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5FSA

Crystal structure of sterol 14-alpha demethylase (CYP51) from a pathogenic yeast Candida albicans in complex with the antifungal drug posaconazole

Functional Information from GO Data
ChainGOidnamespacecontents
A0001766biological_processmembrane raft polarization
A0004497molecular_functionmonooxygenase activity
A0005506molecular_functioniron ion binding
A0005783cellular_componentendoplasmic reticulum
A0005789cellular_componentendoplasmic reticulum membrane
A0005886cellular_componentplasma membrane
A0006696biological_processergosterol biosynthetic process
A0007032biological_processendosome organization
A0008398molecular_functionsterol 14-demethylase activity
A0016020cellular_componentmembrane
A0016126biological_processsterol biosynthetic process
A0016491molecular_functionoxidoreductase activity
A0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
A0020037molecular_functionheme binding
A0032541cellular_componentcortical endoplasmic reticulum
A0036187biological_processcell growth mode switching, budding to filamentous
A0046872molecular_functionmetal ion binding
A0097038cellular_componentperinuclear endoplasmic reticulum
B0001766biological_processmembrane raft polarization
B0004497molecular_functionmonooxygenase activity
B0005506molecular_functioniron ion binding
B0005783cellular_componentendoplasmic reticulum
B0005789cellular_componentendoplasmic reticulum membrane
B0005886cellular_componentplasma membrane
B0006696biological_processergosterol biosynthetic process
B0007032biological_processendosome organization
B0008398molecular_functionsterol 14-demethylase activity
B0016020cellular_componentmembrane
B0016126biological_processsterol biosynthetic process
B0016491molecular_functionoxidoreductase activity
B0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
B0020037molecular_functionheme binding
B0032541cellular_componentcortical endoplasmic reticulum
B0036187biological_processcell growth mode switching, budding to filamentous
B0046872molecular_functionmetal ion binding
B0097038cellular_componentperinuclear endoplasmic reticulum
Functional Information from PDB Data
site_idAC1
Number of Residues16
DetailsBINDING SITE FOR RESIDUE HEM A 580
ChainResidue
ATYR118
APRO462
AHIS468
AARG469
ACYS470
AILE471
AX2N590
AHOH2052
ATYR132
ALEU139
ALYS143
AGLY308
ATHR311
APRO375
AILE379
AARG381

site_idAC2
Number of Residues16
DetailsBINDING SITE FOR RESIDUE X2N A 590
ChainResidue
AALA61
ATYR118
ALEU121
APHE126
AILE131
APHE228
APRO230
APHE233
AGLY307
ALEU376
AHIS377
ASER506
ASER507
AMET508
AHEM580
AHOH2045

site_idAC3
Number of Residues18
DetailsBINDING SITE FOR RESIDUE HEM B 580
ChainResidue
BTYR118
BTYR132
BLYS143
BGLY308
BTHR311
BTHR315
BPRO375
BILE379
BARG381
BPRO462
BPHE463
BHIS468
BCYS470
BILE471
BGLY472
BPHE475
BX2N590
BHOH2057

site_idAC4
Number of Residues16
DetailsBINDING SITE FOR RESIDUE X2N B 590
ChainResidue
BALA61
BTYR64
BGLY65
BGLN66
BLEU121
BPHE126
BPHE228
BPRO230
BGLY303
BGLY307
BLEU376
BHIS377
BSER506
BSER507
BMET508
BHEM580

Functional Information from PROSITE/UniProt
site_idPS00086
Number of Residues10
DetailsCYTOCHROME_P450 Cytochrome P450 cysteine heme-iron ligand signature. FGgGRHRCIG
ChainResidueDetails
APHE463-GLY472

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsBINDING: BINDING => ECO:0007744|PDB:5TZ1
ChainResidueDetails
ATYR64
AHIS377
BTYR64
BHIS377

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0007744|PDB:5V5Z
ChainResidueDetails
ATYR118
BTYR118

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: BINDING => ECO:0007744|PDB:5FSA
ChainResidueDetails
AGLY307
BGLY307

site_idSWS_FT_FI4
Number of Residues2
DetailsBINDING: axial binding residue => ECO:0007744|PDB:5FSA, ECO:0007744|PDB:5TZ1, ECO:0007744|PDB:5V5Z
ChainResidueDetails
ACYS470
BCYS470

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PDB entries from 2024-07-24

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