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2X5K

Structure of an active site mutant of the D-Erythrose-4-Phosphate Dehydrogenase from E. coli

Functional Information from GO Data
ChainGOidnamespacecontents
O0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
O0005737cellular_componentcytoplasm
O0005829cellular_componentcytosol
O0006006biological_processglucose metabolic process
O0008615biological_processpyridoxine biosynthetic process
O0016491molecular_functionoxidoreductase activity
O0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
O0042823biological_processpyridoxal phosphate biosynthetic process
O0048001molecular_functionerythrose-4-phosphate dehydrogenase activity
O0051287molecular_functionNAD binding
P0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
P0005737cellular_componentcytoplasm
P0005829cellular_componentcytosol
P0006006biological_processglucose metabolic process
P0008615biological_processpyridoxine biosynthetic process
P0016491molecular_functionoxidoreductase activity
P0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
P0042823biological_processpyridoxal phosphate biosynthetic process
P0048001molecular_functionerythrose-4-phosphate dehydrogenase activity
P0051287molecular_functionNAD binding
Q0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
Q0005737cellular_componentcytoplasm
Q0005829cellular_componentcytosol
Q0006006biological_processglucose metabolic process
Q0008615biological_processpyridoxine biosynthetic process
Q0016491molecular_functionoxidoreductase activity
Q0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
Q0042823biological_processpyridoxal phosphate biosynthetic process
Q0048001molecular_functionerythrose-4-phosphate dehydrogenase activity
Q0051287molecular_functionNAD binding
R0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
R0005737cellular_componentcytoplasm
R0005829cellular_componentcytosol
R0006006biological_processglucose metabolic process
R0008615biological_processpyridoxine biosynthetic process
R0016491molecular_functionoxidoreductase activity
R0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
R0042823biological_processpyridoxal phosphate biosynthetic process
R0048001molecular_functionerythrose-4-phosphate dehydrogenase activity
R0051287molecular_functionNAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL P 1335
ChainResidue
PASP323
PHOH2022
PHOH2245

site_idAC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE GOL R 1334
ChainResidue
RALA54
RTRP55

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL R 1335
ChainResidue
RHOH2203
OASN123
RLEU33
RALA34
RHIS75

site_idAC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE GOL O 1336
ChainResidue
OALA164
OHOH2147

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL P 1336
ChainResidue
PGLU86
PHOH2029
PHOH2246

site_idAC6
Number of Residues1
DetailsBINDING SITE FOR RESIDUE EDO O 1337
ChainResidue
OVAL98

site_idAC7
Number of Residues1
DetailsBINDING SITE FOR RESIDUE EDO P 1337
ChainResidue
PTRP55

site_idAC8
Number of Residues1
DetailsBINDING SITE FOR RESIDUE EDO R 1336
ChainResidue
RHOH2170

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PG4 O 1338
ChainResidue
OALA38
OHOH2257
PARG142
PARG334
RLEU193

site_idBC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL P 1338
ChainResidue
PTHR48
QARG197
QALA198

site_idBC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL O 1339
ChainResidue
OTHR48
RARG197
RALA198

site_idBC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL Q 1339
ChainResidue
PARG197
PALA198
QTHR48

site_idBC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE PEG P 1340
ChainResidue
PARG58
PGLU60

site_idBC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE PEG P 1341
ChainResidue
QLEU193

site_idBC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE PGE O 1340
ChainResidue
OGLN264
OHIS268

site_idBC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PGE P 1342
ChainResidue
PGLU103
PALA110
PHOH2109
RTYR188
RHIS190

site_idBC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PGE Q 1336
ChainResidue
QGLY97
QVAL98
QGLY100
QHIS120
QSER122

site_idBC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PGE P 1343
ChainResidue
PVAL98
PTYR99
PHIS104
RHOH2075

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Nucleophile => ECO:0000250
ChainResidueDetails
OALA149
PALA149
QALA149
RALA149

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000250
ChainResidueDetails
OARG10
RARG10
RARG77
RASN313
OARG77
OASN313
PARG10
PARG77
PASN313
QARG10
QARG77
QASN313

site_idSWS_FT_FI3
Number of Residues16
DetailsBINDING: BINDING => ECO:0000255
ChainResidueDetails
OSER148
QARG195
QTHR208
QARG231
RSER148
RARG195
RTHR208
RARG231
OARG195
OTHR208
OARG231
PSER148
PARG195
PTHR208
PARG231
QSER148

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Activates thiol group during catalysis => ECO:0000250
ChainResidueDetails
OHIS176
PHIS176
QHIS176
RHIS176

223166

PDB entries from 2024-07-31

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