Align Methylmalonate-semialdehyde dehydrogenase [inositol] (EC 1.2.1.27) (characterized)
to candidate WP_034274777.1 AMYHA_RS23925 gamma-aminobutyraldehyde dehydrogenase
Query= reanno::Caulo:CCNA_01360 (500 letters) >NCBI__GCF_000504245.1:WP_034274777.1 Length = 479 Score = 226 bits (577), Expect = 1e-63 Identities = 158/485 (32%), Positives = 244/485 (50%), Gaps = 22/485 (4%) Query: 2 MRDIPHFIGGQKVDGASGRFGEVFDPNTGKVQARVALASAGELNTAI-ANAKVAQAAWAA 60 +R + +FI G VD A GR E+ DP TG V A L+SA +++TA A A + W Sbjct: 5 VRRLKNFINGAYVDAADGRTSEIVDPATGHVVAEAPLSSADDVDTAFRAAADAFENGWRD 64 Query: 61 TNPQRRARVMFEFKRLLEVHMDELAALLSSEHGKVIADSKGD-IQRGLEVIEFACGVPHL 119 P R + +F +E DEL A + GK +K + I + L+ + F G Sbjct: 65 ATPGERQIALNKFADAVEDRADELVAAEVANCGKPAQMTKDEEIFQVLDALRFFAGASRN 124 Query: 120 LKGEYTQGAGPGIDVYSMRQPLGVVAGITPFNFPAMIPMWMFGPAIATGNAFILKPSERD 179 L+G+ G + R+P+G V ITP+N+P + W GPA+A GN+ +LKPS+ Sbjct: 125 LEGKAAGEYMAGHTSWVRREPIGPVGQITPWNYPMAMAAWKIGPALAAGNSVVLKPSDTT 184 Query: 180 PSVPVRLAELMIEAGLPPGVLNVVHGDKDCVEAILDHPDIKAVSFVGSSDIAQSVFQRAG 239 P + LAE+ E LP GV NVV GD+D A++DHP + +S GS+ + + + Sbjct: 185 PMSTLLLAEIAAEF-LPAGVFNVVTGDRDTGRALVDHPTPRLISLTGSTRAGKEIAEAGA 243 Query: 240 AAGKRVQAMGGAKNHGLVMPDADLDQAVADIIGAAYGSAGERCMALPVVVPVGEKTATAL 299 KR+ G K +V DAD++ A I GA Y +AG+ C A V+ A + Sbjct: 244 KDLKRLHLELGGKAPVVVFDDADIEAAAEGIAGAGYFNAGQDCTAATRVL-----AAPGI 298 Query: 300 REKLVAAIG-GLRVGVSTDP---DAHYGPVVSAAHKARIESYIQMGVDEGAELVVDGRGF 355 + L AA+ R V+ P DA YGP+ + AR+ +I D A+++ G Sbjct: 299 HDDLAAALAEQARKTVTAGPDNADADYGPLNNPNQLARVSGFIDRAPDH-AKILAGGERV 357 Query: 356 SLQGHEEGFFVGPTLFDHVKPTSRSYHDEIFGPVLQMVRAESLEEGIALASRHQYGNGVA 415 + G+F PT+ ++ DE+FGPV+ + R + + + A+ +YG + Sbjct: 358 G----DTGYFYAPTVVAGLRQGDELTTDEVFGPVVTVQRFDDEDTAVNWANSVEYGLASS 413 Query: 416 IFTRNGDAAREFADQVEVGMVGINVPIPVPVAYHSFGGWKRSGFG-DLNQYGMDGVRFYT 474 ++TR+ A + +++ G V IN IP+ +A GG+K SG+G DL+ Y + YT Sbjct: 414 VWTRDHARALRVSRRLDFGCVWINTHIPL-IAEMPHGGFKHSGYGKDLSAYSFEE---YT 469 Query: 475 RTKTV 479 R K V Sbjct: 470 RVKHV 474 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: 613 Number of extensions: 28 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: 479 Length adjustment: 34 Effective length of query: 466 Effective length of database: 445 Effective search space: 207370 Effective search space used: 207370 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 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