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6VC1

Octreotide oxalate

Summary for 6VC1
Entry DOI10.2210/pdb6vc1/pdb
DescriptorOctreotide, OXALATE ION (3 entities in total)
Functional Keywordsoctreotide, de novo protein; somatostatin-14 analogue, de novo protein
Biological sourceunidentified
Total number of polymer chains3
Total formula weight3196.76
Authors
Spiliopoulou, M.,Karavassili, F.,Triandafillidis, D.,Valmas, A.,Kosinas, C.,Fili, S.,Barlos, K.,Barlos, K.K.,Morin, M.,Reinle-Schmitt, M.,Gozzo, F.,Margiolaki, I. (deposition date: 2019-12-20, release date: 2020-12-23, Last modification date: 2021-05-19)
Primary citationSpiliopoulou, M.,Karavassili, F.,Triandafillidis, D.P.,Valmas, A.,Fili, S.,Kosinas, C.,Barlos, K.,Barlos, K.K.,Morin, M.,Reinle-Schmitt, M.L.,Gozzo, F.,Margiolaki, I.
New perspectives in macromolecular powder diffraction using single-photon-counting strip detectors: high-resolution structure of the pharmaceutical peptide octreotide.
Acta Crystallogr.,Sect.A, 77:186-195, 2021
Cited by
PubMed Abstract: Advances in instrumentation, as well as the development of powerful crystallographic software have significantly facilitated the collection of high-resolution diffraction data and have made X-ray powder diffraction (XRPD) particularly useful for the extraction of structural information; this is true even for complex molecules, especially when combined with synchrotron radiation. In this study, in-line with past instrumental profile studies, an improved data collection strategy exploiting the MYTHEN II detector system together with significant beam focusing and tailored data collection options was introduced and optimized for protein samples at the Material Science beamline at the Swiss Light Source. Polycrystalline precipitates of octreotide, a somatostatin analog of particular pharmaceutical interest, were examined with this novel approach. XRPD experiments resulted in high angular and d-spacing (1.87 Å) resolution data, from which electron-density maps of enhanced quality were extracted, revealing the molecule's structural properties. Since microcrystalline precipitates represent a viable alternative for administration of therapeutic macromolecules, XRPD has been acknowledged as the most applicable tool for examining a wide spectrum of physicochemical properties of such materials and performing studies ranging from phase identification to complete structural characterization.
PubMed: 33944797
DOI: 10.1107/S2053273321001698
PDB entries with the same primary citation
Experimental method
POWDER DIFFRACTION
Structure validation

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