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8KME

CRYSTAL STRUCTURE OF HUMAN ALPHA-THROMBIN INHIBITED WITH SEL2770.

Functional Information from GO Data
ChainGOidnamespacecontents
10004252molecular_functionserine-type endopeptidase activity
10005576cellular_componentextracellular region
10006508biological_processproteolysis
10007596biological_processblood coagulation
20004252molecular_functionserine-type endopeptidase activity
20005509molecular_functioncalcium ion binding
20006508biological_processproteolysis
20007596biological_processblood coagulation
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE NA 2 950
ChainResidue
2LYS169
2THR172
2HOH463
2HOH465

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE NA 2 951
ChainResidue
2LYS224
2HOH440
2HOH462
2HOH570

site_idAC3
Number of Residues13
DetailsBINDING SITE FOR CHAIN 3 OF N-ACETYLHIRUDIN
ChainResidue
2LYS36
2GLN38
2LEU65
2ARG73
2THR74
2TYR76
2GLU80
2LYS81
2ILE82
3HOH427
3HOH450
3HOH467
2PHE34

site_idAC4
Number of Residues14
DetailsBINDING SITE FOR CHAIN 4 OF SEL2770
ChainResidue
2LEU99
2ILE174
2ASP189
2ALA190
2GLU192
2SER214
2TRP215
2GLY216
2GLU217
2GLY219
2CYS220
2HOH709
4HOH428
4HOH679

site_idCAT
Number of Residues3
DetailsCATALYTIC SITE
ChainResidue
2HIS57
2ASP102
2SER195

Functional Information from PROSITE/UniProt
site_idPS00134
Number of Residues6
DetailsTRYPSIN_HIS Serine proteases, trypsin family, histidine active site. LTAAHC
ChainResidueDetails
2LEU53-CYS58

site_idPS00135
Number of Residues12
DetailsTRYPSIN_SER Serine proteases, trypsin family, serine active site. DAceGDSGGPFV
ChainResidueDetails
2ASP189-VAL200

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues22
DetailsRegion: {"description":"High affinity receptor-binding region which is also known as the TP508 peptide"}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues3
DetailsActive site: {"description":"Charge relay system"}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues1
DetailsGlycosylation: {"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"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1a0j
ChainResidueDetails
2ASP102
2HIS57

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1a0j
ChainResidueDetails
2SER195
2GLY196

site_idCSA3
Number of Residues2
DetailsAnnotated By Reference To The Literature 1a0j
ChainResidueDetails
2SER195
2GLY193

site_idCSA4
Number of Residues4
DetailsAnnotated By Reference To The Literature 1a0j
ChainResidueDetails
2ASP102
2SER195
2GLY193
2HIS57

site_idCSA5
Number of Residues3
DetailsAnnotated By Reference To The Literature 1a0j
ChainResidueDetails
2ASP102
2SER195
2HIS57

site_idCSA6
Number of Residues4
DetailsAnnotated By Reference To The Literature 1a0j
ChainResidueDetails
2ASP102
2SER195
2HIS57
2GLY196

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PDB entries from 2025-07-30

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