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-Structure paper
Title | BTB domain mutations perturbing KCTD15 oligomerisation cause a distinctive frontonasal dysplasia syndrome. |
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Journal, issue, pages | J Med Genet, Vol. 61, Page 490-501, Year 2024 |
Publish date | Jun 30, 2023 (structure data deposition date) |
Authors | Miller, K.A. / Cruz Walma, D.A. / Pinkas, D.M. / Tooze, R.S. / Bufton, J.C. / Richardson, W. / Manning, C.E. / Hunt, A.E. / Cros, J. / Hartill, V. ...Miller, K.A. / Cruz Walma, D.A. / Pinkas, D.M. / Tooze, R.S. / Bufton, J.C. / Richardson, W. / Manning, C.E. / Hunt, A.E. / Cros, J. / Hartill, V. / Parker, M.J. / McGowan, S.J. / Twigg, S.R.F. / Chalk, R. / Staunton, D. / Johnson, D. / Wilkie, A.O.M. / Bullock, A.N. |
External links | J Med Genet / PubMed:38296633 |
Methods | X-ray diffraction |
Resolution | 1.94 - 2.25 Å |
Structure data | PDB-8pnm: PDB-8pnr: |
Chemicals | ChemComp-HOH: |
Source |
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Keywords | GENE REGULATION / Oligomerisation / BTB domain |