SitesBLAST
Comparing WP_068748960.1 NCBI__GCF_001601575.1:WP_068748960.1 to proteins with known functional sites using BLASTp with E ≤ 0.001.
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Found 20 (the maximum) hits to proteins with known functional sites (download)
8a5eA Cryo-em structure of the electron bifurcating fe-fe hydrogenase hydabc complex from acetobacterium woodii in the reduced state (see paper)
59% identity, 99% coverage: 1:577/582 of query aligns to 1:580/583 of 8a5eA
- binding fe2/s2 (inorganic) cluster: T34 (= T34), C36 (= C36), G45 (= G45), C47 (= C47), C50 (= C50), C64 (= C64)
- binding 2 iron/2 sulfur/5 carbonyl/2 water inorganic cluster: C300 (= C300), P325 (= P325), M354 (= M354), C356 (= C356), K359 (= K359), C506 (= C504)
- binding iron/sulfur cluster: H96 (= H96), N97 (= N97), C100 (= C100), C103 (= C103), S106 (≠ N106), C109 (= C109), C148 (= C148), C151 (= C151), K152 (≠ R152), C154 (= C154), C158 (= C158), V166 (= V166), C191 (= C191), C194 (= C194), G195 (= G195), C197 (= C197), C201 (= C201), P202 (= P202), V203 (= V203), S301 (= S301), C356 (= C356), C502 (= C500), C506 (= C504)
8a6tA Cryo-em structure of the electron bifurcating fe-fe hydrogenase hydabc complex from thermoanaerobacter kivui in the reduced state (see paper)
55% identity, 99% coverage: 1:576/582 of query aligns to 1:567/571 of 8a6tA
- binding fe2/s2 (inorganic) cluster: C36 (= C36), D37 (≠ F37), C47 (= C47), R48 (= R48), C50 (= C50), C63 (= C64)
- binding 2 iron/2 sulfur/5 carbonyl/2 water inorganic cluster: A229 (= A231), P230 (= P232), A231 (= A233), C298 (= C300), P323 (= P325), M352 (= M354), P353 (= P355), K357 (= K359), F412 (= F418), C500 (= C504)
- binding iron/sulfur cluster: H95 (= H96), C99 (= C100), C102 (= C103), C108 (= C109), C146 (= C148), C149 (= C151), G150 (≠ R152), K151 (≠ R153), C152 (= C154), C156 (= C158), C189 (= C191), C192 (= C194), C195 (= C197), C199 (= C201), G202 (= G204), C299 (≠ S301), C354 (= C356), C496 (= C500), C500 (= C504)
4xdcA Active semisynthetic [fefe]-hydrogenase cpi with aza-dithiolato- bridged [2fe] cofactor (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/581 of 4xdcA
- active site: E279 (= E280), E282 (= E283), C299 (= C300), S319 (= S320), K358 (= K359), E361 (= E362), Q366 (≠ E367), C503 (= C504)
- binding dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+): A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding magnesium ion: N40 (= N42), D42 (≠ E43)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R104 (≠ N106), C107 (= C109), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), Q195 (= Q196), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A203 (≠ G204), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504)
8aj6A Cyanide-bound [fefe]-hydrogenase i from clostridium pasteurianum (cpi) (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/580 of 8aj6A
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding magnesium ion: N40 (= N42), D42 (≠ E43)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R104 (≠ N106), C107 (= C109), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), A498 (≠ C499), C499 (= C500), C503 (= C504)
- binding Binuclear [FeFe], di(thiomethyl)amine, carbon monoxide, cyanide cluster (-CN form): A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
5oefA Active semisynthetic [fefe]-hydrogenase cpi with aza-diselenato- bridged [2fe] cofactor (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/574 of 5oefA
- active site: E279 (= E280), E282 (= E283), C299 (= C300), S319 (= S320), K358 (= K359), E361 (= E362), Q366 (≠ E367), C503 (= C504)
- binding dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethaneselenato- 1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+): A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding fe2/s2 (inorganic) cluster: C34 (= C36), F35 (= F37), K45 (≠ A46), C46 (= C47), C49 (= C50), C62 (= C64)
- binding magnesium ion: N40 (= N42), D42 (≠ E43)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R103 (= R105), R104 (≠ N106), C107 (= C109), L110 (≠ Q112), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504)
3c8yA 1.39 angstrom crystal structure of fe-only hydrogenase (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/574 of 3c8yA
- active site: E279 (= E280), E282 (= E283), C299 (= C300), S319 (= S320), K358 (= K359), E361 (= E362), Q366 (≠ E367), C503 (= C504)
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), K45 (≠ A46), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding 2 iron/2 sulfur/3 carbonyl/2 cyanide/water/methylether cluster: A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R104 (≠ N106), C107 (= C109), L110 (≠ Q112), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), Q195 (= Q196), C196 (= C197), C200 (= C201), P201 (= P202), A203 (≠ G204), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504)
1c4cA Binding of exogenously added carbon monoxide at the active site of the fe-only hydrogenase (cpi) from clostridium pasteurianum (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/574 of 1c4cA
- active site: E279 (= E280), E282 (= E283), C299 (= C300), S319 (= S320), K358 (= K359), E361 (= E362), Q366 (≠ E367), C503 (= C504)
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), K45 (≠ A46), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding 2 iron/2 sulfur/6 carbonyl/1 water inorganic cluster: A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R104 (≠ N106), C107 (= C109), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), C153 (= C154), C157 (= C158), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A203 (≠ G204), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504), G506 (= G507)
1c4aA Binding of exogenously added carbon monoxide at the active site of the fe-only hydrogenase (cpi) from clostridium pasteurianum (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/574 of 1c4aA
- active site: E279 (= E280), E282 (= E283), C299 (= C300), S319 (= S320), K358 (= K359), E361 (= E362), Q366 (≠ E367), C503 (= C504)
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), K45 (≠ A46), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding 2 iron/2 sulfur/5 carbonyl/2 water inorganic cluster: A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding iron/sulfur cluster: H94 (= H96), K97 (≠ E99), C98 (= C100), C101 (= C103), R104 (≠ N106), C107 (= C109), L140 (≠ I141), K146 (= K147), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A203 (≠ G204), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504), G506 (= G507)
