Regulation of IGF transport and uptake by IGF binding proteins (Homo sapiens)
From WikiPathways
Description
About 75% of circulating IGFs are in 1500 220 KDa complexes with IGFBP3 and ALS. Such complexes are too large to pass the endothelial barrier. The remaining 20 25% of IGFs are bound to other IGFBPs in 40 50 KDa complexes. IGFs are released from IGF:IGFBP complexes by proteolysis of the IGFBP. IGFs become active after release, however IGFs may also have activity when still bound to some IGFBPs. IGFBP1 is enriched in amniotic fluid and is produced in the liver under control of insulin (insulin suppresses production). IGFBP1 binding stimulates IGF function. It is unknown which if any protease degrades IGFBP1. IGFBP2 is enriched in cerebrospinal fluid; its binding inhibits IGF function. IGFBP2 is not significantly degraded in circulation. IGFB3, which binds most IGF in the body is enriched in follicular fluid and found in many other tissues. IGFBP 3 may be cleaved by plasmin, thrombin, Prostate specific Antigen (PSA, KLK3), Matrix Metalloprotease-1 (MMP1), and Matrix Metalloprotease-2 (MMP2). IGFBP3 also binds extracellular matrix and binding lowers its affinity for IGFs. IGFBP3 binding stimulates the effects of IGFs. IGFBP4 acts to inhibit IGF function and is cleaved by Pregnancy associated Plasma Protein A (PAPPA) to release IGF. IGFBP5 is enriched in bone matrix; its binding stimulates IGF function. IGFBP5 is cleaved by Pregnancy Associated Plasma Protein A2 (PAPPA2), ADAM9, complement C1s from smooth muscle, and thrombin. Only the cleavage site for PAPPA2 is known. IGFBP6 is enriched in cerebrospinal fluid. It is unknown which if any protease degrades IGFBP6.
View original pathway at:Reactome.Quality Tags
Ontology Terms
Bibliography
View all... |
- Collett-Solberg PF, Nunn SE, Gibson TB, Cohen P.; ''Identification of novel high molecular weight insulin-like growth factor-binding protein-3 association proteins in human serum.''; PubMed Europe PMC Scholia
- Bach LA, Hsieh S, Brown AL, Rechler MM.; ''Recombinant human insulin-like growth factor (IGF)-binding protein-6 inhibits IGF-II-induced differentiation of L6A1 myoblasts.''; PubMed Europe PMC Scholia
- Galanis M, Firth SM, Bond J, Nathanielsz A, Kortt AA, Hudson PJ, Baxter RC.; ''Ligand-binding characteristics of recombinant amino- and carboxyl-terminal fragments of human insulin-like growth factor-binding protein-3.''; PubMed Europe PMC Scholia
- Payet LD, Firth SM, Baxter RC.; ''The role of the acid-labile subunit in regulating insulin-like growth factor transport across human umbilical vein endothelial cell monolayers.''; PubMed Europe PMC Scholia
- Kuang Z, Yao S, McNeil KA, Thompson JA, Bach LA, Forbes BE, Wallace JC, Norton RS.; ''Cooperativity of the N- and C-terminal domains of insulin-like growth factor (IGF) binding protein 2 in IGF binding.''; PubMed Europe PMC Scholia
- Headey SJ, Keizer DW, Yao S, Brasier G, Kantharidis P, Bach LA, Norton RS.; ''C-terminal domain of insulin-like growth factor (IGF) binding protein-6: structure and interaction with IGF-II.''; PubMed Europe PMC Scholia
- Butkowski RJ, Elion J, Downing MR, Mann KG.; ''Primary structure of human prethrombin 2 and alpha-thrombin.''; PubMed Europe PMC Scholia
