Align glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate 208821 DVU3294 aldehyde dehydrogenase (NADP) family protein
Query= BRENDA::Q88RC0 (480 letters) >MicrobesOnline__882:208821 Length = 464 Score = 226 bits (576), Expect = 1e-63 Identities = 152/443 (34%), Positives = 224/443 (50%), Gaps = 10/443 (2%) Query: 27 TIKVTNPATGEVIGTVPKMGTAETRRAIEAADKAL--PAWRALTAKERSAKLRRWFELMI 84 +I V NP +G VP M AE A+E A PA R + A ER A L R LM Sbjct: 3 SITVRNPFDLSTVGEVPLMSEAEAFAALERAHALHGDPAHR-IPAHERLAILERLATLMR 61 Query: 85 ENQDDLARLMTTEQGKPLAEAKGEIAYAASFIEWFAEEAKRIYGDTIP-GHQP---DKRL 140 + + L R E GKP A++ E+ A + W A E ++ G +P G P + Sbjct: 62 THAEALVRDAVREGGKPWADSVVEVERAIDGVRWAARELAQLGGREVPMGLTPASAGRLA 121 Query: 141 IVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTPYSALALVELAHRAG 200 +++P GV AI+ +N P +I +A PA AAGC +++KPAS TP S ++ L H AG Sbjct: 122 FTVREPRGVVLAISAFNHPVNLIVHQAVPAFAAGCPVLVKPASATPLSCRNVLRLMHEAG 181 Query: 201 IPAGVLSVVTGSAGEVGGELTGNSLVRKLSFTGSTEIGRQLMEECAKDIKKVSLELGGNA 260 +P +++ +A +L + V LSF GS+ +G L + A +LE GG A Sbjct: 182 VPEAWATMLPCAAA-TAEKLVADPRVAFLSFIGSSRVGWHLRSKLAPGAT-CALEHGGAA 239 Query: 261 PFIVFDDADLDKAVEGAIISKYRNNGQTCVCANRIYVQDGVYDAFAEKLAAAVAKLKIGN 320 P ++ ADLD A+ + + + GQ CV R++ FAE+LAAA A+L G+ Sbjct: 240 PVVLDASADLDAALPLLLKGGFYHAGQVCVSVQRVFAPHETARTFAERLAAAAAQLPTGD 299 Query: 321 GLEEGTTTGPLIDGKAVAKVQEHIEDAVSKGAKVLSGGKLIEGNFFEPTILVDVPKTAAV 380 + T GPLID + V++V E +E+A + G VL GG + + PT++ D P+ + Sbjct: 300 PMRHDTAVGPLIDPREVSRVHEWVEEARAGGGTVLCGGAPLSETLYSPTVVYDPPQGCRL 359 Query: 381 AKEETFGPLAPLFRFKDEAEVIAMSNDTEFGLASYFYARDMSRVFRVAEALEYGMVGINT 440 A+ E FGP+ +F +D E IA +ND F + +ARD+ A L V +N Sbjct: 360 ARNEVFGPVVAVFSTRDRDEAIARANDVPFIFQAAVFARDVDVALDTARRLNATGVMVND 419 Query: 441 GLISN-EVAPFGGIKASGLGREG 462 + PFGG SG+G G Sbjct: 420 HTAFRVDWMPFGGRGESGMGTGG 442 Lambda K H 0.317 0.134 0.384 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: 484 Number of extensions: 25 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: 480 Length of database: 464 Length adjustment: 33 Effective length of query: 447 Effective length of database: 431 Effective search space: 192657 Effective search space used: 192657 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 (21.6 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