SAM-T04: What is new in protein-structure prediction for CASP6

被引:73
作者
Karplus, K [1 ]
Katzman, S [1 ]
Shackleford, G [1 ]
Koeva, M [1 ]
Draper, J [1 ]
Barnes, B [1 ]
Soriano, M [1 ]
Hughey, R [1 ]
机构
[1] Univ Calif Santa Cruz, Dept Biomol Engn, Santa Cruz, CA 95064 USA
关键词
fold recognition/new fold; SAM-T04; hidden Markov models; local structure prediction; UNDERTAKER protein conformation generation; FRAGFINDER protein fragment finder;
D O I
10.1002/prot.20730
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
The SAM-T04 method for predicting protein structures uses a single protocol across the entire range of targets, from comparative modeling to new folds. This protocol is similar to the SAM-T02 protocol used in CASP5, but has improvements in the iterative search for similar sequences in finding and aligning templates, in creating fragment libraries, in generating protein conformations, and in scoring the conformations. The automatic procedure made some improvements over simply selecting an alignment to the highest-scoring template, and human intervention made substantial improvements over the automatic procedure. The main improvements made by human intervention were from adding constraints to build (or retain) beta-sheets and from splitting multidomain proteins into separate domains. The uniform protocol was moderately successful across the entire range of target difficulty, but was somewhat less successful than other approaches in CASP6 on the comparative modeling targets.
引用
收藏
页码:135 / 142
页数:8
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