Align Malonate-semialdehyde dehydrogenase 1; MSA dehydrogenase 1; EC 1.2.1.-; Methylmalonate-semialdehyde dehydrogenase 1; MMSA dehydrogenase 1; MSDH 1; EC 1.2.1.27 (uncharacterized)
to candidate WP_038806127.1 HK29_RS05075 NADP-dependent glyceraldehyde-3-phosphate dehydrogenase
Query= curated2:Q5L025 (488 letters) >NCBI__GCF_000382825.1:WP_038806127.1 Length = 474 Score = 224 bits (572), Expect = 4e-63 Identities = 141/462 (30%), Positives = 240/462 (51%), Gaps = 18/462 (3%) Query: 9 TVLKNYIGGQWVASSGTETLEVPNPATGEVLARVPISTKEDVDQAVQAAKKAFATWKDVP 68 T +N + G W +S + + + +P E L VP ++ +VD+A++AA+ A W+D+ Sbjct: 2 TNYQNLVNGNWKSSE--KEITIYSPINQEKLGTVPAMSQAEVDEAMKAARAALPAWRDLA 59 Query: 69 VPKRARIMFSFHHLLNQHHEELAELVVQENGKAYKEAYGEIQRGIECVEFAAGAPTLLMG 128 +RA + +L + E++ ++ +E K K A GE+ R + + FAA + G Sbjct: 60 PVERAAYLHKTADILERDKEKIGTILAKEVAKGIKAAIGEVVRTADLIRFAAEEGLRITG 119 Query: 129 ESLSNIAEEIDSE-----MFRYPLGVVAGITPFNFPMMVPLWMFPLAIVCGNTFVLKPSE 183 +++ E S+ + R P+GVV I PFN+P+ + A++ GN + KP Sbjct: 120 QAMEGGGFEAASKNKLAVVRREPVGVVLAIAPFNYPVNLSGSKIAPALIAGNVVMFKPPT 179 Query: 184 RTPILANKLAELFTEAGAPPGVLNVVHG-AHEVVNALIDHEDIRAISFVGSQPVAKYVYE 242 + I LA+ F EAG P GV N + G E+ + +I+H+++ I+F GS P+ + + Sbjct: 180 QGSISGLLLAKAFDEAGIPAGVFNTITGRGSEIGDYIIEHKEVNFINFTGSTPIGERIGR 239 Query: 243 RTAAQGKRVQALSGAKNHHIVMPDADVETAVQHVISSAFGSAGQRCMACSAVVIVGE-NE 301 A + + G K+ IV+ DAD+E A + ++ AF +GQRC A V++V + Sbjct: 240 --LAGMRPIMLELGGKDAAIVLEDADLEHAAKQIVGGAFSYSGQRCTAIKRVLVVESVAD 297 Query: 302 TFVRRLKQKADELIIGNGMDPEVLLTPVIRQSHREKVLGYIQKGIEEGAVLLRDGRKEMD 361 L+ + +L +G+ D +TPV+ + + + G IQ E+GA L ++E Sbjct: 298 RLAELLQAEVAKLTVGDPFD-NADITPVVDNASADFIWGLIQDAQEKGAKALSPIKRE-- 354 Query: 362 DRPEGNFLGPTIFDYVTPDMTIAKEEIFAPVLSLLRANDLDEALSYIRKSRYGNGATIYT 421 GN + P +FDYVT DM +A EE+F PVL ++R D +EA++ +S +G ++++T Sbjct: 355 ----GNLIWPGLFDYVTRDMKLAWEELFGPVLPIIRVADANEAVAIANESEFGLQSSVFT 410 Query: 422 KDAKAVRKFREEADAGMLGINVGVPATMAFFPFSGWKDSFYG 463 D K + E+ + G + IN FPF G K S G Sbjct: 411 NDFKKAFEIAEKLEVGTVHINNKTQRGPDNFPFLGVKGSGAG 452 Lambda K H 0.319 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: 512 Number of extensions: 26 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: 488 Length of database: 474 Length adjustment: 34 Effective length of query: 454 Effective length of database: 440 Effective search space: 199760 Effective search space used: 199760 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 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