5XF9
Crystal structure of NAD+-reducing [NiFe]-hydrogenase in the air-oxidized state
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0000166 | molecular_function | nucleotide binding |
| A | 0008137 | molecular_function | NADH dehydrogenase (ubiquinone) activity |
| A | 0010181 | molecular_function | FMN binding |
| A | 0046872 | molecular_function | metal ion binding |
| A | 0051536 | molecular_function | iron-sulfur cluster binding |
| A | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| A | 1902600 | biological_process | proton transmembrane transport |
| B | 0008137 | molecular_function | NADH dehydrogenase (ubiquinone) activity |
| B | 0016020 | cellular_component | membrane |
| B | 0016491 | molecular_function | oxidoreductase activity |
| B | 0042773 | biological_process | ATP synthesis coupled electron transport |
| B | 0046872 | molecular_function | metal ion binding |
| B | 0051536 | molecular_function | iron-sulfur cluster binding |
| B | 0051537 | molecular_function | 2 iron, 2 sulfur cluster binding |
| B | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| B | 1902600 | biological_process | proton transmembrane transport |
| C | 0016491 | molecular_function | oxidoreductase activity |
| C | 0046872 | molecular_function | metal ion binding |
| C | 0051536 | molecular_function | iron-sulfur cluster binding |
| C | 0051538 | molecular_function | 3 iron, 4 sulfur cluster binding |
| C | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| D | 0008901 | molecular_function | ferredoxin hydrogenase activity |
| D | 0016151 | molecular_function | nickel cation binding |
| D | 0016491 | molecular_function | oxidoreductase activity |
| D | 0046872 | molecular_function | metal ion binding |
| E | 0000166 | molecular_function | nucleotide binding |
| E | 0008137 | molecular_function | NADH dehydrogenase (ubiquinone) activity |
| E | 0010181 | molecular_function | FMN binding |
| E | 0046872 | molecular_function | metal ion binding |
| E | 0051536 | molecular_function | iron-sulfur cluster binding |
| E | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| E | 1902600 | biological_process | proton transmembrane transport |
| F | 0008137 | molecular_function | NADH dehydrogenase (ubiquinone) activity |
| F | 0016020 | cellular_component | membrane |
| F | 0016491 | molecular_function | oxidoreductase activity |
| F | 0042773 | biological_process | ATP synthesis coupled electron transport |
| F | 0046872 | molecular_function | metal ion binding |
| F | 0051536 | molecular_function | iron-sulfur cluster binding |
| F | 0051537 | molecular_function | 2 iron, 2 sulfur cluster binding |
| F | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| F | 1902600 | biological_process | proton transmembrane transport |
| G | 0016491 | molecular_function | oxidoreductase activity |
| G | 0046872 | molecular_function | metal ion binding |
| G | 0051536 | molecular_function | iron-sulfur cluster binding |
| G | 0051538 | molecular_function | 3 iron, 4 sulfur cluster binding |
| G | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| H | 0008901 | molecular_function | ferredoxin hydrogenase activity |
