SitesBLAST
Comparing WP_090216759.1 NCBI__GCF_002796795.1:WP_090216759.1 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)
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)
70% identity, 98% coverage: 9:648/651 of query aligns to 6:642/648 of Q89WV5
- G263 (= G267) mutation to I: Loss of activity.
- G266 (= G270) mutation to I: Great decrease in activity.
- K269 (= K273) mutation to G: Great decrease in activity.
- E414 (= E418) mutation to Q: Great decrease in 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)
63% identity, 96% coverage: 21:648/651 of query aligns to 19:645/652 of P27550
- K609 (= K612) 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)
63% identity, 96% coverage: 21:648/651 of query aligns to 19:645/652 of Q8ZKF6
- R194 (≠ K197) 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 (= T312) binding CoA
- N335 (≠ T336) binding CoA
- A357 (= A358) 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 (= D520) 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 (= S526) binding CoA
- G524 (= G527) 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 (= R529) 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 (= R587) 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 (= K612) 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)
63% identity, 96% coverage: 21:648/651 of query aligns to 15:638/640 of 5jrhA
- active site: T260 (= T265), T412 (= T417), E413 (= E418), N517 (= N524), R522 (= R529), K605 (= K612)
- binding (r,r)-2,3-butanediol: W93 (= W99), E140 (= E147), G169 (≠ A176), K266 (≠ Q271), P267 (= P272)
- binding adenosine-3',5'-cyclic-monophosphate: G383 (= G388), E384 (= E389), P385 (= P390), T408 (= T413), W409 (= W414), W410 (= W415), Q411 (= Q416), T412 (= T417), D496 (= D503), I508 (= I515), N517 (= N524), R522 (= R529)
- binding coenzyme a: F159 (= F166), G160 (≠ A167), G161 (= G168), R187 (= R194), S519 (= S526), R580 (= R587), P585 (= P592)
- binding magnesium ion: V533 (= V540), H535 (= H542), I538 (≠ V545)
2p20A Acetyl-coa synthetase, r584a mutation (see paper)
62% identity, 96% coverage: 21:648/651 of query aligns to 15:639/641 of 2p20A
- active site: T260 (= T265), T412 (= T417), E413 (= E418), N517 (= N524), R522 (= R529), K605 (= K612)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G388), E384 (= E389), P385 (= P390), T408 (= T413), W409 (= W414), W410 (= W415), Q411 (= Q416), T412 (= T417), D496 (= D503), I508 (= I515), R511 (= R518), R522 (= R529)
2p2fA Acetyl-coa synthetase, wild-type with acetate, amp, and coa bound (see paper)
62% identity, 96% coverage: 21:648/651 of query aligns to 14:635/637 of 2p2fA
- active site: T259 (= T265), T411 (= T417), E412 (= E418), N516 (= N524), R521 (= R529), K604 (= K612)
- binding adenosine monophosphate: G382 (= G388), E383 (= E389), P384 (= P390), T407 (= T413), W408 (= W414), W409 (= W415), Q410 (= Q416), T411 (= T417), D495 (= D503), I507 (= I515), R510 (= R518), N516 (= N524), R521 (= R529)
- binding coenzyme a: F158 (= F166), R186 (= R194), W304 (= W310), T306 (= T312), P329 (= P335), A352 (= A358), A355 (= A361), S518 (= S526), R579 (= R587), P584 (= P592)
1pg3A Acetyl coa synthetase, acetylated on lys609 (see paper)
61% identity, 96% coverage: 21:648/651 of query aligns to 15:632/634 of 1pg3A
- active site: T260 (= T265), T412 (= T417), E413 (= E418), N517 (= N524), R522 (= R529), K605 (= K612)
- binding coenzyme a: F159 (= F166), G160 (≠ A167), R187 (= R194), R190 (≠ K197), A301 (= A306), T307 (= T312), P330 (= P335), A356 (= A361), S519 (= S526), R580 (= R587), P585 (= P592)
- binding magnesium ion: V533 (= V540), H535 (= H542), I538 (≠ V545)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G388), E384 (= E389), P385 (= P390), T408 (= T413), W409 (= W414), W410 (= W415), Q411 (= Q416), T412 (= T417), D496 (= D503), R511 (= R518), R522 (= R529)
Q9NR19 Acetyl-coenzyme A synthetase, cytoplasmic; Acetate--CoA ligase; Acetyl-CoA synthetase; ACS; AceCS; Acetyl-CoA synthetase 1; AceCS1; Acyl-CoA synthetase short-chain family member 2; Acyl-activating enzyme; Propionate--CoA ligase; EC 6.2.1.1; EC 6.2.1.17 from Homo sapiens (Human) (see paper)
53% identity, 99% coverage: 8:651/651 of query aligns to 28:699/701 of Q9NR19