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PDBsum entry 1kyu
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Endocytosis/exocytosis
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PDB id
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1kyu
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Contents |
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* Residue conservation analysis
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DOI no:
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Structure
10:797-809
(2002)
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PubMed id:
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Accessory protein recruitment motifs in clathrin-mediated endocytosis.
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T.J.Brett,
L.M.Traub,
D.H.Fremont.
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ABSTRACT
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Clathrin-mediated endocytosis depends upon the interaction of accessory proteins
with the alpha-ear of the AP-2 adaptor. We present structural characterization
of these regulatory interactions. DPF and DPW motif peptides derived from eps15
and epsin bind in type I beta turn conformations to a conserved pocket on the
alpha-ear platform. We show evidence for a second binding site that is DPW motif
specific. The structure of a complex with an AP-2 binding segment from
amphiphysin reveals a novel binding motif that we term FxDxF, which is engaged
in an extended conformation by a unique surface of the platform domain. The
FxDxF motif is also used by AP180 and the 170 kDa isoform of synaptojanin and
can be found in several potential endocytic proteins, including HIP1, CD2AP, and
PLAP. A mechanism of clathrin assembly regulation is suggested by three
different AP-2 engagement modes.
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Selected figure(s)
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Figure 1.
Figure 1. Experimental Evidence for DPF, DPW, and FxDxF
Motif Peptides Binding to the a-Ear(A) Ribbon representation of
the a-ear showing the binding sites of the FxDxF (extended
platform site) and DPW2 (distal site) peptides, with the
peptides shown as CPK models.(B-E) The fit of each peptide to
its corresponding simulated annealing omit electron density
contoured at 2.5 s.(B) The FxDxF peptide at 2.15 Å
resolution.(C) The DPF peptide (in P2[1]) at 1.22 Å
resolution.(D) The DPW1 peptide at 2.0 Å resolution.(E) The DPW2
peptide at 2.0 Å resolution. The orientation of the peptides
depicted in B, C, and D were achieved by superposition of the
a-ear platform domain. For the DPW2 peptide in (E), the Ca
coordinates were aligned with those of the DPF peptide. DPF,
cyan; DPW1, steel blue; DPW2, blue-green; FxDxF, magenta.
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The above figure is
reprinted
by permission from Cell Press:
Structure
(2002,
10,
797-809)
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.Harel,
F.Wu,
M.P.Mattson,
C.M.Morris,
and
P.J.Yao
(2008).
Evidence for CALM in Directing VAMP2 Trafficking.
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Traffic,
9,
417-429.
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C.J.DeRegis,
P.B.Rahl,
G.R.Hoffman,
R.A.Cerione,
and
R.N.Collins
(2008).
Mutational analysis of betaCOP (Sec26p) identifies an appendage domain critical for function.
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BMC Cell Biol,
9,
3.
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F.Buss,
and
J.Kendrick-Jones
(2008).
How are the cellular functions of myosin VI regulated within the cell?
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Biochem Biophys Res Commun,
369,
165-175.
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L.E.Olesen,
M.G.Ford,
E.M.Schmid,
Y.Vallis,
M.M.Babu,
P.H.Li,
I.G.Mills,
H.T.McMahon,
and
G.J.Praefcke
(2008).
Solitary and repetitive binding motifs for the AP2 complex alpha-appendage in amphiphysin and other accessory proteins.
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J Biol Chem,
283,
5099-5109.
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PDB code:
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L.Tomassi,
A.Costantini,
S.Corallino,
E.Santonico,
M.Carducci,
G.Cesareni,
and
L.Castagnoli
(2008).
The central proline rich region of POB1/REPS2 plays a regulatory role in epidermal growth factor receptor endocytosis by binding to 14-3-3 and SH3 domain-containing proteins.
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BMC Biochem,
9,
21.
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M.Sato,
K.Sato,
W.Liou,
S.Pant,
A.Harada,
and
B.D.Grant
(2008).
Regulation of endocytic recycling by C. elegans Rab35 and its regulator RME-4, a coated-pit protein.
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EMBO J,
27,
1183-1196.
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P.A.Keyel,
J.R.Thieman,
R.Roth,
E.Erkan,
E.T.Everett,
S.C.Watkins,
J.E.Heuser,
and
L.M.Traub
(2008).
The AP-2 adaptor beta2 appendage scaffolds alternate cargo endocytosis.
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Mol Biol Cell,
19,
5309-5326.
