4K3I
Crystal Structure of the Quinol Form of Methylamine Dehydrogenase in Complex with the Diferrous Form of MauG, C2 Space Group
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0004130 | molecular_function | cytochrome-c peroxidase activity |
A | 0009055 | molecular_function | electron transfer activity |
A | 0016491 | molecular_function | oxidoreductase activity |
A | 0020037 | molecular_function | heme binding |
A | 0042597 | cellular_component | periplasmic space |
A | 0046872 | molecular_function | metal ion binding |
A | 0098869 | biological_process | cellular oxidant detoxification |
B | 0004130 | molecular_function | cytochrome-c peroxidase activity |
B | 0009055 | molecular_function | electron transfer activity |
B | 0016491 | molecular_function | oxidoreductase activity |
B | 0020037 | molecular_function | heme binding |
B | 0042597 | cellular_component | periplasmic space |
B | 0046872 | molecular_function | metal ion binding |
B | 0098869 | biological_process | cellular oxidant detoxification |
C | 0009308 | biological_process | amine metabolic process |
C | 0016491 | molecular_function | oxidoreductase activity |
C | 0016638 | molecular_function | oxidoreductase activity, acting on the CH-NH2 group of donors |
C | 0030058 | molecular_function | aliphatic amine dehydrogenase activity |
C | 0030288 | cellular_component | outer membrane-bounded periplasmic space |
C | 0042597 | cellular_component | periplasmic space |
C | 0052876 | molecular_function | methylamine dehydrogenase (amicyanin) activity |
D | 0016491 | molecular_function | oxidoreductase activity |
D | 0030058 | molecular_function | aliphatic amine dehydrogenase activity |
D | 0030416 | biological_process | methylamine metabolic process |
D | 0042597 | cellular_component | periplasmic space |
D | 0052876 | molecular_function | methylamine dehydrogenase (amicyanin) activity |
E | 0009308 | biological_process | amine metabolic process |
E | 0016491 | molecular_function | oxidoreductase activity |
E | 0016638 | molecular_function | oxidoreductase activity, acting on the CH-NH2 group of donors |
E | 0030058 | molecular_function | aliphatic amine dehydrogenase activity |
E | 0030288 | cellular_component | outer membrane-bounded periplasmic space |
E | 0042597 | cellular_component | periplasmic space |
E | 0052876 | molecular_function | methylamine dehydrogenase (amicyanin) activity |
F | 0016491 | molecular_function | oxidoreductase activity |
F | 0030058 | molecular_function | aliphatic amine dehydrogenase activity |
F | 0030416 | biological_process | methylamine metabolic process |
F | 0042597 | cellular_component | periplasmic space |
F | 0052876 | molecular_function | methylamine dehydrogenase (amicyanin) activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE CA A 401 |
Chain | Residue |
A | ASN66 |
A | THR275 |
A | PRO277 |
A | HOH515 |
A | HOH528 |
A | HOH534 |
A | HOH680 |
site_id | AC2 |
Number of Residues | 24 |
Details | BINDING SITE FOR RESIDUE HEC A 402 |
Chain | Residue |
A | CYS31 |
A | CYS34 |
A | HIS35 |
A | VAL55 |
A | ARG65 |
A | THR67 |
A | PRO68 |
A | LEU70 |
A | GLN91 |
A | PHE92 |
A | TRP93 |
A | ARG96 |
A | LEU100 |
A | GLN103 |
A | ALA104 |
A | PRO107 |
A | GLU113 |
A | GLN163 |
A | LYS265 |
A | HOH710 |
A | HOH779 |
A | HOH783 |
A | GLN29 |
A | SER30 |
site_id | AC3 |
Number of Residues | 20 |
Details | BINDING SITE FOR RESIDUE HEC A 403 |
Chain | Residue |
A | TRP93 |
A | ASN200 |
A | CYS201 |
A | CYS204 |
A | HIS205 |
A | HIS224 |
A | LEU228 |
A | PHE264 |
A | PRO267 |
A | TYR278 |
A | MET279 |
A | HIS280 |
A | LEU287 |
A | TYR294 |
A | SER324 |
A | HOH515 |
A | HOH551 |
A | HOH558 |
A | HOH642 |
