2.Research advances of herpesvirus gB gene and its encoding protein.
Long JIANG ; Hui-juan LIU ; An-chun CHENG ; Ming-shu WANG ; Zheng-li CHEN ; Ren-yong JIA ; De-kang ZHU ; Xiao-yue CHEN
Chinese Journal of Virology 2010;26(5):414-417
Glycoproteins
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genetics
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metabolism
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Herpesviridae
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genetics
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metabolism
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Viral Proteins
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genetics
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metabolism
3.Identification of endoplasmic reticulum-shaping proteins in Plasmodium parasites.
Sha SUN ; Li LV ; Zhi YAO ; Purnima BHANOT ; Junjie HU ; Qian WANG
Protein & Cell 2016;7(8):615-620
4.Oncogene addiction and non-oncogene addiction in glioblastoma therapy.
Chinese Medical Journal 2011;124(17):2565-2568
5.The Mechanism and Influence of AKAP12 in Different Cancers.
Xuan WU ; Tong WU ; Ke LI ; Yuan LI ; Ting Ting HU ; Wei Feng WANG ; Su Jing QIANG ; Shao Bo XUE ; Wei Wei LIU
Biomedical and Environmental Sciences 2018;31(12):927-932
A Kinase Anchor Proteins
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genetics
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metabolism
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Animals
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Cell Cycle Proteins
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genetics
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metabolism
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Humans
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Neoplasms
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genetics
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metabolism
7.The baculovirus enhancin.
Xiao-xia ZHANG ; Xiao-hui CHEN ; Zhen-pu LIANG ; Su-mei CAO ; Fen XU ; Guan-hua QIAO ; Xing-ming YIN
Chinese Journal of Virology 2010;26(5):418-423
Baculoviridae
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genetics
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metabolism
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Phylogeny
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Viral Proteins
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chemistry
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classification
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genetics
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metabolism
8.Advances in UL7 gene of herpesvirus.
Jie HUANG ; An-Chun CHENG ; Ming-Shu WANG
Chinese Journal of Virology 2011;27(5):501-504
Animals
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Herpesviridae
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genetics
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metabolism
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Humans
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Viral Proteins
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chemistry
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genetics
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metabolism
9.Increasing of product specificity of gamma-cyclodextrin by mutating the active domain of alpha-cyclodextrin glucanotransferase from Paenibacillus macerans sp. 602-1.
Ting XIE ; Yang YUE ; Binghong SONG ; Yapeng CHAO ; Shijun QIAN
Chinese Journal of Biotechnology 2013;29(9):1234-1244
We studied the mutation effect of subsites -3(Lys47), -7(146-152), and cyclization center (Tyr195) in active domain on product specificity of alpha-cyclodextrin glucanotransferase (alpha-CGTase) from Paenibacillus macerans sp. 602-1. The Lys47 was replaced by Thr47 and Tyr195 by Ile195, and the amino acids from 146 to 152 were replaced by Ile (named as delta6). All these mutant alpha-CGTases were actively expressed in E. coli BL21. Compared with the wild-type alpha-CGTase, the starch-degrading activities of all the mutant enzymes were declined. For mutant Y195I, the percentage of alpha-CD was decreased from 68% to 30%, and beta-CD was raised from 22.2% to 33.3%. Interestingly, gamma-CD was increased from 8.9% to 36.7% and became the main product, while the actual yield was increased from 0.4 g/L to 1.1 g/L. Mutant K47T and delta6 still produced alpha-CD as main product though the percentage of beta- and gamma-CD increased. Purified Y195I CGTase showed similar optimum temperature with the wild-type alpha-CGTase, but its optimum pH shifted from 5.0 to 6.0 with better pH stability. In summary, mutant Y195I CGTase has the potential to produce gamma-CD as the main product.
Escherichia coli
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genetics
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metabolism
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Glucosyltransferases
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genetics
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metabolism
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Mutant Proteins
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genetics
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metabolism
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Mutation
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Paenibacillus
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enzymology
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Recombinant Proteins
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genetics
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gamma-Cyclodextrins
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metabolism
10.Research advances in CKLF-like MARVEL transmembrane domain containing member 5.
Ye-qing YUAN ; Yun-bei XIAO ; Zhen-hua LIU ; Xiao-wei ZHANG ; Tao XU ; Xiao-feng WANG
Acta Academiae Medicinae Sinicae 2012;34(6):625-628
CKLF-like MARVEL transmembrane domain containing member(CMTM)is a novel generic family firstly reported by Peking University Center for Human Disease Genomics. CMTM5 belongs to this family and has exhibited tumor-inhibiting activities. It can encode proteins approaching to the transmembrane 4 superfamily(TM4SF). CMTM5 is broadly expressed in normal adult and fetal human tissues, but is undetectable or down-regulated in most carcinoma cell lines and tissues. Restoration of CMTM5 may inhibit the proliferation, migration, and invasion of carcinoma cells. Although the exact mechanism of its anti-tumor activity remains unclear, CMTM5 may be involved in various signaling pathways governing the occurrence and development of tumors. CMTM5 may be a new target in the gene therapies for tumors, while further studies on CMTM5 and its anti-tumor mechanisms are warranted.
Chemokines
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genetics
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metabolism
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Humans
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MARVEL Domain-Containing Proteins
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genetics
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metabolism
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Neoplasms
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genetics
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metabolism
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Signal Transduction
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Tumor Suppressor Proteins
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genetics
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metabolism