Align Alpha-ketoglutarate semialdehyde dehydrogenase; KGSADH; EC 1.2.1.26 (characterized)
to candidate WP_017549863.1 C792_RS0112845 aldehyde dehydrogenase family protein
Query= SwissProt::D4GP41 (482 letters) >NCBI__GCF_000330705.1:WP_017549863.1 Length = 488 Score = 426 bits (1095), Expect = e-124 Identities = 216/476 (45%), Positives = 304/476 (63%), Gaps = 3/476 (0%) Query: 6 KNYVNGEWVTSETGETTEVTNPANPSEVVAAYQHSNENDAAAAVDAAVAAEDEWRNTPGP 65 KN++NG W T E + NPAN EVV+++ S D + A+D+A +W++ P P Sbjct: 10 KNFINGTWTTPSGKELKQGVNPANTKEVVSSFYQSTSEDLSDAIDSASKGFQQWKDIPAP 69 Query: 66 ERGRILREAGTLLAQRKDELTEILTAEEGKARPEAAGEVQRAIDIFHYFSSKAADLGGTK 125 +RG L + L+ + KD+L + + EEGK +A EV A I Y++ + L G+ Sbjct: 70 QRGEYLYKISALMEEEKDDLAKTMVQEEGKTYNDAIKEVGYAAGIVKYYAGECRRLKGSI 129 Query: 126 KGASGPNTNLYTRQEPVGVAALITPWNYPIAIPAWKLAPALAAGNTVVLKPASIAPGVVI 185 A P+ + T+ EP+GV ++TPWN+P++IPAWK APALA+GN VVLKP+S P V+ Sbjct: 130 LEADMPDIQIQTKPEPLGVVLVVTPWNFPLSIPAWKTAPALASGNAVVLKPSSETPLTVM 189 Query: 186 EIARALDEAGLPDGVLNVVTGPGSSVGSEFIGNEGTDLVSFTGSSQVGEMVYEQATDAGK 245 + + AG+P GV+N V PG V SE I + V+FTGS+ VGE +Y +A K Sbjct: 190 KFMDIIQRAGVPAGVVNSVIAPGKLV-SEMIHHPAVKAVTFTGSNTVGEKIYAEAAKGMK 248 Query: 246 RVQTELGGKNPTLVADSANPAEAADIVANGGFGTTGQSCTACSRAIVHEDVYDDFVAELV 305 R E+GGKNP ++ + A+ EA I GG+G TGQ+CTA R IVHE V +F +LV Sbjct: 249 RCLLEMGGKNPLIIMEDADIDEAVQIAVTGGYGQTGQACTATGRIIVHEKVVKEFTEKLV 308 Query: 306 DRAESLDVGPGTDH--EMGPQVSESELSSTLEYIDIAEAEGATLVAGGGVPEGEAVETGH 363 R E L VG G +MGPQVS++E STL+ I A+ EGAT++ GGG+P+ +E G+ Sbjct: 309 KRTEQLKVGNGMHEGIDMGPQVSQAERQSTLDLIQSAKDEGATVLTGGGIPQYPELEDGY 368 Query: 364 FVEPTVFTDVDPDMRIAQEEVFGPVVAVIEVSDFDEGLAVANDVDYGLSASIVTDDHTEA 423 F+EPTV ++V P M I+Q+EVFGPV ++IEV D DE ++VANDV+YGLS++I T + Sbjct: 369 FIEPTVISNVKPAMTISQKEVFGPVNSIIEVRDIDEAISVANDVEYGLSSAICTRNIGYM 428 Query: 424 NRFVDEVEAGVVKVNDKTTGLELHVPFGGFKRSSSETWREQGDAGLDFYTIEKTVY 479 N+ + E+EAG+VKVN TTG PFGG+K+SS+ T++E G G+DFY KT Y Sbjct: 429 NKALSEIEAGIVKVNMTTTGTFFQAPFGGYKKSSTGTYKELGSEGMDFYCQYKTRY 484 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: 574 Number of extensions: 25 Number of successful extensions: 3 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: 488 Length adjustment: 34 Effective length of query: 448 Effective length of database: 454 Effective search space: 203392 Effective search space used: 203392 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 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