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Relevant bibliographies by topics / Protein functional analysis

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Academic literature on the topic 'Protein functional analysis'

Author: Grafiati

Published: 5 June 2025

Last updated: 2 August 2025

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Journal articles on the topic "Protein functional analysis"

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Levy-Cohen, Gal, and Michael Blank. "Functional analysis of protein ubiquitination." Analytical Biochemistry 484 (September 2015): 37–39. http://dx.doi.org/10.1016/j.ab.2015.04.040.

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Johri, Parul, Mala Trivedi, and Sujeet Pratap Singh. "Atom based Profiling and Functional Enrichment analysis of Aquaporins." Research Journal of Biotechnology 16, no. 10 (2021): 75–77. http://dx.doi.org/10.25303/1610rjbt7577.

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Sequence analysis is a computational biology method to study protein sequences by comparing amino acids of one protein sequence with the other (residual level comparison). This study reveals a new concept of comparing protein sequences at their basic atomic level. Aquaporins from various origin were compared at their atomic level and the study revealed that all the aquaporin proteins have a closed range of 31.0% to 34.2% of carbon atoms irrespective of their origin and amino acid sequence. Further the protein interaction and functional enrichment analysis of AQP7 showed significant interaction

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Yuan, Fei, Xiaoyong Pan, Lei Chen, Yu-Hang Zhang, Tao Huang, and Yu-Dong Cai. "Analysis of Protein–Protein Functional Associations by Using Gene Ontology and KEGG Pathway." BioMed Research International 2019 (July 18, 2019): 1–10. http://dx.doi.org/10.1155/2019/4963289.

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Protein–protein interaction (PPI) plays an extremely remarkable role in the growth, reproduction, and metabolism of all lives. A thorough investigation of PPI can uncover the mechanism of how proteins express their functions. In this study, we used gene ontology (GO) terms and biological pathways to study an extended version of PPI (protein–protein functional associations) and subsequently identify some essential GO terms and pathways that can indicate the difference between two proteins with and without functional associations. The protein–protein functional associations validated by experime

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Konig, Simone. "Functional Protein Analysis Using Mass Spectrometry." Current Organic Chemistry 9, no. 9 (2005): 875–87. http://dx.doi.org/10.2174/1385272054038291.

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Ranganathan, Vasudevan, and Kainaat Munir Khoja. "Characterization and functional analysis of the hypothetical protein in Yersinia pestis." Journal of Microbiology & Experimentation 10, no. 5 (2022): 170–79. http://dx.doi.org/10.15406/jmen.2022.10.00370.

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A hypothetical protein is a protein which exists but the function is not known. These are the proteins for which there is no experimental evidence that it is expressed in vivo. The usual scenario involving a hypothetical protein is gene identification during genome analysis. The function of a hypothetical protein can also be predicted by domain homology searches with various confidence levels. The Human Genome project and the genome projects of many other organisms has been a source for the information on the sequences and their functional aspects. However, this resulted in identification of m

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Christensen, Stefan Jarl, Silke Flindt Badino, Ana Mafalda Cavaleiro, Kim Borch, and Peter Westh. "Functional analysis of chimeric TrCel6A enzymes with different carbohydrate binding modules." Protein Engineering, Design and Selection 32, no. 9 (2019): 401–9. http://dx.doi.org/10.1093/protein/gzaa003.

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Abstract The glycoside hydrolase (GH) family 6 is an important group of enzymes that constitute an essential part of industrial enzyme cocktails used to convert lignocellulose into fermentable sugars. In nature, enzymes from this family often have a carbohydrate binding module (CBM) from the CBM family 1. These modules are known to promote adsorption to the cellulose surface and influence enzymatic activity. Here, we have investigated the functional diversity of CBMs found within the GH6 family. This was done by constructing five chimeric enzymes based on the model enzyme, TrCel6A, from the so

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A. Rahaman, Siti Nurulnabila, Jastina Mat Yusop, Zeti-Azura Mohamed-Hussein, et al. "Crystal structure and functional analysis of human C1ORF123." PeerJ 6 (September 28, 2018): e5377. http://dx.doi.org/10.7717/peerj.5377.

