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1GYQ

CRYSTAL STRUCTURE OF GLYCOSOMAL GLYCERALDEHYDE FROM LEISHMANIA MEXICANA IN COMPLEX WITH N6-BENZYL-NAD

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 Residues21
DetailsBINDING SITE FOR RESIDUE NBD A 361
ChainResidue
AASN8
AGLN91
AARG92
ASER110
ATHR111
AGLY112
ALEU113
ASER134
AALA135
ACYS166
AALA198
AGLY9
AASN335
ATYR339
APHE10
AGLY11
AARG12
AILE13
AVAL37
AASP38
AMET39

site_idAC2
Number of Residues21
DetailsBINDING SITE FOR RESIDUE NBD B 361
ChainResidue
BASN8
BGLY9
BPHE10
BGLY11
BARG12
BILE13
BVAL37
BASP38
BMET39
BGLN91
BSER110
BTHR111
BGLY112
BLEU113
BSER134
BALA135
BCYS166
BALA198
BASN335
BGLU336
BTYR339

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE NBD C 361
ChainResidue
CASN8
CGLY9
CPHE10
CGLY11
CARG12
CILE13
CASP38
CMET39
CGLN91
CTHR111
CLEU113
CSER134
CALA135
CCYS166
CALA198
CASN335
CTYR339
DVAL206

site_idAC4
Number of Residues19
DetailsBINDING SITE FOR RESIDUE NBD D 361
ChainResidue
DASN8
DGLY9
DPHE10
DGLY11
DARG12
DILE13
DASP38
DMET39
DGLN91
DSER110
DTHR111
DLEU113
DSER134
DALA135
DCYS166
DALA198
DASN335
DGLU336
DTYR339

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
DetailsActive site: {"description":"Nucleophile"}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues20
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"7578111","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"9571030","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues20
DetailsBinding site: {"evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsSite: {"description":"Activates thiol group during catalysis"}
ChainResidueDetails

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

247536

PDB entries from 2026-01-14

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