Align Dihydroxy-acid dehydratase; DAD; EC 4.2.1.9 (uncharacterized)
to candidate WP_038205992.1 Q392_RS10365 IlvD/Edd family dehydratase
Query= curated2:A8AB39 (552 letters) >NCBI__GCF_000745855.1:WP_038205992.1 Length = 580 Score = 377 bits (968), Expect = e-109 Identities = 213/528 (40%), Positives = 321/528 (60%), Gaps = 14/528 (2%) Query: 31 RPLIGVANSWNEIVPGHVHLDKVAEAVKAGIRMAGGTPLEFGTIAVCDGIAMGHEGMRYS 90 RP+IG+ N+++E+ P + H +AE VK G+ AGG PLEF +++ + + + M Y Sbjct: 47 RPVIGICNTFSELTPCNSHFRTLAEQVKIGVYEAGGFPLEFPVMSLGETL-LRPTAMLY- 104 Query: 91 LPSREVIADTVEIMVEAHRLDAVVMVTNCDKITPGFLLAAARLEVPVILINGGPMMPGVY 150 R + + VE + A+ LD VV++ CDK TP ++ AA +++P I ++GGPM+ G + Sbjct: 105 ---RNLASMDVEESIRANPLDGVVLLMGCDKTTPALMMGAASVDLPTIGVSGGPMLSGKW 161 Query: 151 GKERIDFKDLMERMNVLIKEG--RTEELRKLEESALPGPGSCAGLFTANTMNMLSEAMGL 208 + + + +M+ +++ G + ++ + E G C + TA+TM + E++G+ Sbjct: 162 RGQELGSGTGVWQMSEMVRAGTLKLQDFFEAESCMHRSHGHCMTMGTASTMASMVESIGI 221 Query: 209 MLPGASTVPAVEARRLWYAKLTGMRIVKMVEEGLTPDKILTRKALENAIAVDMALGGSTN 268 LPG + PAV+ RR A++ G RIV MV E L +I+TR+A+EN I V+ A+GGSTN Sbjct: 222 GLPGNAAYPAVDGRRNVLARMAGRRIVDMVHEDLVMSRIVTREAMENVIKVNAAIGGSTN 281 Query: 269 SVLHLEALAYELGIDLPLEVFDEISRKVPHIASISPSGRHFVVDLDRAGGIPAVLKELGE 328 V+HL A+A LGIDL L+ FD I ++P + + PSG+H + D AGG+P V+KE+ Sbjct: 282 LVIHLLAIAGRLGIDLTLDDFDRIGSELPCLLDLQPSGKHLMEDFCYAGGLPVVMKEI-- 339 Query: 329 AGLIHKDALTVTGKTVWENVKDAAVLDREVIRPLDNPYSPFGGLAILKGSLAPNGAVVKA 388 A L+HKD +T +G+TVWENVKDA + +VIRPL P+ G+ +L+G+LAPNGA++K Sbjct: 340 AHLLHKDLITASGQTVWENVKDAENYNPQVIRPLAEPFKDKAGICVLRGNLAPNGAIIKP 399 Query: 389 SAVKRELWKFKGVARVFDREEDAVKAI--RGGEIEPGTVIVIRYEGPRGGPGMREM--LT 444 SA EL KG A VF+ +D K I +I+ V+V++ GP+G PGM E + Sbjct: 400 SAATPELLVHKGRAVVFENADDLHKRIDDEDLDIDETCVMVLKNCGPKGYPGMAEAGNMP 459 Query: 445 ATAAVMALGLGDKVALVTDGRFSGATRGPAIGHVSPEAAAGGPIALVQDGDEIVIDIEKR 504 V+ G+ D V V+D R SG G + H +PEAAAGGP+ALV++GD + +D+ R Sbjct: 460 LPPKVLRKGITDMVR-VSDARMSGTAYGTVVLHTAPEAAAGGPLALVKNGDIVELDVPNR 518 Query: 505 RLDLLVDEKELEERRARWKPKVKPLRRGILRRYAKMALSADKGGALEY 552 RL L V ++EL RRA W P PL G + Y L AD+G L + Sbjct: 519 RLHLHVSDEELARRRAEWTPPKPPLDSGYWKLYVDNVLQADEGADLGF 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: 808 Number of extensions: 42 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: 552 Length of database: 580 Length adjustment: 36 Effective length of query: 516 Effective length of database: 544 Effective search space: 280704 Effective search space used: 280704 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