Align L-arabinonate dehydratase; ArDHT; D-fuconate dehydratase; Galactonate dehydratase; L-arabonate dehydratase; EC 4.2.1.25; EC 4.2.1.67; EC 4.2.1.6 (characterized)
to candidate WP_211262552.1 NITAL_RS20450 dihydroxy-acid dehydratase
Query= SwissProt::B5ZZ34 (579 letters) >NCBI__GCF_000969705.1:WP_211262552.1 Length = 560 Score = 323 bits (829), Expect = 9e-93 Identities = 194/530 (36%), Positives = 300/530 (56%), Gaps = 21/530 (3%) Query: 44 RPVIGILNTWSDMTPCNGHLRELAEKVKAGVWEAGGFPLEVPVFSASENTFRP-----TA 98 +P IG+ ++W+++TPCN L LA++ K G+ +AGGFP+E + S+ + Sbjct: 36 KPQIGVASSWNEVTPCNLPLDRLAKQAKLGIRDAGGFPIEFNTIAVSDGISMGHEGMRAS 95 Query: 99 MMYRNLAALAVEEAIRGQPMDGCVLLVGCDKTTPSLLMGAASCDLPSIVVTGGPMLNGYF 158 ++ R + A +VE + + DG V GCDK+ P ++M A D+ S + GG +L G Sbjct: 96 LVSREVIADSVETVMHAERFDGMVTFAGCDKSLPGMVMAAVRLDVASTFLYGGSILPGQH 155 Query: 159 RGERVGSGTHLWKFSEMVKA---GEMTQAEFLEAEASMSRSSGTCNTMGTASTMASMAEA 215 G + + E V A ++ AE E + S G C M TA+TMAS EA Sbjct: 156 DGHDIS----IQDVFEAVGARGRDQIDDAELDRIERAACPSEGACAGMFTANTMASAVEA 211 Query: 216 LGMALSGNAAIPGVDSRRKVMAQLTGRRIVQMVKDDLKPSEIMTKQAFENAIRTNAAIGG 275 LG+AL G++ P D RR A+ +G ++ ++++ + I+T++A ENA A+GG Sbjct: 212 LGLALPGSSTAPAPDPRRDEFARRSGAAVLHLLEEGITARRIVTREALENATSVVMALGG 271 Query: 276 STNAVIHLLAIAGRVGIDLSLDDWDRCGRDVPTIVNLMPSGKYLMEEFFYAGGLPVVLKR 335 STNAV+HL+AIA ++ SLDD+DR GR VP I + P G+Y M + GG+PVVLK Sbjct: 272 STNAVLHLIAIAREAEVEFSLDDFDRIGRRVPHIADTKPGGRYFMTDLDRIGGVPVVLKE 331 Query: 336 LGEAGLLHKDALTVSGETVWDEVK--DVVNWNEDVILPAEKALTSSGGIVVLRGNLAPKG 393 L +AGLLH D LTV+G ++ DE++ DV + +V+ P ++ + + GG+ +LRG+LAP+G Sbjct: 332 LLDAGLLHGDCLTVTGRSLGDEIEAMDVPAPDGEVVHPLDRPIHADGGLAILRGSLAPEG 391 Query: 394 AVLKPSAASPHLLVHKGRAVVFE-DIDDYKAKINDDNLDIDENCIMVMKNCGPKGYPGMA 452 AV+K + +G A VF+ + D +A + +D D ++V++ GPKG PGM Sbjct: 392 AVVKIAGIPEDNHQFEGPARVFDGEQDAMEAVLTGRIVDGD---VIVIRYEGPKGGPGMR 448 Query: 453 EVGNMGLPPKVLKKGI-LDMVRISDARMSGTAYGTVVLHTSPEAAVGGPLAVVKNGDMIE 511 E+ + + V G+ + ++D R SG +G + H +PEA GGP+A V+ GD I Sbjct: 449 EM--LAVTSAVKGAGLGASVALLTDGRFSGATHGFSIGHVAPEATDGGPIAFVREGDRIR 506 Query: 512 LDVPNRRLHLDISDEELARRLAEWQPNHDLPTSGYAFLHQQHVEGADTGA 561 +DVP+R + L + + ELA R WQP T G + + V A GA Sbjct: 507 IDVPSRTMDLLVDEGELATRREGWQPLPPRYTRGVLAKYARTVSSASLGA 556 Lambda K H 0.318 0.135 0.408 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: 820 Number of extensions: 39 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: 579 Length of database: 560 Length adjustment: 36 Effective length of query: 543 Effective length of database: 524 Effective search space: 284532 Effective search space used: 284532 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