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. Author manuscript; available in PMC: 2013 Mar 7.
Published in final edited form as: Structure. 2012 Mar 7;20(3):450–463. doi: 10.1016/j.str.2012.01.008

Table 3.

Pathwalking results on authentic density maps. A summarized table of all pathwalking generated models is presented. As in Table 1, the number of amino acids for each protein, resolution, the Cα RMS deviation, the percent of total Cαs within a 3 and 5 Å radius when compared to the corresponding Cα position in the known structure, the percent of correctly registered Cαs and the topology score from the CLICK webserver (0–1 where 1 corresponds to an identical topology between the known and pathwalker structures) are reported. The results summarized in this table were from the LKH-TSP solver. For RDV P8 and MM-cpn, only the results for the first pathwalker model are reported.

Data set Reported
Resolution
(Å)
Number
of
Amino
Acids

RMSD
(Å)

within

radius
(%)

within

radius
(%)
Correctly
registered
Cαs (%)
Topology
score
Aquaporin-1 3.8 220 4.63 27.3 57.7 25.5 1.00
Rotavirus VP6 3.8 397 3.99 49.6 72.5 40.8 0.93
GroEL 4.0 524 7.51 12 35.8 10.3 0.79
GroEL-Rosetta 4.0 524 6.31 25.8 45.5 25.4 0.98
Ribosome chain P 6.4 84 3.08 4.51.8 83.1 45.8 0.88
Ribosome chain Q 6.4 100 4.42 36.4 69.7 31.3 1.00
Ribosome chain H 6.4 139 8.09 18.8 35.5 15.2 0.93
Ribosome chain B 6.4 220 9.86 3.2 15.4 4.1 0.96
Ribosome chain G 6.4 156 8.75 20 27.1 19.4 1.00
Ribosome chain N 6.4 61 4.89 21.7 47.7 15 1.00
RDV P8* 7.9 421 15.49 3.1 12.4 1 0.27
MM-cpn* 4.3 508 3.13 56.2 84.3 51.9 1.00
Epsilon 15 gp7 4.5 335 9.02 4.2 14 5.1 0.75