Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_068167173.1 HTA01S_RS03325 aldehyde dehydrogenase family protein
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_001592305.1:WP_068167173.1 Length = 506 Score = 311 bits (798), Expect = 2e-89 Identities = 178/474 (37%), Positives = 267/474 (56%), Gaps = 13/474 (2%) Query: 11 LVSGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTPKVRAECLLKL 70 +V +G+ V P +G V + A ++AE ++ A+ AA AA WG+T R+ LLK+ Sbjct: 28 VVPCKGQYFDVITPVSGQVYTQAARSTAEDIELALDAAHAAADAWGKTDAATRSNILLKI 87 Query: 71 ADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAAGEYLEGH 130 AD IE+N ++ A E+ + GK + N +IP VD FR+FAG R G A E Sbjct: 88 ADRIEQNLELLAYAETVDNGKAIRETLNADIPLTVDHFRYFAGCVRAQEG-ALSNIDENT 146 Query: 131 TSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTALKLAELAKD 190 + ++PLGVV I PWN+P++MAAWKLAPAL AGNCVVLKP+E TP++ L LAEL D Sbjct: 147 VAYHIQEPLGVVGQIIPWNFPILMAAWKLAPALGAGNCVVLKPAESTPISILILAELIAD 206 Query: 191 IFPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIKRTHMELGGK 250 + P GV+NI+ G G+ G PL ++ ++ TGS TG I A+++ +ELGGK Sbjct: 207 LLPPGVLNIVNGFGREAGMPLAQSKRIAKIAFTGSTTTGRVIAQAAANNLIPATLELGGK 266 Query: 251 APVIVF------DDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLGAAV 304 +P + F DDA ++ VEG+ F +N G+ CT R Q+ IYD +E++ V Sbjct: 267 SPNVFFADIMDKDDAFLDKCVEGLVLFA-FNQGEVCTCPSRALIQESIYDRFMERVLKRV 325 Query: 305 ATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKG----NGYYY 360 A ++ P D + +G +S L ++ +E KA G +I GG+ G GYY Sbjct: 326 AAIQQANPLDSESMMGAQASKEQLTKILSYLELGKAEGAEVLIGGGQAHLGGDLEGGYYV 385 Query: 361 APTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRAHR 420 PTL G I Q+E+FGPV++VT F +E + + AND+ YGL + VW+++ A+R Sbjct: 386 QPTLFKGH-NKMRIFQEEIFGPVLAVTTFKDEAEALAIANDTLYGLGAGVWSRNGNVAYR 444 Query: 421 VSARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVMVKH 474 + ++ G W N + + GG K SG G++ L+ Y ++++V + Sbjct: 445 MGRAIKAGRVWTNCYHAYPAHAAFGGYKESGIGRETHKMMLDHYQQTKNLLVSY 498 Lambda K H 0.317 0.134 0.397 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: 569 Number of extensions: 29 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: 474 Length of database: 506 Length adjustment: 34 Effective length of query: 440 Effective length of database: 472 Effective search space: 207680 Effective search space used: 207680 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 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