Structure of PDB 2e7z Chain A

Receptor sequence
>2e7zA (length=727) Species: 29542 (Syntrophotalea acetylenica) [Search protein sequence]
KKHVVCQSCDINCVVEAEVKADGKIQTKSISEPHPTTPPNSICMKSVNAD
TIRTHKDRVLYPLKNVGSKRGEQRWERISWDQALDEIAEKLKKIIAKYGP
ESLGVSQTEINQQSEYGTLRRFMNLLGSPNWTSAMYMCIGNTAGVHRVTH
GSYSFASFADSNCLLFIGKNLSNHNWVSQFNDLKAALKRGCKLIVLDPRR
TKVAEMADIWLPLRYGTDAALFLGMINVIINEQLYDKEFVENWCVGFEEL
KERVQEYPLDKVAEITGCDAGEIRKAAVMFATESPASIPWAVSTDMQKNS
CSAIRAQCILRAIVGSFVNGAEILGAPHSDLVPISKIQMHEALPEEKKKL
QLGTETYPFLTYTGMSALEEPSERVYGVKYFHNMGAFMANPTALFTAMAT
EKPYPVKAFFALASNALMGYANQQNALKGLMNQDLVVCYDQFMTPTAQLA
DYVLPGDHWLERPVVQPNWEGIPFGNTSQQVVEPAGEAKDEYYFIRELAV
RMGLEEHFPWKDRLELINYRISPTGMEWEEYQKQYTYMSKLPDYFGPEGV
GVATPSGKVELYSSVFEKLGYDPLPYYHEPLQTEISDPELAKEYPLILFA
GLREDSNFQSCYHQPGILRDAEPDPVALLHPKTAQSLGLPSGEWIWVETT
HGRLKLLLKHDGAQPEGTIRIPHGRWCPEQEGGPETGFSGAMLHNDAMVL
SDDDWNLDPEQGLPNLRGGILAKAYKC
3D structure
PDB2e7z Structure of the non-redox-active tungsten/[4Fe:4S] enzyme acetylene hydratase
ChainA
Resolution1.26 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) K48 T111 I113 W134 C141 I142 V295 S338 K339 I340
Catalytic site (residue number reindexed from 1) K45 T108 I110 W131 C138 I139 V292 S335 K336 I337
Enzyme Commision number 4.2.1.112: acetylene hydratase.
Interaction with ligand
Gene Ontology
Molecular Function
GO:0016491 oxidoreductase activity
GO:0016829 lyase activity
GO:0018818 acetylene hydratase activity
GO:0043546 molybdopterin cofactor binding
GO:0046872 metal ion binding
GO:0051539 4 iron, 4 sulfur cluster binding

View graph for
Molecular Function
External links
PDB RCSB:2e7z, PDBe:2e7z, PDBj:2e7z
PDBsum2e7z
PubMed17360611
UniProtQ71EW5|AHY_SYNAC Acetylene hydratase

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