Dr Guo-Ping Zhou, Ph.D. - Gordon Life Science Institute - Professor & Principal Investigator

Dr Guo-Ping Zhou

Ph.D.

Gordon Life Science Institute

Professor & Principal Investigator

Rocky Mount, NC | United States

Main Specialties: Biochemical Genetics, Biotechnology, Other

Additional Specialties: Biophysics, Structural Biology, Bioinformatics, Medicinal Chemistry

ORCID logohttps://orcid.org/0000-0002-1140-2481


Top Author

Dr Guo-Ping Zhou, Ph.D. - Gordon Life Science Institute - Professor & Principal Investigator

Dr Guo-Ping Zhou

Ph.D.

Introduction

Dr. Guo-Ping Zhou is currently a Distinguished Professor of Gordon Life Science Institute, USA. He is also an Adjunct Professor of several academics in the United States and China. Dr. Zhou received his Ph.D in Biophysics from University of California at Davis, and completed his postdoctoral training at Stanford University and Harvard University, respec-tively. Dr. Zhou determined the 3D NMR structures of some proteins, protein-DNA com-plexes, super lipids such as dolichol and other polyisoprenyls, as well as polyisoprenol recognition sequences. Dr. Zhou has successfully introduced the elegant wenxiang dia-grams to elucidate the mechanisms of the coiled-coil proteins, protein-lipids, protein-DNA interactions, and prion protein misfolding observed by NMR. Meanwhile, he has also pub-lished many papers in Bioinformatics. Dr. Zhou’s current research interests focus on inves-tigation into the intrinsic relationship between the functions and structures of polysialyl-transferases, the suggested targets in metastatic cancer. Recently, a novel model of neural cell adhesion molecule (NCAM) polysialylation and cell migration have been proposed based on the cooperative effects between the intramolecular and intermolecular interactions in Zhou’s laboratory. In addition, Dr. Zhou has also edited some special issues on structur-al biology for several influential scientific journals such as Current Topics in Medicinal Chemistry, Current Medicinal Chemistry, Amino Acids, and as well as Protein & Peptide Letters.

