Brand  (β version)

PDB ID: 3V5L

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Ligands
Code Name Style Show Link
0G1 3-[3-(4-methoxyphenyl)-2-(1h-thieno[3,2-C]pyrazol-3-yl)-1h-indol-6-yl]pentan-3-ol PoSSuM
Non-standard Residues
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Glycosylation
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Structure summary

Code : 3V5L   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : Crystal Structure of Interleukin-2 Inducible T-cell Kinase Itk Catalytic Domain with Thienopyrazolylindole Inhibitor 542
Release Data : 2012-05-02
Compound :
mol_id molecule chains synonym
1 Tyrosine-protein kinase ITK/TSK A,B,C,D Interleukin-2-inducible T cell kinase, IL-2-inducible T cell kinase, Kinase EMT, T-cell-specific kinase, Tyrosine-protein kinase Lyk
ec: 2.7.10.2
fragment: unp residues 357-620
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: ITK, EMT, LYK
expression_system_cell_line: Sf9
expression_system_vector_type: plasmid
expression_system_plasmid: pFastBac1
Authors : McLean, L.R., Zhang, Y.
Keywords : Kinase, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.8600 Å )
Citation :

X-ray crystallographic structure-based design of selective thienopyrazole inhibitors for interleukin-2-inducible tyrosine kinase.

McLean, L.R.,Zhang, Y.,Zaidi, N.  et al.
(2012)  Bioorg.Med.Chem.Lett.  22 : 3296 - 3300

PubMed: 22464456
DOI: 10.1016/j.bmcl.2012.03.016

Reaction

Chain : A, B, C, D
UniProt : Q08881 (ITK_HUMAN)
Reaction: EC: Evidence:
Physiological Direction:
L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H(+) 2.7.10.2 PROSITE-ProRule:PRU10028
-
Cofactor: Evidence: Note:
Zn(2+) ECO:0000250
Binds 1 zinc ion per subunit.