Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_057507768.1 ABB28_RS05980 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-15203 (503 letters) >NCBI__GCF_001431535.1:WP_057507768.1 Length = 454 Score = 199 bits (505), Expect = 2e-55 Identities = 137/467 (29%), Positives = 225/467 (48%), Gaps = 26/467 (5%) Query: 24 EVTNPATGQVTGQVALASQADVDSAVAAAQAAFPAWSDTPPIRRARVMFKFLELLNAHKD 83 E+ NP TG+V + L +A ++ + AA AFPAWS T RA V+ L KD Sbjct: 4 EIVNPTTGRVDYRHELLDKAGIEQRLQAAAGAFPAWSATSLQERAAVLRAIGAQLRERKD 63 Query: 84 ELAEAITREHGKVFTDAQGEVARGIDIVEFACGI------PQLLKGDYTEQVSTGIDNWT 137 ++ A+TRE GK+ +A EV + E+ PQL+ + ++ Sbjct: 64 DIQGAMTREMGKLKVEALAEVEKCAAACEYYADHAADYLKPQLIDTEAQR-------SYV 116 Query: 138 TRQPLGVVAGITPFNFPVMVPMWMFPLAIAAGNSFVLKPSPLDPSASLMMADLLKQAGLP 197 +P+G V + P+NFP+ A AGN +LK + P + ++ ++++ GLP Sbjct: 117 RYEPIGCVFAVMPWNFPIWQVFRFLAPAFMAGNVALLKHASNVPQCADLINEVVRAGGLP 176 Query: 198 DGVFNVVQGDKDSVEALIDHPDVKALSFVGSTPIA-NLIYERGARSGKRIQALGGAKNHM 256 DGVF+V+ D D ++ VKA++ GS ++ G + K + LGG+ + Sbjct: 177 DGVFDVLHIDNDQAADVLRDRRVKAVTLTGSERAGRSIAANAGDQLKKCVMELGGS-DAF 235 Query: 257 VVMPDANLDKAVDALIGAAYGSAGERCMAISVAVLVGDVADKIVPRLAERARDLKIKNGL 316 VV+ DA+LDKA+DA + + + ++G+ C+A ++V VAD R A + + + Sbjct: 236 VVLDDADLDKAIDAAVKSRFDNSGQTCIAAKRFIVVEAVADAFTERFVAAAGERRYGDPA 295 Query: 317 ELDAEMGPIVTSQAHQRITGYIEKGVAEGAEMVVDGRDFDSSVTGEGCADGFWMGGTLFD 376 + + P+ + + ++ VA+GA ++ G D S G T+ D Sbjct: 296 DARTTLAPMARADLRDELHKQVQASVAKGARVLAGGEPVDGSHAG--------YPATVLD 347 Query: 377 HVTPEMTIYREEIFGPVLACVRVPDVATAIQLINDHEFGNGVSCFTESGSVAREFGRRIQ 436 V P M Y EE+FGPV A +RV D A A+++ ND FG G S +T + F ++++ Sbjct: 348 QVGPGMPAYDEELFGPVAAVIRVKDEAEALKVANDTRFGLGGSVWTTDAARGEAFAQQME 407 Query: 437 VGMVGINVPIPVPMAWHGFGGWKRSMFGDTHAYGEEGVRFYTKQKSI 483 G +N + + FGG K S FG E G+ + K+I Sbjct: 408 CGAAFVNSIVKSDVRL-PFGGSKESGFG--RELAEHGIHEFMNIKTI 451 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: 522 Number of extensions: 23 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: 454 Length adjustment: 34 Effective length of query: 469 Effective length of database: 420 Effective search space: 196980 Effective search space used: 196980 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: 51 (24.3 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