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8PBJ

Mutant R1722W of the dihydroorotase domain of human CAD protein bound to the substrate carbamoyl aspartate

Summary for 8PBJ
Entry DOI10.2210/pdb8pbj/pdb
Related8PBE 8PBG 8PBH 8PBI 8PBJ 8PBK 8PBM 8PBN 8PBP 8PBQ 8PBR 8PBS 8PBT 8PBU
DescriptorCAD protein, N-CARBAMOYL-L-ASPARTATE, FORMIC ACID, ... (6 entities in total)
Functional Keywordsnucleotide metabolism, de novo pyrimidine synthesis, cad disease, multienzymatic protein, zinc, carboxylated lysine, biosynthetic protein, hydrolase
Biological sourceHomo sapiens (human)
Total number of polymer chains1
Total formula weight40464.09
Authors
del Cano-Ochoa, F.,Ramon-Maiques, S. (deposition date: 2023-06-09, release date: 2023-11-01, Last modification date: 2023-11-22)
Primary citationDel Cano-Ochoa, F.,Ng, B.G.,Rubio-Del-Campo, A.,Mahajan, S.,Wilson, M.P.,Vilar, M.,Rymen, D.,Sanchez-Pintos, P.,Kenny, J.,Ley Martos, M.,Campos, T.,Wortmann, S.B.,Freeze, H.H.,Ramon-Maiques, S.
Beyond genetics: Deciphering the impact of missense variants in CAD deficiency.
J Inherit Metab Dis, 46:1170-1185, 2023
Cited by
PubMed: 37540500
DOI: 10.1002/jimd.12667
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.55 Å)
Structure validation

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