HCK

HCK
HCK
Protein HCK PDB 1ad5.png
사용 가능한 구조물
PDB직교 검색: PDBe RCSB
식별자
별칭HCK, JTK9, p59Hck, p61Hck, HCK proto-oncogene, Src 계열 tyrosine kinase
외부 IDOMIM: 142370 MGI: 96052 HomoloGene: 20489 GeneCard: HCK
직교체
인간마우스
엔트레스
앙상블
유니프로트
RefSeq(mRNA)

NM_001172117
NM_010407

RefSeq(단백질)

NP_001165588
NP_034537

위치(UCSC)Chr 20: 32.05 – 32.1MbChr 2: 152.95 – 152.99Mb
PubMed 검색[3][4]
위키다타
인간 보기/편집마우스 보기/편집

Tyrosine-단백질 키나아제 HCK는 인간에게 HCK 유전자에 의해 암호화된 효소다.[5]

함수

이 유전자에 의해 인코딩된 단백질은 주로 조혈모세포 유형으로 발현되는 단백질-티로신키나아제로, 티로신키나아제의 src 계열에 속한다.인코딩된 단백질은 Fc 수용체를 호흡기 폭발의 활성화에 결합시키는 데 도움을 줄 수 있다.HCK와 src 계열 키나제스는 또한 약물 내성 암세포에서 세포 생존을 이끄는 데 관여했다.[6] 또한 중성미자의 이동과 중성미자의 분해에도 역할을 할 수 있다.비 AUG(CUG) 코돈을 포함한 대체 번역 개시 사이트 사용은 세포 내 국산화 방법이 다른 두 개의 다른 ISO 형식을 생산하게 된다.[7]

상호작용

HCK는 다음과 상호 작용하는 것으로 나타났다.

참조

  1. ^ a b c GRCh38: 앙상블 릴리스 89: ENSG00000101336 - 앙상블, 2017년 5월
  2. ^ a b c GRCm38: 앙상블 릴리스 89: ENSMUSG00000003283 - 앙상블, 2017년 5월
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ Quintrell N, Lebo R, Varmus H, Bishop JM, Pettenati MJ, Le Beau MM, Diaz MO, Rowley JD (August 1987). "Identification of a human gene (HCK) that encodes a protein-tyrosine kinase and is expressed in hemopoietic cells". Mol Cell Biol. 7 (6): 2267–75. doi:10.1128/mcb.7.6.2267. PMC 365351. PMID 3496523.
  6. ^ Saha, Tanmoy; Mondal, Jayanta; Khiste, Sachin; Lusic, Hrvoje; Hu, Zhang-Wei; Jayabalan, Ruparoshni; Hodgetts, Kevin J.; Jang, Haelin; Sengupta, Shiladitya; Lee, Somin Eunice; Park, Younggeun; Lee, Luke P.; Goldman, Aaron (2021-06-24). "Nanotherapeutic approaches to overcome distinct drug resistance barriers in models of breast cancer". Nanophotonics. 10 (12): 3063–3073. Bibcode:2021Nanop..10..142S. doi:10.1515/nanoph-2021-0142. PMC 8478290. PMID 34589378.
  7. ^ "Entrez Gene: HCK hemopoietic cell kinase".
  8. ^ Poghosyan Z, Robbins SM, Houslay MD, Webster A, Murphy G, Edwards DR (Feb 2002). "Phosphorylation-dependent interactions between ADAM15 cytoplasmic domain and Src family protein-tyrosine kinases". Journal of Biological Chemistry. 277 (7): 4999–5007. doi:10.1074/jbc.M107430200. PMID 11741929.
  9. ^ Stanglmaier M, Warmuth M, Kleinlein I, Reis S, Hallek M (Feb 2003). "The interaction of the Bcr-Abl tyrosine kinase with the Src kinase Hck is mediated by multiple binding domains". Leukemia. 17 (2): 283–9. doi:10.1038/sj.leu.2402778. PMID 12592324.
  10. ^ Lionberger JM, Wilson MB, Smithgall TE (Jun 2000). "Transformation of myeloid leukemia cells to cytokine independence by Bcr-Abl is suppressed by kinase-defective Hck". The Journal of Biological Chemistry. 275 (24): 18581–5. doi:10.1074/jbc.C000126200. PMID 10849448.
  11. ^ Howlett CJ, Robbins SM (Mar 2002). "Membrane-anchored Cbl suppresses Hck protein-tyrosine kinase mediated cellular transformation". Oncogene. 21 (11): 1707–16. doi:10.1038/sj.onc.1205228. PMID 11896602. S2CID 34296309.
  12. ^ Howlett CJ, Bisson SA, Resek ME, Tigley AW, Robbins SM (Apr 1999). "The proto-oncogene p120(Cbl) is a downstream substrate of the Hck protein-tyrosine kinase". Biochemical and Biophysical Research Communications. 257 (1): 129–38. doi:10.1006/bbrc.1999.0427. PMID 10092522.
  13. ^ Scott MP, Zappacosta F, Kim EY, Annan RS, Miller WT (Aug 2002). "Identification of novel SH3 domain ligands for the Src family kinase Hck. Wiskott-Aldrich syndrome protein (WASP), WASP-interacting protein (WIP), and ELMO1". The Journal of Biological Chemistry. 277 (31): 28238–46. doi:10.1074/jbc.M202783200. PMID 12029088.
  14. ^ Ward AC, Monkhouse JL, Csar XF, Touw IP, Bello PA (Oct 1998). "The Src-like tyrosine kinase Hck is activated by granulocyte colony-stimulating factor (G-CSF) and docks to the activated G-CSF receptor". Biochemical and Biophysical Research Communications. 251 (1): 117–23. doi:10.1006/bbrc.1998.9441. PMID 9790917.
  15. ^ Shivakrupa R, Radha V, Sudhakar C, Swarup G (Dec 2003). "Physical and functional interaction between Hck tyrosine kinase and guanine nucleotide exchange factor C3G results in apoptosis, which is independent of C3G catalytic domain". The Journal of Biological Chemistry. 278 (52): 52188–94. doi:10.1074/jbc.M310656200. PMID 14551197.
  16. ^ a b Briggs SD, Bryant SS, Jove R, Sanderson SD, Smithgall TE (Jun 1995). "The Ras GTPase-activating protein (GAP) is an SH3 domain-binding protein and substrate for the Src-related tyrosine kinase, Hck". The Journal of Biological Chemistry. 270 (24): 14718–24. doi:10.1074/jbc.270.24.14718. PMID 7782336.

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