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HUMAN:APOE

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Contents

Species (Taxon ID) Homo sapiens (Human). (taxon:9606)
Gene Name(s) APOE
Protein Name(s)
  • Apolipoprotein E
  • Apo-E
External Links
UniProt Identifier APOE_HUMAN
UniProt Accessions P02649, B2RC15, C0JYY5, Q9P2S4,
EMBL M12529, K00396, M10065, AF050154, AF261279, AK314898, FJ525876, BC003557, AB035149,
PIR A92478,
RefSeq NP_000032.1,
PDB 1B68, 1BZ4, 1EA8, 1GS9, 1H7I, 1LE2, 1LE4, 1LPE, 1NFN, 1NFO, 1OEF, 1OEG, 1OR2, 1OR3, 2KC3, 2KNY,
IntAct P02649,
Ensembl ENST00000252486,
Pfam PF01442,

Annotations

Qualifier GO ID GO term name Reference Evidence Code with/from Aspect Notes Status
GO:0043025

cell soma

NAS: Non-traceable Author Statement

C

Source: UniProtKB

GO:0042627

chylomicron

IEA

C

Source: UniProtKB-KW

GO:0030425

dendrite

NAS: Non-traceable Author Statement

C

Source: UniProtKB

GO:0034364

high-density lipoprotein particle

IEA

C

Source: UniProtKB-KW

GO:0034363

intermediate-density lipoprotein particle

IDA: Inferred from Direct Assay

C

Source: UniProtKB

GO:0034362

low-density lipoprotein particle

IDA: Inferred from Direct Assay

C

Source: UniProtKB

GO:0034361

very-low-density lipoprotein particle

IEA

C

Source: UniProtKB-KW

GO:0016209

antioxidant activity

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0001540

beta-amyloid binding

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0008201

heparin binding

IEA

F

Source: UniProtKB-KW

GO:0050750

low-density lipoprotein receptor binding

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0046911

metal chelating activity

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0005543

phospholipid binding

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0046982

protein heterodimerization activity

IPI: Inferred from Physical Interaction

F

Source: UniProtKB

GO:0042803

protein homodimerization activity

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0048156

tau protein binding

IPI: Inferred from Physical Interaction

F

Source: UniProtKB

GO:0070326

very-low-density lipoprotein receptor binding

IDA: Inferred from Direct Assay

F

Source: UniProtKB

GO:0033344

cholesterol efflux

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0042632

cholesterol homeostasis

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0034382

chylomicron remnant clearance

IMP: Inferred from Mutant Phenotype

P

Source: UniProtKB

GO:0046907

intracellular transport

TAS: Traceable Author Statement

P

Source: UniProtKB

GO:0010875

positive regulation of cholesterol efflux

IDA: Inferred from Direct Assay

P

required field missing

GO:0033700

phospholipid efflux

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0032805

positive regulation of low-density lipoprot...

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0045541

negative regulation of cholesterol biosynthetic process

IDA: Inferred from Direct Assay

P

required field missing

GO:0034375

high-density lipoprotein particle remodeling

IGI: Inferred from Genetic Interaction

P

required field missing

GO:0034380

high-density lipoprotein particle assembly

IDA: Inferred from Direct Assay

P

required field missing

GO:0006898

receptor-mediated endocytosis

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0034384

high-density lipoprotein particle clearance

IDA: Inferred from Direct Assay

P

required field missing

GO:0010873

positive regulation of cholesterol esterification

IMP: Inferred from Mutant Phenotype

P

required field missing

GO:0008203

cholesterol metabolic process

IMP: Inferred from Mutant Phenotype

P

required field missing

GO:0034372

very-low-density lipoprotein particle remodeling

IGI: Inferred from Genetic Interaction

P

required field missing

GO:0043691

reverse cholesterol transport

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0006641

triglyceride metabolic process

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0034447

very-low-density lipoprotein particle clear...

IDA: Inferred from Direct Assay

P

Source: UniProtKB

GO:0000302

response to reactive oxygen species

PMID:11743999[1]

NAS: Non-traceable Author Statement

P

GO:0001540

beta-amyloid binding

PMID:11305869[2]

IDA: Inferred from Direct Assay

F

GO:0001937

negative regulation of endothelial cell proliferation

PMID:9685360[3]

IDA: Inferred from Direct Assay

P

GO:0002021

response to dietary excess

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0005319

lipid transporter activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

F

GO:0005319

lipid transporter activity

PMID:17305370[4]

IDA: Inferred from Direct Assay

F

GO:0005515

protein binding

PMID:21163940[5]

IPI: Inferred from Physical Interaction

UniProtKB:P50502

F

GO:0005515

protein binding

PMID:21163940[5]

IPI: Inferred from Physical Interaction

UniProtKB:Q16543

F

GO:0005515

protein binding

PMID:21163940[5]

IPI: Inferred from Physical Interaction

UniProtKB:Q53EL6

F

GO:0005515

protein binding

PMID:21163940[5]

IPI: Inferred from Physical Interaction

UniProtKB:Q9BQ95

F

GO:0005515

protein binding

PMID:21593558[6]

IPI: Inferred from Physical Interaction

UniProtKB:O75069

F

GO:0005515

protein binding

PMID:7972031[7]

IPI: Inferred from Physical Interaction

UniProtKB:P10636

F

GO:0005543

phospholipid binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

F

GO:0005543

phospholipid binding

PMID:4066713[8]

IDA: Inferred from Direct Assay

F

GO:0005576

extracellular region

GO_REF:0000002

IEA: Inferred from Electronic Annotation

InterPro:IPR000074

C

GO:0005576

extracellular region

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0964

C

GO:0005576

extracellular region

GO_REF:0000023

IEA: Inferred from Electronic Annotation

SP_SL:SL-0243

C

GO:0005576

extracellular region

Reactome:REACT_13783

TAS: Traceable Author Statement

C

GO:0005576

extracellular region

Reactome:REACT_6727

TAS: Traceable Author Statement

C

GO:0005576

extracellular region

Reactome:REACT_6734

TAS: Traceable Author Statement

C

GO:0005576

extracellular region

Reactome:REACT_6849

TAS: Traceable Author Statement

C

GO:0005576

extracellular region

Reactome:REACT_6852

TAS: Traceable Author Statement

C

GO:0005576

extracellular region

Reactome:REACT_6865

TAS: Traceable Author Statement

C

GO:0005615

extracellular space

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

C

GO:0005615

extracellular space

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0005615

extracellular space

PMID:20551380[9]

IDA: Inferred from Direct Assay

C

GO:0005737

cytoplasm

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0005737

cytoplasm

PMID:8083695[10]

NAS: Non-traceable Author Statement

C

GO:0005737

cytoplasm

PMID:9622609[11]

TAS: Traceable Author Statement

C

GO:0005769

early endosome

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0005770

late endosome

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0005794

Golgi apparatus

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0005874

microtubule

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0005886

plasma membrane

Reactome:REACT_6849

TAS: Traceable Author Statement

C

GO:0006629

lipid metabolic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0006629

lipid metabolic process

Reactome:REACT_602

TAS: Traceable Author Statement

P

GO:0006641

triglyceride metabolic process

PMID:3771793[12]

IMP: Inferred from Mutant Phenotype

P

GO:0006641

triglyceride metabolic process

PMID:9649566[13]

IDA: Inferred from Direct Assay

P

GO:0006707

cholesterol catabolic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0006810

transport

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0813

P

GO:0006869

lipid transport

GO_REF:0000002

IEA: Inferred from Electronic Annotation

InterPro:IPR000074

P

GO:0006869

lipid transport

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0445

P

GO:0006869

lipid transport

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

P

GO:0006874

cellular calcium ion homeostasis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0006898

receptor-mediated endocytosis

PMID:1917954[14]

IDA: Inferred from Direct Assay

P

GO:0006916

anti-apoptosis

PMID:9685360[3]

IDA: Inferred from Direct Assay

P

GO:0006917

induction of apoptosis

PMID:12753088[15]

IDA: Inferred from Direct Assay

P

GO:0006979

response to oxidative stress

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0007010

cytoskeleton organization

PMID:9622609[11]

TAS: Traceable Author Statement

P

GO:0007186

G-protein coupled receptor protein signaling pathway

PMID:16443932[16]

IDA: Inferred from Direct Assay

P

GO:0007263

nitric oxide mediated signal transduction

PMID:8995232[17]

IDA: Inferred from Direct Assay

P

GO:0007271

synaptic transmission, cholinergic

PMID:9622609[11]

TAS: Traceable Author Statement

P

GO:0007568

aging

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

P

GO:0008201

heparin binding

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0358

F

GO:0008201

heparin binding

PMID:2745454[18]

IDA: Inferred from Direct Assay

F

GO:0008203

cholesterol metabolic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0008203

cholesterol metabolic process

PMID:3771793[12]

