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Coagulation factor X (EC 3.4.21.6), or Stuart factor, ... The affinity of this protein for factor Xa is increased 1000-fold by the presence of protein Z, ...
Factor X deficiency (X as Roman numeral ten) is a bleeding disorder characterized by a lack in the production of factor X (FX), an enzyme protein that causes blood to clot in the coagulation cascade. Produced in the liver FX when activated cleaves prothrombin to generate thrombin in the intrinsic pathway of coagulation.
7257 53424 Ensembl ENSG00000116918 ENSMUSG00000056820 UniProt Q99598 Q9QZE7 RefSeq (mRNA) NM_005999 NM_016909 RefSeq (protein) NP_005990 NP_058605 Location (UCSC) Chr 1: 231.53 – 231.57 Mb Chr 8: 125.74 – 125.76 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse Translin-associated protein X (abbr. TSNAX or TRAX) is a protein that in humans is encoded by the TSNAX gene. Function ...
The protein product of MAX contains the basic helix-loop-helix and leucine zipper motifs. It is therefore included in the bHLHZ family of transcription factors. It is able to form homodimers with other MAX proteins and heterodimers with other transcription factors, including Mad, Mxl1 and Myc.
19724 Ensembl ENSG00000132005 ENSG00000288283 ENSMUSG00000031706 UniProt P22670 P48377 RefSeq (mRNA) NM_002918 NM_009055 RefSeq (protein) NP_002909 NP_033081 Location (UCSC) Chr 19: 13.96 – 14.01 Mb Chr 8: 84.79 – 84.82 Mb PubMed search Wikidata View/Edit Human View/Edit Mouse MHC class II regulatory factor RFX1 is a protein that, in humans, is encoded by the RFX1 gene located on the short ...
Activated factor X (FXa) is the sole enzyme that catalyzes the conversion of prothrombine into thrombin, which is vital in the coagulation cascade. [1] Draculin is a member of the Lactoferrin family of proteins that functions as an antibacterial protein in other mammals, but has been co-opted in bat evolution to function as an anticoagulant. [3]
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