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We designed numerous models of CnN5− (n = 1 13) using molecular graphics software.
We have designed numerous models of CnP+3 (n=1–8) using molecular graphics software.
Making use of molecular graphics software, we designed numerous models of BeCn− (n = 1 8).
Using molecular graphics software, we have designed numerous models of CnP5− (n=1–7).
Making use of molecular graphics software, we have designed numerous models of HCn+ (n = 1 10) cationic clusters, and performed geometry optimization and vibrational frequency calculation by means of the B3LYP density functional method.
Making use of molecular graphics software, we have designed numerous models of HCnSi+ (n = 1 10), and by means of the B3LYP density functional method, performed geometry optimization and calculation on vibrational frequency.
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The resulting three-dimensional (3D) structure prediction (Protein Data Bank file) was described using the molecular graphic software, Waals 2013 (Altif Laboratories Inc).
The 3D structures were visualized using the molecular-graphics software Yasara (http://www.yasara.org).
Molecular graphics: SHELXTL, software used to prepare material for publication: SHELXTL and PLATON [21].
X-Ray data collection was carried out on Bruker SMART APEX II CCD diffractometer, cell refinement: SAINT; data reduction: SAINT; program used to solve structure: SHELXS; program used to refine structure: SHELXL; molecular graphics: SHELXTL; software used to prepare material for publication: SHELXTL [30] and PLATON [31].
A comparison of protein structures was performed using PyMOL (Molecular Graphics System software, DeLano Scientific, Palo Alto, CA).
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