- Byun D, Mohan S, Yoo M, Sexton C, Baylink DJ, Qin X.; ''Pregnancy-associated plasma protein-A accounts for the insulin-like growth factor (IGF)-binding protein-4 (IGFBP-4) proteolytic activity in human pregnancy serum and enhances the mitogenic activity of IGF by degrading IGFBP-4 in vitro.''; PubMed Europe PMC Scholia
- Booth BA, Boes M, Dake BL, Knudtson KL, Bar RS.; ''IGFBP-3 binding to endothelial cells inhibits plasmin and thrombin proteolysis.''; PubMed Europe PMC Scholia
- Lawrence JB, Oxvig C, Overgaard MT, Sottrup-Jensen L, Gleich GJ, Hays LG, Yates JR, Conover CA.; ''The insulin-like growth factor (IGF)-dependent IGF binding protein-4 protease secreted by human fibroblasts is pregnancy-associated plasma protein-A.''; PubMed Europe PMC Scholia
- Zhou R, Diehl D, Hoeflich A, Lahm H, Wolf E.; ''IGF-binding protein-4: biochemical characteristics and functional consequences.''; PubMed Europe PMC Scholia
- Headey SJ, Leeding KS, Norton RS, Bach LA.; ''Contributions of the N- and C-terminal domains of IGF binding protein-6 to IGF binding.''; PubMed Europe PMC Scholia
- Belgorosky A, Rivarola MA.; ''Insulin-like growth factor binding protein (IGFBP)-3-bound IGF-I and IGFBP-3-bound IGF-II in growth hormone deficiency.''; PubMed Europe PMC Scholia
- Bond JJ, Meka S, Baxter RC.; ''Binding characteristics of pro-insulin-like growth factor-II from cancer patients: binary and ternary complex formation with IGF binding proteins-1 to -6.''; PubMed Europe PMC Scholia
- Jansson M, Andersson G, Uhlén M, Nilsson B, Kördel J.; ''The insulin-like growth factor (IGF)binding protein 1 binding epitope on IGF-I probed by heteronuclear NMR spectroscopy and mutational analysis.''; PubMed Europe PMC Scholia
- Degen SJ, Davie EW.; ''Nucleotide sequence of the gene for human prothrombin.''; PubMed Europe PMC Scholia
- Fowlkes JL, Enghild JJ, Suzuki K, Nagase H.; ''Matrix metalloproteinases degrade insulin-like growth factor-binding protein-3 in dermal fibroblast cultures.''; PubMed Europe PMC Scholia
- Rajah R, Katz L, Nunn S, Solberg P, Beers T, Cohen P.; ''Insulin-like growth factor binding protein (IGFBP) proteases: functional regulators of cell growth.''; PubMed Europe PMC Scholia
- Juul A, Dalgaard P, Blum WF, Bang P, Hall K, Michaelsen KF, Müller J, Skakkebaek NE.; ''Serum levels of insulin-like growth factor (IGF)-binding protein-3 (IGFBP-3) in healthy infants, children, and adolescents: the relation to IGF-I, IGF-II, IGFBP-1, IGFBP-2, age, sex, body mass index, and pubertal maturation.''; PubMed Europe PMC Scholia
- Janosi JB, Firth SM, Bond JJ, Baxter RC, Delhanty PJ.; ''N-Linked glycosylation and sialylation of the acid-labile subunit. Role in complex formation with insulin-like growth factor (IGF)-binding protein-3 and the IGFs.''; PubMed Europe PMC Scholia
- Arai T, Parker A, Busby W, Clemmons DR.; ''Heparin, heparan sulfate, and dermatan sulfate regulate formation of the insulin-like growth factor-I and insulin-like growth factor-binding protein complexes.''; PubMed Europe PMC Scholia
- Firth SM, Baxter RC.; ''Cellular actions of the insulin-like growth factor binding proteins.''; PubMed Europe PMC Scholia
- Qin X, Byun D, Lau KH, Baylink DJ, Mohan S.; ''Evidence that the interaction between insulin-like growth factor (IGF)-II and IGF binding protein (IGFBP)-4 is essential for the action of the IGF-II-dependent IGFBP-4 protease.''; PubMed Europe PMC Scholia