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Proteins of the DUF866 superfamily are exclusively found in eukaryotic cells. A member of the DUF866 superfamily, C1ORF123, is a human protein found in the open reading frame 123 of chromosome 1. The physiological role of C1ORF123 is yet to be determined. The only available protein structure of the DUF866 family shares just 26% sequence similarity and does not contain a zinc binding motif. Here, we present the crystal structure of the recombinant human C1ORF123 protein (rC1ORF123). The structure has a 2-fold internal symmetry dividing the monomeric protein into two mirrored halves that compris

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Buck, B. Logan, Eric Altermann, Tina Svingerud, and Todd R. Klaenhammer. "Functional Analysis of Putative Adhesion Factors in Lactobacillus acidophilus NCFM." Applied and Environmental Microbiology 71, no. 12 (2005): 8344–51. http://dx.doi.org/10.1128/aem.71.12.8344-8351.2005.

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ABSTRACT Lactobacilli are major inhabitants of the normal microflora of the gastrointestinal tract, and some select species have been used extensively as probiotic cultures. One potentially important property of these organisms is their ability to interact with epithelial cells in the intestinal tract, which may promote retention and host-bacterial communication. However, the mechanisms by which they attach to intestinal epithelial cells are unknown. The objective of this study was to investigate cell surface proteins in Lactobacillus acidophilus that may promote attachment to intestinal tissu

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van Staalduinen, Laura, Stefanie Novakowski, and Zongchao Jia. "Structure and Functional Analysis of a Ribosomal Oxygenase." Acta Crystallographica Section A Foundations and Advances 70, a1 (2014): C1408. http://dx.doi.org/10.1107/s205327331408591x.

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The 2-oxoglutarate/Fe(II)-dependent oxygenases (2OG oxygenases) are a large family of proteins that share a similar overall three-dimensional structure and catalyze a diverse array of oxidation reactions. The Jumonji C (JmjC)-domain containing proteins represent an important subclass of the 2OG oxygenase family that typically catalyze protein hydroxylation; however, recently other reactions have been identified, such as tRNA modification. The E. coli gene, ycfD, was predicted to be a JmjC-domain containing protein of unknown function based on primary sequence. Recently YcfD was determined to a

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Zybailov, Boris L., Alicia K. Byrd, Galina V. Glazko, Yasir Rahmatallah, and Kevin D. Raney. "Protein-protein interaction analysis for functional characterization of helicases." Methods 108 (October 2016): 56–64. http://dx.doi.org/10.1016/j.ymeth.2016.04.014.

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Dissertations / Theses on the topic "Protein functional analysis"

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Nguyen, Giang Huong. "A functional analysis of the human LPA₁G protein coupled receptor." Thesis, Available online, Georgia Institute of Technology, 2004:, 2004. http://etd.gatech.edu/theses/available/etd-06072004-131304/unrestricted/nguyen%5Fgiang%5Fh%5F200405%5Fms.pdf.

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Akkoyun, Emrah. "Parallelization Of Functional Flow To Predict Protein Functions." Master's thesis, METU, 2011. http://etd.lib.metu.edu.tr/upload/12612932/index.pdf.

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Protein-protein interaction networks provide important information about what the biological function of proteins whose roles are unknown might be in a cell. These interaction networks were analyzed by a variety of approaches by running them on a single computer and the roles of the proteins identified were used to predict the function of the proteins unidentified. The functional flow is an approach that takes the network connectivity, distance effect, topology of the network with local and global views into account. With these advantages, that the functional flow produces more accurate result

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Tuason, Maria Clarita. "Functional analysis of Proteolipid Protein regulatory sequence." Thesis, McGill University, 2006. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=101805.

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Myelin is an evolutionarily late acquisition of the vertebrate nervous system which speeds electrochemical signaling in mature nerve fibers by providing insulation in the form of a lipid-rich multilammelar sheath. Proteolipid Protein (PLP) is the most abundant protein in mature mammalian central nervous system myelin where it serves as a structural component in addition to other yet undefined roles. It is coordinately regulated at the transcriptional level with other myelin genes such as Myelin Basic Protein (MBP). The major components of MBP transcriptional regulation have been defined using

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Chodagam, Sasidhar. "Functional analysis of the centrosomal protein CP190." Thesis, University of Cambridge, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.619859.

