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3H52

Crystal structure of the antagonist form of human glucocorticoid receptor

Functional Information from PDB Data
site_idAC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE 486 A 3
ChainResidue
AASN564
AMET752
AGLY567
AGLN570
AVAL571
AMET601
AARG611
AGLN642
ALEU732
ATYR735

site_idAC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE 486 B 1
ChainResidue
BMET560
BLEU563
BASN564
BGLY567
BGLY568
BGLN570
BVAL571
BARG611
BMET639
BGLN642
BMET646
BTYR735
BLEU753

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL B 778
ChainResidue
BHIS645
BGLU727
BASN731

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE 486 C 4
ChainResidue
CLEU563
CGLY567
CGLN570
CMET604
CARG611
CPHE623
CMET639
CPHE740

site_idAC5
Number of Residues12
DetailsBINDING SITE FOR RESIDUE 486 D 2
ChainResidue
DLEU563
DASN564
DGLY567
DGLN570
DVAL571
DMET601
DMET604
DARG611
DPHE623
DMET639
DTYR735
DLEU753

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues8
DetailsCROSSLNK: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in SUMO) => ECO:0000269|PubMed:12144530
ChainResidueDetails
ALYS703
BLYS703
CLYS703
DLYS703

226707

PDB entries from 2024-10-30

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