Prediction of the structure of human Janus kinase 2 (JAK2) comprising the two carboxy-terminal domains reveals a mechanism for autoregulation

被引:129
作者
Lindauer, K
Loerting, T
Liedl, KR
Kroemer, RT
机构
[1] Queen Mary Univ London, Dept Chem, London E1 4NS, England
[2] Univ Innsbruck, Inst Gen Inorgan & Theoret Chem, A-6020 Innsbruck, Austria
来源
PROTEIN ENGINEERING | 2001年 / 14卷 / 01期
关键词
amino acid interactions; comparative sequence analysis; homology modelling; JAK2; tyrosine kinase;
D O I
10.1093/protein/14.1.27
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The structure of human Janus kinase 2 (JAK2) comprising the two C-terminal domains (JH1 and JH2) was predicted by application of homology modelling techniques. JH1 and JH2 represent the tyrosine kinase and tyrosine kinase-like domains, respectively, and are crucial for function and regulation of the protein. A comparison between the structures of the two domains is made and structural differences are highlighted. Prediction of the relative orientation of JH1 and JH2 was aided by a newly developed method for the detection of correlated amino acid mutations. Analysis of the interactions between the two domains led to a model for the regulatory effect of JH2 on JH1, The predictions are consistent with available experimental data on JAK2 or related proteins and provide an explanation for inhibition of JH1 tyrosine kinase activity by the adjacent JH2 domain.
引用
收藏
页码:27 / 37
页数:11
相关论文
共 77 条
  • [1] ALEXANDROV NN, 1996, BIOCOMPUTING, P53
  • [2] The SWISS-PROT protein sequence data bank and its supplement TrEMBL
    Bairoch, A
    Apweller, R
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (01) : 31 - 36
  • [3] Jak2-Stat5 interactions analyzed in yeast
    Barahmand-Pour, F
    Meinke, A
    Groner, B
    Decker, T
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) : 12567 - 12575
  • [4] HEMATOPOIETIC RECEPTORS AND HELICAL CYTOKINES
    BAZAN, JF
    [J]. IMMUNOLOGY TODAY, 1990, 11 (10): : 350 - 354
  • [5] Cytokine receptor-independent, constitutively active variants of STAT5
    Berchtold, S
    Moriggl, R
    Gouilleux, F
    Silvennoinen, O
    Beisenherz, C
    Pfitzner, E
    Wissler, M
    Stocklin, E
    Groner, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (48) : 30237 - 30243
  • [6] PROTEIN DATA BANK - COMPUTER-BASED ARCHIVAL FILE FOR MACROMOLECULAR STRUCTURES
    BERNSTEIN, FC
    KOETZLE, TF
    WILLIAMS, GJB
    MEYER, EF
    BRICE, MD
    RODGERS, JR
    KENNARD, O
    SHIMANOUCHI, T
    TASUMI, M
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1977, 112 (03) : 535 - 542
  • [7] JAKs and STATs branch out
    Briscoe, J
    Kohlhuber, F
    Muller, M
    [J]. TRENDS IN CELL BIOLOGY, 1996, 6 (09) : 336 - 340
  • [8] Kinase-negative mutants of JAK1 can sustain interferon-gamma-inducible gene expression but not an antiviral state
    Briscoe, J
    Rogers, NC
    Witthuhn, BA
    Watling, D
    Harpur, AG
    Wilks, A
    Stark, GR
    Ihle, JN
    Kerr, IM
    [J]. EMBO JOURNAL, 1996, 15 (04) : 799 - 809
  • [9] Complex effects of naturally occurring mutations in the JAK3 pseudokinase domain: Evidence for interactions between the kinase and pseudokinase domains
    Chen, M
    Cheng, A
    Candotti, F
    Zhou, YJ
    Hymel, A
    Fasth, A
    Notarangelo, LD
    O'Shea, JJ
    [J]. MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (03) : 947 - 956
  • [10] The amino terminus of JAK3 is necessary and sufficient for binding to the common gamma chain and confers the ability to transmit interleukin 2-mediated signals
    Chen, M
    Cheng, A
    Chen, YQ
    Hymel, A
    Hanson, EP
    Kimmel, L
    Minami, Y
    Taniguchi, T
    Changelian, PS
    OShea, JJ
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (13) : 6910 - 6915