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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
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

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PDB entries from 2024-11-13

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