Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_017359492.1 BA79_RS13175 aldehyde dehydrogenase family protein
Query= BRENDA::P05091 (517 letters) >NCBI__GCF_000691145.1:WP_017359492.1 Length = 494 Score = 518 bits (1334), Expect = e-151 Identities = 258/475 (54%), Positives = 334/475 (70%), Gaps = 3/475 (0%) Query: 38 QIFINNEWHDAVSRKTFPTVNPSTGEVICQVAEGDKEDVDKAVKAARAAFQLGSPWRRMD 97 +++IN ++ + KTF T NP+TGE + V E D+D+AVKAA+ AF PWR M Sbjct: 21 KLYINGQFVTSHDNKTFSTPNPATGETLIDVYEAGAADIDEAVKAAKKAFH--GPWRSMS 78 Query: 98 ASHRGRLLNRLADLIERDRTYLAALETLDNGKPYVISYLVDLDMVLKCLRYYAGWADKYH 157 A+ R RL+ +LADL+E + LA LETLDNGKP + D+ + ++ +RYYAGW K Sbjct: 79 AAERARLMFKLADLMEEHQEELAQLETLDNGKPINETTNADIPLAIEHMRYYAGWTTKMT 138 Query: 158 GKTIPIDGDFFSYTRHEPVGVCGQIIPWNFPLLMQAWKLGPALATGNVVVMKVAEQTPLT 217 G+T+P+ +F+YTRHEPVGV GQIIPWNFPLLM WK+G ALATG +V+K AEQTPL+ Sbjct: 139 GQTLPVSQGYFNYTRHEPVGVVGQIIPWNFPLLMAMWKMGAALATGCTIVLKPAEQTPLS 198 Query: 218 ALYVANLIKEAGFPPGVVNIVPGFGPTAGAAIASHEDVDKVAFTGSTEIGRVIQVAAGSS 277 ALY+A L+ +AGFP GV+NIVPGFG TAG A+ H DV+K+AFTGST +G++I A S Sbjct: 199 ALYLAELVDKAGFPEGVINIVPGFGETAGEALTDHPDVNKLAFTGSTSVGKLIMEKAAKS 258 Query: 278 NLKRVTLELGGKSPNIIMSDADMDWAVEQAHFALFFNQGQCCCAGSRTFVQEDIYDEFVE 337 +KRVTLELGGKSPNII+ DAD+ A+ A + FNQGQ CCAGSR FV YDE V+ Sbjct: 259 -IKRVTLELGGKSPNIILPDADLKKAIPGALNGVMFNQGQVCCAGSRVFVHRSQYDEVVD 317 Query: 338 RSVARAKSRVVGNPFDSKTEQGPQVDETQFKKILGYINTGKQEGAKLLCGGGIAADRGYF 397 + A S G T+ GP V + Q +++LGYI GK EGA + GG + GYF Sbjct: 318 QMAKYATSLKQGAGLHHDTQIGPLVSKEQHERVLGYIEKGKSEGATAVVGGDCPYEAGYF 377 Query: 398 IQPTVFGDVQDGMTIAKEEIFGPVMQILKFKTIEEVVGRANNSTYGLAAAVFTKDLDKAN 457 + PTVF DV+D MTIAKEEIFGPV+ + + +I+EVV RAN S YGLAA ++T++L A+ Sbjct: 378 VSPTVFRDVEDEMTIAKEEIFGPVLSAIPYDSIDEVVERANQSDYGLAAGLWTENLKHAH 437 Query: 458 YLSQALQAGTVWVNCYDVFGAQSPFGGYKMSGSGRELGEYGLQAYTEVKTVTVKV 512 ++ L+AGT+WVNCY+VF A SPFGGYK SG GRE+G Y L YTEVK+V + + Sbjct: 438 DIAARLEAGTIWVNCYNVFDAASPFGGYKQSGLGREMGSYALNNYTEVKSVWINL 492 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: 675 Number of extensions: 22 Number of successful extensions: 3 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: 494 Length adjustment: 34 Effective length of query: 483 Effective length of database: 460 Effective search space: 222180 Effective search space used: 222180 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