Crystal structure of cysteine protease inhibitor, chagasin, in complex with human cathepsin L
The structure was published by Ljunggren, A., Redzynia, I., Alvarez-Fernandez, M., et al., Krupa, J.C., Jaskolski, M., and Bujacz, G., in 2007 in a paper entitled "Crystal structure of the parasite protease inhibitor chagasin in complex with a host target cysteine protease" (abstract).
This crystal structure was determined using X-ray diffraction at a resolution of 1.75 Å and deposited in 2006.
The experimental data on which the structure is based was also deposited.
This PDB entry contains a complex of 2 biomacromolecules, namely Chagasin and Cathepsin L.
It also contains one or more heterogenic compounds (e.g., ligands, co-factors, ions, modified amino acids, etc.); see here for a complete list.
The molecule most likely forms heterodimers.
The following tables show cross-reference information to other databases (to obtain a list of all PDB entries sharing the same property or classification, click on the magnifying glass icon):
This entry contains 2 unique UniProt proteins: