Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_211262411.1 NITAL_RS14175 AMP-binding protein
Query= BRENDA::A4YDT1 (564 letters) >NCBI__GCF_000969705.1:WP_211262411.1 Length = 543 Score = 230 bits (587), Expect = 9e-65 Identities = 166/521 (31%), Positives = 260/521 (49%), Gaps = 29/521 (5%) Query: 47 DIHVKERGSKTALIWRDINTGEEAKLSYHELSLMSNRVLSTLRKHGLKKGDVVYLMTKVH 106 D+H + T+L +I G + ++ ++ SNR+ + L G+ +GD V ++ Sbjct: 26 DVH-----AATSLAMIEIVGGRVREHTFGHITEGSNRLANGLDGLGVTRGDRVGIVLPQG 80 Query: 107 PMHWAVFLAVIKGGFVMVPSATNLTVAEMKYRFSDLKPSAIISDSLRASVMEEALGSLKV 166 LAV K G + VP +++R +D +++D+ V+ E G L Sbjct: 81 FDVAIAHLAVYKLGAIAVPMTQLFGPEAIRHRLADSGARVVVTDTTTLDVVAEVAGELDD 140 Query: 167 EKFLIDGKRET------WNSLEDESSNAEPEDTRGEDVIINYFTSGTTGMPKRVIHTAVS 220 ++ T + LE S AE T +D + +TSGTTG PK +H Sbjct: 141 VTVVVAADTVTSPHVRLQDLLERASVRAEVAPTGPDDPALLIYTSGTTGSPKGALH-GHR 199 Query: 221 YPVGSITTASIVGVR---ESDLHLNLSATGWAKFAWSSFFSPLLVGATVVGINYEGKLDT 277 G ++ ++ R D + W +F G V+ + D Sbjct: 200 VLAGHLSGFDLMFDRFPHPDDRMWTPADWAWIGGLLDAFLPAWSHGRPVIATP-RARFDP 258 Query: 278 RRYLGEVENLGVTSFCAPPTAWRQFITLDLDQFRFERLRSVVSAGEPLNPEVIKIWKDKF 337 + + GVT+ PPTA + D + LRSV+S GE L E++ ++ Sbjct: 259 EWAVALMAEHGVTTAFLPPTALKLMRQADATAGDLQ-LRSVMSGGESLGSEMLSWGREHL 317 Query: 338 NLTIRDFYGQTETTAMVGNFPFL-KVKPGSMGKPHPLYDIRLLDDEGKEITKPYEVGHIT 396 +TI + YGQTE +VGN + V+PGSMG+P+P +++ +L D+G I P G + Sbjct: 318 GVTINEIYGQTEANLLVGNSAAIWDVRPGSMGRPYPGHEVAVLADDGA-IAPPGVEGELV 376 Query: 397 VKLNPRPIGLFLGYSDEKKNMESFRE---------GYYYTGDKAYFDEEGYFYFVGRGDD 447 V+ P P+ + ++ + E F + + TGD D++GYF+F R DD Sbjct: 377 VRA-PDPVLMLRYWNQPEATEEKFVDVPDGAGGTHRWLRTGDVGTVDDDGYFWFTARDDD 435 Query: 448 VIKTSDYRVGPFEVESALLEHPAVAEAAVVGVPDTVRWQLVKAYIVLKKGYMPSKELAEE 507 VI ++ YR+GP E+E ++ HPAVA AA VGVPD VR ++VKA++ L G PS EL +E Sbjct: 436 VIISAGYRIGPAEIEECIIGHPAVALAAAVGVPDEVRGEVVKAFVTLADGVAPSAELRDE 495 Query: 508 IREKMKTLLSPYKVPRIIEFVDELPKTISGKIRRVELRKRE 548 IR++++T L+ Y+ PR +EFVDELP T +GKIRR +LR RE Sbjct: 496 IRQRVRTQLAAYEYPREVEFVDELPLTTTGKIRRRDLRDRE 536 Lambda K H 0.318 0.137 0.402 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: 663 Number of extensions: 26 Number of successful extensions: 4 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: 564 Length of database: 543 Length adjustment: 36 Effective length of query: 528 Effective length of database: 507 Effective search space: 267696 Effective search space used: 267696 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 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