Protein Pink1

URN urn:agi-llid:65018
Total Entities 0
Connectivity 518
Name Pink1
Description PTEN induced putative kinase 1
Notes This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease. [provided by RefSeq, Jul 2008]

GO Molecular Function transferase activity
transferase activity, transferring phosphorus-containing groups
kinase activity
protein kinase activity
calcium-dependent protein kinase activity
protein serine-threonine kinase activity
ubiquitin protein ligase binding
C3HC4-type RING finger domain binding
nucleotide binding
ATP binding
metal ion binding
magnesium ion binding

GO Cellular Component membrane
integral component of membrane
mitochondrial outer membrane
mitochondrial inner membrane
cytoplasm
cytosol
mitochondrion

GO Biological Process cell death
intracellular signal transduction
positive regulation of I-kappaB kinase-NF-kappaB signaling
positive regulation of release of cytochrome c from mitochondria
positive regulation of synaptic transmission, dopaminergic
positive regulation of catecholamine secretion
positive regulation of dopamine secretion
regulation of neuron apoptotic process
negative regulation of neuron apoptotic process
response to stress
cellular response to toxic substance
regulation of protein complex assembly
regulation of protein ubiquitination
protein phosphorylation
peptidyl-serine phosphorylation
phosphorylation
autophagy
mitochondrion degradation

Pathway Mitochondrial Fusion and Fission
Young Onset PARK2, PINK1, and UCHL1 Induced Parkinson's Disease
Proteins Involved in Pathogenesis of Parkinson's Disease
mitochondrial autophagy pathway
altered mitochondrial autophagy pathway
Parkinson disease pathway

Group Protein kinases
cell death
intracellular signal transduction
positive regulation of I-kappaB kinase-NF-kappaB signaling
positive regulation of release of cytochrome c from mitochondria
positive regulation of synaptic transmission, dopaminergic
positive regulation of catecholamine secretion
positive regulation of dopamine secretion
regulation of neuron apoptotic process
negative regulation of neuron apoptotic process
response to stress
cellular response to toxic substance
regulation of protein complex assembly
regulation of protein ubiquitination
transferase activity
transferase activity, transferring phosphorus-containing groups
kinase activity
protein kinase activity
calcium-dependent protein kinase activity
protein serine-threonine kinase activity
protein phosphorylation
peptidyl-serine phosphorylation
phosphorylation
autophagy
mitochondrion degradation
ubiquitin protein ligase binding
C3HC4-type RING finger domain binding
nucleotide binding
ATP binding
metal ion binding
magnesium ion binding
membrane
integral component of membrane
mitochondrial outer membrane
mitochondrial inner membrane
cytoplasm
cytosol
mitochondrion
Genes with Mutations Associated with Parkinson's Disease
Secreted proteins

LocusLink ID 65018
68943
298575

Cell Localization Cytoplasm
Mitochondrion outer membrane
Cytosol

GO ID 0005524
0055131
0010857
0016301
0000287
0004674
0031625
0008219
0097237
0035556
0000422
0043524
0018105
0043123
0033603
0090200
0032226
0006468
0043254
0031396
0006950
0005829
0016021
0005741
0005739
0046872
0000166
0004672
0016740
0016772
0006914
0016310
0033605
0043523
0005737
0016020
0005743

Alias BRPK
PARK6
serine/threonine-protein kinase PINK1, mitochondrial
protein kinase BRPK
PTEN-induced putative kinase protein 1
AU042772
AW557854
mFLJ00387
1190006F07Rik
Parkinson disease 6
phosphatase and tensin homologue-induced kinase 1
PINK1
PTEN induced kinase 1
PTEN induced kinase I
PTEN-induced kinase
serine/threonine-protein kinase PINK1
Parkinson disease VI
Parkinson disease (autosomal recessive) VI
PTEN-induced putative kinase-1
Parkinson disease (autosomal recessive) 6
FLJ27236
MGC189438
OTTHUMP00000002881
PINK I
OTTMUSP00000010580
1190006F07

Mouse chromosome position 4

OMIM ID 608309
605909

Rat chromosome position 5q36

Hugo ID 14581

Human chromosome position 1p36

Swiss-Prot Accession Q9BXM7
Q99MQ3
D3Z9M9
Q8N6T9
Q8NBU3
Q96DE4
A2AM77
Q7TMZ3
Q811I8
Q91XU5

GenBank ID NC_000001
NM_032409
NP_115785
NG_008164
NC_018912
AC_000133
ABBA01059790
AL391357
AMYH02000431
AMYH02000432
CH471134
EAW94934
EAW94935
HH961852
CBX51399
AB053323
BAB55647
AF316873
AAK28062
AK075225
BAC11484
AK130746
BC009534
AAH09534
BC028215
AAH28215
Q9BXM7
DQ891033
ABM81959
DQ893330
ABM84256
DQ894212
ABM85138
DQ896646
ABM87645
NC_000070
NM_026880
NP_081156
AC_000026
AAHY01041112
AAHY01041113
AAHY01041114
AAHY01041115
AAHY01041116
AAHY01041117
AAHY01041118
AAHY01041119
AL807249
CH466615
EDL13260
EDL13261
EDL13262
AB053476
BAB55651
AF316872
AAK28061
AK004507
AK050322
AK155474
BAE33284
AK165480
AK179666
AK181855
AK182588
AK188455
AK190010
AK190338
AK195623
AK196813
AK198589
AK205601
AK212959
AK213324
AK213673
AK213702
AK215426
AK218284
AK219274
AK219694
AK219773
AK220094
AK220318
BAD90392
BC018561
BC018594
BC044743
AAH44743
BC054349
AAH54349
BC067066
AAH67066
BC069968
AAH69968
CX238874
Q99MQ3
NC_005104
NM_001106694
NP_001100164
AC_000073
AABR06040522
AAHX01040404
CH473968
EDL80874
BC169047
AAI69047

Unigene ID Hs.389171
Mm.18539
Rn.219286
Rn.219317

KEGG ID hsa:65018
mmu:68943
rno:298575

Swiss-Prot ID PINK1_HUMAN
PINK1_MOUSE

EC Number 2.7.11.1

Ensembl ID ENSG00000158828
ENSP00000364204
ENST00000321556
ENSMUSG00000028756
ENSMUSP00000030536
ENSMUST00000030536

Homologene ID 32672

Organism Homo sapiens
Mus musculus
Rattus norvegicus

MGI ID 1916193

RGD ID 1305769

MedScan ID 65018