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

1MC5

Ternary complex of Human glutathione-dependent formaldehyde dehydrogenase with S-(hydroxymethyl)glutathione and NADH

Functional Information from GO Data
ChainGOidnamespacecontents
A0001523biological_processretinoid metabolic process
A0003016biological_processrespiratory system process
A0004022molecular_functionalcohol dehydrogenase (NAD+) activity
A0004024molecular_functionalcohol dehydrogenase (NAD+) activity, zinc-dependent
A0005504molecular_functionfatty acid binding
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006629biological_processlipid metabolic process
A0008270molecular_functionzinc ion binding
A0009055molecular_functionelectron transfer activity
A0010430biological_processfatty acid omega-oxidation
A0016491molecular_functionoxidoreductase activity
A0018467molecular_functionformaldehyde dehydrogenase (NAD+) activity
A0032496biological_processresponse to lipopolysaccharide
A0042802molecular_functionidentical protein binding
A0044281biological_processsmall molecule metabolic process
A0045777biological_processpositive regulation of blood pressure
A0046294biological_processformaldehyde catabolic process
A0046872molecular_functionmetal ion binding
A0051409biological_processresponse to nitrosative stress
A0051775biological_processresponse to redox state
A0051903molecular_functionS-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
A0070062cellular_componentextracellular exosome
A0106321molecular_functionS-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity
A0106322molecular_functionS-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity
B0001523biological_processretinoid metabolic process
B0003016biological_processrespiratory system process
B0004022molecular_functionalcohol dehydrogenase (NAD+) activity
B0004024molecular_functionalcohol dehydrogenase (NAD+) activity, zinc-dependent
B0005504molecular_functionfatty acid binding
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006629biological_processlipid metabolic process
B0008270molecular_functionzinc ion binding
B0009055molecular_functionelectron transfer activity
B0010430biological_processfatty acid omega-oxidation
B0016491molecular_functionoxidoreductase activity
B0018467molecular_functionformaldehyde dehydrogenase (NAD+) activity
B0032496biological_processresponse to lipopolysaccharide
B0042802molecular_functionidentical protein binding
B0044281biological_processsmall molecule metabolic process
B0045777biological_processpositive regulation of blood pressure
B0046294biological_processformaldehyde catabolic process
B0046872molecular_functionmetal ion binding
B0051409biological_processresponse to nitrosative stress
B0051775biological_processresponse to redox state
B0051903molecular_functionS-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity
B0070062cellular_componentextracellular exosome
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 375
ChainResidue
ACYS96
ACYS99
ACYS102
ACYS110

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN A 376
ChainResidue
ANAD500
ACYS44
ATHR46
AHIS66
ACYS173
AAHE404

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN B 375
ChainResidue
BCYS96
BCYS99
BCYS102
BCYS110

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ZN B 376
ChainResidue
BCYS44
BHIS66
BGLU67
BCYS173
BHOH667

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE K A 400
ChainResidue
AALA186
ALYS187
AGLU189
ATYR263
AHOH608

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 A 401
ChainResidue
ALYS314
AHOH538
AHOH608
AHOH623
BLYS314

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 B 402
ChainResidue
ALYS83
APO4403
BLYS83
BASP86
BLYS158

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 A 403
ChainResidue
ALYS83
AASP86
ALYS158
BLYS83
BPO4402

site_idAC9
Number of Residues25
DetailsBINDING SITE FOR RESIDUE NAD A 500
ChainResidue
AHIS45
ATHR46
ATYR92
ACYS173
ATHR177
AGLY198
AGLY200
AGLY201
AVAL202
AASP222
AILE223
ALYS227
ACYS267
AILE268
AVAL291
AGLY292
AVAL293
ATHR316
AALA317
APHE318
AARG368
AZN376
AAHE404
AHOH571
AHOH572

site_idBC1
Number of Residues28
DetailsBINDING SITE FOR RESIDUE NAD B 501
ChainResidue
BHIS45
BCYS173
BTHR177
BGLY198
BLEU199
BGLY200
BGLY201
BVAL202
BASP222
BILE223
BLYS227
BCYS267
BILE268
BVAL273
BVAL291
BGLY292
BVAL293
BTHR316
BPHE318
BARG368
BHOH516
BHOH548
BHOH565
BHOH616
BHOH622
BHOH675
BHOH691
BHOH699

site_idBC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE AHE A 404
ChainResidue
ACYS173
AVAL293
AZN376
ANAD500
AHOH529
AHOH606
AHOH611
AHOH644
ATHR46
AASP55
APRO56
AGLU57
AHIS66
ATYR92
AARG114

Functional Information from PROSITE/UniProt
site_idPS00059
Number of Residues15
DetailsADH_ZINC Zinc-containing alcohol dehydrogenases signature. GHEgAGIvesvGegV
ChainResidueDetails
AGLY65-VAL79

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: BINDING => ECO:0000269|PubMed:3365377
ChainResidueDetails
AHIS45
BGLY97
BLYS100
BLEU103
BGLN111
BGLY174
AGLU67
AGLY97
ALYS100
ALEU103
AGLN111
AGLY174
BHIS45
BGLU67

site_idSWS_FT_FI2
Number of Residues2
DetailsSITE: Important for FDH activity and activation by fatty acids => ECO:0000269|PubMed:8460164, ECO:0000269|PubMed:8494891
ChainResidueDetails
AVAL115
BVAL115

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: N-acetylalanine => ECO:0007744|PubMed:19413330
ChainResidueDetails
AASN2
BASN2

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:P28474
ChainResidueDetails
AGLU233
AGLY315
BGLU233
BGLY315

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:24275569
ChainResidueDetails
ALYS247
BLYS247

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163
ChainResidueDetails
AVAL324
APHE351
BVAL324
BPHE351

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1teh
ChainResidueDetails
ATHR46
AHIS45

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1teh
ChainResidueDetails
BTHR46
BHIS45

site_idCSA3
Number of Residues1
DetailsAnnotated By Reference To The Literature 1teh
ChainResidueDetails
AASP55

site_idCSA4
Number of Residues1
DetailsAnnotated By Reference To The Literature 1teh
ChainResidueDetails
BASP55

site_idMCSA1
Number of Residues12
DetailsM-CSA 464
ChainResidueDetails
AHIS45metal ligand
AVAL115activator
AGLY174metal ligand
ATHR369steric role
ATHR46proton shuttle (general acid/base)
AASP47proton shuttle (general acid/base)
AGLU67metal ligand
AGLY68metal ligand
AGLY97metal ligand
ALYS100metal ligand
ALEU103metal ligand
AGLN111metal ligand

site_idMCSA2
Number of Residues12
DetailsM-CSA 464
ChainResidueDetails
BHIS45metal ligand
BVAL115activator
BGLY174metal ligand
BTHR369steric role
BTHR46proton shuttle (general acid/base)
BASP47proton shuttle (general acid/base)
BGLU67metal ligand
BGLY68metal ligand
BGLY97metal ligand
BLYS100metal ligand
BLEU103metal ligand
BGLN111metal ligand

223166

PDB entries from 2024-07-31

PDB statisticsPDBj update infoContact PDBjnumon