5T8K
1.95 Angstrom Crystal Structure of S-adenosylhomocysteinase from Cryptosporidium parvum in Complex with Adenine and NAD
Functional Information from GO Data
Chain | GOid | namespace | contents |
A | 0000166 | molecular_function | nucleotide binding |
A | 0004013 | molecular_function | adenosylhomocysteinase activity |
A | 0005829 | cellular_component | cytosol |
A | 0006730 | biological_process | one-carbon metabolic process |
A | 0016787 | molecular_function | hydrolase activity |
A | 0033353 | biological_process | S-adenosylmethionine cycle |
B | 0000166 | molecular_function | nucleotide binding |
B | 0004013 | molecular_function | adenosylhomocysteinase activity |
B | 0005829 | cellular_component | cytosol |
B | 0006730 | biological_process | one-carbon metabolic process |
B | 0016787 | molecular_function | hydrolase activity |
B | 0033353 | biological_process | S-adenosylmethionine cycle |
C | 0000166 | molecular_function | nucleotide binding |
C | 0004013 | molecular_function | adenosylhomocysteinase activity |
C | 0005829 | cellular_component | cytosol |
C | 0006730 | biological_process | one-carbon metabolic process |
C | 0016787 | molecular_function | hydrolase activity |
C | 0033353 | biological_process | S-adenosylmethionine cycle |
D | 0000166 | molecular_function | nucleotide binding |
D | 0004013 | molecular_function | adenosylhomocysteinase activity |
D | 0005829 | cellular_component | cytosol |
D | 0006730 | biological_process | one-carbon metabolic process |
D | 0016787 | molecular_function | hydrolase activity |
D | 0033353 | biological_process | S-adenosylmethionine cycle |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 6 |
Details | binding site for residue NA A 501 |
Chain | Residue |
A | GLU57 |
A | THR408 |
A | GLY409 |
A | HIS410 |
A | ADE503 |
A | HOH717 |
site_id | AC2 |
Number of Residues | 32 |
Details | binding site for residue NAD A 502 |
Chain | Residue |
A | ASN246 |
A | GLY275 |
A | GLY277 |
A | GLU278 |
A | VAL279 |
A | THR297 |
A | GLU298 |
A | ILE299 |
A | ASP300 |
A | CYS303 |
A | THR331 |
A | GLY332 |
A | ASN333 |
A | VAL336 |
A | ILE354 |
A | GLY355 |
A | HIS356 |
A | ASN403 |
A | HIS410 |
A | ADE503 |
A | HOH625 |
A | HOH731 |
A | HOH744 |
A | HOH824 |
A | HOH827 |
A | HOH872 |
A | HOH928 |
C | LYS489 |
C | TYR493 |
A | THR212 |
A | THR213 |
A | THR214 |
site_id | AC3 |
Number of Residues | 12 |
Details | binding site for residue ADE A 503 |
Chain | Residue |
A | LEU52 |
A | HIS53 |
A | THR55 |
A | GLU57 |
A | THR58 |
A | THR408 |
A | GLY409 |
A | HIS410 |
A | MET415 |
A | NA501 |
A | NAD502 |
A | HOH622 |
site_id | AC4 |
Number of Residues | 3 |
Details | binding site for residue P6G A 504 |
Chain | Residue |
A | LYS36 |
A | GLU452 |
A | TYR456 |
site_id | AC5 |
Number of Residues | 3 |
Details | binding site for residue TRS A 505 |
Chain | Residue |
A | ILE7 |
A | LYS8 |
A | TRP101 |
site_id | AC6 |
Number of Residues | 4 |
Details | binding site for residue GOL A 506 |
Chain | Residue |
A | TYR206 |
A | ARG433 |
A | GLU434 |
A | VAL436 |
site_id | AC7 |
Number of Residues | 6 |
Details | binding site for residue NA B 501 |
Chain | Residue |
B | GLU57 |
B | THR408 |
B | GLY409 |
B | HIS410 |
B | ADE503 |
B | HOH880 |
site_id | AC8 |
Number of Residues | 32 |
Details | binding site for residue NAD B 502 |
Chain | Residue |
B | THR212 |
B | THR213 |
B | THR214 |
B | ASN246 |
B | GLY275 |
B | GLY277 |
B | GLU278 |
B | VAL279 |
B | THR297 |
B | GLU298 |
B | ILE299 |
B | ASP300 |
B | CYS303 |
B | THR331 |
B | GLY332 |
B | ASN333 |
B | VAL336 |
B | ILE354 |
B | GLY355 |
B | HIS356 |
B | ASN403 |
B | HIS410 |
B | ADE503 |
B | HOH624 |
B | HOH776 |
B | HOH785 |
B | HOH792 |
B | HOH793 |
B | HOH863 |
B | HOH925 |
D | LYS489 |
D | TYR493 |
site_id | AC9 |
Number of Residues | 12 |
Details | binding site for residue ADE B 503 |
Chain | Residue |
B | HIS53 |
B | THR55 |
B | GLU57 |
B | THR58 |
B | THR408 |
B | GLY409 |
B | HIS410 |
B | MET415 |
B | NA501 |
B | NAD502 |
B | HOH620 |
B | LEU52 |