- Laursen LS, Overgaard MT, Nielsen CG, Boldt HB, Hopmann KH, Conover CA, Sottrup-Jensen L, Giudice LC, Oxvig C.; ''Substrate specificity of the metalloproteinase pregnancy-associated plasma protein-A (PAPP-A) assessed by mutagenesis and analysis of synthetic peptides: substrate residues distant from the scissile bond are critical for proteolysis.''; PubMed Europe PMC Scholia
- Twigg SM, Baxter RC.; ''Insulin-like growth factor (IGF)-binding protein 5 forms an alternative ternary complex with IGFs and the acid-labile subunit.''; PubMed Europe PMC Scholia
- Cianfarani S, Frost VJ, Savage MO, Holly JM.; ''Glucose does not influence the insulin-like growth factor (JGF) binding to carrier proteins (IGFBPs): analysis of rat and human serum by western ligand blotting.''; PubMed Europe PMC Scholia
- Lalou C, Silve C, Rosato R, Segovia B, Binoux M.; ''Interactions between insulin-like growth factor-I (IGF-I) and the system of plasminogen activators and their inhibitors in the control of IGF-binding protein-3 production and proteolysis in human osteosarcoma cells.''; PubMed Europe PMC Scholia
- Binkert C, Landwehr J, Mary JL, Schwander J, Heinrich G.; ''Cloning, sequence analysis and expression of a cDNA encoding a novel insulin-like growth factor binding protein (IGFBP-2).''; PubMed Europe PMC Scholia
- Hoeflich A, Reisinger R, Lahm H, Kiess W, Blum WF, Kolb HJ, Weber MM, Wolf E.; ''Insulin-like growth factor-binding protein 2 in tumorigenesis: protector or promoter?''; PubMed Europe PMC Scholia
- Bach LA, Hsieh S, Sakano K, Fujiwara H, Perdue JF, Rechler MM.; ''Binding of mutants of human insulin-like growth factor II to insulin-like growth factor binding proteins 1-6.''; PubMed Europe PMC Scholia
- Angelloz-Nicoud P, Harel L, Binoux M.; ''Recombinant human insulin-like growth factor (IGF) binding protein-3 stimulates prostate carcinoma cell proliferation via an IGF-dependent mechanism. Role of serine proteases.''; PubMed Europe PMC Scholia
- Cohen P, Graves HC, Peehl DM, Kamarei M, Giudice LC, Rosenfeld RG.; ''Prostate-specific antigen (PSA) is an insulin-like growth factor binding protein-3 protease found in seminal plasma.''; PubMed Europe PMC Scholia
- Holly J, Perks C.; ''The role of insulin-like growth factor binding proteins.''; PubMed Europe PMC Scholia
- Rajah R, Nachajon RV, Collins MH, Hakonarson H, Grunstein MM, Cohen P.; ''Elevated levels of the IGF-binding protein protease MMP-1 in asthmatic airway smooth muscle.''; PubMed Europe PMC Scholia
- Baxter RC, Martin JL.; ''Structure of the Mr 140,000 growth hormone-dependent insulin-like growth factor binding protein complex: determination by reconstitution and affinity-labeling.''; PubMed Europe PMC Scholia
- Choi KY, Kyung YJ, Lee CY, Lee DH.; ''Characterization of insulin-like growth factor-free interaction between insulin-like growth factor binding protein 3 and acid labile subunit expressed from Xenopus oocytes.''; PubMed Europe PMC Scholia
- Twigg SM, Kiefer MC, Zapf J, Baxter RC.; ''Insulin-like growth factor-binding protein 5 complexes with the acid-labile subunit. Role of the carboxyl-terminal domain.''; PubMed Europe PMC Scholia
- Yan X, Forbes BE, McNeil KA, Baxter RC, Firth SM.; ''Role of N- and C-terminal residues of insulin-like growth factor (IGF)-binding protein-3 in regulating IGF complex formation and receptor activation.''; PubMed Europe PMC Scholia
