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4FXL

Crystal structure of the D76N Beta-2 Microglobulin mutant

Summary for 4FXL
Entry DOI10.2210/pdb4fxl/pdb
DescriptorBeta-2-microglobulin, SODIUM ION, ACETATE ION, ... (5 entities in total)
Functional Keywordsimmunoglobin, beta-sandwitch, amyloidosis, pathologic mutation, genetic disease, mhc class i, immune system
Biological sourceHomo sapiens (human)
Cellular locationSecreted: P61769
Total number of polymer chains1
Total formula weight12066.53
Authors
Ricagno, S.,Bellotti, V.,Pepys, M.B.,Stoppini, M.,Bolognesi, M. (deposition date: 2012-07-03, release date: 2012-08-15, Last modification date: 2023-09-13)
Primary citationValleix, S.,Gillmore, J.D.,Bridoux, F.,Mangione, P.P.,Dogan, A.,Nedelec, B.,Boimard, M.,Touchard, G.,Goujon, J.M.,Lacombe, C.,Lozeron, P.,Adams, D.,Lacroix, C.,Maisonobe, T.,Plante-Bordeneuve, V.,Vrana, J.A.,Theis, J.D.,Giorgetti, S.,Porcari, R.,Ricagno, S.,Bolognesi, M.,Stoppini, M.,Delpech, M.,Pepys, M.B.,Hawkins, P.N.,Bellotti, V.
Hereditary systemic amyloidosis due to Asp76Asn variant beta-2-microglobulin.
N.Engl.J.Med., 366:2276-2283, 2012
Cited by
PubMed: 22693999
DOI: 10.1056/NEJMoa1201356
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.4 Å)
Structure validation

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数据于2024-04-24公开中

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