RECENT LIST OF PUBLICATIONS
[1] Zhou, G.P. & Chou, K.C. Perspectives in Medicinal Chemistry: Two Latest Hot Researches in Medicinal Chemistry. Curr. Top. Med. Chem., 2020, 20, No.4, 1.
[2] Zhou, G.P. Current Advances of Drug Target Research in Medicinal Chemistry. Curr. Top. Med. Chem., 2020, 19(25): 2269 – 2270. DOI: 10.2174/156802661925191114094117.
[3] Zhou, G.P., Liao, S.M., Chen, D., Huang, R.B. The Cooperative Effect between Polybasic Re-gion (PBR) and Polysialyltransferase Domain (PSTD) within Tumor-Target Polysialyltranseferase ST8Sia II. Curr. Top. Med. Chem., 2019, 19(31): 2831-2841. doi: 10.2174/1568026619666191121145924.
[4] Bo Lu, B., Liu, X.H., Lia, S.M., Lu, Z.L., Huang, R.B., Zhou, G.P. A Possible Modulation Mechanism of Intramolecular and Intermolecular Interactions for NCAM Polysialylation and Cell Migration, Curr. Top. Med. Chem., 2019, 19(25), 2271-2282. DOI : 10.2174/1568026619666191018094805.
[5] Zhou, G.P. The Latest Researches of Enzyme Inhibition and Multi-Target Drug Predictors in Me-dicinal Chemistry, Med. Chem., 2019, 15, 572-573.
[6] Zhou, G.P. The Impact of Biophysics on Medicinal Chemistry, Curr Med Chem., 2019, 26, 4916-4917.
[7] Zhou, G.P & Li, Z.Y. Editorial Medicinal Chemistry Driven by the Development of System Bi-ology & Cheminformatics. Med. Chem., 2019, 15:5.
[8] Liao S, Shen, N.K.., Liang, G., Lu, B., Lu, Z.L., Peng L.X., Zhou, F., Du, L.Q., Wei, Y.T., Zhou, G.P., Huang, R.B. Inhibition of ?-amylase Activity by Zn2+: Insights from Spectroscopy and Molecular Dynamics Simulations. Med. Chem., 2019, 15, 5, 1-11.
[9] Liao, S., Liang, G., Zhu, J., Lu, B., Peng, L.X., Wang, Q.Y., Wei, Y.T., Huang, R.B., Zhou, G.P. Influence of Calcium Ions on the Thermal Characteristics of ?-amylase from Thermophilic Anoxybacillus sp. GXS-BL. Protein Pept Lett. 2019 Jan 16. doi: 10.2174/0929866526666190116162958. [Epub ahead of print] PMID:30652633
[10] Li-Xin Peng, Xue-Hui Liu, Bo Lu, Si-Ming Liao, Feng Zhou, Ji-Min Huang, Dong Chen, Frederic A. Troy II, Guo-Ping Zhou, and Ri-Bo Huang. The Inhibition of Polysialyltranseferase ST8SiaIV through Heparin Binding to Polysialyltransferase Domain (PSTD). Med. Chem., 2019, 15, 5.
[11] Huang,R.B.; Cheng, D.; Lu, B.; Liao, S.M.; Troy, F.A.; Zhou, G.P. The Intrinsic Relationship between Structure and Function of the Sialyltransferase ST8Sia Family Members, Curr. Top. Med. Chem., 2017, 17, 2359-2369.
[12] Xie, N.Z.; Chen, X.R.; Wang, Q.Y.; Chen, D.; Du, Q.S.; Zhou, G.P.; Huang, R.B. Microbial Routes to (2R,3R)-2,3-Butanediol: Recent Advances and Future Prospects, Curr. Top. Med. Chem., 2017,17, 2433-2439.
[13] Zhou, G.P. Impacts of computational biology to medicinal chemistry, Med. Chem., 2017, 13:6, 504-505.
[14] Zhou, G.P. Impacts of Biological Science to Medicinal Chemistry, Curr. Top. Med. Chem., 2017, 17, 2335-2336.
[15] Zhou, G.P. and W. Z. Zhong. Perspectives in the Medicinal Chemistry, Curr. Top. Med. Chem., 2016,16, 381-382.

Primary Affiliation: Gordon Life Science Institute - Rocky Mount, NC , United States

Specialties:

Additional Specialties:

Research Interests:


View Dr Guo-Ping Zhou’s Resume / CV

Education

Sep 1996
University of California, Davis, U.S.A.
Ph.D.
Biophysics
Feb 1984
Shanghai Jiaotong University, Shanghai, China.
M.S.
Engineering,
Jul 1981
Shanghai Jiaotong University, China.
B.S.
Engineering,

Publications

33Publications

277Reads

129Profile Views

261PubMed Central Citations

Molecular Interactions of the Polysialytransferase Domain (PSTD) in ST8Sia IV with CMP-Sialic Acid and Polysialic Acid Required for Polysialylation of the Neural Cell Adhesion Molecule Proteins: An NMR Study.

Int J Mol Sci 2020 Feb 26;21(5). Epub 2020 Feb 26.

The National Engineering Research Center for Non-food Biorefinery, Guangxi Academy of Sciences, Nanning, Guangxi 530007, China.

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http://dx.doi.org/10.3390/ijms21051590DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7084582PMC
February 2020
2.862 Impact Factor

The Cooperative Effect between Polybasic Region (PBR) and Polysialyltransferase Domain (PSTD) within Tumor-Target Polysialyltranseferase ST8Sia II.

Curr Top Med Chem 2019 ;19(31):2831-2841

National Engineering Research Center for Non-Food Biorefinery, State Key Laboratory of Non-Food Biomass and Enzyme Technology, Guangxi Key Laboratory of Bio-refinery, Guangxi Academy of Sciences, 98 Daling Road, Nanning, 530007, China.

