Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_068105462.1 I601_RS01380 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_001653335.1:WP_068105462.1 Length = 506 Score = 349 bits (895), Expect = e-100 Identities = 192/485 (39%), Positives = 276/485 (56%), Gaps = 18/485 (3%) Query: 39 IFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMDA 98 ++I+ W DA T P+ G + V+EG ++D AV AAR+AF G PW A Sbjct: 4 LYIDGTWRDAADGATRDIHCPADGHHVVTVSEGGEQDAVAAVVAARSAFDNG-PWPHTPA 62 Query: 99 SHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYHG 158 R LL+RLAD +E D+ +A LE+LD GK +V S +D+D ++ R++A A G Sbjct: 63 PERAALLHRLADRLEADKDEVARLESLDTGKRFVESQ-IDVDDIVSVFRHFASLAQGEAG 121 Query: 159 KTIPID-GDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLT 217 + + S HEP+GVC I PWN+PLL +WK+ P LA GN ++K +E TP T Sbjct: 122 RVVDAGMPGVVSRVVHEPIGVCTLITPWNYPLLQTSWKVAPCLAAGNTFILKPSELTPST 181 Query: 218 ALYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSS 277 A+++ + +AG P GV N+V G G G + +VD V+FTG GR + VAA + Sbjct: 182 AIWLMGALSDAGLPDGVANLVLGAGDRVGPTLTEAPEVDLVSFTGGVVTGRRVMVAA-AP 240 Query: 278 NLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFVE 337 +K+V LELGGK+PN+I +DAD+D A++ A A+F + GQ C AG+R V++ ++D+ V+ Sbjct: 241 TVKKVALELGGKNPNVIFADADLDAAIDNALTAVFLDSGQVCSAGARLVVEDTVHDQVVD 300 Query: 338 RSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAADRGY- 396 V RA +G PFD E GP + K+ Y+ G EGA L GGG GY Sbjct: 301 ELVRRAGRIRLGGPFDDDAETGPLISAAHRDKVEAYVAAGIAEGATLRVGGGRPEGAGYA 360 Query: 397 -------FIQPTVFGDVQDGMTIAKEEIFGPVMQILKF------KTIEEVVGRANNSTYG 443 + PT+ D M+ +EE FGPV+ + +F E V AN++ YG Sbjct: 361 AGLAEGFYYLPTILDDCSADMSCVQEESFGPVLTVERFTGEDADAREEAAVSIANDTVYG 420 Query: 444 LAAAVFTKDLDKANYLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYT 503 LA AV+T D +A ++ L+ GT+W+N Y + AQ+ +GGYK SG+GRELG GL+ Y Sbjct: 421 LAGAVWTSDAGRAERVASRLRHGTIWINDYHPYVAQAEWGGYKQSGTGRELGIAGLEEYR 480 Query: 504 EVKTV 508 E K + Sbjct: 481 ETKHI 485 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: 700 Number of extensions: 37 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: 506 Length adjustment: 35 Effective length of query: 482 Effective length of database: 471 Effective search space: 227022 Effective search space used: 227022 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