Dr.
Harikishore Amaravadhi,
PhD
Nanyang Technological
University
School of Biological Sciences
60 Nanyang Drive
Singapore 637551
Email:
amaravadhi@ntu.edu.sg
Publications:
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Alag, R., Bharatham, N., Dong, A.,
Hills, T., Harikishore, A.,
Widjaja, A.A., Shochat, S.G., Hui,
R. and Yoon, H.S. (2009)
Crystallographic structure of the
tetratricopeptide repeat domain of
Plasmodium falciparum FKBP35 and its
molecular interaction with Hsp90
C-terminal pentapeptide.
Protein Sci. 18, 2115-2124
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Chattopadhaya, S., Harikishore,
A. and Yoon, H.S. (2011) Role
of FK506 binding proteins in
neurodegenerative disorders.
Curr. Med. Chem. 18, 5380-5397
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Chakraborty, G., Shin, J., Nguyen,
Q.T., Harikishore, A., Baek,
K. and Yoon, H.S. (2012) Solution
structure of FK506-binding protein
12 from Aedes aegypti.
Proteins 80, 2476-2481
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Ye, H., Li, B., Subramanian, V.,
Choi, B.H., Liang, Y.,
Harikishore, A., Chakraborty,
G., Baek, K. and Yoon, H.S. (2013)
NMR solution structure of C2
domain of MFG-E8 and insights into
its molecular recognition with
phosphatidylserine.
Biochim. Biophys. Acta 1828,
1083-1093
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Harikishore, A., Niang, M.,
Rajan, S., Preiser, P.R. and Yoon,
H.S. (2013) Small molecule
Plasmodium FKBP35 inhibitor as a
potential antimalaria agent.
Sci. Rep. 3, 2501
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Harikishore, A., Leow, M.L.,
Niang, M., Rajan, S., Pasunooti,
K.K., Preiser, P.R., Liu, X. and
Yoon, H.S. (2013) Adamantyl
derivative as a potent inhibitor of
Plasmodium FK506 binding protein 35.
ACS Med. Chem. Lett. 4, 1097-1101
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Shin, J.C., Jung, H.Y.,
Harikishore, A., Kwon, O.D.,
Yoon, H.S., Kim, K.T. and Choi, B.H.
(2014) The flavonoid myricetin
reduces nocturnal melatonin levels
in the blood through the inhibition
of serotonin N-acetyltransferase.
Biochem. Biophys. Res. Commun. 440,
312-316
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Kwon, H.S., Cho, S.J., Ha, T.J.,
Harikishore, A., Yoon, H.S.,
Park, K.H., Kim, I.S. and Jang, D.S.
(2014) Lipoxygenase inhibitory
effects of dibenzylbutane lignans
from the seeds of Myristica fragrans
(Nutmeg).
Bull. Korean Chem. Soc. 35,
3095-3098
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Rajan, S., Austin, D.,
Harikishore, A., Nguyen, Q.T.,
Baek, K. and Yoon, H.S. (2014)
Crystal structure of Plasmodium
vivax FK506-binding protein 25
reveals conformational changes
responsible for its noncanonical
activity.
Proteins 82, 1235-1244
-
Harikishore, A., Baek, K. and
Yoon, H.S. (2014). Revisiting de
novo drug design: Receptor based
pharmacophore screening.
Curr. Topi. Med. Chem. 14, 1890-1898
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Choi, B.H., Chattopadhaya, S., Thanh,
le. N., Feng, L., Nguyen, Q.T., Lim,
C.B., Harikishore, A., Nanga,
R.P., Bharatham, N., Zhao, Y., Liu,
X. and Yoon, H.S. (2014)
Suprafenacine, an indazole-hydrazide
agent, targets cancer cells through
microtubule destabilization.
PLoS One 9, e110955
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Kim, Y.S., Kim, S.H., Shin, J.,
Harikishore, A., Lim, J.K.,
Jung, Y., Lyu, H.N., Baek, N.I.,
Choi, K.Y., Yoon, H.S. and Kim, K.T.
