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Metal coordination Forms a blue copper complex through defined ligand interactions

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The expression of some paternal genes that shouldn't be expressed leads to Prader-Willi syndrome and can be caused by one of the following factors: Absence of paternal genes on chromosome 15

For GCGR, the lipidated K10 P contributed three hydrogen bonds (with S139 1.37b , Q142 1.40b and R199 2.72b ), extensive hydrophobic contacts (with V143 1.41b , T146 1.44b , L192 2.65b and V193 2.66b ) and lipid membrane where the 16-carbon palmitic chain implanted (Fig

Hurtado I, Robles C, Peir S, Garca-Sempere A, Sanflix-Gimeno G

Weight loss induced bone loss: mechanism of action and clinical implications