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Computational prediction of protein complexes from protein interaction networks / (Record no. 883)

MARC details
000 -LEADER
fixed length control field 06818nam a2200601 i 4500
001 - CONTROL NUMBER
control field 011453064650
003 - CONTROL NUMBER IDENTIFIER
control field MOCL
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20260609132937.0
006 - FIXED-LENGTH DATA ELEMENTS--ADDITIONAL MATERIAL CHARACTERISTICS
fixed length control field m eo d
007 - PHYSICAL DESCRIPTION FIXED FIELD--GENERAL INFORMATION
fixed length control field cr cn |||m|||a
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 170810s2017 nyua fob 000 0deng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number 9781970001532
Qualifying information ebook
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9781970001549
Qualifying information ePub
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9781970001525
Qualifying information paperback
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
Canceled/invalid ISBN 9781970001556
Qualifying information hardcover
024 7# - OTHER STANDARD IDENTIFIER
Standard number or code 10.1145/3064650
Source of number or code doi
035 ## - SYSTEM CONTROL NUMBER
System control number (CaBNVSL)swl00407728
035 ## - SYSTEM CONTROL NUMBER
System control number (OCoLC)1000387350
040 ## - CATALOGING SOURCE
Original cataloging agency CaBNVSL
Language of cataloging eng
Description conventions rda
Transcribing agency CaBNVSL
Modifying agency CaBNVSL
050 #4 - LIBRARY OF CONGRESS CALL NUMBER
Classification number QP551.5
Item number .S753 2017
082 04 - DEWEY DECIMAL CLASSIFICATION NUMBER
Classification number 572.64
Edition information 23
100 1# - MAIN ENTRY--PERSONAL NAME
Personal name Srihari, Sriganesh,
Relator term author.
245 10 - TITLE STATEMENT
Title Computational prediction of protein complexes from protein interaction networks /
Statement of responsibility, etc. Sriganesh Srihari, Chern Han Yong, Limsoon Wong.
250 ## - EDITION STATEMENT
Edition statement First edition.
264 #1 - PRODUCTION, PUBLICATION, DISTRIBUTION, MANUFACTURE, AND COPYRIGHT NOTICE
Place of production, publication, distribution, manufacture [New York] :
Name of producer, publisher, distributor, manufacturer Association for Computing Machinery ;
Place of production, publication, distribution, manufacture [San Rafael, California] :
Name of producer, publisher, distributor, manufacturer Morgan & Claypool,
Date of production, publication, distribution, manufacture, or copyright notice 2017.
300 ## - PHYSICAL DESCRIPTION
Extent 1 PDF (xiv, 281 pages) :
Other physical details illustrations.
336 ## - CONTENT TYPE
Content type term text
Source rdacontent
337 ## - MEDIA TYPE
Media type term electronic
Source isbdmedia
338 ## - CARRIER TYPE
Carrier type term online resource
Source rdacarrier
490 1# - SERIES STATEMENT
Series statement ACM books,
International Standard Serial Number 2374-6777 ;
Volume/sequential designation #16
538 ## - SYSTEM DETAILS NOTE
System details note Mode of access: World Wide Web.
538 ## - SYSTEM DETAILS NOTE
System details note System requirements: Adobe Acrobat Reader.
504 ## - BIBLIOGRAPHY, ETC. NOTE
Bibliography, etc. note Includes bibliographical references (pages 233-278).
