Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
Pt 10
pubmed:dateCreated
2007-10-2
pubmed:databankReference
pubmed:abstractText
Mouse 3(17)alpha-hydroxysteroid dehydrogenase (AKR1C21) is a bifunctional enzyme that catalyses the oxidoreduction of the 3- and 17-hydroxy/keto groups of steroid substrates such as oestrogens, androgens and neurosteroids. The structure of the AKR1C21-NADPH binary complex was determined from an orthorhombic crystal belonging to space group P2(1)2(1)2(1) at a resolution of 1.8 A. In order to identify the factors responsible for the bifunctionality of AKR1C21, three steroid substrates including a 17-keto steroid, a 3-keto steroid and a 3alpha-hydroxysteroid were docked into the substrate-binding cavity. Models of the enzyme-coenzyme-substrate complexes suggest that Lys31, Gly225 and Gly226 are important for ligand recognition and orientation in the active site.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-10441302, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-10496958, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-10843227, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-10998348, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-11306071, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-11514561, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-11720859, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-11996927, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-12604210, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-12861966, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-12899831, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-14993666, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-15299374, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-15299926, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-15572765, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-15577209, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-15645014, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-16018803, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-16511129, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-17034817, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-1734286, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-17442338, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-2417090, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-2691507, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-7552731, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-7578036, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-8146147, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-9261071, http://linkedlifedata.com/resource/pubmed/commentcorrection/17909281-9307009
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
1744-3091
pubmed:author
pubmed:issnType
Electronic
pubmed:day
1
pubmed:volume
63
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
825-30
pubmed:dateRevised
2010-9-15
pubmed:meshHeading
pubmed:year
2007
pubmed:articleTitle
Structure of 3(17)alpha-hydroxysteroid dehydrogenase (AKR1C21) holoenzyme from an orthorhombic crystal form: an insight into the bifunctionality of the enzyme.
pubmed:affiliation
Department of Medicinal Chemistry, Victorian College of Pharmacy, Monash University, Parkville, Victoria 3052, Australia.
pubmed:publicationType
Journal Article