SitesBLAST
Comparing WP_011869271.1 NCBI__GCF_000016125.1:WP_011869271.1 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)
5jrhA Crystal structure of salmonella enterica acetyl-coa synthetase (acs) in complex with camp and coenzyme a (see paper)
48% identity, 97% coverage: 11:629/636 of query aligns to 18:637/640 of 5jrhA
- active site: T260 (= T247), T412 (= T399), E413 (= E400), N517 (= N506), R522 (= R511), K605 (= K596)
- binding (r,r)-2,3-butanediol: W93 (≠ C83), E140 (= E129), G169 (≠ D158), K266 (≠ S253), P267 (= P254)
- binding adenosine-3',5'-cyclic-monophosphate: G383 (= G370), E384 (= E371), P385 (= P372), T408 (≠ C395), W409 (≠ Y396), W410 (= W397), Q411 (= Q398), T412 (= T399), D496 (= D485), I508 (≠ V497), N517 (= N506), R522 (= R511)
- binding coenzyme a: F159 (= F148), G160 (≠ S149), G161 (= G150), R187 (= R176), S519 (= S508), R580 (= R571), P585 (= P576)
- binding magnesium ion: V533 (= V522), H535 (≠ N524), I538 (≠ V527)
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)
47% identity, 97% coverage: 11:629/636 of query aligns to 22:644/652 of Q8ZKF6
- R194 (≠ K179) 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 (= T294) binding CoA
- N335 (≠ D318) binding CoA
- A357 (= A340) 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 (= D502) 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 (= S508) binding CoA
- G524 (= G509) 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 (= R511) 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 (= R571) 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 (= K596) modified: N6-acetyllysine; by Pat; mutation to A: No acetyl-coenzyme A synthetase activity.
2p20A Acetyl-coa synthetase, r584a mutation (see paper)
47% identity, 97% coverage: 11:629/636 of query aligns to 18:638/641 of 2p20A
- active site: T260 (= T247), T412 (= T399), E413 (= E400), N517 (= N506), R522 (= R511), K605 (= K596)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G370), E384 (= E371), P385 (= P372), T408 (≠ C395), W409 (≠ Y396), W410 (= W397), Q411 (= Q398), T412 (= T399), D496 (= D485), I508 (≠ V497), R511 (= R500), R522 (= R511)
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)
47% identity, 97% coverage: 11:629/636 of query aligns to 22:644/652 of P27550
- K609 (= K596) modified: N6-acetyllysine; by autocatalysis
2p2fA Acetyl-coa synthetase, wild-type with acetate, amp, and coa bound (see paper)
47% identity, 97% coverage: 11:629/636 of query aligns to 17:634/637 of 2p2fA
- active site: T259 (= T247), T411 (= T399), E412 (= E400), N516 (= N506), R521 (= R511), K604 (= K596)
- binding adenosine monophosphate: G382 (= G370), E383 (= E371), P384 (= P372), T407 (≠ C395), W408 (≠ Y396), W409 (= W397), Q410 (= Q398), T411 (= T399), D495 (= D485), I507 (≠ V497), R510 (= R500), N516 (= N506), R521 (= R511)
- binding coenzyme a: F158 (= F148), R186 (= R176), W304 (= W292), T306 (= T294), P329 (≠ I317), A352 (= A340), A355 (= A343), S518 (= S508), R579 (= R571), P584 (= P576)
1pg3A Acetyl coa synthetase, acetylated on lys609 (see paper)
48% identity, 94% coverage: 11:609/636 of query aligns to 18:618/634 of 1pg3A
- active site: T260 (= T247), T412 (= T399), E413 (= E400), N517 (= N506), R522 (= R511), K605 (= K596)
- binding coenzyme a: F159 (= F148), G160 (≠ S149), R187 (= R176), R190 (≠ K179), A301 (= A288), T307 (= T294), P330 (≠ I317), A356 (= A343), S519 (= S508), R580 (= R571), P585 (= P576)
- binding magnesium ion: V533 (= V522), H535 (≠ N524), I538 (≠ V527)
- binding adenosine-5'-monophosphate-propyl ester: G383 (= G370), E384 (= E371), P385 (= P372), T408 (≠ C395), W409 (≠ Y396), W410 (= W397), Q411 (= Q398), T412 (= T399), D496 (= D485), R511 (= R500), R522 (= R511)
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)
45% identity, 98% coverage: 12:634/636 of query aligns to 22:646/648 of Q89WV5
- G263 (= G249) mutation to I: Loss of activity.
