1M1Y
Chemical Crosslink of Nitrogenase MoFe Protein and Fe Protein
Functional Information from GO Data
| Chain | GOid | namespace | contents |
| A | 0000166 | molecular_function | nucleotide binding |
| A | 0005524 | molecular_function | ATP binding |
| A | 0009399 | biological_process | nitrogen fixation |
| A | 0016163 | molecular_function | nitrogenase activity |
| A | 0016491 | molecular_function | oxidoreductase activity |
| A | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| A | 0046872 | molecular_function | metal ion binding |
| A | 0051536 | molecular_function | iron-sulfur cluster binding |
| B | 0000166 | molecular_function | nucleotide binding |
| B | 0005524 | molecular_function | ATP binding |
| B | 0009399 | biological_process | nitrogen fixation |
| B | 0016163 | molecular_function | nitrogenase activity |
| B | 0016491 | molecular_function | oxidoreductase activity |
| B | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| B | 0046872 | molecular_function | metal ion binding |
| B | 0051536 | molecular_function | iron-sulfur cluster binding |
| C | 0000166 | molecular_function | nucleotide binding |
| C | 0005524 | molecular_function | ATP binding |
| C | 0009399 | biological_process | nitrogen fixation |
| C | 0016163 | molecular_function | nitrogenase activity |
| C | 0016491 | molecular_function | oxidoreductase activity |
| C | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| C | 0046872 | molecular_function | metal ion binding |
| C | 0051536 | molecular_function | iron-sulfur cluster binding |
| D | 0000166 | molecular_function | nucleotide binding |
| D | 0005524 | molecular_function | ATP binding |
| D | 0009399 | biological_process | nitrogen fixation |
| D | 0016163 | molecular_function | nitrogenase activity |
| D | 0016491 | molecular_function | oxidoreductase activity |
| D | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| D | 0046872 | molecular_function | metal ion binding |
| D | 0051536 | molecular_function | iron-sulfur cluster binding |
| E | 0000166 | molecular_function | nucleotide binding |
| E | 0005524 | molecular_function | ATP binding |
| E | 0009399 | biological_process | nitrogen fixation |
| E | 0016163 | molecular_function | nitrogenase activity |
| E | 0016491 | molecular_function | oxidoreductase activity |
| 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 |
| F | 0000166 | molecular_function | nucleotide binding |
| F | 0005524 | molecular_function | ATP binding |
| F | 0009399 | biological_process | nitrogen fixation |
| F | 0016163 | molecular_function | nitrogenase activity |
| F | 0016491 | molecular_function | oxidoreductase activity |
| F | 0046872 | molecular_function | metal ion binding |
| F | 0051536 | molecular_function | iron-sulfur cluster binding |
| F | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| G | 0000166 | molecular_function | nucleotide binding |
| G | 0005524 | molecular_function | ATP binding |
| G | 0009399 | biological_process | nitrogen fixation |
| G | 0016163 | molecular_function | nitrogenase activity |
| G | 0016491 | molecular_function | oxidoreductase activity |
| G | 0046872 | molecular_function | metal ion binding |
| G | 0051536 | molecular_function | iron-sulfur cluster binding |
| G | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| H | 0000166 | molecular_function | nucleotide binding |
| H | 0005524 | molecular_function | ATP binding |
| H | 0009399 | biological_process | nitrogen fixation |
| H | 0016163 | molecular_function | nitrogenase activity |
| H | 0016491 | molecular_function | oxidoreductase activity |
| H | 0046872 | molecular_function | metal ion binding |
| H | 0051536 | molecular_function | iron-sulfur cluster binding |
| H | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| I | 0000166 | molecular_function | nucleotide binding |
| I | 0005524 | molecular_function | ATP binding |
| I | 0009399 | biological_process | nitrogen fixation |
| I | 0016163 | molecular_function | nitrogenase activity |
| I | 0016491 | molecular_function | oxidoreductase activity |
| I | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| I | 0046872 | molecular_function | metal ion binding |
