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5DPW

Crystal structure of PLEKHM1 LIR in complex with human LC3C_8-125

Summary for 5DPW
Entry DOI10.2210/pdb5dpw/pdb
Related5DPR 5DPS 5DPT
DescriptorMicrotubule-associated proteins 1A/1B light chain 3C, Pleckstrin homology domain-containing family M member 1 (3 entities in total)
Functional Keywordsautophagy, protein binding
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains16
Total formula weight124438.75
Authors
Ravichandran, A.C.,Suzuki, H.,Dobson, R.C.J. (deposition date: 2015-09-14, release date: 2016-09-28, Last modification date: 2024-03-06)
Primary citationRogov, V.V.,Stolz, A.,Ravichandran, A.C.,Rios-Szwed, D.O.,Suzuki, H.,Kniss, A.,Lohr, F.,Wakatsuki, S.,Dotsch, V.,Dikic, I.,Dobson, R.C.,McEwan, D.G.
Structural and functional analysis of the GABARAP interaction motif (GIM).
EMBO Rep., 18:1382-1396, 2017
Cited by
PubMed Abstract: Through the canonical LC3 interaction motif (LIR), [W/F/Y]-X-X-[I/L/V], protein complexes are recruited to autophagosomes to perform their functions as either autophagy adaptors or receptors. How these adaptors/receptors selectively interact with either LC3 or GABARAP families remains unclear. Herein, we determine the range of selectivity of 30 known core LIR motifs towards individual LC3s and GABARAPs. From these, we define a ABARAP nteraction otif (GIM) sequence ([W/F]-[V/I]-X-V) that the adaptor protein PLEKHM1 tightly conforms to. Using biophysical and structural approaches, we show that the PLEKHM1-LIR is indeed 11-fold more specific for GABARAP than LC3B. Selective mutation of the X and X positions either completely abolished the interaction with all LC3 and GABARAPs or increased PLEKHM1-GIM selectivity 20-fold towards LC3B. Finally, we show that conversion of p62/SQSTM1, FUNDC1 and FIP200 LIRs into our newly defined GIM, by introducing two valine residues, enhances their interaction with endogenous GABARAP over LC3B. The identification of a GABARAP-specific interaction motif will aid the identification and characterization of the expanding array of autophagy receptor and adaptor proteins and their functions.
PubMed: 28655748
DOI: 10.15252/embr.201643587
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.185 Å)
Structure validation

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数据于2024-10-30公开中

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