Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_009763662.1 MICLODRAFT_RS20175 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000262405.1:WP_009763662.1 Length = 495 Score = 313 bits (803), Expect = 6e-90 Identities = 164/468 (35%), Positives = 268/468 (57%), Gaps = 1/468 (0%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 Y+ G+++ I V +P A+I +PD + AR+AID A Q +W A ER+ Sbjct: 26 YVAGEWIDAPDGKTIPVTDPFDGALILEVPDLGPDAARRAIDKAHAVQKDWAKRTAKERS 85 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQS 129 + LR+ I A +++ ++ E GK A+ EV A YI++ AE A+R +G++I Sbjct: 86 AILRRWYDLIVANADDLALILTTEQGKPLAEAKGEVISNAAYIEWFAEEAKRIDGDVIPG 145 Query: 130 DRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFA 189 P + I++ K+ +GV I PWNFP +I RK+ PAL G T+V+KP+ TP +A+A A Sbjct: 146 ATPSQRIVVLKQPVGVCAAITPWNFPNGMITRKVGPALAAGCTMVLKPAAQTPLSALALA 205 Query: 190 KIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVC 249 + + G+P+G F++V G + +G+E NPKVA ++ TGS G +M AA I ++ Sbjct: 206 VLAERAGVPKGAFSVVTGEAKPIGEEFCHNPKVAKITFTGSTGVGRWLMKEAADGIKRLS 265 Query: 250 LELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAM 309 LELGG AP IV DDADL+ AV+ + S+ N+GQ C CA R+YVQ+G+ + F +L Sbjct: 266 LELGGNAPFIVFDDADLDAAVEGAMASKFRNAGQTCVCANRIYVQEGVAEAFAEKLAAKA 325 Query: 310 QAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPTL 369 +++ G + + MGPLI+ A+ ++E+ V +++G ++ GGK + ++ PT+ Sbjct: 326 GSLKLGRGTDAG-VTMGPLIDDRAVAKMEEHVRDVLDKGGKLLVGGKRSDLGSTFFEPTV 384 Query: 370 LLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKG 429 + V Q M + EETF P+ P++ F D I+MANDS++GL S Y +++ + + Sbjct: 385 MTGVTQAMKVTKEETFAPLAPIITFKDEADVIAMANDSEFGLASYFYAKDMARVWRVAEA 444 Query: 430 LKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYL 477 L+ G +N G ++SG+G K+G+ +L+ + + L Sbjct: 445 LESGMVGVNTPALANEMAPFGGVKQSGLGREGSKYGIEGFLEIKYINL 492 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: 574 Number of extensions: 34 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: 495 Length adjustment: 34 Effective length of query: 445 Effective length of database: 461 Effective search space: 205145 Effective search space used: 205145 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