IMP: Inferred from Mutant Phenotype

P

GO:0008203

cholesterol metabolic process

PMID:9649566[13]

IDA: Inferred from Direct Assay

P

GO:0008219

cell death

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0523

P

GO:0008289

lipid binding

GO_REF:0000002

IEA: Inferred from Electronic Annotation

InterPro:IPR000074

F

GO:0008289

lipid binding

PMID:4066713[8]

IDA: Inferred from Direct Assay

F

GO:0010468

regulation of gene expression

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0010544

negative regulation of platelet activation

PMID:8995232[17]

IDA: Inferred from Direct Assay

P

GO:0010873

positive regulation of cholesterol esterification

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0010873

positive regulation of cholesterol esterification

PMID:15654758[19]

IDA: Inferred from Direct Assay

P

GO:0010875

positive regulation of cholesterol efflux

PMID:12401887[20]

IGI: Inferred from Genetic Interaction

UniProtKB:P08226

P

GO:0010875

positive regulation of cholesterol efflux

PMID:14754908[21]

IDA: Inferred from Direct Assay

P

GO:0014012

peripheral nervous system axon regeneration

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

P

GO:0016209

antioxidant activity

PMID:9685360[3]

IDA: Inferred from Direct Assay

F

GO:0017127

cholesterol transporter activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

F

GO:0019934

cGMP-mediated signaling

PMID:8995232[17]

IDA: Inferred from Direct Assay

P

GO:0030195

negative regulation of blood coagulation

PMID:8995232[17]

IDA: Inferred from Direct Assay

P

GO:0030425

dendrite

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0030425

dendrite

PMID:8083695[10]

NAS: Non-traceable Author Statement

C

GO:0030516

regulation of axon extension

PMID:9622609[11]

TAS: Traceable Author Statement

P

GO:0030828

positive regulation of cGMP biosynthetic process

PMID:8995232[17]

IDA: Inferred from Direct Assay

P

GO:0031232

extrinsic to external side of plasma membrane

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0032488

Cdc42 protein signal transduction

PMID:16443932[16]

IDA: Inferred from Direct Assay

P

GO:0032805

positive regulation of low-density lipoprotein particle receptor catabolic process

PMID:15950758[22]

IDA: Inferred from Direct Assay

P

GO:0033344

cholesterol efflux

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0033344

cholesterol efflux

PMID:11162594[23]

IDA: Inferred from Direct Assay

P

GO:0033344

cholesterol efflux

PMID:16443932[16]

IDA: Inferred from Direct Assay

P

GO:0033700

phospholipid efflux

PMID:11162594[23]

IDA: Inferred from Direct Assay

P

GO:0034361

very-low-density lipoprotein particle

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0850

C

GO:0034361

very-low-density lipoprotein particle

PMID:17154273[24]

IDA: Inferred from Direct Assay

C

GO:0034361

very-low-density lipoprotein particle

PMID:8245722[25]

IDA: Inferred from Direct Assay

C

GO:0034362

low-density lipoprotein particle

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

C

GO:0034362

low-density lipoprotein particle

PMID:8245722[25]

IDA: Inferred from Direct Assay

C

GO:0034363

intermediate-density lipoprotein particle

PMID:17336988[26]

IDA: Inferred from Direct Assay

C

GO:0034364

high-density lipoprotein particle

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0345

C

GO:0034364

high-density lipoprotein particle

PMID:210174[27]

IDA: Inferred from Direct Assay

C

GO:0034372

very-low-density lipoprotein particle remodeling

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0034372

very-low-density lipoprotein particle remodeling

PMID:12401887[20]

IGI: Inferred from Genetic Interaction

UniProtKB:P08226

P

GO:0034372

very-low-density lipoprotein particle remodeling

PMID:15654758[19]

IDA: Inferred from Direct Assay

P

GO:0034374

low-density lipoprotein particle remodeling

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0034375

high-density lipoprotein particle remodeling

PMID:12401887[20]

IGI: Inferred from Genetic Interaction

UniProtKB:P08226

P

GO:0034380

high-density lipoprotein particle assembly

PMID:17305370[4]

IDA: Inferred from Direct Assay

P

GO:0034382

chylomicron remnant clearance

PMID:7175379[28]

IMP: Inferred from Mutant Phenotype

P

GO:0034384

high-density lipoprotein particle clearance

PMID:210175[29]

IDA: Inferred from Direct Assay

P

GO:0034447

very-low-density lipoprotein particle clearance

PMID:1917954[14]