site_id | AD1 |
Number of Residues | 6 |
Details | binding site for residue P6G B 504 |
Chain | Residue |
B | ASN481 |
B | PRO487 |
B | LYS489 |
B | SER490 |
B | HOH806 |
D | SER224 |
site_id | AD2 |
Number of Residues | 3 |
Details | binding site for residue PEG B 505 |
Chain | Residue |
B | LYS36 |
B | TYR37 |
B | HOH889 |
site_id | AD3 |
Number of Residues | 9 |
Details | binding site for residue GOL B 506 |
Chain | Residue |
B | ARG218 |
B | PHE357 |
B | ASP359 |
B | HOH643 |
B | HOH718 |
B | HOH736 |
B | HOH740 |
B | HOH854 |
D | TYR479 |
site_id | AD4 |
Number of Residues | 6 |
Details | binding site for residue NA C 501 |
Chain | Residue |
C | GLU57 |
C | THR408 |
C | GLY409 |
C | HIS410 |
C | ADE503 |
C | HOH859 |
site_id | AD5 |
Number of Residues | 33 |
Details | binding site for residue NAD C 502 |
Chain | Residue |
A | LYS489 |
A | TYR493 |
C | THR212 |
C | THR213 |
C | THR214 |
C | ASN246 |
C | GLY275 |
C | GLY277 |
C | GLU278 |
C | VAL279 |
C | THR297 |
C | GLU298 |
C | ILE299 |
C | ASP300 |
C | CYS303 |
C | THR331 |
C | GLY332 |
C | ASN333 |
C | VAL336 |
C | ILE354 |
C | GLY355 |
C | HIS356 |
C | LEU401 |
C | ASN403 |
C | HIS410 |
C | ADE503 |
C | HOH712 |
C | HOH734 |
C | HOH812 |
C | HOH831 |
C | HOH861 |
C | HOH877 |
C | HOH954 |
site_id | AD6 |
Number of Residues | 12 |
Details | binding site for residue ADE C 503 |
Chain | Residue |
C | LEU52 |
C | HIS53 |
C | THR55 |
C | GLU57 |
C | THR58 |
C | THR408 |
C | GLY409 |
C | HIS410 |
C | MET415 |
C | NA501 |
C | NAD502 |
C | HOH670 |
site_id | AD7 |
Number of Residues | 7 |
Details | binding site for residue P6G C 504 |
Chain | Residue |
A | SER224 |
C | ASN481 |
C | VAL482 |
C | SER483 |
C | PRO487 |
C | LYS489 |
C | HOH878 |
site_id | AD8 |
Number of Residues | 4 |
Details | binding site for residue P6G C 505 |
Chain | Residue |
C | LYS36 |
C | TYR37 |
C | LEU453 |
C | HOH880 |
site_id | AD9 |
Number of Residues | 1 |
Details | binding site for residue PEG C 506 |
Chain | Residue |
C | ILE7 |
site_id | AE1 |
Number of Residues | 4 |
Details | binding site for residue PEG C 507 |
Chain | Residue |
C | TYR206 |
C | ARG433 |
C | GLU434 |
C | VAL436 |
site_id | AE2 |
Number of Residues | 6 |
Details | binding site for residue NA D 501 |
Chain | Residue |
D | GLU57 |
D | THR408 |
D | GLY409 |
D | HIS410 |
D | ADE503 |
D | HOH950 |
site_id | AE3 |
Number of Residues | 33 |
Details | binding site for residue NAD D 502 |
Chain | Residue |
B | LYS489 |
B | TYR493 |
D | THR212 |
D | THR213 |
D | THR214 |
D | ASN246 |
D | GLY275 |
D | GLY277 |
D | GLU278 |
D | VAL279 |
D | THR297 |
D | GLU298 |
D | ILE299 |
D | ASP300 |
D | CYS303 |
D | THR331 |
D | GLY332 |
D | ASN333 |
D | VAL336 |
D | ILE354 |
D | GLY355 |
D | HIS356 |
D | ASN403 |
D | HIS410 |
D | ADE503 |
D | HOH629 |
D | HOH771 |
D | HOH792 |
D | HOH797 |
D | HOH802 |
D | HOH862 |
D | HOH872 |
D | HOH929 |
site_id | AE4 |
Number of Residues | 12 |
Details | binding site for residue ADE D 503 |
Chain | Residue |
D | LEU52 |
D | HIS53 |
D | THR55 |
D | GLU57 |
D | THR58 |
D | THR408 |
D | GLY409 |
D | HIS410 |
D | MET415 |
D | NA501 |
D | NAD502 |
D | HOH624 |
site_id | AE5 |
Number of Residues | 3 |
Details | binding site for residue PGE D 504 |
Chain | Residue |
D | LYS36 |
D | TYR37 |
D | TYR456 |
site_id | AE6 |
Number of Residues | 2 |
Details | binding site for residue PGE D 505 |
Chain | Residue |
D | ASN481 |
D | SER490 |
site_id | AE7 |
Number of Residues | 3 |
Details | binding site for residue PEG D 506 |
Chain | Residue |
D | ILE7 |
D | TRP101 |
D | HOH736 |
Functional Information from PROSITE/UniProt
site_id | PS00738 |
Number of Residues | 15 |
Details | ADOHCYASE_1 S-adenosyl-L-homocysteine hydrolase signature 1. SCNiYSTQDhAAAAL |
Chain | Residue | Details |
A | SER76-LEU90 | |
C | SER76-LEU90 |
site_id | PS00739 |
Number of Residues | 17 |
Details | ADOHCYASE_2 S-adenosyl-L-homocysteine hydrolase signature 2. GKkivVlGYGeVGKGc.A |
Chain | Residue | Details |
A | GLY268-ALA284 | |
C | GLY268-ALA284 |