ExPASy logo ExPASy Home page Site Map Search ExPASy Contact us Swiss-Prot
Notice: This page will be replaced with www.uniprot.org. Please send us your feedback!
Search for

UniProtKB/Swiss-Prot entry P01189


[Entry info] [Name and origin] [References] [Comments] [Cross-references] [Keywords] [Features] [Sequence] [Tools]

Note: most headings are clickable, even if they don't appear as links. They link to the user manual or other documents.
Entry information
Entry name COLI_HUMAN
Primary accession number P01189
Secondary accession numbers P78442 Q9UD39 Q9UD40
Integrated into Swiss-Prot on July 21, 1986
Sequence was last modified on February 1, 1991 (Sequence version 2)
Annotations were last modified on    November 25, 2008 (Entry version 98)
Name and origin of the protein
Protein name Corticotropin-lipotropin [Precursor]
Synonyms Pro-opiomelanocortin
POMC
Contains NPP
Melanotropin gamma
     (Gamma-MSH)
Potential peptide
Corticotropin
     (Adrenocorticotropic hormone)
     (ACTH)
Melanotropin alpha
     (Alpha-MSH)
Corticotropin-like intermediary peptide
     (CLIP)
Lipotropin beta
     (Beta-LPH)
Lipotropin gamma
     (Gamma-LPH)
Melanotropin beta
     (Beta-MSH)
Beta-endorphin
Met-enkephalin
Gene name
Name: POMC
From
Homo sapiens (Human) [TaxID: 9606] 
Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo.
Protein existence 1: Evidence at protein level;
References
[1]
NUCLEOTIDE SEQUENCE [GENOMIC DNA].
DOI=10.1016/0014-5793(81)80952-0; PubMed=6274691 [NCBI, ExPASy, EBI, Israel, Japan]
Takahashi H., Teranishi Y., Nakanishi S., Numa S.;
"Isolation and structural organization of the human corticotropin-beta-lipotropin precursor gene.";
FEBS Lett. 135:97-102(1981).
[2]
NUCLEOTIDE SEQUENCE [GENOMIC DNA].
PubMed=6299668 [NCBI, ExPASy, EBI, Israel, Japan]
Whitfeld P.L., Seeburg P.H., Shine J.;
"The human pro-opiomelanocortin gene: organization, sequence, and interspersion with repetitive DNA.";
DNA 1:133-143(1982).
[3]
NUCLEOTIDE SEQUENCE.
DOI=10.1093/nar/11.19.6847; PubMed=6314261 [NCBI, ExPASy, EBI, Israel, Japan]
Takahashi H., Hakamata Y., Watanabe Y., Kikuno R., Miyata T., Numa S.;
"Complete nucleotide sequence of the human corticotropin-beta-lipotropin precursor gene.";
Nucleic Acids Res. 11:6847-6858(1983).
[4]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
TISSUE=Pituitary;
DOI=10.1101/gr.2596504; PubMed=15489334 [NCBI, ExPASy, EBI, Israel, Japan]
The MGC Project Team;
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).";
Genome Res. 14:2121-2127(2004).
[5]
NUCLEOTIDE SEQUENCE OF 6-267.
PubMed=3606677 [NCBI, ExPASy, EBI, Israel, Japan]
Golovin S.Y., Karginov V.A., Bondar A.A., Beklemishev A.B., Chekhranova M.K., Mertvetsov N.P., Pankov Y.A.;
"Synthesis, cloning and primary structure of DNA complementary to mRNA for human pituitary pro-opiomelanocortin.";
Bioorg. Khim. 13:562-564(1987).
[6]
NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 46-267.
PubMed=6254047 [NCBI, ExPASy, EBI, Israel, Japan]
Chang A.C.Y., Cochet M., Cohen S.N.;
"Structural organization of human genomic DNA encoding the pro-opiomelanocortin peptide.";
Proc. Natl. Acad. Sci. U.S.A. 77:4890-4894(1980).
[7]
PROTEIN SEQUENCE OF 27-102.
PubMed=6945581 [NCBI, ExPASy, EBI, Israel, Japan]
Seidah N.G., Chretien M.;
"Complete amino acid sequence of a human pituitary glycopeptide: an important maturation product of pro-opiomelanocortin.";
Proc. Natl. Acad. Sci. U.S.A. 78:4236-4240(1981).
[8]
PROTEIN SEQUENCE OF 27-102.
PubMed=6267033 [NCBI, ExPASy, EBI, Israel, Japan]
Seidah N.G., Rochemont J., Hamelin J., Lis M., Chretien M.;
"Primary structure of the major human pituitary pro-opiomelanocortin NH2-terminal glycopeptide. Evidence for an aldosterone-stimulating activity.";
J. Biol. Chem. 256:7977-7984(1981).
[9]
PROTEIN SEQUENCE OF 105-134.
DOI=10.1016/S0006-291X(81)80190-8; PubMed=6272808 [NCBI, ExPASy, EBI, Israel, Japan]
Seidah N.G., Rochemont J., Hamelin J., Benjannet S., Chretien M.;
"The missing fragment of the pro-sequence of human pro-opiomelanocortin: sequence and evidence for C-terminal amidation.";
