Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

5Q0F

FACTOR XIA IN COMPLEX WITH THE INHIBITOR methyl [(4R,5E,8S)-8-({(2E)-3-[5-chloro-2-(1H-tetrazol-1-yl)phenyl]prop-2-enoyl}amino)-4-methyl-2-oxo-1,3,4,7,8,10-hexahydro-2H-12,9-(azeno)-1,10-benzodiazacyclotetradecin-15-yl]carbamate

Functional Information from GO Data
ChainGOidnamespacecontents
A0004252molecular_functionserine-type endopeptidase activity
A0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues25
Detailsbinding site for residue 9FA A 301
ChainResidue
AARG39
ALYS192
AGLY193
AASP194
ASER195
ATRP215
AGLY216
AGLY218
ACYS219
AGLY226
AVAL227
AHIS40
AEDO304
AEDO307
AEDO315
AHOH425
AHOH446
AHOH454
ALEU41
AHIS57
ALEU147
AILE151
AASP189
AALA190
ACYS191

site_idAC2
Number of Residues11
Detailsbinding site for residue SO4 A 302
ChainResidue
AVAL23
AARG24
AGLY25
AGLU26
ATRP27
APRO28
AILE70
ALEU71
ALEU155
AHOH410
AHOH412

site_idAC3
Number of Residues6
Detailsbinding site for residue SO4 A 303
ChainResidue
ALYS169
ALYS169
AARG170
AARG170
AARG184
AARG184

site_idAC4
Number of Residues5
Detailsbinding site for residue EDO A 304
ChainResidue
A9FA301
AEDO307
AEDO308
AEDO315
AHOH511

site_idAC5
Number of Residues5
Detailsbinding site for residue EDO A 305
ChainResidue
AASN49
AVAL112
AGLY113
ATYR114
AHOH450

site_idAC6
Number of Residues9
Detailsbinding site for residue EDO A 306
ChainResidue
AARG24
ASER99
AGLY173
AHIS174
ALYS175
AHOH460
AHOH485
AHOH492
AHOH536

site_idAC7
Number of Residues8
Detailsbinding site for residue EDO A 307
ChainResidue
ASER81
AGLY216
AGLU217
AGLY218
A9FA301
AEDO304
AEDO308
AHOH491

site_idAC8
Number of Residues5
Detailsbinding site for residue EDO A 308
ChainResidue
AGLY216
AGLU217
AEDO304
AEDO307
AHOH422

site_idAC9
Number of Residues1
Detailsbinding site for residue EDO A 309
ChainResidue
AHIS178

site_idAD1
Number of Residues3
Detailsbinding site for residue EDO A 310
ChainResidue
AGLN38
AHOH408
AHOH530

site_idAD2
Number of Residues8
Detailsbinding site for residue EDO A 311
ChainResidue
AGLU167
AARG170
AGLY184
AARG184
AGLU223
AARG224
APRO225
AHOH431

site_idAD3
Number of Residues6
Detailsbinding site for residue EDO A 312
ChainResidue
AHIS178
AMET180
AILE181
AASN230
AHOH539
AHOH546

site_idAD4
Number of Residues5
Detailsbinding site for residue EDO A 313
ChainResidue
ASER99
AGLY100
ATYR101
ATHR177
ALYS179

site_idAD5
Number of Residues4
Detailsbinding site for residue EDO A 314
ChainResidue
ALYS157
AHOH413
AGLU26
ATRP137

site_idAD6
Number of Residues6
Detailsbinding site for residue EDO A 315
ChainResidue
AGLY113
ATYR114
A9FA301
AEDO304
AHOH445
AHOH511

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

225946

PDB entries from 2024-10-09

PDB statisticsPDBj update infoContact PDBjnumon