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4MPX

Human beta-tryptase co-crystal structure with [(1,1,3,3-tetramethyldisiloxane-1,3-diyl)di-1-benzothiene-4,2-diyl]bis({4-[3-(aminomethyl)phenyl]piperidin-1-yl}methanone)

Functional Information from GO Data
ChainGOidnamespacecontents
A0004252molecular_functionserine-type endopeptidase activity
A0005515molecular_functionprotein binding
A0005576cellular_componentextracellular region
A0005615cellular_componentextracellular space
A0006508biological_processproteolysis
A0006952biological_processdefense response
A0008236molecular_functionserine-type peptidase activity
A0022617biological_processextracellular matrix disassembly
A0042802molecular_functionidentical protein binding
A0062023cellular_componentcollagen-containing extracellular matrix
B0004252molecular_functionserine-type endopeptidase activity
B0005515molecular_functionprotein binding
B0005576cellular_componentextracellular region
B0005615cellular_componentextracellular space
B0006508biological_processproteolysis
B0006952biological_processdefense response
B0008236molecular_functionserine-type peptidase activity
B0022617biological_processextracellular matrix disassembly
B0042802molecular_functionidentical protein binding
B0062023cellular_componentcollagen-containing extracellular matrix
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 301
ChainResidue
AHIS138
ATRP236
AHOH460
AHOH530

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 302
ChainResidue
AHIS74
AGLN221
AGLY222
ASER224

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 303
ChainResidue
ALYS179
AARG217
AGLN35

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PGE A 304
ChainResidue
AVAL50
APHE58
ALYS81
AASP82
AALA85
AHOH544

site_idAC5
Number of Residues25
DetailsBINDING SITE FOR RESIDUE 2AV B 301
ChainResidue
ATHR115
AGLN117
AASP218
ASER219
ACYS220
AGLN221
ASER224
ATRP244
AGLY245
AGLU246
AGLY247
AGLY255
AHOH408
BGLN117
BASP218
BSER219
BCYS220
BSER224
BVAL242
BTRP244
BGLY245
BGLU246
BGLY247
BCYS248
BHOH413

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 302
ChainResidue
BHIS74
BGLN221
BGLY222
BSER224

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 B 303
ChainResidue
AHIS136
BGLU128
BHIS186
BARG203
BMES307

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 B 304
ChainResidue
BASN214
BTHR215
BARG216

site_idAC9
Number of Residues1
DetailsBINDING SITE FOR RESIDUE CL B 305
ChainResidue
BASN185

site_idBC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PGE B 306
ChainResidue
BVAL50
BPHE58
BLYS81
BASP82
BALA85
BHOH504

site_idBC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MES B 307
ChainResidue
ALYS132
AHIS136
AHOH468
BARG203
BARG206
BASP207
BSO4303

Functional Information from PROSITE/UniProt
site_idPS00134
Number of Residues6
DetailsTRYPSIN_HIS Serine proteases, trypsin family, histidine active site. LTAAHC
ChainResidueDetails
ALEU70-CYS75

site_idPS00135
Number of Residues12
DetailsTRYPSIN_SER Serine proteases, trypsin family, serine active site. DScqGDSGGPLV
ChainResidueDetails
AASP218-VAL229

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsACT_SITE: Charge relay system
ChainResidueDetails
AHIS74
AASP121
ASER224
BHIS74
BASP121
BSER224

site_idSWS_FT_FI2
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
ALYS132
BLYS132

site_idSWS_FT_FI3
Number of Residues2
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000269|PubMed:19159218
ChainResidueDetails
AASN233
BASN233

222415

PDB entries from 2024-07-10

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