Align Dihydroxy-acid dehydratase; DAD; EC 4.2.1.9 (uncharacterized)
to candidate WP_036259301.1 DL86_RS05900 phosphogluconate dehydratase
Query= curated2:A8AB39 (552 letters) >NCBI__GCF_000746085.1:WP_036259301.1 Length = 603 Score = 258 bits (658), Expect = 6e-73 Identities = 182/509 (35%), Positives = 263/509 (51%), Gaps = 31/509 (6%) Query: 32 PLIGVANSWNEIVPGHVHLDKVAEAVKAGIRMAGGTPLEFGTI-AVCDGIAMGHEGMRYS 90 P + + ++N+++ H ++ +K R G G + A+CDG+ G GM S Sbjct: 67 PNLAIVTAYNDMLSAHQPYERFPAIIKRAAREIGAVAQVAGGVPAMCDGVTQGRAGMELS 126 Query: 91 LPSREVIADTVEIMVEAHRLDAVVMVTNCDKITPGFLLAAARL-EVPVILINGGPMMPGV 149 L SR+VIA I + DAV + CDKI PG ++AA +P + I GPM G+ Sbjct: 127 LFSRDVIAMAAAIALSHDMFDAVAFLGVCDKIVPGLVIAAQAFGHLPAVFIPAGPMPSGI 186 Query: 150 YGKERIDFKDLMERMNVLIKEGRTEELRKLEESALPGPGSCAGLFTANTMNMLSEAMGLM 209 + + M R + + E+L + E ++ PG+C TAN+ ML E MGL Sbjct: 187 PNETKA-----MLRQSYAEGKASREDLLEAEAASYHAPGTCTFYGTANSNQMLMETMGLH 241 Query: 210 LPGASTV-PAVEARRLWYAKLT--GMRIVKMVEEGLTPDKILTRKALENAIAVDMALGGS 266 LPG S V P R A + I + E+ +IL +A N I A GGS Sbjct: 242 LPGGSFVNPDTPLRDALTAAAAQRALAITALGEDYTPVAQILDERAFVNGIVALHATGGS 301 Query: 267 TNSVLHLEALAYELGIDLPLEVFDEISRKVPHIASISPSGRHFVVDLDRAGGIPAVLKEL 326 TN V+HL A+A G+ L L+ F ++S+ VP + I P+G V +AGG ++ +L Sbjct: 302 TNHVIHLVAMARAGGLILTLDDFADLSKAVPLLTRIYPNGGADVNHFTKAGGTGFLIGQL 361 Query: 327 GEAGLIHKDALTVTGKTVWENVKD--------------AAVLDREVIRPLDNPYSPFGGL 372 EAGL+H DA T+ G + V + AA D V+RP P+S GGL Sbjct: 362 LEAGLLHPDAKTIAGHALEGYVVEPYLDGGRLAYRPAAAASSDLSVLRPARRPFSQDGGL 421 Query: 373 AILKGSLAPNGAVVKASAVKRELWKFKGVARVFDREEDAVKAIRGGEIEPGTVIVIRYEG 432 +L+G+L AV+K SAV E K + AR+F +E+ A GE+ V V+R++G Sbjct: 422 KVLEGNL--GRAVIKLSAVAPERRKLRAPARIFHTQEEVEAAFCAGELNLDFVAVVRFQG 479 Query: 433 PR--GGPGMREMLTATAAVMALGLGDKVALVTDGRFSGAT-RGPAIGHVSPEAAAGGPIA 489 R G P + ++ A++MA G +VALVTDGR SGA+ + PA HVSPEA GGPIA Sbjct: 480 ARATGMPELHKLTPLLASLMA--QGHQVALVTDGRMSGASGKVPAAIHVSPEAQDGGPIA 537 Query: 490 LVQDGDEIVIDIEKRRLDLLVDEKELEER 518 ++DGD I +D E L V ++L+ER Sbjct: 538 RLRDGDIISLDAEAGMLMAEVSAQDLQER 566 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: 868 Number of extensions: 49 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: 552 Length of database: 603 Length adjustment: 36 Effective length of query: 516 Effective length of database: 567 Effective search space: 292572 Effective search space used: 292572 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