HUMAN HGPRTASE WITH TRANSITION STATE INHIBITOR
The structure was published by Shi, W., Li, C.M., Tyler, P.C., et al., Grubmeyer, C., Schramm, V.L., and Almo, S.C., in 1999 in a paper entitled "The 2.0 A structure of human hypoxanthine-guanine phosphoribosyltransferase in complex with a transition-state analog inhibitor." (abstract).
This crystal structure was determined using X-ray diffraction at a resolution of 2.0 Å and deposited in 1998.
The experimental data on which the structure is based was also deposited.
This PDB entry contains multiple copies of the structure of HYPOXANTHINE-GUANINE PHOSPHORIBOSYLTRANSFERASE.
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 homotetramers.
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 1 unique UniProt protein: