Align Dihydroxy-acid dehydratase; DAD; EC 4.2.1.9 (uncharacterized)
to candidate AZOBR_RS31260 AZOBR_RS31260 dihydroxy-acid dehydratase
Query= curated2:A8AB39 (552 letters) >FitnessBrowser__azobra:AZOBR_RS31260 Length = 608 Score = 291 bits (745), Expect = 5e-83 Identities = 186/518 (35%), Positives = 281/518 (54%), Gaps = 28/518 (5%) Query: 23 GLIDEELRR--PLIGVANSWNEIVPGHVHLDKVAEAVKAGIRMAGGTPLEFGTIAVCDGI 80 GL EEL+ P+IG+A + +++ P + H +AE ++ GIR AGG +EF + + Sbjct: 45 GLTREELQSGAPIIGIAQTGSDLSPCNRHHLVLAERLREGIRTAGGIAIEFPVHPIQE-- 102 Query: 81 AMGHEGMR--YSLPSREVIADTVEIMVEAHRLDAVVMVTNCDKITPGFLLAAARLEVPVI 138 G R S+ VE++ + LD VV+ CDK TP L+AAA + +P I Sbjct: 103 ----TGKRPTASIDRNLAYLGLVEVL-HGYPLDGVVLTIGCDKTTPACLMAAATVNIPAI 157 Query: 139 LINGGPMMPGVYGKERIDFKDLMERMNVLIKEGRTEELRKLE--ESALPGPGSCAGLFTA 196 ++ GPM+ G + ER ++ + ++ G + +E S+ P G C + TA Sbjct: 158 ALSVGPMLNGWFRGERTGSGTIVWKARQMMAAGEIDYQGFIELVASSAPSTGYCNTMGTA 217 Query: 197 NTMNMLSEAMGLMLPGASTVPAVEARRLWYAKLTGMRIVKMVEEGLTPDKILTRKALENA 256 +TMN L+E +G+ LPG++ +PA R TG RIV+MV E L P ILTR A NA Sbjct: 218 STMNSLAEVLGMQLPGSAAIPAPYRERQQADYETGKRIVEMVREDLKPSDILTRDAFLNA 277 Query: 257 IAVDMALGGSTNSVLHLEALAYELGIDLPLEVFDEISRKVPHIASISPSGRHFVVDLDRA 316 I V+ A+GGSTN+ +H+ A+A +G+ L +E + VP + ++ P+G + D RA Sbjct: 278 IVVNSAIGGSTNAPIHINAIAKHIGVPLTVEDWQTHGHDVPLLVNLQPAGEYLGEDFHRA 337 Query: 317 GGIPAVLKELGEAGLIHKDALTVTGKTVWENVKDAAVLDREVIRPLDNPYSPFGGLAILK 376 GG+PAV+ +L GLI + A TV G+T+ EN + +LD VI P+D P P G +L+ Sbjct: 338 GGVPAVVAQLMGKGLIREGAPTVNGRTIGENCRRQPILDTRVIHPIDEPLMPNAGFVVLR 397 Query: 377 GSLAPNGAVVKASAVKRELWK-----------FKGVARVFDREEDAVKAIRGGE--IEPG 423 G+L A++K S + E + F+G VFD ED I I+ Sbjct: 398 GNLF-GAAIMKTSVISDEFRERYLSNPQDPEAFEGKVVVFDGPEDYHHRIDDPSLGIDAY 456 Query: 424 TVIVIRYEGPRGGPGMREMLTATAAVMALGLG-DKVALVTDGRFSGATRGPAIGHVSPEA 482 T++VIR GP G PG E++ + G + + DGR SG + P+I + SPEA Sbjct: 457 TILVIRGTGPIGYPGAAEVVNMRPPATLIKQGVHSLPCIGDGRQSGTSGSPSILNASPEA 516 Query: 483 AAGGPIALVQDGDEIVIDIEKRRLDLLVDEKELEERRA 520 AAGG +AL++ GD + ID+ + D+L+ E EL +RRA Sbjct: 517 AAGGGLALLRSGDRVRIDLRRGSADILIPEGELADRRA 554 Lambda K H 0.319 0.138 0.401 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: 814 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: 552 Length of database: 608 Length adjustment: 36 Effective length of query: 516 Effective length of database: 572 Effective search space: 295152 Effective search space used: 295152 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 Jul 25 2024. The underlying query database was built on Jul 25 2024.
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