Reaction Details
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Dolichyl-phosphate-mannose--protein mannosyltransferase 1
Ligand
BDBM50149752
Substrate
n/a
Meas. Tech.
ChEMBL_304888 (CHEMBL877327)
IC50
350±n/a nM
Citation
Orchard, MG; Neuss, JC; Galley, CM; Carr, A; Porter, DW; Smith, P; Scopes, DI; Haydon, D; Vousden, K; Stubberfield, CR; Young, K; Page, M Rhodanine-3-acetic acid derivatives as inhibitors of fungal protein mannosyl transferase 1 (PMT1). Bioorg Med Chem Lett 14:3975-8 (2004) [PubMed] Article More Info.:
Target
Name:
Dolichyl-phosphate-mannose--protein mannosyltransferase 1
Synonyms:
PMT1 | PMT1_CANAL
Type:
PROTEIN
Mol. Mass.:
99941.72
Organism:
Candida albicans
Description:
ChEMBL_304888
Residue:
877
Sequence:
MAKKPVTPASKVAAKQAAVRSRHQEDVFTLDPLIDPIFQKGELRSYLVTEPSPSVLKKRSIHTKEYWMLSSLLLIAFYVRMYNLSNPNSVVFDEVHFGGFARKYILGTFFMDVHPPLAKMLFGAVGAIGGFKGDFEFKSIGDKFPDSTPYIFMRQFPALLGVGTVILCYLTLRQSGVRPIIAYITTFLLIIENSNVTISRYILLDSPLIFFIAAAIYAWKKFEIQIPFTFGWYRSLLATGIALGLALSSKWVGLFTVAWVGFLCIYQLWFLIGDLSVSTKKIWGHFFARGIILLGVPIALYLGFFAIHFQLLNKEGDGGAFMSSAFRAGLQGNKIPRDITEQVGLGSVVTIRHVDTQGGYLHSHEHFYQTGSKQQQITLYPHLDSNNKWLIEPYNGTIHNETFVPLINGMKIRLKHINTGRRLHSHDEKPPVSERDWQKECSCYGYDGFAGDANDDWVVEIVNYRSQKGEAQTFVKAINTIFRLRHAMTGHYLFSSEVKLPEWGFGQQEVTSASQGKRALTHWYIETNENSILPPSEAKIINYPKLSLWQKVVESHKRMWKINQGLTSHHHWQSSPSEWPLLLRGINYWNKEHKQVYLLGNAVTWWAATLSIITFGTYVLVTVFRWHLGTPLSTNKHVFNFNVQTFSYVLGWALHYLPFFIMGRQLFLHHYLPALYFGILALGHFFEIFTGYLTSRSKYFQQVAFVLVGLFSILSLVFYVNYSSLIYGTPWTKASCELTKPFSGWDYNCGTFFDTLGEYDIQEKSLASESEIPTETVVVEAKQTPKAEPKLAKQDDHIESPAAAEPVEEKEVKEEVEQLAPPLAVDFEEETPKVEDPQVADVDASSNDEKSVEEKQQQEQQQEQEQVEDESVHQVQQ
Inhibitor
Name:
BDBM50149752
Synonyms:
CHEMBL361718 | {4-Oxo-5-[4-((R)-2-phenyl-butoxy)-3-((R)-2,2,2-trifluoro-1-phenyl-ethoxy)-benzylidene]-2-thioxo-thiazolidin-3-yl}-acetic acid
Type:
Small organic molecule
Emp. Form.:
C30H26F3NO5S2
Mol. Mass.:
601.656
SMILES:
CC[C@@H](COc1ccc(\C=C2/SC(=S)N(CC(O)=O)C2=O)cc1O[C@H](c1ccccc1)C(F)(F)F)c1ccccc1
Structure:
