Gene/Proteome Database (LMPD)

LMPD ID
LMP002626
Gene ID
347
Species
Homo sapiens (Human)
Gene Name
apolipoprotein D
Gene Symbol
Synonyms
-
Alternate Names
apolipoprotein D; apo-D
Chromosome
3
Map Location
3q29
Summary
This gene encodes a component of high density lipoprotein that has no marked similarity to other apolipoprotein sequences. It has a high degree of homology to plasma retinol-binding protein and other members of the alpha 2 microglobulin protein superfamily of carrier proteins, also known as lipocalins. This glycoprotein is closely associated with the enzyme lecithin:cholesterol acyltransferase - an enzyme involved in lipoprotein metabolism. [provided by RefSeq, Aug 2008]
Orthologs

Proteins

apolipoprotein D precursor
Refseq ID NP_001638
Protein GI 4502163
UniProt ID P05090
mRNA ID NM_001647
Length 189
RefSeq Status REVIEWED
MVMLLLLLSALAGLFGAAEGQAFHLGKCPNPPVQENFDVNKYLGRWYEIEKIPTTFENGRCIQANYSLMENGKIKVLNQELRADGTVNQIEGEATPVNLTEPAKLEVKFSWFMPSAPYWILATDYENYALVYSCTCIIQLFHVDFAWILARNPNLPPETVDSLKNILTSNNIDVKKMTVTDQVNCPKLS
sig_peptide: 1..20 inference: COORDINATES: ab initio prediction:SignalP:4.0 calculated_mol_wt: 1991 peptide sequence: MVMLLLLLSALAGLFGAAEG

Gene Information

Entrez Gene ID
347
Gene Name
apolipoprotein D
Gene Symbol
Species
Homo sapiens

Gene Ontology (GO Annotations)

GO ID Source Type Description
GO:0022626 ISS:UniProtKB C cytosolic ribosome
GO:0030425 ISS:UniProtKB C dendrite
GO:0005783 ISS:UniProtKB C endoplasmic reticulum
GO:0005576 NAS:UniProtKB C extracellular region
GO:0005615 IDA:UniProtKB C extracellular space
GO:0070062 IDA:UniProtKB C extracellular vesicular exosome
GO:0043025 ISS:UniProtKB C neuronal cell body
GO:0048471 IDA:UniProtKB C perinuclear region of cytoplasm
GO:0015485 IDA:UniProtKB F cholesterol binding
GO:0005319 NAS:UniProtKB F lipid transporter activity
GO:0007568 NAS:UniProtKB P aging
GO:0001525 NAS:UniProtKB P angiogenesis
GO:0007420 ISS:UniProtKB P brain development
GO:0006006 IDA:UniProtKB P glucose metabolic process
GO:0006629 IDA:UniProtKB P lipid metabolic process
GO:0006869 NAS:GOC P lipid transport
GO:2000405 IDA:UniProtKB P negative regulation of T cell migration
GO:1900016 IDA:UniProtKB P negative regulation of cytokine production involved in inflammatory response
GO:0051895 IMP:UniProtKB P negative regulation of focal adhesion assembly
GO:0060588 IDA:UniProtKB P negative regulation of lipoprotein lipid oxidation
GO:0071638 IDA:UniProtKB P negative regulation of monocyte chemotactic protein-1 production
GO:0010642 IDA:UniProtKB P negative regulation of platelet-derived growth factor receptor signaling pathway
GO:0042308 IDA:UniProtKB P negative regulation of protein import into nucleus
GO:0048662 IDA:UniProtKB P negative regulation of smooth muscle cell proliferation
GO:2000098 IMP:UniProtKB P negative regulation of smooth muscle cell-matrix adhesion
GO:0014012 ISS:UniProtKB P peripheral nervous system axon regeneration
GO:0048678 ISS:UniProtKB P response to axon injury
GO:0042493 ISS:UniProtKB P response to drug
GO:0000302 IDA:UniProtKB P response to reactive oxygen species
GO:0042246 ISS:UniProtKB P tissue regeneration

Domain Information

InterPro Annotations

Accession Description
IPR002969 Apolipoprotein D
IPR026222 Apolipoprotein D, vertebrates
IPR012674 Calycin
IPR011038 Calycin-like
IPR002345 Lipocalin
IPR022272 Lipocalin family conserved site
IPR022271 Lipocalin, ApoD type
IPR000566 Lipocalin/cytosolic fatty-acid binding domain

UniProt Annotations

Entry Information

Gene Name
apolipoprotein D
Protein Entry
APOD_HUMAN
UniProt ID
Species
Human

Comments

Comment Type Description
Function APOD occurs in the macromolecular complex with lecithin- cholesterol acyltransferase. It is probably involved in the transport and binding of bilin. Appears to be able to transport a variety of ligands in a number of different contexts.
Miscellaneous APOD is primarily localized in HDL (60-65%), with most of the remainder in VHDL and only trace amounts in VLDL and LDL.
Ptm N-glycosylatd. N-glycan heterogeneity at Asn-65: Hex5HexNAc4 (major) and Hex6HexNAc5 (minor); at Asn-98: Hex5HexNAc4 (minor), dHex1Hex5HexNAc4 (major), dHex1Hex6HexNAc5 (minor) and dHex1Hex7HexNAc6 (minor). {ECO
Similarity Belongs to the calycin superfamily. Lipocalin family.
Subcellular Location Secreted.
Subunit Homodimer. In plasma, also exists as a disulfide-linked heterodimer with APOA2.
Tissue Specificity Expressed in liver, intestine, pancreas, kidney, placenta, adrenal, spleen, fetal brain tissue and tears.

Identical and Related Proteins

Unique RefSeq proteins for LMP002626 (as displayed in Record Overview)

Protein GI Database Accession Length Protein Name
4502163 RefSeq NP_001638 189 apolipoprotein D precursor

Identical Sequences to LMP002626 proteins

Reference Database Accession Length Protein Name
GI:4502163 GenBank ACM80605.1 189 Sequence 6103 from patent US 6812339
GI:4502163 GenBank ACN00274.1 189 Sequence 224 from patent US 7476723
GI:4502163 GenBank ADS26268.1 189 Sequence 224 from patent US 7777007
GI:4502163 GenBank ADS58649.1 189 Sequence 224 from patent US 7807385
GI:4502163 GenBank AHD75033.1 189 Sequence 16312 from patent US 8586006
GI:4502163 GenBank AIC48280.1 189 APOD, partial [synthetic construct]

Related Sequences to LMP002626 proteins

Reference Database Accession Length Protein Name
GI:4502163 GenBank AAX29138.1 190 apolipoprotein D, partial [synthetic construct]
GI:4502163 GenBank AAX36879.1 190 apolipoprotein D, partial [synthetic construct]
GI:4502163 GenBank JAA08583.1 189 apolipoprotein D [Pan troglodytes]
GI:4502163 GenBank JAA22562.1 189 apolipoprotein D [Pan troglodytes]
GI:4502163 GenBank AGB62526.1 225 Sequence 87 from patent US 8288091
GI:4502163 RefSeq XP_003807686.1 189 PREDICTED: apolipoprotein D [Pan paniscus]