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1P11

CRYSTAL STRUCTURES OF ALPHA-LYTIC PROTEASE COMPLEXES WITH IRREVERSIBLY BOUND PHOSPHONATE ESTERS

Functional Information from GO Data
ChainGOidnamespacecontents
E0004252molecular_functionserine-type endopeptidase activity
E0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 E 1
ChainResidue
EALA15
EASN15
EARG230
EPRO233
EHOH266
EHOH277
EHOH292
EHOH367
EHOH381

site_idAC2
Number of Residues30
DetailsBINDING SITE FOR CHAIN P OF PHOSPHONATE ESTER INHIBITOR A
ChainResidue
ESER40
ELEU41
EHIS57
EARG125
ETHR128
ETYR171
EGLY192
EARG192
EGLY193
EASP194
ESER195
EGLN208
ESER214
EGLY215
EGLY216
EVAL217
EGLY244
EHOH247
EHOH348
IPVA1
IPRO2
IALA3
IALA4
IBOC5
PHOH6
PHOH7
PHOH8
PHOH9
PHOH10
PHOH11

site_idAC3
Number of Residues23
DetailsBINDING SITE FOR CHAIN I OF PHOSPHONATE ESTER INHIBITOR B(TRANSITION STATE)
ChainResidue
EHIS57
EARG125
ETYR171
EGLY192
EGLY193
EASP194
ESER195
ESER214
EGLY215
EGLY216
EVAL217
EGLY244
EHOH348
PLAC-1
PALA-2
PPVA1
PPRO2
PALA3
PALA4
PBOC5
PHOH6
PHOH8
PHOH10

Functional Information from PROSITE/UniProt
site_idPS00134
Number of Residues6
DetailsTRYPSIN_HIS Serine proteases, trypsin family, histidine active site. VTAGHC
ChainResidueDetails
EVAL53-CYS58

site_idPS00135
Number of Residues12
DetailsTRYPSIN_SER Serine proteases, trypsin family, serine active site. CMgrGDSGGSWI
ChainResidueDetails
ECYS191-ILE200

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues3
DetailsActive site: {"description":"Charge relay system","evidences":[{"evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

Catalytic Information from CSA
site_idCSA1
Number of Residues5
DetailsAnnotated By Reference To The Literature 1ssx
ChainResidueDetails
EASP102
ESER195
EGLY193
EHIS57
ESER214

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1ssx
ChainResidueDetails
EASP102
ESER195
EGLY193
EHIS57

site_idMCSA1
Number of Residues5
DetailsM-CSA 609
ChainResidueDetails

248636

PDB entries from 2026-02-04

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