HIGHLIGHTS
- who: Please doChemComm and colleagues from the conformer poorly populated in solutionThis result contrasts to that found for SN-101, for which the structure of the glycopeptide in bound state is identical to its solution NMRderived structure. In conclusion, we have solved the crystal structure of the antitumoral antibody , in complex with its natural epitope. Our findings establish that the main driving force of , mAb binding is the recognition of the GalNAc moiety and to a lesser extent the Thr residue and the neighbouring downstream proline residue. , tolerates well any amino acid at APGST*XP, as well . . .
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