General Information of Target

Target ID LDTP06964
Target Name UMP-CMP kinase 2, mitochondrial (CMPK2)
Gene Name CMPK2
Gene ID 129607
Synonyms
UMP-CMP kinase 2, mitochondrial; EC 2.7.4.14; Nucleoside-diphosphate kinase; EC 2.7.4.6
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MAFARRLLRGPLSGPLLGRRGVCAGAMAPPRRFVLELPDCTLAHFALGADAPGDADAPDP
RLAALLGPPERSYSLCVPVTPDAGCGARVRAARLHQRLLHQLRRGPFQRCQLLRLLCYCP
GGQAGGAQQGFLLRDPLDDPDTRQALLELLGACQEAPRPHLGEFEADPRGQLWQRLWEVQ
DGRRLQVGCAQVVPVPEPPLHPVVPDLPSSVVFPDREAARAVLEECTSFIPEARAVLDLV
DQCPKQIQKGKFQVVAIEGLDATGKTTVTQSVADSLKAVLLKSPPSCIGQWRKIFDDEPT
IIRRAFYSLGNYIVASEIAKESAKSPVIVDRYWHSTATYAIATEVSGGLQHLPPAHHPVY
QWPEDLLKPDLILLLTVSPEERLQRLQGRGMEKTREEAELEANSVFRQKVEMSYQRMENP
GCHVVDASPSREKVLQTVLSLIQNSFSEP
Target Bioclass
Enzyme
Family
Thymidylate kinase family
Subcellular location
Mitochondrion
Function
Mitochondrial nucleotide monophosphate kinase needed for salvage dNTP synthesis that mediates immunomodulatory and antiviral activities through IFN-dependent and IFN-independent pathways. Restricts the replication of multiple viruses including flaviviruses or coronaviruses. Together with viperin/RSAD2 and ddhCTP, suppresses the replication of several coronaviruses through inhibition of the viral RNA-dependent RNA polymerase activities. Concerning flaviviruses, restricts RNA translation when localized to the mitochondria independently of its kinase activity. Is able to phosphorylate dUMP, dCMP, CMP, UMP and monophosphates of the pyrimidine nucleoside analogs ddC, dFdC, araC, BVDU and FdUrd with ATP as phosphate donor. Efficacy is highest for dUMP followed by dCMP while CMP and UMP are poor substrates. Controls therefore mitochondrial DNA synthesis by supplying required deoxyribonucleotides. CMPK2-dependent mitochondrial DNA synthesis is necessary for the production of oxidized mitochondrial DNA fragments after exposure to NLRP3 activators. In turn, cytosolic oxidized mtDNA associates with the NLRP3 inflammasome complex and is required for its activation.
Uniprot ID
Q5EBM0
Ensemble ID
ENST00000256722.10
HGNC ID
HGNC:27015

Target Site Mutations in Different Cell Lines

Cell line Mutation details Probe for labeling this protein in this cell
CMK SNV: p.P429L DBIA    Probe Info 
DU145 SNV: p.V272M .
HEC1B SNV: p.R134C .
HT115 SNV: p.E321Ter .
JHH7 SNV: p.W291C .
NCIH716 SNV: p.S228F .
SKHEP1 SNV: p.D206E .

Probe(s) Labeling This Target

ABPP Probe
Click To Hide/Show 6 Probe Related to This Target
Probe name Structure Binding Site(Ratio) Interaction ID Ref
BTD
 Probe Info 
C110(1.03)  LDD2104  [1]
DBIA
 Probe Info 
C40(9.45)  LDD0209  [2]
4-Iodoacetamidophenylacetylene
 Probe Info 
C243(0.00); C40(0.00); C422(0.00); C287(0.00)  LDD0038  [3]
IA-alkyne
 Probe Info 
C243(0.00); C226(0.00); C40(0.00); C422(0.00)  LDD0036  [3]
Lodoacetamide azide
 Probe Info 
C243(0.00); C226(0.00); C40(0.00); C422(0.00)  LDD0037  [3]
Compound 10
 Probe Info 
N.A.  LDD2216  [4]

Competitor(s) Related to This Target

Competitor ID Name Cell line Binding Site(Ratio) Interaction ID Ref
 LDCM0548  1-(4-(Benzo[d][1,3]dioxol-5-ylmethyl)piperazin-1-yl)-2-nitroethan-1-one MDA-MB-231 C110(0.92)  LDD2142  [1]
 LDCM0519  1-(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)-2-nitroethan-1-one MDA-MB-231 C110(1.08)  LDD2112  [1]
 LDCM0022  KB02 22RV1 C189(0.96)  LDD2243  [5]
 LDCM0023  KB03 Jurkat C40(9.45)  LDD0209  [2]
 LDCM0024  KB05 COLO792 C189(1.19)  LDD3310  [5]
 LDCM0511  Nucleophilic fragment 18b MDA-MB-231 C110(1.03)  LDD2104  [1]
 LDCM0512  Nucleophilic fragment 19a MDA-MB-231 C110(1.01)  LDD2105  [1]
 LDCM0526  Nucleophilic fragment 26a MDA-MB-231 C110(1.50)  LDD2119  [1]
 LDCM0536  Nucleophilic fragment 31 MDA-MB-231 C110(1.20)  LDD2129  [1]
 LDCM0547  Nucleophilic fragment 41 MDA-MB-231 C110(0.79)  LDD2141  [1]
 LDCM0556  Nucleophilic fragment 8a MDA-MB-231 C110(0.62)  LDD2150  [1]

References

1 Nucleophilic covalent ligand discovery for the cysteine redoxome. Nat Chem Biol. 2023 Nov;19(11):1309-1319. doi: 10.1038/s41589-023-01330-5. Epub 2023 May 29.
Mass spectrometry data entry: PXD039908 , PXD029761
2 Covalent Inhibition by a Natural Product-Inspired Latent Electrophile. J Am Chem Soc. 2023 May 24;145(20):11097-11109. doi: 10.1021/jacs.3c00598. Epub 2023 May 15.
3 Enhancing Cysteine Chemoproteomic Coverage through Systematic Assessment of Click Chemistry Product Fragmentation. Anal Chem. 2022 Mar 8;94(9):3800-3810. doi: 10.1021/acs.analchem.1c04402. Epub 2022 Feb 23.
Mass spectrometry data entry: PXD028853
4 Multiplexed CuAAC Suzuki-Miyaura Labeling for Tandem Activity-Based Chemoproteomic Profiling. Anal Chem. 2021 Feb 2;93(4):2610-2618. doi: 10.1021/acs.analchem.0c04726. Epub 2021 Jan 20.
Mass spectrometry data entry: PXD022279
5 DrugMap: A quantitative pan-cancer analysis of cysteine ligandability. Cell. 2024 May 9;187(10):2536-2556.e30. doi: 10.1016/j.cell.2024.03.027. Epub 2024 Apr 22.
Mass spectrometry data entry: PXD047840