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R.I.Johnson,
M.J.Seppa,
and
R.L.Cagan
(2008).
The Drosophila CD2AP/CIN85 orthologue Cindr regulates junctions and cytoskeleton dynamics during tissue patterning.
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J Cell Biol,
180,
1191-1204.
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R.Mattera,
and
J.S.Bonifacino
(2008).
Ubiquitin binding and conjugation regulate the recruitment of Rabex-5 to early endosomes.
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EMBO J,
27,
2484-2494.
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S.Símová,
M.Klíma,
L.Cermak,
V.Sourková,
and
L.Andera
(2008).
Arf and Rho GAP adapter protein ARAP1 participates in the mobilization of TRAIL-R1/DR4 to the plasma membrane.
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Apoptosis,
13,
423-436.
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B.Ritter,
A.Y.Denisov,
J.Philie,
P.D.Allaire,
V.Legendre-Guillemin,
P.Zylbergold,
K.Gehring,
and
P.S.McPherson
(2007).
The NECAP PHear domain increases clathrin accessory protein binding potential.
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EMBO J,
26,
4066-4077.
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E.J.Ungewickell,
and
L.Hinrichsen
(2007).
Endocytosis: clathrin-mediated membrane budding.
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Curr Opin Cell Biol,
19,
417-425.
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G.Spudich,
M.V.Chibalina,
J.S.Au,
S.D.Arden,
F.Buss,
and
J.Kendrick-Jones
(2007).
Myosin VI targeting to clathrin-coated structures and dimerization is mediated by binding to Disabled-2 and PtdIns(4,5)P2.
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Nat Cell Biol,
9,
176-183.
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J.A.Ybe,
S.Mishra,
S.Helms,
and
J.Nix
(2007).
Crystal structure at 2.8 A of the DLLRKN-containing coiled-coil domain of huntingtin-interacting protein 1 (HIP1) reveals a surface suitable for clathrin light chain binding.
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J Mol Biol,
367,
8.
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PDB code:
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M.L.Kuravsky,
and
V.I.Muronetz
(2007).
Somatic and sperm-specific isoenzymes of glyceraldehyde-3-phosphate dehydrogenase: comparative analysis of primary structures and functional features.
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Biochemistry (Mosc),
72,
744-749.
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C.Knuehl,
C.Y.Chen,
V.Manalo,
P.K.Hwang,
N.Ota,
and
F.M.Brodsky
(2006).
Novel binding sites on clathrin and adaptors regulate distinct aspects of coat assembly.
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Traffic,
7,
1688-1700.
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M.A.Edeling,
C.Smith,
and
D.Owen
(2006).
Life of a clathrin coat: insights from clathrin and AP structures.
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Nat Rev Mol Cell Biol,
7,
32-44.
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M.Döring,
A.Loos,
N.Schrader,
B.Pfander,
and
R.Bauerfeind
(2006).
Nerve growth factor-induced phosphorylation of amphiphysin-1 by casein kinase 2 regulates clathrin-amphiphysin interactions.
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J Neurochem,
98,
2013-2022.
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M.J.Hawryluk,
P.A.Keyel,
S.K.Mishra,
S.C.Watkins,
J.E.Heuser,
and
L.M.Traub
(2006).
Epsin 1 is a polyubiquitin-selective clathrin-associated sorting protein.
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Traffic,
7,
262-281.
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S.Bruck,
T.B.Huber,
R.J.Ingham,
K.Kim,
H.Niederstrasser,
P.M.Allen,
T.Pawson,
J.A.Cooper,
and
A.S.Shaw
(2006).
Identification of a novel inhibitory actin-capping protein binding motif in CD2-associated protein.
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J Biol Chem,
281,
19196-19203.
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S.E.Dho,
J.Trejo,
D.P.Siderovski,
and
C.J.McGlade
(2006).
Dynamic regulation of mammalian numb by G protein-coupled receptors and protein kinase C activation: Structural determinants of numb association with the cortical membrane.
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Mol Biol Cell,
17,
4142-4155.
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T.J.Brett,
and
L.M.Traub
(2006).
Molecular structures of coat and coat-associated proteins: function follows form.
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Curr Opin Cell Biol,
18,
395-406.
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T.J.Brett,
V.Legendre-Guillemin,
P.S.McPherson,
and
D.H.Fremont
(2006).
Structural definition of the F-actin-binding THATCH domain from HIP1R.