- G266 (= G252) mutation to I: Great decrease in activity.
- K269 (= K255) mutation to G: Great decrease in activity.
- E414 (= E400) 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)
47% identity, 97% coverage: 14:627/636 of query aligns to 26:648/651 of P9WQD1
- K617 (= K596) modified: N6-acetyllysine; mutation to R: Complete loss of acetyl-coenzyme A synthetase activity.
8w0dA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with an isopropyl amp ester inhibitor
45% identity, 97% coverage: 10:626/636 of query aligns to 34:656/666 of 8w0dA
- binding 5'-O-{(R)-hydroxy[(propan-2-yl)oxy]phosphoryl}adenosine: G398 (= G370), E399 (= E371), P400 (= P372), T423 (≠ C395), Y424 (= Y396), W425 (= W397), Q426 (= Q398), T427 (= T399), D513 (= D485), I525 (≠ V497), R528 (= R500), R539 (= R511)
8v4rA Crystal structure of acetyl-coa synthetase 2 in complex with amp and coa from candida albicans (see paper)
45% identity, 97% coverage: 10:626/636 of query aligns to 34:656/666 of 8v4rA
- binding adenosine monophosphate: G398 (= G370), E399 (= E371), P400 (= P372), T423 (≠ C395), Y424 (= Y396), Q426 (= Q398), T427 (= T399), D513 (= D485), I525 (≠ V497), R528 (= R500), R539 (= R511)
- binding coenzyme a: F175 (= F148), R203 (= R176), R206 (≠ K179), G316 (≠ A288), H538 (= H510), R599 (= R571), F605 (≠ I577)
8w0cA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with a cyclopentyl ester amp inhibitor
45% identity, 97% coverage: 10:626/636 of query aligns to 35:657/667 of 8w0cA
- binding 5'-O-[(S)-(cyclopentyloxy)(hydroxy)phosphoryl]adenosine: G399 (= G370), E400 (= E371), P401 (= P372), T424 (≠ C395), Y425 (= Y396), W426 (= W397), Q427 (= Q398), T428 (= T399), D514 (= D485), R529 (= R500), R540 (= R511)
8w0bA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with a cyclopropyl amp ester inhibitor
45% identity, 97% coverage: 10:626/636 of query aligns to 35:657/667 of 8w0bA
- binding 5'-O-[(R)-(cyclopropyloxy)(hydroxy)phosphoryl]adenosine: V398 (= V369), G399 (= G370), E400 (= E371), P401 (= P372), T424 (≠ C395), Y425 (= Y396), W426 (= W397), Q427 (= Q398), T428 (= T399), D514 (= D485), I526 (≠ V497), R529 (= R500), R540 (= R511)
8w0jA Crystal structure of acetyl-coa synthetase 2 from candida albicans in complex with a propyne amp ester inhibitor
45% identity, 97% coverage: 10:626/636 of query aligns to 35:652/662 of 8w0jA
- binding 5'-O-{(S)-hydroxy[(prop-2-yn-1-yl)oxy]phosphoryl}adenosine: G399 (= G370), E400 (= E371), P401 (= P372), T424 (≠ C395), Y425 (= Y396), W426 (= W397), Q427 (= Q398), T428 (= T399), D514 (= D485), I526 (≠ V497), R529 (= R500), R540 (= R511)
8v4pA Crystal structure of acetyl-coa synthetase 2 in complex with adenosine-5'-allylphosphate from candida albicans
45% identity, 97% coverage: 10:626/636 of query aligns to 34:651/660 of 8v4pA
- binding 5'-O-{(S)-hydroxy[(prop-2-en-1-yl)oxy]phosphoryl}adenosine: P152 (= P125), A176 (≠ S149), G177 (= G150), R203 (= R176), T208 (≠ I181), D317 (= D289), E342 (= E314), G343 (= G315), P345 (≠ I317), G398 (= G370), E399 (= E371), P400 (= P372), T423 (≠ C395), W425 (= W397), Q426 (= Q398), T427 (= T399), D513 (= D485), I525 (≠ V497), R528 (= R500), R539 (= R511)
