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PDBsum entry 1ocs
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Sorting protein
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PDB id
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1ocs
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Contents |
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* Residue conservation analysis
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PDB id:
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Sorting protein
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Title:
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Crystal structure of the yeast px-doamin protein grd19p (sorting nexin3) complexed to phosphatidylinosytol-3-phosphate.
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Structure:
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Sorting nexin grd19. Chain: a. Fragment: px-domain, residues 1-162. Engineered: yes. Other_details: cysteine a91 chemically modified by beta mercapto- ethanol
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Source:
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Saccharomyces cerevisiae. Baker's yeast. Organism_taxid: 4932. Strain: s288c. Expressed in: escherichia coli. Expression_system_taxid: 469008. Other_details: cloned gene
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Resolution:
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2.03Å
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R-factor:
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0.217
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R-free:
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0.247
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Authors:
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C.Z.Zhou,I.Li De La Sierra-Gallay,S.Cheruel,B.Collinet,P.Minard, K.Blondeau,G.Henkes,R.Aufrere,N.Leulliot,M.Graille,I.Sorel, P.Savarin,F.De La Torre,A.Poupon,J.Janin,H.Van Tilbeurgh
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Key ref:
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C.Z.Zhou
et al.
(2003).
Crystal structure of the yeast Phox homology (PX) domain protein Grd19p complexed to phosphatidylinositol-3-phosphate.
J Biol Chem,
278,
50371-50376.
PubMed id:
DOI:
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Date:
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10-Feb-03
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Release date:
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12-Dec-03
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PROCHECK
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Headers
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References
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Q08826
(SNX3_YEAST) -
Sorting nexin-3 from Saccharomyces cerevisiae (strain ATCC 204508 / S288c)
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Seq: Struc:
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162 a.a.
132 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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*
PDB and UniProt seqs differ
at 1 residue position (black
cross)
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DOI no:
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J Biol Chem
278:50371-50376
(2003)
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PubMed id:
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Crystal structure of the yeast Phox homology (PX) domain protein Grd19p complexed to phosphatidylinositol-3-phosphate.
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C.Z.Zhou,
I.L.de La Sierra-Gallay,
S.Quevillon-Cheruel,
B.Collinet,
P.Minard,
K.Blondeau,
G.Henckes,
R.Aufrère,
N.Leulliot,
M.Graille,
I.Sorel,
P.Savarin,
F.de la Torre,
A.Poupon,
J.Janin,
H.van Tilbeurgh.
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ABSTRACT
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Phox homology (PX) domains have been recently identified in a number of
different proteins and are involved in various cellular functions such as
vacuolar targeting and membrane protein trafficking. It was shown that these
modules of about 130 amino acids specifically binding to phosphoinositides and
that this interaction is crucial for their cellular function. The yeast genome
contains 17 PX domain proteins. One of these, Grd19p, is involved in the
localization of the late Golgi membrane proteins DPAP A and Kex2p. Grd19p
consists of the PX domain with 30 extra residues at the N-terminal and is
homologous to the functionally characterized human sorting nexin protein SNX3.
We determined the 2.0 A crystal structure of Grd19p in the free form and in
complex with d-myo-phosphatidylinositol 3-phosphate (diC4PtdIns(3)P),
representing the first case of both free and ligand-bound conformations of the
same PX module. The ligand occupies a well defined positively charged binding
pocket at the interface between the beta-sheet and alpha-helical parts of the
molecule. The structure of the free and bound protein are globally similar but
show some significant differences in a region containing a polyproline peptide
and a putative membrane attachment site.
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Selected figure(s)
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Figure 3.
FIG. 3. A, stereo view of an omitted F[o] - F[c] electron
density map covering the bound diC4PtdIns(3)P, contoured at 3
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B, overall view of binding of diC4PtdIns(3)P to Grd19p. Helices
are colored yellow, strands green, and loop connections purple.
The ligand is represented in sticks (gray, carbon; red, oxygen;
and pink, phosphate). Some of the secondary structure elements
(Fig. 1) are labeled. C, detailed stereo view of diC4PtdIns(3)P
binding to Grd19p (yellow, carbon atoms; green, phosphate; red,
oxygen; and blue, nitrogen). Positions of the phosphate groups
of the ligand on the 1- and 3-OH position are labeled as P1 and
P3, respectively.
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Figure 4.
FIG. 4. A, stereo view of the superposition of the
ligand-bound (C atoms in yellow) and free form (C atoms in
wheat) of Grd19p. Residues in a radius of 5 Å around the
bound ligand are represented. B, stereo view of the
superposition of the ligand-binding sites of Grd19p and
p40^phox. Grd19p, same color code as Fig. 4A. p40^phox has
carbon atoms in green. Only the Grd19p residues are labeled.
