Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate GFF4005 HP15_3945 aldehyde dehydrogenase family protein
Query= BRENDA::Q97YT9 (492 letters) >lcl|FitnessBrowser__Marino:GFF4005 HP15_3945 aldehyde dehydrogenase family protein Length = 471 Score = 231 bits (588), Expect = 5e-65 Identities = 156/461 (33%), Positives = 236/461 (51%), Gaps = 24/461 (5%) Query: 18 YINGEFIDSKTDTIGKAYNPAKDEIIAEVPFSAKDEVEEAIQSAQEAFEKWREVPITTRI 77 YING+++ D I + ++IA VP + DE+E+AI +A AFE W E + RI Sbjct: 8 YINGQWVSWAGDMID-VHEAGTGDVIARVPAAGADEMEQAIAAADAAFESWSESTLEERI 66 Query: 78 QYLFALKNRLEEYSETIARIIVQNHGKTIQEARGDMRRTIENVEAAISAAYTLYKGEHLD 137 + L L L+E + IA + + G I+ A ++A + AA T + L Sbjct: 67 KVLEQLHAGLKERAPEIAETVCREVGMPIKLATP--------IQAGMPAAVTKSYLKLLP 118 Query: 138 Q---VSQEVDETVVREPLGVFGIITPFNFPTMVPFWFLPYAIVLGNTVVVKPSEITPVPM 194 Q + V P+GV G ITP+N+P + AI G TVV+KPSEI P Sbjct: 119 DFPFTEQSGNSEVQYAPVGVVGCITPWNYPLHQVILKIVPAIAAGCTVVLKPSEIAPQTA 178 Query: 195 DFIIRIFDEIKLPRGVVNVVHGAKDVV-DEFLTNKLVQGVTFVGSTRVGKYIYENAGKNG 253 + I D LP+GV N+V G V D + + V+ V+F GSTR G I A + Sbjct: 179 FILAEILDGTDLPKGVFNMVCGYGHTVGDTLIKHPDVRMVSFTGSTRTGNLIAHAAADDF 238 Query: 254 KKAIVQAGAKNFVVVMPDADLNKAIPSIVSAFFGNAGQRCLAAANLVAVGNIYDEVKRKF 313 K+ ++ G K+ V++PDADL A+ ++ N+GQ C A ++ + +DE Sbjct: 239 KRFALEMGGKSASVILPDADLAAAVKGTINNCLLNSGQTCTALTRMLVPADKHDEACELA 298 Query: 314 IEASKQLKIGYGLDESVDMGPVVTKDAKKRIIGYIEKGIEEGAKLLLDGRDVKVPEYP-- 371 A ++ G L+E+ +GP+ + + ++I YI+ G++EGAKL+ G PE P Sbjct: 299 AAAVAKMTPGNPLEETTRLGPLSSAQQRDKVIDYIKLGVQEGAKLIAGG-----PEAPEG 353 Query: 372 --NGYFLGPTVFDEVTPEMVIAKEEIFGPVASIIHVKNLDEAINIINRSNYGNASSIFTT 429 GYF+ TVF V P+ IA+EEIFGPV +I + EA+ I N + YG + ++++ Sbjct: 354 CEKGYFVKATVFGNVKPDSRIAQEEIFGPVLCVIPYNDEAEAVKIANGTQYGLSGAVWSG 413 Query: 430 SGYYARKFRREVNTGNIGINIGVAAPMAFFPFGGRKESFFG 470 A+K ++ TG + +N G PMA PFGG S G Sbjct: 414 DDAKAKKIASKLRTGQVFVNGGAFNPMA--PFGGFGHSGIG 452 Lambda K H 0.319 0.139 0.398 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: 540 Number of extensions: 23 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: 492 Length of database: 471 Length adjustment: 34 Effective length of query: 458 Effective length of database: 437 Effective search space: 200146 Effective search space used: 200146 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 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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