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1C28

THE CRYSTAL STRUCTURE OF A COMPLMENT-1Q FAMILY PROTEIN SUGGESTS AN EVOLUTIONARY LINK TO TUMOR NECROSIS FACTOR

Summary for 1C28
Entry DOI10.2210/pdb1c28/pdb
DescriptorPROTEIN (30 KD ADIPOCYTE COMPLEMENT-RELATED PROTEIN PRECURSOR (ACRP30)) (2 entities in total)
Functional Keywordsacrp30 c1q tnf trimer all-beta, serum protein
Biological sourceMus musculus (house mouse)
Cellular locationSecreted: Q60994
Total number of polymer chains3
Total formula weight46879.21
Authors
Shapiro, L.,Scherer, P. (deposition date: 1999-07-22, release date: 1999-08-04, Last modification date: 2024-02-07)
Primary citationShapiro, L.,Scherer, P.E.
The crystal structure of a complement-1q family protein suggests an evolutionary link to tumor necrosis factor.
Curr.Biol., 8:335-338, 1998
Cited by
PubMed Abstract: ACRP30--adipocyte complement-related protein of 30 kDa or AdipoQ--is an abundant serum protein, secreted exclusively from fat cells, which is implicated in energy homeostasis and obesity [1,2]. ACRP30 is a close homologue of the complement protein C1q, which is involved in the recognition of microbial surfaces [3-5] and antibody-antigen complexes [6,7] in the classical pathway of complement. We have determined the crystal structure of a homotrimeric fragment from ACRP30 at 2.1 A resolution. The structure reveals an unexpected homology to the tumor necrosis factor (TNF) family. Identical folding topologies, key residue conservations, and similarity of trimer interfaces and intron positions firmly establish an evolutionary link between the TNF and C1q families. We suggest that TNFs--which control many aspects of inflammation, adaptive immunity, apoptosis and energy homeostasis--arose by divergence from a primordial recognition molecule of the innate immune system. The evolutionary connection between C1q-like proteins and TNFs illuminates the shared functions of these two important groups of proteins.
PubMed: 9512423
DOI: 10.1016/S0960-9822(98)70133-2
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

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