Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_052668356.1 NITAL_RS21380 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000969705.1:WP_052668356.1 Length = 495 Score = 389 bits (998), Expect = e-112 Identities = 211/464 (45%), Positives = 286/464 (61%), Gaps = 13/464 (2%) Query: 39 IFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMDA 98 +FI E+ D +F T++PST E + +VA G DVD+AVKAAR AF+ W ++ Sbjct: 37 LFIGGEFVDPADGGSFATISPSTEEHLAEVALGTATDVDRAVKAARKAFRT---WSKLPG 93 Query: 99 SHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHG 158 + RG+ L RLA L++ A LE++DNGKP S VD+ L ++AGWADK Sbjct: 94 AERGKYLYRLARLLQERAREFAVLESIDNGKPIRESRDVDVPTAAAHLFHHAGWADKLDW 153 Query: 159 KTIPIDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLTA 218 + P+GV GQ+IPWNFPLLM AWK+ PALA GN VV+K AE TPLTA Sbjct: 154 AGLG--------PAPRPLGVAGQVIPWNFPLLMLAWKVAPALACGNTVVLKPAETTPLTA 205 Query: 219 LYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSSN 278 L A L ++A PPGV+NIV G G T GAA+ H+DVDKVAFTGSTE+G+ IQ A + Sbjct: 206 LLFAELCQQADLPPGVINIVTGAGET-GAAVVGHDDVDKVAFTGSTEVGKAIQRALAGTG 264 Query: 279 LKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFVER 338 KR+TLELGGK+ NI+ DA +D AVE +FFNQG CCAGSR VQE ++D V++ Sbjct: 265 -KRLTLELGGKAANIVFDDAPIDQAVEGIVAGIFFNQGHVCCAGSRLLVQESVHDLVVDK 323 Query: 339 SVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAADRGYFI 398 R ++ +G+P D T+ G Q ++I + G+ EG G++ Sbjct: 324 LQQRLETLRLGDPLDKNTDIGAINSAEQLERITTLVEAGEAEGGTRWESPCELPSSGFWF 383 Query: 399 QPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFTKDLDKANY 458 +PTVF + +A+EEIFGPV+ +L F+T +E V +ANN+ YGL+A V+T+ + + Sbjct: 384 KPTVFTGIGQSSRVAQEEIFGPVLSVLTFRTPDEAVAKANNTPYGLSAGVWTEKGSRILW 443 Query: 459 LSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAY 502 ++ L+AG VW N ++ F SPFGGYK SG GRE G +GL +Y Sbjct: 444 MADRLRAGVVWANTFNRFDPTSPFGGYKESGFGREGGRHGLASY 487 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: 657 Number of extensions: 24 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: 495 Length adjustment: 34 Effective length of query: 483 Effective length of database: 461 Effective search space: 222663 Effective search space used: 222663 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