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6BAW

Structure of GRP94 with a selective resorcinylic inhibitor.

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
C0005524molecular_functionATP binding
C0006457biological_processprotein folding
C0016887molecular_functionATP hydrolysis activity
C0051082molecular_functionunfolded protein binding
C0140662molecular_functionATP-dependent protein folding chaperone
D0005524molecular_functionATP binding
D0006457biological_processprotein folding
D0016887molecular_functionATP hydrolysis activity
D0051082molecular_functionunfolded protein binding
D0140662molecular_functionATP-dependent protein folding chaperone
Functional Information from PDB Data
site_idAC1
Number of Residues11
Detailsbinding site for residue D57 B 401
ChainResidue
BALA111
BHOH508
BHOH516
BASP149
BGLY153
BMET154
BASN162
BLEU163
BPHE195
BTHR245
BILE247

site_idAC2
Number of Residues4
Detailsbinding site for residue EDO B 402
ChainResidue
BARG156
BASP218
BHIS221
BPO4405

site_idAC3
Number of Residues5
Detailsbinding site for residue EDO B 403
ChainResidue
BGLU224
BASP226
BGLU229
BSER231
CARG156

site_idAC4
Number of Residues5
Detailsbinding site for residue PO4 B 404
ChainResidue
BLYS114
BILE118
BGLU158
BHIS215
BHOH518

site_idAC5
Number of Residues5
Detailsbinding site for residue PO4 B 405
ChainResidue
BARG156
BALA234
BEDO402
CLYS208
CGLU224

site_idAC6
Number of Residues13
Detailsbinding site for residue D57 A 401
ChainResidue
AASN107
AALA111
AASP149
AGLY153
AMET154
AASN162
ALEU163
APHE195
ATRP223
ATHR245
AILE247
AHOH505
AHOH507

site_idAC7
Number of Residues5
Detailsbinding site for residue EDO A 402
ChainResidue
AARG156
AASP218
ATHR219
AHIS221
APO4407

site_idAC8
Number of Residues6
Detailsbinding site for residue EDO A 403
ChainResidue
ASER169
AGLU224
AASP226
APHE230
ASER231
DARG156

site_idAC9
Number of Residues3
Detailsbinding site for residue EDO A 404
ChainResidue
ALYS137
ATHR148
AEDO405

site_idAD1
Number of Residues3
Detailsbinding site for residue EDO A 405
ChainResidue
ATHR212
AARG237
AEDO404

site_idAD2
Number of Residues3
Detailsbinding site for residue PO4 A 406
ChainResidue
ALYS114
AGLU158
AHIS215

site_idAD3
Number of Residues5
Detailsbinding site for residue PO4 A 407
ChainResidue
AILE233
AALA234
AEDO402
DLYS208
DGLU224

site_idAD4
Number of Residues11
Detailsbinding site for residue D57 C 401
ChainResidue
CASN107
CALA111
CASP149
CVAL152
CGLY153
CMET154
CASN162
CPHE195
CTHR245
CILE247
CHOH502

site_idAD5
Number of Residues4
Detailsbinding site for residue EDO C 402
ChainResidue
CASP207
CLYS252
CGLU253
CGLU254

site_idAD6
Number of Residues3
Detailsbinding site for residue EDO C 403
ChainResidue
CLYS137
CASP139
CHIS146

site_idAD7
Number of Residues3
Detailsbinding site for residue EDO C 404
ChainResidue
CTHR212
CARG237
CTHR246

site_idAD8
Number of Residues4
Detailsbinding site for residue PO4 C 405
ChainResidue
BLYS208
CARG156
CASP218
CHIS221

site_idAD9
Number of Residues9
Detailsbinding site for residue D57 D 401
ChainResidue
DPHE195
DTHR245
DILE247
DASN107
DALA111
DASP149
DGLY153
DMET154
DASN162

site_idAE1
Number of Residues3
Detailsbinding site for residue EDO D 402
ChainResidue
DLYS137
DASP139
DHIS146

site_idAE2
Number of Residues3
Detailsbinding site for residue EDO D 403
ChainResidue
DTHR212
DARG237
DTHR246

site_idAE3
Number of Residues4
Detailsbinding site for residue PO4 D 404
ChainResidue
DARG156
DASP218
DTHR219
DHIS221

site_idAE4
Number of Residues4
Detailsbinding site for residue PO4 D 405
ChainResidue
CLYS265
CGLU334
DLYS265
DGLU334

Functional Information from PROSITE/UniProt
site_idPS00298
Number of Residues10
DetailsHSP90 Heat shock hsp90 proteins family signature. YkNKEIFLRE
ChainResidueDetails
BTYR94-GLU103

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
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
BASN107
AASN107
CASN107
DASN107

site_idSWS_FT_FI2
Number of Residues8
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
BASP149
BPHE199
AASP149
APHE199
CASP149
CPHE199
DASP149
DPHE199

site_idSWS_FT_FI3
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:2O1U, ECO:0007744|PDB:2O1V
ChainResidueDetails
BASN162
AASN162
CASN162
DASN162

site_idSWS_FT_FI4
Number of Residues4
DetailsMOD_RES: N6-(2-hydroxyisobutyryl)lysine => ECO:0000250|UniProtKB:P14625
ChainResidueDetails
BLYS168
ALYS168
CLYS168
DLYS168

site_idSWS_FT_FI5
Number of Residues4
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q66HD0
ChainResidueDetails
BSER172
ASER172
CSER172
DSER172

site_idSWS_FT_FI6
Number of Residues8
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
BASN107
BASN217
AASN107
AASN217
CASN107
CASN217
DASN107
DASN217

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PDB entries from 2024-11-13

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