Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_011829917.1 MPE_RS11735 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000015725.1:WP_011829917.1 Length = 492 Score = 315 bits (808), Expect = 2e-90 Identities = 177/465 (38%), Positives = 270/465 (58%), Gaps = 12/465 (2%) Query: 22 AWID------VVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERASWLRKI 75 AW+D V +PAT V++++ + A DA A+ AA RA P W A A ERAS L K Sbjct: 26 AWVDRGEHFAVTDPATGQVLAQVANLGAADAEAALAAAARAWPAWRAKTAKERASVLMKW 85 Query: 76 SAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQSDRPGEN 135 + + A +++ ++ E GK A+ EV + A +I++ AE A+R GE + + + Sbjct: 86 YQLLLQHADDLARIMTAEQGKPLAEAKGEVGYGASFIEWFAEEAKRVYGETVPTTDNNKR 145 Query: 136 ILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFAKIVDEI 195 L+ K+A+GV I PWNFP +I RK+APAL G +VIKP+E TP +A+A A++ Sbjct: 146 YLVLKQAMGVCAAITPWNFPIAMITRKVAPALAAGCPVVIKPAEQTPLSALAVAELAQRA 205 Query: 196 GLPRGVFNLVLGRGE---TVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKVCLEL 252 G+P GV N++ E +G L + V +S TGS G +M A I K+ LEL Sbjct: 206 GMPAGVLNVLTADAERSIQIGNVLCASDTVRHLSFTGSTEVGRILMKQCAPTIKKLSLEL 265 Query: 253 GGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEAMQAV 312 GG AP IV DDADL+ AV+ + S+ N+GQ C CA R+YVQ G+YD FV +L ++A+ Sbjct: 266 GGNAPFIVFDDADLDSAVEGAMISKYRNAGQTCVCANRLYVQAGVYDAFVEKLAAKVKAI 325 Query: 313 QFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPTLLLD 372 + GN E + GPLI+ AAL +VE VA A+ +GA++ GG+ + + +Y PT+L Sbjct: 326 KVGNGFEAG-VTQGPLIDEAALAKVESHVADALAKGAKLLTGGQRIGER--FYSPTVLAQ 382 Query: 373 VRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIKGLKF 432 EM EETFGPV PV F+T + +++AND+++GL S Y++++ + + L++ Sbjct: 383 ATGEMLCAREETFGPVAPVFRFETEAEVVALANDTEFGLASYFYSRDVGRIFRVGEALEY 442 Query: 433 GETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYL 477 G IN + G ++SG+G HG+ +Y++ + + L Sbjct: 443 GMVGINTGLISTAEVPFGGVKQSGLGREGSHHGIDDYVEIKYLCL 487 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: 551 Number of extensions: 31 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: 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