Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_034275197.1 AMYHA_RS25345 aldehyde dehydrogenase family protein
Query= BRENDA::Q97YT9 (492 letters) >NCBI__GCF_000504245.1:WP_034275197.1 Length = 487 Score = 233 bits (595), Expect = 9e-66 Identities = 153/458 (33%), Positives = 236/458 (51%), Gaps = 20/458 (4%) Query: 18 YINGEFIDSKTDTIGKAYNPAKDEIIAEVPFSAKDEVEEAIQSAQEAFEK-WREVPITTR 76 +I G F+D + + K NPA E++AEV A +V+ A+ +A++AFE+ W +P R Sbjct: 25 FIGGGFVDGGGEPL-KTLNPATGEVLAEVSTVASSDVDSAVTAARKAFERVWSPMPGAER 83 Query: 77 IQYLFALKNRLEEYSETIARIIVQNHGKTIQEARGDMRRTIENVEAAISAAYTLYKG--- 133 +Y++ + ++E + +A + ++GK I+E+R + + +AA+ Y Sbjct: 84 AKYIYRIARLIQERARELAVLESLDNGKPIKESR--------DADIPTAAAHFFYHAGWA 135 Query: 134 EHLDQVSQEVDETVVREPLGVFGIITPFNFPTMVPFWFLPYAIVLGNTVVVKPSEITPVP 193 + LD +PLGV G + P+NFP ++ W + A+ GNTVV+KP+E TP+ Sbjct: 136 DKLDYAGFSTSTAGPPQPLGVAGQVIPWNFPLLMLAWKIAPALATGNTVVLKPAETTPLT 195 Query: 194 MDFIIRIFDEIKLPRGVVNVVHGAKDVVDEFLTNKLVQGVTFVGSTRVGKYIYENAGKNG 253 I + +LP GVVN+V GA DV + +T+ + V F GST VGK I Sbjct: 196 ALVFAEICQQAELPPGVVNIVPGAGDVGEMLVTHPGIDKVAFTGSTEVGKLIQRQLAGTR 255 Query: 254 KKAIVQAGAKNFVVVMPDADLNKAIPSIVSAFFGNAGQRCLAAANLVAVGNIYDEVKRKF 313 + ++ G K VV DA L++AI IV+ F N G C A + L+ ++ DEV K Sbjct: 256 TRLTLELGGKAANVVFDDAPLDQAIEGIVNGIFFNQGHVCCAGSRLLVQESVADEVLAKL 315 Query: 314 IEASKQLKIGYGLDESVDMGPVVTKDAKKRIIGYIEKGIEEGAKLLLDGRDVKVPEYPNG 373 + L++G LD++ D+G + + + +I + G +EGA+ VPE G Sbjct: 316 RARVETLRLGDPLDKNTDIGAINSAEQLAKIRELVASGEDEGAQRWTS--SCPVPE--KG 371 Query: 374 YFLGPTVFDEVTPEMVIAKEEIFGPVASIIHVKNLDEAINIINRSNYGNASSIFTTSGYY 433 YF PTVF V M IA+EEIFGPV S+ + DEA+ N + YG ++ ++T G Sbjct: 372 YFFAPTVFSGVESSMRIAREEIFGPVLSVQTFRTPDEAVTKANTTPYGLSAGVWTEKGSR 431 Query: 434 ARKFRREVNTGNIGIN-IGVAAPMAFFPFGGRKESFFG 470 + G + N P A PFGG KES FG Sbjct: 432 ILWLSNALRAGVVWANTFNRFDPSA--PFGGYKESGFG 467 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: 514 Number of extensions: 27 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: 492 Length of database: 487 Length adjustment: 34 Effective length of query: 458 Effective length of database: 453 Effective search space: 207474 Effective search space used: 207474 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