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1HX3

CRYSTAL STRUCTURE OF E.COLI ISOPENTENYL DIPHOSPHATE:DIMETHYLALLYL DIPHOSPHATE ISOMERASE

Functional Information from GO Data
ChainGOidnamespacecontents
A0000287molecular_functionmagnesium ion binding
A0003824molecular_functioncatalytic activity
A0004452molecular_functionisopentenyl-diphosphate delta-isomerase activity
A0005737cellular_componentcytoplasm
A0006974biological_processDNA damage response
A0008270molecular_functionzinc ion binding
A0008299biological_processisoprenoid biosynthetic process
A0016853molecular_functionisomerase activity
A0046872molecular_functionmetal ion binding
A0050992biological_processdimethylallyl diphosphate biosynthetic process
B0000287molecular_functionmagnesium ion binding
B0003824molecular_functioncatalytic activity
B0004452molecular_functionisopentenyl-diphosphate delta-isomerase activity
B0005737cellular_componentcytoplasm
B0006974biological_processDNA damage response
B0008270molecular_functionzinc ion binding
B0008299biological_processisoprenoid biosynthetic process
B0016853molecular_functionisomerase activity
B0046872molecular_functionmetal ion binding
B0050992biological_processdimethylallyl diphosphate biosynthetic process
Functional Information from PDB Data
site_idAC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 A 191
ChainResidue
ALYS21
AARG51
AALA67
AHIS69
AIMD202
AHOH211
AHOH222

site_idAC2
Number of Residues9
DetailsBINDING SITE FOR RESIDUE SO4 B 191
ChainResidue
BLYS55
BHIS69
BARG83
BIMD203
BHOH219
BHOH241
BHOH264
BLYS21
BARG51

site_idAC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MN A 201
ChainResidue
AHIS25
AHIS69

site_idAC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE MN B 202
ChainResidue
BHIS25
BHIS69

site_idAC5
Number of Residues4
DetailsBINDING SITE FOR RESIDUE IMD A 202
ChainResidue
AALA67
AHIS69
ATRP161
ASO4191

site_idAC6
Number of Residues2
DetailsBINDING SITE FOR RESIDUE IMD B 203
ChainResidue
BTRP161
BSO4191

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues4
DetailsACT_SITE:
ChainResidueDetails
AALA67
AGLU116
BALA67
BGLU116

site_idSWS_FT_FI2
Number of Residues14
DetailsBINDING:
ChainResidueDetails
ALYS21
BLYS55
BALA67
BHIS69
BARG83
BGLU87
AARG51
ALYS55
AALA67
AHIS69
AARG83
AGLU87
BLYS21
BARG51

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000269|PubMed:12630859, ECO:0000269|PubMed:15643873
ChainResidueDetails
AHIS25
AHIS32
AGLU114
AGLU116
BHIS25
BHIS32
BGLU114
BGLU116

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Essential for catalytic activity
ChainResidueDetails
ATYR104
BTYR104

Catalytic Information from CSA
site_idCSA1
Number of Residues4
DetailsAnnotated By Reference To The Literature 1i9a
ChainResidueDetails
ATRP161
AGLU87
AGLU116
AALA67

site_idCSA2
Number of Residues4
DetailsAnnotated By Reference To The Literature 1i9a
ChainResidueDetails
BTRP161
BGLU87
BGLU116
BALA67

site_idMCSA1
Number of Residues9
DetailsM-CSA 190
ChainResidueDetails
AHIS25metal ligand
AHIS32metal ligand
AALA67hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
AHIS69metal ligand
AGLU87metal ligand
ATYR104hydrogen bond acceptor, hydrogen bond donor, proton donor
AGLU114metal ligand
AGLU116electrostatic stabiliser, hydrogen bond acceptor, metal ligand, proton acceptor, proton donor
ATRP161electrostatic stabiliser, polar/non-polar interaction

site_idMCSA2
Number of Residues9
DetailsM-CSA 190
ChainResidueDetails
BHIS25metal ligand
BHIS32metal ligand
BALA67hydrogen bond acceptor, hydrogen bond donor, proton acceptor, proton donor
BHIS69metal ligand
BGLU87metal ligand
BTYR104hydrogen bond acceptor, hydrogen bond donor, proton donor
BGLU114metal ligand
BGLU116electrostatic stabiliser, hydrogen bond acceptor, metal ligand, proton acceptor, proton donor
BTRP161electrostatic stabiliser, polar/non-polar interaction

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PDB entries from 2024-05-01

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