Biochem. Biophys. Res. Commun. 102:710-716(1981).
[10]
PROTEIN SEQUENCE OF 138-176.
PubMed=4352834 [NCBI, ExPASy, EBI, Israel, Japan]
Bennett H.P.J., Lowry P.J., McMartin C.;
"Confirmation of the 1-20 amino acid sequence of human adrenocorticotrophin.";
Biochem. J. 133:11-13(1973).
[11]
PROTEIN SEQUENCE OF 138-176.
PubMed=14463577 [NCBI, ExPASy, EBI, Israel, Japan]
Lee T.H., Lerner A.B., Buettner-Janusch V.;
"On the structure of human corticotropin (adrenocorticotropic hormone).";
J. Biol. Chem. 236:2970-2974(1961).
[12]
PROTEIN SEQUENCE OF 27-41.
DOI=10.1110/ps.04682504; PubMed=15340161 [NCBI, ExPASy, EBI, Israel, Japan]
Zhang Z., Henzel W.J.;
"Signal peptide prediction based on analysis of experimentally verified cleavage sites.";
Protein Sci. 13:2819-2824(2004).
[13]
SEQUENCE REVISION (CORTICOTROPIN).
PubMed=4334191 [NCBI, ExPASy, EBI, Israel, Japan]
Riniker B., Sieber P., Rittel W., Zuber H.;
"Revised amino-acid sequences for porcine and human adrenocorticotrophic hormone.";
Nature New Biol. 235:114-115(1972).
[14]
SYNTHESIS OF CORTICOTROPIN.
DOI=10.1002/hlca.19720550420; PubMed=4338630 [NCBI, ExPASy, EBI, Israel, Japan]
Sieber P., Rittel W., Riniker B.;
"Synthesis of the human adrenal cortex hormone (alpha-h-ACTH) with a revised amino-acid sequence.";
Helv. Chim. Acta 55:1243-1248(1972).
[15]
SYNTHESIS OF CORTICOTROPIN.
DOI=10.1021/ja00785a049; PubMed=4347148 [NCBI, ExPASy, EBI, Israel, Japan]
Yamashiro D., Li C.H.;
"Adrenocorticotropins. 44. Total synthesis of the human hormone by the solid-phase method.";
J. Am. Chem. Soc. 95:1310-1315(1973).
[16]
PROTEIN SEQUENCE OF 179-267.
DOI=10.1038/260622a0; PubMed=1264228 [NCBI, ExPASy, EBI, Israel, Japan]
Li C.H., Chung D.;
"Primary structure of human beta-lipotropin.";
Nature 260:622-624(1976).
[17]
PROTEIN SEQUENCE OF 217-234.
Harris J.I.;
"Structure of a melanocyte-stimulating hormone from the human pituitary gland.";
Nature 184:167-169(1959).
[18]
PROTEIN SEQUENCE OF 237-267.
PubMed=195688 [NCBI, ExPASy, EBI, Israel, Japan]
Dragon N., Seidah N.G., Lis M., Routhier R., Chretien M.;
"Primary structure and morphine-like activity of human beta-endorphin.";
Can. J. Biochem. 55:666-670(1977).
[19]
NUCLEOTIDE SEQUENCE OF 235-256.
DOI=10.1016/0006-8993(86)90896-6; PubMed=2424570 [NCBI, ExPASy, EBI, Israel, Japan]
Bovenberg R.A.L., Burbach J.P.H., Wiegant V.M., Veeneman G.H., van Boom J.H., Baas P.D., Jansz H.S., de Wied D.;
"Gamma-endorphin and schizophrenia: amino acid composition of gamma-endorphin and nucleotide sequence of gamma-endorphin cDNA from pituitary glands of schizophrenic patients.";
Brain Res. 376:29-37(1986).
[20]
PROTEOLYTIC PROCESSING.
PubMed=2839146 [NCBI, ExPASy, EBI, Israel, Japan]
Fenger M., Johnsen A.H.;
"Alpha-amidated peptides derived from pro-opiomelanocortin in normal human pituitary.";
Biochem. J. 250:781-788(1988).
[21]
NUCLEOTIDE SEQUENCE OF 75-104, AND VARIANT 97-SER--GLY-99 DEL.
TISSUE=Pituitary;
DOI=10.1210/en.136.1.195; PubMed=7828531 [NCBI, ExPASy, EBI, Israel, Japan]
Morris J.C., Savva D., Lowry P.J.;
"Reduced expression of a naturally deleted form of human proopiomelanocortin complementary deoxyribonucleic acid after transfection into Chinese hamster ovary cells.";
Endocrinology 136:195-201(1995).
[22]
INVOLVEMENT IN PRO-OPIOMELANOCORTININ DEFICIENCY.
DOI=10.1038/509; PubMed=9620771 [NCBI, ExPASy, EBI, Israel, Japan]
Krude H., Biebermann H., Luck W., Horn R., Brabant G., Grueters A.;
"Severe early-onset obesity, adrenal insufficiency and red hair pigmentation caused by POMC mutations in humans.";
Nat. Genet. 19:155-157(1998).
[23]
INVOLVEMENT IN ABDOMINAL BODY FAT DISTRIBUTION.
DOI=10.2337/diabetes.54.8.2492; PubMed=16046320 [NCBI, ExPASy, EBI, Israel, Japan]
Baker M., Gaukrodger N., Mayosi B.M., Imrie H., Farrall M., Watkins H., Connell J.M.C., Avery P.J., Keavney B.;
"Association between common polymorphisms of the proopiomelanocortin gene and body fat distribution: a family study.";
Diabetes 54:2492-2496(2005).
[24]
PHOSPHORYLATION [LARGE SCALE ANALYSIS] AT SER-168, AND MASS SPECTROMETRY.
TISSUE=Pituitary;