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The above figures are
reprinted
by permission from the ASBMB:
J Biol Chem
(2003,
278,
50371-50376)
copyright 2003.
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Figures were
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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T.G.Kutateladze
(2010).
Translation of the phosphoinositide code by PI effectors.
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Nat Chem Biol,
6,
507-513.
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C.S.Wood,
K.R.Schmitz,
N.J.Bessman,
T.G.Setty,
K.M.Ferguson,
and
C.G.Burd
(2009).
PtdIns4P recognition by Vps74/GOLPH3 links PtdIns 4-kinase signaling to retrograde Golgi trafficking.
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J Cell Biol,
187,
967-975.
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PDB code:
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L.M.Koharudin,
W.Furey,
H.Liu,
Y.J.Liu,
and
A.M.Gronenborn
(2009).
The phox domain of sorting nexin 5 lacks phosphatidylinositol 3-phosphate (PtdIns(3)P) specificity and preferentially binds to phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2).
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J Biol Chem,
284,
23697-23707.
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F.Dancea,
K.Kami,
and
M.Overduin
(2008).
Lipid interaction networks of peripheral membrane proteins revealed by data-driven micelle docking.
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Biophys J,
94,
515-524.
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G.N.Parkinson,
D.Vines,
P.C.Driscoll,
and
S.Djordjevic
(2008).
Crystal structures of PI3K-C2alpha PX domain indicate conformational change associated with ligand binding.
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BMC Struct Biol,
8,
13.
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PDB codes:
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J.Song,
K.Q.Zhao,
C.L.Newman,
D.A.Vinarov,
and
J.L.Markley
(2007).
Solution structure of human sorting nexin 22.
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Protein Sci,
16,
807-814.
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PDB code:
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N.R.Blatner,
M.I.Wilson,
C.Lei,
W.Hong,
D.Murray,
R.L.Williams,
and
W.Cho
(2007).
The structural basis of novel endosome anchoring activity of KIF16B kinesin.
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EMBO J,
26,
3709-3719.
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PDB code:
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O.Pylypenko,
R.Lundmark,
E.Rasmuson,
S.R.Carlsson,
and
A.Rak
(2007).
The PX-BAR membrane-remodeling unit of sorting nexin 9.
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EMBO J,
26,
4788-4800.
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PDB codes:
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T.G.Kutateladze
(2007).
Mechanistic similarities in docking of the FYVE and PX domains to phosphatidylinositol 3-phosphate containing membranes.
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Prog Lipid Res,
46,
315-327.
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T.I.Strochlic,
T.G.Setty,
A.Sitaram,
and
C.G.Burd
(2007).
Grd19/Snx3p functions as a cargo-specific adapter for retromer-dependent endocytic recycling.
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J Cell Biol,
177,
115-125.
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M.L.Cheever,
T.G.Kutateladze,
and
M.Overduin
(2006).
Increased mobility in the membrane targeting PX domain induced by phosphatidylinositol 3-phosphate.
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Protein Sci,
15,
1873-1882.
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S.A.Lee,
J.Kovacs,
R.V.Stahelin,
M.L.Cheever,
M.Overduin,
T.G.Setty,
C.G.Burd,
W.Cho,
and
T.G.Kutateladze
(2006).
Molecular mechanism of membrane docking by the Vam7p PX domain.
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J Biol Chem,
281,
37091-37101.
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Q.Zhong,
M.J.Watson,
C.S.Lazar,
A.M.Hounslow,
J.P.Waltho,
and
G.N.Gill
(2005).
Determinants of the endosomal localization of sorting nexin 1.
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Mol Biol Cell,
16,
2049-2057.
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PDB code:
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W.Cho,
and
R.V.Stahelin
(2005).
Membrane-protein interactions in cell signaling and membrane trafficking.
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Annu Rev Biophys Biomol Struct,
34,
119-151.
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Y.Ano,
T.Hattori,
M.Oku,
H.Mukaiyama,
M.Baba,
Y.Ohsumi,
N.Kato,
and
Y.Sakai
(2005).
A sorting nexin PpAtg24 regulates vacuolar membrane dynamics during pexophagy via binding to phosphatidylinositol-3-phosphate.
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Mol Biol Cell,
16,
446-457.
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T.T.Tran,
I.Sorel,
and
A.Lewit-Bentley
(2004).
Statistical experimental design of protein crystallization screening revisited.
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Acta Crystallogr D Biol Crystallogr,
60,
1562-1568.
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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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