Align Probable galactarate dehydratase (L-threo-forming); GalcD; EC 4.2.1.42 (uncharacterized)
to candidate CCNA_01555 CCNA_01555 altronate dehydratase
Query= curated2:P42240 (510 letters) >FitnessBrowser__Caulo:CCNA_01555 Length = 502 Score = 238 bits (606), Expect = 5e-67 Identities = 155/454 (34%), Positives = 237/454 (52%), Gaps = 22/454 (4%) Query: 42 VLEEDVPQGHKVALTDLNQGDEIVRYGEVIGFADETIKRGSWIR--EALVRMPAPPALDD 99 ++ DVP+GHK+A + GD++++YG IG A I G + + R+ Sbjct: 42 IVRADVPKGHKIATRVVRSGDDVLKYGWPIGRATADIAVGDHVHVHNVITRLEGVEGYAF 101 Query: 100 LPLANRVPQPRPPLEGYTFEGYRNADGSAGTKNILGITTSVQCVVGVLDYAVKRIKEELL 159 PL P P + TF+G+R +G AGT+N + + +V CV +RI E+ Sbjct: 102 APLP---PAGAPSADTRTFQGFRRKNGRAGTRNEIWVLCTVGCVANT----ARRIAEKAN 154 Query: 160 PKYPN-VDDVVPLHHQYGCGVAINAPDAVIPIRTIQNLAKHPNFGGEVMVIGLGCEKLLP 218 ++ VD V H +GC D + I LA HPN GG V+++GLGCE Sbjct: 155 QRFAGRVDGVYAFPHPFGCSQL--GDDLAHTRKLIAALASHPNAGG-VLILGLGCENNQL 211 Query: 219 ERIASENDDDILSLQDHRGFAA-MIQSILE---MAEERLIRLNSRTRVS-CPVSDLVIGL 273 + + D + + +GF M++ LE A E L+ + + R PVS+LV+GL Sbjct: 212 KALLESAPD--IDRERLKGFTTQMVEDELEDGLAAVEALVEIAEKDRREPVPVSELVVGL 269 Query: 274 QCGGSDAFSGVTANPAVGYAADLLVRAGATVLFSEVTEVRDAIHLLTPRAVSEEVGQSLI 333 +CGGSD FSG+TANP VG AD + AG T + +E+ E+ A ++L RA S EV + + Sbjct: 270 KCGGSDGFSGITANPLVGRIADKVAEAGGTPVLTEIPEIFGAENVLLQRAASREVFDAAV 329 Query: 334 KEMKWYDSYLRRGDADRSANPSPGNKKGGLSNVVEKALGSVAKSGTSPISGVLGPGERAK 393 + + Y + NPSPGN GG++++ EK+LG+V K G +P+ VL GE Sbjct: 330 AVIDDFKRYFIEANQPIYENPSPGNIAGGITSLEEKSLGAVQKGGRAPLVEVLRYGETVG 389 Query: 394 QKGLLFAATPASDFVCGTLQLAAGMNLQVFTTGRGTPYGLAAAPVLKVSTRHSLSEHWAD 453 + GL P +D V T AAG + +FTTGRGTP G AP LK+++ L++ Sbjct: 390 RHGLTLLEAPGNDAVSSTALTAAGATVILFTTGRGTPLGF-PAPTLKIASNSGLAQRKPG 448 Query: 454 LIDINAGRIATGEASIEDVGWEIFRTILDVASGR 487 ID +AG++ G S++ + +++ ASG+ Sbjct: 449 WIDFDAGQVLEG-VSMDVAAENLMDLVIETASGK 481 Lambda K H 0.318 0.136 0.406 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: 660 Number of extensions: 42 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: 510 Length of database: 502 Length adjustment: 34 Effective length of query: 476 Effective length of database: 468 Effective search space: 222768 Effective search space used: 222768 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 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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