Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_012755384.1 RLEG_RS24785 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000023185.1:WP_012755384.1 Length = 495 Score = 313 bits (802), Expect = 8e-90 Identities = 167/470 (35%), Positives = 275/470 (58%), Gaps = 5/470 (1%) Query: 9 MYIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIER 68 +YI G + G+ I+V++P+TEAVI+ +PD DA A++AA A W P +R Sbjct: 24 LYIGGAWRPAAGEGRIEVIDPSTEAVIAAVPDATLADAAAAVEAAASAAESWRETPPRKR 83 Query: 69 ASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQ 128 + LR+ + ER+ ++ LI E GK + A EVA+ A++ + AE A R GE Sbjct: 84 SEILRRCFELMVERSETLARLISLENGKALRDARGEVAYAAEFFRWNAEEAVRISGEFGL 143 Query: 129 SDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAF 188 + G I++ + +G+ I PWNFP + RK+APAL G T+++KP+ TP A A Sbjct: 144 APAGGNRIVVDYQPIGICVLITPWNFPAAMATRKIAPALAAGCTVILKPASETPLTAYAL 203 Query: 189 AKIVDEIGLPRGVFNLVLGR--GETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNIT 246 A + +E G+P GV N++ G + LA +P+V +S TGS G ++A AAKN+ Sbjct: 204 AALYEEAGVPPGVVNVMTTSTPGPVIAAMLA-DPRVRKLSFTGSTGVGRMLLAEAAKNVI 262 Query: 247 KVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLG 306 +ELGG AP +V DDAD++ A++ ++ +++ N+G+ C A R+Y+Q GI+D F + Sbjct: 263 SCSMELGGNAPFVVFDDADIDAAIEGLMVAKMRNAGEACTAANRIYIQSGIHDAFAKKFT 322 Query: 307 EAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYP 366 + M A+ G+ + D GP+I A+E++E+ V A+ GARV GG+++ G+G++Y Sbjct: 323 QRMAALNVGSGVDA-DTECGPMITRKAVEKIERLVEDAISRGARVLCGGRSLAGRGFFYR 381 Query: 367 PTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKA 426 PT+L+DV + EE FGPV P+ F++ + I+ AND++YGL + IYT+++ M+ Sbjct: 382 PTVLVDVSPASDMGCEEIFGPVAPLYRFESEAEVIAAANDTEYGLAAYIYTRDIGRGMRV 441 Query: 427 IKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGK-HGLHEYLQTQVV 475 ++ G +NR G ++SG+G G+ HG+ E+++ + + Sbjct: 442 ASKIEAGMIALNRGLVSDPAAPFGGVKQSGLGREGGQHHGIAEFMEAKYI 491 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: 552 Number of extensions: 30 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 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