Are Hydrophobins and/or Non-Specific Lipid Transfer Proteins
... However, in brewing technology the formation and stability of foam are important criteria concerning beer quality. Sørensen and co-workers (1993) reported that barley LTP1 is involved in beer foam formation. LTP1 purified from beer created a good beer foam with high potential in a foam assay. In con ...
... However, in brewing technology the formation and stability of foam are important criteria concerning beer quality. Sørensen and co-workers (1993) reported that barley LTP1 is involved in beer foam formation. LTP1 purified from beer created a good beer foam with high potential in a foam assay. In con ...
APPLICATION OF PANCREATIC ENZYMES IN HYDROLYSIS OF
... functional properties (data not shown). Furthermore, these proteins are known to be strong allergenic factors. Therefore we proposed enzymatic hydrolysis as a method for utilizing egg-white protein precipitate (EWPP). Hydrolysis of the EWPP was performed using the pancreatic serine proteinases try ...
... functional properties (data not shown). Furthermore, these proteins are known to be strong allergenic factors. Therefore we proposed enzymatic hydrolysis as a method for utilizing egg-white protein precipitate (EWPP). Hydrolysis of the EWPP was performed using the pancreatic serine proteinases try ...
Complementary DNA Sequence of a Human Cytoplasmic Actin
... randomly distributed. but rather are clustered in specific regions (see Fig. 2). This suggests that certain segments of the actin sequence may be very crucial for filament formation. The percentage of nucleotides substituted within the coding regions of these sequences is significantly greater than ...
... randomly distributed. but rather are clustered in specific regions (see Fig. 2). This suggests that certain segments of the actin sequence may be very crucial for filament formation. The percentage of nucleotides substituted within the coding regions of these sequences is significantly greater than ...
TITLE : BLAST
... primary biological sequence information such as nucleotides sequence and amino-acids sequence in order to find regions of local similarity. ...
... primary biological sequence information such as nucleotides sequence and amino-acids sequence in order to find regions of local similarity. ...
IvDimitrov_slides
... Conclusions 1. An alignment-free method for in silico prediction of allergens based on the main physicochemical properties of proteins was developed. 2. The method uses z descriptors for representation of amino acids in the protein sequences and ACC transformation for conversion of proteins into ...
... Conclusions 1. An alignment-free method for in silico prediction of allergens based on the main physicochemical properties of proteins was developed. 2. The method uses z descriptors for representation of amino acids in the protein sequences and ACC transformation for conversion of proteins into ...
PDF
... Department of Biochemistry and Center for Metalloenzyme Studies, University of Georgia, Athens, GA 30602, USA (Received 5 May 1994; revision received 7 June 1994; accepted 8 June 1994) ...
... Department of Biochemistry and Center for Metalloenzyme Studies, University of Georgia, Athens, GA 30602, USA (Received 5 May 1994; revision received 7 June 1994; accepted 8 June 1994) ...
How to obtain labeled proteins and what to do with... Marlon J Hinner and Kai Johnsson
... with lipoic acid ligase. Recent promising advances in the incorporation of unnatural amino acids into proteins are also briefly discussed. We describe new tools using tag-mediated labeling methods including the super-resolution microscopy of tagged proteins, the study of the interactions of proteins ...
... with lipoic acid ligase. Recent promising advances in the incorporation of unnatural amino acids into proteins are also briefly discussed. We describe new tools using tag-mediated labeling methods including the super-resolution microscopy of tagged proteins, the study of the interactions of proteins ...
Protein kinases - Institut de recherches cliniques de Montréal
... How many phosphorylation sites are there? If there are ~10,000 proteins per cell with an average length of 400 aa (~ 17% of which are Ser, Thr or Tyr), then there are ~700,000 potential phosphorylation sites for any given kinase (including hidden residues). Although protein kinases have relatively ...
... How many phosphorylation sites are there? If there are ~10,000 proteins per cell with an average length of 400 aa (~ 17% of which are Ser, Thr or Tyr), then there are ~700,000 potential phosphorylation sites for any given kinase (including hidden residues). Although protein kinases have relatively ...
