Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate 208821 DVU3294 aldehyde dehydrogenase (NADP) family protein
Query= BRENDA::Q9CZS1 (519 letters) >MicrobesOnline__882:208821 Length = 464 Score = 189 bits (481), Expect = 1e-52 Identities = 146/463 (31%), Positives = 213/463 (46%), Gaps = 16/463 (3%) Query: 60 NPTTGEVIGHVAEGDRADVDLAVKAAREAFRLGSPWRRMDASERGRLLNRLADLVERDRV 119 NP +G V A+ A++ A G P R+ A ER +L RLA L+ Sbjct: 8 NPFDLSTVGEVPLMSEAEAFAALERAHALH--GDPAHRIPAHERLAILERLATLMRTHAE 65 Query: 120 YLASLETLDNGKPFQESYVLDLDEVIKVYRYFAGWADKWHGKTIPM-----DGEHFCFTR 174 L + GKP+ +S V++++ I R+ A + G+ +PM FT Sbjct: 66 ALVRDAVREGGKPWADS-VVEVERAIDGVRWAARELAQLGGREVPMGLTPASAGRLAFTV 124 Query: 175 HEPVGVCGQIIPWNFPLVMQGWKLAPALATGNTVVMKVAEQTPLSALYLASLIKEAGFPP 234 EP GV I +N P+ + + PA A G V++K A TPLS + L+ EAG P Sbjct: 125 REPRGVVLAISAFNHPVNLIVHQAVPAFAAGCPVLVKPASATPLSCRNVLRLMHEAGVPE 184 Query: 235 GVVNIITGYGPTAGAAIAQHMDVDKVAFTGSTEVG-HLIQKAAGESNLKRVTLELGGKSP 293 ++ TA +A V ++F GS+ VG HL K A + LE GG +P Sbjct: 185 AWATMLPCAAATAEKLVADPR-VAFLSFIGSSRVGWHLRSKLAPGATC---ALEHGGAAP 240 Query: 294 SIVLADADMEHAVDQCHEALFFNMGQCCCAGSRTFVEESIYREFLERTVEKAKQRKVGNP 353 ++ A AD++ A+ + F++ GQ C + R F R F ER A Q G+P Sbjct: 241 VVLDASADLDAALPLLLKGGFYHAGQVCVSVQRVFAPHETARTFAERLAAAAAQLPTGDP 300 Query: 354 FELDTQQGPQVDKEQFERILGYIRLGQKEGAKLLCGGERLGERGFFIKPTVFGDVQDGMR 413 DT GP +D + R+ ++ + G +LCGG L E PTV D G R Sbjct: 301 MRHDTAVGPLIDPREVSRVHEWVEEARAGGGTVLCGGAPLSET--LYSPTVVYDPPQGCR 358 Query: 414 IAKEEIFGPVQPLFKFKKIEEVIQRANNTRYGLAAAVFTRDLDKAIYFTQALQAGTVWVN 473 +A+ E+FGPV +F + +E I RAN+ + AAVF RD+D A+ + L A V VN Sbjct: 359 LARNEVFGPVVAVFSTRDRDEAIARANDVPFIFQAAVFARDVDVALDTARRLNATGVMVN 418 Query: 474 TYNIVTCH-TPFGGFKESGNGRELGEDGLRAYTEVKTVTIKVP 515 + PFGG ESG G + T K + ++ P Sbjct: 419 DHTAFRVDWMPFGGRGESGMGTGGIGPAMHEMTTEKLIVLRSP 461 Lambda K H 0.320 0.137 0.416 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: 522 Number of extensions: 28 Number of successful extensions: 5 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: 519 Length of database: 464 Length adjustment: 34 Effective length of query: 485 Effective length of database: 430 Effective search space: 208550 Effective search space used: 208550 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 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