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5UFJ

Crystal Structure of Carbonmonoxy Hemoglobin S (Liganded Sickle Cell Hemoglobin) Complexed with GBT Compound 6

Summary for 5UFJ
Entry DOI10.2210/pdb5ufj/pdb
Related5U3I
DescriptorHemoglobin subunit alpha, Hemoglobin subunit beta, PROTOPORPHYRIN IX CONTAINING FE, ... (6 entities in total)
Functional Keywordsr2 quaternary state, oxygen transport
Biological sourceHomo sapiens (Human)
More
Total number of polymer chains4
Total formula weight65165.69
Authors
Partridge, J.R.,Choy, R.M.,Li, Z.,Metcalf, B. (deposition date: 2017-01-04, release date: 2017-02-22, Last modification date: 2024-11-20)
Primary citationMetcalf, B.,Chuang, C.,Dufu, K.,Patel, M.P.,Silva-Garcia, A.,Johnson, C.,Lu, Q.,Partridge, J.R.,Patskovska, L.,Patskovsky, Y.,Almo, S.C.,Jacobson, M.P.,Hua, L.,Xu, Q.,Gwaltney, S.L.,Yee, C.,Harris, J.,Morgan, B.P.,James, J.,Xu, D.,Hutchaleelaha, A.,Paulvannan, K.,Oksenberg, D.,Li, Z.
Discovery of GBT440, an Orally Bioavailable R-State Stabilizer of Sickle Cell Hemoglobin.
ACS Med Chem Lett, 8:321-326, 2017
Cited by
PubMed Abstract: We report the discovery of a new potent allosteric effector of sickle cell hemoglobin, GBT440 (), that increases the affinity of hemoglobin for oxygen and consequently inhibits its polymerization when subjected to hypoxic conditions. Unlike earlier allosteric activators that bind covalently to hemoglobin in a 2:1 stoichiometry, binds with a 1:1 stoichiometry. Compound is orally bioavailable and partitions highly and favorably into the red blood cell with a RBC/plasma ratio of ∼150. This partitioning onto the target protein is anticipated to allow therapeutic concentrations to be achieved in the red blood cell at low plasma concentrations. GBT440 () is in Phase 3 clinical trials for the treatment of sickle cell disease (NCT03036813).
PubMed: 28337324
DOI: 10.1021/acsmedchemlett.6b00491
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.05 Å)
Structure validation

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