Protein one-dimensional (1D) structures such as secondary structure and
contact number provide intuitive pictures to understand how the native
three-dimensional (3D) structure of a protein is encoded in the amino acid
sequence. However, it has not been clear whether a given set of 1D structures
contains sufficient information for recovering the underlying 3D structure.
Here we show that the 3D structure of a protein can be recovered from a set of
three types of 1D structures, namely, secondary structure, contact number and
residue-wise contact order which is introduced here for the first time. Using
simulated annealing molecular dynamics simulations, the structures satisfying
the given native 1D structural restraints were sought for 16 proteins of
various structural classes and of sizes ranging from 56 to 146 residues. By
selecting the structures best satisfying the restraints, all the proteins
showed a coordinate RMS deviation of less than 4\AA{} from the native
structure, and for most of them, the deviation was even less than 2\AA{}. The
present result opens a new possibility to protein structure prediction and our
understanding of the sequence-structure relationship.Comment: Corrected title. No Change In Content