SCUBA

NME4 — NME/NM23 nucleoside diphosphate kinase 4

NME4 belongs to a gene co-expression module in 5 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

NME4's module in each cell type

Cell typeModuleShares the module with
CD4⁺ T cellsTCR signaling
TCR/AP1/NFKb pathway
ACVR1C, ADA2, ANK3, CAMK4, CHD7, GCLM, GNAO1, MPP7 +15 moreView in SCUBA
EndothelialProteasomal Degradation
Protein processing & ER
GNL3, HACD3, MRPL36, NUDT5, PON2, PSMA1, PSMB5, PSMC1 +3 moreView in SCUBA
Hematopoietic progenitor cellsNucleotide Metabolism
Housekeeping
DCTPP1, DNPH1, EIF4EBP1, FKBP4, GCSH, METTL26, MRPL12, NHP2 +2 more
MacrophagesInflammasome Oxidative Stress
Inflammatory
ABI3, ADISSP, AKR1A1, ARHGDIB, ARPC1B, ASCL2, BLVRA, C1orf54 +33 moreView in SCUBA
Smooth muscle cellsmRNA Splicing Factors
RNA processing & translation
ATF4, BEX3, CLIC4, COX20, HNRNPA0, NAP1L1, NDUFA6, PCBP1 +7 moreView in SCUBA

About the gene

SynonymsNDPKD, nm23-H4, NM23H4
Chromosome16: 396725-410367
Predicted locationIntracellular
Essential geneNo
Protein classEnzymes, Metabolic proteins, Plasma proteins, Predicted intracellular proteins
Molecular functionKinase, Transferase
Biological processNucleotide metabolism

Function

Major role in the synthesis of nucleoside triphosphates other than ATP. The ATP gamma phosphate is transferred to the NDP beta phosphate via a ping-pong mechanism, using a phosphorylated active-site intermediate. Through the catalyzed exchange of gamma-phosphate between di- and triphosphonucleosides participates in regulation of intracellular nucleotide homeostasis. Binds to anionic phospholipids, predominantly to cardiolipin; the binding inhibits its phosphotransfer activity. Acts as a mitochondria-specific NDK; its association with cardiolipin-containing mitochondrial inner membrane is coupled to respiration suggesting that ADP locally regenerated in the mitochondrion innermembrane space by its activity is directly taken up via ANT ADP/ATP translocase into the matrix space to stimulate respiratory ATP regeneration. Proposed to increase GTP-loading on dynamin-related GTPase OPA1 in mitochondria. In vitro can induce liposome cross-linking suggesting that it can cross-link inner and outer membranes to form contact sites, and promotes intermembrane migration of anionic phosphoplipids. Promotes the redistribution of cardiolipin between the mitochondrial inner membrane and outer membrane which is implicated in pro-apoptotic signaling.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.