نتایج جستجو برای: fragile histidine triad

تعداد نتایج: 35876  

Journal: :Cancer genomics & proteomics 2012
Selda Samakoglu Dhanvanthri S Deevi Huiling Li Su Wang Mary Murphy Channa Bao Rajiv Bassi Marie Prewett James R Tonra

BACKGROUND Although the addition of epidermal growth factor receptor (EGFR) antibodies to various platinum-based chemotherapy regimens for non-small cell lung cancer (NSCLC) is being actively pursued in the clinic, rationale for the prioritization of specific regimens is lacking. MATERIALS AND METHODS We evaluated the antitumor effects of necitumumab, a recombinant human IgG1 antibody targeti...

2012
Toshiki Kameyama Hitoshi Suzuki Akila Mayeda

Transcripts of the human tumor susceptibility gene 101 (TSG101) are aberrantly spliced in many cancers. A major aberrant splicing event on the TSG101 pre-mRNA involves joining of distant alternative 5' and 3' splice sites within exon 2 and exon 9, respectively, resulting in the extensive elimination of the mRNA. The estimated strengths of the alternative splice sites are much lower than those o...

Journal: :Biochemistry 2013
Xin Zhou Tsui-Fen Chou Brandon E Aubol Chin Ju Park Richard Wolfenden Joseph Adams Carston R Wagner

Human histidine triad nucleotide binding protein 1 (hHint1) is a member of a ubiquitous and ancient branch of the histidine triad protein superfamily. hHint1 is a homodimeric protein that catalyzes the hydrolysis of model substrates, phosphoramidate and acyl adenylate, with a high efficiency. Recently, catalytically inactive hHint1 has been identified as the cause of inherited peripheral neurop...

Journal: :Acta crystallographica. Section D, Biological crystallography 2004
Katherine E McAuley Allan Svendsen Shamkant A Patkar Keith S Wilson

The crystallographic structure of feruloyl esterase from Aspergillus niger has been determined to a resolution of 1.5 A by molecular replacement. The protein has an alpha/beta-hydrolase structure with a Ser-His-Asp catalytic triad; the overall fold of the protein is very similar to that of the fungal lipases. The structure of the enzyme-product complex was determined to a resolution of 1.08 A a...

Journal: :Biochemical Society transactions 2008
Stefan Leitgeb Bernd Nidetzky

The canonical structural motif for co-ordination of non-haem ferrous iron in metal-dependent oxygenases is a facial triad of two histidine residues and one aspartate or glutamate residue. This so-called 2-His-1-carboxylate metallocentre is often accommodated in a double-stranded beta-helix fold with the iron-co-ordinating residues located in the rigid core structure of the protein. At the seque...

Journal: :The Journal of biological chemistry 2002
Pawel Bieganowski Preston N Garrison Santosh C Hodawadekar Gerard Faye Larry D Barnes Charles Brenner

The histidine triad superfamily of nucleotide hydrolases and nucleotide transferases consists of a branch of proteins related to Hint and Aprataxin, a branch of Fhit-related hydrolases, and a branch of galactose-1-phosphate uridylyltransferase (GalT)-related transferases. Although substrates of Fhit and GalT are known and consequences of mutations in Aprataxin, Fhit, and GalT are known, good su...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1981
W W Bachovchin R Kaiser J H Richards J D Roberts

L-Histidine, 90% 13C enriched at the C2 position, was incorporated into the catalytic triad of alpha-lytic protease (EC 3.4.21.12) with the aid of histidine-requiring mutant of Lysobacter enzymogenes (ATC 29487), and the pH dependence of the coupling constant between this carbon atom and its directly bonded proton was reinvestigated. The high degree of specific 13C isotopic enrichment attainabl...

Journal: :Chemical science 2014
David M Nedrud Hui Lin Gilsinia Lopez Santosh K Padhi Graig A Legatt Romas J Kaz-Lauskas

Hevea brasiliensis hydroxynitrile lyase (HbHNL) and salicylic acid binding protein 2 (SABP2, an esterase) share 45% amino acid sequence identity, the same protein fold, and even the same catalytic triad of Ser-His-Asp. However, they catalyze different reactions: cleavage of hydroxynitriles and hydrolysis of esters, respectively. To understand how other active site differences in the two enzymes...

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