Reaction Details |
| Report a problem with these data |
Target | Protein-glutamine gamma-glutamyltransferase 2 |
---|
Ligand | BDBM50342580 |
---|
Substrate/Competitor | n/a |
---|
Meas. Tech. | ChEMBL_744966 (CHEMBL1771981) |
---|
IC50 | 1400±n/a nM |
---|
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 |
---|
More Info.: | Get all data from this article, Assay Method |
---|
|
Protein-glutamine gamma-glutamyltransferase 2 |
---|
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
|
|
|
BDBM50342580 |
---|
n/a |
---|
Name | BDBM50342580 |
Synonyms: | (E)-4-chloro-3-(2-(6-methoxypyridin-3-yl)-2-oxoethylidene)indolin-2-one | CHEMBL1770517 |
Type | Small organic molecule |
Emp. Form. | C16H11ClN2O3 |
Mol. Mass. | 314.723 |
SMILES | COc1ccncc1C(=O)\C=C1\C(=O)Nc2cccc(Cl)c12 |
Structure |
|