The weighting in REFMAC is a function of SigmA ( plotted in log file).
For this example it will be nearly 1 for all resolutions ranges so the
weights are pretty constant. There is also a contribution from the
"experimental" sigma, which in this case seems to be proportional to |F|
Yesterday I attached the wrong TRUNCATE log file - here is the correct
one, and if you look at the plot
"Amplitude Analysis against resolution" it also includes a plot of <F>
<SigF>
Eleanor
Dominika Borek wrote:
> There are many more interesting things about this structure - obvious
> fake - refined against fabricated data.
>
> After running refmac I have noticed discrepancies between R and
> weighted R-factors. However, I do not know how the weights are
> calculated and applied - it could maybe help to find out how these
> data were created. Could you help?
>
> M(4SSQ/LL) NR_used %_obs M(Fo_used) M(Fc_used) Rf_used WR_used
> NR_free M(Fo_free) M(Fc_free) Rf_free WR_free $$
> $$
> 0.005 2205 98.77 3800.5 3687.2 0.12 0.30 121 4133.9
> 4042.7 0.12 0.28
> 0.015 3952 99.90 1932.9 1858.7 0.20 0.60 197 2010.5
> 1880.5 0.21 0.40
> 0.025 5026 99.81 1577.9 1512.3 0.23 0.62 283 1565.0
> 1484.6 0.26 0.54
> 0.034 5988 99.76 1598.0 1541.5 0.23 0.61 307 1625.7
> 1555.6 0.23 0.42
> 0.044 6751 99.79 1521.2 1481.6 0.18 0.41 338 1550.3
> 1523.8 0.18 0.61
> 0.054 7469 99.81 1314.5 1291.2 0.14 0.29 391 1348.3
> 1337.7 0.15 0.27
> 0.064 8078 99.87 1111.5 1089.1 0.16 0.36 465 1096.1
> 1077.9 0.18 0.42
> 0.073 8642 99.84 976.7 959.2 0.15 0.32 488 995.3
> 988.4 0.16 0.50
> 0.083 9255 99.88 866.4 848.0 0.16 0.36 490 856.8
> 846.0 0.17 0.38
> 0.093 9778 99.88 747.6 731.4 0.16 0.36 515 772.8
> 747.3 0.18 0.38
> 0.103 10225 99.86 662.6 649.1 0.17 0.38 547 658.9
> 643.6 0.20 0.36
> 0.113 10768 99.83 597.2 584.7 0.18 0.42 538 593.4
> 590.0 0.20 0.49
> 0.122 11121 99.86 535.5 521.9 0.19 0.48 607 556.2
> 542.0 0.20 0.47
> 0.132 11692 99.85 489.3 479.2 0.19 0.46 607 476.4
> 467.3 0.23 0.42
> 0.142 11999 99.83 453.9 443.1 0.19 0.48 621 455.3
> 440.6 0.22 0.55
> 0.152 12463 99.79 419.2 407.3 0.19 0.44 655 435.3
> 424.3 0.22 0.53
> 0.162 12885 99.78 384.0 373.9 0.20 0.53 632 384.1
> 376.1 0.22 0.43
> 0.171 12698 95.96 357.2 348.5 0.21 0.57 686 353.9
> 338.6 0.24 0.51
> 0.181 11926 87.78 332.0 323.3 0.21 0.66 590 333.4
> 322.6 0.24 0.57
> 0.191 11204 80.39 309.9 299.6 0.22 0.59 600 302.1
> 296.3 0.26 0.77
> $$
>
>
>
>
> Eleanor Dodson wrote:
>> There is a correspondence in last weeks Nature commenting on the
>> disparities between three C3B structures. These are:
>> 2icf solved at 4.0A resolution, 2i07 at 4.1A resolution, and 2hr0
>> at 2.26A resolution.
>>
>> The A chains of all 3 structures agree closely, with each other and
>> other deposited structures.
>> The B chains of 2icf and 2i07 are in reasonable agreement, but there
>> are enormous differences to the B chain of 2hr0.
>> This structure is surprisingly out of step, and by many criteria
>> likely to be wrong.
>>
>> There has been many articles written on validation and it seems worth
>> reminding crystallographers
>> of some of tests which make 2hr0 suspect.
>>
>> 1) The cell content analysis suggests there is 80% solvent in the
>> asymmetric unit.
>> Such crystals have been observed but they rarely diffract to 2.26A.
>>
>> 2) Data Analysis:
>> The reflection data has been deposited so it can be analysed.
>> The plots provided by TRUNCATE showing intensity statistic features
>> are not compatible with such a high solvent ratio. They are too
>> perfect; the moments are perfectly linear, unlikely with such large
>> volumes of the crystal containing solvent, and there is absolutely no
>> evidence of anisotropy, again unlikely with high solvent content.
>>
>> 3) Structure analysis
>> a) The Ramachandran plot is very poor ( 84% allowed) with many
>> residues in disallowed regions.
>> b) The distribution of residue B values is quite unrealistic. There
>> is a very low spread, which is most unusual for a structure with
>> long stretches of exposed chain. The baverage log file is attached.
>>
>> c) There does not seem to be enough contacts to maintain the
>> crystalline state.
>
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