Structure Modeling and Molecular Docking Studies of Schizophrenia Candidate Genes, Synapsins 2 (SYN2) and Trace Amino Acid Receptor (TAAR6)

被引:0
作者
Khattak, Naureen Aslam [1 ,2 ]
Sehgal, Sheikh Arslan [3 ]
Bai, Yongsheng [1 ,2 ]
Deng, Youping [4 ,5 ]
机构
[1] Indiana State Univ, Dept Biol, 600 Chestnut St, Terre Haute, IN 47809 USA
[2] Indiana State Univ, Ctr Genom Advocacy, 600 Chestnut St, Terre Haute, IN 47809 USA
[3] Univ Chinese Acad Sci, Beijing, Peoples R China
[4] Univ Hawaii, John A Burns Sch Med, Dept Complementary & Integrat Med, Honolulu, HI 96813 USA
[5] Nanjing Univ Chinese Med, Affiliated Hosp 3, Nanjing Municipal Hosp Chinese Med, Natl Ctr Colorectal Dis, Nanjing 210001, Jiangsu, Peoples R China
来源
BIOINFORMATICS RESEARCH AND APPLICATIONS (ISBRA 2017) | 2017年 / 10330卷
关键词
Bioinformatics; Computational biology; TAAR6; SYN2; Protein modeling; Molecular docking; Phylogenetic; Schizophrenia; PROTEIN; SUSCEPTIBILITY; GENETICS;
D O I
10.1007/978-3-319-59575-7_26
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Schizophrenia (SZ) is a severe manifesting psychiatric neural disorder with abnormal behavior, disorganized speech and figment of the imagination. The Synapsin II (SYN2) and Trace Amine Associated Receptor (TAAR6) genes has direct association with SZ. In the current study, the 3-dimensional structure of SYN2 and TAAR6 protein is proposed and the protein-protein docking analysis was applied to explore the binding interactions of the candidate proteins. The comparative modeling was performed with the suitable template (Q86VA8 for SYN2 and H0YF79 for TAAR6) which represents the query coverage (71%, 87%), sequence identity (67%, 34%) and the e-value (0.0, 1e-43) respectively. The structure quality of the predicted model of SYN2 and TAAR6 presents 90.7%, and 96.5% residues in the favored region of Ramachandran plot analysis respectively, suggests the good quality models construction. The phylogenetic analysis suggests that the TAAR6 sequence is conserved in chimpanzee and gorilla (> 80% homology) whereas the SYN2 is closely related with macaque. The protein docking analysis of SYN2 shows five ionic interactions with Lys-256, Lys-539, Arg-475, Gln-536 and Gln-529 with His-121, Glu-467, Glu-472, Arg-458 and Asp-477 of CAPON. The TAAR6 have two interactions of Glu-33 and Gly-171 with Arg-85 and Lys-52 of the PPP3CC. Current computational study may play a significant role to recruit, analyze and cure the mysteries of schizophrenia neurodegenerative disorder.
引用
收藏
页码:291 / 301
页数:11
相关论文
共 29 条
[1]   Sex differences in the risk of schizophrenia - Evidence from meta-analysis [J].
Aleman, A ;
Kahn, RS ;
Selten, JP .
ARCHIVES OF GENERAL PSYCHIATRY, 2003, 60 (06) :565-571
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]  
[Anonymous], PYMOL MOL GRAPH SYST
[4]  
Apweiler R, 2004, NUCLEIC ACIDS RES, V32, pD115, DOI [10.1093/nar/gkh131, 10.1093/nar/gkw1099]
[5]  
Austin Jehannine, 2005, J Genet Couns, V14, P329, DOI 10.1007/s10897-005-1622-4
[6]   The Protein Data Bank [J].
Berman, HM ;
Westbrook, J ;
Feng, Z ;
Gilliland, G ;
Bhat, TN ;
Weissig, H ;
Shindyalov, IN ;
Bourne, PE .
NUCLEIC ACIDS RESEARCH, 2000, 28 (01) :235-242
[7]   The structure of psychosis revisited: The role of mood symptoms [J].
Boks, Marco P. M. ;
Leask, Stuart ;
Vermunt, Jeroen K. ;
Kahn, Rene S. .
SCHIZOPHRENIA RESEARCH, 2007, 93 (1-3) :178-185
[8]   VERIFICATION OF PROTEIN STRUCTURES - PATTERNS OF NONBONDED ATOMIC INTERACTIONS [J].
COLOVOS, C ;
YEATES, TO .
PROTEIN SCIENCE, 1993, 2 (09) :1511-1519
[9]   Genes for schizophrenia and bipolar disorder? Implications for psychiatric nosology [J].
Craddock, N ;
O'Donovan, MC ;
Owen, MJ .
SCHIZOPHRENIA BULLETIN, 2006, 32 (01) :9-16
[10]   Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia [J].
Duan, JB ;
Martinez, M ;
Sanders, AR ;
Hou, CP ;
Saitou, N ;
Kitano, T ;
Mowry, BJ ;
Crowe, RR ;
Silverman, JM ;
Levinson, DF ;
Gejman, PV .
AMERICAN JOURNAL OF HUMAN GENETICS, 2004, 75 (04) :624-638