| I | 0051536 | molecular_function | iron-sulfur cluster binding |
| J | 0000166 | molecular_function | nucleotide binding |
| J | 0005524 | molecular_function | ATP binding |
| J | 0009399 | biological_process | nitrogen fixation |
| J | 0016163 | molecular_function | nitrogenase activity |
| J | 0016491 | molecular_function | oxidoreductase activity |
| J | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| J | 0046872 | molecular_function | metal ion binding |
| J | 0051536 | molecular_function | iron-sulfur cluster binding |
| K | 0000166 | molecular_function | nucleotide binding |
| K | 0005524 | molecular_function | ATP binding |
| K | 0009399 | biological_process | nitrogen fixation |
| K | 0016163 | molecular_function | nitrogenase activity |
| K | 0016491 | molecular_function | oxidoreductase activity |
| K | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| K | 0046872 | molecular_function | metal ion binding |
| K | 0051536 | molecular_function | iron-sulfur cluster binding |
| L | 0000166 | molecular_function | nucleotide binding |
| L | 0005524 | molecular_function | ATP binding |
| L | 0009399 | biological_process | nitrogen fixation |
| L | 0016163 | molecular_function | nitrogenase activity |
| L | 0016491 | molecular_function | oxidoreductase activity |
| L | 0016612 | cellular_component | molybdenum-iron nitrogenase complex |
| L | 0046872 | molecular_function | metal ion binding |
| L | 0051536 | molecular_function | iron-sulfur cluster binding |
| M | 0000166 | molecular_function | nucleotide binding |
| M | 0005524 | molecular_function | ATP binding |
| M | 0009399 | biological_process | nitrogen fixation |
| M | 0016163 | molecular_function | nitrogenase activity |
| M | 0016491 | molecular_function | oxidoreductase activity |
| M | 0046872 | molecular_function | metal ion binding |
| M | 0051536 | molecular_function | iron-sulfur cluster binding |
| M | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| N | 0000166 | molecular_function | nucleotide binding |
| N | 0005524 | molecular_function | ATP binding |
| N | 0009399 | biological_process | nitrogen fixation |
| N | 0016163 | molecular_function | nitrogenase activity |
| N | 0016491 | molecular_function | oxidoreductase activity |
| N | 0046872 | molecular_function | metal ion binding |
| N | 0051536 | molecular_function | iron-sulfur cluster binding |
| N | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| O | 0000166 | molecular_function | nucleotide binding |
| O | 0005524 | molecular_function | ATP binding |
| O | 0009399 | biological_process | nitrogen fixation |
| O | 0016163 | molecular_function | nitrogenase activity |
| O | 0016491 | molecular_function | oxidoreductase activity |
| O | 0046872 | molecular_function | metal ion binding |
| O | 0051536 | molecular_function | iron-sulfur cluster binding |
| O | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
| P | 0000166 | molecular_function | nucleotide binding |
| P | 0005524 | molecular_function | ATP binding |
| P | 0009399 | biological_process | nitrogen fixation |
| P | 0016163 | molecular_function | nitrogenase activity |
| P | 0016491 | molecular_function | oxidoreductase activity |
| P | 0046872 | molecular_function | metal ion binding |
| P | 0051536 | molecular_function | iron-sulfur cluster binding |
| P | 0051539 | molecular_function | 4 iron, 4 sulfur cluster binding |
Functional Information from PDB Data
| site_id | AC1 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CA D 6492 |
| Chain | Residue |
| B | ARG108 |
| B | GLU109 |
| D | ASP353 |
| D | ASP357 |
| site_id | AC2 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CA B 7492 |
| Chain | Residue |
| B | ASP353 |
| B | ASP357 |
| D | ARG108 |
| D | GLU109 |
| site_id | AC3 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CA L 8492 |
| Chain | Residue |
| J | GLU109 |
| L | ASP353 |
| L | ASP357 |
| J | ARG108 |
| site_id | AC4 |
| Number of Residues | 4 |
| Details | BINDING SITE FOR RESIDUE CA J 9492 |
| Chain | Residue |
| J | ASP353 |
| J | ASP357 |
| L | ARG108 |
| L | GLU109 |
| site_id | AC5 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE HCA A 6494 |
| Chain | Residue |
| A | GLN191 |
