Reactome | Gould, SJ

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Gould, SJ Show undefined attributes

created	[InstanceEdit:6783876] Jassal, Bijay, 2015-06-17
dbId	6783881
displayName	Gould, SJ
firstname	S J
initial	SJ
publications	[LiteratureReference:9036572] A conserved tripeptide sorts proteins to peroxisomes [LiteratureReference:9036563] Pex13p is an SH3 protein of the peroxisome membrane and a docking factor for the predominantly cytoplasmic PTs1 receptor [LiteratureReference:9036556] A novel, cleavable peroxisomal targeting signal at the amino-terminus of the rat 3-ketoacyl-CoA thiolase [LiteratureReference:8963766] Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: evidence that PTS1 protein import is mediated by a cycling receptor [LiteratureReference:9033067] Identification of PTE2, a human peroxisomal long-chain acyl-CoA thioesterase [LiteratureReference:9603866] Multiple distinct targeting signals in integral peroxisomal membrane proteins [LiteratureReference:9033049] Peroxisomal targeting signal-1 recognition by the TPR domains of human PEX5 [LiteratureReference:9033036] An isoform of pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes [LiteratureReference:9036564] PEX12 interacts with PEX5 and PEX10 and acts downstream of receptor docking in peroxisomal matrix protein import [LiteratureReference:9033609] Domain mapping of human PEX5 reveals functional and structural similarities to Saccharomyces cerevisiae Pex18p and Pex21p [LiteratureReference:9033013] Human PEX7 encodes the peroxisomal PTS2 receptor and is responsible for rhizomelic chondrodysplasia punctata [LiteratureReference:9033031] Mutations in the PTS1 receptor gene, PXR1, define complementation group 2 of the peroxisome biogenesis disorders
schemaClass	Person
surname	Gould

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