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1GYP

CRYSTAL STRUCTURE OF GLYCOSOMAL GLYCERALDEHYDE-3-PHOSPHATE DEHYDROGENASE FROM LEISHMANIA MEXICANA: IMPLICATIONS FOR STRUCTURE-BASED DRUG DESIGN AND A NEW POSITION FOR THE INORGANIC PHOSPHATE BINDING SITE

Functional Information from GO Data
ChainGOidnamespacecontents
A0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
A0005829cellular_componentcytosol
A0006006biological_processglucose metabolic process
A0006096biological_processglycolytic process
A0016491molecular_functionoxidoreductase activity
A0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
A0020015cellular_componentglycosome
A0050661molecular_functionNADP binding
A0051287molecular_functionNAD binding
B0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
B0005829cellular_componentcytosol
B0006006biological_processglucose metabolic process
B0006096biological_processglycolytic process
B0016491molecular_functionoxidoreductase activity
B0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
B0020015cellular_componentglycosome
B0050661molecular_functionNADP binding
B0051287molecular_functionNAD binding
C0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
C0005829cellular_componentcytosol
C0006006biological_processglucose metabolic process
C0006096biological_processglycolytic process
C0016491molecular_functionoxidoreductase activity
C0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
C0020015cellular_componentglycosome
C0050661molecular_functionNADP binding
C0051287molecular_functionNAD binding
D0004365molecular_functionglyceraldehyde-3-phosphate dehydrogenase (NAD+) (phosphorylating) activity
D0005829cellular_componentcytosol
D0006006biological_processglucose metabolic process
D0006096biological_processglycolytic process
D0016491molecular_functionoxidoreductase activity
D0016620molecular_functionoxidoreductase activity, acting on the aldehyde or oxo group of donors, NAD or NADP as acceptor
D0020015cellular_componentglycosome
D0050661molecular_functionNADP binding
D0051287molecular_functionNAD binding
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PO4 A 359
ChainResidue
ASER165
ACYS166
ATHR167
AHIS194
ATHR226
AGLY227
AALA228

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PO4 A 360
ChainResidue
AARG249
ANAD361
ATHR197
ATHR199

site_idAC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 B 359
ChainResidue
BSER165
BCYS166
BTHR167
BTHR226
BGLY227

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PO4 B 360
ChainResidue
BTHR197
BTHR199
BARG249
BNAD361

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PO4 C 359
ChainResidue
CSER165
CCYS166
CTHR167
CTHR226
CGLY227
CALA228

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PO4 C 360
ChainResidue
CTHR197
CTHR199
CARG249
CNAD361

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 D 359
ChainResidue
DSER165
DCYS166
DTHR167
DTHR226
DGLY227

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PO4 D 360
ChainResidue
DTHR197
DTHR199
DARG249
DNAD361

site_idAC9
Number of Residues21
DetailsBINDING SITE FOR RESIDUE NAD A 361
ChainResidue
AASN8
AGLY9
AGLY11
AARG12
AILE13
AVAL37
AASP38
AMET39
AALA90
AGLN91
ASER110
ATHR111
AGLY112
ALEU113
ASER134
AALA135
ACYS166
AALA198
AASN335
APO4360
BVAL206

site_idBC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE NAD B 361
ChainResidue
BASN8
BGLY9
BPHE10
BGLY11
BARG12
BILE13
BVAL37
BASP38
BGLN91
BSER110
BTHR111
BGLY112
BLEU113
BSER134
BALA135
BCYS166
BTHR197
BASN335
BTYR339
BPO4360

site_idBC2
Number of Residues19
DetailsBINDING SITE FOR RESIDUE NAD C 361
ChainResidue
CASN8
CGLY9
CGLY11
CARG12
CILE13
CVAL37
CASP38
CALA90
CGLN91
CGLY112
CLEU113
CSER134
CALA135
CCYS166
CTHR197
CASN335
CTYR339
CPO4360
DVAL206

site_idBC3
Number of Residues17
DetailsBINDING SITE FOR RESIDUE NAD D 361
ChainResidue
DASN8
DGLY9
DPHE10
DGLY11
DARG12
DILE13
DASP38
DALA90
DSER110
DTHR111
DLEU113
DSER134
DALA135
DCYS166
DASN335
DTYR339
DPO4360

Functional Information from PROSITE/UniProt
site_idPS00071
Number of Residues8
DetailsGAPDH Glyceraldehyde 3-phosphate dehydrogenase active site. ASCTTNcL
ChainResidueDetails
AALA164-LEU171

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Nucleophile
ChainResidueDetails
ATHR167
BTHR167
CTHR167
DTHR167

site_idSWS_FT_FI2
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:7578111, ECO:0000269|PubMed:9571030
ChainResidueDetails
AILE13
BGLU336
CILE13
CMET39
CARG92
CALA135
CGLU336
DILE13
DMET39
DARG92
DALA135
AMET39
DGLU336
AARG92
AALA135
AGLU336
BILE13
BMET39
BARG92
BALA135

site_idSWS_FT_FI3
Number of Residues16
DetailsBINDING: BINDING => ECO:0000250
ChainResidueDetails
ACYS166
CALA198
CGLY227
CVAL250
DCYS166
DALA198
DGLY227
DVAL250
AALA198
AGLY227
AVAL250
BCYS166
BALA198
BGLY227
BVAL250
CCYS166

site_idSWS_FT_FI4
Number of Residues4
DetailsSITE: Activates thiol group during catalysis
ChainResidueDetails
ASER195
BSER195
CSER195
DSER195

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
ACYS166
AHIS194

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
BCYS166
BHIS194

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
CCYS166
CHIS194

site_idCSA4
Number of Residues2
DetailsAnnotated By Reference To The Literature 1szj
ChainResidueDetails
DCYS166
DHIS194

226707

PDB entries from 2024-10-30

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