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2AAW

Studies on ligand binding and enzyme inhibition of Plasmodium falciparum glutathione S-transferase

Functional Information from GO Data
ChainGOidnamespacecontents
A0004364molecular_functionglutathione transferase activity
A0006749biological_processglutathione metabolic process
A0016740molecular_functiontransferase activity
C0004364molecular_functionglutathione transferase activity
C0006749biological_processglutathione metabolic process
C0016740molecular_functiontransferase activity
Functional Information from PDB Data
site_idAC1
Number of Residues17
DetailsBINDING SITE FOR RESIDUE GTX A 220
ChainResidue
ATYR9
AP33222
AHOH223
AHOH260
AHOH263
AHOH266
CPHE42
CLYS46
CASP105
ALYS15
APHE45
AGLN58
AVAL59
AGLN71
ASER72
APHE116
ATYR211

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE GTX C 221
ChainResidue
APHE42
AASP105
CTYR9
CLYS15
CGLN58
CVAL59
CGLN71
CSER72
CTYR211
CP33223
CHOH232
CHOH239
CHOH263

site_idAC3
Number of Residues10
DetailsBINDING SITE FOR RESIDUE P33 A 222
ChainResidue
AGLY14
ALYS15
AGLN104
AHIS107
ATYR108
AASN111
AGTX220
CTYR108
CP33223
CHOH295

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE P33 C 223
ChainResidue
AP33222
CGLY14
CLYS15
CGLN104
CHIS107
CASN111
CGTX221
CHOH263

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE DTL C 224
ChainResidue
AHOH300
CLEU26
CHOH306

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING: BINDING => ECO:0000305|PubMed:12972411
ChainResidueDetails
AGLN58
AGLN71
ALYS117
ATHR121
CGLN58
CGLN71
CLYS117
CTHR121

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0007744|PDB:3FR9
ChainResidueDetails
AASP105
CASP105

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1oe8
ChainResidueDetails
ATYR9

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1oe8
ChainResidueDetails
CTYR9

237735

PDB entries from 2025-06-18

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