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

6LQ2

Crystal Structure of E447A Acyl-CoA Dehydrogenase FadE5 mutant from Mycobacteria smegmatis in complex with C10CoA

Functional Information from GO Data
ChainGOidnamespacecontents
A0004466molecular_functionlong-chain fatty acyl-CoA dehydrogenase activity
A0006631biological_processfatty acid metabolic process
A0016491molecular_functionoxidoreductase activity
A0016627molecular_functionoxidoreductase activity, acting on the CH-CH group of donors
A0016937molecular_functionshort-chain fatty acyl-CoA dehydrogenase activity
A0070991molecular_functionmedium-chain fatty acyl-CoA dehydrogenase activity
B0004466molecular_functionlong-chain fatty acyl-CoA dehydrogenase activity
B0006631biological_processfatty acid metabolic process
B0016491molecular_functionoxidoreductase activity
B0016627molecular_functionoxidoreductase activity, acting on the CH-CH group of donors
B0016937molecular_functionshort-chain fatty acyl-CoA dehydrogenase activity
B0070991molecular_functionmedium-chain fatty acyl-CoA dehydrogenase activity
Functional Information from PDB Data
site_idAC1
Number of Residues31
Detailsbinding site for residue FAD A 701
ChainResidue
AMET162
ALEU445
ATYR446
AALA447
ATHR449
ADKA702
ACOA703
AHOH863
AHOH1021
AHOH1036
AHOH1077
ALEU164
AHOH1085
BARG326
BGLN328
BILE345
BHIS348
BGLN420
BTHR421
BGLY423
BGLY424
BHOH819
ATHR165
BHOH884
BHOH904
AGLY170
ASER171
APHE196
ATHR198
ATHR266
AILE442

site_idAC2
Number of Residues31
Detailsbinding site for residue FAD B 701
ChainResidue
AARG326
AGLN328
AILE345
AHIS348
AGLN420
ATHR421
AGLY423
AGLY424
AHOH838
AHOH878
AHOH1025
BMET162
BLEU164
BTHR165
BGLY170
BSER171
BPHE196
BTHR198
BILE442
BLEU445
BTYR446
BALA447
BTHR449
BALA451
BDKA702
BCOA703
BHOH967
BHOH1022
BHOH1052
BHOH1053
BHOH1108

site_idAC3
Number of Residues37
Detailsbinding site for residues DKA A 702 and COA A 703
ChainResidue
AMET130
AMET134
AALA160
AMET162
ASER171
AVAL173
ATHR224
ALYS225
AILE290
APHE294
AGLU298
AARG301
ATYR446
AALA447
AGLY448
AILE452
AASP456
AARG460
ALYS461
AFAD701
AHOH823
AHOH829
AHOH854
AHOH879
AHOH952
AHOH954
AHOH988
AHOH1042
AHOH1045
AHOH1054
AHOH1065
AHOH1093
AHOH1120
AHOH1163
AHOH1168
AHOH1210
BLYS338

site_idAC4
Number of Residues37
Detailsbinding site for residues DKA B 702 and COA B 703
ChainResidue
ALYS338
BMET134
BALA160
BMET162
BSER171
BVAL173
BTHR224
BLYS225
BILE290
BPHE294
BGLU298
BARG301
BMET303
BTYR446
BALA447
BGLY448
BILE452
BASP456
BARG460
BLYS461
BARG464
BFAD701
BHOH832
BHOH843
BHOH856
BHOH859
BHOH864
BHOH907
BHOH917
BHOH934
BHOH935
BHOH948
BHOH1009
BHOH1025
BHOH1067
BHOH1129
BHOH1153

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsACT_SITE: Proton acceptor => ECO:0000305|PubMed:32601219
ChainResidueDetails
AALA447
BALA447

site_idSWS_FT_FI2
Number of Residues24
DetailsBINDING: BINDING => ECO:0000269|PubMed:32601219
ChainResidueDetails
AMET162
ATHR449
AASP456
AARG460
BMET162
BSER171
BTHR198
BTHR224
BARG301
BARG326
BLYS338
ASER171
BGLN420
BALA447
BTHR449
BASP456
BARG460
ATHR198
ATHR224
AARG301
AARG326
ALYS338
AGLN420
AALA447

222926

PDB entries from 2024-07-24

PDB statisticsPDBj update infoContact PDBjnumon