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1DO8

CRYSTAL STRUCTURE OF A CLOSED FORM OF HUMAN MITOCHONDRIAL NAD(P)+-DEPENDENT MALIC ENZYME

Functional Information from GO Data
ChainGOidnamespacecontents
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
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
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
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
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
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
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
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 Residues13
DetailsBINDING SITE FOR RESIDUE OXL A 603
ChainResidue
ATYR112
AASN467
ANAD601
AMN604
AHOH4290
AARG165
ALEU167
ALYS183
AGLU255
AASP256
AASP279
AASN421
AASN466

site_idAC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN A 604
ChainResidue
AARG165
AGLU255
AASP256
AASP279
AOXL603
AHOH606

site_idAC3
Number of Residues12
DetailsBINDING SITE FOR RESIDUE OXL B 1603
ChainResidue
BARG1165
BLEU1167
BLYS1183
BGLU1255
BASP1256
BASP1279
BASN1421
BASN1466
BASN1467
BNAD1601
BMN1604
BHOH4112

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN B 1604
ChainResidue
BARG1165
BGLU1255
BASP1256
BASP1279
BOXL1603
BHOH1606

site_idAC5
Number of Residues12
DetailsBINDING SITE FOR RESIDUE OXL C 2603
ChainResidue
CARG2165
CLEU2167
CLYS2183
CGLU2255
CASP2256
CASP2279
CASN2421
CASN2466
CASN2467
CNAD2601
CMN2604
CHOH4054

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN C 2604
ChainResidue
CARG2165
CGLU2255
CASP2256
CASP2279
COXL2603
CHOH2606

site_idAC7
Number of Residues12
DetailsBINDING SITE FOR RESIDUE OXL D 3603
ChainResidue
DARG3165
DLEU3167
DLYS3183
DGLU3255
DASP3256
DASP3279
DASN3421
DASN3466
DASN3467
DNAD3601
DMN3604
DHOH4119

site_idAC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MN D 3604
ChainResidue
DARG3165
DGLU3255
DASP3256
DASP3279
DOXL3603
DHOH3606

site_idAC9
Number of Residues27
DetailsBINDING SITE FOR RESIDUE NAD A 601
ChainResidue
AHOH4315
AARG165
ALEU167
AGLY168
AASN259
AASP279
ATHR283
AGLY311
AALA312
AGLY313
AGLU314
AALA315
AASP345
ALYS346
AVAL392
AALA393
AGLY394
AALA395
ALEU398
ALEU419
AASN421
AGLY446
AGLY465
AASN466
AASN467
AOXL603
AHOH4007

site_idBC1
Number of Residues13
DetailsBINDING SITE FOR RESIDUE NAD A 602
ChainResidue
AHIS154
AARG194
AARG197
AILE479
ALEU480
AARG542
ATYR552
AARG556
AHOH4739
AHOH4888
DASP3244
DARG3245
DGLY3247

site_idBC2
Number of Residues25
DetailsBINDING SITE FOR RESIDUE NAD B 1601
ChainResidue
BARG1165
BLEU1167
BGLY1168
BASN1259
BTHR1283
BGLY1311
BALA1312
BGLY1313
BGLU1314
BALA1315
BASP1345
BLYS1346
BVAL1392
BALA1393
BGLY1394
BLEU1398
BLEU1419
BASN1421
BGLY1446
BGLY1465
BASN1466
BASN1467
BOXL1603
BHOH4066
BHOH4933

site_idBC3
Number of Residues11
DetailsBINDING SITE FOR RESIDUE NAD B 1602
ChainResidue
BHIS1154
BLYS1156
BGLY1192
BARG1194
BARG1197
BILE1479
BLEU1480
BARG1542
BARG1556
BHOH4443
CARG2245

site_idBC4
Number of Residues27
DetailsBINDING SITE FOR RESIDUE NAD C 2601
ChainResidue
CARG2165
CLEU2167
CGLY2168
CASN2259
CASP2279
CTHR2283
CGLY2311
CALA2312
CGLY2313
CGLU2314
CALA2315
CASP2345
CLYS2346
CVAL2392
CALA2393
CGLY2394
CALA2395
CLEU2419
CASN2421
CGLY2446
CGLY2465
CASN2466
CASN2467
COXL2603
CHOH4017
CHOH4175
CHOH4678

site_idBC5
Number of Residues14
DetailsBINDING SITE FOR RESIDUE NAD C 2602
ChainResidue
BARG1245
BHOH4632
CHIS2154
CLYS2156
CGLY2192
CILE2193
CARG2194
CARG2197
CILE2479
CLEU2480
CARG2542
CTYR2552
CARG2556
CHOH4303

site_idBC6
Number of Residues29
DetailsBINDING SITE FOR RESIDUE NAD D 3601
ChainResidue
DARG3165
DLEU3167
DGLY3168
DASN3259
DASP3279
DTHR3283
DGLY3311
DALA3312
DGLY3313
DGLU3314
DALA3315
DASP3345
DLYS3346
DVAL3392
DALA3393
DGLY3394
DALA3395
DLEU3398
DLEU3419
DASN3421
DGLY3446
DGLY3465
DASN3466
DASN3467
DOXL3603
DHOH4124
DHOH4485
DHOH4533
DHOH4788

site_idBC7
Number of Residues11
DetailsBINDING SITE FOR RESIDUE NAD D 3602
ChainResidue
AASP244
AARG245
DHIS3154
DARG3194
DARG3197
DILE3479
DLEU3480
DASN3482
DARG3542
DTYR3552
DARG3556

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
AARG67
AARG91
BARG1067
BARG1091
CARG2067
CARG2091
DARG3067
DARG3091

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

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

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
ALYS156
BLYS1346
CLYS2156
CLYS2224
CLYS2240
CLYS2272
CLYS2346
DLYS3156
DLYS3224
DLYS3240
DLYS3272
ALYS224
DLYS3346
ALYS240
ALYS272
ALYS346
BLYS1156
BLYS1224
BLYS1240
BLYS1272

Catalytic Information from CSA
site_idCSA1
Number of Residues3
Detailsa catalytic site defined by CSA, PubMed 10700286, 12962632
ChainResidueDetails
AASP278
ALYS183
ATYR112

site_idCSA2
Number of Residues3
Detailsa catalytic site defined by CSA, PubMed 10700286, 12962632
ChainResidueDetails
BLYS1183
BASP1278
BTYR1112

site_idCSA3
Number of Residues3
Detailsa catalytic site defined by CSA, PubMed 10700286, 12962632
ChainResidueDetails
CASP2278
CLYS2183
CTYR2112

site_idCSA4
Number of Residues3
Detailsa catalytic site defined by CSA, PubMed 10700286, 12962632
ChainResidueDetails
DASP3278
DTYR3112
DLYS3183

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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PDB entries from 2024-07-17

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