#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA1034103	B	Inhibition of DMPK2 at 3 uM		1	ALA1142492	single protein format	Scientific Literature
2.	ALA1060242	B	Binding constant for DMPK2 kinase domain	Homo sapiens	38	ALA1150977	single protein format	Scientific Literature
3.	ALA1055294	B	Inhibition of DMPK2 assessed as enzyme activity at 1 uM relative to untreated control		1	ALA1155237	single protein format	Scientific Literature
4.	ALA1168857	B	Inhibition of DMPK2 at 1 uM		10	ALA1165965	single protein format	Scientific Literature
5.	ALA1174319	B	Inhibition of DMPK2 at 10 uM		2	ALA1177794	single protein format	Scientific Literature
6.	ALA1244795	B	Binding affinity to DMPK2		7	ALA1240346	single protein format	Scientific Literature
7.	ALA1827246	B	Activity of DMPK2 kinase at 1 uM		1	ALA1821651	single protein format	Scientific Literature
8.	ALA1908804	B	Binding constant for DMPK2 kinase domain		72	ALA1908390	single protein format	Scientific Literature
9.	ALA2216438	B	Inhibition of DMPK2 assessed as residual activity at 10 uM relative to control		1	ALA2203081	single protein format	Scientific Literature
10.	ALA2428157	B	Competitive binding affinity to DMPK2 (unknown origin) at 10 uM in presence of ATP relative to control	Homo sapiens	3	ALA2424622	single protein format	Scientific Literature
11.	ALA3630349	B	Inhibition of DMPK2 (unknown origin) at 10 uM after 120 mins P33 radiolabeled kinase activity assay	Homo sapiens	3	ALA3627608	single protein format	Scientific Literature
12.	ALA3749007	B	Inhibition of human DMPK2 using [KKRPQRRYSNVF] as substrate	Homo sapiens	1	ALA3745707	single protein format	Scientific Literature
13.	ALA3991648	B	Kinobeads (epsilon), multiple immobilized ATP-competitive broad spectrum kinase inhibitors, used to assess residual binding of ~300 proteins simultaneously from cell lysate in the presence of a compound. Quantitative readout performed by mass spectrometry.	Homo sapiens	218	ALA3991601	subcellular format	Kuster lab chemical proteomics drug profiling
14.	ALA4025094	B	Inhibition of wild-type human partial length DMPK2 (S46 to S408 residues) expressed in bacterial expression system assessed as residual activity at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4024706	assay format	Scientific Literature
15.	ALA4043905	B	Inhibition of wild-type human partial length DMPK2 (S46 to S408 residues) expressed in Escherichia coli BL21 assessed as residual activity at 1000 nM after 30 mins by Kinomescan method relative to control	Homo sapiens	1	ALA4043093	assay format	Scientific Literature
16.	ALA4054921	B	Inhibition of wild-type human partial length DMPK2 (S46 to S408 residues) expressed in bacterial expression system assessed as residual activity at 50 nM by Kinomescan method relative to control	Homo sapiens	2	ALA4052645	assay format	Scientific Literature
17.	ALA4156984	B	Binding affinity to wild-type human partial length DMPK2 (S46 to S408 residues) expressed in bacterial expression system assessed as residual binding at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4152344	assay format	Scientific Literature
18.	ALA4185763	B	Binding affinity to wild-type human partial length DMPK2 (S46 to S408 residues) expressed in Escherichia coli BL21 at 1 uM by Kinomescan method relative to control	Homo sapiens	2	ALA4184148	assay format	Scientific Literature
19.	ALA4230663	B	Binding affinity to wild-type human partial length DMPK2 (S46 to S408 residues) expressed in bacterial expression system assessed as residual binding level at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4229344	assay format	Scientific Literature
20.	ALA4264252	B	Binding affinity to wild-type human partial length DMPK2 (S46 to S408 residues) expressed in bacterial expression system assessed as remaining unbound target protein level at 1000 nM by Kinomescan method relative to control	Homo sapiens	1	ALA4261600	assay format	Scientific Literature