PDBsum entry: 2hqh

Structural protein, protein binding

PDB-id: 2hqh

Contents

Description

Header details

Header records

References

PROCHECK

Protein chains

72 a.a. *

22 a.a. *

Metal ions

_ZN ×4

Waters ×500

* Residue conservation analysis

Tools

Clefts Calculation

PDB id:

2hqh

Name:

Structural protein, protein binding

Title:

Crystal structure of p150glued and clip-170

Structure:

Dynactin-1. Chain: a, b, c, d. Fragment: cap-gly domain, residues 15-107. Synonym: 150 kda dynein-associated polypeptide, dp-150, dap-150, p150-glued, p135. Engineered: yes. Restin. Chain: e, f, g, h. Fragment: second zinc finger domain, residues 1405-1427.

Source:

Homo sapiens. Human. Organism_taxid: 9606. Gene: dctn1. Expressed in: escherichia coli bl21(de3). Expression_system_taxid: 469008. Gene: rsn, cyln1.

UniProt:

Chains A, B, C, D: Q14203 (DCTN1_HUMAN)

Seq:
Struc:
	Seq:
	Struc:
Seq:
Struc:
	Seq:
	Struc:
Seq:
Struc:
	Seq:	1278 a.a.
	Struc:	72 a.a.

Chains E, F, G, H: P30622 (CLIP1_HUMAN)

Seq:

Struc:

Seq:

Struc:

Seq:

Struc:

Seq:

Struc:

Seq:

Struc:

Seq:

1438 a.a.

Struc:

22 a.a.

Key:	PfamA domain	PfamB domain
Secondary structure

Resolution:

1.80Å

R-factor:

0.194

R-free:

0.215

Authors:

I.Hayashi,M.Ikura

Key ref:

I.Hayashi et al. (2007). CLIP170 autoinhibition mimics intermolecular interactions with p150Glued or EB1.. Nat Struct Biol, 14, 980-981. [PubMed id: 17828275] [DOI: 10.1038/nsmb1299]

Date:

18-Jul-06

Release date:

21-Aug-07

Related entries:

1txq
crystal structure of the eb1 c-terminal domain complexed
with the cap-gly domain of p150glued

Quick_links

Procheck

Surface

Key reference

DOI no: 10.1038/nsmb1299

Nat Struct Biol 14:980-981 (2007)

PubMed id: 17828275

CLIP170 autoinhibition mimics intermolecular interactions with p150Glued or EB1.

I.Hayashi, M.J.Plevin, M.Ikura.

ABSTRACT

CLIP170 and p150(Glued) localize to the plus ends of growing microtubules. Using crystallography and NMR, we show that autoinhibitory interactions within CLIP170 use the same binding determinants as CLIP170's intermolecular interactions with p150(Glued). These interactions have both similar and distinct features when compared with the p150(Glued)-EB1 complex. Our data thus demonstrate that regulation of microtubule dynamics by plus end-tracking proteins (+TIPs) occurs through direct competition between homologous binding interfaces.

Selected figure(s)

Figure 1.
(a) Surface representation of p150n with C traces of ClipZn2 (pink) and p150n (green). Key interacting side chains are shown as sticks (green atoms are sulfur). Blue, GKNDG motif; orange, conserved hydrophobic residues (Phe52, Trp57 and Phe88; Supplementary Fig. 3 online). Red circled region is expanded in b. (b) Close-up views of interface between ClipZn2 and p150n. Middle panel has same orientation as in a. Residues discussed in the text are labeled. Orange sphere, water molecule mediating the Arg90-Asn1422 interaction. (c) Pull-down assays of wild-type and mutant ClipZn12 and p150n. p150n proteins were incubated with glutathione S-transferase (GST)-fused ClipZn12 proteins. Left lane contains wild-type p150n, for reference. Mock pull-down is shown as a control (see Supplementary Table 2).

Figure 2.
(a) NMR chemical shift perturbations induced by binding of ClipZn12, mapped onto the surface of ClipCG1 (left; PDB 2CP7) and ClipCG2 (right; PDB 2CP6). The two panels show equivalent views. Purple residues are missing from the HSQC spectra owing to chemical exchanges. See Supplementary Figure 2. (b) Sequence alignments of ClipCG domains. ClipCG1 and ClipCG2 of human, Xenopus laevis and zebrafish CLIP170, human CLIP115 and Drosophila CLIP190 are shown. The single ClipCG domains of p150n, fission yeast Tip1p and budding yeast Bik1 are also shown. Green highlight, GKNDG motif; blue, its invariant lysine residue; red, arginine residues conserved in ClipCG1 (and p150n); orange, lysine and histidine conserved in ClipCG2. (c,d) In vitro assays of wild-type or mutant ClipCG1 and ClipCG2 binding to ClipZn12 (c; see Supplementary Table 2) or MTs (d). ClipCG1, ClipCG2 and mutants were detected by Coomassie staining after SDS-PAGE. Input lanes show wild-type ClipCG domains, for reference. All the mutations abrogate binding to ClipZn12 or MTs.

The above figures are reprinted by permission from Macmillan Publishers Ltd: Nat Struct Biol (2007, 14, 980-981) copyright 2007.