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Molecular structural formula
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Normal/Tumor
Melanoma
Melanoma
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HLA
DR4(用于人类白细胞抗原 II类)
DR4(用于人类白细胞抗原 II类)
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Peptide Sequence
EDLTVKIGDFGLATEKSRWSGSHQFEQLS(其中第二个"E"为独特抗原突变所导致的修饰残基)
EDLTVKIGDFGLATEKSRWSGSHQFEQLS(其中第二个"E"为独特抗原突变所导致的修饰残基)
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Lymphocyte Stimulation
peptide
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NCBI Gene SummaryNCBI
This gene encodes a protein belonging to the RAF family of serine/threonine protein kinases. This protein plays a role in regulating the MAP kinase/ERK signaling pathway, which affects cell division, differentiation, and secretion. Mutations in this gene, most commonly the V600E mutation, are the most frequently identified cancer-causing mutations in melanoma, and have been identified in various other cancers as well, including non-Hodgkin lymphoma, colorectal cancer, thyroid carcinoma, non-small cell lung carcinoma, hairy cell leukemia and adenocarcinoma of lung. Mutations in this gene are also associated with cardiofaciocutaneous, Noonan, and Costello syndromes, which exhibit overlapping phenotypes. A pseudogene of this gene has been identified on the X chromosome. [provided by RefSeq, Aug 2017].
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GeneCards Summary
BRAF (B-Raf Proto-Oncogene, Serine/Threonine Kinase) is a Protein Coding gene. Diseases associated with BRAF include Lung Cancer and Cardiofaciocutaneous Syndrome 1. Among its related pathways are IL-9 Signaling Pathways and Prolactin Signaling. Gene Ontology (GO) annotations related to this gene include calcium ion binding and transferase activity, transferring phosphorus-containing groups. An important paralog of this gene is RAF1.
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UniProtKB SwissProt Summary
Protein kinase involved in the transduction of mitogenic signals from the cell membrane to the nucleus (Probable). Phosphorylates MAP2K1, and thereby activates the MAP kinase signal transduction pathway . Phosphorylates PFKFB2 (PubMed:36402789). May play a role in the postsynaptic responses of hippocampal neurons . ( BRAF_HUMAN,P15056 )
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References
[1].Sharkey MS, Lizée G, Gonzales MI, Patel S, Topalian SL. CD4(+) T-cell recognition of mutated B-RAF in melanoma patients harboring the V599E mutation. Cancer Res. 2004 Mar 1, 64(5):1595-9. (PMID: 14996715).
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