Align Alpha-ketoglutarate semialdehyde dehydrogenase; KGSADH; EC 1.2.1.26 (characterized)
to candidate Ga0059261_3677 Ga0059261_3677 methylmalonic acid semialdehyde dehydrogenase
Query= SwissProt::D4GP41 (482 letters) >FitnessBrowser__Korea:Ga0059261_3677 Length = 503 Score = 249 bits (636), Expect = 2e-70 Identities = 156/471 (33%), Positives = 233/471 (49%), Gaps = 4/471 (0%) Query: 11 GEWVTSETGETTEVTNPANPSEVVAAYQHSNENDAAAAVDAAVAAEDEWRNTPGPERGRI 70 G T+ TG N V A + D AA+ AV A+ W T R R+ Sbjct: 13 GNAATAGTGTRRSDVFDPNTGAVQAQVTLGAQADLDAAMANAVRAQISWAATNPQRRARV 72 Query: 71 LREAGTLLAQRKDELTEILTAEEGKARPEAAGEVQRAIDIFHYFSSKAADLGGTKKGASG 130 + L+ + +EL +L++E GK +A G++QR +++ + L G +G Sbjct: 73 MFNFKALIEKNMEELAHLLSSEHGKVIADAKGDIQRGLEVIEFVCGIPHVLKGEYTQGAG 132 Query: 131 PNTNLYTRQEPVGVAALITPWNYPIAIPAWKLAPALAAGNTVVLKPASIAPGVVIEIARA 190 P ++Y+ ++P+GV A ITP+N+P IP W A+A GN +LKP+ P V + +A Sbjct: 133 PGIDVYSMRQPLGVVAGITPFNFPAMIPMWMFGVAIACGNAFILKPSERDPSVPVRLAEL 192 Query: 191 LDEAGLPDGVLNVVTGPGSSVGSEFIGNEGTDLVSFTGSSQVGEMVYEQATDAGKRVQTE 250 + EAGLP+GVL VV G V + + + VSF GSS + VY + AGKRVQ Sbjct: 193 MLEAGLPEGVLQVVQGDKEMVDA-ILDHPEIKAVSFVGSSDIAHYVYRRGVAAGKRVQAM 251 Query: 251 LGGKNPTLVADSANPAEAADIVANGGFGTTGQSCTACSRAI-VHEDVYDDFVAELVDRAE 309 G KN +V A+ + + +A FG+ G+ C A + V + D A+L+ E Sbjct: 252 GGAKNHGIVMPDADLDQVVNDLAGAAFGSAGERCMALPVVVPVGDKTADALRAKLLPAIE 311 Query: 310 SLDVGPGTD--HEMGPQVSESELSSTLEYIDIAEAEGATLVAGGGVPEGEAVETGHFVEP 367 +L VG TD GP V+ + + YI + EGA LV G + E G FV P Sbjct: 312 ALRVGVSTDAGAHYGPVVTAAHKAKIESYIQMGVDEGAELVVDGRGFTLQGHEQGFFVGP 371 Query: 368 TVFTDVDPDMRIAQEEVFGPVVAVIEVSDFDEGLAVANDVDYGLSASIVTDDHTEANRFV 427 T+F V P M+ QEE+FGPV+ ++ DF+ L + ++ YG +I T + A F Sbjct: 372 TLFDRVTPQMQSYQEEIFGPVLQIVRAPDFETALRLPSEHQYGNGVAIFTRNGHAAREFA 431 Query: 428 DEVEAGVVKVNDKTTGLELHVPFGGFKRSSSETWREQGDAGLDFYTIEKTV 478 V G+V +N + FGG+KRS+ + G G+ F+T KTV Sbjct: 432 ARVNVGMVGINVPIPVPVAYHTFGGWKRSAFGDTNQHGMEGIKFFTKVKTV 482 Lambda K H 0.310 0.130 0.370 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: 556 Number of extensions: 25 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: 482 Length of database: 503 Length adjustment: 34 Effective length of query: 448 Effective length of database: 469 Effective search space: 210112 Effective search space used: 210112 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (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