Fractionation of rice glutelin polypeptides using gel filtration
... these components eluted just prior to the 29KD standard, they appearedpresent as free polypeptides and, as such, would be suitable for further characterization and study. Similarly, fraction 4 most likely contained free basic polypeptides, but this fraction was heavily contaminated with the prolamin ...
... these components eluted just prior to the 29KD standard, they appearedpresent as free polypeptides and, as such, would be suitable for further characterization and study. Similarly, fraction 4 most likely contained free basic polypeptides, but this fraction was heavily contaminated with the prolamin ...
User`s guide to GO
... Biocurators have tried to add GO but there is no functional data available Previously: “process_unknown”, “function_unknown”, “component_unknown” Now: “biological process”, “molecular function”, “cellular component” ...
... Biocurators have tried to add GO but there is no functional data available Previously: “process_unknown”, “function_unknown”, “component_unknown” Now: “biological process”, “molecular function”, “cellular component” ...
Structural and functional study of K453E mutant protective
... only two kinds of missense mutations, reflecting mild phenotype (Y249N and F440V; the numbering is based on the initiation codon being taken as codon no. 1), have been reported so far (Shimmoto et al. 1993; Zhou et al. 1991, ...
... only two kinds of missense mutations, reflecting mild phenotype (Y249N and F440V; the numbering is based on the initiation codon being taken as codon no. 1), have been reported so far (Shimmoto et al. 1993; Zhou et al. 1991, ...
proteins: three-dimensional structure
... be quite complex. The connection between two antiparallel strands may be just a small loop (Fig. 6-13a), but the link between tandem parallel strands must be a crossover connection that is out of the plane of the b sheet (Fig. 6-13b). The connecting link in either case can be extensive, often contai ...
... be quite complex. The connection between two antiparallel strands may be just a small loop (Fig. 6-13a), but the link between tandem parallel strands must be a crossover connection that is out of the plane of the b sheet (Fig. 6-13b). The connecting link in either case can be extensive, often contai ...
A Method To Define the Carboxyl Terminal of Proteins
... residues 22-113, (provided by A. R. Ferre-D'Amare and S. K. Burley) was expressed and purified as described.44 The helixloop-helix region of the Drosphila melanogaster protein hairy, residues 30-96, was provided by S. K. Burley. Human karyopherin R-2, residues 40-510, (provided by E. Conti and J. Ku ...
... residues 22-113, (provided by A. R. Ferre-D'Amare and S. K. Burley) was expressed and purified as described.44 The helixloop-helix region of the Drosphila melanogaster protein hairy, residues 30-96, was provided by S. K. Burley. Human karyopherin R-2, residues 40-510, (provided by E. Conti and J. Ku ...
Bioinformatics Explained
... One of the reasons for this is that protein sequences are evolutionarily more conserved than nucleotide sequences. Another good reason for translating the query sequence before the search is that you get protein hits which are likely to be annotated. Thus you can directly see the protein function of ...
... One of the reasons for this is that protein sequences are evolutionarily more conserved than nucleotide sequences. Another good reason for translating the query sequence before the search is that you get protein hits which are likely to be annotated. Thus you can directly see the protein function of ...
Homology Modelling
... CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS TECHNICAL UNIVERSITY OF DENMARK DTU ...
... CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS TECHNICAL UNIVERSITY OF DENMARK DTU ...
Intersubunit contacts are often facilitated by specificity
... recognition of the interaction partner ...
... recognition of the interaction partner ...
products of the dioxygenase reaction ... useful intermediates for natural-product syntheses ...
... enzymes. Such efforts have been reviewed [1]. Recently, human P450 CYP2D6 has been linked to human NADPHcytochrome P450 oxidoreductase (CPR), which is the first report of a functionally complete human P450 fusion enzyme system [26]. Site-directed mutagenesis at a single residue converted the human P ...
... enzymes. Such efforts have been reviewed [1]. Recently, human P450 CYP2D6 has been linked to human NADPHcytochrome P450 oxidoreductase (CPR), which is the first report of a functionally complete human P450 fusion enzyme system [26]. Site-directed mutagenesis at a single residue converted the human P ...
Insilico Studies on Taste Receptor Gene (Tas2r38) and Tas2r38
... functions based on the observation that the TAS2R genes are expressed at various extra-oral sites.( W. MEYERHOF)Various TAS2Rs show quite specific agonist profiles, like ptc & prop, have certain chemical substructures in common. In the formation of bitterness receptors, the human body uses “blueprin ...
