Related ArticlesStabilized NMR structure of human parathyroid hormone(1-34).
Eur J Biochem. 1993 Jul 15;215(2):315-21
Authors: Barden JA, Cuthbertson RM
The structure of the biologically-active N-terminal region of human parathyroid hormone, PTH(1-34), was investigated in the presence of 10% trifluoroethanol using two-dimensional proton NMR spectroscopy, distance geometry and dynamic simulated annealing. Complete assignments of all backbone and side chain hydrogens were made with the aid of totally correlated spectroscopy (TOCSY) experiments, providing through-bond 1H-1H connectivities, and NOESY providing through-space and sequential backbone connectivities. Distance and angle constraints were used in the distance geometry algorithm DIANA II to generate a family of structures satisfying all inputs. The lowest energy structures were further refined using the dynamic-simulated-annealing protocol XPLOR 3. The major structural features evident in 10% trifluoroethanol are two segments of alpha-helix extending from residues Glu4 to Lys14/His14 and Ser17 to Asp30. A short length of unordered structure joined the two spans of helix. The structures of the N-terminal regions (4-13/14) agreed closely with the structure found in human parathyroid-hormone-related protein (PTHrP)(1-34) obtained earlier by Ray, Barden and Kemp [19]. However, PTHrP(16-19) exhibited a reverse turn which is incorporated in an extended helix in PTH. The consequent interactions between several hydrophobic residues in the C-terminal region in PTHrP are absent in PTH. Moreover, the turn in PTHrP(22-25) at the start of the C-terminal helix is present as a more standard loop of helix in PTH. Comparisons between the structures of the two hormones has enabled the probable location and structure of the PTH receptor-binding site to be placed in the segment of amphiphilic alpha-helix (24-31).
[NMR paper] NMR studies of the backbone flexibility and structure of human growth hormone: a comp
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J Mol Biol. 2002 May 3;318(3):679-95
Authors: Kasimova MR, Kristensen SM, Howe PW, Christensen T, Matthiesen F, Petersen J, Sørensen HH, Led JJ
(15)N NMR relaxation parameters and amide (1)H/(2)H-exchange rates have been used to characterize the structural flexibility of human...
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[NMR paper] Assessment by 1H NMR spectroscopy of the structural behaviour of human parathyroid-ho
Assessment by 1H NMR spectroscopy of the structural behaviour of human parathyroid-hormone-related protein(1-34) and its close relationship with the N-terminal fragments of human parathyroid hormone in solution.
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Biol Chem. 1997 Dec;378(12):1501-8
Authors: Gronwald W, Schomburg D, Tegge W, Wray V
Human...
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[NMR paper] Mono- and bicyclic analogs of parathyroid hormone-related protein. 2. Conformational
Mono- and bicyclic analogs of parathyroid hormone-related protein. 2. Conformational analysis of antagonists by CD, NMR, and distance geometry calculations.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-acspubs.jpg Related Articles Mono- and bicyclic analogs of parathyroid hormone-related protein. 2. Conformational analysis of antagonists by CD, NMR, and distance geometry calculations.
Biochemistry. 1997 Mar 18;36(11):3300-7
Authors: Maretto S, Mammi S, Bissacco E, Peggion E, Bisello A, Rosenblatt M, Chorev M, Mierke DF
...
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[NMR paper] Mono- and bicyclic analogs of parathyroid hormone-related protein. 2. Conformational
Mono- and bicyclic analogs of parathyroid hormone-related protein. 2. Conformational analysis of antagonists by CD, NMR, and distance geometry calculations.
http://www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-acspubs.jpg Related Articles Mono- and bicyclic analogs of parathyroid hormone-related protein. 2. Conformational analysis of antagonists by CD, NMR, and distance geometry calculations.
Biochemistry. 1997 Mar 18;36(11):3300-7
Authors: Maretto S, Mammi S, Bissacco E, Peggion E, Bisello A, Rosenblatt M, Chorev M, Mierke DF
...
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[NMR paper] Conformational differences of ovine and human corticotropin releasing hormone. A CD,
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Int J Pept Protein Res. 1996 May;47(5):383-93
Authors: Dathe M, Fabian H, Gast K, Zirwer D, Winter R, Beyermann M, Schümann M, Bienert M
The differences in the conformational properties of ovine (o) and human (h) CRH in aqueous solution, structure-inducing TFE and in the...
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[NMR paper] Structure of recombinant human parathyroid hormone in solution using multidimensional
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Biol Chem Hoppe Seyler. 1996 Mar;377(3):175-86
Authors: Gronwald W, Schomburg D, Harder MP, Mayer H, Paulsen J, Wingender E, Wray V
The solution structure of human parathyroid hormone, in the form of recombinant prolyl-hPTH(1-84), has been investigated by multidimensional NMR spectroscopy under conditions (aqueous...
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[NMR paper] Conformation of parathyroid hormone antagonists by CD, NMR, and molecular dynamics si
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Biopolymers. 1995 Oct;36(4):485-95
Authors: Chorev M, Behar V, Yang Q, Rosenblatt M, Mammi S, Maretto S, Pellegrini M, Peggion E
The conformation of two highly potent parathyroid hormone (PTH) antagonists was investigated in water/2,2,2-trifluoroethanol mixtures. The two peptides are derived from the sequence (7-34) of PTH and of...
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[NMR paper] NMR solution structure of the [Ala26]parathyroid-hormone-related protein(1-34) expres
NMR solution structure of the parathyroid-hormone-related protein(1-34) expressed in humoral hypercalcemia of malignancy.
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Eur J Biochem. 1993 Jan 15;211(1-2):205-11
Authors: Ray FR, Barden JA, Kemp BE
The structure of the biologically active N-terminal domain of...