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3T2J

Tetragonal thermolysin in the presence of betaine

Functional Information from GO Data
ChainGOidnamespacecontents
E0004222molecular_functionmetalloendopeptidase activity
E0006508biological_processproteolysis
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE CA E 317
ChainResidue
EASP138
EGLU177
EASP185
EGLU187
EGLU190
ECA318
EHOH412

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE CA E 318
ChainResidue
EASP185
EGLU190
ECA317
EHOH419
EHOH460
EGLU177
EASN183

site_idAC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA E 319
ChainResidue
EASP57
EASP59
EGLN61
EHOH449
EHOH467
EHOH472

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA E 320
ChainResidue
ETYR193
ETHR194
EILE197
EASP200
EHOH420
EHOH465

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN E 321
ChainResidue
EHIS142
EHIS146
EGLU166
EZN322
EHOH437
EBET2005

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ZN E 322
ChainResidue
EGLU143
EZN321
EHOH437
EHOH541
EBET2004
EBET2005

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN E 323
ChainResidue
EHIS250
ECL324
ECL325
EBET2006

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CL E 324
ChainResidue
ELYS45
EARG47
EHIS250
ETYR251
EZN323

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL E 325
ChainResidue
EHIS250
EZN323
EBET2006

site_idBC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE NA E 326
ChainResidue
ETYR211
EHOH480
EHOH520
EHOH536
EHOH537
EHOH655

site_idBC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE BET E 2001
ChainResidue
EILE1
ETYR29
EALA209
ELYS210
ETYR211
EGLY212
EHOH538
EHOH701
EHOH707

site_idBC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE BET E 2002
ChainResidue
EVAL7
EASN19
EASN21
EARG35
EHOH417
EHOH459

site_idBC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE BET E 2003
ChainResidue
ETYR179
EASN181
EARG269

site_idBC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE BET E 2004
ChainResidue
EPHE114
ETRP115
EGLU143
ETYR157
EZN322

site_idBC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE BET E 2005
ChainResidue
EASN112
EALA113
EGLU143
EARG203
EHIS231
EZN321
EZN322
EHOH437

site_idBC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE BET E 2006
ChainResidue
EARG47
ESER206
ELYS239
ETHR249
EHIS250
EZN323
ECL325
EHOH742

site_idBC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE DMS E 2011
ChainResidue
EHOH702
EHIS216
ESER218
ETYR251
EHOH609

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
DetailsActive site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10095","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"4808703","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues1
DetailsActive site: {"description":"Proton donor","evidences":[{"source":"PROSITE-ProRule","id":"PRU10095","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"4808703","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues16
DetailsBinding site: {}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues7
DetailsM-CSA 176
ChainResidueDetails

246704

PDB entries from 2025-12-24

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