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6VIE

Structure of caspase-1 in complex with gasdermin D

Functional Information from GO Data
ChainGOidnamespacecontents
A0004197molecular_functioncysteine-type endopeptidase activity
A0006508biological_processproteolysis
A0008234molecular_functioncysteine-type peptidase activity
B0004197molecular_functioncysteine-type endopeptidase activity
B0006508biological_processproteolysis
B0008234molecular_functioncysteine-type peptidase activity
C0001786molecular_functionphosphatidylserine binding
C0005546molecular_functionphosphatidylinositol-4,5-bisphosphate binding
C0005576cellular_componentextracellular region
C0005615cellular_componentextracellular space
C0005634cellular_componentnucleus
C0005654cellular_componentnucleoplasm
C0005737cellular_componentcytoplasm
C0005739cellular_componentmitochondrion
C0005829cellular_componentcytosol
C0005886cellular_componentplasma membrane
C0006954biological_processinflammatory response
C0008289molecular_functionlipid binding
C0009306biological_processprotein secretion
C0012501biological_processprogrammed cell death
C0016020cellular_componentmembrane
C0022829molecular_functionwide pore channel activity
C0031966cellular_componentmitochondrial membrane
C0032731biological_processpositive regulation of interleukin-1 beta production
C0045087biological_processinnate immune response
C0046931biological_processpore complex assembly
C0050729biological_processpositive regulation of inflammatory response
C0050829biological_processdefense response to Gram-negative bacterium
C0050830biological_processdefense response to Gram-positive bacterium
C0051260biological_processprotein homooligomerization
C0055085biological_processtransmembrane transport
C0061702cellular_componentcanonical inflammasome complex
C0070269biological_processpyroptotic inflammatory response
C0070273molecular_functionphosphatidylinositol-4-phosphate binding
C0070300molecular_functionphosphatidic acid binding
C0072559cellular_componentNLRP3 inflammasome complex
C0141201biological_processpyroptotic cell death
C1901612molecular_functioncardiolipin binding
D0001786molecular_functionphosphatidylserine binding
D0005546molecular_functionphosphatidylinositol-4,5-bisphosphate binding
D0005576cellular_componentextracellular region
D0005615cellular_componentextracellular space
D0005634cellular_componentnucleus
D0005654cellular_componentnucleoplasm
D0005737cellular_componentcytoplasm
D0005739cellular_componentmitochondrion
D0005829cellular_componentcytosol
D0005886cellular_componentplasma membrane
D0006954biological_processinflammatory response
D0008289molecular_functionlipid binding
D0009306biological_processprotein secretion
D0012501biological_processprogrammed cell death
D0016020cellular_componentmembrane
D0022829molecular_functionwide pore channel activity
D0031966cellular_componentmitochondrial membrane
D0032731biological_processpositive regulation of interleukin-1 beta production
D0045087biological_processinnate immune response
D0046931biological_processpore complex assembly
D0050729biological_processpositive regulation of inflammatory response
D0050829biological_processdefense response to Gram-negative bacterium
D0050830biological_processdefense response to Gram-positive bacterium
D0051260biological_processprotein homooligomerization
D0055085biological_processtransmembrane transport
D0061702cellular_componentcanonical inflammasome complex
D0070269biological_processpyroptotic inflammatory response
D0070273molecular_functionphosphatidylinositol-4-phosphate binding
D0070300molecular_functionphosphatidic acid binding
D0072559cellular_componentNLRP3 inflammasome complex
D0141201biological_processpyroptotic cell death
D1901612molecular_functioncardiolipin binding
Functional Information from PROSITE/UniProt
site_idPS00455
Number of Residues12
DetailsAMP_BINDING Putative AMP-binding domain signature. MPTSSGSEGnVK
ChainResidueDetails
AMET123-LYS134

site_idPS01121
Number of Residues15
DetailsCASPASE_HIS Caspase family histidine active site. HktsdStfLvFMSHG
ChainResidueDetails
AHIS224-GLY238

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues46
DetailsTRANSMEM: Beta stranded => ECO:0000250|UniProtKB:P57764
ChainResidueDetails
CGLN92-SER98
CLYS104-ALA109
CGLY181-LEU187
CCYS192-LYS198
DGLN92-SER98
DLYS104-ALA109
DGLY181-LEU187
DCYS192-LYS198

site_idSWS_FT_FI2
Number of Residues2
DetailsSITE: Cleavage; by CASP3 or CASP7 => ECO:0000269|PubMed:37327784
ChainResidueDetails
CASP88
DASP88

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Cleavage; by caspases CASP1, CASP4/CASP11 and CASP8 => ECO:0000269|PubMed:26375259, ECO:0000269|PubMed:30361383, ECO:0000269|PubMed:32553275, ECO:0000269|PubMed:38538834, ECO:0000305|PubMed:30135078
ChainResidueDetails
CSER300
DSER300

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Cleavage; by papain => ECO:0000269|PubMed:35794369
ChainResidueDetails
CSER334
DSER334

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:P57764
ChainResidueDetails
CTYR38
DTYR38

site_idSWS_FT_FI6
Number of Residues18
DetailsMOD_RES: S-(2-succinyl)cysteine => ECO:0000269|PubMed:32820063
ChainResidueDetails
CCYS39
DCYS39
DCYS57
DCYS77
DCYS122
DCYS192
DPHE289
DGLN323
DGLN458
CCYS57
CCYS77
CCYS122
CCYS192
CPHE289
CGLN323
CGLN458

site_idSWS_FT_FI7
Number of Residues2
DetailsLIPID: S-palmitoyl cysteine => ECO:0000269|PubMed:38530158, ECO:0000269|PubMed:38538834, ECO:0000269|PubMed:38599239
ChainResidueDetails
CCYS192
DCYS192

Catalytic Information from CSA
site_idMCSA1
Number of Residues1
DetailsM-CSA 718
ChainResidueDetails
BGLU390electrostatic stabiliser
AGLY238electrostatic stabiliser
AALA285nucleofuge, nucleophile, proton acceptor, proton donor
AARG286electrostatic stabiliser

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PDB entries from 2024-09-11

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