SitesBLAST
Comparing WP_044198804.1 NCBI__GCF_000566685.1:WP_044198804.1 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)
4wd1A Acetoacetyl-coa synthetase from streptomyces lividans (see paper)
45% identity, 98% coverage: 10:646/649 of query aligns to 4:636/646 of 4wd1A
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)
27% identity, 93% coverage: 41:642/649 of query aligns to 24:635/652 of Q8ZKF6
- R194 (≠ K208) 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 (≠ M321) binding CoA
- N335 (≠ M343) binding CoA
- A357 (≠ G365) 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 (= D523) 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 (≠ G529) binding CoA
- G524 (= G530) 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 (= R532) 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 (= R590) 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 (= K615) modified: N6-acetyllysine; by Pat; mutation to A: No acetyl-coenzyme A synthetase activity.
2p2fA Acetyl-coa synthetase, wild-type with acetate, amp, and coa bound (see paper)
28% identity, 92% coverage: 41:635/649 of query aligns to 19:624/637 of 2p2fA
- active site: T259 (≠ S274), T411 (≠ S417), E412 (≠ L418), N516 (= N527), R521 (= R532), K604 (= K615)
- binding adenosine monophosphate: G382 (= G394), E383 (≠ S395), P384 (= P396), T407 (≠ V413), W408 (= W414), W409 (≠ L415), Q410 (≠ I416), T411 (≠ S417), D495 (= D506), I507 (= I518), R510 (= R521), N516 (= N527), R521 (= R532)
- binding coenzyme a: F158 (≠ S177), R186 (≠ Y205), W304 (= W319), T306 (≠ M321), P329 (= P342), A352 (≠ G365), A355 (≠ Y368), S518 (≠ G529), R579 (= R590), P584 (= P595)
5jrhA Crystal structure of salmonella enterica acetyl-coa synthetase (acs) in complex with camp and coenzyme a (see paper)
28% identity, 91% coverage: 41:633/649 of query aligns to 20:623/640 of 5jrhA
- active site: T260 (≠ S274), T412 (≠ S417), E413 (≠ L418), N517 (= N527), R522 (= R532), K605 (= K615)
- binding (r,r)-2,3-butanediol: W93 (≠ F112), E140 (= E158), G169 (≠ D187), K266 (= K280), P267 (= P281)
- binding adenosine-3',5'-cyclic-monophosphate: G383 (= G394), E384 (≠ S395), P385 (= P396), T408 (≠ V413), W409 (= W414), W410 (≠ L415), Q411 (≠ I416), T412 (≠ S417), D496 (= D506), I508 (= I518), N517 (= N527), R522 (= R532)
- binding coenzyme a: F159 (≠ S177), G160 (≠ P178), G161 (≠ D179), R187 (≠ Y205), S519 (≠ G529), R580 (= R590), P585 (= P595)
- binding magnesium ion: V533 (≠ E543), H535 (≠ L545), I538 (≠ V548)
2p20A Acetyl-coa synthetase, r584a mutation (see paper)
27% identity, 93% coverage: 41:642/649 of query aligns to 20:629/641 of 2p20A
- active site: T260 (≠ S274), T412 (≠ S417), E413 (≠ L418), N517 (= N527), R522 (= R532), K605 (= K615)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G394), E384 (≠ S395), P385 (= P396), T408 (≠ V413), W409 (= W414), W410 (≠ L415), Q411 (≠ I416), T412 (≠ S417), D496 (= D506), I508 (= I518), R511 (= R521), R522 (= R532)
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)
27% identity, 93% coverage: 39:642/649 of query aligns to 22:635/652 of P27550
- K609 (= K615) modified: N6-acetyllysine; by autocatalysis
1pg3A Acetyl coa synthetase, acetylated on lys609 (see paper)
27% identity, 92% coverage: 41:636/649 of query aligns to 20:628/634 of 1pg3A
- active site: T260 (≠ S274), T412 (≠ S417), E413 (≠ L418), N517 (= N527), R522 (= R532), K605 (= K615)
- binding coenzyme a: F159 (≠ S177), G160 (≠ P178), R187 (≠ Y205), R190 (≠ K208), A301 (≠ S315), T307 (≠ M321), P330 (= P342), A356 (≠ Y368), S519 (≠ G529), R580 (= R590), P585 (= P595)
- binding magnesium ion: V533 (≠ E543), H535 (≠ L545), I538 (≠ V548)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G394), E384 (≠ S395), P385 (= P396), T408 (≠ V413), W409 (= W414), W410 (≠ L415), Q411 (≠ I416), T412 (≠ S417), D496 (= D506), R511 (= R521), R522 (= R532)
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)
28% identity, 94% coverage: 41:649/649 of query aligns to 23:639/648 of Q89WV5