Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_073950325.1 RH94_RS25575 gamma-aminobutyraldehyde dehydrogenase
Query= reanno::pseudo5_N2C3_1:AO356_23175 (500 letters) >NCBI__GCF_001906585.1:WP_073950325.1 Length = 511 Score = 243 bits (621), Expect = 9e-69 Identities = 161/477 (33%), Positives = 246/477 (51%), Gaps = 13/477 (2%) Query: 10 YIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPAWSEQSSLRRS 69 YI GR+ + R V +PATG LA P VDAAVA+A AFP W+ + RS Sbjct: 24 YIAGRLTKGTSGRTHAVVDPATGEEVHTYELAGPDDVDAAVAAAREAFPGWAGATPGDRS 83 Query: 70 RVMFKFKELLDRHHDELAQIISREHGKVLS-DAHGEVTRGIEIVEYACGAPNLLKTDFSD 128 + +F E+L ++ A+ S + GK L +V I+ + GA L+ + Sbjct: 84 DALHRFAEVLADRAEDFARAESLQCGKPLKLTREFDVPGTIDNAAFFAGAARHLQGQSAG 143 Query: 129 NIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERDPSASLLM 188 G ++ R+P+GV + P+N+P+ + W + A+ AGN +LKP+E P SLL Sbjct: 144 EYSGDHTSYVRREPIGVVGSIAPWNYPLQMAAWKVLPAIAAGNTIVLKPAELTPLTSLLF 203 Query: 189 ARLLTEAGLPDGVFNVVQGD-KVAVDALLQHPDIEAISFVGSTPIAEYIHQQGTAQGKRV 247 A+ TEAG+PDGV N+V G K A + L+ HPD+ +SF GST + + + + TA KR+ Sbjct: 204 AQAATEAGIPDGVINIVTGTGKEAGEHLVGHPDVAMVSFTGSTAVGKRVAEIATASVKRL 263 Query: 248 QALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDELIAKLLPR 307 G K +V DADL+ A + + A + G+ C A + A + +E +A+ Sbjct: 264 HLELGGKAPFVVFDDADLEAAVNGAVAGALINTGQDCTAATRAYVQRPLYEEFVARTAAL 323 Query: 308 IDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFKVPGAE--QGF 365 ++ +++G+ PGTD+GPL++ H+ +V GF+D A AR++ G + P E G Sbjct: 324 METVRLGDPFAPGTDLGPLISHVHRDRVAGFVDRARAY-ARVVTGG---EAPQGELKNGA 379 Query: 366 FVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCFTRDGGIA 425 + TL + I Q EIFGPVL ++ + L N +G S ++RD A Sbjct: 380 YYRPTLIAGAAQDSEIVQSEIFGPVLVVLPFDSDDEGIRLANDTAYGLAASAWSRDVYRA 439 Query: 426 RAFARSIKVGMVGINVPIPVPMAWHSFGGWKRSLFG-DHHAYGEEGLRFYSRYKSVM 481 R IK G V +N IP+ ++ GG K+S FG D +Y E Y++ K VM Sbjct: 440 NRATREIKAGCVWVNDHIPI-ISEMPHGGSKQSGFGKDMSSYSFEE---YTQIKHVM 492 Lambda K H 0.320 0.137 0.412 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: 556 Number of extensions: 27 Number of successful extensions: 4 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: 511 Length adjustment: 34 Effective length of query: 466 Effective length of database: 477 Effective search space: 222282 Effective search space used: 222282 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