- Laursen LS, Kjaer-Sorensen K, Andersen MH, Oxvig C.; ''Regulation of insulin-like growth factor (IGF) bioactivity by sequential proteolytic cleavage of IGF binding protein-4 and -5.''; PubMed Europe PMC Scholia
- Bach LA, Rechler MM.; ''Measurement of insulin-like growth factor (IGF)-II binding to purified IGF binding proteins 1-6: comparison of charcoal adsorption and high performance size exclusion chromatography.''; PubMed Europe PMC Scholia
- Twigg SM, Kiefer MC, Zapf J, Baxter RC.; ''A central domain binding site in insulin-like growth factor binding protein-5 for the acid-labile subunit.''; PubMed Europe PMC Scholia
- Overgaard MT, Boldt HB, Laursen LS, Sottrup-Jensen L, Conover CA, Oxvig C.; ''Pregnancy-associated plasma protein-A2 (PAPP-A2), a novel insulin-like growth factor-binding protein-5 proteinase.''; PubMed Europe PMC Scholia
- Gibson TL, Cohen P.; ''Inflammation-related neutrophil proteases, cathepsin G and elastase, function as insulin-like growth factor binding protein proteases.''; PubMed Europe PMC Scholia
- Angelloz-Nicoud P, Lalou C, Binoux M.; ''Prostate carcinoma (PC-3) cell proliferation is stimulated by the 22-25-kDa proteolytic fragment (1-160) and inhibited by the 16-kDa fragment (1-95) of recombinant human insulin-like growth factor binding protein-3.''; PubMed Europe PMC Scholia
- Lalou C, Lassarre C, Binoux M.; ''Isolation and characterization of proteolytic fragments of insulin-like growth factor-binding protein-3.''; PubMed Europe PMC Scholia
- Tagliabracci VS, Wiley SE, Guo X, Kinch LN, Durrant E, Wen J, Xiao J, Cui J, Nguyen KB, Engel JL, Coon JJ, Grishin N, Pinna LA, Pagliarini DJ, Dixon JE.; ''A Single Kinase Generates the Majority of the Secreted Phosphoproteome.''; PubMed Europe PMC Scholia
- Schneider MR, Zhou R, Hoeflich A, Krebs O, Schmidt J, Mohan S, Wolf E, Lahm H.; ''Insulin-like growth factor-binding protein-5 inhibits growth and induces differentiation of mouse osteosarcoma cells.''; PubMed Europe PMC Scholia
- Campbell EJ, Silverman EK, Campbell MA.; ''Elastase and cathepsin G of human monocytes. Quantification of cellular content, release in response to stimuli, and heterogeneity in elastase-mediated proteolytic activity.''; PubMed Europe PMC Scholia
- Firth SM, Clemmons DR, Baxter RC.; ''Mutagenesis of basic amino acids in the carboxyl-terminal region of insulin-like growth factor binding protein-5 affects acid-labile subunit binding.''; PubMed Europe PMC Scholia
- Mohan S, Baylink DJ.; ''IGF-binding proteins are multifunctional and act via IGF-dependent and -independent mechanisms.''; PubMed Europe PMC Scholia
- Baxter RC, Bayne ML, Cascieri MA.; ''Structural determinants for binary and ternary complex formation between insulin-like growth factor-I (IGF-I) and IGF binding protein-3.''; PubMed Europe PMC Scholia
- Angelloz-Nicoud P, Binoux M.; ''Autocrine regulation of cell proliferation by the insulin-like growth factor (IGF) and IGF binding protein-3 protease system in a human prostate carcinoma cell line (PC-3).''; PubMed Europe PMC Scholia
- Marinaro JA, Neumann GM, Russo VC, Leeding KS, Bach LA.; ''O-glycosylation of insulin-like growth factor (IGF) binding protein-6 maintains high IGF-II binding affinity by decreasing binding to glycosaminoglycans and susceptibility to proteolysis.''; PubMed Europe PMC Scholia
- Okabe E, Kajihara J, Usami Y, Hirano K.; ''The cleavage site specificity of human prostate specific antigen for insulin-like growth factor binding protein-3.''; PubMed Europe PMC Scholia
