Align Methylmalonate-semialdehyde dehydrogenase (EC 1.2.1.27) (characterized)
to candidate SMa2213 SMa2213 aldehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_5146 (508 letters) >FitnessBrowser__Smeli:SMa2213 Length = 494 Score = 246 bits (628), Expect = 1e-69 Identities = 163/488 (33%), Positives = 251/488 (51%), Gaps = 28/488 (5%) Query: 14 KVKLLIDGQWVESKTTEWHDIINPATQQVLAKVPFATAEEVDAAISAAHRAFQT--WKLT 71 K+ + IDGQWV + E+ + ++P T + A VP AE+ D A+ AAHRAF W Sbjct: 6 KLSMYIDGQWVAPASGEYIETVDPFTARPWALVPRGNAEDADRAVRAAHRAFSQGPWGKM 65 Query: 72 PIGARMRIMLKLQALIREHSKRIAAVLSAEQGKTIADAEGDIFRGLEVVEHACSIGSLQM 131 R RI+ + ALI EH+ +A + + G+ +A+ I R + H Sbjct: 66 HPTERGRIIQRFAALIEEHADALADIEVRDNGRLLAEMTHQI-RYIPRWYH-------YY 117 Query: 132 GEFAENVAGGVD-------TYTLRQPIGVCAGITPFNFPAMIPLWMFPMAIACGNTFVLK 184 FA+ + G + +++ +P+GVC GI P+N P ++ A+A GNT V+K Sbjct: 118 AGFADKIEGTLHPCDKPALSFSRHEPLGVCVGIVPWNAPLLLFSLKAAPALAAGNTLVMK 177 Query: 185 PSEQDPMSTMLLVELAIEAGIPAGVLNVVHG-GKDVVDGLCTHKDIKAVSFVGSTAVGTH 243 P+E + + L+EL +AG P GV+NVV G G +V + L TH + V F GST G H Sbjct: 178 PAEFTSATALKLMELVEKAGFPTGVINVVTGYGPEVGEPLVTHPLTRHVGFTGSTKTGAH 237 Query: 244 VYDLAGKHGKRVQSMMGAKNHAVVLPDANREQALNALVGAGFGAAGQRCMATS-VVVLVG 302 +Y LA K KRV +G K+ +V DA+ + A+ +VG FGA GQ C+A S ++V Sbjct: 238 LYSLAAKDVKRVSLELGGKSPNIVFGDADLDNAVRGVVGGIFGAVGQTCIAGSRLLVHRS 297 Query: 303 AAKQWLPDLKALAQKLKVNAGSEPGTDVGPVISKKAKARILDLIESGIKEGAKLELDGRE 362 ++L L + ++ + T +GP+ + ++L I+ +EGA+L L G Sbjct: 298 IHDEFLEKLAVFTKTARIGDPRKVETQIGPIANSMQFEKVLGYIDIARREGAELILGGGR 357 Query: 363 ISVPGYEKGNFVGPTLFSGVTTDMQIYTQEIFGPVLVVLEVNTLDEAIALVNANPFGNGT 422 + G F+ PT+F+GV+ DM+I +E+FGPVL + + +EA+A+ N + FG G Sbjct: 358 PDLEECGTGYFIEPTIFAGVSNDMRIAREEVFGPVLSAIVFDEPEEALAIANDSEFGLGA 417 Query: 423 GLFTQSGAAARKFQNEIDVGQVGINI--PIPVPVPFFSFTGSR-GSKLGDLGPYGKQVVQ 479 G++T A K ++ G V +N I PF + S G + G G Y Sbjct: 418 GVWTSDMRLALKMSERLEAGSVWVNTYRDISYTTPFGGYKKSGIGRENGVAGIYE----- 472 Query: 480 FYTQTKTV 487 Y QTK V Sbjct: 473 -YLQTKAV 479 Lambda K H 0.318 0.135 0.395 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: 588 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: 508 Length of database: 494 Length adjustment: 34 Effective length of query: 474 Effective length of database: 460 Effective search space: 218040 Effective search space used: 218040 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: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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