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2FZE

Crystal structure of the binary complex of human glutathione-dependent formaldehyde dehydrogenase with ADP-ribose

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
AHOH4014
ACYS44
ATHR46
AHIS66
AGLU67
ACYS173

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

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN B 376
ChainResidue
BCYS44
BTHR46
BHIS66
BGLU67
BCYS173
BHOH4094

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE K A 3001
ChainResidue
AALA186
ALYS187
AGLU189
ATYR263

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE K B 3002
ChainResidue
BALA186
BLYS187
BGLU189
BTYR263

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PO4 A 4001
ChainResidue
ALYS314
AHOH4229
AHOH4280
AHOH4292
AHOH4296
AHOH4351
AHOH4394
BLYS314

site_idAC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PO4 B 4002
ChainResidue
APO44003
AHOH4250
BLYS83
BLYS158
BHOH4163
BHOH4352

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE PO4 A 4003
ChainResidue
ALYS83
ALYS158
AHOH4335
BLYS83
BPO44002

site_idBC1
Number of Residues31
DetailsBINDING SITE FOR RESIDUE APR A 1377
ChainResidue
ATHR46
AGLY198
AGLY200
AGLY201
AVAL202
AASP222
AILE223
ACYS267
AILE268
AVAL273
AVAL291
AGLY292
AVAL293
AARG368
AHOH4021
AHOH4037
AHOH4043
AHOH4056
AHOH4072
AHOH4089
AHOH4097
AHOH4103
AHOH4110
AHOH4117
AHOH4120
AHOH4121
AHOH4162
AHOH4176
AHOH4195
AHOH4208
AHOH4326

site_idBC2
Number of Residues30
DetailsBINDING SITE FOR RESIDUE APR B 2377
ChainResidue
BHOH4115
BHOH4153
BHOH4155
BHOH4167
BHOH4179
BHOH4235
BHOH4261
BHOH4265
BHOH4434
BHIS45
BTHR46
BGLY198
BGLY200
BGLY201
BVAL202
BASP222
BILE223
BCYS267
BILE268
BVAL273
BVAL291
BGLY292
BVAL293
BARG368
BHOH4033
BHOH4046
BHOH4047
BHOH4050
BHOH4070
BHOH4090

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

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PDB entries from 2024-07-17

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