Align Methylmalonate-semialdehyde dehydrogenase (EC 1.2.1.27) (characterized)
to candidate WP_010529728.1 ON01_RS04100 betaine-aldehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_5146 (508 letters) >NCBI__GCF_000224785.1:WP_010529728.1 Length = 489 Score = 248 bits (632), Expect = 5e-70 Identities = 152/476 (31%), Positives = 253/476 (53%), Gaps = 7/476 (1%) Query: 16 KLLIDGQWVESKTTEWHDIINPATQQVLAKVPFATAEEVDAAISAAHRAFQT--WKLTPI 73 K LIDG WV S + DIINP Q+++A V + + AAI+AA +AF W TP Sbjct: 5 KQLIDGSWVTSNSDAVRDIINPFNQKIVATVTESDESDTKAAITAARKAFDQGDWATTPA 64 Query: 74 GARMRIMLKLQALIREHSKRIAAVLSAEQGKTIADAEGDIFRGLEVVEHACSIGSLQMGE 133 R +I+ K+ LI + +A + S + GKT+ ++ GD+ V + + GE Sbjct: 65 AERGKIVHKIADLIERDREELAELESLDTGKTVEESLGDMDDIAGVFRYFAEMADKDGGE 124 Query: 134 FAENVAGGVDTYTLRQPIGVCAGITPFNFPAMIPLWMFPMAIACGNTFVLKPSEQDPMST 193 E+ + + +P+GVC ITP+N+P + W A+A GNT V+KPSE P+++ Sbjct: 125 IIESPIPNSTSKVVHEPVGVCGQITPWNYPLLQASWKLAPALAAGNTLVMKPSEITPLTS 184 Query: 194 MLLVELAIEAGIPAGVLNVVHGGKDVVDG-LCTHKDIKAVSFVGSTAVGTHVYDLAGKHG 252 + + EL EAG+PAGV+N+V G D V L + ++ +SF G G + A + Sbjct: 185 IKVFELMAEAGVPAGVVNLVLGPGDSVGAELSANDNVDLISFTGGIHTGKKIMQAASSNV 244 Query: 253 KRVQSMMGAKNHAVVLPDANREQALNALVGAGFGAAGQRCMA-TSVVVLVGAAKQWLPDL 311 K + +G KN +V DA+ E A++ + A F AGQ C A T +++ ++ + Sbjct: 245 KNLALELGGKNPNIVFADADFETAVDQAMNAVFFHAGQICSAGTRLIIEESIHDAFVSAI 304 Query: 312 KALAQKLKVNAGSEPGTDVGPVISKKAKARILDLIESGIKEGAKLELDGREISVPGYEKG 371 + +K+ +G + T +GP+IS+ ++++ +E+G +EGA + + G P + G Sbjct: 305 VDRVKNIKLGSGFDESTQMGPLISEDHLNKVVNYVENGKQEGATVAVGGSRPDDPELQNG 364 Query: 372 NFVGPTLFSGVTTDMQIYTQEIFGPVLVVLEVNTLDEAIALVNANPFGNGTGLFTQSGAA 431 F PT+ +G T+DM++ E FGPV+ V + T +EA+ L N + +G G+FT A Sbjct: 365 LFYLPTILTGCTSDMRVVQDEGFGPVITVEKFTTEEEAVRLANDSIYGLSGGVFTNDIAK 424 Query: 432 ARKFQNEIDVGQVGINIPIPVPVPFFSFTGSRGSKLGDLGPYGKQVVQFYTQTKTV 487 A + ++ +G V IN + + P + G + S +G GK ++ Y +TK + Sbjct: 425 AERCVAKLRMGTVWIN-DVNLYFPHAPWGGYKQSGIG--RELGKTGLEEYQETKHI 477 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: 577 Number of extensions: 27 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: 508 Length of database: 489 Length adjustment: 34 Effective length of query: 474 Effective length of database: 455 Effective search space: 215670 Effective search space used: 215670 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 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