Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_017549143.1 C792_RS0108995 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000330705.1:WP_017549143.1 Length = 501 Score = 392 bits (1006), Expect = e-113 Identities = 204/475 (42%), Positives = 300/475 (63%), Gaps = 7/475 (1%) Query: 38 QIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMD 97 ++FIN E ++ T +NP+TGEVI +VA ED ++AV AAR AF+ S W+ Sbjct: 16 ELFINGEKVESSDGGTNDIINPATGEVIAKVAMATGEDAERAVMAARDAFE-NSKWKIYP 74 Query: 98 ASHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYH 157 AS R ++LNR+A ++ L LE L++GK + + ++ ++ YYAG + Sbjct: 75 ASKRAKILNRIASIMRERFKELVELEVLNSGKS-INAATGQINQAVEDFEYYAGAVCNHG 133 Query: 158 GKTIPIDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLT 217 G+T + G F +YT EPVGVC QI+PWN+PL+M AWK+ PALA G VV+K A TPLT Sbjct: 134 GQTNDVPGQFHNYTEKEPVGVCAQIVPWNYPLMMAAWKVAPALAAGCTVVLKPASLTPLT 193 Query: 218 ALYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSS 277 AL + + +EAG P GV+NI+PG G G + H +VDKVAFTGST+ G+ I ++ S Sbjct: 194 ALILGEICQEAGVPDGVINILPGSGSRVGDYLVEHPEVDKVAFTGSTDTGKDI-MSKASR 252 Query: 278 NLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFVE 337 LKR+TLELGGKSP +I DA+++ AV + + ++ N GQ C A SR +V++ IYD+FVE Sbjct: 253 TLKRLTLELGGKSPALIFGDAELENAVASSVYGIYNNTGQSCDARSRIYVEDRIYDKFVE 312 Query: 338 RSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAADRGY- 396 + V + K +G+P +T G +D++Q + + YI T +QEGA + GG + GY Sbjct: 313 QFVEKTKQMKMGDPMSKETHMGSLIDKSQLESVEAYIETARQEGATIAYGGNRLSIEGYE 372 Query: 397 ---FIQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFTKDL 453 +++PT+ DV + MT+ ++EIFGPV+ I +F +E V ANN+ YGLA++++T+D Sbjct: 373 GGFWLEPTIITDVTEDMTVVRDEIFGPVVVISRFSDEKEAVSLANNTIYGLASSIYTEDT 432 Query: 454 DKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVKTV 508 KA ++ ++AG V +NC +PFGGYK SG GREL L Y+E K++ Sbjct: 433 RKAKRVADKIRAGIVMINCPFSAFPGTPFGGYKQSGFGRELSAETLDLYSETKSI 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: 633 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: 517 Length of database: 501 Length adjustment: 34 Effective length of query: 483 Effective length of database: 467 Effective search space: 225561 Effective search space used: 225561 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