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3BUV

Crystal structure of human Delta(4)-3-ketosteroid 5-beta-reductase in complex with NADP and HEPES. Resolution: 1.35 A.

Functional Information from GO Data
ChainGOidnamespacecontents
A0004032molecular_functionaldose reductase (NADPH) activity
A0004033molecular_functionaldo-keto reductase (NADPH) activity
A0005496molecular_functionsteroid binding
A0005737cellular_componentcytoplasm
A0005829cellular_componentcytosol
A0006699biological_processbile acid biosynthetic process
A0006707biological_processcholesterol catabolic process
A0007586biological_processdigestion
A0008202biological_processsteroid metabolic process
A0008207biological_processC21-steroid hormone metabolic process
A0008209biological_processandrogen metabolic process
A0016042biological_processlipid catabolic process
A0016229molecular_functionsteroid dehydrogenase activity
A0016491molecular_functionoxidoreductase activity
A0030573biological_processbile acid catabolic process
A0047086molecular_functionketosteroid monooxygenase activity
A0047787molecular_functionDelta4-3-oxosteroid 5beta-reductase activity
B0004032molecular_functionaldose reductase (NADPH) activity
B0004033molecular_functionaldo-keto reductase (NADPH) activity
B0005496molecular_functionsteroid binding
B0005737cellular_componentcytoplasm
B0005829cellular_componentcytosol
B0006699biological_processbile acid biosynthetic process
B0006707biological_processcholesterol catabolic process
B0007586biological_processdigestion
B0008202biological_processsteroid metabolic process
B0008207biological_processC21-steroid hormone metabolic process
B0008209biological_processandrogen metabolic process
B0016042biological_processlipid catabolic process
B0016229molecular_functionsteroid dehydrogenase activity
B0016491molecular_functionoxidoreductase activity
B0030573biological_processbile acid catabolic process
B0047086molecular_functionketosteroid monooxygenase activity
B0047787molecular_functionDelta4-3-oxosteroid 5beta-reductase activity
Functional Information from PDB Data
site_idAC1
Number of Residues34
DetailsBINDING SITE FOR RESIDUE NAP B 3901
ChainResidue
BGLY24
BTYR219
BSER220
BPRO221
BLEU222
BGLY223
BTHR224
BSER225
BLEU239
BALA256
BILE271
BTHR25
BPRO272
BLYS273
BSER274
BPHE275
BARG279
BGLU282
BASN283
BHOH3941
BHOH3944
BHOH4019
BTYR26
BHOH4041
BHOH4074
BHOH4107
BHOH4125
BHOH4135
BASP53
BTYR58
BLYS87
BSER169
BASN170
BGLN193

site_idAC2
Number of Residues37
DetailsBINDING SITE FOR RESIDUE NAP A 3902
ChainResidue
AGLY24
ATHR25
ATYR26
AASP53
ATYR58
ASER169
AASN170
AGLN193
ATYR219
ASER220
APRO221
ALEU222
AGLY223
ATHR224
ASER225
ALEU239
AALA256
AILE271
APRO272
ALYS273
ASER274
APHE275
AARG279
AGLU282
AASN283
AEPE3999
AHOH4006
AHOH4038
AHOH4072
AHOH4095
AHOH4121
AHOH4148
AHOH4160
AHOH4174
AHOH4206
AHOH4230
AHOH4246

site_idAC3
Number of Residues12
DetailsBINDING SITE FOR RESIDUE EPE A 3999
ChainResidue
ATYR26
AILE57
AILE131
ATYR132
ATRP230
AVAL309
ALEU311
ANAP3902
AHOH4158
AHOH4160
AHOH4174
AHOH4240

site_idAC4
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL B 329
ChainResidue
AGLU103
BASP129
BHOH3923
BHOH4101
BHOH4137

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL B 330
ChainResidue
AASP112
AHOH4053
BMET97
BPRO100
BTHR101
BARG104

Functional Information from PROSITE/UniProt
site_idPS00062
Number of Residues18
DetailsALDOKETO_REDUCTASE_2 Aldo/keto reductase family signature 2. MeackdaglVKSLGVSNF
ChainResidueDetails
BMET154-PHE171

site_idPS00063
Number of Residues16
DetailsALDOKETO_REDUCTASE_3 Aldo/keto reductase family putative active site signature. IPKSFNleRIkENfQI
ChainResidueDetails
BILE271-ILE286

site_idPS00798
Number of Residues18
DetailsALDOKETO_REDUCTASE_1 Aldo/keto reductase family signature 1. GYRHIDGAyiyqnEheVG
ChainResidueDetails
BGLY48-GLY65

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton donor => ECO:0000305|PubMed:18407998
ChainResidueDetails
BTYR58
ATYR58

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:18624455, ECO:0000269|PubMed:18848863, ECO:0000269|PubMed:19075558, ECO:0000269|PubMed:19515843, ECO:0000269|PubMed:22437839
ChainResidueDetails
BSER169
BGLN193
BTYR219
BLYS273
AGLY22
AASP53
ASER169
AGLN193
ATYR219
ALYS273
BGLY22
BASP53

site_idSWS_FT_FI3
Number of Residues12
DetailsBINDING:
ChainResidueDetails
BTYR26
BTYR58
BTRP89
BGLU120
BTYR132
BTRP230
ATYR26
ATYR58
ATRP89
AGLU120
ATYR132
ATRP230

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PDB entries from 2024-06-12

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