Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_003466863.1 J416_RS06115 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000359605.1:WP_003466863.1 Length = 486 Score = 257 bits (656), Expect = 8e-73 Identities = 162/483 (33%), Positives = 257/483 (53%), Gaps = 13/483 (2%) Query: 37 NQIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRM 96 N +I+ +W + S+ + NP E + K D+D A + A+ A + W++ Sbjct: 8 NSQYIDGQWKEGNSQLSMKNQNPYNQETLTTYQAASKTDIDHAYQVAQKAQK---KWQQQ 64 Query: 97 DASHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKY 156 + + + + + +IE + + + G + + ++ +V L+ + + + Sbjct: 65 NPTFQRGIFEQAVHVIEDHHEAIVEVINKEIGGTRLKAEF-EISLVKNMLKEASTFPFRM 123 Query: 157 HGKTIP--IDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQT 214 GK +P DG R P+GV G I P+NFP + + PALATGN VV+K E T Sbjct: 124 DGKILPSMTDGKENQVYRI-PIGVVGVISPFNFPFFLSMKSIAPALATGNGVVVKPHEHT 182 Query: 215 PLTA-LYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVA 273 +T +A + +EAG P G++NIV G A H ++FTGST IGR I Sbjct: 183 VITGGTMIAKIFEEAGLPQGLLNIVTTEISEIGDAFVEHPIPQSISFTGSTAIGRHIGSI 242 Query: 274 AGSSNLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYD 333 AG LK V LELGG S I++ DAD+D AV A F+ F +QGQ C + +R + ED+YD Sbjct: 243 AGRE-LKDVHLELGGNSGLIVLDDADIDLAVSAAIFSRFTHQGQICMSANRIIIHEDVYD 301 Query: 334 EFVERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAAD 393 FVE+ VA+ G+P D T GP ++E Q + I G EGA L G + Sbjct: 302 TFVEKYVAKVNELSCGDPCDDTTIIGPLINEKQVENTKQIIEAGINEGADPLVHGQV--- 358 Query: 394 RGYFIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFTKDL 453 RG ++P VFG+V MT+AKEE+F PV+ + K + EE++ N+++YGL+ AV T+++ Sbjct: 359 RGNVVEPVVFGNVTKNMTVAKEEMFAPVVSLFKASSEEEILDIVNDTSYGLSGAVHTQNI 418 Query: 454 DKANYLSQALQAGTVWVNCYDVFGAQS-PFGGYKMSGSGRELGEYGLQAYTEVKTVTVKV 512 ++ L++ ++ G + +N + + FGG K SG GR GE+ L A+T K ++++ Sbjct: 419 ERGAQLAKQMETGMIHINDGTINDEPNVAFGGMKNSGVGRLNGEWSLDAFTTTKWISIQH 478 Query: 513 PQK 515 +K Sbjct: 479 NRK 481 Lambda K H 0.319 0.136 0.409 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: 31 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: 517 Length of database: 486 Length adjustment: 34 Effective length of query: 483 Effective length of database: 452 Effective search space: 218316 Effective search space used: 218316 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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