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1P9F

NMR Structure of Neurokinin B from DYANA

Summary for 1P9F
Entry DOI10.2210/pdb1p9f/pdb
NMR InformationBMRB: 5864
DescriptorNEUROKININ B (1 entity in total)
Functional Keywordsprotein, structures from dyana, neuropeptide
Cellular locationSecreted: Q9UHF0
Total number of polymer chains1
Total formula weight1212.42
Authors
Mantha, A.K.,Chandrashekar, I.R.,Baquer, N.Z.,Cowsik, S.M. (deposition date: 2003-05-12, release date: 2004-08-10, Last modification date: 2024-05-22)
Primary citationMantha, A.K.,Chandrashekar, I.R.,Baquer, N.Z.,Cowsik, S.M.
Three dimensional structure of Mammalian tachykinin Peptide neurokinin B bound to lipid micelles.
J.Biomol.Struct.Dyn., 22:137-148, 2004
Cited by
PubMed Abstract: Neurokinin B (NKB), a decapeptide of mammalian origin exhibits a variety of biological activities such as regulatory functions in reproduction, pre-eclampsia and neuroprotection in Alzheimer's disease. In order to gain insight into structure-function relationship, three-dimensional structure of NKB has been investigated using CD spectropolarimetry and two-dimensional proton nuclear magnetic resonance (2D 1H-NMR) spectroscopy in aqueous and membrane mimetic solvents. Unambiguous NMR assignments of resonances have been made with the aid of correlation spectroscopy (DQF-COSY and TOCSY) experiments and Nuclear Overhauser Effect Spectroscopy (NOESY) experiments. Distance constraints obtained from the NMR data have been used to generate a family of structures, which have been refined using restrained energy minimization and dynamics. Our data show that a helical structure is induced in NKB, in presence of perdeuterated dodecyl phosphocholine (DPC) micelles, a membrane model system. Further, the conformation adopted by NKB in presence of DPC micelles represents a structural motif typical of neurokinin-3 selective agonists.
PubMed: 15317475
PDB entries with the same primary citation
Experimental method
SOLUTION NMR
Structure validation

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