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6NLH

Structure of human triose phosphate isomerase R189A

Summary for 6NLH
Entry DOI10.2210/pdb6nlh/pdb
DescriptorTriosephosphate isomerase, SODIUM ION, BROMIDE ION, ... (5 entities in total)
Functional Keywordsisomerase
Biological sourceHomo sapiens (Human)
Total number of polymer chains8
Total formula weight210990.36
Authors
Richards, K.R.,Roland, B.P.,Palladino, M.J.,VanDemark, A.P. (deposition date: 2019-01-08, release date: 2019-06-19, Last modification date: 2023-10-11)
Primary citationRoland, B.P.,Richards, K.R.,Hrizo, S.L.,Eicher, S.,Barile, Z.J.,Chang, T.C.,Savon, G.,Bianchi, P.,Fermo, E.,Ricerca, B.M.,Tortorolo, L.,Vockley, J.,VanDemark, A.P.,Palladino, M.J.
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo.
Biochim Biophys Acta Mol Basis Dis, 1865:2257-2266, 2019
Cited by
PubMed: 31075491
DOI: 10.1016/j.bbadis.2019.05.002
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.199 Å)
Structure validation

218500

數據於2024-04-17公開中

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