Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Yeong Joon Jo"'
Autor:
Jong Hyuk Sung, Kwang Il Kim, Min A. Yu, Yeong Joon Jo, Ho Bin Yang, Sang Gyu Park, Jin Gu Cho
Med28 plays a role in transcription, signal transduction, and cell proliferation. The overexpression of med28 is associated with tumor progression in in vitro and in vivo models. Recently it has been reported that the elevated expression of med28 is
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4642a97667f86474e7653c67f784e796
https://europepmc.org/articles/PMC4350139/
https://europepmc.org/articles/PMC4350139/
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 11:965-968
As aminoacyl adenylate surrogates, a series of methionyl and isoleucyl phenolic analogues containing bioisosteric linkers mimicking ribose have been investigated. Inhibition of synthesized compounds to the aminoacylation reaction by the corresponding
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b557b5d3721cef283064ccd51868a871
https://doi.org/10.1016/s0960-894x(01)00096-8
https://doi.org/10.1016/s0960-894x(01)00096-8
Autor:
Kiyotaka Shiba, Yeong Joon Jo, Jong Sang Lee, Sang Gyu Park, Hiromi Motegi, Sunghoon Kim, Keum Hee Jung
Publikováno v:
Journal of Biological Chemistry. 274:16673-16676
Endothelial monocyte activating polypeptide II (EMAPII) is a cytokine that is specifically induced by apoptosis. Its precursor (pro-EMAPII) has been suggested to be identical to p43, which is associated with the multi-tRNA synthetase complex. Herein,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d6c2aa0294a6cff8f173c0f25867aee2
https://doi.org/10.1074/jbc.274.24.16673
https://doi.org/10.1074/jbc.274.24.16673
Autor:
Jin Hwan Kkwak, Moon Woo Chun, Sang Uk Kang, Jeewoo Lee, Yeong Joon Jo, Sunghoon Kim, Mee Kyoung Kang
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 9:1365-1370
Four stable analogues of methionyl adenylate (3-6) were designed as inhibitors of methionyl-tRNA synthetase and synthesized from 2',3'-isopropylideneadenosine. They strongly inhibited aminoacylation activity of methionyl-tRNA synthetases isolated fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2c0d44f2ce1bda2e1930867b2c6e60
https://doi.org/10.1016/s0960-894x(99)00206-1
https://doi.org/10.1016/s0960-894x(99)00206-1
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 8:3511-3514
A series of methionine analogues have been synthesized as inhibitors of methionyl-tRNA synthetase and evaluated for their inhibitory activities of E. coli methionyl-tRNA synthetase and bacterial growth. Among them, L -methionine hydroxamate 20 has pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a5e7e919815721020cd66deb050a0cee
https://doi.org/10.1016/s0960-894x(98)00642-8
https://doi.org/10.1016/s0960-894x(98)00642-8
Publikováno v:
Proceedings of the National Academy of Sciences. 93:10128-10133
Aminoacyl-tRNA synthetases (tRNA synthetases) of higher eukaryotes form a multiprotein complex. Sequence elements that are responsible for the protein assembly were searched by using a yeast two-hybrid system. Human cytoplasmic isoleucyl-tRNA synthet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::538832dcf9f1815c5748a608342c9100
https://doi.org/10.1073/pnas.93.19.10128
https://doi.org/10.1073/pnas.93.19.10128
Monoclonal and polyclonal antibodies specific for foot and mouth disease virus type A and type O VP1
Autor:
Ji Hyeon Hwang, Kwang Nyeong Lee, Jong Hyuk Sung, Jong-Hyeon Park, Sang Gyu Park, Yeong Joon Jo, Jang Kwan Hong, Jin Gu Cho
Publikováno v:
Hybridoma (2005). 31(5)
The foot and mouth disease virus (FMDV) is an RNA virus composed of single stranded positive sense RNA. FMDV has been known to infect cloven-hoofed animals, including pigs, cattle, and sheep. FMDV is rapidly spreading outward to neighboring regions,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::60a5322ad4bd938f569e936d1f3ac14c
https://pubmed.ncbi.nlm.nih.gov/23098303
https://pubmed.ncbi.nlm.nih.gov/23098303
Publikováno v:
ChemInform. 30
A series of methionine analogues have been synthesized as inhibitors of methionyl-tRNA synthetase and evaluated for their inhibitory activities of E. coli methionyl-tRNA synthetase and bacterial growth. Among them, L -methionine hydroxamate 20 has pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0b1f0c5de4f0cdcf3d7baa5de5a27fa7
https://doi.org/10.1002/chin.199917201
https://doi.org/10.1002/chin.199917201
Autor:
Jeewoo Lee, Mee Kyoung Kang, Sang Uk Kang, Yeong Joon Jo, Moon Woo Chun, Sunghoon Kim, Jin Hwan Kwak
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4775e72811f03256c40dbfbbe4e12f0c
https://doi.org/10.1002/chin.199937237
https://doi.org/10.1002/chin.199937237
Autor:
Jeewoo Lee, Sung-Hoon Kim, Mee Kyoung Kang, Sang Uk Kang, Sungeun Kim, Yeong Joon Jo, Su-Yeon Kim
Publikováno v:
ChemInform. 32
The structure activity relationship on a series of ester and hydroxamate analogues of methionyl and isoleucyl adenylate has been investigated through introducing linkers between the 1'-position of ribose and adenine surrogates as methionyl-tRNA, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a47c3f5658661bf24c2a21c17cd44a34
https://doi.org/10.1002/chin.200133242
https://doi.org/10.1002/chin.200133242