Tuesday 21 April 2015

3D structure of Lysine deficient protein kinase present in humans(WNK4)

WNK, s are the protein kinase super family with no lysine residue and are newly identifiable proteins. These proteins have unique replacement of lysine that is involved in the process of ATP binding and phosphorylation that involves phosphoryl transfer . WNK, s occurs in multicellular organisms and their homologs are not present in unicellular organisms. Serine/ threonine protein kinase is an important member of the WNK family and is encoded by WNK4 gene. WNK4 is also known as PHA2B and PRKWNK4. The orthologs of WNK4 protein are mouse (Mus musculus), chicken (Gallus gallus) and lizard ( Anolis carolinensis). The paralogs of WNK4 protein are WNK1, WNK2, and WNK3. WNK4 proteins play an important role in kidneys. These proteins play an important role in Na+ and K+ ions homeostasis by controlling these ion channels in the cell membrane . These channels are involved in transportation of Na+ and K+ ions into and out of the cell, present mainly in kidneys. Na+ channels help in maintaining the  balance of Na+ and their transport to kidney cells and then further into blood, while K+ channels , help in transport of excess K+ by a process known as secretion. WNK4 protein is present mainly in the distal convoluted tubule of kidney and it is part of tight junction. It is mainly expressed in kidney, colon and skin . Mutation in this protein causes inherited hypertension and hyperkelemia (elevated level of K+) disorder known as pseudohypoaldosteronium type II also known as Gordon’s syndrome .

Sequence retreival from NCBI

Protein sequence of WNK lysine deficient protein kinase 4 in humans is retrieved from NCBI (National center for biotechnology information) in FASTA format.TheAccession number of the protein present in NCBI is AAI36665 and total consisting of 1423 total amino acids.

3D structure prediction by SWISS MODEL
To achieve the 3D structure efficient computer programs are required. A huge gap between the protein structures and available protein sequences developed the need of automated, stable and reliable modeling methods . The idea of an internet based automated modeling facility with integrated expert knowledge was first implemented 10 years ago by Peitsch and co-workers and formed the starting point for the SWISS-MODEL server . Swiss model is reachable on World Wide Web.Three models(template sequences were identified from the swiss model but on the  basis of highest sequence similarity model 2 was chosen.
On the basis of sequence identity model 2 was best having sequence identity score of 80.49% and this template sequence was lysine deficient domain of WNK1 present in ratus norvagicus.

Chimera results
for 3D structure visualization chimera tool was used and got the following results  for all the three models.


3D structure of the best model on the basis of RMSD value(Model 3)



Models
RMSD Value

Sequence length


Model  1

0.062


264 269








Model  2
0.062

263 263









Model  3
0.061

271 278



(Table showing RMSD value)

SAVES server Results
SAVES server is a structure analysis and verification tool consisting of six different programs to evaluate the 3D structure of protein whose structure is not predicted yet. To evaluate the 3D structure protein i used following programs.Ramachandaran plot
ERRAT
VERIFY3D
Results  for the best models are given below.
Ramachandaran plot for best model


ERRAT results for best model

Main chain parameter results
3D structure of lysine deficient protein kinase (WNK4 in humans)


Conclusion
The 3D structure prediction is very important to know about the molecular functions of protein. Structural analysis of lysine deficient protein kianse was done using Swiss Model. .  Further experimentation and analysis of structure is needed to study the molecular function of the protein in more detail. The study of the bond lengths, bond energies, bonding interactions and information about the 3D structure of lysine deficient protein kinase is needed to be studied in more detail to get more information about its function.





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