3T9K
Crystal Structure of ACAP1 C-portion mutant S554D fused with integrin beta1 peptide
Summary for 3T9K
Entry DOI | 10.2210/pdb3t9k/pdb |
Descriptor | Arf-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 Keywords | arfgap domain, ank repeat, zinc-binding module, protein transport |
Biological source | Homo sapiens (Human) More |
Cellular location | Cell membrane ; Single-pass type I membrane protein . Isoform 5: Cell membrane, sarcolemma : P05556 |
Total number of polymer chains | 2 |
Total formula weight | 83526.88 |
Authors | |
Primary citation | Bai, 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: 22645133DOI: 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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