Loading
PDBj
MenuPDBj@FacebookPDBj@TwitterPDBj@YouTubewwPDB FoundationwwPDB
RCSB PDBPDBeBMRBAdv. SearchSearch help

1U2O

Crystal Structure Of The N-Domain Of Grp94 Lacking The Charged Domain In Complex With Neca

Replaces:  1QYH
Functional Information from GO Data
ChainGOidnamespacecontents
A0005524molecular_functionATP binding
A0006457biological_processprotein folding
A0016887molecular_functionATP hydrolysis activity
A0051082molecular_functionunfolded protein binding
A0140662molecular_functionATP-dependent protein folding chaperone
B0005524molecular_functionATP binding
B0006457biological_processprotein folding
B0016887molecular_functionATP hydrolysis activity
B0051082molecular_functionunfolded protein binding
B0140662molecular_functionATP-dependent protein folding chaperone
Functional Information from PDB Data
site_idAC1
Number of Residues14
DetailsBINDING SITE FOR RESIDUE NEC A 1001
ChainResidue
AALA111
AHOH2015
AHOH2039
AHOH2059
AHOH2065
AHOH2079
AASP149
AMET154
AASN162
AGLY196
AVAL197
ATYR200
AHOH2004
AHOH2009

site_idAC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE NEC B 1002
ChainResidue
BASN107
BALA111
BASP149
BMET154
BASN162
BLEU163
BGLY196
BVAL197
BTYR200
BHOH2012
BHOH2013
BHOH2014
BHOH2069
BHOH2138
BHOH2141

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE PG4 A 2001
ChainResidue
ATHR212
AARG237
ATHR246
ATHR248
APG42002
AHOH2085
AHOH2134

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE PG4 A 2002
ChainResidue
ALYS137
ATHR148
ATRP282
APG42001
AHOH2046
AHOH2134

site_idAC5
Number of Residues9
DetailsBINDING SITE FOR RESIDUE 1PE B 2006
ChainResidue
AASN83
AMET86
ALYS87
ASER227
BASN83
BLYS87
BILE90
BSER227
BHOH2124

site_idAC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE PG4 B 2008
ChainResidue
BTHR212
BARG237
BTHR240
BTHR248
BPG42009
BHOH2016
BHOH2072
BHOH2112

site_idAC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PG4 B 2009
ChainResidue
BLYS137
BTHR148
BTRP282
BPG42008

site_idAC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PG4 B 2011
ChainResidue
BGLY128
BASN129
BASN239
BGLY242

Functional Information from PROSITE/UniProt
site_idPS00298
Number of Residues10
DetailsHSP90 Heat shock hsp90 proteins family signature. YkNKEIFLRE
ChainResidueDetails
ATYR94-GLU103

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:15292259, ECO:0000269|PubMed:15951571, ECO:0000269|PubMed:17936703, ECO:0007744|PDB:1TC0, ECO:0007744|PDB:1TC6, ECO:0007744|PDB:1YT0, ECO:0007744|PDB:2O1U, ECO:0007744|PDB:2O1V
ChainResidueDetails
AASN107
BASN107

site_idSWS_FT_FI2
Number of Residues4
DetailsBINDING: BINDING => ECO:0000269|PubMed:15292259, ECO:0000269|PubMed:15951571, ECO:0000269|PubMed:17936703, ECO:0007744|PDB:1TBW, ECO:0007744|PDB:1TC0, ECO:0007744|PDB:1TC6, ECO:0007744|PDB:1YT0, ECO:0007744|PDB:2O1U, ECO:0007744|PDB:2O1V
ChainResidueDetails
AASP149
BASP149
BPHE199
APHE199

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:15292259, ECO:0000269|PubMed:15951571, ECO:0000269|PubMed:17936703, ECO:0007744|PDB:1TBW, ECO:0007744|PDB:1TC0, ECO:0007744|PDB:1TC6, ECO:0007744|PDB:2O1U, ECO:0007744|PDB:2O1V
ChainResidueDetails
AASN162
BASN162

site_idSWS_FT_FI4
Number of Residues2
DetailsMOD_RES: N6-(2-hydroxyisobutyryl)lysine => ECO:0000250|UniProtKB:P14625
ChainResidueDetails
ALYS168
BLYS168

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q66HD0
ChainResidueDetails
ASER172
BSER172

site_idSWS_FT_FI6
Number of Residues2
DetailsMOD_RES: Phosphothreonine; by CK2 => ECO:0000255
ChainResidueDetails
AGLY325
BGLY325

site_idSWS_FT_FI7
Number of Residues2
DetailsMOD_RES: Phosphoserine; by CK2 => ECO:0000250|UniProtKB:P14625, ECO:0000255
ChainResidueDetails

site_idSWS_FT_FI8
Number of Residues4
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
AASN107
AASN217
BASN107
BASN217

221051

PDB entries from 2024-06-12

PDB statisticsPDBj update infoContact PDBjnumon