P29166 Iron hydrogenase 1; CpI; Fe-only hydrogenase; [Fe] hydrogenase; EC 1.12.7.2 from Clostridium pasteurianum (see 2 papers)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/574 of P29166
- C34 (= C36) binding [2Fe-2S] cluster
- C46 (= C47) binding [2Fe-2S] cluster
- C49 (= C50) binding [2Fe-2S] cluster
- C62 (= C64) binding [2Fe-2S] cluster
- H94 (= H96) binding [4Fe-4S] cluster
- C98 (= C100) binding [4Fe-4S] cluster
- C101 (= C103) binding [4Fe-4S] cluster
- C107 (= C109) binding [4Fe-4S] cluster
- C147 (= C148) binding [4Fe-4S] cluster
- C150 (= C151) binding [4Fe-4S] cluster
- C153 (= C154) binding [4Fe-4S] cluster
- C157 (= C158) binding [4Fe-4S] cluster
- C190 (= C191) binding [4Fe-4S] cluster
- C193 (= C194) binding [4Fe-4S] cluster
- C196 (= C197) binding [4Fe-4S] cluster
- C200 (= C201) binding [4Fe-4S] cluster
- C300 (≠ S301) binding [4Fe-4S] cluster
- C355 (= C356) binding [4Fe-4S] cluster
- C499 (= C500) binding [4Fe-4S] cluster
- C503 (= C504) binding [4Fe-4S] cluster; binding Fe(2+)
4xddA Apo [fefe]-hydrogenase cpi (see paper)
45% identity, 98% coverage: 3:575/582 of query aligns to 1:574/582 of 4xddA
- active site: E279 (= E280), E282 (= E283), C299 (= C300), S319 (= S320), K358 (= K359), E361 (= E362), Q366 (≠ E367), C503 (= C504)
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding magnesium ion: N40 (= N42), D42 (≠ E43)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R104 (≠ N106), C107 (= C109), L110 (≠ Q112), K146 (= K147), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), Q195 (= Q196), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504)
6h63A Semisynthetic [fefe]-hydrogenase cpi with ethanedithiolate [2fe] cofactor
45% identity, 98% coverage: 5:575/582 of query aligns to 2:573/578 of 6h63A
- active site: E278 (= E280), E281 (= E283), C298 (= C300), S318 (= S320), K357 (= K359), E360 (= E362), Q365 (≠ E367), C502 (= C504)
- binding fe2/s2 (inorganic) cluster: C33 (= C36), F34 (= F37), C45 (= C47), E46 (≠ R48), C48 (= C50), C61 (= C64)
- binding dicarbonyl[bis(cyanide-kappaC)]-mu-(ethanethiolatato-1kappaS:2kappaS)-mu-(ox omethylidene)diiron(2+): A229 (= A231), P230 (= P232), S231 (≠ A233), C298 (= C300), P323 (= P325), Q324 (= Q326), M352 (= M354), P353 (= P355), K357 (= K359), F416 (= F418), M496 (= M498), C502 (= C504)
- binding magnesium ion: N39 (= N42), D41 (≠ E43)
- binding iron/sulfur cluster: H93 (= H96), F95 (≠ L98), K96 (≠ E99), C97 (= C100), C100 (= C103), R102 (= R105), C106 (= C109), C146 (= C148), L147 (≠ I149), L148 (= L150), C149 (= C151), G150 (≠ R152), C152 (= C154), C156 (= C158), T160 (≠ Q162), A164 (≠ V166), M165 (≠ I167), I176 (≠ V178), C189 (= C191), L190 (≠ V192), L191 (≠ N193), C192 (= C194), G193 (= G195), C195 (= C197), C199 (= C201), P200 (= P202), V201 (= V203), A203 (= A205), L204 (= L206), C299 (≠ S301), C354 (= C356), A497 (≠ C499), C498 (= C500), C502 (= C504)
5byqA Semisynthetic [fefe]-hydrogenase cpi with oxodithiolato-bridged [2fe] cofactor (see paper)
45% identity, 98% coverage: 5:575/582 of query aligns to 2:573/580 of 5byqA
- active site: E278 (= E280), E281 (= E283), C298 (= C300), S318 (= S320), K357 (= K359), E360 (= E362), Q365 (≠ E367), C502 (= C504)
- binding bis(cyanido-kappaC)(dicarbonyl)-mu-(oxomethylidene)-mu-(oxydimethanethiolate-1kappaS:2kappaS)diiron(2+): A229 (= A231), P230 (= P232), S231 (≠ A233), C298 (= C300), P323 (= P325), Q324 (= Q326), M352 (= M354), P353 (= P355), K357 (= K359), F416 (= F418), M496 (= M498), C502 (= C504)
- binding fe2/s2 (inorganic) cluster: A31 (≠ T34), C33 (= C36), F34 (= F37), C45 (= C47), E46 (≠ R48), C48 (= C50), C61 (= C64)
- binding magnesium ion: N39 (= N42), D41 (≠ E43)
- binding iron/sulfur cluster: H93 (= H96), F95 (≠ L98), K96 (≠ E99), C97 (= C100), C100 (= C103), R103 (≠ N106), C106 (= C109), K145 (= K147), C146 (= C148), L147 (≠ I149), L148 (= L150), C149 (= C151), G150 (≠ R152), C152 (= C154), C156 (= C158), T160 (≠ Q162), A164 (≠ V166), M165 (≠ I167), I176 (≠ V178), C189 (= C191), L190 (≠ V192), L191 (≠ N193), C192 (= C194), G193 (= G195), Q194 (= Q196), C195 (= C197), C199 (= C201), P200 (= P202), V201 (= V203), A203 (= A205), L204 (= L206), C299 (≠ S301), C354 (= C356), M496 (= M498), A497 (≠ C499), C498 (= C500), C502 (= C504)
5bysA Semisynthetic [fefe]-hydrogenase cpi with sulfur-dithiolato-bridged [2fe] cofactor (see paper)
45% identity, 98% coverage: 5:575/582 of query aligns to 2:573/576 of 5bysA
- active site: E278 (= E280), E281 (= E283), C298 (= C300), S318 (= S320), K357 (= K359), E360 (= E362), Q365 (≠ E367), C502 (= C504)
- binding bis(cyanido-kappaC)(dicarbonyl)-mu-(oxomethylidene)-mu-(sulfanediyldimethanethiolatato-1kappaS:2kappaS)diiron(2+): A229 (= A231), P230 (= P232), S231 (≠ A233), I267 (≠ T269), C298 (= C300), P323 (= P325), Q324 (= Q326), M352 (= M354), P353 (= P355), K357 (= K359), F416 (= F418), V422 (= V424), M496 (= M498), C502 (= C504)
- binding fe2/s2 (inorganic) cluster: A31 (≠ T34), C33 (= C36), F34 (= F37), C45 (= C47), E46 (≠ R48), C48 (= C50), C61 (= C64)
- binding magnesium ion: N39 (= N42), D41 (≠ E43)
- binding iron/sulfur cluster: H93 (= H96), F95 (≠ L98), K96 (≠ E99), C97 (= C100), C100 (= C103), C106 (= C109), K145 (= K147), C146 (= C148), L147 (≠ I149), L148 (= L150), C149 (= C151), G150 (≠ R152), C152 (= C154), C156 (= C158), T160 (≠ Q162), A164 (≠ V166), M165 (≠ I167), I176 (≠ V178), C189 (= C191), L190 (≠ V192), L191 (≠ N193), C192 (= C194), G193 (= G195), C195 (= C197), C199 (= C201), P200 (= P202), V201 (= V203), A202 (≠ G204), A203 (= A205), L204 (= L206), C299 (≠ S301), C354 (= C356), M496 (= M498), A497 (≠ C499), C498 (= C500), C502 (= C504)
8aioA Co-bound [fefe]-hydrogenase i from clostridium pasteurianum (cpi) (see paper)
45% identity, 98% coverage: 3:573/582 of query aligns to 1:572/573 of 8aioA
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding magnesium ion: N40 (= N42), D42 (≠ E43)
- binding Binuclear [FeFe], di(thiomethyl)amine, carbon monoxide, cyanide cluster (-CO form): A230 (= A231), P231 (= P232), S232 (≠ A233), C299 (= C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), C107 (= C109), K146 (= K147), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), C499 (= C500), C503 (= C504)
5byrA Semisynthetic [fefe]-hydrogenase cpi with propane-dithiolato-bridged [2fe] cofactor (see paper)
45% identity, 98% coverage: 5:573/582 of query aligns to 2:571/571 of 5byrA
- active site: E278 (= E280), E281 (= E283), C298 (= C300), S318 (= S320), K357 (= K359), E360 (= E362), Q365 (≠ E367), C502 (= C504)
- binding bis(cyanido-kappaC)(dicarbonyl)-mu-(oxomethylidene)[mu-propane-1,3-bis(thiolate)-1kappa~2~S~1~,S~3~:2kappa~2~S~1~,S~3~]diiron(2+): A229 (= A231), P230 (= P232), S231 (≠ A233), I267 (≠ T269), C298 (= C300), P323 (= P325), Q324 (= Q326), M352 (= M354), P353 (= P355), K357 (= K359), F416 (= F418), M496 (= M498), C502 (= C504)
- binding fe2/s2 (inorganic) cluster: A31 (≠ T34), C33 (= C36), F34 (= F37), C45 (= C47), E46 (≠ R48), C48 (= C50), C61 (= C64)
- binding magnesium ion: N39 (= N42), D41 (≠ E43), E281 (= E283), H564 (= H566), H568 (= H570)
- binding iron/sulfur cluster: H93 (= H96), F95 (≠ L98), K96 (≠ E99), C97 (= C100), C100 (= C103), R103 (≠ N106), C106 (= C109), C146 (= C148), L147 (≠ I149), L148 (= L150), C149 (= C151), G150 (≠ R152), C152 (= C154), C156 (= C158), A164 (≠ V166), M165 (≠ I167), I176 (≠ V178), C189 (= C191), L190 (≠ V192), L191 (≠ N193), C192 (= C194), G193 (= G195), Q194 (= Q196), C195 (= C197), C199 (= C201), P200 (= P202), V201 (= V203), A202 (≠ G204), A203 (= A205), L204 (= L206), C299 (≠ S301), C354 (= C356), M496 (= M498), A497 (≠ C499), C498 (= C500), C502 (= C504)
8pvmA Formaldehyde-inhibited [fefe]-hydrogenase cpi from clostridium pasteurianum, variant c299d (see paper)
45% identity, 98% coverage: 3:573/582 of query aligns to 1:572/573 of 8pvmA
- binding dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+): A230 (= A231), P231 (= P232), S232 (≠ A233), D299 (≠ C300), P324 (= P325), Q325 (= Q326), M353 (= M354), P354 (= P355), K358 (= K359), F417 (= F418), M497 (= M498), C503 (= C504)
- binding methyl radical: N38 (≠ G40), C39 (≠ I41), K159 (= K160)
- binding fe2/s2 (inorganic) cluster: A32 (≠ T34), C34 (= C36), F35 (= F37), K45 (≠ A46), C46 (= C47), E47 (≠ R48), C49 (= C50), C62 (= C64)
- binding magnesium ion: N40 (= N42), D42 (≠ E43)
- binding iron/sulfur cluster: H94 (= H96), F96 (≠ L98), K97 (≠ E99), C98 (= C100), C101 (= C103), R103 (= R105), R104 (≠ N106), C107 (= C109), K146 (= K147), C147 (= C148), L148 (≠ I149), L149 (= L150), C150 (= C151), G151 (≠ R152), C153 (= C154), C157 (= C158), T161 (≠ Q162), A165 (≠ V166), M166 (≠ I167), I177 (≠ V178), C190 (= C191), L191 (≠ V192), L192 (≠ N193), C193 (= C194), G194 (= G195), C196 (= C197), C200 (= C201), P201 (= P202), V202 (= V203), A204 (= A205), L205 (= L206), C300 (≠ S301), C355 (= C356), M497 (= M498), A498 (≠ C499), C499 (= C500), C503 (= C504)
7p8na Tmhydabc- t. Maritima hydrogenase with bridge closed (see paper)
44% identity, 99% coverage: 6:581/582 of query aligns to 3:556/642 of 7p8na
- binding fe2/s2 (inorganic) cluster: N32 (≠ T34), C34 (= C36), Y42 (≠ I44), G43 (= G45), C45 (= C47), R46 (= R48), C48 (= C50), C60 (= C64)
- binding iron/sulfur cluster: H92 (= H96), D95 (≠ E99), C96 (= C100), C99 (= C103), C105 (= C109), Q108 (= Q112), C143 (= C148), I144 (= I149), L145 (= L150), C146 (= C151), G147 (≠ R152), D148 (≠ R153), C149 (= C154), C153 (= C158), V161 (= V166), C186 (= C191), V187 (= V192), L188 (≠ N193), C189 (= C194), G190 (= G195), C192 (= C197), C196 (= C201), P197 (= P202), T198 (≠ V203), A200 (= A205), L201 (= L206), C295 (≠ S301), C350 (= C356), M480 (= M498), A481 (≠ C499), C482 (= C500), C486 (= C504)