505 0# - FORMATTED CONTENTS NOTE
Formatted contents note 1. Introduction to protein complex prediction -- 1.1 From protein interactions to protein complexes -- 1.2 Databases for protein complexes -- 1.3 Organization of the rest of the book --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 2. Constructing reliable protein-protein interaction (PPI) networks -- 2.1 High-throughput experimental systems to infer PPIs -- 2.2 Data sources for PPIs -- 2.3 Topological properties of PPI networks -- 2.4 Theoretical models for PPI networks -- 2.5 Visualizing PPI networks -- 2.6 Building high-confidence PPI networks -- 2.7 Enhancing PPI networks by integrating functional interactions --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 3. Computational methods for protein complex prediction from PPI networks -- 3.1 Basic definitions and terminologies -- 3.2 Taxonomy of methods for protein complex prediction -- 3.3 Methods based solely on PPI network clustering -- 3.4 Methods incorporating core-attachment structure -- 3.5 Methods incorporating functional information --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 4. Evaluating protein complex prediction methods -- 4.1 Evaluation criteria and methodology -- 4.2 Evaluation on unweighted yeast PPI networks -- 4.3 Evaluation on weighted yeast PPI networks -- 4.4 Evaluation on human PPI networks -- 4.5 Case study: prediction of the human mechanistic target of Rapamycin complex -- 4.6 Take-home lessons from evaluating prediction methods --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 5. Open challenges in protein complex prediction -- 5.1 Three main challenges in protein complex prediction -- 5.2 Identifying sparse protein complexes -- 5.3 Identifying overlapping protein complexes -- 5.4 Identifying small protein complexes -- 5.5 Identifying protein sub-complexes -- 5.6 An integrated system for identifying challenging protein complexes -- 5.7 Recent methods for protein complex prediction -- 5.8 Identifying membrane-protein complexes --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 6. Identifying dynamic protein complexes -- 6.1 Dynamism of protein interactions and protein complexes -- 6.2 Identifying temporal protein complexes -- 6.3 Intrinsic disorder in proteins -- 6.4 Intrinsic disorder in protein interactions and protein complexes -- 6.5 Identifying fuzzy protein complexes --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 7. Identifying evolutionarily conserved protein complexes -- 7.1 Inferring evolutionarily conserved PPIs (interologs) -- 7.2 Identifying conserved complexes from interolog networks, I -- 7.3 Identifying conserved complexes from interolog networks, II --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 8. Protein complex prediction in the era of systems biology -- 8.1 Constructing the network of protein complexes -- 8.2 Identifying protein complexes across phenotypes -- 8.3 Identifying protein complexes in diseases -- 8.4 Enhancing quantitative proteomics using PPI networks and protein complexes -- 8.5 Systems biology tools and databases to analyze biomolecular networks --
505 8# - FORMATTED CONTENTS NOTE
Formatted contents note 9. Conclusion -- References -- Authors' biographies.
520 3# - SUMMARY, ETC.
Summary, etc. Complexes of physically interacting proteins constitute fundamental functional units that drive almost all biological processes within cells. A faithful reconstruction of the entire set of protein complexes (the "complexosome") is therefore important not only to understand the composition of complexes but also the higher level functional organization within cells. Advances over the last several years, particularly through the use of high-throughput proteomics techniques, have made it possible to map substantial fractions of protein interactions (the "interactomes") from model organisms including Arabidopsis thaliana (a flowering plant), Caenorhabditis elegans (a nematode), Drosophila melanogaster (fruit fly), and Saccharomyces cerevisiae (budding yeast). These interaction datasets have enabled systematic inquiry into the identification and study of protein complexes from organisms. Computational methods have played a significant role in this context, by contributing accurate, efficient, and exhaustive ways to analyze the enormous amounts of data. These methods have helped to compensate for some of the limitations in experimental datasets including the presence of biological and technical noise and the relative paucity of credible interactions. In this book, we systematically walk through computational methods devised to date (approximately between 2000 and 2016) for identifying protein complexes from the network of protein interactions (the protein-protein interaction (PPI) network). We present a detailed taxonomy of these methods, and comprehensively evaluate them for protein complex identification across a variety of scenarios including the absence of many true interactions and the presence of false-positive interactions (noise) in PPI networks. Based on this evaluation, we highlight challenges faced by the methods, for instance in identifying sparse, sub-, or small complexes and in discerning overlapping complexes, and reveal how a combination of strategies is necessary to accurately reconstruct the entire complexosome.
530 ## - ADDITIONAL PHYSICAL FORM AVAILABLE NOTE
Additional physical form available note Also available in print.
588 ## - SOURCE OF DESCRIPTION NOTE
Source of description note Title from PDF title page (viewed on August 10, 2017).
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Protein-protein interactions
General subdivision Computer simulation.
655 #0 - INDEX TERM--GENRE/FORM
Genre/form data or focus term Electronic books.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Yong, Chern Han,
Relator term author.
700 1# - ADDED ENTRY--PERSONAL NAME
Personal name Wong, Limsoon,
Dates associated with a name 1965-,
Relator term author.
776 08 - ADDITIONAL PHYSICAL FORM ENTRY
Relationship information Print version:
International Standard Book Number 9781970001556
-- 9781970001525
830 #0 - SERIES ADDED ENTRY--UNIFORM TITLE
Uniform title ACM books ;
Volume/sequential designation #16.
International Standard Serial Number 2374-6777
856 48 - ELECTRONIC LOCATION AND ACCESS
Materials specified Abstract with links to full text
Uniform Resource Identifier <a href="http://dx.doi.org/10.1145/3064650">http://dx.doi.org/10.1145/3064650</a>

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