Molecule Information
General Information of the Molecule (ID: Mol02049)
Name |
Bifunctional dihydrofolate reductase-thymidylate synthase (PVDHFR)
,Plasmodium vivax
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Synonyms |
dhfr; dfhr
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Molecule Type |
Protein
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Gene Name |
Pvdhfr
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Sequence |
MEDLSDVFDIYAICACCKVAPTSEGTKNEPFSPRTFRGLGNKGTLPWKCNSVDMKYFRSV
TTYVDESKYEKLKWKRERYLRMEASQGGGDNTSGGDNTHGGDNADKLQNVVVMGRSNWES IPKQYKPLPNRINVVLSKTLTKEDVKEKVFIIDSIDDLLLLLKKLKYYKCFIIGGAQVYR ECLSRNLIKQIYFTRIN Click to Show/Hide
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Function |
Bifunctional enzyme. Involved in de novo dTMP biosynthesis. Key enzyme in folate metabolism. Catalyzes an essential reaction for de novo glycine and purine synthesis, DNA precursor synthesis, and for the conversion of dUMP to dTMP.
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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
Drug Resistance Data Categorized by Drug
Approved Drug(s)
1 drug(s) in total
Pyrimethamine/Sulfadoxine
Drug Resistance Data Categorized by Their Corresponding Mechanisms | ||||
Aberration of the Drug's Therapeutic Target (ADTT) | ||||
Disease Class: Plasmodium vivax malaria | [1] | |||
Resistant Disease | Plasmodium vivax malaria [ICD-11: 1F41.0] | |||
Resistant Drug | Pyrimethamine/Sulfadoxine | |||
Molecule Alteration | SNP | . |
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Experimental Note | Identified from the Human Clinical Data | |||
In Vitro Model | Red blood cells | Blood | Homo sapiens (Human) | N.A. |
Experiment for Molecule Alteration |
Whole genome sequencing assay | |||
Experiment for Drug Resistance |
Giemsa stain assay | |||
Mechanism Description | The lack of copy number variation of pvgch1 suggests that SP-resistant P. vivax may harbor alternative mechanisms to secure sufficient folate.The quadruple mutant haplotypes 57I/L/58R/61M/117T of pvdhfr gene were the most common (comprising 76% of cases in Myitsone and 43.7% of case in Laiza). The double mutant haplotype 383G/553G of pvdhps gene was also prevalent at each site. |
References
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