Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate Ac3H11_3961 Aldehyde dehydrogenase B (EC 1.2.1.22)
Query= metacyc::MONOMER-15203 (503 letters) >FitnessBrowser__acidovorax_3H11:Ac3H11_3961 Length = 512 Score = 265 bits (677), Expect = 3e-75 Identities = 170/475 (35%), Positives = 242/475 (50%), Gaps = 8/475 (1%) Query: 10 INGHKTNGVADSHQEVTNPA-TGQVTGQVALASQADVDSAVAAAQAAFPAWSDTPPIRRA 68 I G T+GV TNP+ T V G A+AS+ AVAAA AAFPAWS + P +R Sbjct: 39 IGGAWTDGVRTYQN--TNPSDTRDVIGDYAVASREQALDAVAAAHAAFPAWSLSTPQQRF 96 Query: 69 RVMFKFLELLNAHKDELAEAITREHGKVFTDAQGEVARGIDIVEFACGIPQLLKGDYTEQ 128 ++ + A K EL + + RE GK +A GEV R I +F G G+ Sbjct: 97 DILDAVGNEIIARKAELGDLLAREEGKTLPEAIGEVGRAAAIFKFFAGEALRPGGEVMPS 156 Query: 129 VSTGIDNWTTRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPSASLMMA 188 V G+ TR+PLG + ITP+NFP+ +P W A+A GN V KP+ + P ++ +A Sbjct: 157 VRPGVGIEITREPLGTIGIITPWNFPIAIPAWKIAPALAYGNCVVFKPAEVVPGSAWALA 216 Query: 189 DLLKQAGLPDGVFNVVQGDKDSVEA-LIDHPDVKALSFVGSTPIANLIYERGARSGKRIQ 247 D+L +AGLP GVFN+V G V A L++ + +SF GS + G ++Q Sbjct: 217 DILHRAGLPAGVFNLVMGRGSDVGAVLLEDERIAGVSFTGSVGTGQRVAAACVPRGAKVQ 276 Query: 248 ALGGAKNHMVVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVPRLAERA 307 G KN VV+ DA+L+ AV A I + + S G+RC A S ++ + D+ V + E+ Sbjct: 277 LEMGGKNPFVVLDDADLNVAVGAAINSGFFSTGQRCTASSRVIVTEGIHDRFVAAMVEKM 336 Query: 308 RDLKIKNGLELDAEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSVTGEGCADG 367 + LK+ + + ++GP+V + + YI G EGA++ G + + G A G Sbjct: 337 KTLKVDDARKAGTDIGPVVDDRQLAQDLEYIGIGQQEGAKLAYGGEALEKNADG---APG 393 Query: 368 FWMGGTLFDHVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFGNGVSCFTESGSV 427 F++ LF TP M I REEIFGPV++ +R + A+ L ND FG T S Sbjct: 394 FYLRPALFTETTPGMRINREEIFGPVVSVLRAKNYEEALALANDTPFGLASGIATTSLKH 453 Query: 428 AREFGRRIQVGMVGINVPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTKQKS 482 A F R Q GMV +N+P FGG K S +G G FYT K+ Sbjct: 454 ATHFKRHAQAGMVMVNLPTAGVDYHVPFGGRKSSSYG-PREQGRYAAEFYTTVKT 507 Lambda K H 0.319 0.136 0.406 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: 645 Number of extensions: 33 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: 503 Length of database: 512 Length adjustment: 34 Effective length of query: 469 Effective length of database: 478 Effective search space: 224182 Effective search space used: 224182 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