Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_012707191.1 NGR_RS14395 aldehyde dehydrogenase
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000018545.1:WP_012707191.1 Length = 492 Score = 407 bits (1046), Expect = e-118 Identities = 217/482 (45%), Positives = 303/482 (62%), Gaps = 8/482 (1%) Query: 38 QIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMD 97 ++ I+ +W DA +TF T NP TG+V + +G KED ++AV+AA AF G+ W ++ Sbjct: 5 KMLIDGQWADAALGETFETRNPYTGDVWAAIPKGTKEDAERAVEAAHKAFTSGT-WPKLT 63 Query: 98 ASHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYH 157 AS RG LL RL DLI + LA +E DNGK + L L + + Y+ G ADK Sbjct: 64 ASDRGHLLRRLGDLIAENAERLARIEVTDNGK-LINEMLFQLKYIPQWYHYFGGLADKIE 122 Query: 158 GKTIPIDG-DFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPL 216 G IPID + F+YTR+EP+GVC I PWN PLL+ ++KL PALA GN V K +E T Sbjct: 123 GAVIPIDKPETFNYTRNEPLGVCVGITPWNSPLLLLSYKLAPALAAGNTFVAKPSEFTSA 182 Query: 217 TALYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGS 276 + L A L+++AGFPPGV N+V GFG G + +H+ V K+AFTGS GR I A + Sbjct: 183 STLEFAKLVEQAGFPPGVFNVVTGFGADVGETLTTHKHVAKIAFTGSEGTGRKIGELA-A 241 Query: 277 SNLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFV 336 N K+VTLELGGKSP+I+ +DA++D AV +F GQ C AGSR V+ I+D+ + Sbjct: 242 RNFKKVTLELGGKSPHIVFADAEIDNAVNGVISGIFAATGQTCIAGSRLLVESKIHDQVL 301 Query: 337 ERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAAD--- 393 E+ +A AK+ +G+P + T+ GP Q +KILGYI+ K EGA+ L GG ++ Sbjct: 302 EKVIALAKTARMGDPLSTSTQVGPVTTPPQLEKILGYIDIAKGEGAECLLGGARPSNSEL 361 Query: 394 -RGYFIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFTKD 452 G+F++PT+F V++ M IA+EE+FGPV+ ++ F T EE + AN++ YGLAA +T+D Sbjct: 362 GNGWFVEPTIFAGVRNSMRIAQEEVFGPVLAVIPFDTEEEAIHIANDTNYGLAAGFWTQD 421 Query: 453 LDKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVKTVTVKV 512 + + +S A+QAGTVWVN Y SP GGYK SG GRE G +Q Y + K+V + Sbjct: 422 MRRMLRVSAAIQAGTVWVNTYRTISYMSPLGGYKHSGIGRENGMASIQNYLQTKSVMIST 481 Query: 513 PQ 514 + Sbjct: 482 AE 483 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: 649 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: 492 Length adjustment: 34 Effective length of query: 483 Effective length of database: 458 Effective search space: 221214 Effective search space used: 221214 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 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