Dear CCP4 community:

I am a beginner to crystallography and therefore my apologies if this question 
is too 
simple.

Basically we obtained several crystal forms of the same molecule, which is a 
hetero-
trimer containing protein A(18kD), protein B(16kD) and a RNA segment(40nt or 
about 
15kD).

We have solved the structure of one crystal form(form_1); its information is as 
follows:
space group = P 42 22;
unit cell = 126.514  126.514   76.766  90.00  90.00  90.00
resolution = 2.7A;
Rwork = 0.25, Rfree = 0.265;
solvent content = 60%;
Number of molecules per Asymmetric Unit = 1;
Data redundancy = 5;
Data Completeness = 94%;

I am now trying to solve the structure of form_2 crystal using molecular 
replacement. So 
far the information I know about form_2 is as follows:
space group = I 422 or I 41 22;
unit cell = 180.096  180.096   152.530  90.00  90.00  90.00
(unit cell is about 4 times the size of form_1)
resolution = 3.3A; (which is low)
Number of molecules per Asymmetric Unit = 2 or 3;
Data redundancy = 4;
Data Completeness = 92%;
There is no twinning(as shown by Sfcheck);
As shown in"Analyse Data for MR", the first peak is 100 and second is 68.92; I 
am not 
sure if this indicates translation in a Asymmetric Unit;

The problem is, I can not get a good solution by MR using Phaser (both I422 and 
I4122 
are tried). When I searched for 3 molecules per Asymmetric Unit, Phaser did not 
give 
solutions at all. 

When I used 2/ASU instead, I was able to get some solutions, with typical 
statistics as 
follows:
RFZ=14, TFZ=35.9, PAK=0, LLG=1036; 
However, these solutions had high R values(like Rwork=0.59 and Rfree=0.58), 
which 
indicated that they are not solutions at all. Still, I tried refinement using 
refmac5, but R 
values did not go down even after 50 rounds; sometimes they even increased 
after 
refinement.

Besides, the RMS values bond length, bond angle and chiral center were all 0 as 
show by 
refmac5.

I tried limiting resolution range to 15-4A in Phaser, which did not help either.

Now I am completely stuck. Could anyone give me some advice? I know this 
situation is 
very strange, because I am using the SAME molecule for MR but can not can a 
solution.

Thanks a lot,

P.S. 
1) Both form_1 and form_2 crystals were grown using Selenomethionine-containing 
samples. There are 3 Sel_Met in protein A and 1 in protein B. 
2) A 10-aa internal segment of protein B is missing in the solved structure, 
which may 
indicate high flexibility.

Chao

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