2FZE
Crystal structure of the binary complex of human glutathione-dependent formaldehyde dehydrogenase with ADP-ribose
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0001523 | biological_process | retinoid metabolic process |
A | 0003016 | biological_process | respiratory system process |
A | 0004022 | molecular_function | alcohol dehydrogenase (NAD+) activity |
A | 0004024 | molecular_function | alcohol dehydrogenase (NAD+) activity, zinc-dependent |
A | 0005504 | molecular_function | fatty acid binding |
A | 0005737 | cellular_component | cytoplasm |
A | 0005739 | cellular_component | mitochondrion |
A | 0005829 | cellular_component | cytosol |
A | 0006629 | biological_process | lipid metabolic process |
A | 0008270 | molecular_function | zinc ion binding |
A | 0009055 | molecular_function | electron transfer activity |
A | 0010430 | biological_process | fatty acid omega-oxidation |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0018467 | molecular_function | formaldehyde dehydrogenase (NAD+) activity |
A | 0032496 | biological_process | response to lipopolysaccharide |
A | 0042802 | molecular_function | identical protein binding |
A | 0044281 | biological_process | small molecule metabolic process |
A | 0045777 | biological_process | positive regulation of blood pressure |
A | 0046294 | biological_process | formaldehyde catabolic process |
A | 0046872 | molecular_function | metal ion binding |
A | 0051409 | biological_process | response to nitrosative stress |
A | 0051775 | biological_process | response to redox state |
A | 0051903 | molecular_function | S-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity |
A | 0070062 | cellular_component | extracellular exosome |
A | 0106321 | molecular_function | S-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity |
A | 0106322 | molecular_function | S-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity |
B | 0001523 | biological_process | retinoid metabolic process |
B | 0003016 | biological_process | respiratory system process |
B | 0004022 | molecular_function | alcohol dehydrogenase (NAD+) activity |
B | 0004024 | molecular_function | alcohol dehydrogenase (NAD+) activity, zinc-dependent |
B | 0005504 | molecular_function | fatty acid binding |
B | 0005737 | cellular_component | cytoplasm |
B | 0005739 | cellular_component | mitochondrion |
B | 0005829 | cellular_component | cytosol |
B | 0006629 | biological_process | lipid metabolic process |
B | 0008270 | molecular_function | zinc ion binding |
B | 0009055 | molecular_function | electron transfer activity |
B | 0010430 | biological_process | fatty acid omega-oxidation |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0018467 | molecular_function | formaldehyde dehydrogenase (NAD+) activity |
B | 0032496 | biological_process | response to lipopolysaccharide |
B | 0042802 | molecular_function | identical protein binding |
B | 0044281 | biological_process | small molecule metabolic process |
B | 0045777 | biological_process | positive regulation of blood pressure |
B | 0046294 | biological_process | formaldehyde catabolic process |
B | 0046872 | molecular_function | metal ion binding |
B | 0051409 | biological_process | response to nitrosative stress |
B | 0051775 | biological_process | response to redox state |
B | 0051903 | molecular_function | S-(hydroxymethyl)glutathione dehydrogenase [NAD(P)+] activity |
B | 0070062 | cellular_component | extracellular exosome |
B | 0106321 | molecular_function | S-(hydroxymethyl)glutathione dehydrogenase (NADP+) activity |
B | 0106322 | molecular_function | S-(hydroxymethyl)glutathione dehydrogenase (NAD+) activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN A 375 |
Chain | Residue |
A | CYS96 |
A | CYS99 |
A | CYS102 |
A | CYS110 |
site_id | AC2 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ZN A 376 |
Chain | Residue |
A | HOH4014 |
A | CYS44 |
A | THR46 |
A | HIS66 |
A | GLU67 |
A | CYS173 |
site_id | AC3 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ZN B 375 |
Chain | Residue |
B | CYS96 |
B | CYS99 |
B | CYS102 |
B | CYS110 |
site_id | AC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE ZN B 376 |
Chain | Residue |
B | CYS44 |
B | THR46 |
B | HIS66 |
B | GLU67 |
B | CYS173 |
B | HOH4094 |
site_id | AC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE K A 3001 |
Chain | Residue |
A | ALA186 |
A | LYS187 |
A | GLU189 |
A | TYR263 |
site_id | AC6 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE K B 3002 |
Chain | Residue |
B | ALA186 |
B | LYS187 |
B | GLU189 |
B | TYR263 |
