Reaction Details |
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Target | Protein-glutamine gamma-glutamyltransferase 2 |
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Ligand | BDBM50342571 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_744966 (CHEMBL1771981) |
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Ki | 3000±n/a nM |
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Citation | Klöck, C; Jin, X; Choi, K; Khosla, C; Madrid, PB; Spencer, A; Raimundo, BC; Boardman, P; Lanza, G; Griffin, JH Acylideneoxoindoles: a new class of reversible inhibitors of human transglutaminase 2. Bioorg Med Chem Lett21:2692-6 (2011) [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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BDBM50342571 |
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n/a |
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Name | BDBM50342571 |
Synonyms: | (E)-5-bromo-3-(2-oxo-2-(pyridin-3-yl)ethylidene)indolin-2-one | CHEMBL1770541 |
Type | Small organic molecule |
Emp. Form. | C15H9BrN2O2 |
Mol. Mass. | 329.148 |
SMILES | Brc1ccc2NC(=O)\C(=C\C(=O)c3cccnc3)c2c1 |
Structure |
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