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http://dx.doi.org/10.2174/1568026619666191121145924DOI Listing
February 2020
3.402 Impact Factor

Two Latest Hot Researches in Medicinal Chemistry

Current Topics in Medicinal Chemistry

Two latest trends in medicinal chemistry are studies on multi-target drugs and inhibition of posttranslational modifications (PTM).

In order to block the growth and spread of cancer by preventing cancer cells from growing and dividing, destroying them directly or helping other therapies work better, the multi-targeted therapies have been proposed to be a better pathway to achieve the desired treatment on cancer, nervous, cardiovascular and immune system diseases [1,2]. Obviously, the discovery of multi-target drugs is an emerging area due to their driving therapeutic benefit by interacting with multiple targets. The net- work analysis tools and computational prediction approaches have been incorporated into the basic research of these disease mechanisms to find possible therapeutic targets. A note-able development in this aspect is that the novel computational ap- proaches are closely associated with the identification of the subcellular localization of the so-called “multi-label” proteins that can simultaneously exist in several different location sites or move between them [3]. To support such a goal, very recently 14 user-friendly web-server predictors were established [4,5] by which users can easily attain their desired results for the multi- label proteins in eukaryotic, human, animal, plant, gram-positive, and gram-negative organisms, respectively, without the need to go through the complicated mathematics.

Inhibition of posttranslational modifications is related to a number of diseases such as cancer, nervous and cardiovascular system diseases. To timely and accurately get the targets’ 3D-structures for rational drug design, both theoretical and experi- mental approaches of structural biology such as PseAAC, PseKNC [4,5], graphical approaches, NMR, x-ray cystography, and cryoelectronic microscopy (Cryo-EM) are used [6-8]. One of the latest advances in PTM research is inhibition of polysialyla- tion of neuronal cell adhesion molecule (NCAM), which is strongly related to the migration and invasion of tumor cells and with aggressive, metastatic disease and poor clinical prognosis in the clinic due to the formation of polysialic acid (poly- Sia) on the surface of NCAM [9]. It has been known that NCAM-polySia expression on cancer cells is catalyzed by two polysialyltransferases (polySTs), ST8SiaIV and ST8SiaII, and specifically two polybasic motifs, polybasic region (PBR) and polysialyltransferase domain (PSTD) within each polyST have been found to be critically important for polyST activity based on recent mutation and molecular modeling analyses [10,11]. Thus, the intermolecular interactions of PBR-NCAM, PSTD- polySia and PSTD-CMP-sialic have been suggested during NCAM polysialylation and tested by more recent NMR studies [12]. Furthermore, a modulation model of NCAM-polysialylation and cell migration has been proposed by incorporating the intramolecular interaction of PBR-PSTD into above intermolecular interaction [12]. These studies may provide new perspec- tives on drug research and development related to the tumor-targeted polysialyltranseferases.

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January 2020

Impact Factor 3.440

3 Reads

A Possible Modulation Mechanism of Intramolecular and Intermolecular Interactions for NCAM Polysialylation and Cell Migration.

Curr Top Med Chem 2019 ;19(25):2271-2282

The National Engineering Research Center for Non-Food Biorefinery, Guangxi Academy of Sciences, Nanning, Guangxi 530007, China.

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http://dx.doi.org/10.2174/1568026619666191018094805DOI Listing
December 2019
3.402 Impact Factor

Influence of Calcium Ions on the Thermal Characteristics of α-amylase from Thermophilic Anoxybacillus sp. GXS-BL.

Protein Pept Lett 2019 ;26(2):148-157

National Engineering Research Center for Non-food Biorefinery, State Key Laboratory of Non-food Biomass and Enzyme Technology, Guangxi Key Laboratory of Bio-refinery, Guangxi Academy of Sciences, 98 Daling Road, Nanning, 530007, China.

