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1PJ2

Crystal structure of human mitochondrial NAD(P)+-dependent malic enzyme in a pentary complex with natural substrate malate, cofactor NADH, Mn++, and allosteric activator fumarate

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0004470molecular_functionmalic enzyme activity
A0004471molecular_functionmalate dehydrogenase (decarboxylating) (NAD+) activity
A0004473molecular_functionmalate dehydrogenase (decarboxylating) (NADP+) activity
A0005739cellular_componentmitochondrion
A0005759cellular_componentmitochondrial matrix
A0006090biological_processpyruvate metabolic process
A0006108biological_processmalate metabolic process
A0008152biological_processmetabolic process
A0008948molecular_functionoxaloacetate decarboxylase activity
A0009055molecular_functionelectron transfer activity
A0016491molecular_functionoxidoreductase activity
A0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
A0043231cellular_componentintracellular membrane-bounded organelle
A0046872molecular_functionmetal ion binding
A0051287molecular_functionNAD binding
A1902031biological_processregulation of NADP metabolic process
B0003824molecular_functioncatalytic activity
B0004470molecular_functionmalic enzyme activity
B0004471molecular_functionmalate dehydrogenase (decarboxylating) (NAD+) activity
B0004473molecular_functionmalate dehydrogenase (decarboxylating) (NADP+) activity
B0005739cellular_componentmitochondrion
B0005759cellular_componentmitochondrial matrix
B0006090biological_processpyruvate metabolic process
B0006108biological_processmalate metabolic process
B0008152biological_processmetabolic process
B0008948molecular_functionoxaloacetate decarboxylase activity
B0009055molecular_functionelectron transfer activity
B0016491molecular_functionoxidoreductase activity
B0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
B0043231cellular_componentintracellular membrane-bounded organelle
B0046872molecular_functionmetal ion binding
B0051287molecular_functionNAD binding
B1902031biological_processregulation of NADP metabolic process
C0003824molecular_functioncatalytic activity
C0004470molecular_functionmalic enzyme activity
C0004471molecular_functionmalate dehydrogenase (decarboxylating) (NAD+) activity
C0004473molecular_functionmalate dehydrogenase (decarboxylating) (NADP+) activity
C0005739cellular_componentmitochondrion
C0005759cellular_componentmitochondrial matrix
C0006090biological_processpyruvate metabolic process
C0006108biological_processmalate metabolic process
C0008152biological_processmetabolic process
C0008948molecular_functionoxaloacetate decarboxylase activity
C0009055molecular_functionelectron transfer activity
C0016491molecular_functionoxidoreductase activity
C0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
C0043231cellular_componentintracellular membrane-bounded organelle
C0046872molecular_functionmetal ion binding
C0051287molecular_functionNAD binding
C1902031biological_processregulation of NADP metabolic process
D0003824molecular_functioncatalytic activity
D0004470molecular_functionmalic enzyme activity
D0004471molecular_functionmalate dehydrogenase (decarboxylating) (NAD+) activity
D0004473molecular_functionmalate dehydrogenase (decarboxylating) (NADP+) activity
D0005739cellular_componentmitochondrion
D0005759cellular_componentmitochondrial matrix
D0006090biological_processpyruvate metabolic process
D0006108biological_processmalate metabolic process
D0008152biological_processmetabolic process
D0008948molecular_functionoxaloacetate decarboxylase activity
D0009055molecular_functionelectron transfer activity
D0016491molecular_functionoxidoreductase activity
D0016616molecular_functionoxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
D0043231cellular_componentintracellular membrane-bounded organelle
D0046872molecular_functionmetal ion binding
D0051287molecular_functionNAD binding
D1902031biological_processregulation of NADP metabolic process
Functional Information from PDB Data
site_idAC1
Number of Residues15
DetailsBINDING SITE FOR RESIDUE MLT A 701
ChainResidue
ATYR112
AASN466
AASN467
ANAI601
AMN604
AHOH4543
AHOH4544
ATHR113
AARG165
ALEU167
ALYS183
AGLU255
AASP256
AASP279
AASN421

site_idAC2
Number of Residues15
DetailsBINDING SITE FOR RESIDUE MLT B 1701
ChainResidue
BTYR1112
BTHR1113
BARG1165
BLEU1167
BLYS1183
BGLU1255
BASP1256
BASP1279
BASN1421
BASN1466
BASN1467
BNAI1601
BMN1604
BHOH4003
BHOH4503

site_idAC3
Number of Residues15
DetailsBINDING SITE FOR RESIDUE MLT C 2701
ChainResidue
CTYR2112
CTHR2113
CARG2165
CLEU2167
CLYS2183
CGLU2255
CASP2256
CASP2279
CASN2421
CASN2466
CASN2467
CNAI2601
CMN2604
CHOH4002
CHOH4116

site_idAC4
Number of Residues15
DetailsBINDING SITE FOR RESIDUE MLT D 3701
ChainResidue
DTYR3112
DTHR3113
DARG3165
DLEU3167
DLYS3183
DGLU3255
DASP3279
DASN3421
DASN3466
DASN3467
DNAI3601
DMN3604
DHOH4335
DHOH4542
DHOH4547