| H | 0016151 | molecular_function | nickel cation binding |
| H | 0016491 | molecular_function | oxidoreductase activity |
| H | 0046872 | molecular_function | metal ion binding |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 23 |
| Details | binding site for residue FMN A 601 |
| Chain | Residue |
| A | GLY202 |
| A | GLY317 |
| A | GLU318 |
| A | GLU319 |
| A | VAL352 |
| A | ASN353 |
| A | ASN354 |
| A | THR357 |
| A | PHE527 |
| A | GLU585 |
| A | HOH703 |
| A | ARG203 |
| A | HOH712 |
| A | HOH721 |
| A | HOH754 |
| A | HOH812 |
| A | GLY204 |
| A | LYS213 |
| A | ASN230 |
| A | ASP232 |
| A | GLU233 |
| A | GLY234 |
| A | TYR314 |
| site_id | AC2 |
| Number of Residues | 9 |
| Details | binding site for residue SF4 A 602 |
| Chain | Residue |
| A | SER478 |
| A | CYS479 |
| A | GLY480 |
| A | PHE481 |
| A | CYS482 |
| A | CYS485 |
| A | ASN524 |
| A | CYS525 |
| A | PHE527 |
| site_id | AC3 |
| Number of Residues | 8 |
| Details | binding site for residue SF4 B 301 |
| Chain | Residue |
| B | PHE98 |
| B | HIS103 |
| B | PHE104 |
| B | CYS105 |
| B | CYS108 |
| B | SER111 |
| B | CYS114 |
| B | GLY209 |
| site_id | AC4 |
| Number of Residues | 8 |
| Details | binding site for residue SF4 B 302 |
| Chain | Residue |
| B | CYS153 |
| B | ILE154 |
| B | CYS156 |
| B | GLY157 |
| B | CYS159 |
| B | CYS206 |
| B | VAL208 |
| B | ALA210 |
| site_id | AC5 |
| Number of Residues | 7 |
| Details | binding site for residue FES B 303 |
| Chain | Residue |
| B | HIS41 |
| B | CYS43 |
| B | GLY52 |
| B | CYS54 |
| B | ARG55 |
| B | CYS57 |
| B | CYS69 |
| site_id | AC6 |
| Number of Residues | 9 |
| Details | binding site for residue SF4 C 201 |
| Chain | Residue |
| C | CYS24 |
| C | CYS27 |
| C | GLU67 |
| C | ALA94 |
| C | CYS95 |
| C | CYS159 |
| C | PRO160 |
| D | ARG78 |
| D | HIS183 |
| site_id | AC7 |
| Number of Residues | 12 |
| Details | binding site for residue FCO D 501 |
| Chain | Residue |
| D | CYS83 |
| D | SER86 |
| D | ALA394 |
| D | PRO395 |
| D | ARG396 |
| D | LEU399 |
| D | VAL418 |
| D | SER419 |
| D | THR420 |
| D | CYS462 |
| D | CYS465 |
| D | 3NI502 |
| site_id | AC8 |
| Number of Residues | 6 |
| Details | binding site for residue 3NI D 502 |
| Chain | Residue |
| D | GLU32 |
| D | CYS80 |
| D | CYS83 |
| D | CYS462 |
| D | CYS465 |
| D | FCO501 |
| site_id | AC9 |
| Number of Residues | 6 |
| Details | binding site for residue MG D 503 |
| Chain | Residue |
| D | GLU61 |
| D | LEU416 |
| D | HIS468 |
| D | HOH609 |
| D | HOH634 |
| D | HOH647 |
| site_id | AD1 |
| Number of Residues | 23 |
| Details | binding site for residue FMN E 601 |
| Chain | Residue |
| E | VAL352 |
| E | ASN353 |
| E | ASN354 |
| E | THR357 |
| E | GLY526 |
| E | PHE527 |
| E | GLU585 |
| E | HOH701 |
| E | HOH708 |
| E | HOH710 |
| E | HOH736 |
| E | HOH737 |
| E | GLY202 |
| E | ARG203 |
| E | GLY204 |
| E | LYS213 |
| E | ASN230 |
| E | ASP232 |
| E | GLY234 |
| E | TYR314 |
| E | GLY317 |
| E | GLU318 |
| E | GLU319 |
| site_id | AD2 |
| Number of Residues | 11 |
| Details | binding site for residue SF4 E 602 |
| Chain | Residue |
