Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_023432784.1 N177_RS12830 betaine-aldehyde dehydrogenase
Query= reanno::Smeli:SMc00781 (498 letters) >NCBI__GCF_000496075.1:WP_023432784.1 Length = 488 Score = 249 bits (637), Expect = 1e-70 Identities = 155/481 (32%), Positives = 247/481 (51%), Gaps = 15/481 (3%) Query: 3 ELGHFIDGKRVAGTSGRVSNIFNPATGEVQGTVALASDADLAAAVESAKAAQPKWAATNP 62 E+ I G+R+ G+ +S+I NPA GE T A+ ++ A+E+A+ A+ W A + Sbjct: 7 EISCHIAGRRIPGSGDALSSI-NPANGETLATGNAAAMPEIEQAIEAAREARRSWMAMSA 65 Query: 63 QRRARVFMKFVQLLNDNMNELAEMLSREHGKTIDDAKG-DIVRGLEVCEFVIGIPHLQKS 121 R RV + +L + ++LA + + GK I +A DI + EF G+ + + Sbjct: 66 AERGRVLARVAAILRERRDDLARLEVLDTGKPIQEAPAADIDSAADCFEFFAGLTQIVQG 125 Query: 122 EFTEGAGPGIDMYSIRQPVGIGAGITPFNFPGMIPMWMFAPAIACGNAFILKPSERDPSV 181 E G Y+ R+P+GI AGI +N+P I W APA+A GNA + KPSE P Sbjct: 126 EHIPFGDDGF-AYTRREPLGICAGIGAWNYPIQIASWKTAPALAAGNAMLFKPSEVTPLT 184 Query: 182 PIRLAELMIEAGLPAGILNVVNGDKGAVDAILTHPDIAAVSFVGSTPIARYVYGTAAMNG 241 + L ++ EAG P G+L+++ G + + + THP IA +S GS P + V +AA Sbjct: 185 ALELGRIVEEAGAPPGLLSILPGGRETGEILSTHPAIAKISVTGSVPTGKAVMASAAGTL 244 Query: 242 KRAQCFGGAKNHMIIMPDADLDQAANALIGAGYGSAGERCMAISVAVPVGEETANRLIDK 301 K G K+ +++ DADLD A +A + A + + GE C V V ++K Sbjct: 245 KHVTMELGGKSALLVFADADLDDAVSAAMLANFYTQGEIC-TNGTRVFVERPVCEAFLEK 303 Query: 302 LVPMVESLRIGPYTDEKADMGPVVTKEAEQRIRSLIDSGIEQGAKLVVDGRDFKLQGYEN 361 E++RIG D + MGP++ + ++ +++G+ +GA+LV G+ + Sbjct: 304 AKARAEAIRIGDPLDPETQMGPLIHAQHLDKVMKFVENGVREGARLVTGGKRLTDGDFAK 363 Query: 362 GHFIGGCLFDDVTPDMDIYKTEIFGPVLSVVRARNYEEALSLPMKHEYGNGVAIYTRDGD 421 G+F+ +F DV M I EIFGPV+SV+ + EEAL +G + TRD Sbjct: 364 GNFMQPTIFADVLDQMTICMQEIFGPVMSVLPFESEEEALRRANDTPFGLAAGVMTRDIS 423 Query: 422 AARDFASRINIGMVGVN----VPIPVPLAYHSFGGWKSSSFGDLNQHGTDSIKFWTRTKT 477 A A+++ G+V VN PIP+P FGG K S G ++G ++ F+T K+ Sbjct: 424 RAHRVAAKLEAGVVWVNHYNLTPIPMP-----FGGSKMSGLG--RENGLAALDFYTERKS 476 Query: 478 I 478 + Sbjct: 477 V 477 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: 612 Number of extensions: 22 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: 498 Length of database: 488 Length adjustment: 34 Effective length of query: 464 Effective length of database: 454 Effective search space: 210656 Effective search space used: 210656 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 Sep 24 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:
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