8KME
CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2770.
Functional Information from GO Data
Chain | GOid | namespace | contents |
1 | 0004252 | molecular_function | serine-type endopeptidase activity |
1 | 0005576 | cellular_component | extracellular region |
1 | 0006508 | biological_process | proteolysis |
1 | 0007596 | biological_process | blood coagulation |
2 | 0004252 | molecular_function | serine-type endopeptidase activity |
2 | 0005509 | molecular_function | calcium ion binding |
2 | 0006508 | biological_process | proteolysis |
2 | 0007596 | biological_process | blood coagulation |
Functional Information from PDB Data
site_id | AC1 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE NA 2 950 |
Chain | Residue |
2 | LYS169 |
2 | THR172 |
2 | HOH463 |
2 | HOH465 |
site_id | AC2 |
Number of Residues | 4 |
Details | BINDING SITE FOR RESIDUE NA 2 951 |
Chain | Residue |
2 | LYS224 |
2 | HOH440 |
2 | HOH462 |
2 | HOH570 |
site_id | AC3 |
Number of Residues | 13 |
Details | BINDING SITE FOR CHAIN 3 OF N-ACETYLHIRUDIN |
Chain | Residue |
2 | LYS36 |
2 | GLN38 |
2 | LEU65 |
2 | ARG73 |
2 | THR74 |
2 | TYR76 |
2 | GLU80 |
2 | LYS81 |
2 | ILE82 |
3 | HOH427 |
3 | HOH450 |
3 | HOH467 |
2 | PHE34 |
site_id | AC4 |
Number of Residues | 14 |
Details | BINDING SITE FOR CHAIN 4 OF SEL2770 |
Chain | Residue |
2 | LEU99 |
2 | ILE174 |
2 | ASP189 |
2 | ALA190 |
2 | GLU192 |
2 | SER214 |
2 | TRP215 |
2 | GLY216 |
2 | GLU217 |
2 | GLY219 |
2 | CYS220 |
2 | HOH709 |
4 | HOH428 |
4 | HOH679 |
site_id | CAT |
Number of Residues | 3 |
Details | CATALYTIC SITE |
Chain | Residue |
2 | HIS57 |
2 | ASP102 |
2 | SER195 |
Functional Information from PROSITE/UniProt
Functional Information from SwissProt/UniProt
site_id | SWS_FT_FI1 |
Number of Residues | 22 |
Details | Region: {"description":"High affinity receptor-binding region which is also known as the TP508 peptide"} |
Chain | Residue | Details |
site_id | SWS_FT_FI2 |
Number of Residues | 3 |
Details | Active site: {"description":"Charge relay system"} |
Chain | Residue | Details |
site_id | SWS_FT_FI3 |
Number of Residues | 1 |
Details | Glycosylation: {"description":"N-linked (GlcNAc...) (complex) asparagine","evidences":[{"source":"PubMed","id":"16335952","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19139490","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19159218","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19838169","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"873923","evidenceCode":"ECO:0000269"}]} |
Chain | Residue | Details |
Catalytic Information from CSA
site_id | CSA1 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1a0j |
Chain | Residue | Details |
2 | ASP102 | |
2 | HIS57 |
site_id | CSA2 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1a0j |
Chain | Residue | Details |
2 | SER195 | |
2 | GLY196 |
site_id | CSA3 |
Number of Residues | 2 |
Details | Annotated By Reference To The Literature 1a0j |
Chain | Residue | Details |
2 | SER195 | |
2 | GLY193 |
site_id | CSA4 |
Number of Residues | 4 |
Details | Annotated By Reference To The Literature 1a0j |
Chain | Residue | Details |
2 | ASP102 | |
2 | SER195 | |
2 | GLY193 | |
2 | HIS57 |
site_id | CSA5 |
Number of Residues | 3 |
Details | Annotated By Reference To The Literature 1a0j |
Chain | Residue | Details |
2 | ASP102 | |
2 | SER195 | |
2 | HIS57 |
site_id | CSA6 |
Number of Residues | 4 |
Details | Annotated By Reference To The Literature 1a0j |
Chain | Residue | Details |
2 | ASP102 | |
2 | SER195 | |
2 | HIS57 | |
2 | GLY196 |