Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_085639722.1 MGEO_RS15320 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_002115805.1:WP_085639722.1 Length = 492 Score = 305 bits (781), Expect = 2e-87 Identities = 163/467 (34%), Positives = 264/467 (56%), Gaps = 2/467 (0%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 YI G++V A V NPA I+ + D + AIDAA AQ +W ERA Sbjct: 23 YIAGEWVDADDGATFSVSNPARGDTIAEVADVTRIETALAIDAAYIAQKDWSKWTGKERA 82 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQS 129 + LRK + E A +++ ++ E GK A E+ + A ++++ AE A+R GE I Sbjct: 83 AVLRKWFDLMVENADDLATILTAEQGKPHAEARGEILYGASFVEWFAEEAKRTYGETIPG 142 Query: 130 DRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFA 189 + + I + K+ +GV I PWNFP +I RK+ PAL G V +P+ TP +A+A Sbjct: 143 HQRDKRITVIKQPIGVAASITPWNFPNAMITRKVGPALAAGCAFVARPAAETPLSALALG 202 Query: 190 KIVDEIGLPRGVFNLV-LGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKV 248 ++ + G+P+GV +++ R +G+E NPKV ++ TGS G ++ AA + K Sbjct: 203 ELAERAGIPKGVLSIIPSSRSSDIGKEFCENPKVRKLTFTGSTEVGRILLKQAADQVMKC 262 Query: 249 CLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEA 308 +ELGG AP IV DDA+L+ AV+ + S+ N+GQ C CA R+YVQ G+YD F +L +A Sbjct: 263 SMELGGNAPFIVFDDANLDAAVEGALISKYRNNGQTCVCANRIYVQAGVYDAFAAKLKDA 322 Query: 309 MQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPT 368 ++A+ G+ + + +GPLIN A+ +VE+ V A+ +G V GGK + G ++ PT Sbjct: 323 VEAMPVGDGLS-DGVQLGPLINEEAVAKVEEHVEDAIAKGGTVISGGKRHDLGGTFFQPT 381 Query: 369 LLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIK 428 ++ +EM+ EETFGP+ P+ FDT+E+ I +AND+ +GL + Y ++L+ + + Sbjct: 382 IVTGATREMAFAQEETFGPLAPLFNFDTVEEVIDLANDTIFGLAAYFYARDLSRVTQVQE 441 Query: 429 GLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVV 475 L++G +N G ++SG+G HG+ E+++ + + Sbjct: 442 ALEYGMVGVNTGLISTEVAPFGGVKQSGLGREGSHHGMDEFMEMKYI 488 Lambda K H 0.318 0.135 0.392 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: 22 Number of successful extensions: 3 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: 479 Length of database: 492 Length adjustment: 34 Effective length of query: 445 Effective length of database: 458 Effective search space: 203810 Effective search space used: 203810 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.3 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.7 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