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3lri

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==Overview==
==Overview==
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Long-[Arg(3)]insulin-like growth factor-I (IGF-I) is a potent analog of, insulin-like growth factor-I that has been modified by a Glu(3) --> Arg, mutation and a 13-amino acid extension appended to the N terminus. We have, determined the solution structure of (15)N-labeled Long-[Arg(3)]-IGF-I, using high resolution NMR and restrained molecular dynamics techniques to, a precision of 0.82 +/- 0.28 A root mean square deviation for the backbone, heavy atoms in the three alpha-helices and 3.5 +/- 0.9 A root mean square, deviation for all backbone heavy atoms excluding the 8 N-terminal residues, and the 8 C-terminal eight residues. Overall, the structure of the IGF-I, domain is consistent with earlier studies of IGF-I with some minor changes, remote from the N terminus. The major variations in the structure, compared with IGF-I, occur at the N terminus with a substantial, reorientation of the N-terminal three residues of the IGF-I domain. These, results are interpreted in terms of the lower binding affinity for, insulin-like growth factor-binding proteins. The backbone dynamics of, Long-[Arg(3)]IGF-I were investigated using (15)N nuclear spin relaxation, and the heteronuclear nuclear Overhauser enhancement (NOE). There is a, considerable degree of flexibility in Long-[Arg(3)]IGF-I, even in the, alpha-helices, as indicated by an average ((1)H)(15)N NOE of 0.55 for the, regions. The largest heteronuclear NOEs are observed in the helical, regions, lower heteronuclear NOEs are observed in the C-domain loop, separating helix 1 from helix 2, and negative heteronuclear NOEs are, observed in the N-terminal extension and at the C terminus. Despite these, data indicating conformational flexibility for the N-terminal extension, slow amide proton exchange was observed for some residues in this region, suggesting some transitory structure does exist, possibly a molten helix., A certain degree of flexibility may be necessary in all insulin-like, growth factors to enable association with various receptors and binding, proteins.
+
Long-[Arg(3)]insulin-like growth factor-I (IGF-I) is a potent analog of insulin-like growth factor-I that has been modified by a Glu(3) --> Arg mutation and a 13-amino acid extension appended to the N terminus. We have determined the solution structure of (15)N-labeled Long-[Arg(3)]-IGF-I using high resolution NMR and restrained molecular dynamics techniques to a precision of 0.82 +/- 0.28 A root mean square deviation for the backbone heavy atoms in the three alpha-helices and 3.5 +/- 0.9 A root mean square deviation for all backbone heavy atoms excluding the 8 N-terminal residues and the 8 C-terminal eight residues. Overall, the structure of the IGF-I domain is consistent with earlier studies of IGF-I with some minor changes remote from the N terminus. The major variations in the structure, compared with IGF-I, occur at the N terminus with a substantial reorientation of the N-terminal three residues of the IGF-I domain. These results are interpreted in terms of the lower binding affinity for insulin-like growth factor-binding proteins. The backbone dynamics of Long-[Arg(3)]IGF-I were investigated using (15)N nuclear spin relaxation and the heteronuclear nuclear Overhauser enhancement (NOE). There is a considerable degree of flexibility in Long-[Arg(3)]IGF-I, even in the alpha-helices, as indicated by an average ((1)H)(15)N NOE of 0.55 for the regions. The largest heteronuclear NOEs are observed in the helical regions, lower heteronuclear NOEs are observed in the C-domain loop separating helix 1 from helix 2, and negative heteronuclear NOEs are observed in the N-terminal extension and at the C terminus. Despite these data indicating conformational flexibility for the N-terminal extension, slow amide proton exchange was observed for some residues in this region, suggesting some transitory structure does exist, possibly a molten helix. A certain degree of flexibility may be necessary in all insulin-like growth factors to enable association with various receptors and binding proteins.
==Disease==
==Disease==
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
[[Category: Single protein]]
[[Category: Single protein]]
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[[Category: Carver, J.A.]]
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[[Category: Carver, J A.]]
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[[Category: Francis, G.L.]]
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[[Category: Francis, G L.]]
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[[Category: Keniry, M.A.]]
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[[Category: Keniry, M A.]]
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[[Category: Laajoki, L.G.]]
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[[Category: Laajoki, L G.]]
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[[Category: Wallace, J.C.]]
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[[Category: Wallace, J C.]]
[[Category: distance geometry]]
[[Category: distance geometry]]
[[Category: growth factor]]
[[Category: growth factor]]
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[[Category: protein structure]]
[[Category: protein structure]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri Feb 15 17:43:55 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 19:10:09 2008''

Revision as of 17:10, 21 February 2008


3lri

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SOLUTION STRUCTURE AND BACKBONE DYNAMICS OF HUMAN LONG-[ARG3]INSULIN-LIKE GROWTH FACTOR 1

Contents

Overview

Long-[Arg(3)]insulin-like growth factor-I (IGF-I) is a potent analog of insulin-like growth factor-I that has been modified by a Glu(3) --> Arg mutation and a 13-amino acid extension appended to the N terminus. We have determined the solution structure of (15)N-labeled Long-[Arg(3)]-IGF-I using high resolution NMR and restrained molecular dynamics techniques to a precision of 0.82 +/- 0.28 A root mean square deviation for the backbone heavy atoms in the three alpha-helices and 3.5 +/- 0.9 A root mean square deviation for all backbone heavy atoms excluding the 8 N-terminal residues and the 8 C-terminal eight residues. Overall, the structure of the IGF-I domain is consistent with earlier studies of IGF-I with some minor changes remote from the N terminus. The major variations in the structure, compared with IGF-I, occur at the N terminus with a substantial reorientation of the N-terminal three residues of the IGF-I domain. These results are interpreted in terms of the lower binding affinity for insulin-like growth factor-binding proteins. The backbone dynamics of Long-[Arg(3)]IGF-I were investigated using (15)N nuclear spin relaxation and the heteronuclear nuclear Overhauser enhancement (NOE). There is a considerable degree of flexibility in Long-[Arg(3)]IGF-I, even in the alpha-helices, as indicated by an average ((1)H)(15)N NOE of 0.55 for the regions. The largest heteronuclear NOEs are observed in the helical regions, lower heteronuclear NOEs are observed in the C-domain loop separating helix 1 from helix 2, and negative heteronuclear NOEs are observed in the N-terminal extension and at the C terminus. Despite these data indicating conformational flexibility for the N-terminal extension, slow amide proton exchange was observed for some residues in this region, suggesting some transitory structure does exist, possibly a molten helix. A certain degree of flexibility may be necessary in all insulin-like growth factors to enable association with various receptors and binding proteins.

Disease

Known disease associated with this structure: Growth retardation with deafness and mental retardation due to IGF1 deficiency OMIM:[147440]

About this Structure

3LRI is a Single protein structure of sequence from Homo sapiens. Full crystallographic information is available from OCA.

Reference

Solution structure and backbone dynamics of long-[Arg(3)]insulin-like growth factor-I., Laajoki LG, Francis GL, Wallace JC, Carver JA, Keniry MA, J Biol Chem. 2000 Apr 7;275(14):10009-15. PMID:10744677

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