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5WB6

FACTOR XIA IN COMPLEX WITH THE INHIBITOR methyl [(11S)-11-({(2E)-3-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]prop-2-enoyl}amino)-6-fluoro-2-oxo-1,3,4,10,11,13-hexahydro-2H-5,9:15,12-di(azeno)-1,13-benzodiazacycloheptadecin-18-yl]carbamate

Functional Information from GO Data
ChainGOidnamespacecontents
A0004252molecular_functionserine-type endopeptidase activity
A0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues29
Detailsbinding site for residue 9ZM A 301
ChainResidue
AARG39
AASP189
AALA190
ACYS191
ALYS192
AGLY193
AASP194
ASER195
ATHR213
ATRP215
AGLY216
AHIS40
AGLY218
ACYS219
AGLY226
AVAL227
AEDO303
AEDO306
AEDO309
AHOH444
AHOH448
AHOH484
ALEU41
AHIS57
ACYS58
ATYR58
ATYR114
ALEU147
AILE151

site_idAC2
Number of Residues4
Detailsbinding site for residue SO4 A 302
ChainResidue
AARG170
AARG170
AARG184
AARG184

site_idAC3
Number of Residues7
Detailsbinding site for residue EDO A 303
ChainResidue
ALYS192
A9ZM301
AEDO306
AEDO307
AEDO309
AHOH406
AHOH519

site_idAC4
Number of Residues6
Detailsbinding site for residue EDO A 304
ChainResidue
AASN49
ATHR111
AVAL112
AGLY113
ATYR114
AHOH483

site_idAC5
Number of Residues6
Detailsbinding site for residue EDO A 305
ChainResidue
AARG24
AGLY25
ATRP27
AILE70
ALEU71
AHOH422

site_idAC6
Number of Residues8
Detailsbinding site for residue EDO A 306
ChainResidue
ASER81
AGLY216
AGLU217
AGLY218
A9ZM301
AEDO303
AEDO307
AHOH445

site_idAC7
Number of Residues6
Detailsbinding site for residue EDO A 307
ChainResidue
AGLU98
AGLY216
AGLU217
AEDO303
AEDO306
AHOH406

site_idAC8
Number of Residues5
Detailsbinding site for residue EDO A 308
ChainResidue
ASER99
AGLY100
ATYR101
ATHR177
ALYS179

site_idAC9
Number of Residues3
Detailsbinding site for residue EDO A 309
ChainResidue
A9ZM301
AEDO303
AHOH474

site_idAD1
Number of Residues10
Detailsbinding site for residue EDO A 310
ChainResidue
AVAL163
AGLU167
AARG170
AGLY184
ATYR184
AARG184
AGLU223
AARG224
APRO225
AHOH413

site_idAD2
Number of Residues5
Detailsbinding site for residue EDO A 311
ChainResidue
AHIS178
AMET180
AILE181
AHOH470
AHOH509

site_idAD3
Number of Residues4
Detailsbinding site for residue EDO A 312
ChainResidue
AGLU26
ATRP137
ALYS157
ATRP207

site_idAD4
Number of Residues2
Detailsbinding site for residue EDO A 313
ChainResidue
AGLN38
AHOH417

site_idAD5
Number of Residues1
Detailsbinding site for residue EDO A 314
ChainResidue
AILE47

site_idAD6
Number of Residues1
Detailsbinding site for residue EDO A 315
ChainResidue
AHIS178

site_idAD7
Number of Residues6
Detailsbinding site for residue EDO A 316
ChainResidue
AGLY173
ALYS175
AHOH429
AHOH449
AARG24
ASER99

Functional Information from PROSITE/UniProt
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. DAckGDSGGPLS
ChainResidueDetails
AASP189-SER200

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues3
DetailsACT_SITE: Charge relay system
ChainResidueDetails
AHIS57
AASP102
ASER195

site_idSWS_FT_FI2
Number of Residues1
DetailsBINDING:
ChainResidueDetails
ALYS169

site_idSWS_FT_FI3
Number of Residues1
DetailsCARBOHYD: N-linked (GlcNAc...) (complex) asparagine => ECO:0000269|PubMed:16335952, ECO:0000269|PubMed:19159218, ECO:0000269|PubMed:25092234
ChainResidueDetails
AASN72

site_idSWS_FT_FI4
Number of Residues1
DetailsCARBOHYD: N-linked (GlcNAc...) (complex) asparagine => ECO:0000269|PubMed:16335952, ECO:0000269|PubMed:19159218, ECO:0000269|PubMed:1998667, ECO:0000269|PubMed:25092234
ChainResidueDetails
AGLY113

219140

PDB entries from 2024-05-01

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