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Khajamohiddin Syed

Researcher at University of Zululand

Publications -  52
Citations -  3982

Khajamohiddin Syed is an academic researcher from University of Zululand. The author has contributed to research in topics: Phanerochaete & Gene. The author has an hindex of 20, co-authored 47 publications receiving 3159 citations. Previous affiliations of Khajamohiddin Syed include University of Cincinnati Academic Health Center & University of Cincinnati.

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Factors Alleviating Cadmium Toxicity in White Rot Fungus

TL;DR: This is the first report on the metal tolerance properties of this organism in a co-contamination scenario as well as on demonstration of a protective effect of PAHs in Cd toxicity.
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Cytochrome P450 monooxygenase analysis in free-living and symbiotic microalgae Coccomyxa sp. C-169 and Chlorella sp. NC64A

TL;DR: In this article, the authors performed genome data-mining, annotation and comparative analysis of P450s in two model algal species and found sixty-nine P450 monooxygenases were found in two different species.
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Comparative analyses and structural insights of new class glutathione transferases in Cryptosporidium species.

TL;DR: The first comparative analysis of glutathione transferase (GST) in Cryptosporidium species is reported, revealing the presence three GSTs in each of the Cryptospora species analyzed in the study.
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Saprophytic to Pathogenic Mycobacteria: Loss of Cytochrome P450s Vis a Vis Their Prominent Involvement in Natural Metabolite Biosynthesis

TL;DR: A comprehensive analysis of P450s and their role in natural metabolite synthesis in 2666 mycobacterial species was carried out in this paper , which revealed the presence of 62,815 P450 enzymes that can be grouped into 182 P450 families and 345 subfamilies.
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The compound (3-{5-[(2,5-dimethoxyphenyl)amino]-1,3,4-thiadiazolidin-2-yl}-5,8-methoxy-2H-chromen-2-one) inhibits the prion protein conversion from PrPC to PrPSc with lower IC50 in ScN2a cells

TL;DR: Virtual screening of a ligand database using the molecular scaffold developed from the set of EBs identified six of the compounds found to be particularly potent in decreasing the accumulation SHaPrPSc in ScN2a cells with an IC50 of ∼35µM and 20µ M.