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http://dx.doi.org/10.2174/0929866526666190116162958DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6416487PMC
October 2019
3 Reads
1.068 Impact Factor

Inhibition of α-amylase Activity by Zn: Insights from Spectroscopy and Molecular Dynamics Simulations.

Med Chem 2019 ;15(5):510-520

Department of Bioengineering, College of Life Science and Technology, Guangxi University, Nanning, Guangxi, 530004, China.

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http://dx.doi.org/10.2174/1573406415666181217114101DOI Listing
July 2019
8 Reads
1.387 Impact Factor

The Inhibition of Polysialyltranseferase ST8SiaIV Through Heparin Binding to Polysialyltransferase Domain (PSTD).

Med Chem 2019 ;15(5):486-495

Life Science and Technology College, Guangxi University, Nanning, Guangxi, 530004 China; 2Institute of Biophysics, Chinese Academy of Sciences, Beijing, China.

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http://www.eurekaselect.com/168414/article
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http://dx.doi.org/10.2174/1573406415666181218101623DOI Listing
July 2019
34 Reads
1.387 Impact Factor

Recent Progresses in Studying Helix-Helix Interactions in Proteins by Incorporating the Wenxiang Diagram into the NMR Spectroscopy.

Curr Top Med Chem 2016 ;16(6):581-90

State Key Laboratory of Non-food Biomass and Enzyme Technology, National Engineering Research Center for Non-food Biorefinery, Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530007, P.R. China.

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http://dx.doi.org/10.2174/1568026615666150819104617DOI Listing
August 2016
4 Reads
3 Citations
3.402 Impact Factor

Editorial: Modulations and their Biological Functions of Protein-Biomolecule Interactions.

Authors:
Guo-Ping Zhou

Curr Top Med Chem 2016 ;16(6):579-80

Guangxi Academy of Sciences Nanning, Guangxi 530004, China University of California Davis, CA 95616 USA.

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http://dx.doi.org/10.2174/1568026616999150918145955DOI Listing
August 2016
12 Reads
3.402 Impact Factor

Perspectives in Medicinal Chemistry.

Curr Top Med Chem 2016 ;16(4):381-2

University of California, Davis, California, USA.

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http://dx.doi.org/10.2174/156802661604151014114030DOI Listing
July 2016
20 Reads
7 Citations
3.402 Impact Factor

Editorial: current progress in structural bioinformatics of protein-biomolecule interactions.

Authors:
Guo-Ping Zhou

Med Chem 2015 ;11(3):216-7

National Engineering Research Center for Non-food Biorefinery, Guangxi Academy of Sciences, Nanning, China; Adjunct Professor, University of California, Davis, CA, USA; Professor & Principal Investigator, Gordon Life Science Institute, Belmont, MA, USA.

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http://dx.doi.org/10.2174/1573406411666141229162618DOI Listing
February 2016
1 Read
3 Citations
1.390 Impact Factor

Perspectives in Medicinal Chemistry.

Curr Top Med Chem 2015 Oct 12. Epub 2015 Oct 12.

Tianchun Lifescience Technology, Nanjing, China.

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October 2015
3 Reads
3.402 Impact Factor

3D structural conformation and functional domains of polysialyltransferase ST8Sia IV required for polysialylation of neural cell adhesion molecules.

Protein Pept Lett 2015 ;22(2):137-48

National Engineering Research Center for Non-food Biorefinery, Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530007, China.

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http://dx.doi.org/10.2174/0929866521666141019192221DOI Listing
October 2015
1 Read
3 Citations
1.070 Impact Factor

The pH-triggered conversion of the PrP(c) to PrP(sc.).

Curr Top Med Chem 2013 ;13(10):1152-63

Gordon Life Science Institute, 53 South Cottage Road, Belmont, MA 02478, USA.

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http://dx.doi.org/10.2174/15680266113139990003DOI Listing
February 2014
11 Reads
10 Citations
3.402 Impact Factor

Mission of randomness.

