Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19); betaine-aldehyde dehydrogenase (EC 1.2.1.8) (characterized)
to candidate WP_033100857.1 JG50_RS0109305 aldehyde dehydrogenase
Query= BRENDA::Q9S795 (501 letters) >NCBI__GCF_000763315.1:WP_033100857.1 Length = 499 Score = 403 bits (1035), Expect = e-117 Identities = 217/486 (44%), Positives = 292/486 (60%), Gaps = 9/486 (1%) Query: 10 LFIDGEWREPILKKRIPIVNPATEEVIGDIPAATTEDVDVAVNAARRALSRNKGKDWAKA 69 L I GE + + NPA E I + AT DVD AV +AR ALS +K WA+ Sbjct: 15 LLIGGEHVPSESGEYFTVYNPANGEAIAQVAKATRADVDRAVQSARDALSNSK---WARW 71 Query: 70 PGAVRAKYLRAIAAKVNERKTDLAKLEALDCGKPLDEAVWDMDDVAGCFEFYADLAEGLD 129 P + R + L IA+ + +R DL +LE L+ GK L A + FE YA + Sbjct: 72 PASRRGQILNKIASIMRQRFNDLVELEVLNSGKALSAAKGQVMQAIEDFELYAGAVTTIQ 131 Query: 130 AKQKAPVSLPMESFKSYVLKQPLGVVGLITPWNYPLLMAVWKVAPSLAAGCTAILKPSEL 189 K PV F Y +K+P+GV I PWNYPL+M WKVAP+LAAGCT ILKP+ L Sbjct: 132 GHTK-PVP---NGFFHYSVKEPVGVCAQIVPWNYPLMMTAWKVAPALAAGCTLILKPASL 187 Query: 190 ASVTCLELADICREVGLPPGVLNVLTGFGSEAGAPLASHPGVDKIAFTGSFATGSKVMTA 249 +T L LADIC E G+P GV+NV+TG G++ G+ L HPGVDK+AFTG TG +M Sbjct: 188 TPLTALVLADICHEAGVPAGVINVITGSGADVGSYLVEHPGVDKVAFTGETTTGKDIMAK 247 Query: 250 AAQLVKPVSMELGGKSPLIVFDDVDLDKAAEWALFGCFWTNGQICSATSRLLVHESIASE 309 A+ +K V++ELGGKSP IVF D DL+ A +++G ++ GQ C A SRL VHE I Sbjct: 248 ASDTLKRVTLELGGKSPNIVFADADLEAAVNGSVYGIYYNTGQSCEARSRLFVHEDIYDA 307 Query: 310 FIEKLVKWSKNIKISDPMEEGCRLGPVVSKGQYEKILKFISTAKSEGATILHGGSRPEHL 369 FIEK V+ +K +K+ DP E +G V+S+GQ++ I ++ A+ EGA +L+GG RPE Sbjct: 308 FIEKFVEQTKKLKLGDPFNEETHVGAVISQGQWDTIDSYVKLAEKEGARVLYGGKRPEGE 367 Query: 370 E--KGFFIEPTIITDVTTSMQIWREEVFGPVLCVKTFASEDEAIELANDSHYGLGAAVIS 427 E KG++ PT+I D T M++ +EE+FGPV+ V F E E ++LAN++ YGL AAV + Sbjct: 368 EFAKGYWYMPTVIVDATNDMRVAQEEIFGPVVVVIKFKDEKEVVKLANETMYGLAAAVWT 427 Query: 428 NDTERCDRISEAFEAGIVWINCSQPCFTQAPWGGVKRSGFGRELGEWGLDNYLSVKQVTL 487 D R R++ +AG+V IN F P+GG K+SGFGREL L+ Y+ K V Sbjct: 428 RDFGRAHRVASQLKAGVVMINNPFSAFPGLPFGGYKQSGFGRELAIESLELYMETKSVLS 487 Query: 488 YTSNDP 493 Y P Sbjct: 488 YVGPKP 493 Lambda K H 0.318 0.135 0.416 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: 629 Number of extensions: 21 Number of successful extensions: 2 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: 501 Length of database: 499 Length adjustment: 34 Effective length of query: 467 Effective length of database: 465 Effective search space: 217155 Effective search space used: 217155 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 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