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Nat Struct Mol Biol,
13,
121-130.
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PDB code:
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A.Meyerholz,
L.Hinrichsen,
S.Groos,
P.C.Esk,
G.Brandes,
and
E.J.Ungewickell
(2005).
Effect of clathrin assembly lymphoid myeloid leukemia protein depletion on clathrin coat formation.
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Traffic,
6,
1225-1234.
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J.D.Mancias,
and
J.Goldberg
(2005).
Exiting the endoplasmic reticulum.
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Traffic,
6,
278-285.
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J.Z.Rappoport,
A.Benmerah,
and
S.M.Simon
(2005).
Analysis of the AP-2 adaptor complex and cargo during clathrin-mediated endocytosis.
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Traffic,
6,
539-547.
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P.Monzo,
N.C.Gauthier,
F.Keslair,
A.Loubat,
C.M.Field,
Y.Le Marchand-Brustel,
and
M.Cormont
(2005).
Clues to CD2-associated protein involvement in cytokinesis.
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Mol Biol Cell,
16,
2891-2902.
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S.E.Holstein,
and
P.Oliviusson
(2005).
Sequence analysis of Arabidopsis thaliana E/ANTH-domain-containing proteins: membrane tethers of the clathrin-dependent vesicle budding machinery.
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Protoplasma,
226,
13-21.
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S.K.Mishra,
P.A.Keyel,
M.A.Edeling,
A.L.Dupin,
D.J.Owen,
and
L.M.Traub
(2005).
Functional dissection of an AP-2 beta2 appendage-binding sequence within the autosomal recessive hypercholesterolemia protein.
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J Biol Chem,
280,
19270-19280.
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A.Jha,
N.R.Agostinelli,
S.K.Mishra,
P.A.Keyel,
M.J.Hawryluk,
and
L.M.Traub
(2004).
A novel AP-2 adaptor interaction motif initially identified in the long-splice isoform of synaptojanin 1, SJ170.
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J Biol Chem,
279,
2281-2290.
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B.Ritter,
A.Y.Denisov,
J.Philie,
C.Deprez,
E.C.Tung,
K.Gehring,
and
P.S.McPherson
(2004).
Two WXXF-based motifs in NECAPs define the specificity of accessory protein binding to AP-1 and AP-2.
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EMBO J,
23,
3701-3710.
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D.J.Owen,
B.M.Collins,
and
P.R.Evans
(2004).
Adaptors for clathrin coats: structure and function.
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Annu Rev Cell Dev Biol,
20,
153-191.
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G.J.Praefcke,
M.G.Ford,
E.M.Schmid,
L.E.Olesen,
J.L.Gallop,
S.Y.Peak-Chew,
Y.Vallis,
M.M.Babu,
I.G.Mills,
and
H.T.McMahon
(2004).
Evolving nature of the AP2 alpha-appendage hub during clathrin-coated vesicle endocytosis.
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EMBO J,
23,
4371-4383.
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PDB code:
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H.T.McMahon,
and
I.G.Mills
(2004).
COP and clathrin-coated vesicle budding: different pathways, common approaches.
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Curr Opin Cell Biol,
16,
379-391.
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J.S.Bonifacino
(2004).
The GGA proteins: adaptors on the move.
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Nat Rev Mol Cell Biol,
5,
23-32.
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P.J.Watson,
G.Frigerio,
B.M.Collins,
R.Duden,
and
D.J.Owen
(2004).
Gamma-COP appendage domain - structure and function.
|
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Traffic,
5,
79-88.
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PDB code:
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R.Mattera,
B.Ritter,
S.S.Sidhu,
P.S.McPherson,
and
J.S.Bonifacino
(2004).
Definition of the consensus motif recognized by gamma-adaptin ear domains.
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J Biol Chem,
279,
8018-8028.
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S.K.Mishra,
M.J.Hawryluk,
T.J.Brett,
P.A.Keyel,
A.L.Dupin,
A.Jha,
J.E.Heuser,
D.H.Fremont,
and
L.M.Traub
(2004).
Dual engagement regulation of protein interactions with the AP-2 adaptor alpha appendage.
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J Biol Chem,
279,
46191-46203.
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T.R.Dafforn,
and
C.J.Smith
(2004).
Natively unfolded domains in endocytosis: hooks, lines and linkers.
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EMBO Rep,
5,
1046-1052.
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W.X.Schulze,
and
M.Mann
(2004).
