Search results for " GENOMICS"

showing 10 items of 390 documents

Protein NMR Structures Refined with Rosetta Have Higher Accuracy Relative to Corresponding X-ray Crystal Structures

2014

We have found that refinement of protein NMR structures using Rosetta with experimental NMR restraints yields more accurate protein NMR structures than those that have been deposited in the PDB using standard refinement protocols. Using 40 pairs of NMR and X-ray crystal structures determined by the Northeast Structural Genomics Consortium, for proteins ranging in size from 5-22 kDa, restrained Rosetta refined structures fit better to the raw experimental data, are in better agreement with their X-ray counterparts, and have better phasing power compared to conventionally determined NMR structures. For 37 proteins for which NMR ensembles were available and which had similar structures in solu…

Models MolecularChemistryProtein ConformationProtein Data Bank (RCSB PDB)X-rayProteinsGeneral ChemistryNuclear magnetic resonance crystallographyCrystal structureCrystallography X-RayBiochemistryCatalysisArticleStructural genomicsCrystalCrystallographyColloid and Surface ChemistryMolecular replacementComputer SimulationNuclear Magnetic Resonance BiomolecularSoftwareJournal of the American Chemical Society
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Evaluating protein structures determined by structural genomics consortia.

2006

Structural genomics projects are providing large quantities of new 3D structural data for proteins. To monitor the quality of these data, we have developed the protein structure validation software suite (PSVS), for assessment of protein structures generated by NMR or X-ray crystallographic methods. PSVS is broadly applicable for structure quality assessment in structural biology projects. The software integrates under a single interface analyses from several widely-used structure quality evaluation tools, including PROCHECK (Laskowski et al., J Appl Crystallog 1993;26:283-291), MolProbity (Lovell et al., Proteins 2003;50:437-450), Verify3D (Luthy et al., Nature 1992;356:83-85), ProsaII (Si…

Models MolecularComputer scienceProtein Data Bank (RCSB PDB)GenomicsComputational biologycomputer.software_genreCrystallography X-RayBiochemistryStructural genomicsProtein structureStructural BiologySoftware DesignHumansDatabases ProteinMolecular BiologyNuclear Magnetic Resonance BiomolecularSoftware suiteComputational BiologyProteinsGenomicsProtein Structure TertiaryCrystallographyStructural biologyQuality ScorecomputerData integrationProteins
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A new evolutionary paradigm for the Parkinson disease gene DJ-1.

2006

The DJ-1 gene is extensively studied because of its involvement in familial Parkinson disease. DJ-1 belongs to a complex superfamily of genes that includes both prokaryotic and eukaryotic representatives. We determine that many prokaryotic groups, such as proteobacteria, cyanobacteria, spirochaetes, firmicutes, or fusobacteria, have genes, often incorrectly called "Thij," that are very close relatives of DJ-1, to the point that they cannot be clearly separated from the eukaryotic DJ-1 genes by phylogenetic analyses of their sequences. In addition, and contrary to a previous study that suggested that DJ-1 genes were animal specific, we show that DJ-1 genes are found in at least 5 of the 6 ma…

Models MolecularGenes FungalMolecular Sequence DataProtein Deglycase DJ-1Genes PlantAmoebozoaEvolution MolecularPhylogeneticsGeneticsAmino Acid SequenceMolecular BiologyGeneEcology Evolution Behavior and SystematicsPhylogenyChromalveolataGeneticsComparative genomicsOncogene ProteinsPhylogenetic treebiologyIntracellular Signaling Peptides and ProteinsFusobacteriaParkinson Diseasebiology.organism_classificationEukaryotic CellsProkaryotic CellsGenes BacterialSchizosaccharomyces pombeSequence AlignmentMolecular biology and evolution
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Assessing model accuracy using the homology modeling automatically software

2007

Homology modeling is a powerful technique that greatly increases the value of experimental structure determination by using the structural information of one protein to predict the structures of homologous proteins. We have previously described a method of homology modeling by satisfaction of spatial restraints (Li et al., Protein Sci 1997;6:956-970). The Homology Modeling Automatically (HOMA) web site,http://www-nmr.cabm.rutgers.edu/HOMA, is a new tool, using this method to predict 3D structure of a target protein based on the sequence alignment of the target protein to a template protein and the structure coordinates of the template. The user is presented with the resulting models, togeth…

Models MolecularProtein Conformationbusiness.industryProteinsSequence alignmentStructure validationComputational biologyProtein superfamilyMachine learningcomputer.software_genreBiochemistryHomology (biology)Structural genomicsProtein structureStructural BiologyArtificial intelligenceTarget proteinHomology modelingbusinessMolecular BiologycomputerSoftwareMathematicsProteins: Structure, Function, and Bioinformatics
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NMR structure of hypothetical protein TA0938 from Thermoplasma acidophilum.