DOI=10.1007/s11102-006-8916-x; PubMed=16807684 [NCBI, ExPASy, EBI, Israel, Japan]
Beranova-Giorgianni S., Zhao Y., Desiderio D.M., Giorgianni F.;
"Phosphoproteomic analysis of the human pituitary.";
Pituitary 9:109-120(2006).
[25]
VARIANTS ASN-106; GLY-214 AND 97-SER--GLY-99 DEL.
DOI=10.1210/jc.83.10.3737; PubMed=9768693 [NCBI, ExPASy, EBI, Israel, Japan]
Hinney A., Becker I., Heibult O., Nottebom K., Schmidt A., Ziegler A., Mayer H., Siegfried W., Blum W.F., Remschmidt H., Hebebrand J.;
"Systematic mutation screening of the pro-opiomelanocortin gene: identification of several genetic variants including three different insertions, one nonsense and two missense point mutations in probands of different weight extremes.";
J. Clin. Endocrinol. Metab. 83:3737-3741(1998).
[26]
VARIANT GLN-236.
DOI=10.1038/sj.ijo.0800814; PubMed=10193875 [NCBI, ExPASy, EBI, Israel, Japan]
Echwald S.M., Sorensen T.I., Andersen T., Tybjaerg-Hansen A., Clausen J.O., Pedersen O.;
"Mutational analysis of the proopiomelanocortin gene in Caucasians with early onset obesity.";
Int. J. Obes. Relat. Metab. Disord. 23:293-298(1999).
[27]
VARIANTS THR-7; LEU-9; GLY-236 AND 97-SER--GLY-99 DEL.
DOI=10.1038/sj.ijo.0801485; PubMed=11244459 [NCBI, ExPASy, EBI, Israel, Japan]
del Giudice E.M., Cirillo G., Santoro N., D'Urso L., Carbone M.T., Toro R.D., Perrone L.;
"Molecular screening of the proopiomelanocortin (POMC) gene in Italian obese children: report of three new mutations.";
Int. J. Obes. Relat. Metab. Disord. 25:61-67(2001).
[28]
VARIANT GLY-236, CHARACTERIZATION OF VARIANT GLY-236, AND POSSIBLE INVOLVEMENT IN OBESITY.
DOI=10.1093/hmg/11.17.1997; PubMed=12165561 [NCBI, ExPASy, EBI, Israel, Japan]
Challis B.G., Pritchard L.E., Creemers J.W.M., Delplanque J., Keogh J.M., Luan J., Wareham N.J., Yeo G.S.H., Bhattacharyya S., Froguel P., White A., Farooqi I.S., O'Rahilly S.;
"A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.";
Hum. Mol. Genet. 11:1997-2004(2002).
Comments
  • FUNCTION: ACTH stimulates the adrenal glands to release cortisol.
  • FUNCTION: MSH (melanocyte-stimulating hormone) increases the pigmentation of skin by increasing melanin production in melanocytes.
  • FUNCTION: Beta-endorphin and Met-enkephalin are endogenous opiates.
  • TISSUE SPECIFICITY: ACTH and MSH are produced by the pituitary gland.
  • PTM: Specific enzymatic cleavages at paired basic residues yield the different active peptides.
  • PTM: O-glycosylated; reducing sugar is probably N-acetylgalactosamine.
  • POLYMORPHISM: Genetic variation in POMC may influence abdominal body fat distribution [MIM:609830].
  • DISEASE: Defects in POMC may be associated with susceptibility to obesity [MIM:601665].
  • DISEASE: Defects in POMC are the cause of pro-opiomelanocortinin deficiency [MIM:609734]. Affected individuals present early-onset obesity, adrenal insufficiency and red hair.
  • SIMILARITY: Belongs to the POMC family.
  • WEB RESOURCE: Name=Wikipedia; Note=Melanocyte-stimulating hormone entry; URL="http://en.wikipedia.org/wiki/Melanocyte-stimulating_hormone";.
Copyright
Copyrighted by the UniProt Consortium, see http://www.uniprot.org/terms. Distributed under the Creative Commons Attribution-NoDerivs License.
Cross-references
Sequence databases
EMBL
M38297; AAA60140.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
J00292; AAB59621.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
J00291; AAB59621.1; JOINED; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
V01510; CAA24754.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
BC065832; AAH65832.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
M25896; AAA35799.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
PIR A17229; CTHUP.
RefSeq NP_000930.1; -.
NP_001030333.1; -.
UniGene Hs.1897
3D structure databases
ModBase P01189.
PTM databases
PhosphoSite P01189; -.
Organism-specific databases
H-InvDB HIX0029971; -.
HGNC HGNC:9201; POMC.
GenAtlas POMC.
HPA CAB002765; -.
MIM 176830; gene. [NCBI / EBI]
601665; phenotype. [NCBI / EBI]
609734; phenotype. [NCBI / EBI]
609830; phenotype. [NCBI / EBI]
