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5LWD

Thermolysin in complex with inhibitor (JC96)

Functional Information from GO Data
ChainGOidnamespacecontents
E0004222molecular_functionmetalloendopeptidase activity
E0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues4
Detailsbinding site for residue ZN E 401
ChainResidue
EHIS142
EHIS146
EGLU166
E79E411

site_idAC2
Number of Residues6
Detailsbinding site for residue CA E 402
ChainResidue
EHOH787
EASP57
EASP59
EGLN61
EHOH578
EHOH582

site_idAC3
Number of Residues6
Detailsbinding site for residue CA E 403
ChainResidue
EASP138
EGLU177
EASP185
EGLU187
EGLU190
EHOH588

site_idAC4
Number of Residues6
Detailsbinding site for residue CA E 404
ChainResidue
EGLU177
EASN183
EASP185
EGLU190
EHOH562
EHOH583

site_idAC5
Number of Residues6
Detailsbinding site for residue CA E 405
ChainResidue
ETYR193
ETHR194
EILE197
EASP200
EHOH604
EHOH761

site_idAC6
Number of Residues7
Detailsbinding site for residue DMS E 406
ChainResidue
ETYR110
EASN112
EPHE114
E79E411
E79E411
EHOH516
EHOH570

site_idAC7
Number of Residues6
Detailsbinding site for residue DMS E 407
ChainResidue
ETYR66
EHIS216
ESER218
ETYR251
EHOH864
EHOH887

site_idAC8
Number of Residues5
Detailsbinding site for residue DMS E 408
ChainResidue
EILE1
ETHR2
EGLY3
EGLN31
EASN33

site_idAC9
Number of Residues8
Detailsbinding site for residue GOL E 409
ChainResidue
EPHE114
ETRP115
EHIS146
ETYR157
E79E411
EHOH510
EHOH557
EHOH703

site_idAD1
Number of Residues7
Detailsbinding site for residue GOL E 410
ChainResidue
EGLY109
ETYR110
EASN111
EASN112
EHOH569
EHOH626
EHOH686

site_idAD2
Number of Residues22
Detailsbinding site for residue 79E E 411
ChainResidue
ETYR106
EASN111
EASN112
EALA113
EPHE114
ETRP115
EPHE130
EHIS142
EGLU143
EHIS146
ETYR157
EGLU166
ELEU202
EARG203
EHIS231
EZN401
EDMS406
EDMS406
EGOL409
EHOH660
EHOH679
EHOH712

Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. VVAHELTHAV
ChainResidueDetails
EVAL139-VAL148

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsACT_SITE: ACT_SITE => ECO:0000255|PROSITE-ProRule:PRU10095, ECO:0000269|PubMed:4808703
ChainResidueDetails
EGLU143

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor => ECO:0000255|PROSITE-ProRule:PRU10095, ECO:0000269|PubMed:4808703
ChainResidueDetails
EHIS231

site_idSWS_FT_FI3
Number of Residues16
DetailsBINDING:
ChainResidueDetails
EASP57
EASP185
EGLU187
EGLU190
ETYR193
ETHR194
EILE197
EASP200
EASP59
EGLN61
EASP138
EHIS142
EHIS146
EGLU166
EGLU177
EASN183

Catalytic Information from CSA
site_idMCSA1
Number of Residues7
DetailsM-CSA 176
ChainResidueDetails
EHIS142metal ligand
EGLU143electrostatic stabiliser, metal ligand
EHIS146metal ligand
ETYR157electrostatic stabiliser, hydrogen bond donor, steric role
EGLU166metal ligand
EASP226activator, electrostatic stabiliser, hydrogen bond acceptor
EHIS231hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor

219140

PDB entries from 2024-05-01

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