| A | GLY424 |
| A | ILE425 |
| A | LYS426 |
| A | HIS442 |
| A | CFM6496 |
| site_id | AC6 |
| Number of Residues | 10 |
| Details | BINDING SITE FOR RESIDUE CFM A 6496 |
| Chain | Residue |
| A | ARG96 |
| A | HIS195 |
| A | TYR229 |
| A | ILE231 |
| A | CYS275 |
| A | GLY356 |
| A | GLY357 |
| A | PHE381 |
| A | HIS442 |
| A | HCA6494 |
| site_id | AC7 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE CLF A 6498 |
| Chain | Residue |
| A | CYS62 |
| A | TYR64 |
| A | GLY87 |
| A | CYS88 |
| A | CYS154 |
| B | CYS70 |
| B | SER92 |
| B | CYS95 |
| B | THR152 |
| B | CYS153 |
| B | SER188 |
| site_id | AC8 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE HCA C 7494 |
| Chain | Residue |
| C | ALA65 |
| C | GLN191 |
| C | GLY424 |
| C | ILE425 |
| C | LYS426 |
| C | HIS442 |
| C | CFM7496 |
| site_id | AC9 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE CFM C 7496 |
| Chain | Residue |
| C | ARG96 |
| C | HIS195 |
| C | TYR229 |
| C | CYS275 |
| C | SER278 |
| C | ILE355 |
| C | GLY356 |
| C | GLY357 |
| C | PHE381 |
| C | HIS442 |
| C | HCA7494 |
| site_id | BC1 |
| Number of Residues | 11 |
| Details | BINDING SITE FOR RESIDUE CLF D 7498 |
| Chain | Residue |
| C | CYS62 |
| C | TYR64 |
| C | GLY87 |
| C | CYS88 |
| C | CYS154 |
| D | CYS70 |
| D | SER92 |
| D | CYS95 |
| D | THR152 |
| D | CYS153 |
| D | SER188 |
| site_id | BC2 |
| Number of Residues | 9 |
| Details | BINDING SITE FOR RESIDUE SF4 E 290 |
| Chain | Residue |
| E | CYS97 |
| E | ALA98 |
| E | CYS132 |
| E | GLY133 |
| E | GLY134 |
| F | CYS97 |
| F | ALA98 |
| F | CYS132 |
| F | GLY134 |
| site_id | BC3 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE SF4 G 1290 |
| Chain | Residue |
| G | CYS97 |
| G | ALA98 |
| G | CYS132 |
| G | GLY134 |
| H | CYS97 |
| H | ALA98 |
| H | CYS132 |
| H | GLY134 |
| site_id | BC4 |
| Number of Residues | 7 |
| Details | BINDING SITE FOR RESIDUE HCA I 8494 |
| Chain | Residue |
| I | ALA65 |
| I | GLN191 |
| I | GLY424 |
| I | ILE425 |
| I | LYS426 |
| I | HIS442 |
| I | CFM8496 |
| site_id | BC5 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE CFM I 8496 |
| Chain | Residue |
| I | TYR229 |
| I | CYS275 |
| I | SER278 |
| I | ILE355 |
| I | GLY356 |
| I | GLY357 |
| I | PHE381 |
| I | HIS442 |
| I | HCA8494 |
| I | VAL70 |
| I | ARG96 |
| I | HIS195 |
| site_id | BC6 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE CLF J 8498 |
| Chain | Residue |
| I | CYS62 |
| I | TYR64 |
| I | PRO85 |
| I | GLY87 |
| I | CYS88 |
| I | CYS154 |
| J | CYS70 |
| J | SER92 |
| J | CYS95 |
| J | THR152 |
| J | CYS153 |
| J | SER188 |
| site_id | BC7 |
| Number of Residues | 6 |
| Details | BINDING SITE FOR RESIDUE HCA K 9494 |
| Chain | Residue |
| K | GLN191 |
| K | GLY424 |
| K | ILE425 |
| K | LYS426 |
| K | HIS442 |
| K | CFM9496 |
| site_id | BC8 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE CFM K 9496 |
| Chain | Residue |
| K | VAL70 |
| K | ARG96 |
| K | HIS195 |
| K | TYR229 |
| K | ILE231 |
| K | CYS275 |
| K | ILE355 |
| K | GLY356 |
| K | GLY357 |
| K | PHE381 |
| K | HIS442 |
| K | HCA9494 |
| site_id | BC9 |
| Number of Residues | 12 |
| Details | BINDING SITE FOR RESIDUE CLF K 9498 |
| Chain | Residue |
| K | CYS62 |
| K | TYR64 |
| K | PRO85 |
| K | GLY87 |
| K | CYS88 |
| K | CYS154 |
| L | CYS70 |
| L | SER92 |
| L | CYS95 |
| L | THR152 |
| L | CYS153 |
| L | SER188 |
| site_id | CC1 |
| Number of Residues | 9 |
| Details | BINDING SITE FOR RESIDUE SF4 N 2290 |
| Chain | Residue |
| M | CYS97 |
| M | ALA98 |
| M | CYS132 |
| M | GLY133 |
| M | GLY134 |
| N | CYS97 |
| N | ALA98 |
| N | CYS132 |
| N | GLY134 |
| site_id | CC2 |
| Number of Residues | 8 |
| Details | BINDING SITE FOR RESIDUE SF4 P 3290 |
| Chain | Residue |
| O | CYS97 |
| O | ALA98 |
| O | CYS132 |
| O | GLY134 |
| P | CYS97 |
| P | ALA98 |
| P | CYS132 |
| P | GLY134 |
Functional Information from PROSITE/UniProt
| site_id | PS00090 |
| Number of Residues | 15 |
| Details | NITROGENASE_1_2 Nitrogenases component 1 alpha and beta subunits signature 2. SECpigliGDDIeSV |
| Chain | Residue | Details |
| A | SER152-VAL166 | |
| B | THR151-PHE165 |
| site_id | PS00692 |
| Number of Residues | 14 |
