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TargetLanosterol synthase
LigandBDBM50128069
Substrate/Competitorn/a
Meas. Tech.ChEMBL_148897 (CHEMBL754981)
IC50 439±n/a nM
Citation Lenhart, AReinert, DJAebi, JDDehmlow, HMorand, OHSchulz, GE Binding structures and potencies of oxidosqualene cyclase inhibitors with the homologous squalene-hopene cyclase. J Med Chem46:2083-92 (2003) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lanosterol synthase
Name:Lanosterol synthase
Synonyms:2,3-epoxysqualene--lanosterol cyclase | LSS | LSS_HUMAN | OSC | Oxidosqualene--lanosterol cyclase
Type:PROTEIN
Mol. Mass.:83309.32
Organism:Homo sapiens (Human)
Description:ChEMBL_11231
Residue:732
Sequence:
MTEGTCLRRRGGPYKTEPATDLGRWRLNCERGRQTWTYLQDERAGREQTGLEAYALGLDT
KNYFKDLPKAHTAFEGALNGMTFYVGLQAEDGHWTGDYGGPLFLLPGLLITCHVARIPLP
AGYREEIVRYLRSVQLPDGGWGLHIEDKSTVFGTALNYVSLRILGVGPDDPDLVRARNIL
HKKGGAVAIPSWGKFWLAVLNVYSWEGLNTLFPEMWLFPDWAPAHPSTLWCHCRQVYLPM
SYCYAVRLSAAEDPLVQSLRQELYVEDFASIDWLAQRNNVAPDELYTPHSWLLRVVYALL
NLYEHHHSAHLRQRAVQKLYEHIVADDRFTKSISIGPISKTINMLVRWYVDGPASTAFQE
HVSRIPDYLWMGLDGMKMQGTNGSQIWDTAFAIQALLEAGGHHRPEFSSCLQKAHEFLRL
SQVPDNPPDYQKYYRQMRKGGFSFSTLDCGWIVSDCTAEALKAVLLLQEKCPHVTEHIPR
ERLCDAVAVLLNMRNPDGGFATYETKRGGHLLELLNPSEVFGDIMIDYTYVECTSAVMQA
LKYFHKRFPEHRAAEIRETLTQGLEFCRRQQRADGSWEGSWGVCFTYGTWFGLEAFACMG
QTYRDGTACAEVSRACDFLLSRQMADGGWGEDFESCEERRYLQSAQSQIHNTCWAMMGLM
AVRHPDIEAQERGVRCLLEKQLPNGDWPQENIAGVFNKSCAISYTSYRNIFPIWALGRFS
QLYPERALAGHP
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50128069
n/a
NameBDBM50128069
Synonyms:(4-Bromo-phenyl)-(4-{2-[(cyclopropyl-methyl-amino)-methyl]-cyclopropylmethoxy}-2-fluoro-phenyl)-methanone | CHEMBL292084 | N-(((1S,2S)-2-((4-(4-bromobenzoyl)-3-fluorophenoxy)methyl)cyclopropyl)methyl)-N-methylcyclopropanaminium
TypeSmall organic molecule
Emp. Form.C22H23BrFNO2
Mol. Mass.432.326
SMILESCN(C[C@H]1C[C@@H]1COc1ccc(C(=O)c2ccc(Br)cc2)c(F)c1)C1CC1
Structure
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