Single-stranded and double-stranded DNA-binding protein prediction using HMM profiles

2021 ◽  
Vol 612 ◽  
pp. 113954
Author(s):  
Ronesh Sharma ◽  
Shiu Kumar ◽  
Tatsuhiko Tsunoda ◽  
Thirumananseri Kumarevel ◽  
Alok Sharma
2018 ◽  
Vol 452 ◽  
pp. 22-34 ◽  
Author(s):  
M. Saifur Rahman ◽  
Swakkhar Shatabda ◽  
Sanjay Saha ◽  
M. Kaykobad ◽  
M. Sohel Rahman

2005 ◽  
Vol 5 (8) ◽  
pp. 1216-1219 ◽  
Author(s):  
Yunfei Bai ◽  
Qinyu Ge ◽  
Quanjun Liu ◽  
Tongxiang Li ◽  
Jinke Wang ◽  
...  

1992 ◽  
Vol 225 (4) ◽  
pp. 999-1011 ◽  
Author(s):  
Maarten H. Stuiver ◽  
Wilma G. Bergsma ◽  
Annika C. Arnberg ◽  
Herbert van Amerongen ◽  
Rienk van Grondelle ◽  
...  

2017 ◽  
Vol 2017 ◽  
pp. 1-10 ◽  
Author(s):  
Rianon Zaman ◽  
Shahana Yasmin Chowdhury ◽  
Mahmood A. Rashid ◽  
Alok Sharma ◽  
Abdollah Dehzangi ◽  
...  

DNA-binding proteins often play important role in various processes within the cell. Over the last decade, a wide range of classification algorithms and feature extraction techniques have been used to solve this problem. In this paper, we propose a novel DNA-binding protein prediction method called HMMBinder. HMMBinder uses monogram and bigram features extracted from the HMM profiles of the protein sequences. To the best of our knowledge, this is the first application of HMM profile based features for the DNA-binding protein prediction problem. We applied Support Vector Machines (SVM) as a classification technique in HMMBinder. Our method was tested on standard benchmark datasets. We experimentally show that our method outperforms the state-of-the-art methods found in the literature.


2001 ◽  
Vol 57 (12) ◽  
pp. 1893-1894 ◽  
Author(s):  
Ben N. Wardleworth ◽  
Rupert J. M. Russell ◽  
Malcolm F. White ◽  
Garry L. Taylor

2005 ◽  
Vol 79 (14) ◽  
pp. 9356-9358 ◽  
Author(s):  
Nina Bacher Reuven ◽  
Sandra K. Weller

ABSTRACT UL12 is a 5′- to 3′-exonuclease encoded by herpes simplex virus type 1 (HSV-1) which degrades single- and double-stranded DNA. UL12 and the single-strand DNA binding protein ICP8 mediate a strand exchange reaction. We found that ICP8 inhibited UL12 digestion of single-stranded DNA but stimulated digestion of double-stranded DNA threefold. The stimulatory effect of ICP8 was independent of a strand exchange reaction; furthermore, the effect was specific to ICP8, as it could not be reproduced by Escherichia coli single-stranded DNA binding protein. The effect of ICP8 on the rate of UL12 double-stranded DNA digestion is attributable to an increase in processivity in the presence of ICP8.


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