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2GCI

The 1,1-proton transfer reaction mechanism by alpha-methylacyl-CoA racemase is catalyzed by an asparte/histidine pair and involves a smooth, methionine-rich surface for binding the fatty acyl moiety

Functional Information from GO Data
ChainGOidnamespacecontents
A0003824molecular_functioncatalytic activity
A0006629biological_processlipid metabolic process
A0006637biological_processacyl-CoA metabolic process
A0008111molecular_functionalpha-methylacyl-CoA racemase activity
A0016853molecular_functionisomerase activity
A0042803molecular_functionprotein homodimerization activity
B0003824molecular_functioncatalytic activity
B0006629biological_processlipid metabolic process
B0006637biological_processacyl-CoA metabolic process
B0008111molecular_functionalpha-methylacyl-CoA racemase activity
B0016853molecular_functionisomerase activity
B0042803molecular_functionprotein homodimerization activity
C0003824molecular_functioncatalytic activity
C0006629biological_processlipid metabolic process
C0006637biological_processacyl-CoA metabolic process
C0008111molecular_functionalpha-methylacyl-CoA racemase activity
C0016853molecular_functionisomerase activity
C0042803molecular_functionprotein homodimerization activity
D0003824molecular_functioncatalytic activity
D0006629biological_processlipid metabolic process
D0006637biological_processacyl-CoA metabolic process
D0008111molecular_functionalpha-methylacyl-CoA racemase activity
D0016853molecular_functionisomerase activity
D0042803molecular_functionprotein homodimerization activity
Functional Information from PDB Data
site_idAC1
Number of Residues21
DetailsBINDING SITE FOR RESIDUE MRR A 1751
ChainResidue
AARG38
ALEU92
AGLY113
AGLY125
AHIS126
AASP127
ATYR130
AASP156
AHOH1845
AHOH1871
AHOH1915
AALA59
AHOH1957
BTYR224
ALEU61
ALYS62
AGLY83
ATYR84
AARG85
AVAL88
AARG91

site_idAC2
Number of Residues38
DetailsBINDING SITE FOR RESIDUE MRR B 1752
ChainResidue
AMET207
AMET216
ATYR224
AILE240
AGLU241
AGOL1306
AHOH1946
BILE16
BARG38
BALA59
BASP60
BLEU61
BLYS62
BGLY83
BTYR84
BARG85
BVAL88
BARG91
BLEU92
BGLY113
BGLY125
BHIS126
BASP127
BTYR130
BASP156
BMET188
BASN263
BASP264
BARG265
BALA266
BGOL1305
BHOH1778
BHOH1853
BHOH1856
BHOH1866
BHOH1954
BHOH1973
BHOH1981

site_idAC3
Number of Residues25
DetailsBINDING SITE FOR RESIDUE MRR C 1753
ChainResidue
CARG38
CALA59
CASP60
CLEU61
CLYS62
CGLY83
CTYR84
CARG85
CVAL88
CARG91
CLEU92
CGLY113
CGLY125
CHIS126
CASP127
CTYR130
CASP156
CHOH1814
CHOH1819
CHOH1907
CHOH1946
CHOH1953
CHOH2015
CHOH2075
DTYR224

site_idAC4
Number of Residues31
DetailsBINDING SITE FOR RESIDUE MRR D 1754
ChainResidue
DGLY113
DGLY125
DHIS126
DASP127
DTYR130
DASP156
DPRO261
DASP264
DHOH1808
DHOH1820
DHOH1929
DHOH1966
DHOH2011
DHOH2042
DHOH2094
DHOH2123
CTYR224
CGLU241
CPRO242
CGOL1302
DARG38
DALA59
DASP60
DLEU61
DLYS62
DGLY83
DTYR84
DARG85
DVAL88
DARG91
DLEU92

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE GOL C 1301
ChainResidue
CASP48
CHOH1810
CHOH2061
CHOH2102
DALA201
DMET202

site_idAC6
Number of Residues10
DetailsBINDING SITE FOR RESIDUE GOL C 1302
ChainResidue
CMET216
CTYR223
CILE240
CGLN262
CASN263
CHOH1930
DPRO261
DASN263
DMRR1754
DHOH1816

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL D 1303
ChainResidue
CHOH1820
CHOH1853
DMET216
DTYR223
DILE240
DPRO242
DGLN262
DASN263

site_idAC8
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL B 1304
ChainResidue
AASN263
AHOH1810
AHOH1864
BMET216
BTYR223
BILE240
BPRO242
BGLN262
BASN263

site_idAC9
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL B 1305
ChainResidue
AMET198
AALA201
AMET202
AMET207
AHOH1912
BASP48
BMET50
BALA266
BMRR1752

site_idBC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE GOL A 1306
ChainResidue
AMET216
ATYR223
AILE240
AGLN262
AASN263
BPRO261
BASN263
BMRR1752

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE: Proton acceptor => ECO:0000305|PubMed:17320106, ECO:0000305|PubMed:22360758
ChainResidueDetails
AHIS126
BHIS126
CHIS126
DHIS126

site_idSWS_FT_FI2
Number of Residues4
DetailsACT_SITE: Proton donor => ECO:0000305|PubMed:17320106, ECO:0000305|PubMed:22360758
ChainResidueDetails
AASP156
BASP156
CASP156
DASP156

site_idSWS_FT_FI3
Number of Residues20
DetailsBINDING: BINDING => ECO:0000269|PubMed:17320106, ECO:0000269|PubMed:22360758
ChainResidueDetails
AARG38
BGLY125
CARG38
CALA59
CGLY83
CARG91
CGLY125
DARG38
DALA59
DGLY83
DARG91
AALA59
DGLY125
AGLY83
AARG91
AGLY125
BARG38
BALA59
BGLY83
BARG91

Catalytic Information from CSA
site_idCSA1
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
AASP156

site_idCSA2
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
BASP156

site_idCSA3
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
CASP156

site_idCSA4
Number of Residues1
DetailsAnnotated By Reference To The Literature 1xvt
ChainResidueDetails
DASP156

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PDB entries from 2024-07-31

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