2D depiction of protein - Ligand complexes

被引:135
作者
Clark, Alex M. [1 ]
Labute, Paul [1 ]
机构
[1] Chem Comp Grp Inc, Montreal, PQ H3A 2R7, Canada
关键词
D O I
10.1021/ci7001473
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
A method is presented for the automated preparation of schematic diagrams for protein-ligand complexes, in which the ligand is displayed in conventional 2D form, and the interactions to and between the residues in its vicinity are summarized in a concise and information-rich manner. The structural entities are arranged to maximize aesthetic ideals and to properly convey important distance relationships. The diagram is annotated with calculated hydrogen bonds, a substitution contour, solvent exposure, chelated metals, covalently bound linkages, pi-pi and pi-cation interactions, and, for series of complexes, conserved residues and interactions. Residues, cofactors, ions, and solvent components are drawn in cartoon form as adjuncts to the ligand. The method can be applied to aligned sets which contain multiple ligands, or multiple members of a protein family, in which case the ligand orientations and protein residue placement will show consistent trends throughout the series.
引用
收藏
页码:1933 / 1944
页数:12
相关论文
共 21 条
[1]   PROTEIN DATA BANK - COMPUTER-BASED ARCHIVAL FILE FOR MACROMOLECULAR STRUCTURES [J].
BERNSTEIN, FC ;
KOETZLE, TF ;
WILLIAMS, GJB ;
MEYER, EF ;
BRICE, MD ;
RODGERS, JR ;
KENNARD, O ;
SHIMANOUCHI, T ;
TASUMI, M .
JOURNAL OF MOLECULAR BIOLOGY, 1977, 112 (03) :535-542
[2]   Macromolecular crystallographic information file [J].
Bourne, PE ;
Berman, HM ;
McMahon, B ;
Watenpaugh, KD ;
Westbrook, JD ;
Fitzgerald, PMD .
MACROMOLECULAR CRYSTALLOGRAPHY, PT B, 1997, 277 :571-590
[3]   Crystal structures of active Src kinase domain complexes [J].
Breitenlechner, CB ;
Kairies, NA ;
Honold, K ;
Scheiblich, S ;
Koll, H ;
Greiter, E ;
Koch, S ;
Schäfer, W ;
Huber, R ;
Engh, RA .
JOURNAL OF MOLECULAR BIOLOGY, 2005, 353 (02) :222-231
[4]   2D structure depiction [J].
Clark, AM ;
Labute, P ;
Santavy, M .
JOURNAL OF CHEMICAL INFORMATION AND MODELING, 2006, 46 (03) :1107-1123
[5]   Structural basis of Src tyrosine kinase inhibition with a new class of potent and selective trisubstituted purine-based compounds [J].
Dalgarno, D ;
Stehle, T ;
Narula, S ;
Schelling, P ;
van Schravendijk, MR ;
Adams, S ;
Andrade, L ;
Keats, J ;
Ram, M ;
Jin, L ;
Grossman, T ;
MacNeil, I ;
Metcalf, C ;
Shakespeare, W ;
Wang, Y ;
Keenan, T ;
Sundaramoorthi, R ;
Bohacek, R ;
Weigele, M ;
Sawyer, T .
CHEMICAL BIOLOGY & DRUG DESIGN, 2006, 67 (01) :46-57
[6]  
Gill P. E., 1981, PRACTICAL OPTIMIZATI
[7]   Crystal structure of Drosophila angiotensin I-converting enzyme bound to captopril and lisinopril [J].
Kim, HM ;
Shin, DR ;
Yoo, OJ ;
Lee, H ;
Lee, JO .
FEBS LETTERS, 2003, 538 (1-3) :65-70
[8]   Toward understanding the structural basis of cyclin-dependent kinase 6 specific inhibition [J].
Lu, Heshu ;
Schulze-Gahmen, Ursula .
JOURNAL OF MEDICINAL CHEMISTRY, 2006, 49 (13) :3826-3831
[9]   Interactions with aromatic rings in chemical and biological recognition [J].
Meyer, EA ;
Castellano, RK ;
Diederich, F .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2003, 42 (11) :1210-1250
[10]  
Nagar B, 2002, CANCER RES, V62, P4236