Cell Reactant:
BDBM2579
Syringe Reactant:
Serine/threonine-protein kinase PIM
Meas. Tech.:
Isothermal Titration Calorimetry
Entry Date.:
10/29/06
ΔG°:
-48.07±n/a (kJ/mole)
pH:
7.5±n/a
Log10Kb:
8.5
Temperature:
283.15±n/a (K)
ΔHobs :
-33.858±0.418 (kJ/mole)
Corrected for ΔHioniz:
no
Stoich. Param.:
0.85
ΔS° :
0.0493±n/a (kJ/mole-K)
Citation
of the article is missing
Cell React
Source:
LC Laboratories
Name:
Serine/threonine-protein kinase pim-1
Synonyms:
PIM-1 Kinase | PIM1 | PIM1_HUMAN | Proto-oncogene serine/threonine-protein kinase Pim-1 | Serine/threonine-protein kinase (PIM1) | Serine/threonine-protein kinase PIM | Serine/threonine-protein kinase PIM1 | Serine/threonine-protein kinase pim-1 (PIM1)
Type:
Protein
Mol. Mass.:
35681.82
Organism:
Homo sapiens (Human)
Description:
P11309
Residue:
313
Sequence:
MLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILERPEPVQDLFDFITERGALQEELARSFFWQVLEAVRHCHNCGVLHRDIKDENILIDLNRGELKLIDFGSGALLKDTVYTDFDGTRVYSPPEWIRYHRYHGRSAAVWSLGILLYDMVCGDIPFEHDEEIIRGQVFFRQRVSSECQHLIRWCLALRPSDRPTFEEIQNHPWMQDVLLPQETAEIHLHSLSPGPSK
  
Syringe React
Source:
Full-length human PIM-1 was subcloned and expressed in E. coli cells.
Prep. Method:
Cells were lysed, and the lysate was purified by Ni-NTA chromatography. The protein was further purified on a monoQ column and resolved into two species, shown by ESI-MS to be homogeneous nonphosphorylated and singularly phosphorylated PIM-1.
Name:
Serine/threonine-protein kinase PIM1
Synonyms:
PIM1 | PIM1_HUMAN | Pim-1L
Type:
Enzyme
Mol. Mass.:
45417.87
Organism:
Homo sapiens (Human)
Description:
P11309-2
Residue:
404
Sequence:
MPHEPHEPLTPPFSALPDPAGAPSRRQSRQRPQLSSDSPSAFRASRSHSRNATRSHSHSHSPRHSLRHSPGSGSCGSSSGHRPCADILEVGMLLSKINSLAHLRAAPCNDLHATKLAPGKEKEPLESQYQVGPLLGSGGFGSVYSGIRVSDNLPVAIKHVEKDRISDWGELPNGTRVPMEVVLLKKVSSGFSGVIRLLDWFERPDSFVLILERPEPVQDLFDFITERGALQEELARSFFWQVLEAVRHCHNCGVLHRDIKDENILIDLNRGELKLIDFGSGALLKDTVYTDFDGTRVYSPPEWIRYHRYHGRSAAVWSLGILLYDMVCGDIPFEHDEEIIRGQVFFRQRVSSECQHLIRWCLALRPSDRPTFEEIQNHPWMQDVLLPQETAEIHLHSLSPGPSK