Align 2-methylbutanoyl-CoA dehydrogenase (EC 1.3.8.5) (characterized)
to candidate 3606773 Dshi_0204 acyl-CoA dehydrogenase domain protein (RefSeq)
Query= reanno::pseudo6_N2E2:Pf6N2E2_1146 (375 letters) >FitnessBrowser__Dino:3606773 Length = 564 Score = 205 bits (521), Expect = 3e-57 Identities = 128/384 (33%), Positives = 207/384 (53%), Gaps = 15/384 (3%) Query: 5 EEQTQIRDMARQFAEERLKPFAAEWD-REHRFPREAIDEMAELGFFGMLVPEQWGGCDTG 63 +E IR+ R+F+ ++++P A EW ++ P E I+E+AE+G FG+ +PE++GG Sbjct: 181 DELEMIREQFRRFSVDKVEPHAHEWHLKDELIPMEIIEELAEMGVFGLTIPEEYGGFGLS 240 Query: 64 YLAYAMTLEEIAAGDGACSTIMSVHNSVGCVPILKFGNDEQKAKFLTPLASGAMLGAFAL 123 + + EE++ G ++ + + I+ G +EQK K+L LAS L Sbjct: 241 KASMCVVSEELSRGYIGVGSL-GTRSEIAAELIICGGTEEQKQKWLPRLASAETLPTAVF 299 Query: 124 TEPQAGSDASSLKTRA-RLEGDHYVLNGCKQFITSGQNAGVVIVFAVTDP-SAGKRGISA 181 TEP GSD +L+TRA + E + + G K +IT V+ + A T P + RG+S Sbjct: 300 TEPNTGSDLGALRTRAVQDENGDWKVTGNKTWITHAARTHVMTLLARTKPDTTDHRGLSM 359 Query: 182 FIV---------PTDSPGYSVARVEDKLGQHASDTCQILFEDLKVPVGNRLG-EEGEGYK 231 F+ P + G + +E LG ++ F++ V N LG EEG+G+K Sbjct: 360 FLAEKTPGTDEAPFPTEGMTGGEIE-VLGYRGMKEYELAFDNFHVKGENLLGGEEGKGFK 418 Query: 232 IALANLEGGRVGIAAQAVGMARAAFEAARDYARERSSFGKPIIEHQAVAFRLADMATQIA 291 + E R+ AA+A+G+A++A + + YA +R FGK +I V+ +LA MA +I Sbjct: 419 QLMETFESARIQTAARAIGVAQSALDVSMQYAIDRKQFGKSLINFPRVSGKLAMMAVEIM 478 Query: 292 VARQMVHYAAALRDSGQPALVEASMAKLFASEMAEKVCSMALQTLGGYGYLNDFPLERIY 351 VARQ+ +++A +D G+ VEA MAKL + +A LQ GG G+ ++ + RI Sbjct: 479 VARQLTYFSAFEKDEGRRCDVEAGMAKLLGARVAWAAADNGLQIHGGNGFALEYGISRIL 538 Query: 352 RDVRVCQIYEGTSDIQRMVISRNL 375 D R+ I+EG ++IQ VI+R L Sbjct: 539 CDARILNIFEGAAEIQAQVIARRL 562 Score = 26.2 bits (56), Expect = 0.002 Identities = 16/44 (36%), Positives = 22/44 (50%) Query: 270 GKPIIEHQAVAFRLADMATQIAVARQMVHYAAALRDSGQPALVE 313 G + EHQ + LA +AT RQM +A L+ G+ VE Sbjct: 55 GALVEEHQTASHGLAWLATYAQSLRQMQKWAETLQADGKFGEVE 98 Lambda K H 0.320 0.134 0.388 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: 450 Number of extensions: 25 Number of successful extensions: 5 Number of sequences better than 1.0e-02: 1 Number of HSP's gapped: 2 Number of HSP's successfully gapped: 2 Length of query: 375 Length of database: 564 Length adjustment: 33 Effective length of query: 342 Effective length of database: 531 Effective search space: 181602 Effective search space used: 181602 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: 51 (24.3 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