SitesBLAST
Comparing WP_110207905.1 NCBI__GCF_003194585.1:WP_110207905.1 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)
P9WQD1 Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Mycobacterium tuberculosis (strain ATCC 25618 / H37Rv) (see 2 papers)
63% identity, 98% coverage: 7:635/644 of query aligns to 12:648/651 of P9WQD1
- K617 (= K604) modified: N6-acetyllysine; mutation to R: Complete loss of acetyl-coenzyme A synthetase activity.
Q89WV5 Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Bradyrhizobium diazoefficiens (strain JCM 10833 / BCRC 13528 / IAM 13628 / NBRC 14792 / USDA 110) (see paper)
53% identity, 95% coverage: 21:631/644 of query aligns to 24:635/648 of Q89WV5
- G263 (= G259) mutation to I: Loss of activity.
- G266 (= G262) mutation to I: Great decrease in activity.
- K269 (= K265) mutation to G: Great decrease in activity.
- E414 (= E411) mutation to Q: Great decrease in activity.
8rplB Amp-forming acetyl-coa synthetase from chloroflexota bacterium with bound acetyl amp (see paper)
51% identity, 96% coverage: 3:623/644 of query aligns to 3:630/630 of 8rplB
- binding [[(2~{R},3~{S},4~{R},5~{R})-5-(6-aminopurin-9-yl)-3,4-bis(oxidanyl)oxolan-2-yl]methoxy-oxidanyl-phosphoryl] ethanoate: G391 (= G381), E392 (= E382), P393 (= P383), T416 (= T406), W417 (= W407), W418 (= W408), Q419 (= Q409), T420 (= T410), D502 (= D494), R517 (= R509), K523 (≠ N515), R528 (= R520)
- binding magnesium ion: V539 (= V531), H541 (= H533)
P27550 Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Escherichia coli (strain K12) (see paper)
52% identity, 95% coverage: 21:631/644 of query aligns to 25:638/652 of P27550
- K609 (= K604) modified: N6-acetyllysine; by autocatalysis
2p20A Acetyl-coa synthetase, r584a mutation (see paper)
51% identity, 95% coverage: 21:631/644 of query aligns to 21:632/641 of 2p20A
- active site: T260 (= T257), T412 (= T410), E413 (= E411), N517 (= N515), R522 (= R520), K605 (= K604)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G381), E384 (= E382), P385 (= P383), T408 (= T406), W409 (= W407), W410 (= W408), Q411 (= Q409), T412 (= T410), D496 (= D494), I508 (≠ V506), R511 (= R509), R522 (= R520)
Q8ZKF6 Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Salmonella typhimurium (strain LT2 / SGSC1412 / ATCC 700720) (see 4 papers)
51% identity, 95% coverage: 21:631/644 of query aligns to 25:638/652 of Q8ZKF6
- R194 (≠ A188) mutation to A: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 2-fold increase in the affinity for ATP and 3-fold reduction for CoA.; mutation to E: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 2-fold increase in the affinity for ATP and 2-fold reduction for CoA.
- T311 (= T305) binding CoA
- N335 (≠ D329) binding CoA
- A357 (= A351) mutation to V: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 3-fold increase in the affinity for ATP and 3-fold reduction for CoA.
- D517 (= D511) mutation to G: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 2-fold increase in the affinity for ATP and 10-fold reduction for CoA.; mutation to P: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 3-fold reduction in the affinity for ATP and 4.5-fold reduction for CoA.
- S523 (= S517) binding CoA
- G524 (= G518) mutation to L: No acetyl-coenzyme A synthetase activity.; mutation to S: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. Almost the same affinity as the wild-type for ATP, but 9-fold reduction in the affinity for CoA.
- R526 (= R520) mutation to A: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 3-fold increase in the affinity for ATP and 4-fold reduction for CoA.
- R584 (≠ A579) binding CoA; mutation to A: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 2-fold increase in the affinity for ATP and 7-fold reduction for CoA.; mutation to E: Results in a 2-fold reduction in the catalytic efficiency for both ATP and CoA. 3-fold increase in the affinity for ATP and 8-fold reduction for CoA.
- K609 (= K604) modified: N6-acetyllysine; by Pat; mutation to A: No acetyl-coenzyme A synthetase activity.
5jrhA Crystal structure of salmonella enterica acetyl-coa synthetase (acs) in complex with camp and coenzyme a (see paper)
51% identity, 95% coverage: 21:631/644 of query aligns to 21:631/640 of 5jrhA
- active site: T260 (= T257), T412 (= T410), E413 (= E411), N517 (= N515), R522 (= R520), K605 (= K604)
- binding (r,r)-2,3-butanediol: W93 (= W91), E140 (= E138), G169 (≠ S167), K266 (= K263), P267 (= P264)
- binding adenosine-3',5'-cyclic-monophosphate: G383 (= G381), E384 (= E382), P385 (= P383), T408 (= T406), W409 (= W407), W410 (= W408), Q411 (= Q409), T412 (= T410), D496 (= D494), I508 (≠ V506), N517 (= N515), R522 (= R520)
- binding coenzyme a: F159 (= F157), G160 (= G158), G161 (= G159), R187 (= R185), S519 (= S517), R580 (≠ A579), P585 (≠ A584)
- binding magnesium ion: V533 (= V531), H535 (= H533), I538 (≠ V536)
2p2fA Acetyl-coa synthetase, wild-type with acetate, amp, and coa bound (see paper)
51% identity, 95% coverage: 21:631/644 of query aligns to 20:628/637 of 2p2fA