Align Methylmalonate-semialdehyde dehydrogenase [inositol] (EC 1.2.1.27) (characterized)
to candidate WP_085636095.1 MGEO_RS07470 aldehyde dehydrogenase
Query= reanno::Caulo:CCNA_01360 (500 letters) >NCBI__GCF_002115805.1:WP_085636095.1 Length = 498 Score = 216 bits (551), Expect = 1e-60 Identities = 153/483 (31%), Positives = 246/483 (50%), Gaps = 32/483 (6%) Query: 8 FIGGQKVDGASGRFGEVFDPNTGKVQARVALASAGELNTAIANAKVA--QAAWAATNPQR 65 FI G ASG + +P TG+V A++A A +++ A+ A+ A W+A P Sbjct: 24 FINGGFRSAASGSTFDTINPATGEVLAKIAACGAADVDFAVQKARDAFEDGRWSALPPAE 83 Query: 66 RARVMFEFKRLLEVHMDELAALLSSEHGKVIADSKG-DIQRGLEVIEFACGVPHLLKGEY 124 R V+ +L+ + ELA + S + GK I D + D+ + +++ + + Sbjct: 84 RKDVLIRLCKLMSRNARELAVMESLDSGKTIFDCETVDVPETIHCLKWHAEAIDKIYDQV 143 Query: 125 TQGAGPGIDVYSMRQPLGVVAGITPFNFPAMIPMWMFGPAIATGNAFILKPSERDPSVPV 184 + + I + +R+P+GVV + P+NFP ++ W GPA+A G + ++KP+E + Sbjct: 144 SPASDDHIAMI-VREPVGVVGLVLPWNFPLLMLAWKIGPALAAGCSVVVKPAEETSLTAL 202 Query: 185 RLAELMIEAGLPPGVLNVVHGD-KDCVEAILDHPDIKAVSFVGSSDIAQSVFQRAGAAG- 242 R+AEL +EAG+PPGVLNVV G+ + E + H D+ +SF GS++ + AG + Sbjct: 203 RVAELAMEAGVPPGVLNVVTGNGPEVGEPLGRHMDVDMISFTGSTETGRRFLTYAGESNL 262 Query: 243 KRVQAMGGAKNHGLVMPDAD-LDQAVADIIGAAYGSAGERCMALP-VVVPVGEKTATALR 300 K V G KN +V+ DA+ LD+ A ++ A+ + GE C A ++V G K AL Sbjct: 263 KEVTLEMGGKNPAIVLDDAENLDRVAAHVVNGAFWNMGENCSASSRLIVQAGVK--DALL 320 Query: 301 EKLVAAIGGLRVGVSTDPDAHYGPVVSAAHKARIESYIQMGVDEGAELVVDGRGFSLQGH 360 E++ A + +G DP+ G +VSAAH ++ Y++ G+ + G Sbjct: 321 ERIAAHLREWPMGDPLDPEMRVGALVSAAHFDKVCGYLK------------GQTVLVGGA 368 Query: 361 EEGFFVGPTLFDHVKPTSRSYHDEIFGPVLQMVRAESLEEGIALASRHQYGNGVAIFTRN 420 + FV PT+ D + +EIFGPVL ++ S +E IALA+ YG +IFT N Sbjct: 369 TQKGFVEPTVLDITDRNAPQVREEIFGPVLSVLTVHSFDEAIALANDTHYGLAASIFTAN 428 Query: 421 GDAAREFADQVEVGMVGINV----PIPVPVAYHSFGGWKRSGFGDLNQYGMDGVRFYTRT 476 A A + G V +N I P FGG+++SGFG + G+ YT+ Sbjct: 429 VKRAIRGARALRAGTVTVNAFGEGDISTP-----FGGYRQSGFGGRDN-GVHAHDQYTQL 482 Query: 477 KTV 479 KT+ Sbjct: 483 KTI 485 Lambda K H 0.320 0.137 0.409 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: 613 Number of extensions: 39 Number of successful extensions: 8 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: 500 Length of database: 498 Length adjustment: 34 Effective length of query: 466 Effective length of database: 464 Effective search space: 216224 Effective search space used: 216224 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 (21.8 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