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DESCRIBE <http://purl.uniprot.org/SHA-384/4B519CA57F5437D2635F5DEDDB0781DCF65357530B631FDF3D3192D52A710EDCF5F024E2C069E2F7AC445EBA0120FD69>
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http://purl.uniprot.org/SHA-384/4B519CA57F5437D2635F5DEDDB0781DCF65357530B631FDF3D3192D52A710EDCF5F024E2C069E2F7AC445EBA0120FD69
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/4B519CA57F5437D2635F5DEDDB0781DCF65357530B631FDF3D3192D52A710EDCF5F024E2C069E2F7AC445EBA0120FD69
http://www.w3.org/2000/01/rdf-schema#comment
"The ability of constitutively-active human MEK1 to stimulate ERK phosphorylation and to induce the neoplastic transformation of NIH 3T3 cells required the integrity of the D-site was found."
xsd:string
http://purl.uniprot.org/uniprot/#_916D3C9A6D30163A1E77B9BD323FC774FE678427B0CEEB6D945F78838087239C3228CF96551CB0D40F224B44E57E394C
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/4B519CA57F5437D2635F5DEDDB0781DCF65357530B631FDF3D3192D52A710EDCF5F024E2C069E2F7AC445EBA0120FD69
http://purl.uniprot.org/uniprot/A4QPA9
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4B519CA57F5437D2635F5DEDDB0781DCF65357530B631FDF3D3192D52A710EDCF5F024E2C069E2F7AC445EBA0120FD69
http://purl.uniprot.org/uniprot/#_A4QPA9-mappedCitation-15979847
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/4B519CA57F5437D2635F5DEDDB0781DCF65357530B631FDF3D3192D52A710EDCF5F024E2C069E2F7AC445EBA0120FD69