Authors:
Guo-Ping Zhou

Virulence 2013 Nov 12;4(8):669-70. Epub 2013 Nov 12.

Gordon Life Science Institute; Belmont, MA USA.

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http://dx.doi.org/10.4161/viru.27136DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3925698PMC
November 2013
17 Reads
4.220 Impact Factor

The structural determinations of the leucine zipper coiled-coil domains of the cGMP-dependent protein kinase Iα and its interaction with the myosin binding subunit of the myosin light chains phosphase.

Authors:
Guo-Ping Zhou

Protein Pept Lett 2011 Oct;18(10):966-78

Department of Chemistry, North Carolina State University, NC 27695, USA.

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http://dx.doi.org/10.2174/0929866511107010966DOI Listing
October 2011
1 Read
13 Citations
1.070 Impact Factor

Predictions and determinations of protein and peptide structures.

Authors:
Guo-Ping Zhou

Protein Pept Lett 2011 Oct;18(10):964-5

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http://dx.doi.org/10.2174/092986611796378738DOI Listing
October 2011
3 Reads
1.070 Impact Factor

The disposition of the LZCC protein residues in wenxiang diagram provides new insights into the protein-protein interaction mechanism.

Authors:
Guo-Ping Zhou

J Theor Biol 2011 Sep 22;284(1):142-8. Epub 2011 Jun 22.

Gordon Life Science Institute, 13784 Torrey Del Mar Drive, San Diego, CA 92130, USA.

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http://dx.doi.org/10.1016/j.jtbi.2011.06.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7094099PMC
September 2011
1 Read
25 Citations
2.120 Impact Factor

Authors:
Guo-Ping Zhou

Protein Pept Lett 2011 May 19. Epub 2011 May 19.

Department of Chemistry, North Carolina State University, NC 27695, USA.

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May 2011
3 Reads
1.070 Impact Factor

Detailed biophysical characterization of the acid-induced PrP(c) to PrP(β) conversion process.

Biochemistry 2011 Feb 27;50(7):1162-73. Epub 2011 Jan 27.

Department of Biological Sciences, University of Alberta, Edmonton, Alberta, Canada T6G 2E8.

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http://dx.doi.org/10.1021/bi101435cDOI Listing
February 2011
2 Reads
22 Citations
3.020 Impact Factor

WITHDRAWN: Some insights into conversion process of the PrP(c) to PrP(beta).

Authors:
Guo-Ping Zhou

Biochem Biophys Res Commun 2009 Oct 13. Epub 2009 Oct 13.

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA Guangxi Academy of Sciences, 98 Daling Road, Nanning, Guangxi 530007, China.

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http://dx.doi.org/10.1016/j.bbrc.2009.09.084DOI Listing
October 2009
3 Reads
2.300 Impact Factor

Probing the interaction between the coiled coil leucine zipper of cGMP-dependent protein kinase Ialpha and the C terminus of the myosin binding subunit of the myosin light chain phosphatase.

J Biol Chem 2008 Nov 9;283(47):32860-9. Epub 2008 Sep 9.

Divison of Molecular and Vascular Medicine, Center for Vascular Biology Research, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.

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http://dx.doi.org/10.1074/jbc.M804916200DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2583292PMC
November 2008
35 Reads
18 Citations
4.573 Impact Factor

Protein structure and function: structural biology, bioinformatics, and system biology. Editorial.

Authors:
Guo-Ping Zhou

Amino Acids 2008 Oct;35(3):513-5

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http://dx.doi.org/10.1007/s00726-008-0078-xDOI Listing
October 2008
2 Reads
3.293 Impact Factor

Predicting protease types by hybridizing gene ontology and pseudo amino acid composition.

Proteins 2006 May;63(3):681-4

Center for Vascular Biology Research, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02115, USA.