IDA: Inferred from Direct Assay

P

GO:0034447

very-low-density lipoprotein particle clearance

PMID:9649566[13]

IMP: Inferred from Mutant Phenotype

P

GO:0042157

lipoprotein metabolic process

GO_REF:0000002

IEA: Inferred from Electronic Annotation

InterPro:IPR000074

P

GO:0042157

lipoprotein metabolic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0042157

lipoprotein metabolic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

P

GO:0042157

lipoprotein metabolic process

Reactome:REACT_13621

TAS: Traceable Author Statement

P

GO:0042157

lipoprotein metabolic process

Reactome:REACT_6823

TAS: Traceable Author Statement

P

GO:0042157

lipoprotein metabolic process

Reactome:REACT_6841

TAS: Traceable Author Statement

P

GO:0042158

lipoprotein biosynthetic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0042159

lipoprotein catabolic process

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0042311

vasodilation

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0042627

chylomicron

GO_REF:0000004

IEA: Inferred from Electronic Annotation

SP_KW:KW-0162

C

GO:0042627

chylomicron

PMID:16935699[30]

IDA: Inferred from Direct Assay

C

GO:0042627

chylomicron

PMID:8245722[25]

IDA: Inferred from Direct Assay

C

GO:0042632

cholesterol homeostasis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0042632

cholesterol homeostasis

PMID:9649566[13]

IDA: Inferred from Direct Assay

P

GO:0042802

identical protein binding

PMID:4066713[8]

IDA: Inferred from Direct Assay

F

GO:0042803

protein homodimerization activity

PMID:8245722[25]

IDA: Inferred from Direct Assay

F

GO:0043025

neuronal cell body

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

C

GO:0043025

neuronal cell body

PMID:8083695[10]

NAS: Non-traceable Author Statement

C

GO:0043407

negative regulation of MAP kinase activity

PMID:9685360[3]

IDA: Inferred from Direct Assay

P

GO:0043537

negative regulation of blood vessel endothelial cell migration

PMID:9685360[3]

IDA: Inferred from Direct Assay

P

GO:0043691

reverse cholesterol transport

PMID:8127890[31]

IDA: Inferred from Direct Assay

P

GO:0045471

response to ethanol

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

P

GO:0045541

negative regulation of cholesterol biosynthetic process

PMID:1917954[14]

IDA: Inferred from Direct Assay

P

GO:0046907

intracellular transport

PMID:9622609[11]

TAS: Traceable Author Statement

P

GO:0046911

metal chelating activity

PMID:9685360[3]

IDA: Inferred from Direct Assay

F

GO:0046982

protein heterodimerization activity

PMID:8245722[25]

IPI: Inferred from Physical Interaction

UniProtKB:P02652

F

GO:0048156

tau protein binding

PMID:7566652[32]

IPI: Inferred from Physical Interaction

UniProtKB:P10636

F

GO:0048168

regulation of neuronal synaptic plasticity

PMID:9622609[11]

TAS: Traceable Author Statement

P

GO:0048844

artery morphogenesis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0050728

negative regulation of inflammatory response

PMID:8995232[17]

IC: Inferred by Curator

GO:0051000

P

GO:0050750

low-density lipoprotein particle receptor binding

PMID:17326667[33]

IPI: Inferred from Physical Interaction

UniProtKB:Q92673

F

GO:0050750

low-density lipoprotein particle receptor binding

PMID:210175[29]

IDA: Inferred from Direct Assay

F

GO:0051000

positive regulation of nitric-oxide synthase activity

PMID:8995232[17]

IDA: Inferred from Direct Assay

P

GO:0051044

positive regulation of membrane protein ectodomain proteolysis

PMID:15950758[22]

IDA: Inferred from Direct Assay

P

GO:0051651

maintenance of location in cell

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0055088

lipid homeostasis

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P

GO:0060228

phosphatidylcholine-sterol O-acyltransferase activator activity

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

F

GO:0060228

phosphatidylcholine-sterol O-acyltransferase activator activity

PMID:15654758[19]

IDA: Inferred from Direct Assay

F

GO:0070326

very-low-density lipoprotein particle receptor binding

PMID:12950167[34]

IPI: Inferred from Physical Interaction

UniProtKB:Q14114

F

GO:0070326

very-low-density lipoprotein particle receptor binding

PMID:1384047[35]

IDA: Inferred from Direct Assay

F

GO:0071363

cellular response to growth factor stimulus

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSRNOP00000050968

P

GO:0071813

lipoprotein particle binding

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

F

GO:0072358

cardiovascular system development

GO_REF:0000019

IEA: Inferred from Electronic Annotation

Ensembl:ENSMUSP00000003066

P


Notes

References

See Help:References for how to manage references in GONUTS.

