Merge branch 'prerelease-3.2.1' into czarek

[unres.git] / doc / 3.2.1 / latex / unresman.tex

diff --git a/doc/3.2.1/latex/unresman.tex b/doc/3.2.1/latex/unresman.tex
index caaa183..6ec0dc5 100644 (file)
--- a/doc/3.2.1/latex/unresman.tex
+++ b/doc/3.2.1/latex/unresman.tex
@@ -958,13 +958,13 @@ to generate random conformations:
 THETPARPDB thetaml.5parm\\
 ROTPARPDB scgauss.parm
 
-For CSA, the best force field is 4P. For MD, the 1L2Y\_1LE1 force field is best for
+For CSA, the best force field is 4P. For MD, the E0LL2Y force field is best for
 ab initio prediction but provides medium resolution (5 A for 60-residue proteins) and 
 overemphasizes $\beta$-structures and has to be run with secondary-structure-prediction
 information. For prediction of the structure of mostly $\alpha$-protein, and for running
 dynamics of large proteins, the best is the GAB force field. All these force fields
 were trained by using our procedure of hierarchical optimization \cite{oldziej_2004,oldziej_2004_02}.
-The 4P and 1L2Y\_1LE1 force fields have considerable power independent of structural class. 
+The 4P and E0LL2Y force fields have considerable power independent of structural class. 
 The ALPHA, BETA, and ALPHABETA force fields (for CSA) were used in the CASP4 exercises
 and the CASP5 force field was used in the CASP5 exercise with some success; ALPHA 
 predicts reasonably the structure of $\alpha$-helical proteins and is still not obsolete,