- Wolf E, Lahm H, Wu M, Wanke R, Hoeflich A.; ''Effects of IGFBP-2 overexpression in vitro and in vivo.''; PubMed Europe PMC Scholia
- Andrade D, Assis DM, Santos JA, Alves FM, Hirata IY, Araujo MS, Blaber SI, Blaber M, Juliano MA, Juliano L.; ''Substrate specificity of kallikrein-related peptidase 13 activated by salts or glycosaminoglycans and a search for natural substrate candidates.''; PubMed Europe PMC Scholia
- Baxter RC, Meka S, Firth SM.; ''Molecular distribution of IGF binding protein-5 in human serum.''; PubMed Europe PMC Scholia
- Cohen P, Peehl DM, Graves HC, Rosenfeld RG.; ''Biological effects of prostate specific antigen as an insulin-like growth factor binding protein-3 protease.''; PubMed Europe PMC Scholia
- Payet LD, Wang XH, Baxter RC, Firth SM.; ''Amino- and carboxyl-terminal fragments of insulin-like growth factor (IGF) binding protein-3 cooperate to bind IGFs with high affinity and inhibit IGF receptor interactions.''; PubMed Europe PMC Scholia
- Gyrup C, Oxvig C.; ''Quantitative analysis of insulin-like growth factor-modulated proteolysis of insulin-like growth factor binding protein-4 and -5 by pregnancy-associated plasma protein-A.''; PubMed Europe PMC Scholia
- Laursen LS, Overgaard MT, Søe R, Boldt HB, Sottrup-Jensen L, Giudice LC, Conover CA, Oxvig C.; ''Pregnancy-associated plasma protein-A (PAPP-A) cleaves insulin-like growth factor binding protein (IGFBP)-5 independent of IGF: implications for the mechanism of IGFBP-4 proteolysis by PAPP-A.''; PubMed Europe PMC Scholia
- Siwanowicz I, Popowicz GM, Wisniewska M, Huber R, Kuenkele KP, Lang K, Engh RA, Holak TA.; ''Structural basis for the regulation of insulin-like growth factors by IGF binding proteins.''; PubMed Europe PMC Scholia
- Lee KO, Oh Y, Giudice LC, Cohen P, Peehl DM, Rosenfeld RG.; ''Identification of insulin-like growth factor-binding protein-3 (IGFBP-3) fragments and IGFBP-5 proteolytic activity in human seminal plasma: a comparison of normal and vasectomized patients.''; PubMed Europe PMC Scholia
- Fielder PJ, Rosenfeld RG, Graves HC, Grandbois K, Maack CA, Sawamura S, Ogawa Y, Sommer A, Cohen P.; ''Biochemical analysis of prostate specific antigen-proteolyzed insulin-like growth factor binding protein-3.''; PubMed Europe PMC Scholia
History
View all... |
External references
DataNodes
View all... |
Name | Type | Database reference | Comment |
---|---|---|---|
CTSG | Protein | P08311 (Uniprot-TrEMBL) | After secretion Cathepsin G is extracellular and associated with the plasma membrane. |
CTSG | Protein | P08311 (Uniprot-TrEMBL) | After secretion Cathepsin G is extracellular and associated with the plasma membrane. |
Ca2+ | Metabolite | CHEBI:29108 (ChEBI) | |
Cathepsin G | Complex | R-HSA-2990877 (Reactome) | This CandidateSet contains sequences identified by William Pearson's analysis of Reactome catalyst entities. Catalyst entity sequences were used to identify analagous sequences that shared overall homology and active site homology. Sequences in this Candidate set were identified in an April 24, 2012 analysis. |
GZMH | Protein | P20718 (Uniprot-TrEMBL) | |
IGF1 | Protein | P05019 (Uniprot-TrEMBL) | |
IGF1,2 | Complex | R-HSA-381451 (Reactome) | |
IGF2(25-91) | Protein | P01344 (Uniprot-TrEMBL) | |
IGF:IGFBP1 | Complex | R-HSA-381539 (Reactome) | |
IGF:IGFBP2 | Complex | R-HSA-381473 (Reactome) | |
