Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate SMa1415 SMa1415 aldehyde dehydrogenase
Query= reanno::WCS417:GFF2142 (499 letters) >FitnessBrowser__Smeli:SMa1415 Length = 498 Score = 243 bits (620), Expect = 1e-68 Identities = 159/466 (34%), Positives = 247/466 (53%), Gaps = 26/466 (5%) Query: 25 NPATGEKTGRVALASRQTVSEAVAAAQAAFAG--WADTPPIRRARVLFEYLHLLRERKDD 82 +P G R A S ++ AVAAA+ AF W+ P RA VL +LR R+D+ Sbjct: 36 SPGHGVAVTRTAKCSVDDLNAAVAAARRAFEDRRWSGLPGGSRASVLLRVAEILRTRRDE 95 Query: 83 LARIIVAEHGKVFTDAQGEVDRGIDILEFACGIPNLLKGEHSDQVSRGMDNWTMRQPLGV 142 LA E+GK A+GE+D I E G LL G+ + + G+ +R+P+GV Sbjct: 96 LAYWETLENGKPIAQARGEIDHCIACFEVGAGAARLLHGDSFNSLGDGLFGMVLREPIGV 155 Query: 143 VAGVTPFNFPVMVPMWMYPIAIAAGNTFILKPSPTDPSASLFMAELLREAGLPKGVFNVV 202 V +TP+NFP ++ P +A+G T ++KPS + +L +AE+L EAGLP GV+NV+ Sbjct: 156 VGLITPWNFPFLILCERVPFILASGCTMVVKPSEVTSATTLILAEVLAEAGLPDGVYNVI 215 Query: 203 QGDKESV-DALIEHPDVKAVSFVGSTPIAQYIYETGARNGKRVQGLG-GAKNHMVVMPDA 260 G ++ A+ EHPD+ +SF GST + + A + + GL G KN ++V D+ Sbjct: 216 TGSGRTIGQAMSEHPDIDMLSFTGSTAVGRSCVHAAADSNFKKLGLELGGKNPIIVFADS 275 Query: 261 DIEKTVDALMGAAYG---SAGERCMAISVAVLVGDVGDKVIAALTERAKHLRITDGRDLK 317 D+E DA GAA+G + G+ C++ S ++ V + A L E+ K +R+ D D Sbjct: 276 DLE---DAADGAAFGISFNTGQCCVSSSRLIVERSVAREFEALLAEKMKRIRVGDPLDET 332 Query: 318 AEMGPIVSRAALERISGYIEQGVQAGAQLLLDGRDYVPTEPGLENGFWLGATLFDHVTEE 377 ++G I + A I YI +G GA+L+ G T L G ++ TLF V+ E Sbjct: 333 TQVGAITTEAQNTTILDYIAKGKTEGAELVTGG-----TAIDLGRGQYIAPTLFSGVSRE 387 Query: 378 MSIYREEIFGPVLACVRVNDFAEAIKLVNAHEFGNGVSCFTRDGNIAREFARRIEVGMVG 437 M+I R+EIFGPVL + + +A++L N +G S +T++ + A RR+ G Sbjct: 388 MAIARDEIFGPVLCSMTFDTVEQAVELANDTVYGLAASVWTKNIDKALTVTRRVRAGRFW 447 Query: 438 INVPIS----VPMAWHGFGGWKKSLFGDMHAYGTEGVRFYTKQKSI 479 +N ++ +P+ GG+K+S +G G GV YT+ KS+ Sbjct: 448 VNTMMAGGPEMPL-----GGFKQSGWG--REAGMYGVEEYTQVKSV 486 Lambda K H 0.320 0.136 0.407 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: 571 Number of extensions: 28 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: 499 Length of database: 498 Length adjustment: 34 Effective length of query: 465 Effective length of database: 464 Effective search space: 215760 Effective search space used: 215760 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