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN A 604
ChainResidue
AARG165
AGLU255
AASP256
AASP279
ALMR701
AHOH4544

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN B 1604
ChainResidue
BARG1165
BGLU1255
BASP1256
BASP1279
BLMR1701
BHOH4003

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN C 2604
ChainResidue
CARG2165
CGLU2255
CASP2256
CASP2279
CLMR2701
CHOH4002

site_idAC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN D 3604
ChainResidue
DARG3165
DGLU3255
DASP3256
DASP3279
DLMR3701
DHOH4547

site_idAC9
Number of Residues30
DetailsBINDING SITE FOR RESIDUE NAI A 601
ChainResidue
AGLY394
AALA395
ALEU419
ASER420
AASN421
AGLY446
AGLY465
AASN466
AASN467
ALMR701
AHOH4007
AHOH4174
AHOH4281
AHOH4317
AHOH4733
AARG165
ALEU167
AGLY168
AASN259
AASP279
ATHR283
AGLY311
AALA312
AGLY313
AGLU314
AALA315
AASP345
ALYS346
AVAL392
AALA393

site_idBC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE NAI A 602
ChainResidue
AHIS154
AGLY192
AILE193
AARG194
AARG197
AILE479
ALEU480
AASN482
AARG542
ATYR552
AARG556
DASP3244
DARG3245

site_idBC2
Number of Residues26
DetailsBINDING SITE FOR RESIDUE NAI B 1601
ChainResidue
BARG1165
BLEU1167
BGLY1168
BASN1259
BASP1279
BTHR1283
BGLY1311
BALA1312
BGLY1313
BGLU1314
BALA1315
BASP1345
BLYS1346
BVAL1392
BALA1393
BGLY1394
BALA1395
BLEU1398
BLEU1419
BASN1421
BGLY1446
BGLY1465
BASN1466
BASN1467
BLMR1701
BHOH4073

site_idBC3
Number of Residues13
DetailsBINDING SITE FOR RESIDUE NAI B 1602
ChainResidue
BHIS1154
BLYS1156
BGLY1192
BILE1193
BARG1194
BARG1197
BILE1479
BLEU1480
BASN1482
BARG1542
BTYR1552
BARG1556
BHOH4180

site_idBC4
Number of Residues30
DetailsBINDING SITE FOR RESIDUE NAI C 2601
ChainResidue
CARG2165
CLEU2167
CGLY2168
CASN2259
CTHR2283
CGLY2311
CALA2312
CGLY2313
CGLU2314
CALA2315
CASP2345
CLYS2346
CVAL2392
CALA2393
CGLY2394
CALA2395
CLEU2398
CLEU2419
CASN2421
CGLY2446
CGLY2465
CASN2466
CASN2467
CLMR2701
CHOH4006
CHOH4085
CHOH4352
CHOH4371
CHOH4492
CHOH4654

site_idBC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE NAI C 2602
ChainResidue
BASP1244
BARG1245
BARG1248
CHIS2154
CLYS2156
CGLY2192
CILE2193
CARG2194
CARG2197
CILE2479
CLEU2480
CARG2542
CTYR2552
CARG2556

site_idBC6
Number of Residues27
DetailsBINDING SITE FOR RESIDUE NAI D 3601
ChainResidue
DARG3165
DLEU3167
DGLY3168
DASN3259
DTHR3283
DLEU3310
DGLY3311
DALA3312
DGLY3313
DGLU3314
DALA3315
DASP3345
DLYS3346
DVAL3392
DALA3393
DGLY3394
DALA3395
DLEU3398
DLEU3419
DSER3420
DASN3421
DGLY3446
DGLY3465
DASN3466
DASN3467
DLMR3701
DHOH4099

site_idBC7
Number of Residues14
DetailsBINDING SITE FOR RESIDUE NAI D 3602
ChainResidue
AARG245
AGLY247
DHIS3154
DLYS3156
DGLY3192
DILE3193
DARG3194
DARG3197
DILE3479
DLEU3480
DARG3542
DTYR3552
DARG3556
DHOH4500

site_idBC8
Number of Residues8
DetailsBINDING SITE FOR RESIDUE FUM A 700
ChainResidue
AGLN64
AARG67
AARG91
AHOH4029
AHOH4042
AHOH4132
BPHE1127
BARG1128

site_idBC9
Number of Residues9
DetailsBINDING SITE FOR RESIDUE FUM B 1700
ChainResidue
APHE127
AARG128
BGLN1064
BARG1067
BILE1088
BARG1091
BHOH4047
BHOH4104
BHOH4540

site_idCC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE FUM C 2700
ChainResidue
CGLN2064
CARG2067
CARG2091
CHOH4017
CHOH4028
CHOH4031
CHOH4051
DPHE3127
DARG3128
DHOH4613

site_idCC2
Number of Residues10
DetailsBINDING SITE FOR RESIDUE FUM D 3700
ChainResidue
CPHE2127
CARG2128
DGLN3064
DARG3067
DARG3091
DHOH4010
DHOH4096
DHOH4130
DHOH4252
DHOH4279

