Align methylmalonate-semialdehyde dehydrogenase (CoA-acylating) (EC 1.2.1.27) (characterized)
to candidate WP_110207793.1 DNK54_RS15005 aldehyde dehydrogenase
Query= BRENDA::P42412 (487 letters) >NCBI__GCF_003194585.1:WP_110207793.1 Length = 501 Score = 254 bits (649), Expect = 5e-72 Identities = 165/483 (34%), Positives = 250/483 (51%), Gaps = 20/483 (4%) Query: 8 KNYINGEWVESKTDQYEDVVNPATKEVLCQVPISTKEDID--YAAQTAAEAFKTWSKVAV 65 +N+ING W ++ Q +V +PAT E++ V +ID AA AA A W Sbjct: 7 QNFINGAWTDN--GQVLEVRSPATGELVATVAKGGAAEIDAAVAAAKAAHAAGVWRNTPP 64 Query: 66 PRRARILFNFQQLLSQHKEELAHLITIENGKNTKEALG-EVGRGIENVEFAAGAPSLMMG 124 RA ++ L+ EELA L + ENG + VG I N++F A + Sbjct: 65 AERAALINAVAGDLAGRLEELAALQSRENGATIRVTGALHVGLSIANMQFIAAQAAEYEF 124 Query: 125 DSLASIATDVEAANY--RYPIGVVGGIAPFNFPMMVPCWMFPMAIALGNTFILKPSERTP 182 + V A R P+GVVG I P+N P++ W A+A GNT +LKP E P Sbjct: 125 EKAGPEIGPVPAEGILRREPLGVVGAIVPWNIPLLTIVWKVTPALAAGNTVVLKPDEHAP 184 Query: 183 LLTEKLVELFEKAGLPKGVFNVVYG-AHDVVNGILEHPEIKAISFVGSKPVGEYVYKKGS 241 LL +L + FE AGLP GV NVV G HD + +HP+++ I F GS VG+ + + Sbjct: 185 LLALELAKAFEAAGLPAGVLNVVVGEGHDAGARLSQHPDVRKIGFTGSTEVGKSILGASA 244 Query: 242 ENLKRVQSLTGAKNHTIVLNDANLEDTVTNIVGAAFGSAGERCMACAVVTVEEGIADEFM 301 +N+KRV G K I+L+DA+L+ + + A + GE C A + V DE + Sbjct: 245 DNMKRVTLELGGKGPNILLDDADLDVAIDGAIYACMANNGEACEAGTRLLVPNSRKDEIV 304 Query: 302 AKLQEKVADIKIGNGLDDGVFLGPVIREDNKKRTLSYIEKGLEEGARLVCDGRENVSDD- 360 +L +V +KIGN LD +GP+I D + R L++I K +GA++ G ++ Sbjct: 305 ERLVARVGTMKIGNPLDPATDIGPLITADQRDRVLAHIAKAETQGAKVAIGGSAPAGEEF 364 Query: 361 --GYFVGPTIFDNVTTEMTIWKDEIFAPVLSVIRVKNLKEAIEIANKSEFANGACLFTSN 418 GYFV PT+ +VT MT+ +E+F PVLSV+ + EAI IAN +E+ A ++ ++ Sbjct: 365 ANGYFVEPTVLTDVTPSMTVACEEVFGPVLSVLGYDTVDEAIAIANDTEYGLSAGVWGTD 424 Query: 419 SNAIRYFRENIDAGMLGIN---LGVPAPMAFFPFSGWKSSFFGTLHANGKDSVDFYTRKK 475 + ++AGM+ +N + PA +PF G+K S G G +++D YT +K Sbjct: 425 ETRVLDVARQLEAGMIYVNDWHVLHPA----YPFGGYKQSGLG--REGGPNALDAYTEQK 478 Query: 476 VVT 478 ++ Sbjct: 479 YIS 481 Lambda K H 0.318 0.136 0.396 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: 603 Number of extensions: 28 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: 487 Length of database: 501 Length adjustment: 34 Effective length of query: 453 Effective length of database: 467 Effective search space: 211551 Effective search space used: 211551 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