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http://dx.doi.org/10.1002/prot.20898DOI Listing
May 2006
1 Read
3 Citations
2.630 Impact Factor

NMR studies on how the binding complex of polyisoprenol recognition sequence peptides and polyisoprenols can modulate membrane structure.

Curr Protein Pept Sci 2005 Oct;6(5):399-411

Center for Hemostasis, Thrombosis and Vascular Biology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.2174/138920305774329377DOI Listing
October 2005
1 Read
12 Citations
3.154 Impact Factor

Rapid and accurate structure determination of coiled-coil domains using NMR dipolar couplings: application to cGMP-dependent protein kinase Ialpha.

Protein Sci 2005 Sep;14(9):2421-8

Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.1110/ps.051528905DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2253468PMC
September 2005
5 Reads
13 Citations
2.854 Impact Factor

Predicting enzyme family classes by hybridizing gene product composition and pseudo-amino acid composition.

J Theor Biol 2005 May 26;234(1):145-9. Epub 2005 Jan 26.

Biomolecular Sciences Department, University of Manchester Institute of Science & Technology, PO Box 88, Manchester, M60 1QD, UK

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http://dx.doi.org/10.1016/j.jtbi.2004.11.017DOI Listing
May 2005
3 Reads
7 Citations
2.120 Impact Factor

NMR study of the preferred membrane orientation of polyisoprenols (dolichol) and the impact of their complex with polyisoprenyl recognition sequence peptides on membrane structure.

Glycobiology 2005 Apr 24;15(4):347-59. Epub 2004 Nov 24.

The Center for Hemostasis, Thrombosis and Vascular Biology, Beth Israel Deaconess Medical Center Harvard Medical School, Boston, MA 02115, USA.

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http://dx.doi.org/10.1093/glycob/cwi016DOI Listing
April 2005
4 Reads
14 Citations
3.150 Impact Factor

Identify catalytic triads of serine hydrolases by support vector machines.

J Theor Biol 2004 Jun;228(4):551-7

Shanghai Research Center of Biotechnology, Chinese Academy of Sciences, Shanghai 200233, China.

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http://dx.doi.org/10.1016/j.jtbi.2004.02.019DOI Listing
June 2004
3 Reads
3 Citations
2.120 Impact Factor

Support vector machines for predicting membrane protein types by using functional domain composition.

Biophys J 2003 May;84(5):3257-63

Shanghai Research Centre of Biotechnology, Chinese Academy of Sciences, Shanghai 200233, China.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1302886PMC
http://dx.doi.org/10.1016/S0006-3495(03)70050-2DOI Listing
May 2003
46 Citations
3.972 Impact Factor

Characterization by NMR and molecular modeling of the binding of polyisoprenols and polyisoprenyl recognition sequence peptides: 3D structure of the complexes reveals sites of specific interactions.

Glycobiology 2003 Feb 1;13(2):51-71. Epub 2002 Nov 1.

Department of Biological Chemistry, University of California Schoolof Medicine, One Shields Avenue, Davis, CA 95616-8635, USA.

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http://dx.doi.org/10.1093/glycob/cwg008DOI Listing
February 2003
3 Reads
10 Citations
3.150 Impact Factor

Subcellular location prediction of apoptosis proteins.

Proteins 2003 Jan;50(1):44-8

Department of Medicine, Harvard Medical School, Boston, Massachusetts 02115, USA.

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http://dx.doi.org/10.1002/prot.10251DOI Listing
January 2003
54 Reads
46 Citations
2.630 Impact Factor

Top co-authors

Ri-Bo Huang
Ri-Bo Huang

Guangxi University

9
Dong Chen
Dong Chen

Huaihe Hospital of Henan University

5
Bo Lu
Bo Lu

Thomas Jefferson University

5
Yu-Dong Cai
Yu-Dong Cai

Shanghai Institutes for Biological Sciences

3
Alan C Rigby
Alan C Rigby

Harvard Medical School

3
Li-Xin Peng
Li-Xin Peng

Tianjin Agricultural College

3