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6YYK

Crystal Structure of 1,5-dimethylindoline-2,3-dione covalently bound to the PH domain of Bruton's tyrosine kinase mutant R28C

Functional Information from GO Data
ChainGOidnamespacecontents
A0035556biological_processintracellular signal transduction
B0035556biological_processintracellular signal transduction
Functional Information from PDB Data
site_idAC1
Number of Residues4
Detailsbinding site for residue ZN A 201
ChainResidue
AHIS143
ACYS154
ACYS155
ACYS165

site_idAC2
Number of Residues1
Detailsbinding site for residue MG A 202
ChainResidue
BGLU96

site_idAC3
Number of Residues4
Detailsbinding site for residue ZN B 201
ChainResidue
BHIS143
BCYS154
BCYS155
BCYS165

site_idAC4
Number of Residues2
Detailsbinding site for residue MG B 202
ChainResidue
AGLU96
BGLU7

site_idAC5
Number of Residues9
Detailsbinding site for Di-peptide IS7 B 203 and LYS B 12
ChainResidue
BLEU11
BARG13
BSER14
BGLN15
BPHE25
BLYS26
BTYR39
BLEU111
BTYR112

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:10196129
ChainResidueDetails
ALYS26
ACYS28
ATYR39
ALYS53
BLYS26
BCYS28
BTYR39
BLYS53

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: BINDING => ECO:0000255|PROSITE-ProRule:PRU00432, ECO:0000269|PubMed:10196129, ECO:0000269|PubMed:9218782, ECO:0000269|Ref.48
ChainResidueDetails
AHIS143
ACYS154
ACYS155
ACYS165
BHIS143
BCYS154
BCYS155
BCYS165

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: N-acetylalanine => ECO:0000269|Ref.11, ECO:0007744|PubMed:25944712
ChainResidueDetails
AALA2
BALA2

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0000269|PubMed:16644721
ChainResidueDetails
ASER21
ASER115
BSER21
BSER115

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphotyrosine => ECO:0000250|UniProtKB:P35991
ChainResidueDetails
ATYR40
BTYR40

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0007744|PubMed:19369195
ChainResidueDetails
ASER55
BSER55

222624

PDB entries from 2024-07-17

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