| Details | NIFH_FRXC_2 NifH/frxC family signature 2. DvLGDVVCGGFAmP |
| Chain | Residue | Details |
| E | ASP125-PRO138 |
| site_id | PS00699 |
| Number of Residues | 8 |
| Details | NITROGENASE_1_1 Nitrogenases component 1 alpha and beta subunits signature 1. ISHGPVGC |
| Chain | Residue | Details |
| A | ILE81-CYS88 | |
| B | TYR88-CYS95 |
| site_id | PS00746 |
| Number of Residues | 13 |
| Details | NIFH_FRXC_1 NifH/frxC family signature 1. EsGGPepGvGCAG |
| Chain | Residue | Details |
| E | GLU87-GLY99 |
Functional Information from SwissProt/UniProt
| site_id | SWS_FT_FI1 |
| Number of Residues | 108 |
| Details | Binding site: {} |
| Chain | Residue | Details |
| site_id | SWS_FT_FI2 |
| Number of Residues | 8 |
| Details | Modified residue: {"description":"ADP-ribosylarginine; by dinitrogenase reductase ADP-ribosyltransferase","evidences":[{"evidenceCode":"ECO:0000250"}]} |
| Chain | Residue | Details |
Catalytic Information from CSA
| site_id | CSA1 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| E | LYS15 | |
| E | GLY12 |
| site_id | CSA2 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| F | LYS15 | |
| F | GLY12 |
| site_id | CSA3 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| G | LYS15 | |
| G | GLY12 |
| site_id | CSA4 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| H | LYS15 | |
| H | GLY12 |
| site_id | CSA5 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| M | LYS15 | |
| M | GLY12 |
| site_id | CSA6 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| N | LYS15 | |
| N | GLY12 |
| site_id | CSA7 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| O | LYS15 | |
| O | GLY12 |
| site_id | CSA8 |
| Number of Residues | 2 |
| Details | Annotated By Reference To The Literature 1f48 |
| Chain | Residue | Details |
| P | LYS15 | |
| P | GLY12 |
| site_id | MCSA1 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| E | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| E | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| E | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| E | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA2 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| F | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| F | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| F | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| F | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA3 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| G | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| G | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| G | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| G | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA4 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| H | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| H | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| H | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| H | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA5 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| M | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| M | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| M | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| M | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA6 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| N | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| N | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| N | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| N | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA7 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| O | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| O | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| O | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| O | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |
| site_id | MCSA8 |
| Number of Residues | 4 |
| Details | M-CSA 212 |
| Chain | Residue | Details |
| P | LYS10 | electrostatic stabiliser, hydrogen bond donor |
| P | LYS15 | electrostatic stabiliser, hydrogen bond donor |
| P | LYS41 | electrostatic stabiliser, hydrogen bond donor |
| P | ASP129 | hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor |






