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 |