Align Methylmalonate-semialdehyde dehydrogenase (EC 1.2.1.27) (characterized)
to candidate WP_023430602.1 N177_RS02270 NAD-dependent succinate-semialdehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_5146 (508 letters) >NCBI__GCF_000496075.1:WP_023430602.1 Length = 480 Score = 261 bits (668), Expect = 3e-74 Identities = 157/475 (33%), Positives = 251/475 (52%), Gaps = 9/475 (1%) Query: 17 LLIDGQWVESKTTEWHDIINPATQQVLAKVPFATAEEVDAAISAAHRAFQTWKLTPIGAR 76 LLIDG+W + + + ++NPAT++V+ KV +A ++DAA+ A + F+ W T R Sbjct: 10 LLIDGEWRPAASGKTIPVVNPATEEVIGKVAWAEKADLDAALEAVAKGFRVWSQTSAYER 69 Query: 77 MRIMLKLQALIREHSKRIAAVLSAEQGKTIADAEGDIFRGLEVVEHACSIGSLQMGEFAE 136 + M K L+RE + IAAV++ EQGK +A+A + G +++E G+ Sbjct: 70 AKTMRKAAGLLRERADEIAAVMTLEQGKPVAEAMMETMAGADIIEWFAGEAQRVYGQIIA 129 Query: 137 NVAGGVDTYTLRQPIGVCAGITPFNFPAMIPLWMFPMAIACGNTFVLKPSEQDPMSTMLL 196 AGGV ++QP+G A TP+NFP + A+A G + ++K E+ P + L Sbjct: 130 PRAGGVTQLAMKQPVGPVAAFTPWNFPINQVVRKLSAALATGCSIIVKAPEETPAAPAAL 189 Query: 197 VELAIEAGIPAGVLNVVHG-GKDVVDGLCTHKDIKAVSFVGSTAVGTHVYDLAGKHGKRV 255 + ++AG+PAGV+N+V+G ++ + L H I+ +SF GST VG H+ LAG+H KR Sbjct: 190 IRAFVDAGVPAGVVNLVYGVPAEISEYLIPHPVIRKISFTGSTPVGKHLAALAGQHMKRA 249 Query: 256 QSMMGAKNHAVVLPDANREQALNALVGAGFGAAGQRCMA-TSVVVLVGAAKQWLPDLKAL 314 +G +V DA+ +A+ L + F AGQ C++ T ++ G K +L Sbjct: 250 TMELGGHAPVIVTEDADVSKAVKLLAASKFRNAGQVCISPTRFLIQDGVKKDFLKGFTEA 309 Query: 315 AQKLKVNAGSEPGTDVGPVISKKAKARILDLIESGIKEGAKLELDGREISVPGYEKGNFV 374 A+ +KV G + GT +GP+ +++ + +LI+ + GA LE GR I KG F+ Sbjct: 310 AKAVKVGNGLDEGTTMGPLANERRVPFLEELIQDAVDSGASLETGGRRIG----NKGYFM 365 Query: 375 GPTLFSGVTTDMQIYTQEIFGPVLVVLEVNTLDEAIALVNANPFGNGTGLFTQSGAAARK 434 PT+ + ++ +E FGP+ VV + LDE I N P+G + FT S A + Sbjct: 366 EPTVIADAPLSSRVMNEEPFGPLAVVNSFSDLDEVIEEANRLPYGLASYAFTGSQKTAHE 425 Query: 435 FQNEIDVGQVGINIPIPVPVPFFSFTGSRGSKLGDLGPYGKQVVQFYTQTKTVTS 489 I+ G IN I + +P F G + S G G G + V+ Y T+ VT+ Sbjct: 426 LTMRIESGMTTIN-HIGLALPEVPFGGMKDSGYGSEG--GSEAVEPYLVTRFVTT 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: 558 Number of extensions: 28 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: 508 Length of database: 480 Length adjustment: 34 Effective length of query: 474 Effective length of database: 446 Effective search space: 211404 Effective search space used: 211404 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