Brand  (β version)

PDB ID: 4E6Q

Hetero Atom Contents

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hetatm:

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information
centroid:
interaction residue:

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Ligands
Code Name Link
0NV 1-(1-benzylpiperidin-4-yl)-1,6-dihydroimidazo[4,5-D]pyrrolo[2,3-B]pyridine PoSSuM
Modified Residues
Code Name Link
PTR O-phosphotyrosine PoSSuM

Structure summary

Code : 4E6Q   PDBj   RCSB PDB   PDBe
Header : TRANSFERASE/TRANSFERASE INHIBITOR
Title : JAK2 kinase (JH1 domain) triple mutant in complex with compound 12
Release Data : 2012-05-30
Compound :
mol_id molecule chains synonym
1 Tyrosine-protein kinase JAK2 A,B Janus kinase 2, JAK-2
ec: 2.7.10.2
fragment: kinase domain, UNP residues 835-1132
mutation: Q853R, Y931F, D939E
Source :
mol_id organism_scientific organism_common expression_system
1 Homo sapiens  (taxid:9606) Human Spodoptera frugiperda  (taxid:7108)
gene: JAK2
expression_system_common: Fall armyworm
expression_system_vector: Baculovirus
Authors : Murray, J.M.
Keywords : JAK2, kinase domain, TRANSFERASE-TRANSFERASE INHIBITOR complex
Exp. method : X-RAY DIFFRACTION ( 1.9480 Å )
Citation :

Identification of Imidazo-Pyrrolopyridines as Novel and Potent JAK1 Inhibitors.

Kulagowski, J.J.,Blair, W.,Bull, R.J.  et al.
(2012)  J.Med.Chem.  55 : 5901 - 5921

PubMed: 22591402
DOI: 10.1021/jm300438j

Reaction

Chain : A, B
UniProt : O60674 (JAK2_HUMAN)
Reaction : Reaction=ATP + L-tyrosyl-[protein] = ADP + H(+) + O-phospho-L-tyrosyl- [protein]; Xref=Rhea:RHEA:10596, Rhea:RHEA-COMP:10136, Rhea:RHEA- COMP:10137, ChEBI:CHEBI:15378, ChEBI:CHEBI:30616, ChEBI:CHEBI:46858, ChEBI:CHEBI:82620, ChEBI:CHEBI:456216; EC=2.7.10.2; Evidence={ECO:0000255|PROSITE-ProRule:PRU10028, ECO:0000269|PubMed:7615558, ECO:0000269|PubMed:9618263};