Align lactaldehyde dehydrogenase (EC 1.2.1.22); 2,5-dioxovalerate dehydrogenase (EC 1.2.1.26) (characterized)
to candidate WP_078210708.1 BXU11_RS01185 aldehyde dehydrogenase family protein
Query= BRENDA::Q97UA1 (478 letters) >NCBI__GCF_002017945.1:WP_078210708.1 Length = 517 Score = 220 bits (561), Expect = 8e-62 Identities = 145/471 (30%), Positives = 247/471 (52%), Gaps = 19/471 (4%) Query: 15 SGEEYLDINPADKDHVLAKIRLYTKDDVKEAINKAVAKFDEWSRTPAPKRGSILLKAGEL 74 SG +P D ++A + + D ++ + A A F + PAP+RG I+ + GE Sbjct: 35 SGSLLESYSPVD-GQLIASVTTSSAADYEKVMQTATAAFKTFRLMPAPQRGEIVRQFGEK 93 Query: 75 MEQEAQEFALLMTLEEGKTLKDSMFEVTRSYNLLKFYGALAFKISGKTLPSADPNTRIFT 134 + + + L++ E GK+L++ EV ++ F L+ ++ G T+ S P R++ Sbjct: 94 LRKNKEALGKLVSYEMGKSLQEGYGEVQEMIDICDFAVGLSRQLHGLTMHSERPGHRMYE 153 Query: 135 VKEPLGVVALITPWNFPLSIPVWKLAPALAAGNTAVIKPATKTPLMVAK----LVEVLSK 190 LGVV +I+ +NFP+++ W A A G+ V KP+ KTPL + EVL + Sbjct: 154 QYHSLGVVGIISAFNFPVAVWAWNTALAWICGDVCVWKPSEKTPLCGVACQNIIAEVLKE 213 Query: 191 AGLPEGVVNLVVGKGSEVGDTIVSDDNIAAVSFTGSTEVGKRIYKLVGNKNRMTRIQLEL 250 LPEG+ L+ G + +G+ + D + +S TGST +GK + + V R+ + LEL Sbjct: 214 NNLPEGISCLINGDYT-IGEMLTKDTRVPLISATGSTRMGKIVAQTVA--GRLGKSLLEL 270 Query: 251 GGKNALYVDKSADLTLAAELAVRGGFGLTGQSCTATSRLIINKDVYTQFKQRLLERVKKW 310 GG NA+ V AD+ + AV G G GQ CT+T RLII++ +Y + K ++ + Sbjct: 271 GGNNAIIVTPDADIKMTVIGAVFGAVGTAGQRCTSTRRLIIHESMYDKVKDTIVAAYGQL 330 Query: 311 RVG-PGTEDVDMGPVVDEGQFKKDLEYIEYGKNVGAKLIYGGNIIPGKGY----FLEPTI 365 R+G P E +GP++D+ + + + G K++ G ++ G+GY +++P I Sbjct: 331 RIGNPLDEKNHVGPLIDKQAVEMYNQALTKVVAEGGKILVEGGVLSGEGYESGCYVKPAI 390 Query: 366 FEGVTSDMRLFKEEIFGPVLSVTE-AKDLDEAIRLVNAVDYGHTAGIVASDIKAINEFVS 424 E S + + E F PVL + + + D+D AI+L N V G ++ I+ ++++ F+S Sbjct: 391 AEAQNS-FEIVQHETFAPVLYLLKYSGDVDNAIKLQNGVAQGLSSAIMTNNLREAERFLS 449 Query: 425 RV--EAGVIKVNKPTVGLELQAPFGGFKNSGATTWKEMGEDALEFYLKEKT 473 + G+ VN T G E+ FGG K +G +E G DA + Y++ +T Sbjct: 450 VAGSDCGIANVNIGTSGAEIGGAFGGEKETGG--GRESGSDAWKVYMRRQT 498 Lambda K H 0.316 0.135 0.389 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: 566 Number of extensions: 30 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: 478 Length of database: 517 Length adjustment: 34 Effective length of query: 444 Effective length of database: 483 Effective search space: 214452 Effective search space used: 214452 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 (21.6 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