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2AA2

Mineralocorticoid Receptor with Bound Aldosterone

Summary for 2AA2
Entry DOI10.2210/pdb2aa2/pdb
Related2AA5 2AA6 2AA7
DescriptorMineralocorticoid receptor, octyl beta-D-glucopyranoside, SULFATE ION, ... (6 entities in total)
Functional Keywordsmineralocorticoid, mr, nuclear receptor, steroid receptor, aldosterone, transcription
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight32543.58
Authors
Bledsoe, R.K.,Madauss, K.P.,Holt, J.A.,Apolito, C.J.,Lambert, M.H.,Pearce, K.H.,Stanley, T.B.,Stewart, E.L.,Trump, R.P.,Willson, T.M.,Williams, S.P. (deposition date: 2005-07-13, release date: 2005-07-26, Last modification date: 2024-02-14)
Primary citationBledsoe, R.K.,Madauss, K.P.,Holt, J.A.,Apolito, C.J.,Lambert, M.H.,Pearce, K.H.,Stanley, T.B.,Stewart, E.L.,Trump, R.P.,Willson, T.M.,Williams, S.P.
A Ligand-mediated Hydrogen Bond Network Required for the Activation of the Mineralocorticoid Receptor
J.Biol.Chem., 280:31283-31293, 2005
Cited by
PubMed Abstract: Ligand binding is the first step in hormone regulation of mineralocorticoid receptor (MR) activity. Here, we report multiple crystal structures of MR (NR3C2) bound to both agonist and antagonists. These structures combined with mutagenesis studies reveal that maximal receptor activation involves an intricate ligand-mediated hydrogen bond network with Asn770 which serves dual roles: stabilization of the loop preceding the C-terminal activation function-2 helix and direct contact with the hormone ligand. In addition, most activating ligands hydrogen bond to Thr945 on helix 10. Structural characterization of the naturally occurring S810L mutant explains how stabilization of a helix 3/helix 5 interaction can circumvent the requirement for this hydrogen bond network. Taken together, these results explain the potency of MR activation by aldosterone, the weak activation induced by progesterone and the antihypertensive agent spironolactone, and the binding selectivity of cortisol over cortisone.
PubMed: 15967794
DOI: 10.1074/jbc.M504098200
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.95 Å)
Structure validation

237735

数据于2025-06-18公开中

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