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1 e other heavy atom derivative data (multiple isomorphous replacement).
2 c structure of type II collagen via multiple isomorphous replacement.
3 riophage at 2.4 A resolution, using multiple isomorphous replacement.
4 e) has been determined to 1.71 A by multiple isomorphous replacement.
5 chrysanthemi has been determined by multiple isomorphous replacement.
6 sence of sulfate and solved its structure by isomorphous replacement.
7 A and the structure was solved using single isomorphous replacement.
9 coli enzyme to 2.5 A resolution using single isomorphous replacement and 3-fold non-crystallographic
10 ution and the structure was phased by single isomorphous replacement and anomalous scattering (SIRAS)
11 cture of AXEII has been determined by single isomorphous replacement and anomalous scattering, and re
12 ynapse was solved using phases from multiple isomorphous replacement and anomalous scattering, and re
13 EBS) was solved by a combination of multiple isomorphous replacement and multiwavelength anomalous di
14 minase I to a resolution of 2.8 A, solved by isomorphous replacement and pseudo-two-wavelength multiw
15 ovora ssp. carotovora was solved by multiple isomorphous replacement and refined at 1.9 A to a conven
16 th cellotetraose has been solved by multiple isomorphous replacement and refined at 2.4 A resolution
17 a chrysanthemi enzyme was solved by multiple isomorphous replacement and refined at 2.4 A to a conven
18 discoideum, has been determined by multiple isomorphous replacement and refined to 1.75 A resolution
19 The crystal structure was solved by multiple isomorphous replacement and refined to a crystallographi
20 been solved at 2.3 A resolution by multiple isomorphous replacement and refined to a final R-factor
21 se family 5, has been determined by multiple isomorphous replacement and refined to a resolution of 1
22 crystallized and its structure determined by isomorphous replacement and refined to a resolution of 1
23 s determined at 2.5 A resolution by multiple isomorphous replacement and refined to an R factor of 0.
24 g a combination of molecular replacement and isomorphous replacement and refined using data from 10 A
25 P from Vibrio harveyi was solved by multiple isomorphous replacement and reveals that the enzyme is a
26 of the native enzyme was solved by multiple isomorphous replacement, and refined at a resolution of
28 udomonas putida, has been solved by multiple isomorphous replacement at 1.6 A resolution and refined
34 c=45.55 A), determined initially by multiple isomorphous replacement, has been refined to R=0.183 and
35 structure of apo OSBS was solved by multiple isomorphous replacement in space group P2(1)2(1)2(1); th
36 minase ADAR1 at 0.97 A, determined by single isomorphous replacement including anomalous scattering.
37 n in two crystal forms by using the multiple isomorphous replacement method and the multiwavelength a
38 oxidase (DHP) was determined by the multiple isomorphous replacement method and was refined at 1.8-A
39 B2, has been solved by conventional multiple isomorphous replacement methods and refined to an R fact
40 conformational state has been determined by isomorphous replacement methods and refined to an R-valu
41 rmined to 2.6 A resolution by usine multiple isomorphous replacement methods and simulated annealing
42 rystal structure has been solved by multiple isomorphous replacement methods at a resolution of 2.75
43 ure of the repressor, determined by multiple isomorphous replacement methods, reveals an unusual over
44 n determined using a combination of multiple isomorphous replacement (MIR) and multiwavelength anomal
46 se with NADP+ has been solved using multiple isomorphous replacement procedures and noncrystallograph
47 ution of 1.8 A using a combination of single isomorphous replacement (SIR) and multi-wavelength anoma
48 lex was solved by the techniques of multiple isomorphous replacement, solvent flattening, and molecul
49 structure of SmtB was solved using multiple isomorphous replacement techniques and refined at 2.2 A
50 n determined at 3.0 A resolution by multiple isomorphous replacement using a uranium derivative and t
51 coli determined by the technique of multiple isomorphous replacement using anomalous scattering at 2.
52 in the protoxin form has been determined by isomorphous replacement using heavy-atom derivatives of
53 lved at 1.9 A resolution by iterative single isomorphous replacement, using the brominated derivative
54 iple anomalous dispersion (MAD) and multiple isomorphous replacement with anomalous scattering (MIRAS
56 res of yeast PPX1, solved using the multiple isomorphous replacement with anomalous scattering (MIRAS
58 bidopsis thaliana, has been solved by single isomorphous replacement with anomalous scattering and re
59 Cry4Ba toxin has been determined by multiple isomorphous replacement with anomalous scattering and re
60 n complex with GSH has been solved by single isomorphous replacement with anomalous scattering at a r
61 n determined at 1.4A resolution using single isomorphous replacement with anomalous scattering method
62 tal structure of LpdA was solved by multiple isomorphous replacement with anomalous scattering, which
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