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5EAJ

Crystal structure of DHFR in 0% 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
A0009257biological_process10-formyltetrahydrofolate biosynthetic process
A0009410biological_processresponse to xenobiotic stimulus
A0016491molecular_functionoxidoreductase activity
A0031427biological_processresponse to methotrexate
A0044281biological_processsmall molecule metabolic process
A0046452biological_processdihydrofolate metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0046655biological_processfolic acid metabolic process
A0046656biological_processfolic acid biosynthetic 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
B0009257biological_process10-formyltetrahydrofolate biosynthetic process
B0009410biological_processresponse to xenobiotic stimulus
B0016491molecular_functionoxidoreductase activity
B0031427biological_processresponse to methotrexate
B0044281biological_processsmall molecule metabolic process
B0046452biological_processdihydrofolate metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0046655biological_processfolic acid metabolic process
B0046656biological_processfolic acid biosynthetic 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 Residues17
Detailsbinding site for residue FOL B 201
ChainResidue
BILE5
BARG57
BILE94
BTYR100
BTHR113
BHOH318
BHOH322
BHOH368
BHOH412
BALA6
BALA7
BASP27
BPHE31
BLYS32
BTHR46
BILE50
BARG52

site_idAC2
Number of Residues7
Detailsbinding site for residue CA B 202
ChainResidue
AHOH302
AHOH370
BSER135
BHOH312
BHOH319
BHOH348
BHOH352

site_idAC3
Number of Residues5
Detailsbinding site for residue CL B 203
ChainResidue
BGLY43
BHIS45
BTHR46
BGLY96
BHOH413

site_idAC4
Number of Residues3
Detailsbinding site for residue CL B 204
ChainResidue
BSER135
BARG159
BHOH352

site_idAC5
Number of Residues4
Detailsbinding site for residue CL B 205
ChainResidue
AARG98
BTRP30
BARG33
BHOH354

site_idAC6
Number of Residues20
Detailsbinding site for residue FOL A 201
ChainResidue
AILE5
AALA6
AALA7
AASP27
ALEU28
APHE31
ALYS32
ATHR46
AILE50
AARG52
ALEU54
AARG57
AILE94
ATYR100
ATHR113
AHOH320
AHOH324
AHOH355
AHOH374
AHOH395

site_idAC7
Number of Residues5
Detailsbinding site for residue CL A 202
ChainResidue
AGLY43
AHIS45
ATHR46
AGLY96
AHOH388

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 Residues314
DetailsDomain: {"description":"DHFR","evidences":[{"source":"PROSITE-ProRule","id":"PRU00660","evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues10
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"9012674","evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues34
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"19374017","evidenceCode":"ECO:0000269"}]}
ChainResidueDetails

238895

PDB entries from 2025-07-16

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