Identification |
HMDB Protein ID
| CDBP00431 |
Secondary Accession Numbers
| Not Available |
Name
| Non-specific lipid-transfer protein |
Description
| Not Available |
Synonyms
|
- NSL-TP
- Propanoyl-CoA C-acyltransferase
- SCP-2
- SCP-X
- SCP-chi
- SCPX
- Sterol carrier protein 2
- Sterol carrier protein X
|
Gene Name
| SCP2 |
Protein Type
| Enzyme |
Biological Properties |
General Function
| Involved in oxidoreductase activity |
Specific Function
| Mediates in vitro the transfer of all common phospholipids, cholesterol and gangliosides between membranes. May play a role in regulating steroidogenesis.
|
GO Classification
|
Biological Process |
progesterone biosynthetic process |
alpha-linolenic acid metabolic process |
fatty acid beta-oxidation using acyl-CoA oxidase |
lipid transport |
inositol trisphosphate biosynthetic process |
lipid hydroperoxide transport |
peroxisome organization |
positive regulation of intracellular cholesterol transport |
positive regulation of steroid metabolic process |
protein localization to plasma membrane |
bile acid biosynthetic process |
Cellular Component |
cytoplasm |
mitochondrion |
nucleus |
peroxisomal matrix |
protein complex |
Function |
catalytic activity |
transferase activity |
transferase activity, transferring acyl groups |
transferase activity, transferring acyl groups other than amino-acyl groups |
oxidoreductase activity |
steroid binding |
sterol binding |
lipid binding |
binding |
Molecular Function |
cholesterol binding |
long-chain fatty acyl-CoA binding |
oleic acid binding |
phosphatidylinositol transporter activity |
propanoyl-CoA C-acyltransferase activity |
transferase activity, transferring acyl groups other than amino-acyl groups |
sterol binding |
Process |
metabolic process |
|
Cellular Location
|
- Isoform SCP2:Mitochondrion (Probable)
|
Pathways
|
Name | SMPDB/Pathwhiz | KEGG | Primary bile acid biosynthesis | Not Available | | PPAR signaling pathway | Not Available | | Peroxisome | Not Available | | Bile Acid Biosynthesis | | | Congenital Bile Acid Synthesis Defect Type II | | Not Available |
|
Gene Properties |
Chromosome Location
| 1 |
Locus
| 1p32 |
SNPs
| SCP2 |
Gene Sequence
|
>1644 bp
ATGTCCTCTTCCCCGTGGGAGCCTGCGACCCTGCGCCGGGTGTTCGTGGTGGGGGTTGGC
ATGACCAAGTTTGTGAAGCCTGGAGCTGAGAATTCAAGAGACTACCCTGACTTGGCAGAA
GAAGCAGGCAAGAAGGCTTTAGCTGATGCACAGATCCCTTATTCAGCAGTGGACCAGGCA
TGTGTTGGCTATGTTTTTGGTGACTCTACCTGTGGGCAGAGGGCTATCTATCACAGTTTG
GGAATGACTGGAATTCCTATAATCAATGTCAACAATAACTGTGCTACTGGTTCTACTGCT