IGF:IGFBP3:ALS | Complex | R-HSA-381536 (Reactome) | |
IGF:IGFBP4 | Complex | R-HSA-381509 (Reactome) | |
IGF:IGFBP5:ALS | Complex | R-HSA-381423 (Reactome) | |
IGF:IGFBP6 | Complex | R-HSA-381482 (Reactome) | |
IGFALS | Protein | P35858 (Uniprot-TrEMBL) | |
IGFALS | Protein | P35858 (Uniprot-TrEMBL) | |
IGFBP1 | Protein | P08833 (Uniprot-TrEMBL) | |
IGFBP1 | Protein | P08833 (Uniprot-TrEMBL) | |
IGFBP2 | Protein | P18065 (Uniprot-TrEMBL) | |
IGFBP2 | Protein | P18065 (Uniprot-TrEMBL) | |
IGFBP3 | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(125-187) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(125-233) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(127-291) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(169-226) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(188-291) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(227-291) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(234-291) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(28-124) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(28-126) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(28-168) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(28-186) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3(291-187) | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP3 | Protein | P17936 (Uniprot-TrEMBL) | |
IGFBP4 | Protein | P22692 (Uniprot-TrEMBL) | |
IGFBP4(157-237) | Protein | P22692 (Uniprot-TrEMBL) | |
IGFBP4(22-156) | Protein | P22692 (Uniprot-TrEMBL) | |
IGFBP4 | Protein | P22692 (Uniprot-TrEMBL) | |
IGFBP5 | Protein | P24593 (Uniprot-TrEMBL) | |
IGFBP5(164-272) | Protein | P24593 (Uniprot-TrEMBL) | |
IGFBP5(21-163) | Protein | P24593 (Uniprot-TrEMBL) | |
IGFBP5 | Protein | P24593 (Uniprot-TrEMBL) | |
IGFBP6 | Protein | P24592 (Uniprot-TrEMBL) | |
IGFBP6 | Protein | P24592 (Uniprot-TrEMBL) | |
KLK1 | Protein | P06870 (Uniprot-TrEMBL) | |
KLK13 | Protein | Q9UKR3 (Uniprot-TrEMBL) | |
KLK2 | Protein | P20151 (Uniprot-TrEMBL) | |
KLK3 | Protein | P07288 (Uniprot-TrEMBL) | |
MMP1(100-469) | Protein | P03956 (Uniprot-TrEMBL) | |
MMP1,2 | Complex | R-HSA-381470 (Reactome) | |
MMP2(110-660) | Protein | P08253 (Uniprot-TrEMBL) | |
PAPPA | Protein | Q13219 (Uniprot-TrEMBL) | |
PAPPA,PAPPA2 | Complex | R-HSA-381483 (Reactome) | |
PAPPA2 | Protein | Q9BXP8 (Uniprot-TrEMBL) | |
PLG(20-580) | Protein | P00747 (Uniprot-TrEMBL) | |
PLG(581-810) | Protein | P00747 (Uniprot-TrEMBL) | |
Plasmin | Complex | R-HSA-158770 (Reactome) | |
Prostate Specific Antigen | Complex | R-HSA-2990872 (Reactome) | This CandidateSet contains sequences identified by William Pearson's analysis of Reactome catalyst entities. Catalyst entity sequences were used to identify analagous sequences that shared overall homology and active site homology. Sequences in this Candidate set were identified in an April 24, 2012 analysis. |
activated thrombin (factor IIa) | Complex | R-HSA-156786 (Reactome) | |
thrombin heavy chain | Protein | P00734 (Uniprot-TrEMBL) | |
thrombin light chain | Protein | P00734 (Uniprot-TrEMBL) |
Annotated Interactions
View all... |
Source | Target | Type | Database reference | Comment |
---|---|---|---|---|