(2014) Luteolin suppresses cancer
cell proliferation by targeting
vaccinia-related kinase 1.
PLoS One 9, e109655
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Harikishore, A. and Yoon, H.S.
(2015) Immunophilins: structures,
mechanisms and ligands.
Curr. Mol. Pharmacol. 8, 1-11
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Harikishore, A., Li, E., Lee,
J.J., Cho, N.J. and Yoon, H.S.
(2015) Combination of
pharmacophore hypothesis and
molecular docking to identify novel
inhibitors targeting thumb site II
of HCV NS5B polymerase.
Molec. Divers., in press
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Saw, W.-G.1, Wu, M.-L1, Ragunathan,
P.1, Biuković, G, Lau, A.-M., Shin,
J., Harikishore, A., Cheung,
C.-Y., Hards, K., Sarathy, J. P.,
Bates, R. W., Cook, G. M. C., Dick,
T.*, and Grüber, G.* (2019)
Disrupting coupling within
mycobacterial F-ATPsynthase subunit
ε causes dysregulated energy
production and cell wall
biosynthesis.
Sci. Rep.
9, 16759
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Harikishore, A., Chong, S. S.
M., Ragunathan, P., Bates, R. W.,
and Grüber, G.* (2020) Targeting
the menaquinol binding loop of
mycobacterial cytochrome bd oxidase.
Mol. Div.,
doi: 10.1007/s11030-020-10034-0
-
Hotra, A.,
Ragunathan P., Ng, P.S., Seankongsuk, P., Harikishore, A., Sarathy, J.P., Saw, W.-G., Lakshmanan, U., Sae-Lao, P., Kalia,
N.P., Shin, J., Kalyanasundaram, R., Anbarasu, S., Parthasarathy,
K., Pradeep, C.N., Makhija, H., Dröge, P., Poulsen, A., Tan,
J.H.L., Pethe, K., Dick, T., Bates, R.W., and Grüber, G.* (2020)
Discovery of a novel Mycobacterial F-ATP synthase inhibitor and
its potency in combination with diarylquinolines.
Angewandte
Chemie i.Ed, 132, 13397-13406
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Wong,
C.-F., Lau, A.-M., Harikishore, A., Saw, W.-G., Shin J.,
Ragunathan, P., Bhushan, S., Ngan, S. F. C., Sze, S. K., Bates,
R.W., Dick, T., and Grüber, G.* (2021) A systematic
assessment of mycobacterial F1-ATPase subunit ε’s role in latent
ATPase hydrolysis.
FEBS J. 288,
818-836
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Harikishore, A., Wong, C.-F., Ragunathan, P., Litty, D.,
Müller, V., and Grüber, G.* (2021) Targeting mycobacterial
F-ATP synthase C-terminal α subunit interaction motif on rotary
subunit γ.
Antibiotics 10, 1456
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Harikishore, A., Saw, W.-G., Ragunathan, P., Litty, D.,
Dick, T., Müller, V., and Grüber, G.* (2022) Mutational
analysis of mycobacterial F-ATP synthase subunit δ leads to a
potent δ enzyme inhibitor.
ACS Chem. Biol.
17, 529-535
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Shin, J.,
Harikishore, A., Wong, C.-F., Ragunathan, P., Dick, T.,
and Grüber, G.* (2022) Atomic solution structure of
Mycobacterium abscessus F-ATP synthase subunit ε and
identification of Ep1MabF1 as a targeted inhibitor.
FEBS J. in press
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Saw, W.-G.,
Leow, C.Y., Harikishore, A., Shin, J., Cole, M., Aragaw,
W.W., Ragunathan, P., Hegde, P., Aldrich, C.C., Dick, T., and
Grüber, G.* (2022) Structural and mechanistic insights into
Mycobacterium abscessus aspartate decarboxylase PanD and a
pyrazinoic acid-derived inhibitor.
ACS Infect. Dis.,
in press
1
(Authors have equal contribution) |