Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

2X50

Crystal structure of Trypanothione reductase from Leishmania infantum in complex with NADPH and silver

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0004362molecular_functionglutathione-disulfide reductase (NADPH) activity
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006749biological_processglutathione metabolic process
A0015036molecular_functiondisulfide oxidoreductase activity
A0015042molecular_functiontrypanothione-disulfide reductase (NADPH) activity
A0016491molecular_functionoxidoreductase activity
A0016668molecular_functionoxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
A0034599biological_processcellular response to oxidative stress
A0045454biological_processcell redox homeostasis
A0050660molecular_functionflavin adenine dinucleotide binding
A0098869biological_processcellular oxidant detoxification
B0000166molecular_functionnucleotide binding
B0004362molecular_functionglutathione-disulfide reductase (NADPH) activity
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006749biological_processglutathione metabolic process
B0015036molecular_functiondisulfide oxidoreductase activity
B0015042molecular_functiontrypanothione-disulfide reductase (NADPH) activity
B0016491molecular_functionoxidoreductase activity
B0016668molecular_functionoxidoreductase activity, acting on a sulfur group of donors, NAD(P) as acceptor
B0034599biological_processcellular response to oxidative stress
B0045454biological_processcell redox homeostasis
B0050660molecular_functionflavin adenine dinucleotide binding
B0098869biological_processcellular oxidant detoxification
Functional Information from PDB Data
site_idAC1
Number of Residues32
DetailsBINDING SITE FOR RESIDUE FAD A 1487
ChainResidue
AGLY11
AGLY50
ATHR51
ACYS52
AVAL55
AGLY56
ACYS57
ALYS60
APHE126
AGLY127
AALA159
AGLY13
ATHR160
AGLY161
AARG287
AARG290
ALEU294
AGLY326
AASP327
AMET333
ALEU334
ATHR335
ASER14
APRO336
ANDP1488
BPRO462
AGLY15
AVAL34
AASP35
AVAL36
AALA46
AALA47

site_idAC2
Number of Residues32
DetailsBINDING SITE FOR RESIDUE FAD B 1489
ChainResidue
APRO462
BGLY11
BGLY13
BSER14
BGLY15
BVAL34
BASP35
BVAL36
BALA46
BALA47
BGLY50
BTHR51
BCYS52
BVAL55
BGLY56
BCYS57
BLYS60
BPHE126
BGLY127
BALA159
BTHR160
BGLY161
BARG287
BARG290
BLEU294
BGLY326
BASP327
BMET333
BLEU334
BTHR335
BPRO336
BNDP1492

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE NDP A 1488
ChainResidue
ALYS60
AGLY196
AGLY197
ATYR198
AILE199
AGLU202
ATYR221
AARG222
AARG228
AASN254
AALA284
AILE285
AGLY286
AMET333
ALEU334
AALA365
APHE367
AFAD1487

site_idAC4
Number of Residues18
DetailsBINDING SITE FOR RESIDUE NDP B 1492
ChainResidue
BFAD1489
BLYS60
BGLY196
BGLY197
BTYR198
BILE199
BGLU202
BTYR221
BARG222
BARG228
BASN254
BALA284
BILE285
BGLY286
BMET333
BLEU334
BALA365
BPHE367

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE AG B 1490
ChainResidue
AHIS461
BCYS52
BCYS57
BTHR335

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE AG A 1489
ChainResidue
ACYS52
ACYS57
ATHR335
BHIS461

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE AG A 1490
ChainResidue
ASER440
ACYS444
BSER440
BCYS444
BAG1491

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE AG B 1491
ChainResidue
ACYS444
AMET447
AAG1490
BCYS444
BMET447

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 1493
ChainResidue
BGLN37
BALA38
BTHR39
BMET124

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 1491
ChainResidue
AGLN37
AALA38
ATHR39
AMET124

Functional Information from PROSITE/UniProt
site_idPS00076
Number of Residues11
DetailsPYRIDINE_REDOX_1 Pyridine nucleotide-disulphide oxidoreductases class-I active site. GGtCVnvGCVP
ChainResidueDetails
AGLY49-PRO59

219140

PDB entries from 2024-05-01

PDB statisticsPDBj update infoContact PDBjnumon