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PDBsum entry 1luf
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* Residue conservation analysis
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PDB id:
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Transferase
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Title:
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Crystal structure of the musk tyrosine kinase: insights into receptor autoregulation
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Structure:
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Muscle-specific tyrosine kinase receptor musk. Chain: a. Fragment: cytoplasmic region (residues 526-868). Engineered: yes
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Source:
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Rattus norvegicus. Norway rat. Organism_taxid: 10116. Expressed in: spodoptera frugiperda. Expression_system_taxid: 7108.
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Resolution:
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2.05Å
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R-factor:
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0.231
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R-free:
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0.246
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Authors:
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J.H.Till,M.Becerra,A.Watty,Y.Lu,Y.Ma,T.A.Neubert,S.J.Burden, S.R.Hubbard
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Key ref:
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J.H.Till
et al.
(2002).
Crystal structure of the MuSK tyrosine kinase: insights into receptor autoregulation.
Structure,
10,
1187-1196.
PubMed id:
DOI:
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Date:
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22-May-02
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Release date:
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11-Sep-02
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PROCHECK
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Headers
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References
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Q62838
(MUSK_RAT) -
Muscle, skeletal receptor tyrosine protein kinase from Rattus norvegicus
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Seq: Struc:
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868 a.a.
275 a.a.
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Key: |
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PfamA domain |
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Secondary structure |
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CATH domain |
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Enzyme class:
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E.C.2.7.10.1
- receptor protein-tyrosine kinase.
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Reaction:
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L-tyrosyl-[protein] + ATP = O-phospho-L-tyrosyl-[protein] + ADP + H+
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L-tyrosyl-[protein]
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+
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ATP
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=
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O-phospho-L-tyrosyl-[protein]
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+
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ADP
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+
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H(+)
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Molecule diagrams generated from .mol files obtained from the
KEGG ftp site
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DOI no:
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Structure
10:1187-1196
(2002)
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PubMed id:
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Crystal structure of the MuSK tyrosine kinase: insights into receptor autoregulation.
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J.H.Till,
M.Becerra,
A.Watty,
Y.Lu,
Y.Ma,
T.A.Neubert,
S.J.Burden,
S.R.Hubbard.
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ABSTRACT
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Muscle-specific kinase (MuSK) is a receptor tyrosine kinase expressed
selectively in skeletal muscle. During neuromuscular synapse formation, agrin
released from motor neurons stimulates MuSK autophosphorylation in the kinase
activation loop and in the juxtamembrane region, leading to clustering of
acetylcholine receptors. We have determined the crystal structure of the
cytoplasmic domain of unphosphorylated MuSK at 2.05 A resolution. The structure
reveals an autoinhibited kinase domain in which the activation loop obstructs
ATP and substrate binding. Steady-state kinetic analysis demonstrates that
autophosphorylation results in a 200-fold increase in k(cat) and a 10-fold
decrease in the K(m) for ATP. These studies provide a molecular basis for
understanding the regulation of MuSK catalytic activity and suggest that an
additional in vivo component may contribute to regulation via the juxtamembrane
region.
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Selected figure(s)
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Figure 1.
Figure 1. Overall Structure of the MuSK Cytoplasmic
Domain(A) A ribbon diagram of the MuSK crystal structure, with b
strands (numbered) shown in cyan and a helices (lettered) shown
in red. The juxtamembrane segment (N terminal) and the
activation loop (containing aAL) are colored green. The
activation loop tyrosines, Tyr-750/754/755, are shown in ball
and stick representation (black).(B) A stereo view of a Ca trace
of MuSK in the same orientation as the diagram in (A). Every
10th residue is marked with a closed circle, and every 20th
residue is labeled with the residue number.
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The above figure is
reprinted
by permission from Cell Press:
Structure
(2002,
10,
1187-1196)
copyright 2002.
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Figure was
selected
by an automated process.
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Literature references that cite this PDB file's key reference
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PubMed id
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Reference
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A.R.Punga,
M.Maj,
S.Lin,
S.Meinen,
and
M.A.Rüegg
(2011).
MuSK levels differ between adult skeletal muscles and influence postsynaptic plasticity.
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Eur J Neurosci,
33,
890-898.
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N.Ghazanfari,
K.J.Fernandez,
Y.Murata,
M.Morsch,
S.T.Ngo,
S.W.Reddel,
P.G.Noakes,
and
W.D.Phillips
(2011).
Muscle specific kinase: organiser of synaptic membrane domains.
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Int J Biochem Cell Biol,
43,
295-298.
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C.C.Lee,
Y.Jia,
N.Li,
X.Sun,
K.Ng,
E.Ambing,
M.Y.Gao,
S.Hua,
C.Chen,
S.Kim,
P.Y.Michellys,
S.A.Lesley,
J.L.Harris,
and
G.Spraggon
(2010).
Crystal structure of the ALK (anaplastic lymphoma kinase) catalytic domain.
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Biochem J,
430,
425-437.
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PDB codes:
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E.Bergamin,
P.T.Hallock,
S.J.Burden,
and
S.R.Hubbard
(2010).
The cytoplasmic adaptor protein Dok7 activates the receptor tyrosine kinase MuSK via dimerization.
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Mol Cell,
39,
100-109.
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PDB code:
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F.Shi,
S.E.Telesco,
Y.Liu,
R.Radhakrishnan,
and
M.A.Lemmon
(2010).
ErbB3/HER3 intracellular domain is competent to bind ATP and catalyze autophosphorylation.
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Proc Natl Acad Sci U S A,
107,
7692-7697.