8v4oA Crystal structure of acetyl-coa synthetase 2 in complex with amp from candida albicans
45% identity, 97% coverage: 10:626/636 of query aligns to 34:651/660 of 8v4oA
- binding adenosine monophosphate: G398 (= G370), E399 (= E371), P400 (= P372), T423 (≠ C395), Y424 (= Y396), W425 (= W397), Q426 (= Q398), T427 (= T399), D513 (= D485), I525 (≠ V497), R528 (= R500), R539 (= R511)
8rwjD Cryoem structure of acs1 filament determined by filamentid (see paper)
46% identity, 96% coverage: 10:619/636 of query aligns to 36:663/676 of 8rwjD
- 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: G406 (= G370), P408 (= P372), T431 (≠ C395), Y432 (= Y396), Q434 (= Q398), T435 (= T399), D522 (= D485), R537 (= R500), K638 (= K596)
P78773 Probable acetyl-coenzyme A synthetase; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 from Schizosaccharomyces pombe (strain 972 / ATCC 24843) (Fission yeast) (see paper)
44% identity, 97% coverage: 10:626/636 of query aligns to 32:650/662 of P78773
- T596 (= T573) modified: Phosphothreonine
7kdsA Crystal structure of acetyl-coa synthetase 2 in complex with adenosine-5'-propylphosphate from candida albicans
44% identity, 97% coverage: 10:626/636 of query aligns to 34:646/654 of 7kdsA
- active site: T275 (= T247), T427 (= T399), E428 (= E400), N534 (= N506), R539 (= R511), K620 (= K596)
- binding adenosine-5'-monophosphate-propyl ester: I321 (= I293), G398 (= G370), E399 (= E371), P400 (= P372), D422 (= D394), T423 (≠ C395), Y424 (= Y396), W425 (= W397), Q426 (= Q398), T427 (= T399), D513 (= D485), R528 (= R500), N534 (= N506), R539 (= R511)
8rplB Amp-forming acetyl-coa synthetase from chloroflexota bacterium with bound acetyl amp (see paper)
46% identity, 95% coverage: 10:615/636 of query aligns to 28:630/630 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 (= G370), E392 (= E371), P393 (= P372), T416 (≠ C395), W417 (≠ Y396), W418 (= W397), Q419 (= Q398), T420 (= T399), D502 (= D485), R517 (= R500), K523 (≠ N506), R528 (= R511)
- binding magnesium ion: V539 (= V522), H541 (≠ N524)
P52910 Acetyl-coenzyme A synthetase 2; Acetate--CoA ligase 2; Acyl-activating enzyme 2; EC 6.2.1.1 from Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast) (see paper)
43% identity, 97% coverage: 2:619/636 of query aligns to 28:662/683 of P52910
- K506 (≠ D475) modified: Glycyl lysine isopeptide (Lys-Gly) (interchain with G-Cter in ubiquitin)
Query Sequence
>WP_011869271.1 NCBI__GCF_000016125.1:WP_011869271.1
MKTGDKYILLEKYSEMQQKALEDPEKFWGEQAKCLEWDKTWDNVLEWNPPYAKWFKSGSL
NASYNCVDRHIKGNRRNKAAIICEKEDGSCGILTYYELYREINKFANVLENLGVEKGDVV
TIYMPMMTEAIIAMLACSRIGVIHNVVFSGFSSDALADRINDSKSKILVTTNLLYRRGKE
IELKKILDKALLNCNSIKHVVYVKRGIEEFNLVSGKEYFWDELMGGAKSYVEPVPVESDH
PLFILYTSGTTGSPKGVVHSTGGYLTYATKTMDWTWGLNEMDVFWCTADIGWITGHTYVV
YGPLSLGATIVLYEGAIDYPEPDRLWGIVENHGVTLLYTAPTAIRMLMMYGEKWVNTHDL
STLRLLGSVGEPINPRAWKWYYKVIGKEKCPICDCYWQTETGGHMIYPAIGIQSVPLKPG
SATFPGIGIDVDVVDNEGNPVEANIKGNLIIKRPWPGMLAGLWNNDERYRAAYWDRFKNN
FSTSDYAIKDQDGYIWVLGRSDEVLNVSGHRIGTAELEHELVSNKMVAESAVVGKPDDVK
GEVPVAFVILNERYRELPSNEVKATLIRHIRDTVGPIGTPAMIFFVNKLPKTRSGKIMRR
ILKKLIIGEEIGDVTTLEDNTSLEDVKKELEDFKYD
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