Nomenclature
Short Name:
HSPA5
Full Name:
78 kDa glucose-regulated protein
Alias:
- BiP
- Heat shock 70kDa protein 5
- Heat-shock 70kD protein-5 (glucose-regulated protein, 78kD
- Immunoglobulin heavy chain binding protein
- MIF2
- Endoplasmic reticulum lumenal Ca
- Glucose-regulated protein
- GRP 78
- GRP78
Classification
Type:
Protein-serine/threonine kinase
Group:
Atypical
Family:
HSP
SubFamily:
NA
Specific Links
Kinexus Products: | HSPA5 |
Structure
Mol. Mass (Da):
72,333
# Amino Acids:
654
# mRNA Isoforms:
1
mRNA Isoforms:
72,333 Da (654 AA; P11021)
4D Structure:
1D Structure:
3D Image (rendered using PV Viewer):
PDB ID
Subfamily Alignment
Domain Distribution:
Start | End | Domain |
---|
Kinexus Products
Click on entries below for direct links to relevant products from Kinexus for this protein kinase.
hiddentext
Post-translation Modifications
For detailed information on phosphorylation of this kinase go to PhosphoNET
Acetylated:
K96, K113, K118, K122, K123, K125, K138, K152, K154, K163, K268, K340, K352, K353, K376, K547, K579, K585, K601, K617, K619, K633, K651.
Methylated:
K581, K585, K591.
O-GalNAcylated:
T69, T203, T643.
Serine phosphorylated:
S4, S14, S86, S107, S146, S354, S365, S448, S567, S587, S588, S637.
Threonine phosphorylated:
T37, T85, T91, T139, T189, T203, T229, T366, T441, T485, T518.
Tyrosine phosphorylated:
Y39, Y65, Y127, Y160, Y466, Y570, Y635.
Ubiquitinated:
K81, K96, K113, K118, K123, K125, K138, K152, K163, K185, K213, K268, K326, K340, K352, K353, K370, K376, K447, K464, K474, K523, K547, K573, K601.
Distribution
Based on gene microarray analysis from the NCBI
Human Tissue Distribution
% Max Expression:
Mean Expression:
Number of Samples:
Standard Deviation:
% Max Expression:
Mean Expression:
Number of Samples:
Standard Deviation:
- 73
1494
22
877
- 25
516
11
180
- 32
645
8
220
- 35
717
74
578
- 64
1312
24
731
- 34
688
46
440
- 44
898
29
738
- 52
1071
26
634
- 72
1462
10
666
- 26
534
78
440
- 45
916
23
355
- 61
1253
99
686
- 32
655
19
203
- 29
599
9
270
- 74
1512
20
594
- 48
984
13
832
- 27
543
171
416
- 42
861
15
410
- 16
324
85
272
- 63
1277
84
810
- 34
689
19
243
- 24
493
21
279
- 35
718
17
355
- 49
1007
15
333
- 24
484
19
256
- 100
2041
47
857
- 37
753
22
185
- 51
1038
15
387
- 33
675
15
274
- 4
86
28
92
- 61
1239
18
500
- 35
705
20
743
- 79
1621
68
1572
- 75
1531
57
930
- 14
282
35
392
Evolution
Species Conservation
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
PhosphoNET % Identity:
PhosphoNET % Similarity:
Homologene %
Identity:
- 100
100
100 - 94
94
100 - -
-
100 - -
-
99 - -
-
- - 97.4
98
99 - -
-
- - 98.4
99
99 - 98.4
99
98.5 - -
-
- - -
-
- - 96.4
98.6
97 - 92.7
96.1
96 - 91.7
96
93.5 - -
-
- - 80.6
90.6
82.5 - 80.8
90.1
- - 77.4
88.8
78 - -
-
- - -
-
- - 67.8
82.8
- - -
-
71 - 67.1
80.5
71 - 64.6
77.8
69 - 67
81
-
For a wider analysis go to PhosphoNET Evolution in PhosphoNET
Regulation
Activation:
NA
Inhibition:
NA
Synthesis:
NA
Degradation:
NA
Disease Linkage
General Disease Association:
Neurological, and endocrine disorders
Specific Diseases (Non-cancerous):
Spinocerebellar ataxia Type 17 (HDL4); Wolfram syndrome (WFS)
Comments:
Spinocerebellar Ataxia Type 17 (HDL4) is rare, and is related to Parkinson’s, involves the retinoblastoma regulation, and the Parkinson disease pathways. HDL4 typically affects the eye. Wolfram Syndrome (WFS) is a rare disease characterized by high blood pressure induced by lack of insulin, and progresses to blindness after optic atrophy (loss of nerves leading from the eye to the brain). WFS can affect the eye, brain, and the lung. Borna Disease results from a viral infection, it affects the brain, and is characterized by mood, behaviour, cognitive, and neurological changes, along with impaired ability to move. In vitro methylation by METTL21A is inhibited with a K585R mutation in HSPA5.
Gene Expression in Cancers:
The COSMIC website notes an up-regulated expression score for HSPA5 in diverse human cancers of 436, which is close to the average score of 462 for the human protein kinases. The down-regulated expression score of 15 for this protein kinase in human cancers was 0.3-fold of the average score of 60 for the human protein kinases.
Mutagenesis Experiments:
Insertional mutagenesis studies in mice support a role for this protein kinase in mouse cancer oncogenesis.
Mutation Rate in All Cancers:
Percent mutation rates per 100 amino acids length in human cancers: 0.04 % in 24615 diverse cancer specimens. This rate is -41 % lower than the average rate of 0.075 % calculated for human protein kinases in general.
Mutation Rate in Specific Cancers:
Highest percent mutation rates per 100 amino acids length in human cancers: 0.19 % in 1063 large intestine cancers tested.
Frequency of Mutated Sites:
None > 3 in 19,898 cancer specimens
Comments:
No deletions, insertions or complex mutations are noted on the COSMIC website.