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3T9K

Crystal Structure of ACAP1 C-portion mutant S554D fused with integrin beta1 peptide

Summary for 3T9K
Entry DOI10.2210/pdb3t9k/pdb
DescriptorArf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 1,Peptide from Integrin beta-1, ZINC ION, SULFATE ION, ... (4 entities in total)
Functional Keywordsarfgap domain, ank repeat, zinc-binding module, protein transport
Biological sourceHomo sapiens (Human)
More
Cellular locationCell membrane ; Single-pass type I membrane protein . Isoform 5: Cell membrane, sarcolemma : P05556
Total number of polymer chains2
Total formula weight83526.88
Authors
Sun, F.,Pang, X.,Zhang, K.,Ma, J.,Zhou, Q. (deposition date: 2011-08-03, release date: 2012-07-18, Last modification date: 2023-11-01)
Primary citationBai, M.,Pang, X.,Lou, J.,Zhou, Q.,Zhang, K.,Ma, J.,Li, J.,Sun, F.,Hsu, V.W.
Mechanistic insights into regulated cargo binding by ACAP1 protein
J.Biol.Chem., 287:28675-28685, 2012
Cited by
PubMed Abstract: Coat complexes sort protein cargoes into vesicular transport pathways. An emerging class of coat components has been the GTPase-activating proteins (GAPs) that act on the ADP-ribosylation factor (ARF) family of small GTPases. ACAP1 (ArfGAP with coiled-coil, ankyrin repeat, and PH domains protein 1) is an ARF6 GAP that also acts as a key component of a recently defined clathrin complex for endocytic recycling. Phosphorylation by Akt has been shown to enhance cargo binding by ACAP1 in explaining how integrin recycling is an example of regulated transport. We now shed further mechanistic insights into how this regulation is achieved at the level of cargo binding by ACAP1. We initially defined a critical sequence in the cytoplasmic domain of integrin β1 recognized by ACAP1 and showed that this sequence acts as a recycling sorting signal. We then pursued a combination of structural, modeling, and functional studies, which suggest that phosphorylation of ACAP1 relieves a localized mechanism of autoinhibition in regulating cargo binding. Thus, we have elucidated a key regulatory juncture that controls integrin recycling and also advanced the understanding of how regulated cargo binding can lead to regulated transport.
PubMed: 22645133
DOI: 10.1074/jbc.M112.378810
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.3 Å)
Structure validation

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数据于2024-10-30公开中

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