靶点信息55(本栏目收费,不能显示细节,电话13136136841)
靶点信息
标题
内容
相关药物
状态
TARGETID
T60857
FORMERID
TTDR00033
UNIPROID
AK1C3_HUMAN
TARGNAME
Dihydrodiol dehydrogenase type I (AKR1C3)
GENENAME
AKR1C3
TARGTYPE
Successful target
SYNONYMS
Trans-1,2-dihydrobenzene-1,2-diol dehydrogenase; Testosterone 17-beta-dehydrogenase 5; Prostaglandin F synthase; PGFS; KIAA0119; Indanol dehydrogenase; HSD17B5; HA1753; Dihydrodiol dehydrogenase 3; DDH1; DD3; DD-3; Chlordecone reductase homolog HAKRb; Aldo-keto reductase family 1 member C3; 3-alpha-hydroxysteroid dehydrogenase type 2; 3-alpha-HSD type II, brain; 3-alpha-HSD type 2; 17-beta-hydroxysteroid dehydrogenase type 5; 17-beta-HSD 5
FUNCTION
Catalyzes the conversion of aldehydes and ketones to alcohols. Catalyzes the reduction of prostaglandin (PG) D2, PGH2 and phenanthrenequinone (PQ) and the oxidation of 9-alpha,11-beta-PGF2 to PGD2. Functions as a bi-directional 3-alpha-, 17-beta- and 20-alpha HSD. Can interconvert active androgens, estrogens and progestins with their cognate inactive metabolites. Preferentially transforms androstenedione (4-dione) to testosterone.
PDBSTRUC
6GXK; 6F78; 6F2U; 5JM5; 5HNU
BIOCLASS
Short-chain dehydrogenases reductase
ECNUMBER
EC 1.-.-.-
SEQUENCE
MDSKHQCVKLNDGHFMPVLGFGTYAPPEVPRSKALEVTKLAIEAGFRHIDSAHLYNNEEQVGLAIRSKIADGSVKREDIFYTSKLWSTFHRPELVRPALENSLKKAQLDYVDLYLIHSPMSLKPGEELSPTDENGKVIFDIVDLCTTWEAMEKCKDAGLAKSIGVSNFNRRQLEMILNKPGLKYKPVCNQVECHPYFNRSKLLDFCKSKDIVLVAYSALGSQRDKRWVDPNSPVLLEDPVLCALAKKHKRTPALIALRYQLQRGVVVLAKSYNEQRIRQNVQVFEFQLTAEDMKAIDGLDRNLHYFNSDSFASHPNYPYSDEY
DRUGINFO
Flufenamic Acid
DRUGINFO
ASP-9521
DRUGINFO
Beta-naphthylacetic acids derivative 1
DRUGINFO
Indomethacin analog 1
DRUGINFO
Indomethacin analog 2
DRUGINFO
Indomethacin analog 3
DRUGINFO
Isoquinolone derivative 1
DRUGINFO
N-(benzimidazole/indole) benzoic acid derivative 1
目标的 KEGG 通路数据
标题内容
hsa00140
hsa00590
hsa01100
hsa04913
目标的 Wiki 路径数据
标题内容
WP702
WP696
WP2650
目标的蛋白质ID
标题内容
TARGETID
UNIPROID
TARGNAME
TARGTYPE
目标的序列数据
标题内容
Dihydrodiol dehydrogenase type I (AKR1C3)
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