Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate BWI76_RS07615 BWI76_RS07615 betaine-aldehyde dehydrogenase
Query= reanno::Smeli:SMc00781 (498 letters) >FitnessBrowser__Koxy:BWI76_RS07615 Length = 490 Score = 254 bits (648), Expect = 6e-72 Identities = 169/487 (34%), Positives = 255/487 (52%), Gaps = 20/487 (4%) Query: 1 MYELGHFIDGKRVAGTSGRVSNIFNPATGEVQGTVALASDADLAAAVESAKAAQPKWAAT 60 M E +IDG V+ TSG+ NPA GEV TV A D+ AV+SA+ Q WAA Sbjct: 4 MAEQQLYIDGGYVSATSGKTFETINPANGEVLATVQAAGREDVDRAVKSAQKGQKIWAAM 63 Query: 61 NPQRRARVFMKFVQLLNDNMNELAEMLSREHGKTIDD-AKGDIVRGLEVCEFVIG-IPHL 118 + R+R+ K V +L +ELA + + + GK + + A DIV G +V E+ G IP L Sbjct: 64 SAMERSRILRKAVDILRARNDELARLETLDTGKPLSETAAVDIVTGADVLEYYAGLIPAL 123 Query: 119 QKSEFTEGAGPGIDMYSIRQPVGIGAGITPFNFPGMIPMWMFAPAIACGNAFILKPSERD 178 + S+ + Y+ R+P+G+ AGI +N+P I +W APA+A GNA I KPSE Sbjct: 124 EGSQIPLRDSSFV--YTRREPLGVVAGIGAWNYPIQIALWKSAPALAAGNAMIFKPSEVT 181 Query: 179 PSVPIRLAELMIEAGLPAGILNVVNGDKGAVDAILT-HPDIAAVSFVGSTPIARYVYGTA 237 P ++LAE+ EAGLPAG+ NV+ G LT HPDIA +SF G + V A Sbjct: 182 PLTALKLAEIYREAGLPAGVFNVLPGTGAETGQYLTEHPDIAKISFTGGVASGKKVMANA 241 Query: 238 AMNG-KRAQCFGGAKNHMIIMPDADLDQAANALIGAGYGSAGERCM-AISVAVPVGEETA 295 A + K G K+ +I+ DA LD AA+ + A + S+G+ C V VP + A Sbjct: 242 AASSLKEVTMELGGKSPLIVCEDASLDLAADIAMMANFYSSGQVCTNGTRVFVPTRLKAA 301 Query: 296 NRLIDKLVPMVESLRIGPYTDEKADMGPVVTKEAEQRIRSLIDSGIEQGAKLVVDGRDFK 355 +K++ V +R G E + GP+V+ + I++G ++GA+L+ G K Sbjct: 302 --FEEKILARVARIRPGDLFAESTNFGPLVSFPHRDNVLRYIETGKQEGARLLCGGEALK 359 Query: 356 LQGYENGHFIGGCLFDDVTPDMDIYKTEIFGPVLSVVRARNYEEALSLPMKHEYGNGVAI 415 +G++ G ++ +F D M I + EIFGPV+S++ + EEAL EYG + Sbjct: 360 GEGFDRGAWVAPTVFTDCDDQMTIVREEIFGPVMSILSYDDEEEALRRANATEYGLAAGV 419 Query: 416 YTRDGDAARDFASRINIGMVGVNV----PIPVPLAYHSFGGWKSSSFGDLNQHGTDSIKF 471 T D + A R+ G+ +N P +P+ GG+K S G ++G ++ Sbjct: 420 VTPDLNRAHRLIHRLEAGICWINTWGESPAEMPV-----GGYKHSGIG--RENGVQTLHS 472 Query: 472 WTRTKTI 478 +T+ K+I Sbjct: 473 YTQIKSI 479 Lambda K H 0.319 0.137 0.409 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: 573 Number of extensions: 27 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: 498 Length of database: 490 Length adjustment: 34 Effective length of query: 464 Effective length of database: 456 Effective search space: 211584 Effective search space used: 211584 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 (21.7 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