![]() (Glu1)-Fibrinopeptide B (human) structure
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Common Name | (Glu1)-Fibrinopeptide B (human) | ||
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CAS Number | 103213-49-6 | Molecular Weight | 1570.572 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 1624.1±75.0 °C at 760 mmHg | |
Molecular Formula | C66H95N19O26 | Melting Point | N/A | |
MSDS | USA | Flash Point | 936.0±37.1 °C |
An integrated workflow for charting the human interaction proteome: insights into the PP2A system.
Mol. Syst. Biol. 5 , 237, (2009) Protein complexes represent major functional units for the execution of biological processes. Systematic affinity purification coupled with mass spectrometry (AP-MS) yielded a wealth of information on the compendium of protein complexes expressed in Saccharom... |
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Albumin is synthesized in epididymis and aggregates in a high molecular mass glycoprotein complex involved in sperm-egg fertilization.
PLoS ONE 9(8) , e103566, (2014) The epididymis has an important role in the maturation of sperm for fertilization, but little is known about the epididymal molecules involved in sperm modifications during this process. We have previously described the expression pattern for an antigen in ep... |
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Radioimmunoassay of human fibrinopeptide B and kinetics of fibrinopeptide cleavage by different enzymes.
J. Clin. Invest. 56(2) , 438-45, (1975) Thrombin converts fibrinogen to fibrin monomer by cleaving fibrinopeptides A and B (FPA and FPB) from the amino terminal ends of the A (alpha) and B (beta) chains. A radioimmunoassay capable of measuring the A peptide in human blood as an index of thrombin ac... |
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Effects of fibrinogen derivatives upon the inflammatory response. Studies with human fibrinopeptide B.
J. Clin. Invest. 77(3) , 1014-9, (1986) Fibrin formation and turnover are intimately associated with inflammation and wound healing. To explore whether fibrin(ogen)-derived peptides exert direct effects upon cells involved in inflammation and tissue repair we examined the capacity of human fibrinop... |
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Plasticity of human protein disulfide isomerase: evidence for mobility around the X-linker region and its functional significance.
J. Biol. Chem. 285(35) , 26788-97, (2010) Protein disulfide isomerase (PDI), which consists of multiple domains arranged as abb'xa'c, is a key enzyme responsible for oxidative folding in the endoplasmic reticulum. In this work we focus on the conformational plasticity of this enzyme. Proteolysis of n... |
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Insight into the Sialome of the Bed Bug, Cimex lectularius.
J. Proteome Res. 9(8) , 3820-31, (2010) The evolution of insects to a blood diet leads to the development of a saliva that antagonizes their hosts' hemostasis and inflammation. Hemostasis and inflammation are redundant processes, and thus a complex salivary potion composed of dozens or near 100 dif... |
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SuperHirn - a novel tool for high resolution LC-MS-based peptide/protein profiling.
Proteomics 7(19) , 3470-80, (2007) Label-free quantification of high mass resolution LC-MS data has emerged as a promising technology for proteome analysis. Computational methods are required for the accurate extraction of peptide signals from LC-MS data and the tracking of these features acro... |
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Proteasomal protein degradation in Mycobacteria is dependent upon a prokaryotic ubiquitin-like protein.
J. Bacteriol. 284 , 3069-75, (2009) The striking identification of an apparent proteasome core in Mycobacteria and allied actinomycetes suggested that additional elements of this otherwise strictly eukaryotic system for regulated protein degradation might be conserved. The genes encoding this p... |
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Mass spectral characterization of organophosphate-labeled, tyrosine-containing peptides: characteristic mass fragments and a new binding motif for organophosphates.
J. Chromatogr. B. Analyt. Technol. Biomed. Life Sci. 878 , 1297-311, (2010) We have identified organophosphorus agent (OP)-tyrosine adducts on 12 different proteins labeled with six different OP. Labeling was achieved by treating pure proteins with up to 40-fold molar excess of OP at pH 8-8.6. OP-treated proteins were digested with t... |
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Towards a rational approach for heavy-atom derivative screening in protein crystallography.
Acta Crystallogr. D Biol. Crystallogr. 64 , 354-67, (2008) Heavy-atom derivatization is routinely used in protein structure determination and is thus of critical importance in structural biology. In order to replace the current trial-and-error heavy-atom derivative screening with a knowledge-based rational derivative... |