... functions based on the observation that the TAS2R genes are expressed at various extra-oral sites.( W. MEYERHOF)Various TAS2Rs show quite specific agonist profiles, like ptc & prop, have certain chemical substructures in common. In the formation of bitterness receptors, the human body uses “blueprin ...
Pharmacophore screening of the Protein Data Bank for specific
... searching the PDB for pockets lined by clusters of aromatic and acidic residues. For each PDB structure, the protein is first stripped of water molecules, ligands (including nucleic acids) and bound peptides (any chain shorter than 25 residues is removed), converted to an ICM object (using the makeB ...
... searching the PDB for pockets lined by clusters of aromatic and acidic residues. For each PDB structure, the protein is first stripped of water molecules, ligands (including nucleic acids) and bound peptides (any chain shorter than 25 residues is removed), converted to an ICM object (using the makeB ...
The complete nucleotide sequence of the RNA coding for the
... long) located approximately 400 nucleotides from the 5' end (1). Unlike most eukaryotlc mRNAs, FMDV RNA is not capped at its 51 end but has a small viral-coded protein (VPg) covalently attached to the terminal 5' uridine residue (2, 3 i The VPg protein is not required for translation and, by correla ...
... long) located approximately 400 nucleotides from the 5' end (1). Unlike most eukaryotlc mRNAs, FMDV RNA is not capped at its 51 end but has a small viral-coded protein (VPg) covalently attached to the terminal 5' uridine residue (2, 3 i The VPg protein is not required for translation and, by correla ...
Identification of fungal oxaloacetate hydrolyase within the
... ability of fungi to produce oxalate with the presence of an oah gene in their genome. This task was made difficult by the fact that fungal genomes encode several OAH homologs having an unusually high level of shared sequence identity. Thus, identification of OAH activity in the gene product would re ...
... ability of fungi to produce oxalate with the presence of an oah gene in their genome. This task was made difficult by the fact that fungal genomes encode several OAH homologs having an unusually high level of shared sequence identity. Thus, identification of OAH activity in the gene product would re ...
Protein Li SDS PAGE
... unknown molecular weight comparing to the ladder. This method is proper to determine the purification of proteins. Staining of samples to become visible Pure proteins and nucleic acids are colourless. To become visible, different methods are used. Dyes that bind aspecifically to every protein is app ...
... unknown molecular weight comparing to the ladder. This method is proper to determine the purification of proteins. Staining of samples to become visible Pure proteins and nucleic acids are colourless. To become visible, different methods are used. Dyes that bind aspecifically to every protein is app ...
Lecture 1 – Classification - LCQB
... organisms. It does not need to follow the evolutionary path of organismic reproduction. Rather, the evolution of proteins is directly related to improved , unaltered or diversified molecular functions, and the protein function is directly related to protein structure. Structures tend to diverge less ...
... organisms. It does not need to follow the evolutionary path of organismic reproduction. Rather, the evolution of proteins is directly related to improved , unaltered or diversified molecular functions, and the protein function is directly related to protein structure. Structures tend to diverge less ...
Lecture 1 – Classification - LCQB
... organisms. It does not need to follow the evolutionary path of organismic reproduction. Rather, the evolution of proteins is directly related to improved , unaltered or diversified molecular functions, and the protein function is directly related to protein structure. Structures tend to diverge less ...
... organisms. It does not need to follow the evolutionary path of organismic reproduction. Rather, the evolution of proteins is directly related to improved , unaltered or diversified molecular functions, and the protein function is directly related to protein structure. Structures tend to diverge less ...
Expressway™ Cell-Free E. coli Expression System
... to allow high-level synthesis of your recombinant protein of interest. At one or several time points after initiating the protein synthesis reaction, the reaction is supplemented with an optimized Feed Buffer containing a proprietary mixture of salts, amino acids, and other substrates that are deple ...
... to allow high-level synthesis of your recombinant protein of interest. At one or several time points after initiating the protein synthesis reaction, the reaction is supplemented with an optimized Feed Buffer containing a proprietary mixture of salts, amino acids, and other substrates that are deple ...