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1NQA

Glyceraldehyde-3-Phosphate Dehydrogenase Mutant With Cys 149 Replaced By Ala Complexed With Nad+ and D-Glyceraldehyde-3-Phosphate

Functional Information from GO Data
ChainGOidnamespacecontents
O0000166molecular_functionnucleotide binding
O0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
O0005737cellular_componentcytoplasm
O0006006biological_processglucose metabolic process
O0006096biological_processglycolytic process
O0016491molecular_functionoxidoreductase activity
O0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
O0030554molecular_functionadenyl nucleotide binding
O0050661molecular_functionNADP binding
O0051287molecular_functionNAD binding
P0000166molecular_functionnucleotide binding
P0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
P0005737cellular_componentcytoplasm
P0006006biological_processglucose metabolic process
P0006096biological_processglycolytic process
P0016491molecular_functionoxidoreductase activity
P0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
P0030554molecular_functionadenyl nucleotide binding
P0050661molecular_functionNADP binding
P0051287molecular_functionNAD binding
Q0000166molecular_functionnucleotide binding
Q0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
Q0005737cellular_componentcytoplasm
Q0006006biological_processglucose metabolic process
Q0006096biological_processglycolytic process
Q0016491molecular_functionoxidoreductase activity
Q0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
Q0030554molecular_functionadenyl nucleotide binding
Q0050661molecular_functionNADP binding
Q0051287molecular_functionNAD binding
R0000166molecular_functionnucleotide binding
R0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
R0005737cellular_componentcytoplasm
R0006006biological_processglucose metabolic process
R0006096biological_processglycolytic process
R0016491molecular_functionoxidoreductase activity
R0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
R0030554molecular_functionadenyl nucleotide binding
R0050661molecular_functionNADP binding
R0051287molecular_functionNAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues30
DetailsBINDING SITE FOR RESIDUE NAD O 1336
ChainResidue
OGLY7
OTHR96
OGLY97
OPHE99
OSER119
OALA120
OASN180
OASN313
OTYR317
OG3H1337
OHOH1353
OGLY9
OHOH1354
OHOH1356
OHOH1367
OHOH1380
OHOH1388
OHOH1560
OHOH1561
OHOH1572
OHOH1621
OHOH4504
OARG10
OHOH4506
OILE11
OASN31
OASP32
OGLU76
OARG77
OSER95

site_idAC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE G3H O 1337
ChainResidue
OALA149
OTHR150
OHIS176
OTHR179
OARG195
OARG231
ONAD1336
OHOH1353
OHOH1440
OHOH1621

site_idAC3
Number of Residues31
DetailsBINDING SITE FOR RESIDUE NAD P 2336
ChainResidue
PGLY7
PGLY9
PARG10
PILE11
PASN31
PASP32
PGLU76
PARG77
PSER95
PTHR96
PGLY97
PARG98
PPHE99
PSER119
PALA120
PASN180
PASN313
PTYR317
PG3H2337
PHOH2353
PHOH2354
PHOH2356
PHOH2366
PHOH2367
PHOH2380
PHOH2388
PHOH2416
PHOH2541
PHOH2555
PHOH2563
QHOH2373

site_idAC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE G3H P 2337
ChainResidue
PALA149
PTHR150
PHIS176
PTHR179
PARG195
PARG231
PNAD2336
PHOH2353
PHOH2608
PHOH2621

site_idAC5
Number of Residues32
DetailsBINDING SITE FOR RESIDUE NAD Q 3336
ChainResidue
QTYR317
QHOH2508
QHOH2514
QHOH2578
QG3H3337
QHOH3353
QHOH3354
QHOH3356
QHOH3367
QHOH3373
QHOH3380
QHOH3388
QHOH3430
QHOH3534
QGLY7
QGLY9
QARG10
QILE11
QASN31
QASP32
QLEU33
QGLU76
QARG77
QSER95
QTHR96
QGLY97
QARG98
QPHE99
QSER119
QALA120
QASN180
QASN313

site_idAC6
Number of Residues11
DetailsBINDING SITE FOR RESIDUE G3H Q 3337
ChainResidue
QALA149
QTHR150
QHIS176
QTHR179
QARG195
QARG231
QNAD3336
QHOH3353
QHOH3410
QHOH3440
QHOH3621

site_idAC7
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NAD R 4336
ChainResidue
RGLY7
RGLY9
RARG10
RILE11
RASN31
RASP32
RLEU33
RARG77
RSER95
RTHR96
RGLY97
RSER119
RALA120
RASN180
RASN313
RTYR317
RG3H4337
RHOH4353
RHOH4354
RHOH4356
RHOH4366
RHOH4367
RHOH4373
RHOH4380
RHOH4388
RHOH4390
RHOH4430
RHOH4578
RHOH4621

site_idAC8
Number of Residues11
DetailsBINDING SITE FOR RESIDUE G3H R 4337
ChainResidue
RALA149
RTHR150
RHIS176
RTHR179
RARG195
RARG231
RNAD4336
RHOH4353
RHOH4440
RHOH4578
RHOH4621

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Nucleophile => ECO:0000269|PubMed:18480053, ECO:0000305|PubMed:12569100
ChainResidueDetails
OTHR150
PTHR150
QTHR150
RTHR150

site_idSWS_FT_FI2
Number of Residues24
DetailsBINDING: BINDING => ECO:0000269|PubMed:12569100, ECO:0000269|PubMed:18480053, ECO:0000269|PubMed:3586018, ECO:0000269|PubMed:9175858
ChainResidueDetails
OILE11
PALA120
PASP181
PGLU314
QILE11
QLEU33
QASP78
QALA120
QASP181
QGLU314
RILE11
OLEU33
RLEU33
RASP78
RALA120
RASP181
RGLU314
OASP78
OALA120
OASP181
OGLU314
PILE11
PLEU33
PASP78

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:12569100, ECO:0000269|PubMed:18480053, ECO:0000269|PubMed:3210237, ECO:0000269|PubMed:3586018, ECO:0000269|PubMed:9175858
ChainResidueDetails
OALA149
RALA149
RASN180
RVAL232
OASN180
OVAL232
PALA149
PASN180
PVAL232
QALA149
QASN180
QVAL232

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:12569100, ECO:0000269|PubMed:18480053, ECO:0000269|PubMed:9175858
ChainResidueDetails
OALA196
PALA196
QALA196
RALA196

site_idSWS_FT_FI5
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:18480053, ECO:0000269|PubMed:3210237, ECO:0000269|PubMed:3586018, ECO:0000269|PubMed:9175858
ChainResidueDetails
OGLY209
PGLY209
QGLY209
RGLY209

site_idSWS_FT_FI6
Number of Residues4
DetailsSITE: Activates thiol group during catalysis => ECO:0000250|UniProtKB:Q6GIL8
ChainResidueDetails
OSER177
PSER177
QSER177
RSER177

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
OALA149
OHIS176

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
PALA149
PHIS176

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
QALA149
QHIS176

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
RALA149
RHIS176

224931

PDB entries from 2024-09-11

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