Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_164924503.1 NGR_RS26215 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000018545.1:WP_164924503.1 Length = 491 Score = 382 bits (982), Expect = e-110 Identities = 213/479 (44%), Positives = 294/479 (61%), Gaps = 9/479 (1%) Query: 37 NQIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRM 96 ++++I+ +W A +TF VNP+T EVI ++A EDVD AVKAAR AF W ++ Sbjct: 3 SELYIDGKWTAAAKGRTFDVVNPATEEVIHRIAAATPEDVDVAVKAARRAFDKDG-WPKL 61 Query: 97 DASHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKY 156 + R + L +AD I ++ +A LE +DNGKP+ + D+ C +YAG A++ Sbjct: 62 SGAQRAKYLRAIADGIRARQSEIARLEVIDNGKPFPEADW-DVADAAGCFDFYAGLAEQL 120 Query: 157 -HGKTIPI---DGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAE 212 + PI D F S EP+GV G IIPWN+PLLM AWK+ PALA G +V+K AE Sbjct: 121 DNNPEEPIALADARFTSKAVKEPIGVAGAIIPWNYPLLMAAWKVAPALAAGCTIVLKPAE 180 Query: 213 QTPLTALYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQV 272 T LTAL +A + EAG PPGV+NI+ G G AG AI H+ VDK+AFTGS +G I + Sbjct: 181 VTSLTALELAAIADEAGLPPGVLNILTGSGSVAGQAIIDHKHVDKLAFTGSGPVGSKI-M 239 Query: 273 AAGSSNLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIY 332 AA + ++KRV+LELGGKSP ++ DAD+D AVE F +F+NQGQ C A SR VQE IY Sbjct: 240 AAAARDIKRVSLELGGKSPFVVFDDADIDEAVEWIMFGIFWNQGQVCSATSRILVQEGIY 299 Query: 333 DEFVERSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGG--GI 390 D + R V K +G+ + GP V + Q ++++ I K GA + CGG Sbjct: 300 DRLLARLVEETKKIRIGDGLEDGVLLGPLVSKRQHEQVVAAIEAAKTAGATVACGGKRPE 359 Query: 391 AADRGYFIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFT 450 D+GY+++PT+ +V +EEIFGPV+ I F T E + AN+S +GLAAAV + Sbjct: 360 GFDKGYYLEPTILTEVPLESDAWREEIFGPVVCIRPFSTEAEAIELANDSRFGLAAAVMS 419 Query: 451 KDLDKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVKTVT 509 KD +A ++ A +AG VW+NC ++P+GGYK SG GRELG +GL+ Y E K +T Sbjct: 420 KDDVRAERVASAFRAGIVWINCSQPTFTEAPWGGYKESGIGRELGRWGLENYLETKQIT 478 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: 677 Number of extensions: 33 Number of successful extensions: 5 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: 491 Length adjustment: 34 Effective length of query: 483 Effective length of database: 457 Effective search space: 220731 Effective search space used: 220731 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