Analysis of light spectra.

Slides:



Advertisements
Similar presentations
Derivative Review Part 1 3.3,3.5,3.6,3.8,3.9. Find the derivative of the function p. 181 #1.
Advertisements

3.1 Definition of the Derivative & Graphing the Derivative
Journal of Vision. 2016;16(15):21. doi: / Figure Legend:
Statistical colorings of 1H NMR estimates of biochemical variables.
Growth rate‐dependent gene expression under glucose limitation.
Waves.
Abundance of proteins matching selected subcellular locations and functions in CaCo‐2 cells. Abundance of proteins matching selected subcellular locations.
Principles of using neural networks for predicting molecular traits from DNA sequence Principles of using neural networks for predicting molecular traits.
Simulation of oxygen and substrate demands for ammonia detoxification.
Summary of clinical and metabolic characteristics.
Quantitative proteomics reveals daf‐16‐mediated reduction in protein metabolism in long‐lived daf‐2(e1370) mutants. Quantitative proteomics reveals daf‐16‐mediated.
Usage of l‐carnitine antimetabolites for the treatment of HCCl‐Carnitine and metabolites in the l‐carnitine biosynthetic pathway, as well as two essential.
Analysis of mutational effects of parameters on the phenotype (i. e
Most promoters preserve their relative activity levels across conditions. Most promoters preserve their relative activity levels across conditions. (A)
(A) Graph depicting interaction between the five regulatory motifs measured by synergy and cooccurrence. (A) Graph depicting interaction between the five.
Analysis of in silico flux changes along the exponential growth phase: (A) In silico flux changes from 24 to 36 h, from 36 to 48 h, and from 48 to 60 h.
Volume 112, Issue 2, Pages (January 2017)
Illustration of the reactions and metabolites obtained from random sampling. Illustration of the reactions and metabolites obtained from random sampling.
Motif detectability corresponds to the phylogenetic profile of the cognate transcription factor. Motif detectability corresponds to the phylogenetic profile.
Heatmaps of the gene mutation distributions in oncogene‐signaling blocks for six representative cancer types. Heatmaps of the gene mutation distributions.
Predicted and measured double‐ring formation.
Validation of the CCE associations by mass spectrometry.
Comparative analysis of RNA and protein profiles.
Confirmation of pool data with isogenic culture
Model training of generalized Lotka–Volterra (gLV) to time‐resolved measurements of monospecies and pairwise assemblages Model training of generalized.
ATOMIC SPECTRA.
Solar spectrum and absorption profiles of chlorophyll and bacteriochlorophyll pigments Solar spectrum and absorption profiles of chlorophyll and bacteriochlorophyll.
Network derived from large‐scale fractionation predicts 48 protein complexes and communities Network derived from large‐scale fractionation predicts 48.
Overview of lysine‐acetylated proteins in the light reactions (A) and the Calvin–Benson cycle (B) identified in this study in Arabidopsis Overview of lysine‐acetylated.
Intracellular noise in the cAMP circuit drives observed population behaviors Firing rate phase diagrams for single cells in a population (top) and the.
FLAME TEST.
Protein–lipid map in yeast.
Detection of specific interacting partners of CBL and CBLB in peripheral CD4+ T cells prior to and following TCR stimulation Detection of specific interacting.
Alignment time for Clustal Omega (red), MAFFT (blue), MUSCLE (green) and Kalign (purple) against the number of sequences of HomFam test sets. Alignment.
Consequences of reducing SF3B2 expression.
The limiting, degrading entity hypothesis
Visualization of a global auxin‐response gradient in the root meristem
Examples for intrachromosomal mRNA co‐regulation patches
Effect of the loss of Kar4 on the induction of various promoters
Characterization of Factor 5 (oxidative stress response factor) in the CLL data Characterization of Factor 5 (oxidative stress response factor) in the.
Patient organoids respond more diverse to drugs and with lower therapeutic potential than 2D cultured patient cells Patient organoids respond more diverse.
Shared components define the ‘ancient’ phagosome.
Antisense transcription, measurement, and correction
Transcriptomic and epigenetic changes associated with Factor 1 in the scMT data Transcriptomic and epigenetic changes associated with Factor 1 in the scMT.
Comparison of proteomics and RNA‐Seq data.
Determination of mRNA synthesis and decay rates.
Simulation showing that the cell length variability of the entire population can mask abnormal cell length variability at a specific cell cycle period.
An integrated NHR network.
The metabolic network of arachidonic acid in human PMN, EC and PLT
Stage‐dependent diurnal transcript changes.
Example transcript and protein patterns.
Reproducibility of DeathPro drug screens
Cluster analysis of all identified models.
Community diversity and metagenome depth interact to influence assembly quality. Community diversity and metagenome depth interact to influence assembly.
Melting behavior of protein complexes
Correlations between metabolic pathway abundances and environmental conditions deduced from the ocean samples in this study, at various levels of model.
Dynamic transcriptome analysis in yeast.
Schematic representation of the data structure.
Global and focused views of human interaction map.
Patterns and regulation of age‐related splicing changes.
Functional metabolic rearrangements in chloramphenicol‐resistant populations Functional metabolic rearrangements in chloramphenicol‐resistant populations.
Correlation of flux and enzyme concentration (inferred from transcripts) changes for reactions in central metabolism. Correlation of flux and enzyme concentration.
Integration of proteomic data into the model
MinD tethers DNA to liposomes in an ATP‐dependent manner.
Many of the diseases associated with high coevolution scores share genetic components. Many of the diseases associated with high coevolution scores share.
Metabolic differences in the small intestine AMetabolic genes as well as the associated reactions involved in the formation of glutathione (GSH) are presented.B,
NMR spectra of Erk. NMR spectra of Erk. (A) Superimposed 1H/15N HSQC spectra of Erk‐pTpY (black) and Erk‐TY (red). Blue circles and arrows mark the C‐terminal.
Oscillations in isotopic labeling of TCA cycle metabolites throughout the cell cycle from [U‐13C]‐glucose show induced glycolytic flux into TCA cycle in.
Contribution of amino‐acid production to the catabolism of BCAAs and AAAs, and to ATP generation under slow‐growing conditions. Contribution of amino‐acid.
Volume 75, Issue 2, Pages (August 1998)
Presentation transcript:

Analysis of light spectra. Analysis of light spectra. (A) Activity and irradiance spectra. The top graph displays activity spectra for photon‐utilizing reactions included in iRC1080. The abbreviated reactions are defined as follows: VITD3, vitamin D3 synthesis; OPSIN, rhodopsin photoisomerase; PCHLD, both protochlorophyllide photoreductase and divinylprotochlorophyllide photoreductase; PSI, photosystem I; PSII, photosystem II. The y axis for the activity spectra is the fraction of maximum‐measured activity with respect to each noted reaction. Four of the eleven sample irradiance spectra (Supplementary Figure S3) are depicted with y axes set as the percentage of total visible photon flux at each wavelength (x axis). Effective spectral bandwidths are denoted by vertical dashed lines color coded to match the activity spectra for each reaction. (B) Prism reaction derivation. The photon flux from wavelengths a to b is normalized by the total visible photon flux from 380 to 750 nm to yield the effective spectral bandwidth coefficient C. The coefficients for each range are compiled into a single prism reaction for a given light source, representing the composition of emitted light as defined by photon‐utilizing metabolic reactions. Equation variables are defined at top. Roger L Chang et al. Mol Syst Biol 2011;7:518 © as stated in the article, figure or figure legend