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Mizuno, Nobuhiro. "Structure-based functional analysis of DsrD protein." 京都大学 (Kyoto University), 2004. http://hdl.handle.net/2433/147845.

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Adams, Vicki 1976. "Functional analysis of the clostridial large resolvase TnpX." Monash University, Dept. of Microbiology, 2003. http://arrow.monash.edu.au/hdl/1959.1/5729.

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Giorgini, Flaviano. "Functional analysis of the murine sequence-specific RNA binding protein MSY4 /." Thesis, Connect to this title online; UW restricted, 2002. http://hdl.handle.net/1773/10293.

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Caufield, J. Harry. "Interactomics-Based Functional Analysis: Using Interaction Conservation To Probe Bacterial Protein Functions." VCU Scholars Compass, 2016. http://scholarscompass.vcu.edu/etd/4580.

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The emergence of genomics as a discrete field of biology has changed humanity’s understanding of our relationship with bacteria. Sequencing the genome of each newly-discovered bacterial species can reveal novel gene sequences, though the genome may contain genes coding for hundreds or thousands of proteins of unknown function (PUFs). In some cases, these coding sequences appear to be conserved across nearly all bacteria. Exploring the functional roles of these cases ideally requires an integrative, cross-species approach involving not only gene sequences but knowledge of interactions among the

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Yang, Long 1976. "Functional analysis of the loki serinethreonine protein kinase." Thesis, McGill University, 2001. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=33859.

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In cell cycle checkpoint control, the Chk2 family protein kinases play a central role in mediating the cellular responses to DNA damage or DNA replication block. However, at the beginning of this project, there was no evidence for a Drosophila homologue of Chk2. loki was identified in a screen for serine/threonine protein kinases that are expressed in the ovary. Using a phylogenetic analysis, I showed that loki is a Drosophila chk2 orthologue. To characterize the checkpoint function of loki in Drosophila development, we created a loki null mutant and generated anti-Loki antibodies. Under norma

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Finnie, Nicholas James. "Functional analysis of the DNA-dependent protein kinase." Thesis, University of Cambridge, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.243027.

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Books on the topic "Protein functional analysis"

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1927-, Jollès Pierre, and Jörnvall Hans, eds. Proteomics in functional genomics: Protein structure analysis. Birkhäuser Verlag, 2000.

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1964-, Predki Paul F., ed. Functional protein microarrays in drug discovery. CRC Press, 2007.

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Muley, Vijaykumar Yogesh, and Vishal Acharya. Genome-Wide Prediction and Analysis of Protein-Protein Functional Linkages in Bacteria. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-4705-4.

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Ganapathy-Kanniappan, Shanmugasundaram. Advances in GAPDH Protein Analysis: A Functional and Biochemical Approach. Springer Singapore, 2017. http://dx.doi.org/10.1007/978-981-10-7342-7.

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Perbal, Marie-Christine. A functional analysis of the cauliflower mosaic virus movement protein. University ofEast Anglia, 1994.

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6

Christoph, Kannicht, ed. Post-translational modifications of proteins: Tools for functional proteomics. 2nd ed. Humana Press, 2008.

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1967-, Wilkins M. R., ed. Proteome research: New frontiers in functional genomics. Springer, 1997.

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Christoph, Kannicht, ed. Posttranslational modifications of proteins: Tools for functional proteomics. Humana Press, 2002.

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9

Cutz, Jean-Claude. Effect of amygdala kindling on G protein-coupled gas-subunit levels: Immunobolt and functional analysis. National Library of Canada, 1993.

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Schneider, Marlon Roberto. Functional analysis of insulin-like growth factor-binding protein-5 in transfected cells and transgenic mice. [s.n.], 2001.

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Book chapters on the topic "Protein functional analysis"

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Persson, Bengt. "Bioinformatics in protein analysis." In Proteomics in Functional Genomics. Birkhäuser Basel, 2000. http://dx.doi.org/10.1007/978-3-0348-8458-7_14.

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Hykollari, Alba, Daniel Malzl, Iain B. H. Wilson, and Katharina Paschinger. "Protein-Specific Analysis of Invertebrate Glycoproteins." In Functional Proteomics. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-8814-3_24.

