Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

7STA

X-ray Crystal Structure of Truncated Human Chemokine CCL19 (7-70)

Summary for 7STA
Entry DOI10.2210/pdb7sta/pdb
DescriptorC-C motif chemokine 19 (2 entities in total)
Functional Keywordsccl19, chemokine, signaling protein
Biological sourceHomo sapiens (Human)
Total number of polymer chains4
Total formula weight29394.58
Authors
Lewandowski, E.M.,Kroeck, K.,Chen, Y. (deposition date: 2021-11-12, release date: 2022-02-23, Last modification date: 2024-11-13)
Primary citationLewandowski, E.M.,Kroeck, K.G.,Jacobs, L.M.C.,Fenske, T.G.,Witt, R.N.,Hintz, A.M.,Ramsden, E.R.,Zhang, X.,Peterson, F.,Volkman, B.F.,Veldkamp, C.T.,Chen, Y.
Structural Insights into Molecular Recognition by Human Chemokine CCL19.
Biochemistry, 61:311-318, 2022
Cited by
PubMed Abstract: The human chemokines CCL19 and CCL21 bind to the G protein-coupled receptor (GPCR) CCR7 and play an important role in the trafficking of immune cells as well as cancer metastasis. Conserved binding sites for sulfotyrosine residues on the receptor contribute significantly to the chemokine/GPCR interaction and have been shown to provide promising targets for new drug-discovery efforts to disrupt the chemokine/GPCR interaction and, consequently, tumor metastasis. Here, we report the first X-ray crystal structure of a truncated CCL19 (residues 7-70) at 2.50 Å resolution, revealing molecular details crucial for protein-protein interactions. Although the overall structure is similar to the previously determined NMR model, there are important variations, particularly near the N terminus and the so-called 30's and 40's loops. Computational analysis using the FTMap server indicates the potential importance of these areas in ligand binding and the differences in binding hotspots compared to CCL21. NMR titration experiments using a CCR7-derived peptide (residues 5-11, TDDYIGD) further demonstrate potential receptor recognition sites, such as those near the C terminus and 40's loop, which consist of both positively charged and hydrophobic residues that may be important for receptor binding. Taken together, the X-ray, NMR, and computational analysis herein provide insights into the overall structure and molecular features of CCL19 and enables investigation into this chemokine's function and inhibitor development.
PubMed: 35156805
DOI: 10.1021/acs.biochem.1c00759
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.5 Å)
Structure validation

246704

PDB entries from 2025-12-24

PDB statisticsPDBj update infoContact PDBjnumon