2007

Models MolecularbiologySequence Homology Amino AcidChemistryThermoplasmaArchaeal ProteinsArchaeal ProteinsHypothetical proteinThermoplasmaMolecular Sequence DataThermoplasma acidophilumSequence alignmentComputational biologybiology.organism_classificationBiochemistryStructural genomicsProtein Structure TertiaryStructural BiologyAmino Acid SequenceMolecular BiologyPeptide sequenceNuclear Magnetic Resonance BiomolecularSequence AlignmentProteins
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Comparative genomic sequencing reveals a strikingly similar architecture of a conserved syntenic region on human chromosome 11p15.3 (including gene S…

2001

Comparative genomics is a superior way to identify phylogenetically conserved features like genes or regions involved in gene regulation. The comparison of extended orthologous chromosomal regions should also reveal other characteristic traits essential for chromosome or gene function. In the present study we have sequenced and compared a region of conserved synteny from human chromosome 11p15.3 and mouse chromosome 7. In human, this region is known to contain several genes involved in the development of various disorders like Beckwith-Wiedemann overgrowth syndrome and other tumor diseases. Furthermore, in the neighboring chromosome region 11p15.5 extensive imprinting of genes has been repo…

Molecular Sequence DataeducationGenomicsBiologyChromosomesContig MappingMiceGene OrderGeneticsAnimalsHumansCloning MolecularMolecular BiologyGeneConserved SequenceGenetics (clinical)Repetitive Sequences Nucleic AcidSyntenyRegulation of gene expressionChromosome 7 (human)Comparative genomicsGeneticsChromosomes Human Pair 11Tumor Suppressor ProteinsGenomic sequencingChromosomeSequence Analysis DNAGC Rich SequenceDNA-Binding ProteinsCytogenetic and Genome Research
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Primate Cytogenetics and Comparative Genomics

2006

This volume is a collection of contributions of a Florentine post congress symposium on "Primate Cytogenetics and Comparative Genomics" held on occasion of the XX International Primatological Congress (Turin in 2004). Comparative Molecular Cytogenetics and Genomics are two rapidly expanding fields. Researchers from Italy, Germany, Spain, United States and Japan meet in Florence to discuss over a two day period recent advances and summarize the current state of the science.

Molecular cytogeneticsComparative genomicsmedicine.medical_specialtyHistoryeducationCytogeneticsmedicineLibrary scienceState of the sciencehealth care economics and organizations
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Gadolinium-chelating nanogels as MR contrast agents specifically targeting tumor cells

2014

Aims and objectives Methods and materials Results Conclusion Personal information References

Molecular imaging Diagnostic procedure MR-Functional imaging MR Contrast agentsMolecular genomics and proteomicsgenetic structuresMolecular imagingMRDiagnostic procedureContrast agentsMR-Functional imaging
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Small genomes and the difficulty to define minimal translation and metabolic machineries

2015

The notion of minimal life has sparked the interest of scientists in different fields, ranging from the origin-of-life research to biotechnology-oriented synthetic biology. Whether the interest is focused on the emergence of protocells out of prebiotic systems or the design of a cell chassis ready to incorporate new devices and functions, proposing minimal combinations of genes for life is not a trivial task. Using comparative genomics and biochemistry of endosymbionts (i.e., intracellular mutualistic symbionts) and intracellular parasites, a decade ago we proposed the core of a minimal gene set for a simple heterotrophic cell adapted to a chemically complex environment. In this work, we di…

Muller’s ratchettRNA post-transcriptional modificationslcsh:EvolutionMetabolic networkComputational biologyBiologyGenomeMicrobiology03 medical and health sciencesSynthetic biologylcsh:QH540-549.5lcsh:QH359-425GeneEcology Evolution Behavior and Systematics030304 developmental biologyComparative genomicsGenetics0303 health sciencesstreamlining hypothesisEcology030306 microbiologyMuller's ratchetminimal metabolismminimal cellMuller's ratchetMinimal genomeSynthetic Biologylcsh:EcologyFlux (metabolism)Black Queen HypothesisFrontiers in Ecology and Evolution
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The Relationship Between Polygenic Risk Scores and Cognition in Schizophrenia

2020

Abstract Background Cognitive impairment is a clinically important feature of schizophrenia. Polygenic risk score (PRS) methods have demonstrated genetic overlap between schizophrenia, bipolar disorder (BD), major depressive disorder (MDD), educational attainment (EA), and IQ, but very few studies have examined associations between these PRS and cognitive phenotypes within schizophrenia cases. Methods We combined genetic and cognitive data in 3034 schizophrenia cases from 11 samples using the general intelligence factor g as the primary measure of cognition. We used linear regression to examine the association between cognition and PRS for EA, IQ, schizophrenia, BD, and MDD. The results wer…

Multifactorial InheritanceBipolar DisorderDatasets as TopicINTELLIGENCEGenome-wide association study0302 clinical medicinegenetics [Schizophrenia]education.field_of_studyHERITABILITYCOMMON VARIANTSCognitionbioinformaticsintelligencepsychiatryABILITYPsychiatry and Mental healthSchizophreniaMajor depressive disorderEducational Statuspsychiatry genomics intelligence bioinformaticsClinical psychologyPopulationgenetics [Psychotic Disorders]behavioral disciplines and activities03 medical and health sciencesmental disordersgenomicsmedicineHumansBipolar disorderddc:610GENOME-WIDE ASSOCIATIONeducationSettore MED/25 - PsichiatriaMETAANALYSISGenetic associationDepressive Disorder MajorENDOPHENOTYPESbusiness.industryMEMORYCONSORTIUMgenetics [Depressive Disorder Major]PERFORMANCEmedicine.disease030227 psychiatryPsychotic Disordersgenetics [Intelligence]EndophenotypeSchizophreniabusiness030217 neurology & neurosurgerygenetics [Bipolar Disorder]Regular ArticlesGenome-Wide Association Study
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