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Minguez, Pablo, and Peer Bork. "Bioinformatics Analysis of Functional Associations of PTMs." In Protein Bioinformatics. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6783-4_14.

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Bradbury, Louis M. T. "Functional Analysis by Protein Biochemistry." In Methods in Molecular Biology. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-715-0_13.

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Shively, John E. "The chemistry of protein sequence analysis." In Proteomics in Functional Genomics. Birkhäuser Basel, 2000. http://dx.doi.org/10.1007/978-3-0348-8458-7_7.

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Wu, Guanming, and Robin Haw. "Functional Interaction Network Construction and Analysis for Disease Discovery." In Protein Bioinformatics. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-6783-4_11.

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Sljoka, Adnan. "Structural and Functional Analysis of Proteins Using Rigidity Theory." In Sublinear Computation Paradigm. Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-16-4095-7_14.

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AbstractOver the past two decades, we have witnessed an unprecedented explosion in available biological data. In the age of big data, large biological datasets have created an urgent need for the development of bioinformatics methods and innovative fast algorithms. Bioinformatics tools can enable data-driven hypothesis and interpretation of complex biological data that can advance biological and medicinal knowledge discovery. Advances in structural biology and computational modelling have led to the characterization of atomistic structures of many biomolecular components of cells. Proteins in

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SHI, LEI, XIUJUAN LEI, and AIDONG ZHANG. "Protein Functional Module Analysis With Protein-Protein Interaction (PPI) Networks." In Algorithmic and Artificial Intelligence Methods for Protein Bioinformatics. John Wiley & Sons, Inc., 2013. http://dx.doi.org/10.1002/9781118567869.ch20.

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Nölting, Bengt. "Proteomics: high throughput protein functional analysis." In Methods in Modern Biophysics. Springer Berlin Heidelberg, 2004. http://dx.doi.org/10.1007/978-3-662-05367-6_9.

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Nölting, Bengt. "Proteomics: high throughput protein functional analysis." In Methods in Modern Biophysics. Springer Berlin Heidelberg, 2009. http://dx.doi.org/10.1007/978-3-642-03022-2_9.

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Conference papers on the topic "Protein functional analysis"

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Ye, Bowei, and Jie Liang. "Predicting Functional Surface Topographies Combining Topological Data Analysis and Deep Learning Across the Human Protein Universe." In 2024 46th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC). IEEE, 2024. https://doi.org/10.1109/embc53108.2024.10782681.

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Shahbazi, Zahra, Horea T. Ilies¸, and Kazem Kazerounian. "Protein Molecules as Natural Nano Bio Devices: Mobility Analysis." In ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13021.

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Proteins are nature’s nano-robots in the form of functional molecular components of living cells. The function of these natural nano-robots often requires conformational transitions between two or more native conformations that are made possible by the intrinsic mobility of the proteins. Understanding these transitions is essential to the understanding of how proteins function, as well as to the ability to design and manipulate protein-based nano-mechanical systems [1]. Modeling protein molecules as kinematic chains provides the foundation for developing powerful approaches to the design, mani

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Hu, Pingzhao, Hui Jiang, and Andrew Emili. "A topology-sharing based method for protein function prediction via analysis of protein functional association networks." In 2009 IEEE International Conference on Bioinformatics and Biomedicine Workshop, BIBMW. IEEE, 2009. http://dx.doi.org/10.1109/bibmw.2009.5332102.

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Shi, Lei, Young-Rae Cho, and Aidong Zhang. "Functional Flow Simulation Based Analysis of Protein Interaction Network." In 2010 IEEE International Conference on BioInformatics and BioEngineering. IEEE, 2010. http://dx.doi.org/10.1109/bibe.2010.32.

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Walker, F. J. "REGULATION OF THE ANTICOAGULANT ACTIVITY OF ACTIVATED PROTEIN C BY PROTEIN S AND PROTEIN S BINDING PROTEIN." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1642964.