Sites not aligning to the query:
7qv7D Cryo-em structure of hydrogen-dependent co2 reductase. (see paper)
48% identity, 74% coverage: 144:576/582 of query aligns to 6:447/448 of 7qv7D
- binding dicarbonyl[bis(cyanide-kappaC)]-mu-(iminodimethanethiolatato-1kappaS:2kappaS)-mu-(oxomethylidene)diiron(2+): T147 (= T269), C178 (= C300), Q204 (= Q326), M232 (= M354), K237 (= K359), C382 (= C504)
- binding iron/sulfur cluster: C10 (= C148), T11 (≠ I149), G12 (≠ L150), C13 (= C151), R14 (= R152), C16 (= C154), C20 (= C158), P21 (≠ K160), A24 (≠ G163), I35 (≠ F174), C40 (= C191), V41 (= V192), C43 (= C194), G44 (= G195), C46 (= C197), C50 (= C201), C179 (≠ S301), C234 (= C356), C236 (≠ A358), K237 (= K359), C378 (= C500), G381 (= G503), C382 (= C504)
8ru6B Desulfovibrio desulfuricans [fefe]-hydrogenase variant with both subunits linked by a 4 amino acid linker peptide derived from cpi of clostridium pasteurianum
48% identity, 78% coverage: 120:573/582 of query aligns to 4:448/484 of 8ru6B
- binding Binuclear [FeFe], di(thiomethyl)amine, carbon monoxide, cyanide cluster (-CO form): A105 (= A231), P106 (= P232), A107 (= A233), C176 (= C300), P201 (= P325), I202 (≠ Q326), M230 (= M354), P231 (= P355), K235 (= K359), F294 (= F418), M374 (= M498), C380 (= C504)
- binding iron/sulfur cluster: C33 (= C148), I34 (= I149), G35 (≠ L150), C36 (= C151), D37 (≠ R152), C39 (= C154), C43 (= C158), P44 (= P169), I48 (≠ G173), H56 (≠ K184), I58 (≠ L186), C64 (= C191), I65 (≠ V192), N66 (= N193), C67 (= C194), G68 (= G195), C70 (= C197), C74 (= C201), E76 (≠ V203), I79 (≠ L206), C177 (≠ S301), C232 (= C356), M374 (= M498), A375 (≠ C499), C376 (= C500), C380 (= C504)
6gl6A Apo [fefe]-hydrogenase hyda1 from chlamydomonas reinhardtii, variant c377h (see paper)
46% identity, 63% coverage: 207:573/582 of query aligns to 13:401/406 of 6gl6A
- active site: E77 (= E280), E80 (= E283), C100 (= C300), S120 (= S320), K159 (= K359), E162 (= E362), W167 (vs. gap), C337 (= C504)
- binding iron/sulfur cluster: C101 (≠ S301), C156 (= C356), R158 (≠ A358), M331 (= M498), H333 (≠ C500), C337 (= C504)
- binding sulfite ion: C156 (= C356), T157 (= T357), R158 (≠ A358), H333 (≠ C500), G341 (= G508)
Query Sequence
>WP_068748960.1 NCBI__GCF_001601575.1:WP_068748960.1
MEMVTLTIDGQKVQVPKGTTVLEAARKLGIKIPTLCFLKGINEIGACRMCVVEVKGARNL
QASCVYPVSEGMEVLTNTPRVRESRKTTLELLLSDHNLECPTCVRNLNCELQKLSEELGI
KSIRYQGEKHKPKYDDFSPSIVRDTSKCILCRRCVSACHKIQGVGVISPNHRGFNTMVAP
VFDKSLSEVACVNCGQCILVCPVGALKEKDDTDRVWQALADPEKHVIVQIAPAVRVSLGE
EFGLGRGAIVTKKIPAALRRMGFDRVFDTDFTADLTIMEEGNEFLERLNHGGKLPLITSC
SPGWIKFCEHYYPEFLENLSTCKSPQQMFGAVAKTYYAEKMGIDPSKIFVVSVMPCTAKK
YEAQRPEMRASGYQDVDVVLTTREIARMLKEAGIDLALMPDEEFDEPLGISTGAGAIFGA
TGGVMEAALRTVYEVVTGKELERIDFTEVRGVEGIKEATIEIDGLKVNVAVAHGLSNAKK
VLDRVKNGEANYHFIEIMCCPGGCVGGGGQPILNADERMELDYREVRGNAIYEVDRNMPL
RKSHENPVVQQLYKEFLGHPLSEKSHELLHTHYTKRPLYPES
Or try a new SitesBLAST search
SitesBLAST's Database
SitesBLAST's database includes
(1) SwissProt
entries with experimentally-supported functional features;
and (2) protein structures with bound ligands, from the
BioLip database.
by Morgan Price,
Arkin group
Lawrence Berkeley National Laboratory