نتایج جستجو برای: single deepest pocket

تعداد نتایج: 890132  

2010
Lin Sun Daqing Zhang Bin Li Bin Guo Shijian Li

This paper uses accelerometer-embedded mobile phones to monitor one’s daily physical activities for sake of changing people’s sedentary lifestyle. In contrast to the previous work of recognizing user’s physical activities by using a single accelerometer-embedded device and placing it in a known position or fixed orientation, this paper intends to recognize the physical activities in the natural...

2010
Qing Zhou Ladan Gheiratmand Yixin Chen Teck Kwang Lim Jun Zhang Shaowei Li Ningshao Xia Binghai Liu Qingsong Lin Cynthia Y. He

A Golgi-associated bi-lobed structure was previously found to be important for Golgi duplication and cell division in Trypanosoma brucei. To further understand its functions, comparative proteomics was performed on extracted flagellar complexes (including the flagellum and flagellum-associated structures such as the basal bodies and the bi-lobe) and purified flagella to identify new bi-lobe pro...

Journal: :Biochemistry 1993
D G Lambright S Balasubramanian S G Boxer

We have recently reported spectroscopic evidence for structural relaxation of myoglobin (Mb) following photodissociation of MbCO [Lambright, D. G., Balasubramanian, S., & Boxer, S. G. (1991) Chem. Phys. 158, 249-260]. In this paper we report measurements for a series of single amino acid mutants of human myoglobin on the distal side of the heme pocket (positions 45, 64, and 68) in order to exam...

2015
Claire Breslin Peter Hornyak Andrew Ridley Stuart L. Rulten Hana Hanzlikova Antony W. Oliver Keith W. Caldecott

Poly (ADP-ribose) is synthesized at DNA single-strand breaks and can promote the recruitment of the scaffold protein, XRCC1. However, the mechanism and importance of this process has been challenged. To address this issue, we have characterized the mechanism of poly (ADP-ribose) binding by XRCC1 and examined its importance for XRCC1 function. We show that the phosphate-binding pocket in the cen...

Journal: :Journal of computer-aided molecular design 2012
Marco A. C. Neves Maxim Totrov Ruben Abagyan

Flexible docking and scoring using the internal coordinate mechanics software (ICM) was benchmarked for ligand binding mode prediction against the 85 co-crystal structures in the modified Astex data set. The ICM virtual ligand screening was tested against the 40 DUD target benchmarks and 11-target WOMBAT sets. The self-docking accuracy was evaluated for the top 1 and top 3 scoring poses at each...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1988
J Badger I Minor M J Kremer M A Oliveira T J Smith J P Griffith D M Guerin S Krishnaswamy M Luo M G Rossmann

The binding to human rhinovirus 14 of a series of eight antiviral agents that inhibit picornaviral uncoating after entry into host cells has been characterized crystallographically. All of these bind into the same hydrophobic pocket within the viral protein VP1 beta-barrel structure, although the orientation and position of each compound within the pocket was found to differ. The compounds caus...

Journal: :Biochemical Society transactions 2010
Matthew J Belousoff Chen Davidovich Ella Zimmerman Yaron Caspi Itai Wekselman Lin Rozenszajn Tal Shapira Ofir Sade-Falk Leena Taha Anat Bashan Manfred S Weiss Ada Yonath

Structural analysis, supported by biochemical, mutagenesis and computational evidence, indicates that the peptidyltransferase centre of the contemporary ribosome is a universal symmetrical pocket composed solely of rRNA. This pocket seems to be a relic of the proto-ribosome, an ancient ribozyme, which was a dimeric RNA assembly formed from self-folded RNA chains of identical, similar or differe...

Journal: :Molecular pharmacology 1998
M Bläker Y Ren M C Gordon J E Hsu M Beinborn A S Kopin

We have reported previously that the transmembrane domains of the cholecystokinin-B/gastrin receptor (CCK-BR) comprise a putative ligand binding pocket. In the present study, we examined whether amino acid substitutions within the CCK-BR pocket altered the affinities and/or functional activities of L-365,260 (the prototypical nonpeptide CCK-BR antagonist) and two structural derivatives, YM022 (...

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