Align L-arabonate dehydratase (EC 4.2.1.25) (characterized)
to candidate WP_073038792.1 BUB04_RS09665 dihydroxy-acid dehydratase
Query= reanno::Smeli:SM_b20890 (579 letters) >NCBI__GCF_900129305.1:WP_073038792.1 Length = 552 Score = 360 bits (923), Expect = e-103 Identities = 214/552 (38%), Positives = 316/552 (57%), Gaps = 16/552 (2%) Query: 21 GKNAIMHRSWMKNQGLPADTFDGRPIIGICNTWSELTPCNAHLRDLAERVKRGVYEAGGF 80 G HRS K G + + RPI+GI N+++E+ P + HL +A+ VK GV AGG Sbjct: 9 GPEKAPHRSLFKAMGYTREELE-RPIVGIVNSFNEIIPGHIHLDKIAQAVKAGVRMAGGT 67 Query: 81 PVEFPVFSTGES-TLRPTAMMF----RNLAAMDVEESIRGNPVDGVVLLGGCDKTTPSLL 135 PVEF + + M + R L A VE +P DG+VL+ CDK P +L Sbjct: 68 PVEFSTIGVCDGIAMNHDGMRYSLASRELIADSVEVMATAHPFDGLVLIPNCDKIIPGML 127 Query: 136 MGAASVDIPAIVVSGGPMLNGKWRGKDVGSGTAIWQFSEMVKSGEMSLEEFMDAEQGMAR 195 M A ++IP I+VSGGPML G+ + V ++++ K+G ++ EE + E Sbjct: 128 MAAFRLNIPTILVSGGPMLAGRVGNRPVDL-ISVFEGVGAYKAGTLTAEELEELEDCACP 186 Query: 196 SAGSCMTMGTASTMASMAEALGMTLSGNAAIPAVDARRRVISQLTGRRIVEMVKEDLKPS 255 GSC M TA++M ++EALG+ L GN IPAV A R +++ G +I++++ + +P Sbjct: 187 GCGSCAGMFTANSMNCLSEALGLALPGNGTIPAVSAARFRLAKTAGMKIMDLIAANKRPR 246 Query: 256 DILTKEAFENAIRVNGAVGGSTNAVLHLLALAGRVGVDLSLDDWDRLGRDVPTIVNLQPS 315 D++T ++FENAI V+ A+G STN VLH+ A+A G+ L LD ++ + P + +L+P Sbjct: 247 DLITLKSFENAIAVDMALGCSTNTVLHVPAIAHEAGITLDLDLFNAMSARTPHLCSLRPG 306 Query: 316 GKYLMEEFYYAGGLPVVIKAVAEMGLLHNDAITVSGDTIWNDVKGVVNYNEDVILPREKA 375 G + +E+ AGG+ V+K +A+ GL+H D +TV+GDT+ +++ V + +VI P + Sbjct: 307 GPHFLEDLNAAGGVQAVMKELAKGGLIHLDVLTVTGDTVGANLERVKAVDHNVIRPLDNP 366 Query: 376 LTKSGGIAVLRGNLAPRGAVLKPSAASPHLMQHKGRAVVFESIEDYHARINREDLDIDET 435 + GGIA+L GNLAP+GAV+K SA +P ++Q GRA VFES + + I D I Sbjct: 367 YHREGGIAILYGNLAPQGAVVKQSAVAPEMLQRTGRARVFESENEAASAI--LDGKIRPG 424 Query: 436 CIMVLKYCGPKGYPGMAEVGNMGLPPKVLKKGI---TDMIRISDARMSGTAYGTVILHTA 492 ++V++Y GPKG PGM E+ L P G+ D+ I+D R SG G I H + Sbjct: 425 DVVVIRYEGPKGGPGMQEM----LTPTAAIMGMGLGKDVALITDGRFSGGTQGAAIGHIS 480 Query: 493 PEAAEGGPLALVENGDLIEVDIPNRTLHLHVSDEELARRRAAWVSPVKPLTGGYGGLYIK 552 PEAA GGP+ LVE GD I +DIPN+ L L V + L RRA W + GY Y + Sbjct: 481 PEAAAGGPIGLVEEGDEIVIDIPNKKLELKVDEATLEARRAKWQPKEPKIRHGYLARYAR 540 Query: 553 TVMQADAGADLD 564 V GA L+ Sbjct: 541 MVTSGARGAVLE 552 Lambda K H 0.318 0.135 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: 866 Number of extensions: 45 Number of successful extensions: 5 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: 579 Length of database: 552 Length adjustment: 36 Effective length of query: 543 Effective length of database: 516 Effective search space: 280188 Effective search space used: 280188 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