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DESCRIBE <http://purl.uniprot.org/SHA-384/90F50C55D2C91975FEF1EB7DB3B8DDF0A1E8943C796585C34A82D13E92DA8918F59FD9EDAF869F1FDF844F27D175A704>
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http://purl.uniprot.org/SHA-384/90F50C55D2C91975FEF1EB7DB3B8DDF0A1E8943C796585C34A82D13E92DA8918F59FD9EDAF869F1FDF844F27D175A704
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://purl.uniprot.org/core/Annotation
http://purl.uniprot.org/SHA-384/90F50C55D2C91975FEF1EB7DB3B8DDF0A1E8943C796585C34A82D13E92DA8918F59FD9EDAF869F1FDF844F27D175A704
http://www.w3.org/2000/01/rdf-schema#comment
"Selective inhibition of NQO2 over NQO1 can be attributed to the bulky aminoalkylamino substituent at the 5-position which blocks entrance of the indolequinones into the NQO1 active site."
xsd:string
http://purl.uniprot.org/uniprot/#_F275ECB0AADDB19CF09565A73D7E72D277C233A4D9048EF19DB170A69B828B6835CD83BA7F834BDAE34A2ECBB8A0AA60
http://www.w3.org/1999/02/22-rdf-syntax-ns#subject
http://purl.uniprot.org/SHA-384/90F50C55D2C91975FEF1EB7DB3B8DDF0A1E8943C796585C34A82D13E92DA8918F59FD9EDAF869F1FDF844F27D175A704
http://purl.uniprot.org/uniprot/P16083
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/90F50C55D2C91975FEF1EB7DB3B8DDF0A1E8943C796585C34A82D13E92DA8918F59FD9EDAF869F1FDF844F27D175A704
http://purl.uniprot.org/uniprot/#_P16083-mappedCitation-21718050
http://purl.uniprot.org/core/mappedAnnotation
http://purl.uniprot.org/SHA-384/90F50C55D2C91975FEF1EB7DB3B8DDF0A1E8943C796585C34A82D13E92DA8918F59FD9EDAF869F1FDF844F27D175A704