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

6OYW

ASK1 kinase domain in complex with Compound 11

Functional Information from GO Data
ChainGOidnamespacecontents
A0004672molecular_functionprotein kinase activity
A0005524molecular_functionATP binding
A0006468biological_processprotein phosphorylation
B0004672molecular_functionprotein kinase activity
B0005524molecular_functionATP binding
B0006468biological_processprotein phosphorylation
C0004672molecular_functionprotein kinase activity
C0005524molecular_functionATP binding
C0006468biological_processprotein phosphorylation
D0004672molecular_functionprotein kinase activity
D0005524molecular_functionATP binding
D0006468biological_processprotein phosphorylation
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue NKJ A 1001
ChainResidue
ALEU686
AGLY760
AASP807
AASN808
ALEU810
ASER821
AASP822
AHOH1125
AGLY689
AALA707
ALYS709
AVAL738
AMET754
AGLU755
AGLN756
AVAL757

site_idAC2
Number of Residues16
Detailsbinding site for residue NKJ B 1001
ChainResidue
BLEU686
BLYS688
BGLY689
BALA707
BLYS709
BMET754
BGLU755
BGLN756
BVAL757
BGLY760
BASP807
BASN808
BLEU810
BSER821
BASP822
BHOH1133

site_idAC3
Number of Residues15
Detailsbinding site for residue NKJ C 1001
ChainResidue
CLEU686
CLYS688
CGLY689
CALA707
CLYS709
CMET754
CGLU755
CGLN756
CVAL757
CGLY760
CASP807
CLEU810
CSER821
CASP822
CHOH1116

site_idAC4
Number of Residues1
Detailsbinding site for residue MG C 1002
ChainResidue
CASP699

site_idAC5
Number of Residues16
Detailsbinding site for residue NKJ D 1001
ChainResidue
DLEU686
DLYS688
DGLY689
DALA707
DLYS709
DVAL738
DMET754
DGLU755
DGLN756
DVAL757
DASP807
DASN808
DLEU810
DSER821
DASP822
DHOH1136

Functional Information from PROSITE/UniProt
site_idPS00107
Number of Residues24
DetailsPROTEIN_KINASE_ATP Protein kinases ATP-binding region signature. LGKGTYGIVYaGrdlsnqvr..........IAIK
ChainResidueDetails
ALEU686-LYS709

site_idPS00108
Number of Residues13
DetailsPROTEIN_KINASE_ST Serine/Threonine protein kinases active-site signature. IvHrDIKgdNVLI
ChainResidueDetails
AILE799-ILE811

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsActive site: {"description":"Proton acceptor","evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"},{"source":"PROSITE-ProRule","id":"PRU10027","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues32
DetailsBinding site: {"evidences":[{"source":"PROSITE-ProRule","id":"PRU00159","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues4
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues4
DetailsModified residue: {"description":"Phosphotyrosine","evidences":[{"source":"PubMed","id":"16407264","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues8
DetailsModified residue: {"description":"Phosphothreonine; by autocatalysis","evidences":[{"source":"PubMed","id":"17937911","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues3
DetailsModified residue: {"description":"Phosphothreonine; by autocatalysis, MELK and MAP3K6","evidences":[{"source":"PubMed","id":"11920685","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17210579","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"17937911","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"18948261","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"19590015","evidenceCode":"ECO:0000269"},{"source":"PubMed","id":"23102700","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

248636

PDB entries from 2026-02-04

PDB statisticsPDBj update infoContact PDBjnumon