Align Acetyl-coenzyme A synthetase; AcCoA synthetase; Acs; Acetate--CoA ligase; Acyl-activating enzyme; EC 6.2.1.1 (characterized)
to candidate WP_084058613.1 B9A12_RS13385 acyl-CoA synthetase
Query= SwissProt::P39062 (572 letters) >NCBI__GCF_900176285.1:WP_084058613.1 Length = 546 Score = 249 bits (636), Expect = 2e-70 Identities = 170/526 (32%), Positives = 277/526 (52%), Gaps = 20/526 (3%) Query: 41 KLNAAYEAIDRHAESFRKNKVALYYKDAKRDEKYTFKEMKEESNRAGNVLRRYGNVEKGD 100 +LN A +DRH R + A+ + D + +TF ++++ N+ GN L+ G VE D Sbjct: 30 ELNLADYLLDRHVREGRGDNPAVKFMD----KVFTFAQIQQMVNKFGNALKEAG-VEPQD 84 Query: 101 RVFIFMPRSPELYFIMLGAIKIGAIAGPLFEAFMEGAVKDRLENSEAKVVVTTPELLERI 160 RV I + SP+ + KIGAI P + + V + N+E K LL + Sbjct: 85 RVGIRLVNSPQALVTIFAIEKIGAIPVPTSPLWSKEEVAFVVNNAEMKYFAVNAPLLPPV 144 Query: 161 PVDKLPHLQH---VFVVGG---EAESGTNIINYDEAAKQESTRLDIEWMDKKDGFLLHYT 214 K P ++ V V+GG E ++ N++ ++E ++ S LD + D ++ YT Sbjct: 145 EEAK-PDFEYGTRVIVIGGNPDEVKAQGNLV-FEEMLEKGSPDLDAVMLKADDIGVILYT 202 Query: 215 SGSTGTPKGVLH-VHEAMIQQYQTGKWVLDLKEEDIYWCTADPGWVTGTVYGIFAPWLNG 273 SG+TG PKG +H V +I+ K+V +L D+ A + G P+ G Sbjct: 203 SGTTGMPKGCVHFVRPIIIEARLVNKYVYNLGPGDVLGGAAPVSFAAGFGTFTLIPFEGG 262 Query: 274 ATNVIVGGRFSPESWYGTIEQLGVNVWYSAPTAFRMLMGAGDEMAAKYDLTSLRHVLSVG 333 + ++ +F+P I++ + V PTA+R LM D KYD +S+R S G Sbjct: 263 SAISLIP-KFAPADMMDLIQKHKITVLTGLPTAYRALMKFPD--FKKYDFSSVRLCTSGG 319 Query: 334 EPLNPEVIRWGHKVFNKRIHDTWWMTETGSQLICNYPCMDIKPGSMGKPIPGVEAAIVDN 393 + L E + ++ + I + TE L N + P S+GK +PGV+ +VD Sbjct: 320 DALGAETLEAWTQLTGQPIWEGLGGTEMLHLLTSNTMNPEPVPNSIGKALPGVQIRVVDP 379 Query: 394 QGNELPPYRMGNLAIKKGWPSMMHTIWNNPE---KYESYFMPGGWYVSGDSAYMDEEGYF 450 + N+ P +G++ IK ++ + + E K + + GW GD+ YM+E+G Sbjct: 380 EWNDCKPNEVGSMIIKGPSGTLYWKPYVDDERLLKSQQKGVKNGWNQMGDAVYMNEDGNL 439 Query: 451 WFQGRVDDVIMTSGERVGPFEVESKLVEHPAIAEAGVIGKPDPVRGEIIKAFIALREGFE 510 +F R DD+I +SG R+GP EVE +++HPA+A+AGV+G PDP +G++ KAF+ L+ G E Sbjct: 440 FFVSREDDMIKSSGYRIGPAEVEEAILKHPAVADAGVVGVPDPEKGQVTKAFVVLKPGHE 499 Query: 511 PSDKLKEEIRLFVKQGLAAHAAPREIEFKDKLPKTRSGKIMRRVLK 556 SD+ EE++ F+KQ +A + PR IE+ D LP+T +GK++RR L+ Sbjct: 500 GSDEFFEELKEFLKQHIAVYKLPRLIEYVDALPRTPTGKLLRRKLR 545 Lambda K H 0.318 0.136 0.425 Gapped Lambda K H 0.267 0.0410 0.140 Matrix: BLOSUM62 Gap Penalties: Existence: 11, Extension: 1 Number of Sequences: 1 Number of Hits to DB: 880 Number of extensions: 40 Number of successful extensions: 6 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 1 Number of HSP's successfully gapped: 1 Length of query: 572 Length of database: 546 Length adjustment: 36 Effective length of query: 536 Effective length of database: 510 Effective search space: 273360 Effective search space used: 273360 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 53 (25.0 bits)
This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.
Each pathway is defined by a set of rules based on individual steps or genes. Candidates for each step are identified by using ublast (a fast alternative to protein BLAST) against a database of manually-curated proteins (most of which are experimentally characterized) or by using HMMer with enzyme models (usually from TIGRFam). Ublast hits may be split across two different proteins.
A candidate for a step is "high confidence" if either:
Otherwise, a candidate is "medium confidence" if either:
Other blast hits with at least 50% coverage are "low confidence."
Steps with no high- or medium-confidence candidates may be considered "gaps." For the typical bacterium that can make all 20 amino acids, there are 1-2 gaps in amino acid biosynthesis pathways. For diverse bacteria and archaea that can utilize a carbon source, there is a complete high-confidence catabolic pathway (including a transporter) just 38% of the time, and there is a complete medium-confidence pathway 63% of the time. Gaps may be due to:
GapMind relies on the predicted proteins in the genome and does not search the six-frame translation. In most cases, you can search the six-frame translation by clicking on links to Curated BLAST for each step definition (in the per-step page).
For more information, see:
If you notice any errors or omissions in the step descriptions, or any questionable results, please let us know
by Morgan Price, Arkin group, Lawrence Berkeley National Laboratory