TTGTTTATGGCCCGCCAGCTGATTCAGGGTGGTGTGGCAGAATGTGTCTTGGCTCTTGGG
TTTGAGAAGATGAGTAAGGGAAGCCTTGGAATAAAATTTTCAGATAGAACCATTCCCACT
GATAAGCATGTTGACCTCCTGATCAATAAGTATGGATTGTCTGCTCACCCAGTTGCTCCT
CAGATGTTTGGGTATGCTGGAAAAGAACATATGGAAAAATATGGAACAAAAATTGAACAC
TTTGCAAAAATTGGATGGAAAAATCATAAACATTCAGTTAATAACCCGTATTCCCAGTTC
CAAGATGAATACAGTTTAGATGAAGTGATGGCATCTAAAGAAGTTTTTGATTTTTTGACT
ATCTTACAATGTTGTCCCACTTCAGATGGTGCTGCAGCAGCAATTTTGGCCAGTGAAGCA
TTTGTACAGAAGTATGGCCTGCAATCCAAAGCTGTGGAAATTTTGGCACAAGAAATGATG
ACTGATTTGCCAAGCTCGTTTGAAGAAAAAAGCATTATTAAAATGGTTGGCTTTGATATG
AGTAAAGAAGCTGCAAGAAAATGCTATGAGAAATCTGGCCTGACACCAAATGATATTGAC
GTAATAGAACTTCACGATTGCTTTTCTACCAACGAACTCCTGACTTATGAAGCACTCGGA
CTCTGTCCAGAAGGACAAGGTGCAACGCTGGTTGATAGAGGAGATAATACATATGGAGGA
AAGTGGGTCATAAATCCTAGTGGTGGACTGATTTCAAAGGGACACCCACTAGGCGCTACA
GGTCTTGCTCAGTGTGCAGAACTCTGCTGGCAGCTGAGAGGGGAAGCCGGAAAGAGGCAA
GTTCCTGGTGCAAAGGTGGCTCTGCAGCATAATTTAGGCATTGGAGGAGCTGTGGTTGTA
ACACTCTACAAGATGGGTTTTCCGGAAGCCGCCAGTTCTTTTAGAACTCATCAAATTGAA
GCTGTTCCAACCAGCTCTGCAAGTGATGGATTTAAGGCAAATCTTGTTTTTAAGGAGATT
GAGAAGAAACTTGAAGAGGAAGGGGAACAGTTTGTGAAGAAAATCGGTGGTATTTTTGCC
TTCAAGGTGAAAGATGGCCCTGGGGGTAAAGAGGCCACCTGGGTGGTGGATGTGAAGAAT
GGCAAAGGATCAGTGCTTCCTAACTCAGATAAGAAGGCTGACTGCACAATCACAATGGCT
GACTCAGACTTCCTGGCTTTAATGACTGGTAAAATGAATCCTCAGTCGGCCTTCTTTCAA
GGCAAATTGAAAATCACTGGCAACATGGGTCTCGCTATGAAGTTACAAAATCTTCAGCTT
CAGCCAGGCAACGCTAAGCTCTGA
|
Protein Properties |
Number of Residues
| 547 |
Molecular Weight
| 34974.505 |
Theoretical pI
| 5.658 |
Pfam Domain Function
|
|
Signals
|
Not Available
|
Transmembrane Regions
|
Not Available
|
Protein Sequence
|
>Non-specific lipid-transfer protein
MSSSPWEPATLRRVFVVGVGMTKFVKPGAENSRDYPDLAEEAGKKALADAQIPYSAVDQA
CVGYVFGDSTCGQRAIYHSLGMTGIPIINVNNNCATGSTALFMARQLIQGGVAECVLALG
FEKMSKGSLGIKFSDRTIPTDKHVDLLINKYGLSAHPVAPQMFGYAGKEHMEKYGTKIEH
FAKIGWKNHKHSVNNPYSQFQDEYSLDEVMASKEVFDFLTILQCCPTSDGAAAAILASEA
FVQKYGLQSKAVEILAQEMMTDLPSSFEEKSIIKMVGFDMSKEAARKCYEKSGLTPNDID
VIELHDCFSTNELLTYEALGLCPEGQGATLVDRGDNTYGGKWVINPSGGLISKGHPLGAT
GLAQCAELCWQLRGEAGKRQVPGAKVALQHNLGIGGAVVVTLYKMGFPEAASSFRTHQIE
AVPTSSASDGFKANLVFKEIEKKLEEEGEQFVKKIGGIFAFKVKDGPGGKEATWVVDVKN
GKGSVLPNSDKKADCTITMADSDFLALMTGKMNPQSAFFQGKLKITGNMGLAMKLQNLQL
QPGNAKL
|
External Links |
GenBank ID Protein
| Not Available |
UniProtKB/Swiss-Prot ID
| P22307 |
UniProtKB/Swiss-Prot Entry Name
| NLTP_HUMAN |
PDB IDs
|
|
GenBank Gene ID
| M75883 |
GeneCard ID
| SCP2 |
GenAtlas ID
| SCP2 |
HGNC ID
| HGNC:10606 |
References |
General References
| Not Available |