6OP1
Selenium incorporated, carbon monoxide inhibited FeMo-cofactor of azotobacter vinelandii
Functional Information from GO Data
Chain | GOid | namespace | contents |
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 | 0018697 | molecular_function | obsolete carbonyl sulfide nitrogenase activity |
A | 0046872 | molecular_function | metal ion binding |
A | 0051536 | molecular_function | iron-sulfur cluster 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 | 0018697 | molecular_function | obsolete carbonyl sulfide nitrogenase activity |
B | 0046872 | molecular_function | metal ion binding |
B | 0051536 | molecular_function | iron-sulfur cluster 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 | 0018697 | molecular_function | obsolete carbonyl sulfide nitrogenase activity |
C | 0046872 | molecular_function | metal ion binding |
C | 0051536 | molecular_function | iron-sulfur cluster 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 | 0018697 | molecular_function | obsolete carbonyl sulfide nitrogenase activity |
D | 0046872 | molecular_function | metal ion binding |
D | 0051536 | molecular_function | iron-sulfur cluster binding |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 17 |
Details | binding site for residue HCA A 501 |
Chain | Residue |
A | ALA65 |
A | HOH730 |
A | HOH748 |
A | HOH750 |
A | HOH761 |
A | HOH793 |
A | HOH818 |
B | HOH775 |
B | HOH842 |
A | ARG96 |
A | GLN191 |
A | GLY424 |
A | ILE425 |
A | HIS442 |
A | ICS502 |
A | HOH623 |
A | HOH635 |
site_id | AC2 |
Number of Residues | 11 |
Details | binding site for residue ICS A 502 |
Chain | Residue |
A | VAL70 |
A | ARG96 |
A | TYR229 |
A | CYS275 |
A | GLY356 |
A | GLY357 |
A | LEU358 |
A | ARG359 |
A | HIS442 |
A | HCA501 |
A | CMO505 |
site_id | AC3 |
Number of Residues | 4 |
Details | binding site for residue IMD A 503 |
Chain | Residue |
A | GLU287 |
A | TRP294 |
A | HOH687 |
A | HOH784 |
site_id | AC4 |
Number of Residues | 7 |
Details | binding site for residue IMD A 504 |
Chain | Residue |
A | ARG96 |
A | ASN98 |
A | TYR99 |
A | THR111 |
A | HOH849 |
D | HOH907 |
D | HOH986 |
site_id | AC5 |
Number of Residues | 4 |
Details | binding site for residue CMO A 505 |
Chain | Residue |
A | VAL70 |
A | HIS195 |
A | PHE381 |
A | ICS502 |
site_id | AC6 |
Number of Residues | 6 |
Details | binding site for residue MG A 506 |
Chain | Residue |
A | ARG93 |
A | ALA94 |
A | VAL110 |
A | MET112 |
A | HOH707 |
A | HOH819 |
site_id | AC7 |
Number of Residues | 4 |
Details | binding site for residue MG A 507 |
Chain | Residue |
A | ILE306 |
A | ILE328 |
A | LYS332 |
A | TRP335 |
site_id | AC8 |
Number of Residues | 14 |
Details | binding site for residue CLF A 508 |
Chain | Residue |
A | CYS62 |
A | TYR64 |
A | PRO85 |
A | GLY87 |
A | CYS88 |
A | TYR91 |
A | CYS154 |
A | GLY185 |
B | CYS70 |
B | SER92 |
B | CYS95 |
B | TYR98 |
B | CYS153 |
B | SER188 |
site_id | AC9 |
Number of Residues | 6 |
Details | binding site for residue CA B 601 |
Chain | Residue |
B | ASP353 |
B | ASP357 |
B | HOH727 |
D | ARG108 |
D | GLU109 |
D | HOH894 |
site_id | AD1 |
Number of Residues | 5 |
Details | binding site for residue IMD B 602 |
Chain | Residue |
B | SER482 |
B | THR483 |
B | GLN492 |
B | THR496 |
B | HOH738 |
site_id | AD2 |
Number of Residues | 4 |
Details | binding site for residue IMD B 603 |
Chain | Residue |
A | GLY157 |
B | GLU120 |
B | ALA123 |
C | LYS44 |
site_id | AD3 |
Number of Residues | 3 |
Details | binding site for residue MG B 604 |
Chain | Residue |
B | LYS365 |
B | HOH986 |
B | HOH1009 |
