PAR-3D: a server to predict protein active site residues

被引:27
作者
Goyal, Kshama [1 ]
Mohanty, Debasisa [2 ]
Mande, Shekhar C. [1 ]
机构
[1] Ctr DNA Fingerprinting & Diagnost, Hyderabad 500076, Andhra Pradesh, India
[2] Natl Inst Immunol, New Delhi 1100067, India
基金
英国惠康基金;
关键词
D O I
10.1093/nar/gkm252
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PAR-3D (http://sunserver.cdfd.org.in:8080/protease/PAR_3D/index.html) is a web-based tool that exploits the fact that relative juxtaposition of active site residues is a conserved feature in functionally related protein families. The server uses previously calculated and stored values of geometrical parameters of a set of known proteins (training set) for prediction of active site residues in a query protein structure. PAR-3D stores motifs for different classes of proteases, the ten glycolytic pathway enzymes and metal-binding sites. The server accepts the structures in the pdb format. The first step during the prediction is the extraction of probable active site residues from the query structure. Spatial arrangement of the probable active site residues is then determined in terms of geometrical parameters. These are compared with stored geometries of the different motifs. Its speed and efficiency make it a beneficial tool for structural genomics projects, especially when the biochemical function of the protein has not been characterized.
引用
收藏
页码:W503 / W505
页数:3
相关论文
共 12 条
[1]   A GRAPH-THEORETIC APPROACH TO THE IDENTIFICATION OF 3-DIMENSIONAL PATTERNS OF AMINO-ACID SIDE-CHAINS IN PROTEIN STRUCTURES [J].
ARTYMIUK, PJ ;
POIRRETTE, AR ;
GRINDLEY, HM ;
RICE, DW ;
WILLETT, P .
JOURNAL OF MOLECULAR BIOLOGY, 1994, 243 (02) :327-344
[2]   Structure-based functional motif identifies a potential disulfide oxidoreductase active site in the serine/threonine protein phosphatase-1 subfamily [J].
Fetrow, JS ;
Siew, N ;
Skolnick, J .
FASEB JOURNAL, 1999, 13 (13) :1866-1874
[3]  
FISCHER D, 1994, PROTEIN SCI, V3, P769
[4]   Knowledge-based modeling of the serine protease triad into non-proteases [J].
Iengar, P ;
Ramakrishnan, C .
PROTEIN ENGINEERING, 1999, 12 (08) :649-655
[5]   Identification of protein biochemical functions by similarity search using the molecular surface database eF-site [J].
Kinoshita, K ;
Nakamura, H .
PROTEIN SCIENCE, 2003, 12 (08) :1589-1595
[6]   Common Structural Cliques: a tool for protein structure and function analysis [J].
Milik, M ;
Szalma, S ;
Olszewski, KA .
PROTEIN ENGINEERING, 2003, 16 (08) :543-552
[7]  
Rawlings ND, 2004, NUCLEIC ACIDS RES, V32, pD160, DOI [10.1093/nar/gkh071, 10.1093/nar/gkp971]
[8]   MEROPS: the peptidase database [J].
Rawlings, Neil D. ;
Morton, Fraser R. ;
Barrett, Alan J. .
NUCLEIC ACIDS RESEARCH, 2006, 34 :D270-D272
[9]   Parameterization and classification of the protein universe via geometric techniques [J].
Tendulkar, AV ;
Wangikar, PP ;
Sohoni, MA ;
Samant, VV ;
Mone, CY .
JOURNAL OF MOLECULAR BIOLOGY, 2003, 334 (01) :157-172
[10]   Evolution of function in protein superfamilies, from a structural perspective [J].
Todd, AE ;
Orengo, CA ;
Thornton, JM .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (04) :1113-1143