PDB Information

PDB6NLH
MethodX-RAY DIFFRACTION
Host OrganismEscherichia coli BL21(DE3)
Gene SourceHomo sapiens
Primary Citation
Missense variant in TPI1 (Arg189Gln) causes neurologic deficits through structural changes in the triosephosphate isomerase catalytic site and reduced enzyme levels in vivo.
Roland, 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.
Biochim Biophys Acta Mol Basis Dis
HeaderIsomerase
Released2019-01-08
Resolution2.200
CATH Insert Date23 Jun, 2019

PDB Images (9)

PDB Prints

PDB Chains (8)

Chain ID Date inserted into CATH CATH Status
A 23 Jun, 2019 New
B 23 Jun, 2019 New
C 23 Jun, 2019 New
D 23 Jun, 2019 New
E 23 Jun, 2019 New
F 23 Jun, 2019 New
G 23 Jun, 2019 New
H 23 Jun, 2019 New

CATH Domains (0)

Domain ID Date inserted into CATH Superfamily CATH Status

UniProtKB Entries (8)

Accession Gene ID Taxon Description
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase
P60174 TPIS_HUMAN Homo sapiens Triosephosphate isomerase