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Mitochondrial NM23-H4/NDPK-D: a bifunctional nanoswitch for bioenergetics and lipid signaling
miR (show MLXIP Proteins)-196 performed it's their function by inhibiting NME4 expression and further activating p-JNK (show MAPK8 Proteins), suppressing TIMP1 (show TIMP1 Proteins), and augmenting MMP1 (show MMP1 Proteins)/9.
NDPK-B and NDPK-D were shown to bind efficiently to liposomes mimicking plasma membrane and mitochondrial inner membrane
findings show NDPKs (NM23-H1 (show NME1 Proteins)/H2/H4) interact with and provide GTP (show AK3 Proteins) to dynamins, allowing these motor proteins to work with high thermodynamic efficiency for membrane remodeling
Nm23-H4 acts as a lipid-dependent mitochondrial switch with dual function in phosphotransfer serving local GTP (show AK3 Proteins) supply and cardiolipin transfer for apoptotic signaling and putative other functions
High expression of ERCC1 (show ERCC1 Proteins), FLT1 (show FLT1 Proteins), NME4 and PCNA (show PCNA Proteins) in myelodysplastic syndrome was associated with poor prognosis and disease progression along the sequence of 5q-syndrome/RCMD/RAEB/de novo AML (show RUNX1 Proteins)
The nucleoside diphosphate (NDP) kinases (EC 126.96.36.199) are ubiquitous enzymes that catalyze transfer of gamma-phosphates, via a phosphohistidine intermediate, between nucleoside and dioxynucleoside tri- and diphosphates. The enzymes are products of the nm23 gene family, which includes NME4 (Milon et al., 1997
, NDP kinase D
, NDP kinase, mitochondrial
, non-metastatic cells 4, protein expressed in
, nucleoside diphosphate kinase D
, nucleoside diphosphate kinase, mitochondrial
, expressed in non-metastatic cells 4, protein