5NX8
Crystal structure of Neanderthal Adenylosuccinate Lyase (ADSL)
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0003824 | molecular_function | catalytic activity |
A | 0004018 | molecular_function | N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity |
A | 0005829 | cellular_component | cytosol |
A | 0006164 | biological_process | purine nucleotide biosynthetic process |
A | 0006167 | biological_process | AMP biosynthetic process |
A | 0006189 | biological_process | 'de novo' IMP biosynthetic process |
A | 0009152 | biological_process | purine ribonucleotide biosynthetic process |
A | 0016829 | molecular_function | lyase activity |
A | 0044208 | biological_process | 'de novo' AMP biosynthetic process |
A | 0070626 | molecular_function | (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity |
B | 0000166 | molecular_function | nucleotide binding |
B | 0003824 | molecular_function | catalytic activity |
B | 0004018 | molecular_function | N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity |
B | 0005829 | cellular_component | cytosol |
B | 0006164 | biological_process | purine nucleotide biosynthetic process |
B | 0006167 | biological_process | AMP biosynthetic process |
B | 0006189 | biological_process | 'de novo' IMP biosynthetic process |
B | 0009152 | biological_process | purine ribonucleotide biosynthetic process |
B | 0016829 | molecular_function | lyase activity |
B | 0044208 | biological_process | 'de novo' AMP biosynthetic process |
B | 0070626 | molecular_function | (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity |
C | 0000166 | molecular_function | nucleotide binding |
C | 0003824 | molecular_function | catalytic activity |
C | 0004018 | molecular_function | N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity |
C | 0005829 | cellular_component | cytosol |
C | 0006164 | biological_process | purine nucleotide biosynthetic process |
C | 0006167 | biological_process | AMP biosynthetic process |
C | 0006189 | biological_process | 'de novo' IMP biosynthetic process |
C | 0009152 | biological_process | purine ribonucleotide biosynthetic process |
C | 0016829 | molecular_function | lyase activity |
C | 0044208 | biological_process | 'de novo' AMP biosynthetic process |
C | 0070626 | molecular_function | (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity |
D | 0000166 | molecular_function | nucleotide binding |
D | 0003824 | molecular_function | catalytic activity |
D | 0004018 | molecular_function | N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity |
D | 0005829 | cellular_component | cytosol |
D | 0006164 | biological_process | purine nucleotide biosynthetic process |
D | 0006167 | biological_process | AMP biosynthetic process |
D | 0006189 | biological_process | 'de novo' IMP biosynthetic process |
D | 0009152 | biological_process | purine ribonucleotide biosynthetic process |
D | 0016829 | molecular_function | lyase activity |
D | 0044208 | biological_process | 'de novo' AMP biosynthetic process |
D | 0070626 | molecular_function | (S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | binding site for residue PEG A 501 |
Chain | Residue |
A | LEU55 |
A | PRO56 |
A | HOH699 |
A | HOH835 |
site_id | AC2 |
Number of Residues | 10 |
Details | binding site for residue PEG A 502 |
Chain | Residue |
A | VAL247 |
A | GLU250 |
A | HOH604 |
A | HOH669 |