Orphanet 71526; Obesity due to pro-opiomelanocortin deficiency.
PharmGKB PA33526; -.
GeneCards P01189.
Gene expression databases
ArrayExpress P01189; -.
CleanEx HS_POMC; -.
GermOnline ENSG00000115138; Homo sapiens.
Ontologies
GO
GO:0005576; Cellular component: extracellular region (inferred from electronic annotation from InterPro).
GO:0005625; Cellular component: soluble fraction (traceable author statement from ProtInc).
GO:0005179; Molecular function: hormone activity (traceable author statement from ProtInc).
GO:0007267; Biological process: cell-cell signaling (traceable author statement from ProtInc).
GO:0006091; Biological process: generation of precursor metabolites and energy (traceable author statement from ProtInc).
GO:0007218; Biological process: neuropeptide signaling pathway (inferred from electronic annotation from UniProtKB-KW).
QuickGo view.
Family and domain databases
InterPro IPR001941; Mcortin_ACTH.
IPR013533; Mcortin_ACTH_C.
IPR013531; Mcrtin_ACTH_cent.
IPR013593; Melanocortin_N.
IPR013532; Opioid_neuropept.
Graphical view of domain structure.
PANTHER PTHR11416; Mcortin_ACTH; 1.
Pfam PF00976; ACTH_domain; 1.
PF08384; NPP; 1.
PF08035; Op_neuropeptide; 1.
Pfam graphical view of domain structure.
PRINTS PR00383; MELANOCORTIN.
ProDom PD003250; Mcortin_ACTH; 1.
[Domain structure / List of seq. sharing at least 1 domain]
ProtoNet P01189.
Genome annotation databases
Ensembl ENSG00000115138; Homo sapiens. [Contig view]
GeneID 5443; -.
KEGG hsa:5443; -.
Phylogenomic databases
HOGENOM P01189; -.
HOVERGEN P01189; -.
Other
DrugBank DB00741; Hydrocortisone.
DB00836; Loperamide.
DB01108; Trilostane.
NextBio 21063; -.
SOURCE POMC; Homo sapiens.
UniRef View cluster of proteins with at least 50% / 90% / 100% identity.
Keywords
Amidation; Cleavage on pair of basic residues; Direct protein sequencing; Endorphin; Glycoprotein; Hormone; Obesity; Phosphoprotein; Polymorphism; Signal.
Features
SEVIEWER logo Feature table viewer FT aligner logo Feature aligner
KeyFrom   To Length Description FTId
SIGNAL   1    26  26      
PEPTIDE   27   102  76     NPP. PRO_0000024966
PEPTIDE   77    87  11     Melanotropin gamma. PRO_0000024967
PEPTIDE   105   134  30     Potential peptide. PRO_0000024968
PEPTIDE   138   176  39     Corticotropin. PRO_0000024969
PEPTIDE   138   150  13     Melanotropin alpha. PRO_0000024970
PEPTIDE   156   176  21     Corticotropin-like intermediary peptide. PRO_0000024971
PEPTIDE   179   267  89     Lipotropin beta. PRO_0000024972
PEPTIDE   179   234  56     Lipotropin gamma. PRO_0000024973
PEPTIDE   217   234  18     Melanotropin beta. PRO_0000024974
PEPTIDE   237   267  31     Beta-endorphin. PRO_0000024975
PEPTIDE   237   241  5     Met-enkephalin. PRO_0000024976
MOD_RES   87    87        Phenylalanine amide. 
MOD_RES   134   134        Glutamic acid 1-amide. 
MOD_RES   150   150        Valine amide. 
MOD_RES   168   168        Phosphoserine. 
CARBOHYD   71    71        O-linked (HexNAc...). 
CARBOHYD   91    91        N-linked (GlcNAc...). 
DISULFID   28    50        By similarity. 
VARIANT   7     7  1     S -> T. VAR_010699 
VARIANT   9     9  1     S -> L. VAR_010700 
VARIANT   62    62  1     P -> L (in dbSNP:rs28932471 [NCBI]). VAR_029762 
VARIANT   97    99  3     Missing. VAR_010714
VARIANT   106   106  1     D -> N. VAR_010715 
VARIANT   132   132  1     P -> A (in dbSNP:rs8192606 [NCBI]). VAR_029314 
VARIANT   214   214  1     E -> G. VAR_010716 
VARIANT   236   236  1     R -> G (may confer susceptibility to obesity; reduces the ability to activate melanocortin receptor 4; dbSNP:rs28932472 [NCBI]). VAR_010701 
VARIANT   236   236  1     R -> Q. VAR_012201 
CONFLICT   48    48        R -> G (in Ref. 6). 
CONFLICT   115   115        P -> T (in Ref. 2). 
Sequence information
Length: 267 AA [This is the length of the unprocessed precursor] Molecular weight: 29424 Da [This is the MW of the unprocessed precursor] CRC64: B927323474A67536 [This is a checksum on the sequence]
        10         20         30         40         50         60 
MPRSCCSRSG ALLLALLLQA SMEVRGWCLE SSQCQDLTTE SNLLECIRAC KPDLSAETPM 

