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3T87

Thermolysin In Complex With UBTLN28

Functional Information from GO Data
ChainGOidnamespacecontents
A0004222molecular_functionmetalloendopeptidase activity
A0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE UBZ A 317
ChainResidue
ATYR106
AGLU166
ALEU202
AARG203
AHIS231
AGOL319
ADMS321
ADMS321
AZN326
AHOH621
AHOH633
AASN112
AHOH683
AALA113
APHE114
ATRP115
AHIS142
AGLU143
AHIS146
ATYR157

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL A 318
ChainResidue
AGLY109
ATYR110
AASN111
AASN112
AHOH674
AHOH713

site_idAC3
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 319
ChainResidue
APHE114
ATRP115
AHIS146
ATYR157
AUBZ317
AHOH490
AHOH515
AHOH537

site_idAC4
Number of Residues11
DetailsBINDING SITE FOR RESIDUE GOL A 320
ChainResidue
AGLY247
AGLY248
ATHR249
AVAL255
AGLN273
ALEU275
AHOH535
AHOH573
AHOH588
AHOH635
AHOH658

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE DMS A 321
ChainResidue
ATYR110
AASN112
APHE114
AUBZ317
AUBZ317
AHOH793
AHOH802

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE DMS A 322
ChainResidue
AILE1
ATHR2
AGLY3
AGLN31
AASN33

site_idAC7
Number of Residues7
DetailsBINDING SITE FOR RESIDUE DMS A 323
ChainResidue
ATYR66
AHIS216
ASER218
ATYR251
AHOH351
AHOH412
AHOH647

site_idAC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE DMS A 324
ChainResidue
ATHR4
ATYR24
ATYR24
ASER25
ATYR28
AHOH717
AHOH722

site_idAC9
Number of Residues6
DetailsBINDING SITE FOR RESIDUE DMS A 325
ChainResidue
AGLY95
APRO184
ATRP186
AHOH570
AHOH732
AHOH739

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 326
ChainResidue
AHIS142
AHIS146
AGLU166
AUBZ317

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 327
ChainResidue
AASP138
AGLU177
AASP185
AGLU187
AGLU190
AHOH785

site_idBC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 328
ChainResidue
AGLU177
AASN183
AASP185
AGLU190
AHOH790
AHOH791

site_idBC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 329
ChainResidue
ATYR193
ATHR194
AILE197
AASP200
AHOH788
AHOH792

site_idBC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 330
ChainResidue
AASP57
AASP59
AGLN61
AHOH786
AHOH787
AHOH789

Functional Information from PROSITE/UniProt
site_idPS00142
Number of Residues10
DetailsZINC_PROTEASE Neutral zinc metallopeptidases, zinc-binding region signature. VVAHELTHAV
ChainResidueDetails
AVAL139-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
AGLU143

site_idSWS_FT_FI2
Number of Residues1
DetailsACT_SITE: Proton donor => ECO:0000255|PROSITE-ProRule:PRU10095, ECO:0000269|PubMed:4808703
ChainResidueDetails
AHIS231

site_idSWS_FT_FI3
Number of Residues16
DetailsBINDING:
ChainResidueDetails
AGLN61
AASP138
AHIS142
AHIS146
AGLU166
AGLU177
AASN183
AASP185
AGLU187
AGLU190
ATYR193
ATHR194
AILE197
AASP200
AASP57
AASP59

Catalytic Information from CSA
site_idMCSA1
Number of Residues7
DetailsM-CSA 176
ChainResidueDetails
AHIS142metal ligand
AGLU143electrostatic stabiliser, metal ligand
AHIS146metal ligand
ATYR157electrostatic stabiliser, hydrogen bond donor, steric role
AGLU166metal ligand
AASP226activator, electrostatic stabiliser, hydrogen bond acceptor
AHIS231hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor

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PDB entries from 2024-05-29

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