نتایج جستجو برای: proadrenomedullin n terminal 20 peptide

تعداد نتایج: 1704817  

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1972
N K Chatterjee S S Kerwar H Weissbach

Initiation of protein synthesis in HeLa cells has been synchronized by exposure of the cells to fluoride. Double-labeling of such cells for short pulses with [(35)S]methionine and a tritiated amino acid, followed by Edman degradation of the puromycin-released nascent peptides, has shown that the percent of N-terminal methionine incorporated compared to total incorporation is significantly highe...

Journal: :Biochimica et biophysica acta 2009
Masaki Takahashi Mineyuki Mizuguchi Hiroyuki Shinoda Tomoyasu Aizawa Makoto Demura Hitoshi Okazawa Keiichi Kawano

Polyglutamine tract binding protein-1 (PQBP-1) is a nuclear protein that interacts with disease proteins containing expanded polyglutamine repeats. PQBP-1 also interacts with RNA polymerase II and a spliceosomal protein U5-15kD. In the present study, we demonstrate that PQBP-1 is composed of a large unstructured region and a small folded core. Intriguingly, the large unstructured region encompa...

Journal: :Chemical communications 2011
Damodara N Reddy Ravula Thirupathi Erode N Prabhakaran

Selective modification of the C-terminal amide in peptides to dihydrooxazine (a novel stable imidate isostere) by intramolecular nucleophilic cyclo-O-alkylation of the corresponding N-(3-bromopropyl)amides results in constraining of the C-terminal residue in natively disallowed conformations both in crystals and in solution.

Journal: :Biochimica et biophysica acta 2014
Christopher E Jones Claire B Otara Nadine D Younan John H Viles Maurice R Elphick

The starfish SALMFamide neuropeptides S1 (GFNSALMFamide) and S2 (SGPYSFNSGLTFamide) are the prototypical members of a family of neuropeptides that act as muscle relaxants in echinoderms. Comparison of the bioactivity of S1 and S2 as muscle relaxants has revealed that S2 is ten times more potent than S1. Here we investigated a structural basis for this difference in potency by comparing the bioa...

A new biological active hexapeptide of C-terminal of nocistatin, contains Glu-Gln-Lys-Gln-Leu-Gln sequence was synthesized according to solid phase peptide synthesis on the surface of 2-chloro tritylchloride resin and using fmoc-protected amino acids in the presence of TBTU (O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyl uranium tetrafluoroborate) as a coupling reagent. Then, amidation of the C-te...

2005
T. A. Blasingame J. A. Rushing

This paper presents a systematic method for the direct estimation of gas-in-place and reserves using only gas production data. The fundamental concept used in this work is "quadratic" rate-cumulative relation, which is given as: 2 2 1 p i p i gi g G G D G D q q + − = ................................................... (1) Where we define the decline constant, Di, for this case as:

Journal: :Organic letters 2005
Yi-An Lu James P Tam

[reaction: see text] Peptide ligation of noncysteinyl residues can be achieved conveniently by a reversible C-terminal thiol handle together with a Ag(+) ion-assisted S,N-acyl migration. The regenerated C-terminal handle permits tandem ligation of multiple segment.

Journal: :FEBS Journal 2021

Lanthipeptides are ribosomally synthesized and posttranslationally modified peptides. Their precursor peptide comprises of an N‐terminal leader a C‐terminal core peptide. Here, the is crucial for enzyme recognition especially modification enzymes acts furthermore as secretion signal lanthipeptide exporter. The target site posttranslational modifications contains dehydrated amino acids lanthioni...

      Kawasaki disease (KD) is characterized as the leading cause of acquired cardiac disease in children. Accurate and timely diagnosis of KD is of high importance for preventing its cardiac complications. However, diagnosis merely based on clinical findings has a number of challenges and, limitations. Therefore, researchers are investigating to find more object...

Journal: :Chemical communications 2011
Valeria Castelletto Ge Cheng Ian W Hamley

A series of heptapeptides comprising the core sequence Aβ(16-20), KLVFF, of the amyloid β peptide coupled with paired N-terminal γ-amino acids are investigated in terms of cytotoxicity reduction and binding to the full Aβ peptide, both pointing to inhibition of fibrillisation for selected compounds. This is related to the self-assembly capacity of the heptapeptides.

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