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The P174L mutation in human Sco1 severely compromises Cox17..:
Cobine, Paul A
;
Pierrel, Fabien
;
Leary, Scot C
...
info:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.M600496200. , 2006
Link:
https://hal.science/hal-00376137
RT Journal T1 <Title>The P174L mutation in human Sco1 severely compromises Cox17-dependent metallation but does not impair copper binding</Title> UL https://suche.suub.uni-bremen.de/peid=base-ftceafr:oai:HAL:hal-00376137v1&Exemplar=1&LAN=DE A1 Cobine, Paul A A1 Pierrel, Fabien A1 Leary, Scot C A1 Sasarman, Florin A1 Horng, Yih-Chern A1 Shoubridge, Eric, A A1 Winge, Dennis R PB HAL CCSD; American Society for Biochemistry and Molecular Biology YR 2006 K1 MESH: Binding Sites K1 MESH: Carrier Proteins K1 MESH: Protein Binding K1 MESH: Recombinant Proteins K1 MESH: Copper K1 MESH: Electron Transport Complex IV K1 MESH: Fibroblasts K1 MESH: Humans K1 MESH: Membrane Proteins K1 MESH: Mitochondria K1 MESH: Mutation K1 Missense K1 [SDV.BBM]Life Sciences [q-bio]/Biochemistry K1 Molecular Biology JF info:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.M600496200 LK http://dx.doi.org/https://hal.science/hal-00376137 DO https://hal.science/hal-00376137 SF ELIB - SuUB Bremen
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