A | HOH680 |
site_id | AC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE NA A 404 |
Chain | Residue |
A | ASN231 |
A | THR233 |
A | HOH816 |
A | HOH821 |
A | HOH826 |
A | HOH850 |
site_id | AC5 |
Number of Residues | 1 |
Details | BINDING SITE FOR RESIDUE EDO A 405 |
Chain | Residue |
A | LEU139 |
site_id | AC6 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE NA A 407 |
Chain | Residue |
A | LEU250 |
A | ARG252 |
A | ILE255 |
A | HOH774 |
A | HOH820 |
A | HOH866 |
site_id | AC7 |
Number of Residues | 5 |
Details | BINDING SITE FOR RESIDUE EDO A 408 |
Chain | Residue |
A | ALA78 |
A | HIS80 |
A | HOH556 |
A | HOH890 |
A | HOH891 |
site_id | AC8 |
Number of Residues | 7 |
Details | BINDING SITE FOR RESIDUE CA B 401 |
Chain | Residue |
B | ASN66 |
B | THR275 |
B | PRO277 |
B | HOH542 |
B | HOH556 |
B | HOH588 |
B | HOH595 |
site_id | AC9 |
Number of Residues | 22 |
Details | BINDING SITE FOR RESIDUE HEC B 402 |
Chain | Residue |
B | GLN29 |
B | SER30 |
B | CYS31 |
B | CYS34 |
B | HIS35 |
B | ARG65 |
B | THR67 |
B | PRO68 |
B | LEU70 |
B | GLN91 |
B | PHE92 |
B | TRP93 |
B | ARG96 |
B | LEU100 |
B | GLN103 |
B | ALA104 |
B | PRO107 |
B | GLN163 |
B | LYS265 |
B | HOH756 |
B | HOH767 |
B | HOH777 |
site_id | BC1 |
Number of Residues | 20 |
Details | BINDING SITE FOR RESIDUE HEC B 403 |
Chain | Residue |
B | ASN200 |
B | CYS201 |
B | CYS204 |
B | HIS205 |
B | HIS224 |
B | LEU228 |
B | PHE264 |
B | PRO267 |
B | TYR278 |
B | MET279 |
B | HIS280 |
B | LEU287 |
B | TYR294 |
B | GLU327 |
B | HOH509 |
B | HOH540 |
B | HOH556 |
B | HOH579 |
B | HOH588 |
B | TRP93 |
site_id | BC2 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE NA B 404 |
Chain | Residue |
B | ASN231 |
B | THR233 |
B | HOH738 |
B | HOH745 |
B | HOH770 |
B | HOH775 |
site_id | BC3 |
Number of Residues | 2 |
Details | BINDING SITE FOR RESIDUE EDO B 405 |
Chain | Residue |
B | HOH706 |
B | HOH736 |
site_id | BC4 |
Number of Residues | 6 |
Details | BINDING SITE FOR RESIDUE NA B 406 |
Chain | Residue |
B | LEU250 |
B | ARG252 |
B | ILE255 |
B | HOH700 |
B | HOH743 |
B | HOH744 |
site_id | BC5 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE ACT D 401 |
Chain | Residue |
D | ARG174 |
D | LEU176 |
D | ASP177 |
D | PRO212 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 2 |
Details | MOD_RES: Tryptophylquinone => ECO:0000269|PubMed:1409575 |
Chain | Residue | Details |
C | TOQ57 | |
E | TOQ57 | |
A | CYS201 | |
A | CYS204 | |
B | CYS31 | |
B | CYS34 | |
B | CYS201 | |
B | CYS204 |
site_id | SWS_FT_FI2 |
Number of Residues | 4 |
Details | CROSSLNK: Tryptophan tryptophylquinone (Trp-Trp) => ECO:0000269|PubMed:1409575 |
Chain | Residue | Details |
C | TOQ57 | |
C | TRP108 | |
E | TOQ57 | |
E | TRP108 | |
B | HIS205 | |
B | HIS280 |
Catalytic Information from CSA
site_id | MCSA1 |
Number of Residues | 6 |
Details | M-CSA 13 |
Chain | Residue | Details |
C | ASP32 | electrostatic stabiliser, proton acceptor, proton donor |
C | TOQ57 | proton acceptor, proton donor, proton relay |
C | ASP76 | electrostatic stabiliser, proton acceptor, proton donor |
C | TRP108 | proton acceptor, proton donor, proton relay, single electron donor |
C | TYR119 | steric role |
C | THR122 | electrostatic stabiliser |
site_id | MCSA2 |
Number of Residues | 6 |
Details | M-CSA 13 |
Chain | Residue | Details |
E | ASP32 | electrostatic stabiliser, proton acceptor, proton donor |
E | TOQ57 | proton acceptor, proton donor, proton relay |
E | ASP76 | electrostatic stabiliser, proton acceptor, proton donor |
E | TRP108 | proton acceptor, proton donor, proton relay, single electron donor |
E | TYR119 | steric role |
E | THR122 | electrostatic stabiliser |