Align Methylmalonate-semialdehyde dehydrogenase (EC 1.2.1.27) (characterized)
to candidate WP_085634733.1 MGEO_RS00465 aldehyde dehydrogenase family protein
Query= reanno::pseudo13_GW456_L13:PfGW456L13_5146 (508 letters) >NCBI__GCF_002115805.1:WP_085634733.1 Length = 508 Score = 252 bits (644), Expect = 2e-71 Identities = 165/478 (34%), Positives = 257/478 (53%), Gaps = 12/478 (2%) Query: 18 LIDGQWVESKTTEWHDIINPATQQVLAKVPFATAEEVDAAISAAHRAFQTWKLTPIGARM 77 LIDG WV + T D ++P+ V++ EE DAAI AA RAF + I R Sbjct: 23 LIDGAWVTGRET--FDRVSPSHGTVVSTSSKGGPEETDAAIKAARRAFDAGIWSRISGRE 80 Query: 78 R--IMLKLQALIREHSKRIAAVLSAEQGKTIADAEGDIFRGLEVVEHACSIGSLQMGEFA 135 R ++L++ LI + RIA + E GK I+ ++G++ ++ +A ++ G+ Sbjct: 81 RAAVLLRVADLIEANVDRIALQETLESGKPISQSKGEVAGAADLWRYAAALARTSQGDSH 140 Query: 136 ENVAGGVDTYTLRQPIGVCAGITPFNFPAMIPLWMFPMAIACGNTFVLKPSEQDPMSTML 195 + + ++ PIGV + ITP+NFP I P A+A G T V+KPSE P ST++ Sbjct: 141 NTLGSDMLGVVVKDPIGVVSVITPWNFPFWILSQKLPFALAAGCTVVVKPSEMTPSSTVM 200 Query: 196 LVELAIEAGIPAGVLNVVHGGKDVVDGL-CTHKDIKAVSFVGSTAVGTHVYDLAGKHGKR 254 + EL ++AG+PAGV N+V G D V L TH D+ V+F GSTAVG + A K+ Sbjct: 201 MGELLMQAGLPAGVCNIVLGYGDPVGSLKSTHPDVDMVTFTGSTAVGKLITKAASDTLKK 260 Query: 255 VQSMMGAKNHAVVLPDANREQALNALVGAGFGAAGQRCMATS-VVVLVGAAKQWLPDLKA 313 V +G KN V+ PDA+ E A +A+ + GQ C ++S ++V A+ ++ + A Sbjct: 261 VALELGGKNPQVIFPDADLENAADAVTFGVYFNVGQCCNSSSRIIVHEDIAEDFVARVVA 320 Query: 314 LAQKLKVNAGSEPGTDVGPVISKKAKARILDLIESGIKEGAKLELDGREISVPGYEKGNF 373 L++K+K +P T VG +++ + ARI ++ + GA+LEL G + V G F Sbjct: 321 LSKKVKFGDPLDPTTQVGAIVTPEHNARIDGYVQEAVAAGARLELGGAYLDVEGL-GDQF 379 Query: 374 VGPTLFSGVTTDMQIYTQEIFGPVLVVLEVNTLDEAIALVNANPFGNGTGLFTQSGAAAR 433 PT+ S V+ DM + +E+FGPVL VL TLD+AIAL N + +G G++++S Sbjct: 380 YQPTVISSVSADMAVAREEVFGPVLSVLTFRTLDDAIALTNDSEYGLSAGVWSESVHTCL 439 Query: 434 KFQNEIDVGQVGINIPIPVPVPFFSFTGSRGSKLG-DLGPYGKQVVQFYTQTKTVTSR 490 +F G V N + P +F G + S G ++G YG + + + K+V R Sbjct: 440 EFARRAQAGTVWTNTWMD-GYPELAFGGMKQSGTGREIGKYG---FEEFLEVKSVVMR 493 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: 592 Number of extensions: 35 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: 508 Length adjustment: 34 Effective length of query: 474 Effective length of database: 474 Effective search space: 224676 Effective search space used: 224676 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