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4KBN

human dihydrofolate reductase complexed with NADPH and 5-{3-[3-(3,5-pyrimidine)]-phenyl-prop-1-yn-1-yl}-6-ethyl-pyrimidine-2,4diamine

Functional Information from GO Data
ChainGOidnamespacecontents
A0000900molecular_functionmRNA regulatory element binding translation repressor activity
A0003723molecular_functionRNA binding
A0003729molecular_functionmRNA binding
A0004146molecular_functiondihydrofolate reductase activity
A0005542molecular_functionfolic acid binding
A0005737cellular_componentcytoplasm
A0005739cellular_componentmitochondrion
A0005829cellular_componentcytosol
A0006545biological_processglycine biosynthetic process
A0006729biological_processtetrahydrobiopterin biosynthetic process
A0006730biological_processone-carbon metabolic process
A0008144molecular_functionobsolete drug binding
A0016491molecular_functionoxidoreductase activity
A0017148biological_processnegative regulation of translation
A0031103biological_processaxon regeneration
A0031427biological_processresponse to methotrexate
A0046452biological_processdihydrofolate metabolic process
A0046653biological_processtetrahydrofolate metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0046655biological_processfolic acid metabolic process
A0050661molecular_functionNADP binding
A0051000biological_processpositive regulation of nitric-oxide synthase activity
A0070402molecular_functionNADPH binding
A1990825molecular_functionsequence-specific mRNA binding
A2000121biological_processregulation of removal of superoxide radicals
B0000900molecular_functionmRNA regulatory element binding translation repressor activity
B0003723molecular_functionRNA binding
B0003729molecular_functionmRNA binding
B0004146molecular_functiondihydrofolate reductase activity
B0005542molecular_functionfolic acid binding
B0005737cellular_componentcytoplasm
B0005739cellular_componentmitochondrion
B0005829cellular_componentcytosol
B0006545biological_processglycine biosynthetic process
B0006729biological_processtetrahydrobiopterin biosynthetic process
B0006730biological_processone-carbon metabolic process
B0008144molecular_functionobsolete drug binding
B0016491molecular_functionoxidoreductase activity
B0017148biological_processnegative regulation of translation
B0031103biological_processaxon regeneration
B0031427biological_processresponse to methotrexate
B0046452biological_processdihydrofolate metabolic process
B0046653biological_processtetrahydrofolate metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0046655biological_processfolic acid metabolic process
B0050661molecular_functionNADP binding
B0051000biological_processpositive regulation of nitric-oxide synthase activity
B0070402molecular_functionNADPH binding
B1990825molecular_functionsequence-specific mRNA binding
B2000121biological_processregulation of removal of superoxide radicals
Functional Information from PDB Data
site_idAC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE 25U A 201
ChainResidue
AILE7
ATYR121
ATHR136
ANDP210
AHOH325
AVAL8
AALA9
AGLU30
APHE34
ATHR56
AILE60
APRO61
ALEU67

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EOH A 202
ChainResidue
AVAL10
ASER11
AGLN12
AMET14
AARG137
AHOH481

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 203
ChainResidue
AMG209
AHOH461
AHOH464

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 204
ChainResidue
AGLU171
ALYS173
AGLY174

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG A 205
ChainResidue
APRO160
ASER167
AHOH425

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL A 206
ChainResidue
ASER42
AVAL43
AHOH469
BMET139

site_idAC7
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL A 207
ChainResidue
AGLN35
AARG70

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 208
ChainResidue
AASN29
AARG32
AHOH318

site_idAC9
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG A 209
ChainResidue
AASP168
AGLN170
ACL203

site_idBC1
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NDP A 210
ChainResidue
AVAL8
AALA9
AILE16
AGLY20
AASP21
AGLY53
ALYS54
ALYS55
ATHR56
ALEU75
ASER76
AARG77
AGLU78
AARG91
AVAL115
AGLY117
ASER118
ASER119
AVAL120
ATYR121
AGLU123
ATHR146
A25U201
AHOH307
AHOH322
AHOH327
AHOH350
AHOH403
AHOH440

site_idBC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE MG A 211
ChainResidue
AASP168
AVAL169
AHOH450

site_idBC3
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SR B 201
ChainResidue
AGLU171
AGLY174
BVAL1
BGLY2
BSER3
BCL205

site_idBC4
Number of Residues17
DetailsBINDING SITE FOR RESIDUE 25U B 202
ChainResidue
BILE7
BVAL8
BALA9
BLEU22
BGLU30
BPHE31
BPHE34
BTHR56
BILE60
BPRO61
BLEU67
BVAL115
BTYR121
BTHR136
BNDP214
BHOH327
BHOH358

site_idBC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EOH B 203
ChainResidue
AASN185
BLYS173
BHOH456

site_idBC6
Number of Residues1
DetailsBINDING SITE FOR RESIDUE EOH B 204
ChainResidue
BGLU62

site_idBC7
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL B 205
ChainResidue
BSER3
BASN5
BSR201
BHOH308

site_idBC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MG B 206
ChainResidue
BASP21
BNH4211

site_idBC9
Number of Residues1
DetailsBINDING SITE FOR RESIDUE CL B 207
ChainResidue
BPRO163

site_idCC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL B 208
ChainResidue
BGLN35
BHOH346
BHOH366

site_idCC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MG B 210
ChainResidue
AGLN140
BASP110

site_idCC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE NH4 B 211
ChainResidue
BLEU22
BTRP24
BMG206

site_idCC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE MG B 212
ChainResidue
BLYS18
BASN19
BGLY20
BASP145
BTHR146
BNDP214
BHOH413

site_idCC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG B 213
ChainResidue
BLEU153
BTYR156
BHOH336
BHOH445

site_idCC6
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NDP B 214
ChainResidue
BVAL8
BALA9
BILE16
BGLY20
BASP21
BGLY53
BLYS54
BLYS55
BTHR56
BLEU75
BSER76
BARG77
BGLU78
BARG91
BVAL115
BGLY117
BSER118
BSER119
BVAL120
BTYR121
BGLU123
BTHR146
B25U202
BMG212
BHOH317
BHOH355
BHOH378
BHOH381
BHOH413

Functional Information from PROSITE/UniProt
site_idPS00075
Number of Residues24
DetailsDHFR_1 Dihydrofolate reductase (DHFR) domain signature. GIGkngdLPWpplrnEfryFqrmT
ChainResidueDetails
AGLY15-THR38

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:15039552, ECO:0000269|PubMed:16222560, ECO:0000269|PubMed:19478082
ChainResidueDetails
AALA9
BGLY116
AGLY15
ALYS54
ASER76
AGLY116
BALA9
BGLY15
BLYS54
BSER76

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000305|PubMed:2248959
ChainResidueDetails
AGLU30
AASN64
AARG70
BGLU30
BASN64
BARG70

Catalytic Information from CSA
site_idMCSA1
Number of Residues2
DetailsM-CSA 490
ChainResidueDetails
ALEU22electrostatic stabiliser
AGLU30electrostatic stabiliser

site_idMCSA2
Number of Residues2
DetailsM-CSA 490
ChainResidueDetails
BLEU22electrostatic stabiliser
BGLU30electrostatic stabiliser

218853

PDB entries from 2024-04-24

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