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120000 - 170000
analytical ultracentrifugation
152000
Pigeon
-
gel filtration
180000 - 190000
-
gel filtration
194000
-
native enzyme, gel filtration
195000 - 205000
-
gel filtration
209400
-
sedimentation equilibrium method
216000
-
isozyme PK1, PAGE
220000 - 240000
gel filtration
225000 - 240000
-
isozyme PK I
227000
-
average MW of all 5 isoforms, PAGE
232600
Busycotypus canaliculatum
-
PK-anoxic, gel filtration
237000
-
sucrose density gradient centrifugation
237500
Busycotypus canaliculatum
-
PK-aerobic, gel filtration
239000
-
isozyme PK5, PAGE
242000
-
sedimentation analysis
265000
-
liver, gel filtration
286000
Busycotypus canaliculatum
-
PK-aerobic, gel filtration
299800
Busycotypus canaliculatum
-
PK-anoxic, gel filtration
400000
-
growing and resting cells, FPLC gel filtration
44000
-
4 * 44000, SDS-PAGE
47000
-
4 * 47000, isozyme II, SDS-PAGE
48000
-
4 * 48000, SDS-PAGE
49800
x * 50000, SDS-PAGE, x * 49800, calculated
50500
-
4 * 50500, PykF, SDS-PAGE, circular dichroism spectroscopy, and gel filtration, 4 * 51500, PykA, SDS-PAGE, circular dichroism spectroscopy, and gel filtration
51300
4 * 51300, SDS-PAGE
51400
-
calculated from amino acid sequence
51500
-
4 * 50500, PykF, SDS-PAGE, circular dichroism spectroscopy, and gel filtration, 4 * 51500, PykA, SDS-PAGE, circular dichroism spectroscopy, and gel filtration
52000
-
4 * 52000, L-type isozyme
53100
4 * 65100, about, full-length enzyme, sequence calculation, 4 * 53100, about, C-terminally truncated enzyme mutant, sequence calculation
53500
-
x * 53500, SDS-PAGE
55400
2 * 55400, SDS-PAGE, predominantly a dimer, but also some tetramer
57590
calculated from amino acid sequence
580000
-
resting cells, FPLC gel filtration
58600
-
4 * 58600, M4-type isozyme, SDS-PAGE
59500
-
4 * 59500, K4-type isozyme, SDS-PAGE
61940
x * 61940, deduced from gene sequence
62200
-
calculated from amino acid sequence
62570
x * 62570, deduced from gene sequence
63000
-
4 * 63000, SDS-PAGE
64400
Busycotypus canaliculatum
-
4 * 64400, PK-aerobic, SDS-PAGE
64500
-
SDS-PAGE, subunit
65000
-
4 * 65000, SDS-PAGE
65100
4 * 65100, about, full-length enzyme, sequence calculation, 4 * 53100, about, C-terminally truncated enzyme mutant, sequence calculation
71000
Busycotypus canaliculatum
-
4 * 71000, PK-aerobic, SDS-PAGE
72600
Busycotypus canaliculatum
-
4 * 72600, PK-anoxic, SDS-PAGE
73000
-
4 * 73000, SDS-PAGE
77000
-
purified recombinant protein
100000
-
gel filtration
100000
-
sucrose density gradient centrifugation
190000
-
-
190000
-
recombinant enzyme, gel filtration
190000
-
isozyme PKII, gel filtration
200000
-
gel filtration
200000
recombinant His-tagged VcIIPK, native PAGE
200000
recombinant His-tagged VcIPK, native PAGE
203000
-
gel filtration
203000
-
calculated from amino acid sequence
210000
-
PK II, sucrose density gradient centrifugation
210000
-
1 * 210000, isozyme PKp, SDS-PAGE
215000
-
L-type isozyme
215000
His-tagged C-terminally truncated enzyme mutant, gel filtration
220000
gel filtration
220000
-
isozyme PKII, gel filtration
220000
-
M4-type isozyme, glycerol density gradient sedimentation
224000
-
gel filtration
224000
-
native molecular mass
225500
-
sedimentation equilibrium method
225500
-
M4-type isozyme, PAGE
230000
-
-
230000
-
K4-type isozyme, glycerol density gradient sedimentation, PAGE
230000
-
sucrose density gradient centrifugation, M1 isozyme
235000
-
-
235000
-
equilibrium sedimentation
235000
-
isozyme PKp, FPLC gel filtration
238000
-
K4-type isozyme, gel filtration
240000
-
gel filtration
240000
Musa cavendishii
-
gel filtration
250000
-
-
250000
His-tagged full-length enzyme, gel filtration
