Align aldehyde dehydrogenase ALDH; EC 1.2.1.3 (characterized)
to candidate CA265_RS24850 CA265_RS24850 aldehyde dehydrogenase
Query= CharProtDB::CH_007936 (497 letters) >FitnessBrowser__Pedo557:CA265_RS24850 Length = 454 Score = 244 bits (624), Expect = 4e-69 Identities = 151/456 (33%), Positives = 238/456 (52%), Gaps = 6/456 (1%) Query: 37 QVINPSNEKVITSVHEATEKDVDVAVAAARAAFEGPWRQVTPSERGILINKLADLMERDI 96 Q+INP+ ++ITS+ E + + A + A + W T ER +I +DL+E +I Sbjct: 2 QIINPATAEIITSLEEDNLSTLQLKFDALQKA-QPQWAGKTLQERIAVITHFSDLLEVEI 60 Query: 97 DTLAAIESLDNGKAFTMAKVDLANSIGCLRYYAGWADKIHGQTIDTN-PETLTYTRHEPV 155 + LA++ + + GK ++ ++ + +++ A+K + T+ P ++EP+ Sbjct: 61 EKLASVLTSEVGKPLQQSRNEINGARARIKWMLANAEKYLADEVMTDEPGIKEIIKYEPL 120 Query: 156 GVCGQIIPWNFPLLMWSWKIGPAVAAGNTVVLKTAEQTPLSALYAAKLIKEAGFPAGVIN 215 GV I WN+P L+ PA+ +GNTV+ K +E L+ + KL+K+AG P V + Sbjct: 121 GVVCNISAWNYPYLVGVNVFIPALLSGNTVMYKPSEYATLTGIEIEKLLKKAGVPDDVFH 180 Query: 216 VISGFGRTAGAAISSHMDIDKVAFTGSTLVGRTILQAAAKSNLKKVTLELGGKSPNIVFD 275 + G T A ++ MD + FTGS G+ I + A + + LELGGK P + D Sbjct: 181 IAIGAKETGSALLN--MDFNGYFFTGSYKTGKLIYEKVA-AKMVPCQLELGGKDPLYITD 237 Query: 276 DA-DIDNAISWANFGIFFNHGQCCCAGSRILVQEGIYDKFVARFKERAQKNKVGNPFEQD 334 D D+ A G F+N+GQ CCA RI VQE YD + F + K G P + Sbjct: 238 DVTDVAAAAIGTADGAFYNNGQSCCAVERIYVQEKNYDDYCNAFVTEVKSWKTGIPTAEG 297 Query: 335 TFQGPQVSQLQFDRIMEYINHGKKAGATVATGGDRHGNEGYFIQPTVFTDVTSDMKIAQE 394 + G + Q + + GA + TGG +GY+ +PTV TDVT+DM + QE Sbjct: 298 VYIGALTRKEQISVLENQVKDALNKGAKLLTGGKAVEGKGYYFEPTVLTDVTNDMLVMQE 357 Query: 395 EIFGPVVTIQKFKDEAEAIKIGNSTDYGLAAAVHTKNVNTAIRVSNALKAGTVWINNYNM 454 E FGP++ I K KD+AEA+K+ TDYGL A+V+T + A ++ L AG+ + N + Sbjct: 358 ESFGPIIGIMKVKDDAEALKMMKDTDYGLTASVYTASQERAEKILAQLDAGSGYWNCCDR 417 Query: 455 ISYQAPFGGFKQSGLGRELGSYALENYTQIKTVHYR 490 +S P+ G K SG+G L + +T+ K H R Sbjct: 418 VSAALPWSGRKYSGIGATLSHQGIRAFTKPKGYHLR 453 Lambda K H 0.318 0.134 0.397 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: 496 Number of extensions: 27 Number of successful extensions: 4 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: 497 Length of database: 454 Length adjustment: 33 Effective length of query: 464 Effective length of database: 421 Effective search space: 195344 Effective search space used: 195344 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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