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1MSO

T6 Human Insulin at 1.0 A Resolution

Summary for 1MSO
Entry DOI10.2210/pdb1mso/pdb
Related4INS
DescriptorInsulin A-Chain, Insulin B-Chain, ZINC ION, ... (4 entities in total)
Functional Keywordst6 conformation, hormone-growth factor complex, hormone/growth factor
Cellular locationSecreted: P01308 P01308
Total number of polymer chains4
Total formula weight11766.12
Authors
Smith, G.D.,Pangborn, W.A.,Blessing, R.H. (deposition date: 2002-09-19, release date: 2003-03-04, Last modification date: 2024-10-16)
Primary citationSmith, G.D.,Pangborn, W.A.,Blessing, R.H.
The structure of T6 human insulin at 1.0 A resolution.
Acta Crystallogr.,Sect.D, 59:474-482, 2003
Cited by
PubMed Abstract: The structure of T(6) human insulin has been determined at 120 K at a resolution of 1.0 A and refined to a residual of 0.183. As a result of cryofreezing, the first four residues of the B chain in one of the two crystallographically independent AB monomers in the hexameric [Zn(1/3)(AB)(2)Zn(1/3)](3) complex undergo a conformational shift that displaces the C(alpha) atom of PheB1 by 7.86 A relative to the room-temperature structure. A least-squares superposition of all backbone atoms of the room-temperature and low-temperature structures yielded a mean displacement of 0.422 A. Omitting the first four residues of the B chain reduced the mean displacement to 0.272 A. At 120 K, nine residues were found to exhibit two discrete side-chain conformations, but only two of these residues are in common with the seven residues found to have disordered side chains in the room-temperature structure. As a result of freezing, the disorder observed at room temperature in both ArgB22 side chains is eliminated. The close contact between pairs of O( epsilon 2) atoms in GluB13 observed at room temperature is maintained at cryotemperature and suggests that a carboxylate-carboxylic acid centered hydrogen bond exists [-C(=O)-O.H.O-C(=O)-] such that the H atom is equally shared between the two partially charged O atoms.
PubMed: 12595704
DOI: 10.1107/S0907444902023685
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1 Å)
Structure validation

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