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3T8H

Thermolysin In Complex With UBTLN29

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 UBS A 317
ChainResidue
ATYR106
AGLU166
ALEU202
AARG203
AHIS231
ADMS318
ADMS318
AGOL323
AZN326
AHOH549
AHOH570
AASN112
AHOH614
AALA113
APHE114
ATRP115
AHIS142
AGLU143
AHIS146
ATYR157

site_idAC2
Number of Residues8
DetailsBINDING SITE FOR RESIDUE DMS A 318
ChainResidue
ATYR110
AASN112
APHE114
AUBS317
AUBS317
AGOL324
AHOH373
AHOH505

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE DMS A 319
ChainResidue
AHIS216
ASER218
ATYR251
AHOH604

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE DMS A 320
ChainResidue
AGLY95
APRO184
ATRP186
AHOH510
AHOH520

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE DMS A 321
ChainResidue
AGLY3
ATYR24
ATYR24
ASER25
ATYR28
AHOH593

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

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 323
ChainResidue
APHE114
ATRP115
AHIS146
ATYR157
AUBS317
AHOH442
AHOH450
AHOH489

site_idAC8
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 324
ChainResidue
AGLY109
ATYR110
AASN111
AASN112
AGLN158
ADMS318
AHOH617
AHOH625

site_idAC9
Number of Residues12
DetailsBINDING SITE FOR RESIDUE GOL A 325
ChainResidue
ATHR152
AGLY247
AGLY248
AVAL255
AGLN273
ATYR274
ALEU275
AHOH487
AHOH526
AHOH552
AHOH563
AHOH680

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 326
ChainResidue
AHIS142
AHIS146
AGLU166
AUBS317

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 327
ChainResidue
AASP138
AGLU177
AASP185
AGLU187
AGLU190
AHOH720

site_idBC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 328
ChainResidue
AGLU177
AASN183
AASP185
AGLU190
AHOH726
AHOH727

site_idBC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 329
ChainResidue
ATYR193
ATHR194
AILE197
AASP200
AHOH721
AHOH728

site_idBC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 330
ChainResidue
AASP59
AGLN61
AHOH722
AHOH723
AHOH724
AASP57

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
AASP57
AASP185
AGLU187
AGLU190
ATYR193
ATHR194
AILE197
AASP200
AASP59
AGLN61
AASP138
AHIS142
AHIS146
AGLU166
AGLU177
AASN183

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

219140

PDB entries from 2024-05-01

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