Loading
PDBj
MenuPDBj@FacebookPDBj@X(formerly Twitter)PDBj@BlueSkyPDBj@YouTubewwPDB FoundationwwPDBDonate
RCSB PDBPDBeBMRBAdv. SearchSearch help

3S3P

Transglutaminase 2 in complex with a novel inhibitor

Functional Information from GO Data
ChainGOidnamespacecontents
A0000166molecular_functionnucleotide binding
A0000785cellular_componentchromatin
A0000786cellular_componentnucleosome
A0003810molecular_functionprotein-glutamine gamma-glutamyltransferase activity
A0005509molecular_functioncalcium ion binding
A0005515molecular_functionprotein binding
A0005525molecular_functionGTP binding
A0005634cellular_componentnucleus
A0005694cellular_componentchromosome
A0005739cellular_componentmitochondrion
A0005783cellular_componentendoplasmic reticulum
A0005829cellular_componentcytosol
A0005886cellular_componentplasma membrane
A0005925cellular_componentfocal adhesion
A0006338biological_processchromatin remodeling
A0006508biological_processproteolysis
A0007200biological_processphospholipase C-activating G protein-coupled receptor signaling pathway
A0008233molecular_functionpeptidase activity
A0016740molecular_functiontransferase activity
A0016746molecular_functionacyltransferase activity
A0016787molecular_functionhydrolase activity
A0018149biological_processpeptide cross-linking
A0018277biological_processprotein deamination
A0031012cellular_componentextracellular matrix
A0032471biological_processnegative regulation of endoplasmic reticulum calcium ion concentration
A0042981biological_processregulation of apoptotic process
A0043065biological_processpositive regulation of apoptotic process
A0043277biological_processapoptotic cell clearance
A0043547biological_processpositive regulation of GTPase activity
A0045785biological_processpositive regulation of cell adhesion
A0046872molecular_functionmetal ion binding
A0048471cellular_componentperinuclear region of cytoplasm
A0050568molecular_functionprotein-glutamine glutaminase activity
A0050769biological_processpositive regulation of neurogenesis
A0051057biological_processpositive regulation of small GTPase mediated signal transduction
A0051561biological_processpositive regulation of mitochondrial calcium ion concentration
A0060348biological_processbone development
A0060445biological_processbranching involved in salivary gland morphogenesis
A0060662biological_processsalivary gland cavitation
A0070062cellular_componentextracellular exosome
A0071314biological_processcellular response to cocaine
A0120294molecular_functionpeptide serotonyltransferase activity
A0120295molecular_functionhistone serotonyltransferase activity
A0120296molecular_functionpeptide dopaminyltransferase activity
A0120297molecular_functionhistone dopaminyltransferase activity
A0120298molecular_functionpeptide noradrenalinyltransferase activity
A0120299molecular_functionpeptide histaminyltransferase activity
A1903351biological_processcellular response to dopamine
A1903672biological_processpositive regulation of sprouting angiogenesis
A1904015biological_processcellular response to serotonin
A2000425biological_processregulation of apoptotic cell clearance
Functional Information from PDB Data
site_idAC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE SO4 A 701
ChainResidue
ALYS202
AARG222

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 702
ChainResidue
ALYS202
AARG209
ATYR219

site_idAC3
Number of Residues1
DetailsBINDING SITE FOR RESIDUE SO4 A 703
ChainResidue
AARG80

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 704
ChainResidue
AARG80
AASP81
AALA82

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 A 705
ChainResidue
AARG478
AVAL479
AGLY480
AARG580

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 706
ChainResidue
ASER68
AGLN69
ALYS74

site_idAC7
Number of Residues14
DetailsBINDING SITE FOR CHAIN B OF PEPTIDE INHIBITOR
ChainResidue
AGLN169
AGLY170
ACYS277
ASER303
AMET330
AILE331
ATRP332
AASN333
APHE334
AHIS335
ALEU420
ATYR516
AASN517
AGLU557

Functional Information from PROSITE/UniProt
site_idPS00547
Number of Residues18
DetailsTRANSGLUTAMINASES Transglutaminases active site. GQCWVfAAVacTvLRCLG
ChainResidueDetails
AGLY275-GLY292

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues1
DetailsActive site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10024","evidenceCode":"ECO:0000255"},{"source":"PubMed","id":"7649299","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"8943303","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues2
DetailsActive site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU10024","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {"evidences":[{"source":"UniProtKB","id":"P00488","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues2
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"31991788","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues10
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"25192068","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"30321187","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"31991788","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"11867708","evidenceCode":"ECO:0000305"},{"source":"PubMed","id":"20450932","evidenceCode":"ECO:0000305"},{"source":"PDB","id":"1KV3","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"3LY6","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"4PYG","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6A8P","evidenceCode":"ECO:0007744"},{"source":"PDB","id":"6KZB","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues1
DetailsSite: {"description":"Important for catalytic activity","evidences":[{"source":"UniProtKB","id":"P52181","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues1
DetailsModified residue: {"description":"N-acetylalanine","evidences":[{"source":"Reference","evidenceCode":"ECO:0000269","citation":{"citationType":"submission","publicationDate":"DEC-2008","submissionDatabase":"UniProtKB","authors":["Bienvenut W.V.","Lilla S.","von Kriegsheim A.","Lempens A.","Kolch W."]}},{"source":"PubMed","id":"22814378","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues1
DetailsModified residue: {"description":"Phosphoserine","evidences":[{"source":"PubMed","id":"24275569","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

site_idSWS_FT_FI9
Number of Residues2
DetailsCross-link: {"description":"Isoglutamyl lysine isopeptide (Gln-Lys) (interchain with K-?)","evidences":[{"source":"UniProtKB","id":"P08587","evidenceCode":"ECO:0000250"}]}
ChainResidueDetails

242842

PDB entries from 2025-10-08

PDB statisticsPDBj update infoContact PDBjnumon