PXD008987 is an
original dataset announced via ProteomeXchange.
Dataset Summary
Title | Chemoproteomic identification of molecular targets of antifungal prototypes, thiosemicarbazide and a camphene derivative of thiosemicarbazide, in Paracoccidioides brasiliensis |
Description | Paracoccidioidomycosis (PCM) is a neglected human systemic disease caused by species of the genus Paracoccidioides. The disease attacks the host’s lungs and may disseminate to many other organs. Treatment involves amphotericin B, sulfadiazine, trimethoprim-sulfamethoxazole, itraconazole, ketoconazole, or fluconazole. The treatment duration is usually long, from 6 months to 2 years, and many adverse effects may occur in relation to the treatment; co-morbidities and poor treatment adherence have been noted. Therefore, the discovery of more effective and less toxic drugs is needed. Thiosemicarbazide (TSC) and a camphene derivative of thiosemicarbazide (TSC-C) were able to inhibit P. lutzii growth at a low dosage and were not toxic to fibroblast cells. In order to investigate the mode of action of those compounds, we used a chemoproteomic approach to determine which fungal proteins were bound to each of these compounds. The compounds were able to inhibit the activities of the enzymes formamidase and β-1,3-glucosidase and interfered in P. brasiliensis dimorphism. In comparison with the transcriptomic and proteomic data previously obtained by our group, we determined that TSC and TSC-C were multitarget compounds that exerted effects on the electron-transport chain and cell cycle regulation, increased ROS formation, inhibited proteasomes and peptidases, modulated glycolysis, lipid, protein and carbohydrate metabolisms, and caused suppressed the mycelium to yeast transition. |
HostingRepository | PRIDE |
AnnounceDate | 2018-10-19 |
AnnouncementXML | Submission_2018-10-19_12:09:57.xml |
DigitalObjectIdentifier | |
ReviewLevel | Peer-reviewed dataset |
DatasetOrigin | Original dataset |
RepositorySupport | Unsupported dataset by repository |
PrimarySubmitter | Joyce Borba |
SpeciesList | scientific name: Paracoccidioides brasiliensis (strain Pb18); NCBI TaxID: 502780; |
ModificationList | No PTMs are included in the dataset |
Instrument | ACQUITY UPLC |
Dataset History
Revision | Datetime | Status | ChangeLog Entry |
0 | 2018-02-20 01:29:46 | ID requested | |
⏵ 1 | 2018-10-19 12:09:58 | announced | |
Publication List
Borba JVVB, Tauhata SBF, Oliveira CMA, Ferreira Marques M, Bail, ã, o AM, Soares CMA, Pereira M, Chemoproteomic identification of molecular targets of antifungal prototypes, thiosemicarbazide and a camphene derivative of thiosemicarbazide, in Paracoccidioides brasiliensis. PLoS One, 13(8):e0201948(2018) [pubmed] |
Keyword List
curator keyword: Biomedical |
submitter keyword: Paracoccidioidomycosis, chemoproteomic, thiosemicarbazide, camphene |
Contact List
Joyce Borba |
contact affiliation | Universidade Federal de Goias |
contact email | joycevillaverde@gmail.com |
lab head | |
Joyce Borba |
contact affiliation | Universidade Federal de Goiás |
contact email | joycevillaverde@gmail.com |
dataset submitter | |
Full Dataset Link List
Dataset FTP location
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PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD008987
- Label: PRIDE project
- Name: Chemoproteomic identification of molecular targets of antifungal prototypes, thiosemicarbazide and a camphene derivative of thiosemicarbazide, in Paracoccidioides brasiliensis