Align Altronate dehydratase; EC 4.2.1.7; D-altronate hydro-lyase (uncharacterized)
to candidate WP_068173723.1 HTA01S_RS16155 galactarate dehydratase
Query= curated2:O34673 (497 letters) >NCBI__GCF_001592305.1:WP_068173723.1 Length = 516 Score = 219 bits (558), Expect = 2e-61 Identities = 159/490 (32%), Positives = 247/490 (50%), Gaps = 23/490 (4%) Query: 5 IKIHKQDNVLLALRD--IQKGERLHAYGVSIEVKDDIKRGHKIALQSIKENDSIVKYGFP 62 I++H DNV + + D ++ G A G + + + +GHK+AL + ++ +Y Sbjct: 10 IRMHPADNVAIVVNDGGLKPGA---APGDGPVLVEAVPQGHKVALVDLPAGSAVRRYNVV 66 Query: 63 IGHASQDISIGEHIHVHNT--KTNLSDIQLYSYTPRFDENPYSNENRTFKGFRRENGDAG 120 IGH I G ++ S L + P + P + TF+G+R +G G Sbjct: 67 IGHTGVAIPAGGWVNEQRLVMPAARSLEGLPASNPPAELPPLTGH--TFQGYRNADGSVG 124 Query: 121 VRNELWIVPTVGCVNGIAEKMLQRFVRETGDIAP-FDNVLVLKHQYGCSQLGDDHENTKQ 179 RN L I TV CV G+ + ++R E + P D V+ L+H YGC D + Sbjct: 125 TRNLLAITTTVQCVAGVLDFAVERIRSELLPLYPNVDGVVGLEHTYGCGVAIDAPDAIIP 184 Query: 180 I--LLNAIRHPNAGG-VLVLGLGCENNELARM-KEALQDVNLKRVKFLESQSVTDEMEAG 235 I L N +PN GG V+VL LGCE + R+ ++ +R L+ + DE G Sbjct: 185 IRTLRNISSNPNFGGEVMVLSLGCEKLQPERLLPPGSIPISDQRDSELDVVMLQDEAHVG 244 Query: 236 V-----ALLKE--IH-EAAKGDKREDIPLSELKIGLKCGGSDGFSGITANPLLGRFSDYL 287 ++L++ +H E +R P S+L +G++CGGSD FSG+TANP +G +D L Sbjct: 245 FMSMIDSILRQARVHLERLNRRQRTTCPASDLVVGVQCGGSDAFSGVTANPAVGFATDLL 304 Query: 288 IAQGGSTVLTEVPEMFGAETILMQRAANEEVFHKIVDLINDFKQYFIKHDQPVYENPSPG 347 + G + + +EV E+ +L RAA+ +V +V + + Y K N +PG Sbjct: 305 VRAGATVMFSEVTEVRDGIDLLTTRAASPDVAEAMVREMAWYDAYLNKGRVDRSANTTPG 364 Query: 348 NKAGGISTLEDKSLGCTQKAGISPVTDVLKYGEVLKTKGLTLLSAPGNDLIASSALAAAG 407 NK GG+S + +K++G K+G P+ V+ GE +K KGL + P +D I + AAG Sbjct: 365 NKKGGLSNIVEKAMGSIVKSGTGPIHGVIAPGEKVKQKGLIFAATPASDFICGTLQLAAG 424 Query: 408 CQIVLFTTGRGTPFG-TFVPTVKVATNTELYEAKPHWIDFNAGLLAEDDVHEEYVLREFI 466 + +FTTGRGTP+G P +KVAT +L +D NAG +A + E V E Sbjct: 425 MNLHVFTTGRGTPYGLAECPVIKVATRDDLARRWHDLMDVNAGRIASGEASIEDVGCELF 484 Query: 467 HYMIEVASGQ 476 +++VASGQ Sbjct: 485 QLLLDVASGQ 494 Lambda K H 0.317 0.137 0.394 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: 568 Number of extensions: 21 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: 497 Length of database: 516 Length adjustment: 34 Effective length of query: 463 Effective length of database: 482 Effective search space: 223166 Effective search space used: 223166 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 (21.6 bits) S2: 52 (24.6 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