TY - JOUR
T1 - An efficient automated computer vision based technique for detection of three dimensional structural motifs in proteins
AU - Fischer, Daniel
AU - Bachar, Orly
AU - Nussinov, Ruth
AU - Wolfson, Haim
N1 - Funding Information:
Research sponsored at least in part by the National Cancer Institute, DHHS, under contract No. 1-C0-74102 with Program Resources, Inc. The contents of this publication do not necessarily reflect the views or policies of the DHHS, nor does mention of trade names, commercial products, or organizations imply endorsement of the U.S. Government.
PY - 1992/1/1
Y1 - 1992/1/1
N2 - As the number of available three dimensional coordinates of proteins increases, it is now recognized that proteins from different families and topologies are constructed from independent motifs. Detection of specific structural motifs within proteins aids in understanding their role and the mechanism of their operation. To aid in identification and use of these motifs it has become necessary to develop efficient methods for systematic scanning of structural databases. To date, methods of structural protein comparison suffer from at least one of the following limitations: (1) are not fully automated (require human intervention), (2) are limited to relatively similar structures, (3) are constrained to linear alignments of the structures, (4) are sensitive to insertions, deletions or gaps in the sequences or (5) are very time consuming.
AB - As the number of available three dimensional coordinates of proteins increases, it is now recognized that proteins from different families and topologies are constructed from independent motifs. Detection of specific structural motifs within proteins aids in understanding their role and the mechanism of their operation. To aid in identification and use of these motifs it has become necessary to develop efficient methods for systematic scanning of structural databases. To date, methods of structural protein comparison suffer from at least one of the following limitations: (1) are not fully automated (require human intervention), (2) are limited to relatively similar structures, (3) are constrained to linear alignments of the structures, (4) are sensitive to insertions, deletions or gaps in the sequences or (5) are very time consuming.
UR - http://www.scopus.com/inward/record.url?scp=0026345280&partnerID=8YFLogxK
U2 - 10.1080/07391102.1992.10507955
DO - 10.1080/07391102.1992.10507955
M3 - Article
AN - SCOPUS:0026345280
SN - 0739-1102
VL - 9
SP - 769
EP - 788
JO - Journal of Biomolecular Structure and Dynamics
JF - Journal of Biomolecular Structure and Dynamics
IS - 4
ER -