  1. ↑ Lauderback CM et al. (2002) Apolipoprotein E modulates Alzheimer's Abeta(1-42)-induced oxidative damage to synaptosomes in an allele-specific manner. Brain Res 924: 90-7 PubMed GONUTS page
  2. ↑ Cho HS et al. (2001) Quantitation of apoE domains in Alzheimer disease brain suggests a role for apoE in Abeta aggregation. J Neuropathol Exp Neurol 60: 342-9 PubMed GONUTS page
  3. ↑ 3.0 3.1 3.2 3.3 3.4 3.5 Ishigami M et al. (1998) Apolipoprotein E inhibits platelet-derived growth factor-induced vascular smooth muscle cell migration and proliferation by suppressing signal transduction and preventing cell entry to G1 phase. J Biol Chem 273: 20156-61 PubMed GONUTS page
  4. ↑ 4.0 4.1 Vedhachalam C et al. (2007) The C-terminal lipid-binding domain of apolipoprotein E is a highly efficient mediator of ABCA1-dependent cholesterol efflux that promotes the assembly of high-density lipoproteins. Biochemistry 46: 2583-93 PubMed GONUTS page
  5. ↑ 5.0 5.1 5.2 5.3 Soler-López M et al. (2011) Interactome mapping suggests new mechanistic details underlying Alzheimer's disease. Genome Res 21: 364-76 PubMed GONUTS page
  6. ↑ Hopkins PC et al. (2011) The Impact of a Novel Apolipoprotein E and Amyloid-β Protein Precursor-Interacting Protein on the Production of Amyloid-β J Alzheimers Dis PubMed GONUTS page
  7. ↑ Strittmatter WJ et al. (1994) Isoform-specific interactions of apolipoprotein E with microtubule-associated protein tau: implications for Alzheimer disease. Proc Natl Acad Sci U S A 91: 11183-6 PubMed GONUTS page
  8. ↑ 8.0 8.1 8.2 Yokoyama S et al. (1985) Behavior of human apolipoprotein E in aqueous solutions and at interfaces. J Biol Chem 260: 16375-82 PubMed GONUTS page
  9. ↑ Didangelos A et al. (2010) Proteomics characterization of extracellular space components in the human aorta. Mol Cell Proteomics 9: 2048-62 PubMed GONUTS page
  10. ↑ 10.0 10.1 10.2 Han SH et al. (1994) Apolipoprotein E is localized to the cytoplasm of human cortical neurons: a light and electron microscopic study. J Neuropathol Exp Neurol 53: 535-44 PubMed GONUTS page
  11. ↑ 11.0 11.1 11.2 11.3 11.4 11.5 Beffert U et al. (1998) The neurobiology of apolipoproteins and their receptors in the CNS and Alzheimer's disease. Brain Res Brain Res Rev 27: 119-42 PubMed GONUTS page
  12. ↑ 12.0 12.1 Schaefer EJ et al. (1986) Familial apolipoprotein E deficiency. J Clin Invest 78: 1206-19 PubMed GONUTS page
  13. ↑ 13.0 13.1 13.2 13.3 Sullivan PM et al. (1998) Type III hyperlipoproteinemia and spontaneous atherosclerosis in mice resulting from gene replacement of mouse Apoe with human Apoe*2. J Clin Invest 102: 130-5 PubMed GONUTS page
  14. ↑ 14.0 14.1 14.2 Sehayek E & Eisenberg S (1991) Mechanisms of inhibition by apolipoprotein C of apolipoprotein E-dependent cellular metabolism of human triglyceride-rich lipoproteins through the low density lipoprotein receptor pathway. J Biol Chem 266: 18259-67 PubMed GONUTS page
  15. ↑ Eugenin EA et al. (2003) MCP-1 (CCL2) protects human neurons and astrocytes from NMDA or HIV-tat-induced apoptosis. J Neurochem 85: 1299-311 PubMed GONUTS page
  16. ↑ 16.0 16.1 16.2 Nofer JR et al. (2006) Apolipoprotein A-I activates Cdc42 signaling through the ABCA1 transporter. J Lipid Res 47: 794-803 PubMed GONUTS page
  17. ↑ 17.0 17.1 17.2 17.3 17.4 17.5 17.6 Riddell DR et al. (1997) Apolipoprotein E inhibits platelet aggregation through the L-arginine:nitric oxide pathway. Implications for vascular disease. J Biol Chem 272: 89-95 PubMed GONUTS page
