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5G1W

Apo Structure of Linalool Dehydratase-Isomerase

Functional Information from GO Data
ChainGOidnamespacecontents
A0016098biological_processmonoterpenoid metabolic process
A0016829molecular_functionlyase activity
A0016836molecular_functionhydro-lyase activity
A0016853molecular_functionisomerase activity
A0042597cellular_componentperiplasmic space
A0043694biological_processmonoterpene catabolic process
A0050486molecular_functionintramolecular hydroxytransferase activity
B0016098biological_processmonoterpenoid metabolic process
B0016829molecular_functionlyase activity
B0016836molecular_functionhydro-lyase activity
B0016853molecular_functionisomerase activity
B0042597cellular_componentperiplasmic space
B0043694biological_processmonoterpene catabolic process
B0050486molecular_functionintramolecular hydroxytransferase activity
C0016098biological_processmonoterpenoid metabolic process
C0016829molecular_functionlyase activity
C0016836molecular_functionhydro-lyase activity
C0016853molecular_functionisomerase activity
C0042597cellular_componentperiplasmic space
C0043694biological_processmonoterpene catabolic process
C0050486molecular_functionintramolecular hydroxytransferase activity
D0016098biological_processmonoterpenoid metabolic process
D0016829molecular_functionlyase activity
D0016836molecular_functionhydro-lyase activity
D0016853molecular_functionisomerase activity
D0042597cellular_componentperiplasmic space
D0043694biological_processmonoterpene catabolic process
D0050486molecular_functionintramolecular hydroxytransferase activity
E0016098biological_processmonoterpenoid metabolic process
E0016829molecular_functionlyase activity
E0016836molecular_functionhydro-lyase activity
E0016853molecular_functionisomerase activity
E0042597cellular_componentperiplasmic space
E0043694biological_processmonoterpene catabolic process
E0050486molecular_functionintramolecular hydroxytransferase activity
Functional Information from PDB Data
site_idAC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO D 1366
ChainResidue
DPHE209
DLYS212
DASP213
DLEU214
DHOH2425

site_idAC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO A 1366
ChainResidue
AEDO1369
ADXX1370
ADXX1370
AGLU147
AARG155
AHIS195
ATYR199

site_idAC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 1366
ChainResidue
BARG155
BTYR199
BDXX1369
BHOH2406
DGLU147
DHIS195
DHOH2256

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EDO C 1366
ChainResidue
CPHE51
CTRP54
CTHR59
CILE64
CARG104
CHOH2092

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO B 1367
ChainResidue
BPHE51
BTRP54
BTHR59
BILE64
BARG104

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO A 1367
ChainResidue
APHE209
ALYS212
AASP213
ALEU214

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE EDO D 1367
ChainResidue
DPHE51
DTRP54
DTHR59
DILE64
DARG104

site_idAC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 1368
ChainResidue
BGLU147
BHIS195
BDXX1369
BHOH2407
DARG155
DTHR197
DTYR199

site_idAC9
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO A 1368
ChainResidue
APHE51
ATRP54
AGLU55
ATHR59
AILE64
AARG104
AHOH2120

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE EDO A 1369
ChainResidue
ATHR197
AASP198
AEDO1366
AHOH2466

site_idBC2
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO E 1366
ChainResidue
EPHE51
ETRP54
EGLU55
ETHR59
EILE64
EARG104
EHOH2090

site_idBC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE DXX B 1369
ChainResidue
BARG155
BTYR191
BHIS195
BEDO1366
BEDO1368
DARG155
DTYR191
DHIS195
DTHR197

site_idBC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE DXX A 1370
ChainResidue
AARG155
AARG155
ATYR191
ATYR191
AHIS195
AHIS195
AEDO1366
AEDO1366

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues5
DetailsActive site: {"description":"Proton donor/acceptor","evidences":[{"source":"Reference","evidenceCode":"ECO:0000305","citation":{"citationType":"journal article","publicationDate":"2020","firstPage":"0","lastPage":"0","volume":"0","journal":"ACS Catal.","title":"Mutational analysis of linalool dehydratase isomerase suggests that alcohol and alkene transformations are catalyzed using noncovalent mechanisms.","authors":["Cuetos A.","Iglesias-Fernandez J.","Danesh-Azari H.R.","Zukic E.","Dowle A.","Osuna S.","Grogan G."],"citationCrossReferences":[{"database":"DOI","id":"10.1021/acscatal.0c02958"}]}}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues5
DetailsBinding site: {"evidences":[{"source":"PubMed","id":"27062179","evidenceCode":"ECO:0000269"},{"source":"PDB","id":"5HSS","evidenceCode":"ECO:0007744"}]}
ChainResidueDetails

248636

PDB entries from 2026-02-04

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