        70         80         90        100        110        120 
FPGNGDEQPL TENPRKYVMG HFRWDRFGRR NSSSSGSSGA GQKREDVSAG EDCGPLPEGG 

       130        140        150        160        170        180 
PEPRSDGAKP GPREGKRSYS MEHFRWGKPV GKKRRPVKVY PNGAEDESAE AFPLEFKREL 

       190        200        210        220        230        240 
TGQRLREGDG PDGPADDGAG AQADLEHSLL VAAEKKDEGP YRMEHFRWGS PPKDKRYGGF 

       250        260 
MTSEKSQTPL VTLFKNAIIK NAYKKGE 

P01189 in FASTA format

View entry in original UniProtKB/Swiss-Prot format
View entry in raw text format (no links)
Report form for errors/updates in this UniProtKB/Swiss-Prot entry

BLAST logo BLAST submission on ExPASy/SIB
or at NCBI (USA)
Tools Sequence analysis tools: ProtParam, ProtScale, Compute pI/Mw, PeptideMass, PeptideCutter, Dotlet (Java)
PROSITE logo ScanProsite, MotifScan SWISS-MODEL Submit a homology modeling request to SWISS-MODEL
NPSA logo NPSA Sequence analysis tools

ExPASy logo ExPASy Home page Site Map Search ExPASy Contact us Swiss-Prot
 Hosted by ch flag SIB Switzerland Mirror sites: Australia  Brazil  Canada  China  Korea
Notice: This page will be replaced with www.uniprot.org. Please send us your feedback!