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4B1B

Crystal structure of Plasmodium falciparum oxidised Thioredoxin Reductase at 2.9 angstrom

Functional Information from GO Data
ChainGOidnamespacecontents
A0004791molecular_functionthioredoxin-disulfide reductase (NADPH) activity
A0016491molecular_functionoxidoreductase activity
A0016668molecular_functionoxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
A0045454biological_processcell redox homeostasis
A0050660molecular_functionflavin adenine dinucleotide binding
B0004791molecular_functionthioredoxin-disulfide reductase (NADPH) activity
B0016491molecular_functionoxidoreductase activity
B0016668molecular_functionoxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
B0045454biological_processcell redox homeostasis
B0050660molecular_functionflavin adenine dinucleotide binding
Functional Information from PDB Data
site_idAC1
Number of Residues31
DetailsBINDING SITE FOR RESIDUE FAD A 1506
ChainResidue
AGLY48
ATHR87
ACYS88
AGLY92
ACYS93
ALYS96
AGLY159
ALEU160
AALA161
AALA191
ATHR192
AGLY49
AGLY193
ATYR232
AASP319
ALEU323
AGLY356
AASP357
AGLU364
ALEU365
AALA366
APRO367
AGLY50
AHOH2001
AHOH2002
APRO51
AGLY52
AASP71
ATYR72
AVAL73
AGLY86

site_idAC2
Number of Residues33
DetailsBINDING SITE FOR RESIDUE FAD B 1506
ChainResidue
BGLY48
BGLY49
BGLY50
BPRO51
BGLY52
BASP71
BTYR72
BVAL73
BGLY86
BTHR87
BCYS88
BVAL91
BGLY92
BCYS93
BLYS96
BLYS97
BGLY159
BLEU160
BALA161
BALA191
BTHR192
BGLY193
BTYR232
BARG316
BASP319
BLEU323
BGLY356
BASP357
BGLU364
BLEU365
BALA366
BPRO367
BHOH2001

Functional Information from PROSITE/UniProt
site_idPS00076
Number of Residues11
DetailsPYRIDINE_REDOX_1 Pyridine nucleotide-disulphide oxidoreductases class-I active site. GGtCVnvGCVP
ChainResidueDetails
AGLY85-PRO95

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000269|PubMed:9368022
ChainResidueDetails
AHIS509
BHIS509

site_idSWS_FT_FI2
Number of Residues14
DetailsBINDING: in other chain => ECO:0000269|PubMed:22889878, ECO:0000269|PubMed:23845423, ECO:0007744|PDB:4B1B, ECO:0007744|PDB:4J56, ECO:0007744|PDB:4J57
ChainResidueDetails
APRO51
BTHR87
BGLY92
BALA161
BASP357
BGLU364
AASP71
ATHR87
AGLY92
AALA161
AASP357
AGLU364
BPRO51
BASP71

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:23845423, ECO:0007744|PDB:4J56, ECO:0007744|PDB:4J57
ChainResidueDetails
AHIS509
BHIS509

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PDB entries from 2024-07-17

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