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Protein S is a vitamin K-dependent protein that acts as a cofactor for the anticoagulant activity of activated protein C both in the proteolytic inactivation of factor V and VIII. Protein S is a single chain protein with a molecular weight of approximately 62 kDa. When the molecular weight of protein S in plasma was determined it was found to be much larger than the single chain protein. The molecular weight of functional protein S when measured by sedimentation equilibrium with the air-driven ultracentrifuge was observed to be between 115 and 130 kDa. In high salt or in the presence of copper

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Mokin, Y. I., O. I. Povarova, I. A. Antifeeva, K. K. Turoverov, I. M. Kuznetsova, and A. V. Fonin. "COMPARATIVE BIOINFORMATICS ANALYSIS OF NUCLEAR AND CYTOPLASMIC ACTIN-BINDING PROTEINS." In XI МЕЖДУНАРОДНАЯ КОНФЕРЕНЦИЯ МОЛОДЫХ УЧЕНЫХ: БИОИНФОРМАТИКОВ, БИОТЕХНОЛОГОВ, БИОФИЗИКОВ, ВИРУСОЛОГОВ, МОЛЕКУЛЯРНЫХ БИОЛОГОВ И СПЕЦИАЛИСТОВ ФУНДАМЕНТАЛЬНОЙ МЕДИЦИНЫ. IPC NSU, 2024. https://doi.org/10.25205/978-5-4437-1691-6-29.

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Actin is an important protein present in the cytoplasm and nucleus of every eukaryotic cell. Its functional diversity is provided by interaction with actin-binding proteins. The work provides a comparative analysis of nuclear and cytoplasmic actin-binding proteins, including 3 stages: analysis of gene ontology, analysis of physical interactions of proteins, analysis of structural features.

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Masso, Majid, Ewy Mathe, Nida Parvez, Kahkeshan Hijazi, and Iosif I. Vaisman. "Structure Based Functional Analysis of Bacteriophage f1 Gene V Protein." In 2008 IEEE International Conference on Bioinformatics and Biomedicine. IEEE, 2008. http://dx.doi.org/10.1109/bibm.2008.14.

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Zhang Fan, Liu Zhicheng, Li Xia, Gao Zhiwen, and Su Xuan. "Functional Site Analysis in Proteins of G Protein Signaling Pathways Using Fuzzy Evolutionary Trace Method." In 2005 IEEE Engineering in Medicine and Biology 27th Annual Conference. IEEE, 2005. http://dx.doi.org/10.1109/iembs.2005.1615537.

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Vatansever, Serap, Rachel Mitacek, Vaidehi Narkar, and Pam Ismail. "Comparing the Structural and Functional Characteristics of Novel Proteins from Pennycress (Thlaspi Arvense) and Camelina Sativa." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/xbog8744.

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Justification:Global demand sustainable plant protein ingredients is peaking. Camelina and pennycress are sustainable, short season cover crops with high protein content (25-35% protein) and are thus great potential sources of protein ingredients. Developing commercially viable protein ingredients may expand the use of these sustainable crops for various food applications. Objective: The objective was to evaluate and compare the structural and functional attributes of both proteins extracted under optimized and industry feasible conditions. Methods: Defatted meals from seeds of both crops were

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Jeganathan, Brasathe, Feral Temelli, and Thavaratnam Vasanthan. "Functional properties of faba bean proteins extracted by different aqueous processes for food applications." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/phkb7574.

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Dry fractionation of faba bean protein is a sustainable alternative to energy-intensive wet fractionation approaches. However, it can only lead to relatively modest enrichment in protein content. The primary goal of this study was to compare the impact of aqueous protein extraction processes on the functionalities of faba bean proteins for food applications. Proteins from two Canadian faba bean cultivars Snowbird (zero-tannin, ZT) and Athena (high-tannin, HT) were extracted by dialysis following water extraction (W) and salt extraction (S) processes, and conventional alkali-acid approach (A).

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Reports on the topic "Protein functional analysis"

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Matthews, Lisa, Guanming Wu, Robin Haw, et al. Illuminating Dark Proteins using Reactome Pathways. Reactome, 2022. http://dx.doi.org/10.3180/poster/20221027matthews.