site_id | AD4 |
Number of Residues | 5 |
Details | binding site for residue IMD B 605 |
Chain | Residue |
B | LEU253 |
B | ASP256 |
B | GLY275 |
B | GLU280 |
B | HOH958 |
site_id | AD5 |
Number of Residues | 6 |
Details | binding site for residue CA B 606 |
Chain | Residue |
B | ARG108 |
B | GLU109 |
B | HOH962 |
D | ASP353 |
D | ASP357 |
D | HOH803 |
site_id | AD6 |
Number of Residues | 17 |
Details | binding site for residue HCA C 501 |
Chain | Residue |
C | GLY424 |
C | ILE425 |
C | HIS442 |
C | ICS502 |
C | HOH626 |
C | HOH703 |
C | HOH711 |
C | HOH712 |
C | HOH752 |
C | HOH770 |
C | HOH808 |
C | HOH826 |
D | HOH739 |
D | HOH819 |
C | ALA65 |
C | ARG96 |
C | GLN191 |
site_id | AD7 |
Number of Residues | 11 |
Details | binding site for residue ICS C 502 |
Chain | Residue |
C | VAL70 |
C | ARG96 |
C | TYR229 |
C | CYS275 |
C | GLY356 |
C | GLY357 |
C | LEU358 |
C | ARG359 |
C | HIS442 |
C | HCA501 |
C | CMO504 |
site_id | AD8 |
Number of Residues | 3 |
Details | binding site for residue IMD C 503 |
Chain | Residue |
C | TRP294 |
C | HOH661 |
C | HOH692 |
site_id | AD9 |
Number of Residues | 4 |
Details | binding site for residue CMO C 504 |
Chain | Residue |
C | VAL70 |
C | HIS195 |
C | PHE381 |
C | ICS502 |
site_id | AE1 |
Number of Residues | 13 |
Details | binding site for residue CLF C 505 |
Chain | Residue |
C | CYS62 |
C | PRO85 |
C | GLY87 |
C | CYS88 |
C | TYR91 |
C | CYS154 |
C | GLY185 |
D | CYS70 |
D | SER92 |
D | CYS95 |
D | TYR98 |
D | CYS153 |
D | SER188 |
site_id | AE2 |
Number of Residues | 3 |
Details | binding site for residue IMD D 601 |
Chain | Residue |
A | LYS44 |
D | GLU120 |
D | ALA123 |
site_id | AE3 |
Number of Residues | 5 |
Details | binding site for residue IMD D 602 |
Chain | Residue |
D | SER482 |
D | THR483 |
D | GLN492 |
D | THR496 |
D | HOH758 |
site_id | AE4 |
Number of Residues | 5 |
Details | binding site for residue IMD D 603 |
Chain | Residue |
D | LEU253 |
D | ASP256 |
D | GLY275 |
D | GLU280 |
D | HOH985 |
site_id | AE5 |
Number of Residues | 2 |
Details | binding site for residue MG D 604 |
Chain | Residue |
D | LYS9 |
D | HOH781 |
site_id | AE6 |
Number of Residues | 4 |
Details | binding site for residue MG D 605 |
Chain | Residue |
C | HOH784 |
C | HOH826 |
D | TYR98 |
D | HOH1111 |
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. TTCmaeviGDDLnAF |
Chain | Residue | Details |
B | THR151-PHE165 | |
A | SER152-VAL166 |
site_id | PS00699 |
Number of Residues | 8 |
Details | NITROGENASE_1_1 Nitrogenases component 1 alpha and beta subunits signature 1. YVHGSQGC |
Chain | Residue | Details |
B | TYR88-CYS95 | |
A | ILE81-CYS88 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 8 |
Details | BINDING: |
Chain | Residue | Details |
B | CYS70 | |
C | HIS442 | |
B | CYS95 | |
B | CYS153 | |
B | SER188 | |
D | CYS70 | |
D | CYS95 | |
D | CYS153 | |
D | SER188 | |
C | CYS275 |
Catalytic Information from CSA
site_id | MCSA1 |
Number of Residues | 2 |
Details | M-CSA 212 |
Chain | Residue | Details |
B | CYS153 | metal ligand |
B | VAL157 | polar interaction, single electron acceptor, single electron donor, single electron relay |
A | ARG96 | activator, hydrogen bond donor |
A | HIS195 | activator, polar interaction |
site_id | MCSA2 |
Number of Residues | 2 |
Details | M-CSA 212 |
Chain | Residue | Details |
D | CYS153 | metal ligand |
D | VAL157 | polar interaction, single electron acceptor, single electron donor, single electron relay |
C | ARG96 | activator, hydrogen bond donor |
C | HIS195 | activator, polar interaction |