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_084058850.1 B9A12_RS14640 L-glutamate gamma-semialdehyde dehydrogenase
Query= curated2:Q5L025 (488 letters) >NCBI__GCF_900176285.1:WP_084058850.1 Length = 994 Score = 245 bits (626), Expect = 5e-69 Identities = 160/450 (35%), Positives = 242/450 (53%), Gaps = 18/450 (4%) Query: 26 ETLEVPNP-ATGEVLARVPISTKEDVDQAVQAAKKAFATWKDVPVPKRARIMFSFHHLLN 84 ET NP T +V+ V + ++ +AV AAK+AFA W+D P +RA +F Sbjct: 519 ETFSSTNPNRTDQVVGVVASAGEKKAREAVAAAKEAFAAWRDTPPRERAEYLFRAAQAAR 578 Query: 85 QHHEELAELVVQENGKAYKEAYGEIQRGIECVEFAAGAPTLLMG--ESLSNIAEEIDSEM 142 ELA L V E GK++KEA G++ I+ +E+ G + +G + N+ E+ S + Sbjct: 579 SRRYELAALQVYEVGKSWKEADGDVCEAIDFLEYY-GREMIRLGAPRRMGNVPGEV-SHL 636 Query: 143 FRYPLGVVAGITPFNFPMMVPLWMFPLAIVCGNTFVLKPSERTPILANKLAELFTEAGAP 202 F P GV A + P+NFP + + M A+V GNT V KP+ ++P++ L +F EA P Sbjct: 637 FYEPRGVAAVVAPWNFPFAISVGMTSAALVTGNTVVYKPASQSPVIGYWLYRIFQEAKLP 696 Query: 203 PGVLNVVHG-AHEVVNALIDHEDIRAISFVGSQPVAKYVYERTAAQG------KRVQALS 255 GVLN + G ++ + L+ H D+ I+F GS+ V + ER A K V A Sbjct: 697 KGVLNFLPGPGAKIGDFLVTHPDVAMIAFTGSKEVGLRIIERAAKTPPDAHFVKNVVAEM 756 Query: 256 GAKNHHIVMPDADVETAVQHVISSAFGSAGQRCMACSAVVIVGEN-ETFVRRLKQKADEL 314 G KN I+ DAD++ AV HV+ SAFG GQ+C ACS ++++ EN + RL+ A+ L Sbjct: 757 GGKNAIIIDADADLDEAVVHVLHSAFGYQGQKCSACSRLIVLEENYHKLLERLRAAAESL 816 Query: 315 IIGNGMDPEVLLTPVIRQSHREKVLGYIQKGIEEGAVLLRDGRKEMDDRPEGNFLGPTIF 374 +G D + ++ VI REK+L YI+ G EG VL+ + + G F+ TIF Sbjct: 817 ELGPVEDAKNVMGAVIDAKAREKILEYIEIGKREGKVLV----ERPVEGSNGYFVPLTIF 872 Query: 375 DYVTPDMTIAKEEIFAPVLSLLRANDLDEALSYIRKSRYGNGATIYTKDAKAVRKFREEA 434 + P+ +A+EEIF PVLS+++ D DEAL ++Y ++++ + + K R Sbjct: 873 TDIRPEHRLAQEEIFGPVLSVMKVRDFDEALEVANSTQYALTGAVFSRSPENIEKARRRF 932 Query: 435 DAGMLGINVG-VPATMAFFPFSGWKDSFYG 463 G L IN G A + PF G+K S G Sbjct: 933 RVGNLYINRGSTGAIVERHPFGGFKMSGVG 962 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: 1038 Number of extensions: 49 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: 994 Length adjustment: 39 Effective length of query: 449 Effective length of database: 955 Effective search space: 428795 Effective search space used: 428795 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: 54 (25.4 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