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2J95

CRYSTAL STRUCTURE OF A HUMAN FACTOR XA INHIBITOR COMPLEX

Functional Information from GO Data
ChainGOidnamespacecontents
A0004252molecular_functionserine-type endopeptidase activity
A0006508biological_processproteolysis
B0005509molecular_functioncalcium ion binding
B0005576cellular_componentextracellular region
Functional Information from PDB Data
site_idAC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A1246
ChainResidue
AASP70
AASN72
AGLN75
AGLU80
AHOH2021
AHOH2022

site_idAC2
Number of Residues16
DetailsBINDING SITE FOR RESIDUE GSX A1245
ChainResidue
ATYR99
APHE174
AASP189
AALA190
AGLN192
ASER195
AVAL213
ATRP215
AGLY216
AGLY219
AGLY226
AILE227
ATYR228
ALYS96
AGLU97
ATHR98

Functional Information from PROSITE/UniProt
site_idPS00010
Number of Residues12
DetailsASX_HYDROXYL Aspartic acid and asparagine hydroxylation site. CkDglgeYtCtC
ChainResidueDetails
BCYS-27-CYS-16

site_idPS00011
Number of Residues26
DetailsGLA_1 Vitamin K-dependent carboxylation domain. EcmEEtCsyeearEvfedsdktne.FW
ChainResidueDetails
BGLU-72-TRP-47

site_idPS00022
Number of Residues12
DetailsEGF_1 EGF-like domain signature 1. CtCleGfeGKnC
ChainResidueDetails
BCYS-18-CYS-7

site_idPS01186
Number of Residues12
DetailsEGF_2 EGF-like domain signature 2. CtCleGFegkn....C
ChainResidueDetails
BCYS-18-CYS-7
BCYS21-CYS36

site_idPS01187
Number of Residues25
DetailsEGF_CA Calcium-binding EGF-like domain signature. DgDQCetsp..........Cqnqgk..CkDglgeYtC
ChainResidueDetails
BASP-42-CYS-18

site_idPS00134
Number of Residues6
DetailsTRYPSIN_HIS Serine proteases, trypsin family, histidine active site. LTAAHC
ChainResidueDetails
ALEU53-CYS58

site_idPS00135
Number of Residues12
DetailsTRYPSIN_SER Serine proteases, trypsin family, serine active site. DAcqGDSGGPHV
ChainResidueDetails
AASP189-VAL200

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues11
DetailsMOD_RES: 4-carboxyglutamate => ECO:0000255|PROSITE-ProRule:PRU00463, ECO:0000269|PubMed:6871167
ChainResidueDetails
BGLU-82
BGLU-81
BGLU-74
BGLU-72
BGLU-69
BGLU-68
BGLU-63
BGLU-62
BGLU-59
BGLU-56
BGLU-49

site_idSWS_FT_FI2
Number of Residues1
DetailsMOD_RES: (3R)-3-hydroxyaspartate => ECO:0000269|PubMed:6871167
ChainResidueDetails
BASP-25

218500

PDB entries from 2024-04-17

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