A novel proteomic screen for peptide-protein interactions.
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J Biol Chem,
279,
10756-10764.
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B.M.Collins,
G.J.Praefcke,
M.S.Robinson,
and
D.J.Owen
(2003).
Structural basis for binding of accessory proteins by the appendage domain of GGAs.
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Nat Struct Biol,
10,
607-613.
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PDB code:
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B.Ritter,
J.Philie,
M.Girard,
E.C.Tung,
F.Blondeau,
and
P.S.McPherson
(2003).
Identification of a family of endocytic proteins that define a new alpha-adaptin ear-binding motif.
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EMBO Rep,
4,
1089-1095.
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C.Knuehl,
and
F.M.Brodsky
(2003).
The long and short of adaptor appendages.
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Nat Struct Biol,
10,
580-582.
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G.J.Miller,
R.Mattera,
J.S.Bonifacino,
and
J.H.Hurley
(2003).
Recognition of accessory protein motifs by the gamma-adaptin ear domain of GGA3.
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Nat Struct Biol,
10,
599-606.
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PDB code:
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G.R.Hoffman,
P.B.Rahl,
R.N.Collins,
and
R.A.Cerione
(2003).
Conserved structural motifs in intracellular trafficking pathways: structure of the gammaCOP appendage domain.
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Mol Cell,
12,
615-625.
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PDB code:
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I.G.Mills,
G.J.Praefcke,
Y.Vallis,
B.J.Peter,
L.E.Olesen,
J.L.Gallop,
P.J.Butler,
P.R.Evans,
and
H.T.McMahon
(2003).
EpsinR: an AP1/clathrin interacting protein involved in vesicle trafficking.
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J Cell Biol,
160,
213-222.
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J.S.Bonifacino,
and
L.M.Traub
(2003).
Signals for sorting of transmembrane proteins to endosomes and lysosomes.
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Annu Rev Biochem,
72,
395-447.
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K.Farsad,
and
P.De Camilli
(2003).
Mechanisms of membrane deformation.
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Curr Opin Cell Biol,
15,
372-381.
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K.Nakayama,
and
S.Wakatsuki
(2003).
The structure and function of GGAs, the traffic controllers at the TGN sorting crossroads.
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Cell Struct Funct,
28,
431-442.
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M.C.Duncan,
G.Costaguta,
and
G.S.Payne
(2003).
Yeast epsin-related proteins required for Golgi-endosome traffic define a gamma-adaptin ear-binding motif.
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Nat Cell Biol,
5,
77-81.
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M.C.Duncan,
and
G.S.Payne
(2003).
ENTH/ANTH domains expand to the Golgi.
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Trends Cell Biol,
13,
211-215.
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R.Mattera,
C.N.Arighi,
R.Lodge,
M.Zerial,
and
J.S.Bonifacino
(2003).
Divalent interaction of the GGAs with the Rabaptin-5-Rabex-5 complex.
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EMBO J,
22,
78-88.
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T.B.Huber,
M.Schmidts,
P.Gerke,
B.Schermer,
A.Zahn,
B.Hartleben,
L.Sellin,
G.Walz,
and
T.Benzing
(2003).
The carboxyl terminus of Neph family members binds to the PDZ domain protein zonula occludens-1.
|
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J Biol Chem,
278,
13417-13421.
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U.Andag,
and
H.D.Schmitt
(2003).
Dsl1p, an essential component of the Golgi-endoplasmic reticulum retrieval system in yeast, uses the same sequence motif to interact with different subunits of the COPI vesicle coat.
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J Biol Chem,
278,
51722-51734.
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U.Scheele,
J.Alves,
R.Frank,
M.Duwel,
C.Kalthoff,
and
E.Ungewickell
(2003).
Molecular and functional characterization of clathrin- and AP-2-binding determinants within a disordered domain of auxilin.
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J Biol Chem,
278,
25357-25368.
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B.Wendland
(2002).
Epsins: adaptors in endocytosis?
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Nat Rev Mol Cell Biol,
3,
971-977.
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S.K.Mishra,
P.A.Keyel,
M.J.Hawryluk,
N.R.Agostinelli,
S.C.Watkins,
and
L.M.Traub
(2002).
Disabled-2 exhibits the properties of a cargo-selective endocytic clathrin adaptor.
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EMBO J,
21,
4915-4926.
|
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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
code is
shown on the right.
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}
}
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