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4U30

Human mesotrypsin complexed with bikunin Kunitz domain 2

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
W0004867molecular_functionserine-type endopeptidase inhibitor activity
X0004867molecular_functionserine-type endopeptidase inhibitor activity
Y0004867molecular_functionserine-type endopeptidase inhibitor activity
Z0004867molecular_functionserine-type endopeptidase inhibitor activity
Functional Information from PDB Data
site_idAC1
Number of Residues6
Detailsbinding site for residue CA A 301
ChainResidue
AGLU70
AASN72
AVAL75
AGLU77
AGLU80
AHOH423

site_idAC2
Number of Residues6
Detailsbinding site for residue CA B 301
ChainResidue
BGLU77
BGLU80
BHOH408
BGLU70
BASN72
BVAL75

site_idAC3
Number of Residues6
Detailsbinding site for residue CA C 301
ChainResidue
CGLU70
CASN72
CVAL75
CGLU77
CGLU80
CHOH414

site_idAC4
Number of Residues6
Detailsbinding site for residue CA D 301
ChainResidue
DGLU70
DASN72
DVAL75
DGLU77
DGLU80
DHOH441

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. FpyGGCqgngnkFysekeC
ChainResidueDetails
XPHE33-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

226707

PDB entries from 2024-10-30

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