2014
DOI: 10.1186/1752-0509-8-8
|View full text |Cite
|
Sign up to set email alerts
|

Exploring metabolism flexibility in complex organisms through quantitative study of precursor sets for system outputs

Abstract: BackgroundWhen studying metabolism at the organ level, a major challenge is to understand the matter exchanges between the input and output components of the system. For example, in nutrition, biochemical models have been developed to study the metabolism of the mammary gland in relation to the synthesis of milk components. These models were designed to account for the quantitative constraints observed on inputs and outputs of the system. In these models, a compatible flux distribution is first selected. Alter… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
5
0

Year Published

2015
2015
2024
2024

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(5 citation statements)
references
References 52 publications
0
5
0
Order By: Relevance
“…Topological analysis and flux balance analysis have been used to describe metabolism based on static approaches (Jeong et al, 2000;Wagner and Fell, 2001;Blavy et al, 2014;Abdou-Arbi et al, 2014). At the cellular scale, the main metabolic pathways have been notably integrated into a generic stoichiometric model by our group (van Milgen, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…Topological analysis and flux balance analysis have been used to describe metabolism based on static approaches (Jeong et al, 2000;Wagner and Fell, 2001;Blavy et al, 2014;Abdou-Arbi et al, 2014). At the cellular scale, the main metabolic pathways have been notably integrated into a generic stoichiometric model by our group (van Milgen, 2002).…”
Section: Introductionmentioning
confidence: 99%
“…NETSIM2 is evaluated based on the EC number (Enzyme Commission) group information, which has been used in previous research [ 18 ]. The idea is that genes that are labeled by the same EC number have the similar function.…”
Section: Resultsmentioning
confidence: 99%
“…Then, we test whether the genes in the same category have higher similarity than genes in different categories. Mathematically, we use the logged fold change (LFC) measure [ 18 ] for quantitative evaluation. The LFC score of EC number e i is calculated as follows: …”
Section: Resultsmentioning
confidence: 99%
“…The cytoHubba plug-in was employed to explore important nodes using several topological algorithms, such as Degree, Maximum Neighborhood Component (MNC) and centralities based on shortest paths, including bottleneck (BN), betweenness, and radiality. 16 Proteins with high degree and betweenness might be important candidate genes which have key physiological regulatory functions.…”
Section: Methodsmentioning
confidence: 99%