B | MET181 |
A | LEU121 |
A | ASP192 |
A | LEU193 |
A | ARG194 |
A | PHE236 |
site_id | AC3 |
Number of Residues | 8 |
Details | binding site for residue GOL A 503 |
Chain | Residue |
A | ASP120 |
A | ARG337 |
A | ARG338 |
A | LEU341 |
A | ALA342 |
A | HOH635 |
A | HOH640 |
A | HOH643 |
site_id | AC4 |
Number of Residues | 6 |
Details | binding site for residue GOL A 504 |
Chain | Residue |
A | ASP216 |
A | HOH657 |
B | GLY451 |
B | ARG452 |
B | GLN455 |
B | HOH668 |
site_id | AC5 |
Number of Residues | 4 |
Details | binding site for residue CL A 505 |
Chain | Residue |
A | GLY200 |
A | THR201 |
A | SER207 |
A | HOH778 |
site_id | AC6 |
Number of Residues | 5 |
Details | binding site for residue CL A 506 |
Chain | Residue |
A | THR111 |
A | TYR114 |
A | ARG196 |
A | LYS199 |
A | GLY200 |
site_id | AC7 |
Number of Residues | 8 |
Details | binding site for residue GOL B 501 |
Chain | Residue |
B | ASP120 |
B | ARG337 |
B | ARG338 |
B | LEU341 |
B | ALA342 |
B | HOH638 |
B | HOH644 |
B | HOH659 |
site_id | AC8 |
Number of Residues | 4 |
Details | binding site for residue CL B 502 |
Chain | Residue |
B | THR111 |
B | ARG196 |
B | LYS199 |
B | GLY200 |
site_id | AC9 |
Number of Residues | 5 |
Details | binding site for residue CL B 503 |
Chain | Residue |
B | GLY200 |
B | THR201 |
B | ALA206 |
B | SER207 |
B | HOH763 |
site_id | AD1 |
Number of Residues | 6 |
Details | binding site for residue PEG C 501 |
Chain | Residue |
A | GLN51 |
A | HOH630 |
C | HIS217 |
C | LYS218 |
C | GLN221 |
C | HOH602 |
site_id | AD2 |
Number of Residues | 10 |
Details | binding site for residue PEG C 502 |
Chain | Residue |
C | LEU121 |
C | ASP192 |
C | LEU193 |
C | ARG194 |
C | PHE236 |
C | VAL247 |
C | GLU250 |
C | HOH601 |
C | HOH633 |
D | MET181 |
site_id | AD3 |
Number of Residues | 8 |
Details | binding site for residue GOL C 503 |
Chain | Residue |
C | ASP120 |
C | ARG337 |
C | ARG338 |
C | LEU341 |
C | ALA342 |
C | HOH648 |
C | HOH662 |
C | HOH691 |
site_id | AD4 |
Number of Residues | 4 |
Details | binding site for residue GOL C 504 |
Chain | Residue |
C | ASP216 |
C | HOH635 |
D | GLY451 |
D | GLN455 |
site_id | AD5 |
Number of Residues | 4 |
Details | binding site for residue CL C 505 |
Chain | Residue |
C | GLY200 |
C | THR201 |
C | SER207 |
C | HOH728 |
site_id | AD6 |
Number of Residues | 4 |
Details | binding site for residue CL C 506 |
Chain | Residue |
C | THR111 |
C | ARG196 |
C | LYS199 |
C | GLY200 |
site_id | AD7 |
Number of Residues | 9 |
Details | binding site for residue GOL D 502 |
Chain | Residue |
D | ASP120 |
D | ILE123 |
D | ARG337 |
D | ARG338 |
D | LEU341 |
D | ALA342 |
D | HOH641 |
D | HOH692 |
D | HOH696 |
site_id | AD8 |
Number of Residues | 5 |
Details | binding site for residue GOL D 503 |
Chain | Residue |
C | GLY451 |
C | GLN455 |
D | ARG83 |
D | ASP216 |
D | HOH647 |
site_id | AD9 |
Number of Residues | 5 |
Details | binding site for residue CL D 504 |
Chain | Residue |
D | THR111 |
D | TYR114 |
D | ARG196 |
D | LYS199 |
D | GLY200 |
site_id | AE1 |
Number of Residues | 4 |
Details | binding site for residue CL D 505 |
Chain | Residue |
D | GLY200 |
D | THR201 |
D | ALA206 |
D | SER207 |
Functional Information from PROSITE/UniProt
site_id | PS00163 |
Number of Residues | 10 |
Details | FUMARATE_LYASES Fumarate lyases signature. GSsaMpYKrN |
Chain | Residue | Details |
A | GLY288-ASN297 |