Molecular modeling and simulation study of homoserine kinase as an effective leishmanial drug target

Meshram, Rohan J.; Shirsath, Akshay M; Aouti, Snehal; Bagul, Kamini T; Gacche, Rajesh N.

doi:10.1007/s00894-020-04473-7

Cited by 7 publications

(5 citation statements)

References 71 publications

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“…Overall, the most stable model was SwissModel_2, followed by Mult1_lr and Mult1_lig. One possible explanation for the low stability of the Mult1_lig model would be that the model was built with an existing ligand that contributed to its stability and the protein was more flexible or disordered without it, as described in other previous studies [ 34 , 35 ]. In addition, our study showed that the average RMSD values corresponding to Lmj_04_BRCT models were similar to those reported for other BRCT domains ranging 3–4 Å [ 36 ].…”

Section: Discussionmentioning

confidence: 99%

“…Figure 11A shows the dynamical correlation between all residues in the complex of multi_lr and inhibitor CPE2 during the MD simulation. It can be observed that the initial residues had a positive correlation with residues in domain regions 35 , Å) for all the residues in the MD simulation of multi_lr in complex with CPE2. Blue-shaded regions corresponded to alpha helices, magenta-shaded regions corresponded to beta sheets.…”

Section: Characterization Of Mult1_lr-cpe2 Interactionmentioning

confidence: 91%

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Discovery and Validation of Lmj_04_BRCT Domain, a Novel Therapeutic Target: Identification of Candidate Drugs for Leishmaniasis

Peña-Guerrero

Fernández-Rubio

Burguete-Mikeo

et al. 2021

IJMS

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Since many of the currently available antileishmanial treatments exhibit toxicity, low effectiveness, and resistance, search and validation of new therapeutic targets allowing the development of innovative drugs have become a worldwide priority. This work presents a structure-based drug discovery strategy to validate the Lmj_04_BRCT domain as a novel therapeutic target in Leishmania spp. The structure of this domain was explored using homology modeling, virtual screening, and molecular dynamics studies. Candidate compounds were validated in vitro using promastigotes of Leishmania major, L. amazonensis, and L. infantum, as well as primary mouse macrophages infected with L. major. The novel inhibitor CPE2 emerged as the most active of a group of compounds against Leishmania, being able to significantly reduce the viability of promastigotes. CPE2 was also active against the intracellular forms of the parasites and significantly reduced parasite burden in murine macrophages without exhibiting toxicity in host cells. Furthermore, L. major promastigotes treated with CPE2 showed significant lower expression levels of several genes (α-tubulin, Cyclin CYCA, and Yip1) related to proliferation and treatment resistance. Our in silico and in vitro studies suggest that the Lmj_04_BRCT domain and its here disclosed inhibitors are new potential therapeutic options against leishmaniasis.

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Section: Discussionmentioning

confidence: 99%

Section: Characterization Of Mult1_lr-cpe2 Interactionmentioning

confidence: 91%

Discovery and Validation of Lmj_04_BRCT Domain, a Novel Therapeutic Target: Identification of Candidate Drugs for Leishmaniasis

Peña-Guerrero

Fernández-Rubio

Burguete-Mikeo

et al. 2021

IJMS

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“…Furthermore, antidepressants like sertraline have been evaluated and shown significant leishmanicidal action with a multi-target mechanism of action [ 67 ]. In silico studies have identified several drugs, including rifabutin, lamivudine, and metformin, as having the potential to eradicate the Leishmania parasite [ 68 , 69 , 70 ].…”

Section: Resultsmentioning

confidence: 99%

Overview of Research on Leishmaniasis in Africa: Current Status, Diagnosis, Therapeutics, and Recent Advances Using By-Products of the Sargassaceae Family

Abdoul-Latif,

Oumaskour,

Abdallah

et al. 2024

Pharmaceuticals

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Leishmaniasis in Africa, which has been designated as a priority neglected tropical disease by various global organizations, exerts its impact on millions of individuals, primarily concentrated within this particular region of the world. As a result of the progressively grave epidemiological data, numerous governmental sectors and civil organizations have concentrated their endeavors on this widespread outbreak with the objective of devising appropriate remedies. This comprehensive examination delves into multiple facets of this parasitic ailment, scrutinizing the associated perils, diagnostic intricacies, and deficiencies within the existing therapeutic protocols. Despite the established efficacy of current treatments, they are not immune to deleterious incidents, particularly concerning toxicity and the emergence of parasitic resistance, thus accentuating the necessity of exploring alternative avenues. Consequently, this research not only encompasses conventional therapeutic approaches, but also extends its scope to encompass complementary and alternative medicinal techniques, thereby striving to identify innovative solutions. A particularly auspicious dimension of this study lies in the exploration of natural substances and by-products derived from some brown algae of the Sargassaceae family. These resources possess the potential to assume a pivotal role in the management of leishmaniasis.

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“…17,18 Interestingly, the mechanistic studies of the kinase activity of HSK propose no involvement of histidine or a base in the catalysis; instead, it is believed that a phosphoryl transfer reaction is initiated by the direct attack of the hydroxyl group of homoserine to γ-phosphate of ATP in the absence of a base. 15,19 However, it raises a mechanistic enigma: if HSK doesn't need a histidine or a base for its catalytic activity, then how does the mutation of H139 result in the diversification of the catalytic function of HSK? Additionally, H139 is conserved among all known HSK families; therefore, nature must have chosen it for some specific function.…”

Section: Introductionmentioning

confidence: 99%

A single site mutation can induce functional promiscuity in homoserine kinase

Dubey

Tripathi

2023

Org. Biomol. Chem.

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Molecular modeling and simulation study of homoserine kinase as an effective leishmanial drug target

Cited by 7 publications

References 71 publications

Discovery and Validation of Lmj_04_BRCT Domain, a Novel Therapeutic Target: Identification of Candidate Drugs for Leishmaniasis

Discovery and Validation of Lmj_04_BRCT Domain, a Novel Therapeutic Target: Identification of Candidate Drugs for Leishmaniasis

Overview of Research on Leishmaniasis in Africa: Current Status, Diagnosis, Therapeutics, and Recent Advances Using By-Products of the Sargassaceae Family

A single site mutation can induce functional promiscuity in homoserine kinase

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