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PDB code:
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B.S.Lipska,
E.Drozynska,
P.Scaruffi,
G.P.Tonini,
E.Izycka-Swieszewska,
S.Zietkiewicz,
A.Balcerska,
D.Perek,
A.Chybicka,
W.Biernat,
and
J.Limon
(2009).
c.1810C>T polymorphism of NTRK1 gene is associated with reduced survival in neuroblastoma patients.
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BMC Cancer,
9,
436.
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C.W.Ward,
and
M.C.Lawrence
(2009).
Ligand-induced activation of the insulin receptor: a multi-step process involving structural changes in both the ligand and the receptor.
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Bioessays,
31,
422-434.
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E.D.Lew,
C.M.Furdui,
K.S.Anderson,
and
J.Schlessinger
(2009).
The precise sequence of FGF receptor autophosphorylation is kinetically driven and is disrupted by oncogenic mutations.
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Sci Signal,
2,
ra6.
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S.T.Lee,
J.Lee,
M.Lee,
J.W.Kim,
and
C.S.Ki
(2009).
Clinical and genetic analysis of Korean patients with congenital insensitivity to pain with anhidrosis.
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Muscle Nerve,
40,
855-859.
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B.P.Craddock,
C.Cotter,
and
W.T.Miller
(2007).
Autoinhibition of the insulin-like growth factor I receptor by the juxtamembrane region.
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FEBS Lett,
581,
3235-3240.
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C.O.Sallum,
R.A.Kammerer,
and
A.T.Alexandrescu
(2007).
Thermodynamic and structural studies of carbohydrate binding by the agrin-G3 domain.
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Biochemistry,
46,
9541-9550.
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N.Jones,
W.R.Hardy,
M.B.Friese,
C.Jorgensen,
M.J.Smith,
N.M.Woody,
S.J.Burden,
and
T.Pawson
(2007).
Analysis of a Shc family adaptor protein, ShcD/Shc4, that associates with muscle-specific kinase.
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Mol Cell Biol,
27,
4759-4773.
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C.M.Furdui,
E.D.Lew,
J.Schlessinger,
and
K.S.Anderson
(2006).
Autophosphorylation of FGFR1 kinase is mediated by a sequential and precisely ordered reaction.
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Mol Cell,
21,
711-717.
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N.Rahimi
(2006).
VEGFR-1 and VEGFR-2: two non-identical twins with a unique physiognomy.
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Front Biosci,
11,
818-829.
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N.Rahimi
(2006).
Vascular endothelial growth factor receptors: molecular mechanisms of activation and therapeutic potentials.
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Exp Eye Res,
83,
1005-1016.
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T.Cheusova,
M.A.Khan,
S.W.Schubert,
A.C.Gavin,
T.Buchou,
G.Jacob,
H.Sticht,
J.Allende,
B.Boldyreff,
H.R.Brenner,
and
S.Hashemolhosseini
(2006).
Casein kinase 2-dependent serine phosphorylation of MuSK regulates acetylcholine receptor aggregation at the neuromuscular junction.
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Genes Dev,
20,
1800-1816.
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E.D.Scheeff,
and
P.E.Bourne
(2005).
Structural evolution of the protein kinase-like superfamily.
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PLoS Comput Biol,
1,
e49.
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J.P.Vainonen,
M.Hansson,
and
A.V.Vener
(2005).
STN8 protein kinase in Arabidopsis thaliana is specific in phosphorylation of photosystem II core proteins.
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J Biol Chem,
280,
33679-33686.
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N.Yokoyama,
I.Ischenko,
M.J.Hayman,
and
W.T.Miller
(2005).
The C terminus of RON tyrosine kinase plays an autoinhibitory role.
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J Biol Chem,
280,
8893-8900.
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C.D.Mol,
D.R.Dougan,
T.R.Schneider,
R.J.Skene,
M.L.Kraus,
D.N.Scheibe,
G.P.Snell,
H.Zou,
B.C.Sang,
and
K.P.Wilson
(2004).
Structural basis for the autoinhibition and STI-571 inhibition of c-Kit tyrosine kinase.
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J Biol Chem,
279,
31655-31663.
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PDB codes:
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C.M.Rohde,
J.Schrum,
and
A.W.Lee
(2004).
A juxtamembrane tyrosine in the colony stimulating factor-1 receptor regulates ligand-induced Src association, receptor kinase function, and down-regulation.
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J Biol Chem,
279,
43448-43461.
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J.C.Lougheed,
R.H.Chen,
P.Mak,
and
T.J.Stout
(2004).
Crystal structures of the phosphorylated and unphosphorylated kinase domains of the Cdc42-associated tyrosine kinase ACK1.
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J Biol Chem,
279,
44039-44045.
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PDB codes:
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J.Griffith,
J.Black,
C.Faerman,
L.Swenson,
M.Wynn,
F.Lu,
J.Lippke,
and
K.Saxena
(2004).
The structural basis for autoinhibition of FLT3 by the juxtamembrane domain.
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Mol Cell,
13,
169-178.
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PDB code:
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S.R.Hubbard
(2004).
Juxtamembrane autoinhibition in receptor tyrosine kinases.
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Nat Rev Mol Cell Biol,
5,
464-471.
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S.Li,
N.D.Covino,
E.G.Stein,
J.H.Till,
and
S.R.Hubbard
(2003).
Structural and biochemical evidence for an autoinhibitory role for tyrosine 984 in the juxtamembrane region of the insulin receptor.
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J Biol Chem,
278,
26007-26014.
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PDB code:
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The most recent references are shown first.
Citation data come partly from CiteXplore and partly
from an automated harvesting procedure. Note that this is likely to be
only a partial list as not all journals are covered by
either method. However, we are continually building up the citation data
so more and more references will be included with time.
Where a reference describes a PDB structure, the PDB
codes are
shown on the right.
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}
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