270000
-
gel filtration
300000
-
gel filtration
300000
-
PK I, gel filtration
49000
-
4 * 49000, SDS-PAGE
49000
-
4 * 49000, SDS-PAGE
50000
-
4 * 50000, SDS-PAGE
50000
x * 50000, SDS-PAGE, x * 49800, calculated
51000
-
4 * 51000, SDS-PAGE
51000
-
4 * 51000, isozyme PK I, SDS-PAGE
51000
-
4 * 51000, native enzyme, SDS-PAGE
54000
-
SDS-PAGE
54000
-
4 * 54000, isozyme I, SDS-PAGE
54400
-
4 * 54400, isozyme PK1, SDS-PAGE
54400
x * 54400, calculated
55000
SDS-PAGE
55000
-
x * 55000, SDS-PAGE
55000
-
x * 55000 + 4-x * 57000, SDS-PAGE
56000
-
4 * 56000, SDS-PAGE
56000
-
2 * 56000 + 2 * 57000, SDS-PAGE
56000
-
4 * 56000, isozyme PK II, SDS-PAGE
56000
-
x * 56000 + x * 57000, SDS-PAGE
56000
-
4 * 56000, recombinant enzyme, SDS-PAGE
56000
-
4 * 56000, gel filtration
56000
-
4 * 56000, gel filtration
57000
-
2 * 57000, SDS-PAGE
57000
-
x * 57000, SDS-PAGE
57000
-
x * 57000, SDS-PAGE
57000
-
4 * 57000, SDS-PAGE
57000
Musa cavendishii
-
4 * 57000, SDS-PAGE
57000
-
4 * 57000, SDS-PAGE
57000
4 * 57000, SDS-PAGE
57000
-
2 * 56000 + 2 * 57000, SDS-PAGE
57000
-
x * 55000 + 4-x * 57000, SDS-PAGE
57000
-
x * 56000 + x * 57000, SDS-PAGE
57000
-
10 * 57000, isozyme PK2, SDS-PAGE
57000
-
4 * 60000 + 4 * 57000, gel filtration
57900
-
calculated from amino acid sequence
57900
-
native enzyme, MALDI-TOF mass spectrometry
58000
-
recombinant enzyme, gel filtration
58000
-
most of the protein recognized by the anti-M2-PK antibodies runs at 58000 Da, SDS-PAGE
58000
-
4 * 58000, SDS-PAGE
58000
-
4 * 58000, SDS-PAGE
58000
-
x * 58000, SDS-PAGE
58000
-
4 * 58000, SDS-PAGE, isozyme PK5
58000
-
3 * 58000 + 3 64000, SDS-PAGE
58000
x * 58000, calculated
59000
-
native enzyme, gel filtration
59000
-
4 * 59000, SDS-PAGE
59000
-
4 * 59000, SDS-PAGE
60000
recombinant enzyme, gel filtration
60000
-
x * 60000, SDS-PAGE
60000
-
4 * 60000, SDS-PAGE, M1 isozyme
60000
-
4 * 60000, L-type isozyme, SDS-PAGE
60000
-
2 * 60000 + 2 * 57000-58000, most important of the "aged" isozymes, PKR2, SDS-PAGE, derived from erythroblast homotetramer by partial proteolysis and transformation into various active heterotetrameric forms with two partially proteolyzed subunits
60000
-
4 * 60000 + 4 * 57000, gel filtration
62000
-
SDS-PAGE
62000
4 * 62000, SDS-PAGE
62000
-
4 * 62000, liver enzyme, SDS-PAGE
66000
-
4 * 66000, SDS-PAGE
66000
-
4 * 66000, tetrameric in low ionic strength buffer
70000
recombinant enzyme, gel filtration
80000
-
M2-PK-SUMO-1 conjugate, SDS-PAGE
80000
-
4 * 80000, SDS-PAGE
additional information
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additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
Antarctic fish
-
overview
additional information
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overview
additional information
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overview
additional information
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overview
additional information
-
amino acid composition
additional information
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amino acid composition
additional information
-
amino acid composition
additional information
-
3-dimensional structure of cat M-type isozyme
additional information
-
structure of liver and erythrocyte L-type kinases seems to be identical with an additional fragment present in erythrocytic enzyme
additional information
-
comparison of amino acid sequences
additional information
-
in vitro addition of substrates leads to higher MW enzyme species with MW of 730000, 1050000 and 1400000
additional information
-
molecular weight fractions I and II are 135000 Da and 260000 Da in normal breast tissue and 72000 Da and 250000 Da in tumor breast tissue