  18. ↑ Fielding PE et al. (1989) Apolipoprotein E mediates binding of normal very low density lipoprotein to heparin but is not required for high affinity receptor binding. J Biol Chem 264: 12462-6 PubMed GONUTS page
  19. ↑ 19.0 19.1 19.2 Zhao Y et al. (2005) Apolipoprotein E is the major physiological activator of lecithin-cholesterol acyltransferase (LCAT) on apolipoprotein B lipoproteins. Biochemistry 44: 1013-25 PubMed GONUTS page
  20. ↑ 20.0 20.1 20.2 Hopkins PC et al. (2002) Evidence for differential effects of apoE3 and apoE4 on HDL metabolism. J Lipid Res 43: 1881-9 PubMed GONUTS page
  21. ↑ Krimbou L et al. (2004) Molecular interactions between apoE and ABCA1: impact on apoE lipidation. J Lipid Res 45: 839-48 PubMed GONUTS page
  22. ↑ 22.0 22.1 Hoe HS & Rebeck GW (2005) Regulation of ApoE receptor proteolysis by ligand binding. Brain Res Mol Brain Res 137: 31-9 PubMed GONUTS page
  23. ↑ 23.0 23.1 Remaley AT et al. (2001) Apolipoprotein specificity for lipid efflux by the human ABCAI transporter. Biochem Biophys Res Commun 280: 818-23 PubMed GONUTS page
  24. ↑ Mancone C et al. (2007) Proteomic analysis of human very low-density lipoprotein by two-dimensional gel electrophoresis and MALDI-TOF/TOF. Proteomics 7: 143-54 PubMed GONUTS page
  25. ↑ 25.0 25.1 25.2 25.3 25.4 Connelly PW et al. (1993) Identification of disulfide-linked apolipoprotein species in human lipoproteins. J Lipid Res 34: 1717-27 PubMed GONUTS page
  26. ↑ Meyer BJ et al. (2007) Fractionation of cholesteryl ester rich intermediate density lipoprotein subpopulations by chondroitin sulphate. Atherosclerosis 195: e28-34 PubMed GONUTS page
  27. ↑ Weisgraber KH & Mahley RW (1978) Apoprotein (E--A-II) complex of human plasma lipoproteins. I. Characterization of this mixed disulfide and its identification in a high density lipoprotein subfraction. J Biol Chem 253: 6281-8 PubMed GONUTS page
  28. ↑ Breslow JL et al. (1982) Studies of familial type III hyperlipoproteinemia using as a genetic marker the apoE phenotype E2/2. J Lipid Res 23: 1224-35 PubMed GONUTS page
  29. ↑ 29.0 29.1 Innerarity TL et al. (1978) Apoprotein (E--A-II) complex of human plasma lipoproteins. II. Receptor binding activity of a high density lipoprotein subfraction modulated by the apo(E--A-II) complex. J Biol Chem 253: 6289-95 PubMed GONUTS page
  30. ↑ Jackson KG et al. (2006) Apolipoprotein E enrichment of immuno-separated chylomicron and chylomicron remnants following saturated fatty acids. Nutr Metab Cardiovasc Dis 16: 405-17 PubMed GONUTS page
  31. ↑ Huang Y et al. (1994) A plasma lipoprotein containing only apolipoprotein E and with gamma mobility on electrophoresis releases cholesterol from cells. Proc Natl Acad Sci U S A 91: 1834-8 PubMed GONUTS page
  32. ↑ Huang DY et al. (1995) ApoE3 binding to tau tandem repeat I is abolished by tau serine262 phosphorylation. Neurosci Lett 192: 209-12 PubMed GONUTS page
  33. ↑ Nilsson SK et al. (2007) Apolipoprotein A-V interaction with members of the low density lipoprotein receptor gene family. Biochemistry 46: 3896-904 PubMed GONUTS page
  34. ↑ Li X et al. (2003) Domains of apoE required for binding to apoE receptor 2 and to phospholipids: implications for the functions of apoE in the brain. Biochemistry 42: 10406-17 PubMed GONUTS page
  35. ↑ Takahashi S et al. (1992) Rabbit very low density lipoprotein receptor: a low density lipoprotein receptor-like protein with distinct ligand specificity. Proc Natl Acad Sci U S A 89: 9252-6 PubMed GONUTS page
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