Align Methylmalonate-semialdehyde dehydrogenase [inositol] (EC 1.2.1.27) (characterized)
to candidate WP_015934068.1 MNOD_RS36935 betaine-aldehyde dehydrogenase
Query= reanno::Caulo:CCNA_01360 (500 letters) >NCBI__GCF_000022085.1:WP_015934068.1 Length = 489 Score = 243 bits (619), Expect = 1e-68 Identities = 169/483 (34%), Positives = 254/483 (52%), Gaps = 25/483 (5%) Query: 8 FIGGQKVDGASGRFGEVFDPNTGKVQARVALASAGELNTAIANAKVAQAAWAATNPQRRA 67 FIGG+ + A +P TG++ A V A+ +L A+A A QA WAAT + R Sbjct: 10 FIGGRLAEEAGRCTFRSVNPATGEILAEVEHATREDLEAAVAAAARGQAVWAATPARERG 69 Query: 68 RVMFEFKRLLEVHMDELAALLSSEHGKVIADSKG-DIQRGLEVIEFACGVPHLLKGEYTQ 126 RV+ LL DELA L S + GK IA+++ D+ G +V+E+ G+ ++G Sbjct: 70 RVLMRAVALLRARNDELARLESLDTGKPIAETRVVDVATGADVLEYYAGLAAAIEGRQIP 129 Query: 127 GAGPGIDVYSMRQPLGVVAGITPFNFPAMIPMWMFGPAIATGNAFILKPSERDPSVPVRL 186 VY+ R+PLG+VAGI +N+P I +W PA+A GNA I KPSE P L Sbjct: 130 LRETSF-VYTRREPLGIVAGIGAWNYPIQIALWKSAPALAAGNAMIFKPSEVTPLTAFAL 188 Query: 187 AELMIEAGLPPGVLNVVHGDKDCVEA-ILDHPDIKAVSFVGSSDIAQSVFQRAGAAG--- 242 A + EAGLP GV +V+ G + A + +HP I VSF G + V AGAA Sbjct: 189 AGIYAEAGLPDGVFSVLPGLGGEIGAWLTEHPAIAKVSFTGGTLTGAKVM--AGAARSTL 246 Query: 243 KRVQAMGGAKNHGLVMPDADLDQAVADIIGAAYGSAGERCM-ALPVVVPVGEKTATALRE 301 K V G K+ +V+ DADLD+A + A + S+G+ C V VP K A Sbjct: 247 KEVTMELGGKSPLIVLDDADLDRAADIAVAANFFSSGQICTNGTRVFVPAPLK--AAFEA 304 Query: 302 KLVAAIGGLRVGVSTDPDAHYGPVVSAAHKARIESYIQMGVDEGAELVVDGRGFSLQGH- 360 +++ + +R+G D ++GP+ S AH+ ++ ++I+ GV++GA L++ G +L+G Sbjct: 305 RVLKRVARIRIGDPLDEATNFGPLASHAHRDKVLAFIRSGVEQGARLLIGGH--ALEGRF 362 Query: 361 EEGFFVGPTLFDHVKPTSRSYHDEIFGPVLQMVRAESLEEGIALASRHQYGNGVAIFTRN 420 G +V PT+F + +EIFGPV+ ++ ES E +A A+ YG + TR+ Sbjct: 363 AAGAYVAPTVFTDCRDDMEIVREEIFGPVMSLLPYESEAEALARANATLYGLAAGVVTRD 422 Query: 421 GDAAREFADQVEVGMVGINV----PIPVPVAYHSFGGWKRSGFGDLNQYGMDGVRFYTRT 476 A ++ G+ IN P +PV GG K+SG G N G++ + YTRT Sbjct: 423 LARAHRITHGLQAGICWINTWGESPPEMPV-----GGTKQSGIGREN--GIETLERYTRT 475 Query: 477 KTV 479 K++ Sbjct: 476 KSI 478 Lambda K H 0.320 0.137 0.409 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: 597 Number of extensions: 31 Number of successful extensions: 6 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: 500 Length of database: 489 Length adjustment: 34 Effective length of query: 466 Effective length of database: 455 Effective search space: 212030 Effective search space used: 212030 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: 52 (24.6 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