Align 4-hydroxybutyrate-CoA ligase (EC 6.2.1.40) (characterized)
to candidate WP_047214219.1 PATSB16_RS11270 AMP-binding protein
Query= BRENDA::A4YDT1 (564 letters) >NCBI__GCF_001931675.1:WP_047214219.1 Length = 561 Score = 417 bits (1073), Expect = e-121 Identities = 237/535 (44%), Positives = 322/535 (60%), Gaps = 20/535 (3%) Query: 35 LRRFNWVRDVFEDIHVKERGSKTALIWRDINTGEEAKLSYHELSLMSNRVLSTLRKHGLK 94 L+ FNW D F+ V+ RG+ T +W G E KL+Y E+S SNRV + LR+ G+ Sbjct: 33 LKEFNWALDFFD---VQARGNDTLALWVVEEDGSERKLTYAEMSARSNRVANFLRQQGVA 89 Query: 95 KGDVVYLMTKVHPMHWAVFLAVIKGGFVMVPSATNLTVAEMKYRFSDLKPSAIISDSLRA 154 +GD V +M W + LA IK G VM+P+ T LT ++ R + + I++ Sbjct: 90 RGDRVLIMIPNQVELWDLMLACIKLGAVMIPATTLLTPEDLADRLTRGQVKHIVTTVAET 149 Query: 155 SVMEEALGSLKVEKFLIDGKRETWNSLED--ESSNA-EPED-TRGEDVIINYFTSGTTGM 210 + + L + + G+ W D E+ A EP T +D ++ YFTSGTT Sbjct: 150 AKFAQLPSGLT--RLCVGGEAPGWLRFADAYEAGEAFEPSGKTMADDPLLLYFTSGTTSK 207 Query: 211 PKRVIHTAVSYPVGSITTASIVGVRESDLHLNLSATGWAKFAWSSFFSPLLVGATVVGIN 270 PK V+H+ SYPVG +TT +G++ D+H N+S+ GWAK AWS FF+P + GAT+ N Sbjct: 208 PKLVLHSHQSYPVGHLTTMYFIGLQPGDVHWNISSPGWAKHAWSCFFAPWIAGATIFIYN 267 Query: 271 YEGKLDTRRYLGEVENLGVTSFCAPPTAWRQFITLDLDQFRFERLRSVVSAGEPLNPEVI 330 + + + + L + VT+ CAPPT WR I DL + +LR +V AGEPLNPEVI Sbjct: 268 F-ARFNAKAVLDTICRCEVTTLCAPPTVWRMLIQEDLASYPV-KLRELVGAGEPLNPEVI 325 Query: 331 KIWKDKFNLTIRDFYGQTETTAMVGNFPFLKVKPGSMGKPHPLYDIRLLDDEGKEITKPY 390 + +N+TIRD YGQTET +GN P +KPGSMG+P P Y + LLD +G P Sbjct: 326 DQVRRAWNITIRDGYGQTETCCQIGNSPGQPIKPGSMGRPMPGYRVALLDHDGH----PV 381 Query: 391 EVGHITVKLNPRPIGLFLGYS-DEKKNMESFREGYYYTGDKAYFDEEGYFYFVGRGDDVI 449 + G I + L RP GL LGY DE KN E R+G+Y+TGD A D+ GYF +VGR DDV Sbjct: 382 QEGEIALSLAQRPTGLMLGYEGDEGKNREVMRDGHYHTGDVAMCDDSGYFTYVGRADDVF 441 Query: 450 KTSDYRVGPFEVESALLEHPAVAEAAVVGVPDTVRWQLVKAYIVLKKGYMPSKELAEEIR 509 K SDYR+ PFE+ES L++HPAVAE VV PD +R + KAY+ L+ G+ PS+ELA +I Sbjct: 442 KASDYRISPFELESELIKHPAVAETGVVPSPDPLRLSVPKAYVALRAGFTPSRELALDIL 501 Query: 510 EKMKTLLSPYKVPRIIEFVDELPKTISGKIRRVELRKREEEKRKKGEVGQNEYVF 564 + + L+PYK R +EF ELPKTISGKIRRVELR+ EE +G+ G+ F Sbjct: 502 KFARAQLAPYKRVRRLEFC-ELPKTISGKIRRVELRRAEE---NRGDAGRRPQEF 552 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: 762 Number of extensions: 30 Number of successful extensions: 7 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: 561 Length adjustment: 36 Effective length of query: 528 Effective length of database: 525 Effective search space: 277200 Effective search space used: 277200 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 Sep 24 2021. 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