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2WAP

3D-crystal structure of humanized-rat fatty acid amide hydrolase (FAAH) conjugated with the drug-like urea inhibitor PF-3845

Functional Information from GO Data
ChainGOidnamespacecontents
A0000139cellular_componentGolgi membrane
A0004040molecular_functionamidase activity
A0005515molecular_functionprotein binding
A0005543molecular_functionphospholipid binding
A0005783cellular_componentendoplasmic reticulum
A0005789cellular_componentendoplasmic reticulum membrane
A0005794cellular_componentGolgi apparatus
A0006631biological_processfatty acid metabolic process
A0008289molecular_functionlipid binding
A0009062biological_processfatty acid catabolic process
A0016020cellular_componentmembrane
A0016042biological_processlipid catabolic process
A0016787molecular_functionhydrolase activity
A0016788molecular_functionhydrolase activity, acting on ester bonds
A0017064molecular_functionfatty acid amide hydrolase activity
A0031090cellular_componentorganelle membrane
A0042802molecular_functionidentical protein binding
A0045907biological_processpositive regulation of vasoconstriction
A0047372molecular_functionacylglycerol lipase activity
A0052651biological_processmonoacylglycerol catabolic process
A0098793cellular_componentpresynapse
A0098794cellular_componentpostsynapse
B0000139cellular_componentGolgi membrane
B0004040molecular_functionamidase activity
B0005515molecular_functionprotein binding
B0005543molecular_functionphospholipid binding
B0005783cellular_componentendoplasmic reticulum
B0005789cellular_componentendoplasmic reticulum membrane
B0005794cellular_componentGolgi apparatus
B0006631biological_processfatty acid metabolic process
B0008289molecular_functionlipid binding
B0009062biological_processfatty acid catabolic process
B0016020cellular_componentmembrane
B0016042biological_processlipid catabolic process
B0016787molecular_functionhydrolase activity
B0016788molecular_functionhydrolase activity, acting on ester bonds
B0017064molecular_functionfatty acid amide hydrolase activity
B0031090cellular_componentorganelle membrane
B0042802molecular_functionidentical protein binding
B0045907biological_processpositive regulation of vasoconstriction
B0047372molecular_functionacylglycerol lipase activity
B0052651biological_processmonoacylglycerol catabolic process
B0098793cellular_componentpresynapse
B0098794cellular_componentpostsynapse
Functional Information from PDB Data
site_idAC1
Number of Residues20
DetailsBINDING SITE FOR RESIDUE PIX A 1574
ChainResidue
AMET191
ATYR335
ALEU372
AGLU373
ATHR377
ALEU380
APHE381
APHE432
ATHR488
AVAL491
AMET495
APHE192
ATRP531
ASER193
ATYR194
ASER217
AILE238
AGLY239
AGLY240
ASER241

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 1575
ChainResidue
AASN259
BASN259
BTRP556

site_idAC3
Number of Residues1
DetailsBINDING SITE FOR RESIDUE NA A 1576
ChainResidue
AGLU373

site_idAC4
Number of Residues17
DetailsBINDING SITE FOR RESIDUE PIX B 1574
ChainResidue
BMET191
BPHE192
BSER193
BTYR194
BILE238
BGLY239
BGLY240
BSER241
BTYR335
BLEU372
BGLU373
BTHR377
BLEU380
BTHR488
BVAL491
BMET495
BTRP531

site_idAC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE NA B 1575
ChainResidue
BGLU373

site_idAC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE NA B 1576
ChainResidue
BASN434
BASN435

Functional Information from PROSITE/UniProt
site_idPS00571
Number of Residues32
DetailsAMIDASES Amidases signature. GGSSGGeGAlIGsggsplGlGtDiGgSIRfPS
ChainResidueDetails
AGLY215-SER246

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues58
DetailsINTRAMEM: INTRAMEM => ECO:0000305
ChainResidueDetails
ALEU404-LEU433
BLEU404-LEU433

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Charge relay system
ChainResidueDetails
ALYS142
ASER217
BLYS142
BSER217

site_idSWS_FT_FI3
Number of Residues2
DetailsACT_SITE: Acyl-ester intermediate
ChainResidueDetails
ASER241
BSER241

site_idSWS_FT_FI4
Number of Residues6
DetailsBINDING:
ChainResidueDetails
AMET191
ASER217
AILE238
BMET191
BSER217
BILE238

site_idSWS_FT_FI5
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:O00519
ChainResidueDetails
ASER241
BSER241

Catalytic Information from CSA
site_idMCSA1
Number of Residues7
DetailsM-CSA 731
ChainResidueDetails
ALYS142proton acceptor, proton donor
ASER217proton acceptor, proton donor, proton relay
ASER218electrostatic stabiliser
AILE238electrostatic stabiliser
AGLY239electrostatic stabiliser
AGLY240electrostatic stabiliser
ASER241nucleofuge, nucleophile, proton acceptor, proton donor

site_idMCSA2
Number of Residues7
DetailsM-CSA 731
ChainResidueDetails
BLYS142proton acceptor, proton donor
BSER217proton acceptor, proton donor, proton relay
BSER218electrostatic stabiliser
BILE238electrostatic stabiliser
BGLY239electrostatic stabiliser
BGLY240electrostatic stabiliser
BSER241nucleofuge, nucleophile, proton acceptor, proton donor

219140

PDB entries from 2024-05-01

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