Reaction Details |
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Target | Protein-glutamine gamma-glutamyltransferase 2 |
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Ligand | BDBM50200147 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_422560 (CHEMBL912249) |
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Ki | 22000±n/a nM |
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Citation | Watts, RE; Siegel, M; Khosla, C Structure-activity relationship analysis of the selective inhibition of transglutaminase 2 by dihydroisoxazoles. J Med Chem49:7493-501 (2006) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Protein-glutamine gamma-glutamyltransferase 2 |
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Name: | Protein-glutamine gamma-glutamyltransferase 2 |
Synonyms: | Protein-glutamine gamma-glutamyltransferase | Protein-glutamine gamma-glutamyltransferase 2 (TG2) | TGM2 | TGM2_HUMAN | Tissue transglutaminase | Tissue transglutaminase (TG2) | Transglutaminase 2 (TGM2) | Transglutaminase C | Transglutaminase-2 |
Type: | Protein |
Mol. Mass.: | 77309.30 |
Organism: | Homo sapiens (Human) |
Description: | P21980 |
Residue: | 687 |
Sequence: | MAEELVLERCDLELETNGRDHHTADLCREKLVVRRGQPFWLTLHFEGRNYEASVDSLTFS
VVTGPAPSQEAGTKARFPLRDAVEEGDWTATVVDQQDCTLSLQLTTPANAPIGLYRLSLE
ASTGYQGSSFVLGHFILLFNAWCPADAVYLDSEEERQEYVLTQQGFIYQGSAKFIKNIPW
NFGQFEDGILDICLILLDVNPKFLKNAGRDCSRRSSPVYVGRVVSGMVNCNDDQGVLLGR
WDNNYGDGVSPMSWIGSVDILRRWKNHGCQRVKYGQCWVFAAVACTVLRCLGIPTRVVTN
YNSAHDQNSNLLIEYFRNEFGEIQGDKSEMIWNFHCWVESWMTRPDLQPGYEGWQALDPT
PQEKSEGTYCCGPVPVRAIKEGDLSTKYDAPFVFAEVNADVVDWIQQDDGSVHKSINRSL
IVGLKISTKSVGRDEREDITHTYKYPEGSSEEREAFTRANHLNKLAEKEETGMAMRIRVG
QSMNMGSDFDVFAHITNNTAEEYVCRLLLCARTVSYNGILGPECGTKYLLNLNLEPFSEK
SVPLCILYEKYRDCLTESNLIKVRALLVEPVINSYLLAERDLYLENPEIKIRILGEPKQK
RKLVAEVSLQNPLPVALEGCTFTVEGAGLTEEQKTVEIPDPVEAGEEVKVRMDLLPLHMG
LHKLVVNFESDKLKAVKGFRNVIIGPA
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BDBM50200147 |
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n/a |
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Name | BDBM50200147 |
Synonyms: | CHEMBL410077 | [1-[(3-bromo-4,5-dihydroisoxazol-5-ylmethyl)carbamoyl]-2-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethyl]carbamic acid benzyl ester |
Type | Small organic molecule |
Emp. Form. | C22H22BrN5O4 |
Mol. Mass. | 500.345 |
SMILES | BrC1=NOC(CNC(=O)C(Cc2c[nH]c3ncccc23)NC(=O)OCc2ccccc2)C1 |t:1| |
Structure |
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