Align 2-methylbutanoyl-CoA dehydrogenase / butanoyl-CoA dehydrogenase / isobutyryl-CoA dehydrogenase (EC 1.3.8.1; EC 1.3.8.5) (characterized)
to candidate WP_012978109.1 AZL_RS29840 isobutyryl-CoA dehydrogenase
Query= reanno::pseudo3_N2E3:AO353_25680 (375 letters) >NCBI__GCF_000010725.1:WP_012978109.1 Length = 381 Score = 286 bits (732), Expect = 7e-82 Identities = 156/372 (41%), Positives = 234/372 (62%), Gaps = 3/372 (0%) Query: 4 TDEQLQISDAARQFAQERLKPFAAEWDREHRFPKEAIGEMAELGFFGMLVPEQWGGCDTG 63 T++Q+ I D A FA++ L P A +WD++ FP + + LG G+ V E GG Sbjct: 6 TEDQVAIRDMALSFARDELAPNAVDWDQKKHFPIDTLRAAGALGMGGIYVSEDQGGSALS 65 Query: 64 YLAYAMALEEIAAGDGACSTIMSVHNSVGCVPILKFGNDDQKERFLKPLASGAMLGAFAL 123 L + E ++ G ++ +S+HN V + + +FG+D QK +L L + L ++ L Sbjct: 66 RLDAVVIFEALSQGCPTIASYISIHNMVAGM-VDRFGDDAQKAHWLPRLCTMDWLASYCL 124 Query: 124 TEPQAGSDASSLKTRARLNGDHYVLNGCKQFITSGQNAGVVIVFAVTDPSAGKRGISAFI 183 TE AGSDA++L+TRA +GD Y+LNG KQFI+ ++ + +V A T G GISAF+ Sbjct: 125 TEANAGSDAAALRTRAVRDGDGYILNGAKQFISGAGSSDLYLVMARTGED-GPGGISAFL 183 Query: 184 VPTDSPGYKVARVEDKLGQHASDTCQILFEDVQVPVANRLGEEGEGYKIALANLEGGRVG 243 VP D+ G E K+G +A T ++ ED +VP RLG+EG G+K A+A L+GGR+ Sbjct: 184 VPKDTAGLSFGSNEHKMGWNAQPTRAVILEDARVPATARLGQEGMGFKFAMAGLDGGRIN 243 Query: 244 IASQSVGMARAAFEAARDYARERESFGKPIIEHQAVAFRLADMATQIAVARQMVHYAAAL 303 IA+ S+G A+AA + A Y ER++FG+ + QA+ FR+ADMAT++ AR VH AA+ Sbjct: 244 IAACSIGGAQAALDKALTYMSERKAFGQTLDRFQALQFRIADMATELEAARTFVHRAASA 303 Query: 304 RDSG-KPALVEASMAKLFASEMAEKVCSTALQTLGGYGYLSDFPLERIYRDVRVCQIYEG 362 D+G K A +MAK FA++ +V + ALQ GGYGYL+D+ +E+I RD+RV QI EG Sbjct: 304 LDAGAKDATRLCAMAKRFATDTGFEVANNALQLFGGYGYLADYGVEKIVRDLRVHQILEG 363 Query: 363 TSDIQRMVISRN 374 T++I R+++SR+ Sbjct: 364 TNEIMRLIVSRS 375 Lambda K H 0.319 0.134 0.389 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: 381 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: 375 Length of database: 381 Length adjustment: 30 Effective length of query: 345 Effective length of database: 351 Effective search space: 121095 Effective search space used: 121095 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 (21.8 bits) S2: 50 (23.9 bits)
This GapMind analysis is from Apr 09 2024. 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