Cathepsin G | mim-catalysis | R-HSA-381500 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381435 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381446 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381461 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381466 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381500 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381518 (Reactome) | ||
IGF1,2 | Arrow | R-HSA-381537 (Reactome) | ||
IGF1,2 | R-HSA-381412 (Reactome) | |||
IGF1,2 | R-HSA-381487 (Reactome) | |||
IGF1,2 | R-HSA-381496 (Reactome) | |||
IGF1,2 | R-HSA-381503 (Reactome) | |||
IGF1,2 | R-HSA-381543 (Reactome) | |||
IGF1,2 | R-HSA-381545 (Reactome) | |||
IGF:IGFBP1 | Arrow | R-HSA-381487 (Reactome) | ||
IGF:IGFBP2 | Arrow | R-HSA-381412 (Reactome) | ||
IGF:IGFBP3:ALS | Arrow | R-HSA-381496 (Reactome) | ||
IGF:IGFBP3:ALS | R-HSA-381435 (Reactome) | |||
IGF:IGFBP3:ALS | R-HSA-381446 (Reactome) | |||
IGF:IGFBP3:ALS | R-HSA-381461 (Reactome) | |||
IGF:IGFBP3:ALS | R-HSA-381466 (Reactome) | |||
IGF:IGFBP3:ALS | R-HSA-381500 (Reactome) | |||
IGF:IGFBP4 | Arrow | R-HSA-381543 (Reactome) | ||
IGF:IGFBP4 | R-HSA-381518 (Reactome) | |||
IGF:IGFBP5:ALS | Arrow | R-HSA-381545 (Reactome) | ||
IGF:IGFBP5:ALS | R-HSA-381537 (Reactome) | |||
IGF:IGFBP6 | Arrow | R-HSA-381503 (Reactome) | ||
IGFALS | Arrow | R-HSA-381435 (Reactome) | ||
IGFALS | Arrow | R-HSA-381446 (Reactome) | ||
IGFALS | Arrow | R-HSA-381461 (Reactome) | ||
IGFALS | Arrow | R-HSA-381466 (Reactome) | ||
IGFALS | Arrow | R-HSA-381500 (Reactome) | ||
IGFALS | Arrow | R-HSA-381537 (Reactome) | ||
IGFALS | R-HSA-381496 (Reactome) | |||
IGFALS | R-HSA-381545 (Reactome) | |||
IGFBP1 | R-HSA-381487 (Reactome) | |||
IGFBP1 | mim-catalysis | R-HSA-381487 (Reactome) | ||
IGFBP2 | R-HSA-381412 (Reactome) | |||
IGFBP2 | mim-catalysis | R-HSA-381412 (Reactome) | ||
IGFBP3(125-187) | Arrow | R-HSA-381461 (Reactome) | ||
IGFBP3(125-233) | Arrow | R-HSA-381446 (Reactome) | ||
IGFBP3(127-291) | Arrow | R-HSA-381435 (Reactome) | ||
IGFBP3(169-226) | Arrow | R-HSA-381500 (Reactome) | ||
IGFBP3(188-291) | Arrow | R-HSA-381461 (Reactome) | ||
IGFBP3(227-291) | Arrow | R-HSA-381500 (Reactome) | ||
IGFBP3(234-291) | Arrow | R-HSA-381446 (Reactome) | ||
IGFBP3(28-124) | Arrow | R-HSA-381446 (Reactome) | ||
IGFBP3(28-124) | Arrow | R-HSA-381461 (Reactome) | ||
IGFBP3(28-126) | Arrow | R-HSA-381435 (Reactome) | ||
IGFBP3(28-168) | Arrow | R-HSA-381500 (Reactome) | ||
IGFBP3(28-186) | Arrow | R-HSA-381466 (Reactome) | ||
IGFBP3(291-187) | Arrow | R-HSA-381466 (Reactome) | ||
IGFBP3 | R-HSA-381496 (Reactome) | |||
IGFBP3 | mim-catalysis | R-HSA-381496 (Reactome) | ||
IGFBP4(157-237) | Arrow | R-HSA-381518 (Reactome) | ||
IGFBP4(22-156) | Arrow | R-HSA-381518 (Reactome) | ||
IGFBP4 | R-HSA-381543 (Reactome) | |||
IGFBP4 | mim-catalysis | R-HSA-381543 (Reactome) | ||
IGFBP5(164-272) | Arrow | R-HSA-381537 (Reactome) | ||
IGFBP5(21-163) | Arrow | R-HSA-381537 (Reactome) | ||
IGFBP5 | R-HSA-381545 (Reactome) | |||
IGFBP5 | mim-catalysis | R-HSA-381545 (Reactome) | ||
IGFBP6 | R-HSA-381503 (Reactome) | |||
IGFBP6 | mim-catalysis | R-HSA-381503 (Reactome) | ||
MMP1,2 | mim-catalysis | R-HSA-381435 (Reactome) | ||
PAPPA,PAPPA2 | mim-catalysis | R-HSA-381518 (Reactome) | ||
PAPPA,PAPPA2 | mim-catalysis | R-HSA-381537 (Reactome) | ||
Plasmin | mim-catalysis | R-HSA-381461 (Reactome) | ||
Prostate Specific Antigen | mim-catalysis | R-HSA-381466 (Reactome) | ||
R-HSA-381412 (Reactome) | IGFBP 2 binds IGF I or IGF II via the conserved N terminus and C terminus of IGFBP 2.
