Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Kevin W. Hallgren"'
Autor:
Mark A. Rishavy, Kevin W. Hallgren, Lee A. Wilson, James M. Hiznay, Kurt W. Runge, Kathleen L. Berkner
Publikováno v:
Blood. 140:1710-1722
γ-Glutamyl carboxylase (GGCX) generates multiple carboxylated Glus (Glas) in vitamin K–dependent (VKD) proteins that are required for their functions. GGCX is processive, remaining bound to VKD proteins throughout multiple Glu carboxylations, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::45761f7fdb31320bb052e1bcf188e39d
https://doi.org/10.1182/blood.2021014275
https://doi.org/10.1182/blood.2021014275
Autor:
Kevin W. Hallgren, Savita Singh, Kurt W. Runge, Kathleen L. Berkner, Lee Wilson, Mark A. Rishavy
Publikováno v:
Blood. 131:2826-2835
The anticoagulant warfarin inhibits the vitamin K oxidoreductase (VKORC1), which generates vitamin K hydroquinone (KH2) required for the carboxylation and consequent activation of vitamin K-dependent (VKD) proteins. VKORC1 produces KH2 in 2 reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c48183e184a475827a01d121373f113
https://doi.org/10.1182/blood-2017-09-804666
https://doi.org/10.1182/blood-2017-09-804666
Vitamin K-dependent (VKD) protein activities require carboxylated Glus (Glas) generated by the gamma-glutamyl carboxylase. Some carboxylase mutations cause severe bleeding, while others cause pseudoxanthoma elasticum (PXE)-like associated with excess
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fc5564bfc5fef3fccbfd45f0071160f
Publikováno v:
J Thromb Haemost
Essentials A carboxylase mutation that impairs splicing to delete exon 2 sequences was previously reported. We found that the mutant was inactive for vitamin K-dependent (VKD) protein carboxylation. An incomplete splicing defect likely accounts for V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cca2cf601db58f0847e9841dc4abda05
https://pubmed.ncbi.nlm.nih.gov/31009158
https://pubmed.ncbi.nlm.nih.gov/31009158
Autor:
Kurt W. Runge, Lee Wilson, Aisulu Usubalieva, Kevin W. Hallgren, Mark A. Rishavy, Kathleen L. Berkner
Publikováno v:
Journal of Biological Chemistry. 288:31556-31566
The vitamin K oxidoreductase (VKORC1) recycles vitamin K to support the activation of vitamin K-dependent (VKD) proteins, which have diverse functions that include hemostasis and calcification. VKD proteins are activated by Glu carboxylation, which d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::004f8e22c59579f7787efb6d4738cfc7
https://doi.org/10.1074/jbc.m113.497297
https://doi.org/10.1074/jbc.m113.497297
Publikováno v:
Journal of Biological Chemistry. 286:7267-7278
The vitamin K oxidoreductase (VKOR) reduces vitamin K to support the carboxylation and consequent activation of vitamin K-dependent proteins, but the mechanism of reduction is poorly understood. VKOR is an integral membrane protein that reduces vitam
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b318c3327cc577a4260be5bc4f4b1ba5
https://doi.org/10.1074/jbc.m110.172213
https://doi.org/10.1074/jbc.m110.172213
Autor:
Alison J. Whelan, Qiaoli Li, Nicole L. Armstrong, Jouni Uitto, Kathleen L. Berkner, Kevin W. Hallgren, Leon J. Schurgers, Mark A. Rishavy, Qiujie Jiang, Maria Yadira Hurley, Dorothy K. Grange
Publikováno v:
Journal of Investigative Dermatology. 129:553-563
A characteristic feature of classic pseudoxanthoma elasticum (PXE), an autosomal recessive disorder caused by mutations in the ABCC6 gene, is aberrant mineralization of connective tissues, particularly the elastic fibers. Here, we report a family wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73d7baa8370d5d440ca6740211106ceb
https://doi.org/10.1038/jid.2008.271
https://doi.org/10.1038/jid.2008.271
Autor:
Dhouha Darghouth, Kevin W. Hallgren, Sophie Lericousse, Jean Rosa, Kathleen L. Berkner, Youssef Gharbi, Radhia Kastally, Amel Mrad, Rebecca L. Shtofman, Ahmed Maherzi
Publikováno v:
Blood. 108:1925-1931
Hereditary combined vitamin K–dependent (VKD) coagulation factor deficiency is an autosomal recessive bleeding disorder associated with defects in either the γ-carboxylase, which carboxylates VKD proteins to render them active, or the vitamin K ep
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::22887a0bda1c7f5305f6ceab8cddda56
https://doi.org/10.1182/blood-2005-12-010660
https://doi.org/10.1182/blood-2005-12-010660
Autor:
Kurt W. Runge, Richard L. Zuerner, Kevin W. Hallgren, Anna V. Yakubenko, Mark A. Rishavy, Kathleen L. Berkner
Publikováno v:
Journal of Biological Chemistry. 280:34870-34877
Leptospirosis is an emerging infectious disease whose pathology includes a hemorrhagic response, and sequencing of the Leptospira interrogans genome revealed an ortholog of the vitamin K-dependent (VKD) carboxylase as one of several hemostatic protei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a7786a5975f7f639e9fcfcc07fdd0fb
https://doi.org/10.1074/jbc.m504345200
https://doi.org/10.1074/jbc.m504345200
Publikováno v:
Biochemistry. 41:15045-15055
Vitamin K-dependent (VKD) proteins are modified by the VKD carboxylase as they transit through the endoplasmic reticulum. In a reaction required for their activity, clusters of Glu's are converted to Gla's, and fully carboxylated VKD proteins are nor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e7c02e3ea31b6e3aa14dcc39b01f59
https://doi.org/10.1021/bi026016e
https://doi.org/10.1021/bi026016e