6IJY
Crystal structure of human MTH1(G2K/C87A/C104S mutant) in complex with 8-oxo-dGTP determined using a crystal obtained under microgravity
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0003723 | molecular_function | RNA binding |
A | 0005515 | molecular_function | protein binding |
A | 0005634 | cellular_component | nucleus |
A | 0005737 | cellular_component | cytoplasm |
A | 0005739 | cellular_component | mitochondrion |
A | 0005759 | cellular_component | mitochondrial matrix |
A | 0005829 | cellular_component | cytosol |
A | 0006152 | biological_process | purine nucleoside catabolic process |
A | 0006281 | biological_process | DNA repair |
A | 0006979 | biological_process | response to oxidative stress |
A | 0008413 | molecular_function | 8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity |
A | 0008828 | molecular_function | dATP diphosphatase activity |
A | 0016787 | molecular_function | hydrolase activity |
A | 0016818 | molecular_function | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides |
A | 0030515 | molecular_function | snoRNA binding |
A | 0035539 | molecular_function | 8-oxo-7,8-dihydrodeoxyguanosine triphosphate pyrophosphatase activity |
A | 0042262 | biological_process | DNA protection |
A | 0046872 | molecular_function | metal ion binding |
A | 0047693 | molecular_function | ATP diphosphatase activity |
A | 0106377 | molecular_function | 2-hydroxy-ATP hydrolase activity |
A | 0106378 | molecular_function | 2-hydroxy-dATP hydrolase activity |
A | 0106431 | molecular_function | N6-methyl-(d)ATP hydrolase activity |
A | 0106433 | molecular_function | O6-methyl-dGTP hydrolase activity |
A | 0140933 | molecular_function | 5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase activity |
B | 0003723 | molecular_function | RNA binding |
B | 0005515 | molecular_function | protein binding |
B | 0005634 | cellular_component | nucleus |
B | 0005737 | cellular_component | cytoplasm |
B | 0005739 | cellular_component | mitochondrion |
B | 0005759 | cellular_component | mitochondrial matrix |
B | 0005829 | cellular_component | cytosol |
B | 0006152 | biological_process | purine nucleoside catabolic process |
B | 0006281 | biological_process | DNA repair |
B | 0006979 | biological_process | response to oxidative stress |
B | 0008413 | molecular_function | 8-oxo-7,8-dihydroguanosine triphosphate pyrophosphatase activity |
B | 0008828 | molecular_function | dATP diphosphatase activity |
B | 0016787 | molecular_function | hydrolase activity |
B | 0016818 | molecular_function | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides |
B | 0030515 | molecular_function | snoRNA binding |
B | 0035539 | molecular_function | 8-oxo-7,8-dihydrodeoxyguanosine triphosphate pyrophosphatase activity |
B | 0042262 | biological_process | DNA protection |
B | 0046872 | molecular_function | metal ion binding |
B | 0047693 | molecular_function | ATP diphosphatase activity |
B | 0106377 | molecular_function | 2-hydroxy-ATP hydrolase activity |
B | 0106378 | molecular_function | 2-hydroxy-dATP hydrolase activity |
B | 0106431 | molecular_function | N6-methyl-(d)ATP hydrolase activity |
B | 0106433 | molecular_function | O6-methyl-dGTP hydrolase activity |
B | 0140933 | molecular_function | 5'-(N(7)-methylguanosine 5'-triphospho)-[mRNA] hydrolase activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 29 |
Details | binding site for residue 8DG A 201 |
Chain | Residue |
A | TYR7 |
A | LYS38 |
A | GLU56 |
A | PHE72 |
A | MET81 |
A | TRP117 |
A | ASP119 |
A | ASP120 |
A | TRP123 |
A | NA202 |
A | NA204 |
A | THR8 |
A | HOH311 |
A | HOH314 |
A | HOH326 |
A | HOH331 |
A | HOH336 |
A | HOH363 |
A | HOH381 |
A | HOH390 |
A | HOH405 |
B | LYS130 |
A | LEU9 |
A | LYS23 |
A | ARG25 |
A | PHE27 |
A | ASN33 |
A | GLY36 |
A | GLY37 |
site_id | AC2 |
Number of Residues | 5 |
Details | binding site for residue NA A 202 |
Chain | Residue |
A | GLY36 |
A | GLU56 |
A | 8DG201 |
A | NA204 |
A | HOH395 |
site_id | AC3 |
Number of Residues | 4 |
Details | binding site for residue NA A 203 |
Chain | Residue |
A | PHE113 |
A | MET116 |
A | HOH388 |
B | HOH411 |
site_id | AC4 |
Number of Residues | 7 |
Details | binding site for residue NA A 204 |
Chain | Residue |
A | GLU52 |
A | GLU56 |
A | 8DG201 |
A | NA202 |
A | HOH303 |
A | HOH311 |
A | HOH314 |
site_id | AC5 |
Number of Residues | 7 |
Details | binding site for residue GOL A 205 |
Chain | Residue |
A | LYS2 |
A | VAL75 |
A | GLY76 |
A | SER121 |
A | TYR122 |
A | HOH456 |
B | HOH320 |
site_id | AC6 |
Number of Residues | 8 |
Details | binding site for residue GOL A 206 |
Chain | Residue |
A | HOH426 |
B | LYS2 |
B | GLU73 |
B | VAL75 |
B | GLY76 |
B | GLU77 |
B | TYR122 |
B | HOH452 |
site_id | AC7 |
Number of Residues | 28 |
Details | binding site for residue 8DG B 201 |
Chain | Residue |
A | LYS130 |
A | HOH309 |
A | HOH320 |
A | HOH325 |
A | HOH385 |
B | TYR7 |
B | THR8 |
B | LEU9 |
B | ASN33 |
B | GLY36 |
B | GLY37 |
B | LYS38 |
B | GLU52 |
B | GLU56 |
B | PHE72 |
B | PHE74 |
B | MET81 |
B | TRP117 |
B | ASP119 |
B | ASP120 |
B | TRP123 |
B | PHE139 |
B | NA202 |
B | HOH313 |
B | HOH316 |
B | HOH342 |
B | HOH343 |
B | HOH344 |
site_id | AC8 |
Number of Residues | 5 |
Details | binding site for residue NA B 202 |
Chain | Residue |
B | TRP117 |
B | ASP119 |
B | ASP120 |
B | 8DG201 |
B | HOH343 |
Functional Information from PROSITE/UniProt
site_id | PS00893 |
Number of Residues | 22 |
Details | NUDIX_BOX Nudix box signature. GkvqegEtiedGArRELqEEsG |
Chain | Residue | Details |
A | GLY37-GLY58 |
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 258 |
Details | Domain: {"description":"Nudix hydrolase","evidences":[{"source":"PROSITE-ProRule","id":"PRU00794","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 42 |
Details | Motif: {"description":"Nudix box","evidences":[{"source":"PROSITE-ProRule","id":"PRU00794","evidenceCode":"ECO:0000255"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 12 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"30304478","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"5OTM","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI4 |
Number of Residues | 2 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"26999531","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"5FSK","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI5 |
Number of Residues | 6 |
Details | Binding site: {"evidences":[{"source":"PubMed","id":"26999531","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"28035004","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"5FSI","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5GHI","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"5GHM","evidenceCode":"ECO:0007744"}]} |
Chain | Residue | Details |
site_id | SWS_FT_FI6 |
Number of Residues | 10 |
Details | Binding site: {"evidences":[{"source":"UniProtKB","id":"Q7ZWC3","evidenceCode":"ECO:0000250"}]} |
Chain | Residue | Details |