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3L3T

Human mesotrypsin complexed with amyloid precursor protein inhibitor variant (APPIR15K)

Functional Information from GO Data
ChainGOidnamespacecontents
A0004252molecular_functionserine-type endopeptidase activity
A0006508biological_processproteolysis
B0004252molecular_functionserine-type endopeptidase activity
B0006508biological_processproteolysis
C0004252molecular_functionserine-type endopeptidase activity
C0006508biological_processproteolysis
D0004252molecular_functionserine-type endopeptidase activity
D0006508biological_processproteolysis
E0004867molecular_functionserine-type endopeptidase inhibitor activity
F0004867molecular_functionserine-type endopeptidase inhibitor activity
G0004867molecular_functionserine-type endopeptidase inhibitor activity
H0004867molecular_functionserine-type endopeptidase inhibitor activity
Functional Information from PDB Data
site_idAC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE FMT A 1
ChainResidue
ALEU163
AHOH300

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE FMT A 2
ChainResidue
AARG66
AILE73
AHOH269
AHOH341

site_idAC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE FMT B 3
ChainResidue
BPRO129
BLEU163

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FMT A 4
ChainResidue
ATYR234
AVAL235
AASP236
ATRP237
AASN233

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE FMT A 247
ChainResidue
AALA221
ATRP221
ALYS222
AHOH327

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE FMT A 248
ChainResidue
ASER119
ATHR120
AHOH205
AHOH301
CSER122
CGLY203

site_idAC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE FMT C 247
ChainResidue
CPRO129
CLYS230

site_idAC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE FMT B 10
ChainResidue
BSER171
BASN223

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE FMT B 11
ChainResidue
BHIS91
BLYS93
CGLY174

site_idBC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE FMT B 12
ChainResidue
ATHR164
BTHR164

site_idBC2
Number of Residues1
DetailsBINDING SITE FOR RESIDUE FMT A 13
ChainResidue
AGLY219

site_idBC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA B 1
ChainResidue
BGLU70
BASN72
BVAL75
BGLU77
BGLU80

site_idBC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 250
ChainResidue
AGLU70
AASN72
AVAL75
AGLU77
AGLU80
AHOH269

site_idBC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA C 3
ChainResidue
CGLU70
CASN72
CVAL75
CGLU77
CGLU80
CHOH289

site_idBC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CA D 4
ChainResidue
DGLU70
DASN72
DVAL75
DGLU80
DHOH267

Functional Information from PROSITE/UniProt
site_idPS00134
Number of Residues6
DetailsTRYPSIN_HIS Serine proteases, trypsin family, histidine active site. VSAAHC
ChainResidueDetails
AVAL53-CYS58

site_idPS00280
Number of Residues19
DetailsBPTI_KUNITZ_1 Pancreatic trypsin inhibitor (Kunitz) family signature. FfyGGCggnrnnFdteeyC
ChainResidueDetails
EPHE33-CYS51

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues12
DetailsACT_SITE: Charge relay system => ECO:0000255|PROSITE-ProRule:PRU00274, ECO:0000305|PubMed:27810896
ChainResidueDetails
AHIS57
DHIS57
DASP102
DALA195
AASP102
AALA195
BHIS57
BASP102
BALA195
CHIS57
CASP102
CALA195

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:11827488, ECO:0000269|PubMed:25301953, ECO:0000269|PubMed:27810896, ECO:0007744|PDB:1H4W, ECO:0007744|PDB:3L33, ECO:0007744|PDB:3L3T, ECO:0007744|PDB:3P92, ECO:0007744|PDB:3P95, ECO:0007744|PDB:4U30, ECO:0007744|PDB:4U32, ECO:0007744|PDB:5JBT, ECO:0007744|PDB:5TP0
ChainResidueDetails
AGLU70
DGLU70
DASN72
DVAL75
AASN72
AVAL75
BGLU70
BASN72
BVAL75
CGLU70
CASN72
CVAL75

site_idSWS_FT_FI3
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:11827488, ECO:0000269|PubMed:25301953, ECO:0000269|PubMed:27810896, ECO:0007744|PDB:1H4W, ECO:0007744|PDB:3L33, ECO:0007744|PDB:3L3T, ECO:0007744|PDB:3P92, ECO:0007744|PDB:3P95, ECO:0007744|PDB:4U30, ECO:0007744|PDB:4U32, ECO:0007744|PDB:5JBT
ChainResidueDetails
AGLU77
BGLU77
CGLU77
DGLU77

site_idSWS_FT_FI4
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:11827488, ECO:0000269|PubMed:25301953, ECO:0000269|PubMed:27810896, ECO:0007744|PDB:1H4W, ECO:0007744|PDB:3L33, ECO:0007744|PDB:3L3T, ECO:0007744|PDB:3P92, ECO:0007744|PDB:3P95, ECO:0007744|PDB:4U32, ECO:0007744|PDB:5JBT, ECO:0007744|PDB:5TP0
ChainResidueDetails
AGLU80
BGLU80
CGLU80
DGLU80

site_idSWS_FT_FI5
Number of Residues4
DetailsSITE: Required for specificity => ECO:0000250
ChainResidueDetails
AASP189
BASP189
CASP189
DASP189

site_idSWS_FT_FI6
Number of Residues4
DetailsMOD_RES: Sulfotyrosine => ECO:0000250
ChainResidueDetails
ATYR151
BTYR151
CTYR151
DTYR151

221716

PDB entries from 2024-06-26

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