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2VYA

Crystal Structure of fatty acid amide hydrolase conjugated with the drug-like inhibitor PF-750

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
A0006629biological_processlipid metabolic process
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
B0000139cellular_componentGolgi membrane
B0004040molecular_functionamidase activity
B0005515molecular_functionprotein binding
B0005543molecular_functionphospholipid binding
B0005783cellular_componentendoplasmic reticulum
B0005789cellular_componentendoplasmic reticulum membrane
B0005794cellular_componentGolgi apparatus
B0006629biological_processlipid metabolic process
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
Functional Information from PDB Data
site_idAC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CL B 1577
ChainResidue
AASN259
BASN259

site_idAC2
Number of Residues14
DetailsBINDING SITE FOR RESIDUE PF7 A 1578
ChainResidue
ASER241
ATHR377
APHE381
APHE432
AMET436
ATHR488
AVAL491
AMET191
APHE192
ASER193
ATYR194
AILE238
AGLY239
AGLY240

site_idAC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE PF7 B 1578
ChainResidue
BMET191
BPHE192
BSER193
BTYR194
BILE238
BGLY239
BGLY240
BSER241
BTHR377
BPHE381
BPHE432

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 Residues290
DetailsTOPO_DOM: Cytoplasmic => ECO:0000305
ChainResidueDetails
AASN434-SER579
BASN434-SER579

site_idSWS_FT_FI3
Number of Residues4
DetailsACT_SITE: Charge relay system
ChainResidueDetails
ALYS142
ASER217
BLYS142
BSER217

site_idSWS_FT_FI4
Number of Residues2
DetailsACT_SITE: Acyl-ester intermediate
ChainResidueDetails
ASER241
BSER241

site_idSWS_FT_FI5
Number of Residues6
DetailsBINDING:
ChainResidueDetails
AMET191
AILE238
BMET191
BSER217
BILE238
ASER217

site_idSWS_FT_FI6
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

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PDB entries from 2024-04-17

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