site_id | AC7 |
Number of Residues | 8 |
Details | BINDING SITE FOR RESIDUE PO4 A 4001 |
Chain | Residue |
A | LYS314 |
A | HOH4229 |
A | HOH4280 |
A | HOH4292 |
A | HOH4296 |
A | HOH4351 |
A | HOH4394 |
B | LYS314 |
site_id | AC8 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE PO4 B 4002 |
Chain | Residue |
A | PO44003 |
A | HOH4250 |
B | LYS83 |
B | LYS158 |
B | HOH4163 |
B | HOH4352 |
site_id | AC9 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE PO4 A 4003 |
Chain | Residue |
A | LYS83 |
A | LYS158 |
A | HOH4335 |
B | LYS83 |
B | PO44002 |
site_id | BC1 |
Number of Residues | 31 |
Details | BINDING SITE FOR RESIDUE APR A 1377 |
Chain | Residue |
A | THR46 |
A | GLY198 |
A | GLY200 |
A | GLY201 |
A | VAL202 |
A | ASP222 |
A | ILE223 |
A | CYS267 |
A | ILE268 |
A | VAL273 |
A | VAL291 |
A | GLY292 |
A | VAL293 |
A | ARG368 |
A | HOH4021 |
A | HOH4037 |
A | HOH4043 |
A | HOH4056 |
A | HOH4072 |
A | HOH4089 |
A | HOH4097 |
A | HOH4103 |
A | HOH4110 |
A | HOH4117 |
A | HOH4120 |
A | HOH4121 |
A | HOH4162 |
A | HOH4176 |
A | HOH4195 |
A | HOH4208 |
A | HOH4326 |
site_id | BC2 |
Number of Residues | 30 |
Details | BINDING SITE FOR RESIDUE APR B 2377 |
Chain | Residue |
B | HOH4115 |
B | HOH4153 |
B | HOH4155 |
B | HOH4167 |
B | HOH4179 |
B | HOH4235 |
B | HOH4261 |
B | HOH4265 |
B | HOH4434 |
B | HIS45 |
B | THR46 |
B | GLY198 |
B | GLY200 |
B | GLY201 |
B | VAL202 |
B | ASP222 |
B | ILE223 |
B | CYS267 |
B | ILE268 |
B | VAL273 |
B | VAL291 |
B | GLY292 |
B | VAL293 |
B | ARG368 |
B | HOH4033 |
B | HOH4046 |
B | HOH4047 |
B | HOH4050 |
B | HOH4070 |
B | HOH4090 |
Functional Information from PROSITE/UniProt
site_id | PS00059 |
Number of Residues | 15 |
Details | ADH_ZINC Zinc-containing alcohol dehydrogenases signature. GHEgAGIvesvGegV |
Chain | Residue | Details |
A | GLY65-VAL79 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 14 |
Details | BINDING: BINDING => ECO:0000269|PubMed:3365377 |
Chain | Residue | Details |
A | HIS45 | |
B | GLY97 | |
B | LYS100 | |
B | LEU103 | |
B | GLN111 | |
B | GLY174 | |
A | GLU67 | |
A | GLY97 | |
A | LYS100 | |
A | LEU103 | |
A | GLN111 | |
A | GLY174 | |
B | HIS45 | |
B | GLU67 |
site_id | SWS_FT_FI2 |
Number of Residues | 2 |
Details | SITE: Important for FDH activity and activation by fatty acids => ECO:0000269|PubMed:8460164, ECO:0000269|PubMed:8494891 |
Chain | Residue | Details |
A | VAL115 | |
B | VAL115 |
site_id | SWS_FT_FI3 |
Number of Residues | 2 |
Details | MOD_RES: N-acetylalanine => ECO:0007744|PubMed:19413330 |
Chain | Residue | Details |
A | ASN2 | |
B | ASN2 |
site_id | SWS_FT_FI4 |
Number of Residues | 4 |
Details | MOD_RES: N6-succinyllysine => ECO:0000250|UniProtKB:P28474 |
Chain | Residue | Details |
A | GLU233 | |
A | GLY315 | |
B | GLU233 | |
B | GLY315 |
site_id | SWS_FT_FI5 |
Number of Residues | 2 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:24275569 |
Chain | Residue | Details |
A | LYS247 | |
B | LYS247 |
site_id | SWS_FT_FI6 |
Number of Residues | 4 |
Details | MOD_RES: Phosphoserine => ECO:0007744|PubMed:23186163 |
Chain | Residue | Details |
A | VAL324 | |
A | PHE351 | |
B | VAL324 | |
B | PHE351 |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1teh |
Chain | Residue | Details |
A | THR46 | |
A | HIS45 |
site_id | CSA2 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1teh |
Chain | Residue | Details |
B | THR46 | |
B | HIS45 |
site_id | CSA3 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1teh |
Chain | Residue | Details |
A | ASP55 |
site_id | CSA4 |
Number of Residues | 1 |
Details | Annotated By Reference To The Literature 1teh |
Chain | Residue | Details |
B | ASP55 |
site_id | MCSA1 |
Number of Residues | 12 |
Details | M-CSA 464 |
Chain | Residue | Details |
A | HIS45 | metal ligand |
A | VAL115 | activator |
A | GLY174 | metal ligand |
A | THR369 | steric role |
A | THR46 | proton shuttle (general acid/base) |
A | ASP47 | proton shuttle (general acid/base) |
A | GLU67 | metal ligand |
A | GLY68 | metal ligand |
A | GLY97 | metal ligand |
A | LYS100 | metal ligand |
A | LEU103 | metal ligand |
A | GLN111 | metal ligand |
site_id | MCSA2 |
Number of Residues | 12 |
Details | M-CSA 464 |
Chain | Residue | Details |
B | HIS45 | metal ligand |
B | VAL115 | activator |
B | GLY174 | metal ligand |
B | THR369 | steric role |
B | THR46 | proton shuttle (general acid/base) |
B | ASP47 | proton shuttle (general acid/base) |
B | GLU67 | metal ligand |
B | GLY68 | metal ligand |
B | GLY97 | metal ligand |
B | LYS100 | metal ligand |
B | LEU103 | metal ligand |
B | GLN111 | metal ligand |