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5UJX

Crystal structure of DHFR in 20% Isopropanol

Functional Information from GO Data
ChainGOidnamespacecontents
A0004146molecular_functiondihydrofolate reductase activity
A0005515molecular_functionprotein binding
A0005542molecular_functionfolic acid binding
A0005829cellular_componentcytosol
A0006730biological_processone-carbon metabolic process
A0009410biological_processresponse to xenobiotic stimulus
A0016491molecular_functionoxidoreductase activity
A0031427biological_processresponse to methotrexate
A0046452biological_processdihydrofolate metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0046655biological_processfolic acid metabolic process
A0046677biological_processresponse to antibiotic
A0050661molecular_functionNADP binding
A0051870molecular_functionmethotrexate binding
A0051871molecular_functiondihydrofolic acid binding
A0070401molecular_functionNADP+ binding
A0070402molecular_functionNADPH binding
B0004146molecular_functiondihydrofolate reductase activity
B0005515molecular_functionprotein binding
B0005542molecular_functionfolic acid binding
B0005829cellular_componentcytosol
B0006730biological_processone-carbon metabolic process
B0009410biological_processresponse to xenobiotic stimulus
B0016491molecular_functionoxidoreductase activity
B0031427biological_processresponse to methotrexate
B0046452biological_processdihydrofolate metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0046655biological_processfolic acid metabolic process
B0046677biological_processresponse to antibiotic
B0050661molecular_functionNADP binding
B0051870molecular_functionmethotrexate binding
B0051871molecular_functiondihydrofolic acid binding
B0070401molecular_functionNADP+ binding
B0070402molecular_functionNADPH binding
Functional Information from PDB Data
site_idAC1
Number of Residues16
Detailsbinding site for residue FOL B 201
ChainResidue
BILE5
BARG52
BARG57
BILE94
BTHR113
BHOH318
BHOH337
BHOH400
BALA6
BALA7
BASP27
BLEU28
BPHE31
BLYS32
BTHR46
BILE50

site_idAC2
Number of Residues4
Detailsbinding site for residue IPA B 202
ChainResidue
BALA117
BGLU118
BHIS149
BHOH342

site_idAC3
Number of Residues6
Detailsbinding site for residue CA B 203
ChainResidue
AHOH313
BSER135
BHOH347
BHOH349
BHOH393
BHOH435

site_idAC4
Number of Residues5
Detailsbinding site for residue CL B 204
ChainResidue
BGLY43
BHIS45
BTHR46
BGLY96
BHOH414

site_idAC5
Number of Residues3
Detailsbinding site for residue CL B 205
ChainResidue
BSER135
BARG159
BHOH393

site_idAC6
Number of Residues5
Detailsbinding site for residue CL B 206
ChainResidue
AARG98
BTRP30
BARG33
BHOH355
BHOH391

site_idAC7
Number of Residues17
Detailsbinding site for residue FOL A 201
ChainResidue
AILE5
AALA6
AALA7
AASP27
ALEU28
APHE31
ALYS32
ATHR46
AARG52
ALEU54
AARG57
AILE94
ATYR100
ATHR113
AHOH323
AHOH327
AHOH381

site_idAC8
Number of Residues4
Detailsbinding site for residue CL A 202
ChainResidue
AGLY43
AHIS45
ATHR46
AGLY96

Functional Information from PROSITE/UniProt
site_idPS00075
Number of Residues23
DetailsDHFR_1 Dihydrofolate reductase (DHFR) domain signature. VIGmenaMPWnlpa.DlawFkrnT
ChainResidueDetails
BVAL13-THR35

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues10
DetailsBINDING: BINDING => ECO:0000305|PubMed:9012674
ChainResidueDetails
BILE5
ATHR113
BASP27
BARG52
BARG57
BTHR113
AILE5
AASP27
AARG52
AARG57

site_idSWS_FT_FI2
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:19374017
ChainResidueDetails
BALA7
ASER63
ALYS76
AGLY95
BVAL13
BHIS45
BSER63
BLYS76
BGLY95
AALA7
AVAL13
AHIS45

219140

PDB entries from 2024-05-01

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