Localization of metallocarboxypeptidase D in AtT-20 cells. Potential role in prohormone processing.
about
Characterization of a novel, cytokine-inducible carboxypeptidase D isoform in haematopoietic tumour cellsFurin at the cutting edge: from protein traffic to embryogenesis and diseaseImmunohistochemical localization and comparison of carboxypeptidases D, E, and Z, alpha-MSH, ACTH, and MIB-1 between human anterior and corticotroph cell "basophil invasion" of the posterior pituitarySignaling mediated by the cytosolic domain of peptidylglycine alpha-amidating monooxygenaseMembrane-bound carboxypeptidase E facilitates the entry of eosinophil cationic protein into neuroendocrine cellsGene expression profiling of differentially expressed genes in granulosa cells of bovine dominant follicles using suppression subtractive hybridization.Identification of peptides from brain and pituitary of Cpe(fat)/Cpe(fat) miceSUPPRESSOR OF LLP1 1-mediated C-terminal processing is critical for CLE19 peptide activity.Individual carboxypeptidase D domains have both redundant and unique functions in Drosophila development and behavior.Prolactin/Stat5 and androgen R1881 coactivate carboxypeptidase-D gene in breast cancer cellsDissecting carboxypeptidase E: properties, functions and pathophysiological roles in disease.Immunohistochemical localization of carboxypeptidases D, E, and Z in pituitary adenomas and normal human pituitary.Palmitoylation of carboxypeptidase D. Implications for intracellular trafficking.AP-1A controls secretory granule biogenesis and trafficking of membrane secretory granule proteinsRole of cytoplasmic domain serines in intracellular trafficking of furin.At the crossroads of homoeostasis and disease: roles of the PACS proteins in membrane traffic and apoptosis.Cathepsin L and Arg/Lys aminopeptidase: a distinct prohormone processing pathway for the biosynthesis of peptide neurotransmitters and hormones.Neuropeptide-processing enzymes: applications for drug discovery.Proteomic analysis of pancreatic zymogen granules: identification of new granule proteins.Role of adaptor proteins in secretory granule biogenesis and maturationPeptidomics of Cpe(fat/fat) mouse brain regions: implications for neuropeptide processingProhormone-convertase 1 processing enhances post-Golgi sorting of prothyrotropin-releasing hormone-derived peptides.Roles of myosin Va and Rab3D in membrane remodeling of immature secretory granules.GGA function is required for maturation of neuroendocrine secretory granules.Neuropeptidomic analysis establishes a major role for prohormone convertase-2 in neuropeptide biosynthesis.Copper, zinc and calcium: imaging and quantification in anterior pituitary secretory granules.Characterization of the enzymatic properties of the first and second domains of metallocarboxypeptidase D.Substrate specificity of human metallocarboxypeptidase D: Comparison of the two active carboxypeptidase domains.Characterization of the molecular basis of the Drosophila mutations in carboxypeptidase D. Effect on enzyme activity and expression.Deficiencies in pro-thyrotropin-releasing hormone processing and abnormalities in thermoregulation in Cpefat/fat mice.Peptidomics of Cpe fat/fat mouse hypothalamus: effect of food deprivation and exercise on peptide levels.Altered neuropeptide processing in prefrontal cortex of Cpe (fat/fat) mice: implications for neuropeptide discovery.The C-terminal Region of proSAAS Is a Potent Inhibitor of Prohormone Convertase 1
P2860
Q24531849-C8C05EE6-FAEB-49CE-9FF1-73867D5B7D30Q24670432-7EB2926B-5AD1-49B8-8C2D-5BE828405242Q28190535-40A441EE-98B3-42AB-B910-B97B818FE428Q28565137-BAA64E4F-3868-4CEF-A4A5-5BAADA66CC36Q28581228-7EE49EC6-C7F5-4BAF-995E-B9BF4D2E42B5Q31015091-3F990208-5DA8-4C89-8575-3819890CF43EQ31942417-BA0025C7-8CDE-4AB6-8990-F749335A0769Q33356700-FA777143-3036-4B10-9B7B-5574F6C0C2C8Q33553558-6E84713E-A4D2-4CC6-BF6B-2BCDD431D8ACQ33632218-DE7102C1-A5F5-40E2-9E88-82F9C7E10D53Q33697577-74A11D99-761F-4986-AF92-C8C7C61295C6Q34157843-0B86BCE5-9312-4AC6-A2D8-890B8C040AF4Q34184352-201E5B31-97B1-4F04-8FC1-B72F5B2D3243Q34207067-C12E7FF8-85E2-48B6-89FB-F8BD3DF520B5Q34359883-9D89E523-007D-4022-A855-1311EE512A56Q34999872-A522FFFB-EA94-4A00-B85F-71DF76FFCD14Q35837221-2F85BE5D-263B-4106-87F8-30BABA1A4C81Q36341621-C4E3C363-CAB6-41A1-8E4C-3FDE337E7045Q36969936-8559BEC8-606E-46CB-8305-D85973393A73Q37094181-E6CCC099-D20E-465A-8443-220AC7FB70BDQ37146747-DC6A8BD4-0D6B-42C7-8C8A-B9F3B3FBDA94Q40365652-168E5474-937F-4489-8D20-2CDB2388FBBAQ41441239-ED641F62-2420-4A7A-BCF5-7B59A0308338Q41864335-F8B4E01C-ED51-4799-ABAE-9325A6D2DD02Q42165641-CB9BF421-EBA6-48C1-8F43-6CCD8A526F80Q42374606-41AAD3E5-2054-4353-BA66-36244CF8CEB1Q44525678-32EB49A1-F34C-4579-82BF-91C5BA7CC6D6Q44748766-0FA1064B-8540-451D-B846-29BF00DA14EEQ47070801-34B8542B-0679-40C9-94E1-C169FD34284DQ48482162-6D7ED54B-1BB7-4B59-9C9A-54A738F3C554Q48511415-D1242739-9134-4631-AAA4-662CB05A935AQ48685492-441A7B62-890D-4476-AD91-BB67C7208B27Q57268727-66FF0006-799A-4A0A-B30D-F8F061597C8C
P2860
Localization of metallocarboxypeptidase D in AtT-20 cells. Potential role in prohormone processing.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
Localization of metallocarboxy ...... role in prohormone processing.
@en
Localization of metallocarboxy ...... role in prohormone processing.
@nl
type
label
Localization of metallocarboxy ...... role in prohormone processing.
@en
Localization of metallocarboxy ...... role in prohormone processing.
@nl
prefLabel
Localization of metallocarboxy ...... role in prohormone processing.
@en
Localization of metallocarboxy ...... role in prohormone processing.
@nl
P2093
P2860
P356
P1476
Localization of metallocarboxy ...... role in prohormone processing.
@en
P2093
P2860
P304
14759-14767
P356
10.1074/JBC.274.21.14759
P407
P577
1999-05-01T00:00:00Z