SitesBLAST
Comparing WP_017367863.1 NCBI__GCF_000691145.1:WP_017367863.1 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)
8rplB Amp-forming acetyl-coa synthetase from chloroflexota bacterium with bound acetyl amp (see paper)
41% identity, 97% coverage: 15:570/574 of query aligns to 53:630/630 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 (= G335), E392 (= E336), P393 (= P337), T416 (= T357), W417 (= W358), W418 (= W359), Q419 (≠ M360), T420 (= T361), D502 (= D442), R517 (= R457), K523 (≠ M463), R528 (= R468)
- binding magnesium ion: V539 (= V479), H541 (= H481)
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)
39% identity, 96% coverage: 23:574/574 of query aligns to 55:631/648 of Q89WV5
- G263 (= G218) mutation to I: Loss of activity.
- G266 (= G221) mutation to I: Great decrease in activity.
- K269 (= K224) mutation to G: Great decrease in activity.
- E414 (= E362) mutation to Q: Great decrease in activity.
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)
38% identity, 94% coverage: 36:574/574 of query aligns to 67:640/651 of P9WQD1
- K617 (= K551) modified: N6-acetyllysine; mutation to R: Complete loss of acetyl-coenzyme A synthetase activity.
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)
38% identity, 97% coverage: 20:574/574 of query aligns to 53:628/652 of P27550
- K609 (= K551) modified: N6-acetyllysine; by autocatalysis
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)
38% identity, 97% coverage: 20:574/574 of query aligns to 53:628/652 of Q8ZKF6
- R194 (vs. gap) 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 (= T262) binding CoA
- N335 (= N286) binding CoA
- A357 (= A305) 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 (= D459) 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 (= S465) binding CoA
- G524 (= G466) 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 (= R468) 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 (≠ K526) 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 (= K551) modified: N6-acetyllysine; by Pat; mutation to A: No acetyl-coenzyme A synthetase activity.
2p20A Acetyl-coa synthetase, r584a mutation (see paper)
37% identity, 97% coverage: 20:574/574 of query aligns to 49:628/641 of 2p20A
- active site: T260 (= T216), T412 (= T361), E413 (= E362), N517 (≠ M463), R522 (= R468), K605 (= K551)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G335), E384 (= E336), P385 (= P337), T408 (= T357), W409 (= W358), W410 (= W359), Q411 (≠ M360), T412 (= T361), D496 (= D442), I508 (≠ F454), R511 (= R457), R522 (= R468)
5jrhA Crystal structure of salmonella enterica acetyl-coa synthetase (acs) in complex with camp and coenzyme a (see paper)
38% identity, 97% coverage: 20:574/574 of query aligns to 49:627/640 of 5jrhA
- active site: T260 (= T216), T412 (= T361), E413 (= E362), N517 (≠ M463), R522 (= R468), K605 (= K551)
- binding (r,r)-2,3-butanediol: W93 (≠ L63), E140 (= E111), G169 (≠ D140), K266 (≠ T222), P267 (= P223)
- binding adenosine-3',5'-cyclic-monophosphate: G383 (= G335), E384 (= E336), P385 (= P337), T408 (= T357), W409 (= W358), W410 (= W359), Q411 (≠ M360), T412 (= T361), D496 (= D442), I508 (≠ F454), N517 (≠ M463), R522 (= R468)
- binding coenzyme a: F159 (= F130), G160 (≠ E131), G161 (≠ A132), R187 (≠ E158), S519 (= S465), R580 (≠ K526), P585 (≠ A531)
- binding magnesium ion: V533 (= V479), H535 (= H481), I538 (= I484)
2p2fA Acetyl-coa synthetase, wild-type with acetate, amp, and coa bound (see paper)
38% identity, 96% coverage: 20:571/574 of query aligns to 48:620/637 of 2p2fA