Phascolarctos cinereus (koala): 110207663
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Entry
110207663 CDS
T05867
Symbol
PPP3R1
Name
(RefSeq) calcineurin subunit B type 1 isoform X1
KO
K06268
serine/threonine-protein phosphatase 2B regulatory subunit
Organism
pcw
Phascolarctos cinereus (koala)
Pathway
pcw04010
MAPK signaling pathway
pcw04020
Calcium signaling pathway
pcw04022
cGMP-PKG signaling pathway
pcw04114
Oocyte meiosis
pcw04218
Cellular senescence
pcw04310
Wnt signaling pathway
pcw04360
Axon guidance
pcw04370
VEGF signaling pathway
pcw04380
Osteoclast differentiation
pcw04625
C-type lectin receptor signaling pathway
pcw04650
Natural killer cell mediated cytotoxicity
pcw04658
Th1 and Th2 cell differentiation
pcw04659
Th17 cell differentiation
pcw04660
T cell receptor signaling pathway
pcw04662
B cell receptor signaling pathway
pcw04720
Long-term potentiation
pcw04724
Glutamatergic synapse
pcw04921
Oxytocin signaling pathway
pcw04922
Glucagon signaling pathway
pcw04924
Renin secretion
pcw05010
Alzheimer disease
pcw05014
Amyotrophic lateral sclerosis
pcw05020
Prion disease
pcw05022
Pathways of neurodegeneration - multiple diseases
pcw05031
Amphetamine addiction
pcw05152
Tuberculosis
pcw05163
Human cytomegalovirus infection
pcw05166
Human T-cell leukemia virus 1 infection
pcw05167
Kaposi sarcoma-associated herpesvirus infection
pcw05170
Human immunodeficiency virus 1 infection
pcw05235
PD-L1 expression and PD-1 checkpoint pathway in cancer
pcw05417
Lipid and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
pcw00001
]
09130 Environmental Information Processing
09132 Signal transduction
04310 Wnt signaling pathway
110207663 (PPP3R1)
04022 cGMP-PKG signaling pathway
110207663 (PPP3R1)
09150 Organismal Systems
09151 Immune system
04650 Natural killer cell mediated cytotoxicity
110207663 (PPP3R1)
04660 T cell receptor signaling pathway
110207663 (PPP3R1)
04658 Th1 and Th2 cell differentiation
110207663 (PPP3R1)
04659 Th17 cell differentiation
110207663 (PPP3R1)
04662 B cell receptor signaling pathway
110207663 (PPP3R1)
09152 Endocrine system
04922 Glucagon signaling pathway
110207663 (PPP3R1)
04921 Oxytocin signaling pathway
110207663 (PPP3R1)
04924 Renin secretion
110207663 (PPP3R1)
09156 Nervous system
04724 Glutamatergic synapse
110207663 (PPP3R1)
04720 Long-term potentiation
110207663 (PPP3R1)
09158 Development and regeneration
04360 Axon guidance
110207663 (PPP3R1)
04380 Osteoclast differentiation
110207663 (PPP3R1)
09160 Human Diseases
09161 Cancer: overview
05235 PD-L1 expression and PD-1 checkpoint pathway in cancer
110207663 (PPP3R1)
09172 Infectious disease: viral
05166 Human T-cell leukemia virus 1 infection
110207663 (PPP3R1)
05170 Human immunodeficiency virus 1 infection
110207663 (PPP3R1)
05163 Human cytomegalovirus infection
110207663 (PPP3R1)
05167 Kaposi sarcoma-associated herpesvirus infection
110207663 (PPP3R1)
09171 Infectious disease: bacterial
05152 Tuberculosis
110207663 (PPP3R1)
09164 Neurodegenerative disease
05010 Alzheimer disease
110207663 (PPP3R1)
05014 Amyotrophic lateral sclerosis
110207663 (PPP3R1)
05020 Prion disease
110207663 (PPP3R1)
05022 Pathways of neurodegeneration - multiple diseases
110207663 (PPP3R1)
09165 Substance dependence
05031 Amphetamine addiction
110207663 (PPP3R1)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
110207663 (PPP3R1)
09180 Brite Hierarchies
09181 Protein families: metabolism
01009 Protein phosphatases and associated proteins [BR:
pcw01009
]
110207663 (PPP3R1)
Protein phosphatases and associated proteins [BR:
pcw01009
]
Protein serine/threonine phosphatases
Phosphoprotein phosphatases (PPPs)
Calcineurin (PPP3/ PP2B)
Regulatory subunits
110207663 (PPP3R1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
EF-hand_7
EF-hand_1
EF-hand_6
EF-hand_5
EF-hand_8
EH
SPARC_Ca_bdg
EF-hand_9
Motif
Other DBs
NCBI-GeneID:
110207663
NCBI-ProteinID:
XP_020841066
UniProt:
A0A6P5K8X3
LinkDB
All DBs
Position
Unknown
AA seq
181 aa
AA seq
DB search
MAKAHSSQTARKGNEASYPLEMCSHFDADEIKRLGKRFKKLDLDNSGSLSVEEFMSLPEL
QQNPLVQRVIDIFDTDGNGEVDFKEFIEGVSQFSVKGDKEQKLRFAFRIYDMDKDGYISN
GELFQVLKMMVGNNLKDTQLQQIVDKTIINADKDGDGRISFEEFCAVVGGLDIHKKMVVD
V
NT seq
546 nt
NT seq
+upstream
nt +downstream
nt
atggctaaggcccacagttcacaaacagcccgtaagggaaatgaagcaagctaccccctg
gaaatgtgctcacattttgatgctgatgaaattaaaaggctaggaaagagatttaagaag
cttgatttggacaactctggttctttgagtgtggaagagttcatgtctttgcctgagttg
caacagaacccattagttcagcgagtaatagatatatttgacacagatggcaatggagaa
gtagacttcaaagaattcattgaaggagtttctcagttcagtgtcaaaggagataaggaa
cagaaattaaggtttgctttccgaatctatgacatggataaagatggctatatttccaat
ggggagctcttccaggtgctgaagatgatggtggggaacaatctgaaagatacacagtta
caacaaattgtagacaaaaccataattaatgcagataaggatggagatggaagaatatcc
tttgaagaattctgtgctgttgtaggaggcctagatatccacaaaaagatggtggtagat
gtgtga
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