Align Altronate dehydratase; D-altronate hydro-lyase; EC 4.2.1.7 (characterized)
to candidate WP_009140717.1 HMPREF9452_RS03440 altronate dehydratase
Query= SwissProt::P42604 (495 letters) >NCBI__GCF_000225705.1:WP_009140717.1 Length = 494 Score = 484 bits (1246), Expect = e-141 Identities = 249/497 (50%), Positives = 324/497 (65%), Gaps = 5/497 (1%) Query: 1 MQYIKIHALDNVAVALADLAEGTEVSVDNQ-TVTLRQDVARGHKFALTDIAKGANVIKYG 59 M+ I+I+ DNV VAL LA GT VSV VT +D+ +GHK A+ IA G NVIKYG Sbjct: 1 MKTIQINPADNVIVALEPLAAGTVVSVPGAGEVTATEDIPQGHKMAVRSIAAGDNVIKYG 60 Query: 60 LPIGYALADIAAGVHVHAHNTRTNLSDLDQYRYQPDFQDLPAQAADREVQIYRRANGDVG 119 LPIG+ D+ AG +H HN +TNLS Y Y P L A + Q +RRA+G Sbjct: 61 LPIGHVTCDVQAGSWLHTHNVKTNLSGEVDYEYHPSRPVLRA-IEPKTFQGFRRADGRAA 119 Query: 120 VRNELWILPTVGCVNGIARQIQNRFLKETNNAEGTDGVFLFSHTYGCSQLGDDHINTRTM 179 RNELWI+PTVGCVN +AR + + + + +GV+ F H +GCSQ G DH TR + Sbjct: 120 TRNELWIIPTVGCVNEVARAMCEQ--AQDLVGDSLEGVYYFPHPFGCSQTGADHAQTRKL 177 Query: 180 LQNMVRHPNAGAVLVIGLGCENNQVAAFRETLGDIDPERVHFMICQQQDDEIEAGIEHLH 239 L + RH NA VL + LGCEN E LG+ D +RV F+ CQ +DE+ G + L Sbjct: 178 LVALSRHANAAGVLFLSLGCENCTHDQVLEELGNYDAQRVRFLTCQDVEDELVEGHKILS 237 Query: 240 QLYNVMRNDKREPGKLSELKFGLECGGSDGLSGITANPMLGRFSDYVIANGGTTVLTEVP 299 +L + KRE SEL GL+CGGSDGLSGITANP++GR SD +A GGT+VLTEVP Sbjct: 238 ELATHAKTFKRETISASELAIGLKCGGSDGLSGITANPVIGRVSDIAVAGGGTSVLTEVP 297 Query: 300 EMFGAEQLLMDHCRDEATFEKLVTMVNDFKQYFIAHDQPIYENPSPGNKAGGITTLEDKS 359 EMFGAE +L+D C + F+ M+N FK YFI+H + +YENPSPGNK GGITTLEDKS Sbjct: 298 EMFGAESILLDRCEGQDVFDAAADMLNGFKDYFISHGEVVYENPSPGNKDGGITTLEDKS 357 Query: 360 LGCTQKAGSSVVVDVLRYGERLKTPGLNLLSAPGNDAVATSALAGAGCHMVLFSTGRGTP 419 GC QK G + +VDVL YG+ ++ PGL +L PGND V+T+AL AGCH++LFSTGRGTP Sbjct: 358 CGCVQKGGDAPIVDVLGYGDTVRKPGLQMLCCPGNDMVSTTALTAAGCHVILFSTGRGTP 417 Query: 420 YGGFVPTVKIATNSELAAKKKHWIDFDAGQLIHG-KAMPQLLEEFIDTIVEFANGKQTCN 478 +G PT+K+ TN L K +W+DF+AG + G + + + E+ D ++E A+G+QT Sbjct: 418 FGAPAPTLKVFTNERLCQHKANWMDFNAGVVATGERTIDEAAEDLWDLVLETASGRQTSA 477 Query: 479 ERNDFRELAIFKSGVTL 495 ER E++I+K GVTL Sbjct: 478 ERRGCHEISIWKDGVTL 494 Lambda K H 0.319 0.136 0.403 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: 702 Number of extensions: 30 Number of successful extensions: 4 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: 495 Length of database: 494 Length adjustment: 34 Effective length of query: 461 Effective length of database: 460 Effective search space: 212060 Effective search space used: 212060 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: 52 (24.6 bits)
This GapMind analysis is from Sep 24 2021. 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