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3GPC

Crystal structure of human Acyl-CoA synthetase medium-chain family member 2A (L64P mutation) in a complex with CoA

Replaces:  3EYN
Functional Information from GO Data
ChainGOidnamespacecontents
A0004321molecular_functionfatty-acyl-CoA synthase activity
A0005524molecular_functionATP binding
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0006631biological_processfatty acid metabolic process
A0006633biological_processfatty acid biosynthetic process
A0006637biological_processacyl-CoA metabolic process
A0015645molecular_functionfatty acid ligase activity
A0016405molecular_functionCoA-ligase activity
A0016874molecular_functionligase activity
A0016878molecular_functionacid-thiol ligase activity
A0018858molecular_functionbenzoate-CoA ligase activity
A0031956molecular_functionmedium-chain fatty acid-CoA ligase activity
A0036112biological_processmedium-chain fatty-acyl-CoA metabolic process
A0042593biological_processglucose homeostasis
A0046872molecular_functionmetal ion binding
A0070328biological_processtriglyceride homeostasis
A0102391molecular_functiondecanoate-CoA ligase activity
B0004321molecular_functionfatty-acyl-CoA synthase activity
B0005524molecular_functionATP binding
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0006631biological_processfatty acid metabolic process
B0006633biological_processfatty acid biosynthetic process
B0006637biological_processacyl-CoA metabolic process
B0015645molecular_functionfatty acid ligase activity
B0016405molecular_functionCoA-ligase activity
B0016874molecular_functionligase activity
B0016878molecular_functionacid-thiol ligase activity
B0018858molecular_functionbenzoate-CoA ligase activity
B0031956molecular_functionmedium-chain fatty acid-CoA ligase activity
B0036112biological_processmedium-chain fatty-acyl-CoA metabolic process
B0042593biological_processglucose homeostasis
B0046872molecular_functionmetal ion binding
B0070328biological_processtriglyceride homeostasis
B0102391molecular_functiondecanoate-CoA ligase activity
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG A 901
ChainResidue
AMET483
AHIS485
AVAL488
AHOH957

site_idAC2
Number of Residues25
DetailsBINDING SITE FOR RESIDUE COA A 578
ChainResidue
ATYR361
AGLY362
AGLN363
ATHR364
ALEU444
AASP446
APHE458
AARG461
ATHR553
ATHR555
ALYS557
AGLN559
AHOH590
AHOH687
AHOH697
AHOH780
AHOH781
AHOH785
AHOH918
AHOH1143
AGLY338
AGLU339
ASER340
AGLU359
ASER360

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE MG B 901
ChainResidue
BMET483
BHIS485
BVAL488
BHOH611

site_idAC4
Number of Residues19
DetailsBINDING SITE FOR RESIDUE COA B 902
ChainResidue
BTRP265
BGLY338
BGLU339
BSER340
BGLU359
BSER360
BTYR361
BGLY362
BGLN363
BTHR364
BASP446
BPHE458
BARG461
BTHR555
BHOH718
BHOH787
BHOH788
BHOH794
BHOH1192

Functional Information from PROSITE/UniProt
site_idPS00455
Number of Residues12
DetailsAMP_BINDING Putative AMP-binding domain signature. IYFTSGTSGlPK
ChainResidueDetails
AILE218-LYS229

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues14
DetailsBINDING: BINDING => ECO:0000269|PubMed:19345228
ChainResidueDetails
AGLN139
BSER469
BARG472
BARG501
BLYS532
BTYR540
ATHR364
ASER469
AARG472
AARG501
ALYS532
ATYR540
BGLN139
BTHR364

site_idSWS_FT_FI2
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:19345228, ECO:0000269|Ref.7
ChainResidueDetails
ATHR221
BLYS557
AGLU359
AASP446
AARG461
ALYS557
BTHR221
BGLU359
BASP446
BARG461

site_idSWS_FT_FI3
Number of Residues2
DetailsMOD_RES: Phosphoserine => ECO:0000250|UniProtKB:Q68CK6
ChainResidueDetails
ASER513
BSER513

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PDB entries from 2024-11-06

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