Imipenem | |||
Molecule Alteration | Expression | Inherence |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | A. xylosoxydans AX22 exhibited broad-spectrum resistance to Beta-lactams and aminoglycosides. The Beta-lactam resistance pattern (including piperacillin, ceftazidime, and carbapenem resistance) was unusual for this species, and the high-level carbapenem resistance suggested the production of an acquired carbapenemase. In fact, carbapenemase activity was detected in a crude extract of AX22 (specific activity, 184 +/- 12 U/mg of protein), and this activity was reduced (>80%) after incubation of the crude extract with 2 mM EDTA, suggesting the presence of a metallo-Beta-lactamase determinant. | |||
Disease Class: Escherichia coli infection | [1] | |||
Resistant Disease | Escherichia coli infection [ICD-11: 1A03.0] | |||
Resistant Drug | Imipenem | |||
Molecule Alteration | Expression | Acquired |
||
Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Escherichia coli | 668369 | ||
Achromobacter xylosoxydans subsp. denitrificans AX-22 | 85698 | |||
Escherichia coli MkD-135 | 562 | |||
Pseudomonas aeruginosa 10145/3 | 287 | |||
Experiment for Molecule Alteration |
DNA extraction and Sequencing assay | |||
Experiment for Drug Resistance |
Macrodilution broth method assay | |||
Mechanism Description | Electroporation of Escherichia coli DH5alpha with the purified plasmid preparation yielded ampicillin-resistant transformants which contained a plasmid apparently identical to pAX22 (data not shown). DH5alpha(pAX22) produced carbapenemase activity (specific activity of crude extract, 202 +/- 14 U/mg of protein) and, compared to DH5alpha, exhibited a decreased susceptibility to several Beta-lactams. |
References
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