scholarly journals The Binding Mechanism Between Inositol Phosphate (InsP) and the Jasmonate Receptor Complex: A Computational Study

2018 ◽  
Vol 9 ◽  
Author(s):  
Mengqi Cui ◽  
Juan Du ◽  
XiaoJun Yao
2013 ◽  
Vol 86 (12) ◽  
pp. 1426-1434
Author(s):  
Toshiaki Matsubara ◽  
Chisato Sasamoto

2017 ◽  
Vol 121 ◽  
pp. 59-72 ◽  
Author(s):  
Thangaraj Sindhu ◽  
Thiruvengadam Venkatesan ◽  
Gandhi R. Gracy ◽  
Sushil Kumar Jalali ◽  
Anil Rai

PLoS ONE ◽  
2016 ◽  
Vol 11 (7) ◽  
pp. e0159053 ◽  
Author(s):  
Juan Du ◽  
Xue Wang ◽  
Chun-Hai Dong ◽  
Jian Ming Yang ◽  
Xiao Jun Yao

2012 ◽  
Vol 116 (51) ◽  
pp. 14754-14759 ◽  
Author(s):  
Siamkhanthang Neihsial ◽  
Ganga Periyasamy ◽  
Pralok K. Samanta ◽  
Swapan K. Pati

2020 ◽  
Author(s):  
John Patterson ◽  
Charles C. David ◽  
Marion Wood ◽  
Xiaolin Sun ◽  
Donald J. Jacobs ◽  
...  

The hormone gibberellin (GA) promotes arabidopsis growth by enhancing binding between GA Insensitive DELLA transcriptional repressors and GA Insensitive Dwarf 1 (GID1) receptors to regulate DELLA degradation. The binding mechanism for GA was elucidated by employing a computational study of dissociations of the N-terminus of the DELLA family member GAI (GA Insensitive transcriptional repressor) from the GID1A receptor in the presence and absence of bound GA, and of GA from GID1A in the presence and absence of GAI. The tRAMD method was employed to deduce egression pathways for a diverse set of GA molecules (GA (x) ). Two pathways in the form of a newly identified cleft and a previously identified channel are prevalent. The cleft pathway is open in the absence of GAI. Upon GAI binding, the cleft route is blocked, resulting in a slower process for GA (x) to exit and enter the binding pocket through the channel. Several binding pocket residues are identified as gate-keepers to the channel. Molecular recognition features (MoRFs) found in the disordered signaling protein GAI affect GA (x) binding and GID1A dynamics. A three-step synergistic binding cycle is proposed where GAI MoRFs regulate the process. Rapid binding takes place through the cleft where little to no distinctions are made between major and less active forms of GA (x) . After GAI is bound to the GA (x) [[EQUATION]] GID1A complex, the channel supports a rectification process that increases the retention of major active forms of GA within the binding pocket. Both the cleft and channel contact residues to GA (x) are markedly conserved in a GID1 phylogeny, suggesting this binding process in the GID1 [[EQUATION]] DELLA GA-receptor complex represents a general paradigm for GA binding. Non-specific GA binding assists binding of GAI, which then helps to select the major active forms of the hormone and induce a downstream signalling cascade in response to bioactive GA.


2003 ◽  
Vol 370 (3) ◽  
pp. 829-838 ◽  
Author(s):  
Antony A. BOUCARD ◽  
Simon S. SAUVÉ ◽  
Gaétan GUILLEMETTE ◽  
Emanuel ESCHER ◽  
Richard LEDUC

A urotensin II (U-II) peptide analogue containing the photoreactive p-benzoyl-l-phenylalanine (Bz-Phe) in the sixth position was used to identify ligand-binding sites of the rat U-II receptor, also known as GPR14. [Bz-Phe6]U-II bound the receptor expressed in COS-7 cells with high affinity (IC50 0.7nM) and was as potent as U-II in the agonist-induced production of inositol phosphate. Photolabelling of the U-II receptor with 125I-[Bz-Phe6]U-II resulted in the specific formation of a glycosylated 125I-[Bz-Phe6]U-II—U-II receptor complex of 60kDa. Digestion of the 60kDa complex with endoproteinase Glu-C generated a fragment of 17kDa circumscribing the labelled fragment to residues 148—286. Digestion of the ligand—receptor complex with endoproteinase Arg-C produced a short peptide of 4kDa corresponding to fragments 125—148, 167—192 or 210—233. CNBr treatment of the endoproteinase-Glu-C and -Arg-C fragments yielded 2kDa fragments, defining the labelling site to methionine residues 184/185 of the fourth transmembrane domain. Photolabelling of two mutant receptors, M184L/M185L and M184A/M185A, led to a significant decrease in the overall yield of covalent labelling. Taken together, our results indicate that position 6 of U-II normally occupied by phenylalanine would interact with Met184 and/or Met185 of the fourth transmembrane domain of the U-II receptor. This information should be of significant value in the study of the interactions between U-II and its cognate receptor.


RSC Advances ◽  
2015 ◽  
Vol 5 (99) ◽  
pp. 81523-81532 ◽  
Author(s):  
Shaojie Ma ◽  
Shepei Tan ◽  
Danqing Fang ◽  
Rong Zhang ◽  
Shengfu Zhou ◽  
...  

Potent dual NF-κB/AP-1 inhibitors could effectively treat immunoinflammatory diseases. An integrated computational study was carried out to identify the most favourable binding sites, the structural features and the interaction mechanisms.


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