Crystal Structure of the E596A V617F Mutant JAK2 Pseudokinase Domain Bound to Mg-ATP. Determined by X-ray diffraction at 1.54 Å resolution. Released 13 Apr 2016.
Explore 5I4N in 3D Show helices and sheets RCSB PDB PDBe
5I4N contains 22 α-helices and 12 β-strands across 1 chain. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 539 | 1 | 1 |
| α-helix | 542-544 | 3 | |
| β-strand | 545-554 | 10 | 1 |
| β-strand | 557-567 | 11 | 1 |
| α-helix | 569-571 | 3 | |
| β-strand | 573-584 | 12 | 1 |
| α-helix | 588-602 | 15 | |
| β-strand | 609 | 1 | 2 |
| α-helix | 610-611 | 2 | |
| β-strand | 612-616 | 5 | 1 |
| β-strand | 621-627 | 7 | 1 |
| α-helix | 628-629 | 2 | |
| β-strand | 633 | 1 | 2 |
| α-helix | 634-640 | 7 | |
| α-helix | 647-666 | 20 | |
| α-helix | 676-678 | 3 | |
| β-strand | 679-683 | 5 | 2 |
| β-strand | 686 | 1 | 3 |
| β-strand | 691 | 1 | 3 |
| α-helix | 692-693 | 2 | |
| β-strand | 694-697 | 4 | 2 |
| α-helix | 698-699 | 2 | |
| α-helix | 709-714 | 6 | |
| α-helix | 721-725 | 5 | |
| α-helix | 727-729 | 3 | |
| α-helix | 732-746 | 15 | |
| α-helix | 751-752 | 2 | |
| α-helix | 759-767 | 9 | |
| α-helix | 772-775 | 4 | |
| α-helix | 778-780 | 3 | |
| α-helix | 781-787 | 7 | |
| α-helix | 792-794 | 3 | |
| α-helix | 796-797 | 2 | |
| α-helix | 798-808 | 11 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Tyrosine-protein kinase JAK2 | A | protein | 290 | Homo sapiens | O60674 (AlphaFold model) |
>5I4N_1 Tyrosine-protein kinase JAK2 (chains A) MVFHKIRNEDLIFNESLGQGTFTKIFKGVRREVGDYGQLHETEVLLKVLDKAHRNYSESF FAAASMMSKLSHKHLVLNYGVCFCGDENILVQEFVKFGSLDTYLKKNKNCINILWKLEVA KQLAAAMHFLEENTLIHGNVCAKNILLIREEDRKTGNPPFIKLSDPGISITVLPKDILQE RIPWVPPECIENPKNLNLATDKWSFGTTLWEICSGGDKPLSALDSQRKLQFYEDRHQLPA PKAAELANLINNCMDYEPDHRPSFRAIIRDLNSLFTPDLVPRGSHHHHHH
Water and common crystallization additives (GOL) are not listed.
Uncoupling JAK2 V617F activation from cytokine-induced signalling by modulation of JH2 alpha C helix. Leroy, E., Dusa, A., Colau, D. et al. Biochem J (2016) 473:1579-1591. DOI 10.1042/BCJ20160085 · PubMed
Other PDB entries of the same protein (UniProt O60674 (AlphaFold model), which also has an AlphaFold model), best resolution first:
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