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

1DDR

MOLECULE: DIHYDROFOLATE REDUCTASE (E.C.1.5.1.3) COMPLEXED WITH METHOTREXATE AND UREA

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
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
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 Residues3
DetailsBINDING SITE FOR RESIDUE CL A 201
ChainResidue
AGLY43
AARG44
AHIS45

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CL B 202
ChainResidue
BGLY43
BARG44
BHIS45
BTHR46

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CA B 203
ChainResidue
BALA143
BHOH808
AASN18
BSER135

site_idAC4
Number of Residues12
DetailsBINDING SITE FOR RESIDUE MTX A 200
ChainResidue
AILE5
AALA6
AASP27
APHE31
ALYS32
ATHR46
AARG52
ALEU54
AARG57
AILE94
ATYR100
ATHR113

site_idAC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE MTX B 200
ChainResidue
BILE5
BALA6
BASP27
BLEU28
BTRP30
BPHE31
BLYS32
BILE50
BARG52
BLEU54
BARG57
BILE94
BTYR100
BTHR113

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE URE A 211
ChainResidue
AARG44
ASER63
AGLN65
AHOH800
BGLU139
BPHE140

site_idAC7
Number of Residues1
DetailsBINDING SITE FOR RESIDUE URE A 212
ChainResidue
AARG52

site_idAC8
Number of Residues1
DetailsBINDING SITE FOR RESIDUE URE A 213
ChainResidue
ALYS76

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE URE B 214
ChainResidue
BGLY56
BASP122
BTHR123
BHIS124
BHOH803

site_idBC1
Number of Residues6
DetailsBINDING SITE FOR RESIDUE URE B 215
ChainResidue
BARG57
BLYS58
BASN59
BARG71
BVAL72
BARG98

Functional Information from PROSITE/UniProt
site_idPS00075
Number of Residues23
DetailsDHFR_1 Dihydrofolate reductase (DHFR) domain signature. VIGmenaMPWnlpa.DlawFkrnT
ChainResidueDetails
AVAL13-THR35

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

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

Catalytic Information from CSA
site_idCSA1
Number of Residues7
DetailsAnnotated By Reference To The Literature 1ra2
ChainResidueDetails
ALEU54
ALEU28
APHE31
AASP27
AILE5
AMET20
AILE94

site_idCSA2
Number of Residues7
DetailsAnnotated By Reference To The Literature 1ra2
ChainResidueDetails
BLEU54
BLEU28
BPHE31
BASP27
BILE5
BMET20
BILE94

224201

PDB entries from 2024-08-28

PDB statisticsPDBj update infoContact PDBjnumon