Functional Information from PROSITE/UniProt
site_idPS00331
Number of Residues17
DetailsMALIC_ENZYMES Malic enzymes signature. FnDDiqGTAaVaLAGLL
ChainResidueDetails
APHE276-LEU292

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton donor => ECO:0000269|PubMed:12962632
ChainResidueDetails
ATYR112
BTYR1112
CTYR2112
DTYR3112

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000269|PubMed:12962632
ChainResidueDetails
ALYS183
BLYS1183
CLYS2183
DLYS3183

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:12121650, ECO:0000269|PubMed:12962632
ChainResidueDetails
CARG2067
CARG2091
DARG3067
DARG3091
AARG67
AARG91
BARG1067
BARG1091

site_idSWS_FT_FI4
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:12962632
ChainResidueDetails
AARG165
AASN421
AASN466
BARG1165
BASN1421
BASN1466
CARG2165
CASN2421
CASN2466
DARG3165
DASN3421
DASN3466

site_idSWS_FT_FI5
Number of Residues12
DetailsBINDING: BINDING => ECO:0000269|PubMed:10700286, ECO:0000269|PubMed:12121650, ECO:0000269|PubMed:12962632
ChainResidueDetails
CASP2279
DGLU3255
DASP3256
DASP3279
AGLU255
AASP256
AASP279
BGLU1255
BASP1256
BASP1279
CGLU2255
CASP2256

site_idSWS_FT_FI6
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:10700286, ECO:0000269|PubMed:12962632
ChainResidueDetails
AASN259
AGLY311
BASN1259
BGLY1311
CASN2259
CGLY2311
DASN3259
DGLY3311

site_idSWS_FT_FI7
Number of Residues20
DetailsMOD_RES: N6-acetyllysine => ECO:0007744|PubMed:19608861
ChainResidueDetails
ALYS346
BLYS1156
BLYS1224
BLYS1240
BLYS1272
BLYS1346
CLYS2156
CLYS2224
CLYS2240
CLYS2272
CLYS2346
DLYS3156
DLYS3224
DLYS3240
DLYS3272
DLYS3346
ALYS156
ALYS224
ALYS240
ALYS272

Catalytic Information from CSA
site_idMCSA1
Number of Residues8
DetailsM-CSA 21
ChainResidueDetails
ATYR112electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AARG165electrostatic stabiliser, hydrogen bond donor
ALYS183electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
AGLU255metal ligand
AASP256metal ligand
AASP278hydrogen bond acceptor, proton acceptor, proton donor
AASP279metal ligand
AASN421electrostatic stabiliser, hydrogen bond donor

site_idMCSA2
Number of Residues8
DetailsM-CSA 21
ChainResidueDetails
BTYR1112electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BARG1165electrostatic stabiliser, hydrogen bond donor
BLYS1183electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
BGLU1255metal ligand
BASP1256metal ligand
BASP1278hydrogen bond acceptor, proton acceptor, proton donor
BASP1279metal ligand
BASN1421electrostatic stabiliser, hydrogen bond donor

site_idMCSA3
Number of Residues8
DetailsM-CSA 21
ChainResidueDetails
CTYR2112electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
CARG2165electrostatic stabiliser, hydrogen bond donor
CLYS2183electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
CGLU2255metal ligand
CASP2256metal ligand
CASP2278hydrogen bond acceptor, proton acceptor, proton donor
CASP2279metal ligand
CASN2421electrostatic stabiliser, hydrogen bond donor

site_idMCSA4
Number of Residues8
DetailsM-CSA 21
ChainResidueDetails
DTYR3112electrostatic stabiliser, hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
DARG3165electrostatic stabiliser, hydrogen bond donor
DLYS3183electrostatic stabiliser, hydrogen bond donor, proton acceptor, proton donor, proton relay
DGLU3255metal ligand
DASP3256metal ligand
DASP3278hydrogen bond acceptor, proton acceptor, proton donor
DASP3279metal ligand
DASN3421electrostatic stabiliser, hydrogen bond donor

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数据于2024-04-17公开中

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