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

4JJI

Crystal structure of S-nitrosoglutathione reductase from Arabidopsis thalina, complex with NAD+

Functional Information from GO Data
ChainGOidnamespacecontents
A0004022molecular_functionalcohol dehydrogenase (NAD+) activity
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0008270molecular_functionzinc ion binding
A0016491molecular_functionoxidoreductase activity
A0044281biological_processsmall molecule metabolic process
A0046294biological_processformaldehyde catabolic process
A0046872molecular_functionmetal ion binding
A0051903molecular_functionS-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
A0080007molecular_functionS-nitrosoglutathione reductase (NADH) activity
A0106321molecular_functionS-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity
A0106322molecular_functionS-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity
B0004022molecular_functionalcohol dehydrogenase (NAD+) activity
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0008270molecular_functionzinc ion binding
B0016491molecular_functionoxidoreductase activity
B0044281biological_processsmall molecule metabolic process
B0046294biological_processformaldehyde catabolic process
B0046872molecular_functionmetal ion binding
B0051903molecular_functionS-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
B0080007molecular_functionS-nitrosoglutathione reductase (NADH) activity
B0106321molecular_functionS-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity
B0106322molecular_functionS-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 401
ChainResidue
ACYS99
ACYS102
ACYS105
ACYS113

site_idAC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN A 402
ChainResidue
ACYS47
AHIS69
AGLU70
ACYS177
AHOH714

site_idAC3
Number of Residues32
DetailsBINDING SITE FOR RESIDUE NAD A 403
ChainResidue
ATYR95
ACYS177
ATHR181
AGLY202
AGLY204
ATHR205
AVAL206
AASP226
AILE227
ALYS231
ACYS271
AILE272
AVAL277
AVAL295
AGLY296
AVAL297
ATHR320
AALA321
APHE322
AARG372
AHOH517
AHOH524
AHOH585
AHOH631
AHOH637
AHOH639
AHOH640
AHOH641
AHOH642
AHOH655
AHOH666
AHOH688

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 404
ChainResidue
ALYS318
AHOH557
AHOH582
AHOH601
BLYS318

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 405
ChainResidue
ASER276
AARG279
AHOH504
AHOH609

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 406
ChainResidue
AHIS249
AASP250
ALYS251

site_idAC7
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 407
ChainResidue
ACYS102
ALYS103
AHOH701

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 A 408
ChainResidue
AARG307
APRO308
APHE309
AHOH616
AHOH654
BALA298
BALA299
BSER300
BGLY301

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 401
ChainResidue
BCYS99
BCYS102
BCYS105
BCYS113

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 402
ChainResidue
BCYS47
BHIS69
BGLU70
BCYS177

site_idBC2
Number of Residues27
DetailsBINDING SITE FOR RESIDUE NAD B 403
ChainResidue
BHOH695
BHIS48
BTYR52
BGLY202
BGLY204
BTHR205
BVAL206
BASP226
BILE227
BLYS231
BCYS271
BILE272
BVAL277
BVAL295
BGLY296
BVAL297
BALA298
BARG372
BHOH508
BHOH571
BHOH574
BHOH581
BHOH588
BHOH662
BHOH666
BHOH677
BHOH694

site_idBC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 B 404
ChainResidue
BHIS249
BASP250
BLYS251

site_idBC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 405
ChainResidue
BSER276
BARG279
BHOH528
BHOH659

site_idBC5
Number of Residues8
DetailsBINDING SITE FOR RESIDUE SO4 B 406
ChainResidue
BASN197
BARG221
BTRP333
BGLU336
BHOH518
BHOH523
BHOH586
BHOH642

site_idBC6
Number of Residues12
DetailsBINDING SITE FOR RESIDUE SO4 B 407
ChainResidue
AVAL312
BLYS109
BASN111
BTHR320
BALA321
BPHE322
BGLY323
BGLY324
BHOH529
BHOH600
BHOH665
BHOH693

Functional Information from PROSITE/UniProt
site_idPS00059
Number of Residues15
DetailsADH_ZINC Zinc-containing alcohol dehydrogenases signature. GHEaAGIvesvGegV
ChainResidueDetails
AGLY68-VAL82

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: BINDING => ECO:0000269|PubMed:38308388, ECO:0000269|Ref.13, ECO:0007744|PDB:3UKO, ECO:0007744|PDB:4GL4, ECO:0007744|PDB:4JJI, ECO:0007744|PDB:4L0Q, ECO:0007744|PDB:8CO4
ChainResidueDetails
ACYS47
BCYS99
BCYS102
BCYS105
BCYS113
BCYS177
AHIS69
ACYS99
ACYS102
ACYS105
ACYS113
ACYS177
BCYS47
BHIS69

site_idSWS_FT_FI2
Number of Residues14
DetailsBINDING: BINDING => ECO:0000269|Ref.13, ECO:0007744|PDB:3UKO, ECO:0007744|PDB:4GL4, ECO:0007744|PDB:4JJI, ECO:0007744|PDB:4L0Q
ChainResidueDetails
AHIS48
BGLY202
BASP226
BILE272
BVAL295
BTHR320
AGLU70
AGLY202
AASP226
AILE272
AVAL295
ATHR320
BHIS48
BGLU70

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P06525
ChainResidueDetails
ATHR49
BTHR49

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|Ref.13, ECO:0007744|PDB:3UKO, ECO:0007744|PDB:4JJI, ECO:0007744|PDB:4L0Q
ChainResidueDetails
ALYS231
AARG372
BLYS231
BARG372

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: N-acetylalanine => ECO:0007744|PubMed:22223895
ChainResidueDetails
AALA2
BALA2

227111

PDB entries from 2024-11-06

PDB statisticsPDBj update infoContact PDBjnumon