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

5QIJ

CRYSTAL STRUCTURE OF MURINE 11B- HYDROXYSTEROIDDEHYDROGENASE COMPLEXED WITH 2-(3-(1-(4- CHLOROPHENYL)CYCLOPROPYL)-[1,2,4]TRIAZOLO[4,3-A]PYRIDIN-8- YL)PROPAN-2-OL

Functional Information from GO Data
ChainGOidnamespacecontents
A0005496molecular_functionsteroid binding
A0005783cellular_componentendoplasmic reticulum
A0005789cellular_componentendoplasmic reticulum membrane
A0006704biological_processglucocorticoid biosynthetic process
A0006706biological_processsteroid catabolic process
A0006713biological_processglucocorticoid catabolic process
A0008202biological_processsteroid metabolic process
A0008212biological_processmineralocorticoid metabolic process
A0016020cellular_componentmembrane
A0016491molecular_functionoxidoreductase activity
A0030324biological_processlung development
A0031965cellular_componentnuclear membrane
A0042803molecular_functionprotein homodimerization activity
A0043231cellular_componentintracellular membrane-bounded organelle
A0043456biological_processregulation of pentose-phosphate shunt
A0045177cellular_componentapical part of cell
A0047022molecular_function7-beta-hydroxysteroid dehydrogenase (NADP+) activity
A0050661molecular_functionNADP binding
A0070524molecular_function11-beta-hydroxysteroid dehydrogenase (NADP+) activity
A0102196molecular_functioncortisol dehydrogenase activity
B0005496molecular_functionsteroid binding
B0005783cellular_componentendoplasmic reticulum
B0005789cellular_componentendoplasmic reticulum membrane
B0006704biological_processglucocorticoid biosynthetic process
B0006706biological_processsteroid catabolic process
B0006713biological_processglucocorticoid catabolic process
B0008202biological_processsteroid metabolic process
B0008212biological_processmineralocorticoid metabolic process
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0030324biological_processlung development
B0031965cellular_componentnuclear membrane
B0042803molecular_functionprotein homodimerization activity
B0043231cellular_componentintracellular membrane-bounded organelle
B0043456biological_processregulation of pentose-phosphate shunt
B0045177cellular_componentapical part of cell
B0047022molecular_function7-beta-hydroxysteroid dehydrogenase (NADP+) activity
B0050661molecular_functionNADP binding
B0070524molecular_function11-beta-hydroxysteroid dehydrogenase (NADP+) activity
B0102196molecular_functioncortisol dehydrogenase activity
Functional Information from PDB Data
site_idAC1
Number of Residues27
Detailsbinding site for residue NAP A 301
ChainResidue
AGLY41
ATHR92
AMET93
AASN119
AHIS120
AILE121
AILE168
ASER169
ASER170
ATYR183
ALYS187
AALA42
ALEU215
AGLY216
AILE218
ATHR220
ATHR222
AALA223
AHJG302
AHOH410
ASER43
ALYS44
AGLY45
AILE46
AALA65
AARG66
ASER67

site_idAC2
Number of Residues14
Detailsbinding site for residue HJG A 302
ChainResidue
ATHR124
ASER125
ALEU126
ASER170
ALEU171
AALA172
AGLN177
AILE180
ATYR183
ALEU217
AALA223
AILE227
ANAP301
BHJG301

site_idAC3
Number of Residues6
Detailsbinding site for residue SO4 A 303
ChainResidue
AGLY45
AARG48
ATHR220
AGLU221
ALYS238
AHOH409

site_idAC4
Number of Residues2
Detailsbinding site for residue SO4 A 304
ChainResidue
AARG66
AGLN123

site_idAC5
Number of Residues2
Detailsbinding site for residue SO4 A 305
ChainResidue
ASER254
AGLU255

site_idAC6
Number of Residues1
Detailsbinding site for residue SO4 A 306
ChainResidue
AARG48

site_idAC7
Number of Residues11
Detailsbinding site for residue HJG B 301
ChainResidue
ALEU171
AMET175
AGLN177
AALA233
AASP259
ASER261
AHJG302
BMET276
BPHE279
BSER280
BTYR283

site_idAC8
Number of Residues28
Detailsbinding site for residue NAP B 302
ChainResidue
BGLY41
BALA42
BSER43
BLYS44
BGLY45
BILE46
BALA65
BARG66
BSER67
BTHR92
BMET93
BASN119
BHIS120
BILE121
BILE168
BSER169
BSER170
BTYR183
BLYS187
BLEU215
BGLY216
BILE218
BTHR220
BTHR222
BALA223
BHJG303
BHOH401
BHOH415

site_idAC9
Number of Residues15
Detailsbinding site for residue HJG B 303
ChainResidue
BLEU217
BALA223
BGLU226
BILE227
BNAP302
BHJG304
BHOH417
BTHR124
BSER125
BLEU126
BSER170
BLEU171
BALA172
BILE180
BTYR183

site_idAD1
Number of Residues9
Detailsbinding site for residue HJG B 304
ChainResidue
AMET276
ASER280
ATYR283
BLEU171
BMET175
BGLN177
BALA233
BASP259
BHJG303

site_idAD2
Number of Residues8
Detailsbinding site for residue SO4 B 305
ChainResidue
BLYS44
BGLY45
BARG48
BTHR220
BGLU221
BLYS238
BHOH401
BHOH411

site_idAD3
Number of Residues3
Detailsbinding site for residue SO4 B 306
ChainResidue
BARG66
BGLN123
BHOH404

site_idAD4
Number of Residues3
Detailsbinding site for residue SO4 B 307
ChainResidue
BLYS253
BSER254
BGLU255

Functional Information from PROSITE/UniProt
site_idPS00061
Number of Residues29
DetailsADH_SHORT Short-chain dehydrogenases/reductases family signature. SlagkmtqpmIapYSASKFALdGFFsTIR
ChainResidueDetails
ASER170-ARG198

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues534
DetailsTOPO_DOM: Lumenal => ECO:0000255
ChainResidueDetails
AGLU25-ASN292
BGLU25-ASN292

site_idSWS_FT_FI2
Number of Residues2
DetailsACT_SITE: Proton acceptor
ChainResidueDetails
ATYR183
BTYR183

site_idSWS_FT_FI3
Number of Residues10
DetailsBINDING:
ChainResidueDetails
AGLY41
BTYR183
ATHR92
AASN119
ASER170
ATYR183
BGLY41
BTHR92
BASN119
BSER170

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: BINDING => ECO:0000250|UniProtKB:P28845
ChainResidueDetails
AILE218
BILE218

site_idSWS_FT_FI5
Number of Residues4
DetailsCARBOHYD: N-linked (GlcNAc...) asparagine => ECO:0000255
ChainResidueDetails
AASN162
AASN207
BASN162
BASN207

223166

PDB entries from 2024-07-31

PDB statisticsPDBj update infoContact PDBjnumon