IGFBP 2 is enriched in cerebrospinal fluid and inhibits IGF function. IGFBP 2 is not significantly degraded in circulation. | |||
R-HSA-381435 (Reactome) | Matrix Metalloprotease-1 and -2 cleave IGFBP-3 in the IGF:IGFBP-3:ALS Complex between amino acids 126 and 127, releasing IGF. The reaction has been demonstrated in vivo. | |||
R-HSA-381446 (Reactome) | Thrombin cleaves IGFBP-3 in the IGF:IGFBP-3:ALS Complex between amino acids 124 and 125 and between amino acids 233 and 234, releasing IGF. | |||
R-HSA-381461 (Reactome) | Plasmin cleaves IGFBP-3 in the IGF:IGFBP-3:ALS Complex between amino acids 124 and 125 and between amino acids 187 and 188, releasing IGF. | |||
R-HSA-381466 (Reactome) | Prostate specific Antigen (PSA, KLK3) cleaves IGFBP-3 in the IGF:IGFBP-3:ALS Complex between amino acids 186 and 187. Other cleavage sites were observed but not reproducibly. These may have been caused by impurities in the PSA preparation. | |||
R-HSA-381487 (Reactome) | IGFBP 1 binds IGF I or IGF II via the conserved N terminus and C terminus of IGFBP 1.
IGFBP 1 is enriched in amniotic fluid and is produced in the liver under control of insulin (insulin suppresses production). IGFBP 1 acts to stimulate IGF function. It is unknown which if any protease degrades IGFBP 1. | |||
R-HSA-381496 (Reactome) | IGFBP3 binds IGF I or IGF II via the conserved N terminus and C terminus of IGFBP 3. IGFBP3 also binds ALS via the C terminal portion of IGFBP3. The interaction is dependent on the glycosylation of ALS. IGFBP3, which binds most IGF in the body, is enriched in follicular fluid and found in many other tissues. IGFBP3 may be cleaved by plasmin, thrombin, Prostate specific Antigen (PSA, KLK3), Matrix Metalloprotease-1 (MMP1), and Matrix Metalloprotease-2 (MMP2). IGFBP3 also binds extracellular matrix and binding lowers its affinity for IGFs. IGFBP3 stimulates the effects of IGFs. | |||
R-HSA-381500 (Reactome) | Cathepsin G cleaves IGFBP-3 between amino acids 168 and 169 and between amino acids 226 and 227, releasing IGF from the IGF:IGFBP-3:ALS Complex. | |||
R-HSA-381503 (Reactome) | IGFBP-6 binds IGF I or IGF II via the conserved N terminus and C terminus of IGFBP-6. IGFBP-6 binds IGF II with greater affinity than IGF I. | |||
R-HSA-381518 (Reactome) | Pregnancy associated Plasma Protein A (PPAP-A) cleaves IGFBP-4 in the IGF:IGFBP-4 Complex between amino acids 156 and 157, releasing IGF. | |||
R-HSA-381537 (Reactome) | Both Pregnancy Associated Plasma Protein A (PAPP-A) and A2 (PAPP-A2) cleave IGFBP-5 in the IGF:IGFBP-5:ALS Complex between amino acids 163 and 164, releasing IGF. PPAP-A has also been shown to cleave IGFBP-5 that is not complexed with IGF. | |||
R-HSA-381543 (Reactome) | IGFBP 4 binds IGF I or IGF II via the conserved N terminus and C terminus of IGFBP 4. | |||
R-HSA-381545 (Reactome) | IGFBP 5 binds IGF I or IGF II via the conserved N terminus and C terminus of IGFBP 5. IGFBP 5 also binds ALS via the central portion of IGFBP 5. About 55% of IGF:IGFBP 5 complexes contain ALS.
IGFBP 5 is enriched in bone matrix and acts to stimulate IGF function. IGFBP 5 is cleaved by Pregnancy associated Plasma Protein A2 (PAPP A2), ADAM 9, complement C1s from smooth muscle, and thrombin. Only the cleavage site for PAPP A2 is known. About 55% of IGF:IGFBP 5 complexes contain ALS; 45% contain only IGF and IGFBP 5. | |||
activated thrombin (factor IIa) | mim-catalysis | R-HSA-381446 (Reactome) |