| E | SER478 |
| E | CYS479 |
| E | GLY480 |
| E | PHE481 |
| E | CYS482 |
| E | CYS485 |
| E | SER523 |
| E | ASN524 |
| E | CYS525 |
| E | PHE527 |
| E | GLY528 |
| site_id | AD3 |
| Number of Residues | 8 |
| Details | binding site for residue SF4 F 301 |
| Chain | Residue |
| F | HIS103 |
| F | PHE104 |
| F | CYS105 |
| F | CYS108 |
| F | SER111 |
| F | CYS114 |
| F | GLN117 |
| F | GLY209 |
| site_id | AD4 |
| Number of Residues | 7 |
| Details | binding site for residue SF4 F 302 |
| Chain | Residue |
| F | CYS153 |
| F | ILE154 |
| F | CYS156 |
| F | GLY157 |
| F | CYS159 |
| F | CYS206 |
| F | VAL208 |
| site_id | AD5 |
| Number of Residues | 7 |
| Details | binding site for residue FES F 303 |
| Chain | Residue |
| F | HIS41 |
| F | CYS43 |
| F | GLY52 |
| F | CYS54 |
| F | ARG55 |
| F | CYS57 |
| F | CYS69 |
| site_id | AD6 |
| Number of Residues | 12 |
| Details | binding site for residue SF4 G 201 |
| Chain | Residue |
| G | GLY23 |
| G | CYS24 |
| G | CYS27 |
| G | GLU67 |
| G | GLY93 |
| G | ALA94 |
| G | CYS95 |
| G | GLY158 |
| G | CYS159 |
| G | PRO160 |
| H | ARG78 |
| H | HIS183 |
| site_id | AD7 |
| Number of Residues | 13 |
| Details | binding site for residue FCO H 501 |
| Chain | Residue |
| H | CYS83 |
| H | SER86 |
| H | HIS87 |
| H | ALA394 |
| H | PRO395 |
| H | ARG396 |
| H | LEU399 |
| H | VAL418 |
| H | SER419 |
| H | THR420 |
| H | CYS462 |
| H | CYS465 |
| H | 3NI502 |
| site_id | AD8 |
| Number of Residues | 6 |
| Details | binding site for residue 3NI H 502 |
| Chain | Residue |
| H | GLU32 |
| H | CYS80 |
| H | CYS83 |
| H | CYS462 |
| H | CYS465 |
| H | FCO501 |
| site_id | AD9 |
| Number of Residues | 6 |
| Details | binding site for residue MG H 503 |
| Chain | Residue |
| H | GLU61 |
| H | LEU416 |
| H | HIS468 |
| H | HOH641 |
| H | HOH667 |
| H | HOH669 |
Functional Information from PROSITE/UniProt
| site_id | PS00507 |
| Number of Residues | 26 |
| Details | NI_HGENASE_L_1 Nickel-dependent hydrogenases large subunit signature 1. RGFEafivgrpyweapvvvQRlCGIC |
| Chain | Residue | Details |
| D | ARG58-CYS83 |
| site_id | PS00508 |
| Number of Residues | 10 |
| Details | NI_HGENASE_L_2 Nickel-dependent hydrogenases large subunit signature 2. FDPCLSCat.H |
| Chain | Residue | Details |
| D | PHE459-HIS468 |
| site_id | PS00641 |
| Number of Residues | 18 |
| Details | COMPLEX1_75K_1 Respiratory-chain NADH dehydrogenase 75 Kd subunit signature 1. PhlCWhpemgnhGsCRlC |
| Chain | Residue | Details |
| B | PRO40-CYS57 |
| site_id | PS00642 |
| Number of Residues | 13 |
| Details | COMPLEX1_75K_2 Respiratory-chain NADH dehydrogenase 75 Kd subunit signature 2. CPgCEkSGdClLQ |
| Chain | Residue | Details |
| B | CYS105-GLN117 |
| site_id | PS00644 |
| Number of Residues | 16 |
| Details | COMPLEX1_51K_1 Respiratory-chain NADH dehydrogenase 51 Kd subunit signature 1. GAGAYVCGEESALIES |
| Chain | Residue | Details |
| A | GLY310-SER325 |
| site_id | PS00645 |
| Number of Residues | 12 |
| Details | COMPLEX1_51K_2 Respiratory-chain NADH dehydrogenase 51 Kd subunit signature 2. ESCGfCtPCRvG |
| Chain | Residue | Details |
| A | GLU477-GLY488 |