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Diseases are often the consequence of proteins or protein complexes that are non-functional or that function improperly. An active area of research has focused on the identification of molecules that can interact with defective proteins and restore their function. While 22% percent of human proteins are estimated to be druggable, less than fifteen percent are targeted by FDA-approved drugs, and the vast majority of untargeted proteins are understudied or so-called "dark" proteins. Elucidation of the function of these dark proteins, particularly those in commonly drug-targeted protein families,

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Yaswen, Paul. Functional Analysis of BORIS, A Novel DNA Binding Protein. Defense Technical Information Center, 2006. http://dx.doi.org/10.21236/ada448330.

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Yaswen, Paul. Functional Analysis of BORIS, a Novel DNA Binding Protein. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada435433.

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Yaswen, Paul. Functional Analysis of BORIS, a Novel DNA Binding Protein. Defense Technical Information Center, 2007. http://dx.doi.org/10.21236/ada477978.

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Yaswen, Paul. Functional Analysis of BORIS, a Novel DNA Binding Protein. Defense Technical Information Center, 2008. http://dx.doi.org/10.21236/ada481004.

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Anderson, Ryan M. Functional Analysis of TGF-alpha/beta Regulated Protein (TGFRP) in Breast Cancer Angiogenesis. Defense Technical Information Center, 2002. http://dx.doi.org/10.21236/ada412099.

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Newton, Ronald, Joseph Riov, and John Cairney. Isolation and Functional Analysis of Drought-Induced Genes in Pinus. United States Department of Agriculture, 1993. http://dx.doi.org/10.32747/1993.7568752.bard.

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Drought is a common factor limiting timber production in the U.S. and Israel. Loblolly (Pinus taeda) and alleppo pine (Pinus halepensis) seedling survival is reduced when out planted, and growth and reproduction are often hindered by periodic droughts during later stages of tree development. Molecular and gene responses to drought stress have not been characterized. The objectives were to characterize drought-induced gene clones from these pines, to determine the effects of a growth regulator on drought tolerance, ABA levels, and drought-induced gene expression in alleppo pine, and to develop

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Whitham, Steven A., Amit Gal-On, and Tzahi Arazi. Functional analysis of virus and host components that mediate potyvirus-induced diseases. United States Department of Agriculture, 2008. http://dx.doi.org/10.32747/2008.7591732.bard.

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The mechanisms underlying the development of symptoms in response to virus infection remain to be discovered in plants. Insight into symptoms induced by potyviruses comes from evidence implicating the potyviral HC-Pro protein in symptom development. In particular, recent studies link the development of symptoms in infected plants to HC-Pro's ability to interfere with small RNA metabolism and function in plant hosts. Moreover, mutation of the highly conserved FRNK amino acid motif to FINK in the HC-Pro of Zucchini yellow mosaic virus (ZYMV) converts a severe strain into an asymptomatic strain,

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McClure, Michael A., Yitzhak Spiegel, David M. Bird, R. Salomon, and R. H. C. Curtis. Functional Analysis of Root-Knot Nematode Surface Coat Proteins to Develop Rational Targets for Plantibodies. United States Department of Agriculture, 2001. http://dx.doi.org/10.32747/2001.7575284.bard.

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The goal of this research was to provide a better understanding of the interface between root-knot nematodes, Meloidogyne spp., and their host in order to develop rational targets for plantibodies and other novel methods of nematode control directed against the nematode surface coat (SC). Specific objectives were: 1. To produce additional monoclonal SC antibodies for use in Objectives 2, 3, and 4 and as candidates for development of plantibodies. 2. To determine the production and distribution of SC proteins during the infection process. 3. To use biochemical and immunological methods to pertu

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Avni, Adi, and Kirankumar S. Mysore. Functional Genomics Approach to Identify Signaling Components Involved in Defense Responses Induced by the Ethylene Inducing Xyalanase Elicitor. United States Department of Agriculture, 2009. http://dx.doi.org/10.32747/2009.7697100.bard.

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Plant-microbe interactions involve a large number of global regulatory systems, which are essential for plants to protect themselves against pathogen attack. An ethylene-inducing xylanase (EIX) of Trichoderma viride is a potent elicitor of plant defense responses, like hypersensitive response (HR), in specific cultivars of tobacco (Nicotiana tabacum) and tomato (Lycopersicon esculentum). The central goal of this proposal was to investigate the molecular mechanisms that allow plants to specifically activate defense responses after EIX treatment. We proposed to identify cellular signaling compon

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