Align Alpha-ketoglutaric semialdehyde dehydrogenase; alphaKGSA dehydrogenase; 2,5-dioxovalerate dehydrogenase; EC 1.2.1.26 (characterized)
to candidate 202599 SO3496 aldehyde dehydrogenase (NCBI ptt file)
Query= SwissProt::P42236 (488 letters) >FitnessBrowser__MR1:202599 Length = 498 Score = 290 bits (742), Expect = 8e-83 Identities = 175/480 (36%), Positives = 273/480 (56%), Gaps = 13/480 (2%) Query: 13 FINGEWVKSQSGDMVKVENPADVNDIVGYVQNSTAEDVERAVTAANEA--KTAWRKLTGA 70 FINGE+ + SG+ +P D ++ V + D AV A E W K Sbjct: 24 FINGEYRDASSGNTFDCISPID-GRLLAPVASCDLMDANIAVANAREVFDSGVWSKAAPV 82 Query: 71 ERGQYLYKTADIMEQRLEEIAACATREMGKTLPEAKGETARGIAILRYYAGEGMRKTGDV 130 +R Q + + A+++E+ E+A T +MGK + +K G A ++GE + K D Sbjct: 83 KRKQVMIRFAELLEENANELALLETLDMGKPIRFSKAVDVAGAARAIRWSGEAIDKLYDE 142 Query: 131 IPSTDKDALMFTTRVPLGVVGVISPWNFPVAIPIWKMAPALVYGNTVVIKPATETAVTCA 190 + T + + TR P+GVV I PWNFP+ + WK+ PALV GN+V++KP+ ++ +T Sbjct: 143 LAPTAHNEIGMITREPVGVVAAIVPWNFPLLMACWKLGPALVTGNSVILKPSEKSPLTAI 202 Query: 191 KIIACFEEAGLPAGVINLVTGPGSVVGQGLAEHDGVNAVTFTGSNQVGK-IIGQAALARG 249 +I +AG+P GV+N++ G G VG+ LA H V+ + FTGS ++ K ++ A + Sbjct: 203 RIAELAVQAGIPKGVLNVLPGYGHTVGKALALHMDVDTLVFTGSTKIAKQLMIYAGESNM 262 Query: 250 AKYQLEMGGKNPVIVADDA-DLEAAAEAVITGAFRSTGQKCTATSRVIVQSGIYERFKEK 308 + LE GGK+P IV +DA DL+AAA A + G+ CTA SR++V+SG+ + Sbjct: 263 KRVWLEAGGKSPNIVFNDAPDLKAAAVAAAEAIGFNQGEVCTAGSRLLVESGVKDELVGL 322 Query: 309 LLQRTKDITIGDSLKEDVWMGPIASKNQLDNCLSYIEKGKQEGASLLIGGEKL--ENGKY 366 + + G L+ G + K QLD LSYI+ G+ EGASL+ GG+++ E G Sbjct: 323 IAEELASWQPGHPLEPTTVSGAVVDKQQLDTILSYIKAGQNEGASLVYGGQQVLAETG-- 380 Query: 367 QNGYYVQPAIFDNVTSEMTIAQEEIFGPVIALIKVDSIEEALNIANDVKFGLSASIFTEN 426 G YVQP +F NV ++M IA EEIFGPV+++I+ + +EEA+ IAND +GL+A ++T + Sbjct: 381 --GVYVQPTVFSNVKNQMKIASEEIFGPVLSVIEFNGMEEAIAIANDTIYGLAAGVWTAD 438 Query: 427 IGRMLSFIDEIDAGLVRINAESAGVELQAPFGGMKQSSSHSREQGEAAKDFFTAIKTVFV 486 I + + +G+V IN G ++ APFGG KQ S + R++ + D +T IK ++ Sbjct: 439 ISKAHKTAKALRSGMVWINHYDGG-DMTAPFGGYKQ-SGNGRDKSLHSFDKYTEIKATWI 496 Lambda K H 0.315 0.132 0.374 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: 581 Number of extensions: 27 Number of successful extensions: 6 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: 488 Length of database: 498 Length adjustment: 34 Effective length of query: 454 Effective length of database: 464 Effective search space: 210656 Effective search space used: 210656 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 (21.5 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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