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

6NNH

Structure of Closed state of Dihydrofolate reductase from Mycobacterium tuberculosis in complex with NADPH and cycloguanil

Functional Information from GO Data
ChainGOidnamespacecontents
A0004146molecular_functiondihydrofolate reductase activity
A0005829cellular_componentcytosol
A0006730biological_processone-carbon metabolic process
A0016491molecular_functionoxidoreductase activity
A0046452biological_processdihydrofolate metabolic process
A0046654biological_processtetrahydrofolate biosynthetic process
A0046655biological_processfolic acid metabolic process
A0050661molecular_functionNADP binding
A0070401molecular_functionNADP+ binding
B0004146molecular_functiondihydrofolate reductase activity
B0005829cellular_componentcytosol
B0006730biological_processone-carbon metabolic process
B0016491molecular_functionoxidoreductase activity
B0046452biological_processdihydrofolate metabolic process
B0046654biological_processtetrahydrofolate biosynthetic process
B0046655biological_processfolic acid metabolic process
B0050661molecular_functionNADP binding
B0070401molecular_functionNADP+ binding
Functional Information from PDB Data
site_idAC1
Number of Residues11
Detailsbinding site for residue 1CY A 201
ChainResidue
AILE5
ANDP202
AHOH385
ATRP6
AALA7
AASP27
APHE31
ATHR46
ALEU50
AILE94
ATHR113

site_idAC2
Number of Residues36
Detailsbinding site for residue NDP A 202
ChainResidue
ATRP6
AALA7
AILE14
AGLY15
AARG16
AGLY18
AASP19
AILE20
AGLY43
AARG44
AARG45
ATHR46
ALEU65
ASER66
AARG67
AGLN68
AGLY80
AILE94
AGLY95
AGLY96
AGLY97
AGLN98
AVAL99
ATYR100
ALEU102
AALA126
A1CY201
AHOH307
AHOH318
AHOH326
AHOH331
AHOH338
AHOH347
AHOH364
AHOH387
AHOH401

site_idAC3
Number of Residues4
Detailsbinding site for residue SO4 A 203
ChainResidue
AARG136
BGLU26
BALA29
BARG146

site_idAC4
Number of Residues5
Detailsbinding site for residue SO4 A 204
ChainResidue
AARG67
AHOH307
AHOH328
BARG67
BHOH360

site_idAC5
Number of Residues4
Detailsbinding site for residue SO4 A 205
ChainResidue
AHOH326
BARG67
BNDP202
BHOH371

site_idAC6
Number of Residues6
Detailsbinding site for residue CO A 206
ChainResidue
AHIS38
AHOH316
AHOH344
BHIS157
BHOH380
BHOH386

site_idAC7
Number of Residues12
Detailsbinding site for residue 1CY B 201
ChainResidue
BILE5
BTRP6
BALA7
BASP27
BPHE31
BTHR46
BLEU50
BILE94
BTYR100
BTHR113
BNDP202
BHOH385

site_idAC8
Number of Residues39
Detailsbinding site for residue NDP B 202
ChainResidue
BGLY97
BGLN98
BVAL99
BTYR100
BLEU102
BALA126
B1CY201
BHOH321
BHOH330
BHOH340
BHOH343
BHOH349
BHOH360
BHOH364
BHOH371
BHOH378
BHOH401
BHOH414
ASO4205
AHOH328
BTRP6
BALA7
BILE14
BGLY15
BARG16
BGLY18
BASP19
BILE20
BGLY43
BARG44
BARG45
BTHR46
BLEU65
BSER66
BARG67
BGLY80
BILE94
BGLY95
BGLY96

site_idAC9
Number of Residues4
Detailsbinding site for residue SO4 B 203
ChainResidue
BPRO51
BALA52
BHOH307
BHOH316

site_idAD1
Number of Residues5
Detailsbinding site for residue SO4 B 204
ChainResidue
BPHE31
BARG32
BARG60
BHOH305
BHOH306

site_idAD2
Number of Residues6
Detailsbinding site for residue CO B 205
ChainResidue
AHOH356
BHIS38
BHOH317
BHOH362
BHOH367
BHOH413

site_idAD3
Number of Residues5
Detailsbinding site for residue GOL B 206
ChainResidue
BTRP22
BARG23
BLEU24
BASP27
BHOH350

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

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues24
DetailsBINDING:
ChainResidueDetails
ATYR100
ATHR113
BILE5
BTRP6
BILE14
BASP27
BARG32
BGLY43
BARG60
BLEU65
BGLY80
BILE94
BTYR100
BTHR113
AILE5
ATRP6
AILE14
AASP27
AARG32
AGLY43
AARG60
ALEU65
AGLY80
AILE94

221051

PDB entries from 2024-06-12

PDB statisticsPDBj update infoContact PDBjnumon