Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_012536595.1 AFE_RS07230 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000021485.1:WP_012536595.1 Length = 475 Score = 246 bits (629), Expect = 9e-70 Identities = 152/471 (32%), Positives = 251/471 (53%), Gaps = 9/471 (1%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 +IDG + R A V +P + +++ + D +A A+ AA A W +RA Sbjct: 9 FIDGCWTDLR--ARFVVQSPVNQQMLAEVSDCGPREADAAVQAATVAFAAWRQTTVYQRA 66 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQS 129 L + + I+ A +++ LI E GK + + E+ + AE +R GE I S Sbjct: 67 LILSRWADLIQVHAEDLARLITWEMGKPIRQSRAEIKTAVALARWYAEECKRVTGESIPS 126 Query: 130 DRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFA 189 P + + ++K +G I PWN P ++ RK+APAL G T+++KP E TP +A+ A Sbjct: 127 QFPDKRLQIWKVPIGPVFAITPWNSPVSMVVRKIAPALAAGCTVILKPDEQTPLSALKLA 186 Query: 190 KIVDEIGLPRGVFNLVLGRGET-VGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKV 248 ++ P G ++ + + L + ++A +S TGS + G+K+ A + I ++ Sbjct: 187 ELWAAAEGPAGTLQVLPSADPAPLAERLMADSRIAKLSFTGSTAVGQKLYAQGSPTIKRL 246 Query: 249 CLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEA 308 LELGG AP ++ DAD++ AV + ++ +GQ C A R+YV + I +F R EA Sbjct: 247 SLELGGHAPVLIFADADIDAAVAMTIHAKFRYAGQSCVAANRLYVDEAILPEFTARYLEA 306 Query: 309 MQAVQFGNP-AERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPP 367 M ++ G+P AE DI GPL++ A+++ + ++ A+ GAR+ GG A +G + P Sbjct: 307 MGHLKVGDPFAEDTDI--GPLVSEVAVQKFKAQLQDAMARGARLLCGGDA---QGLWCSP 361 Query: 368 TLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAI 427 TLL D+ + I HEE+F P+LP+ F + +A++ AND+ YGL + ++T++L A + Sbjct: 362 TLLADLDPQSRIFHEESFSPLLPIQGFRSEAEAVARANDTPYGLAAYLWTRDLGRAYRIA 421 Query: 428 KGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYLQ 478 + L+ G +N Q G + SG+G GK GL EYLQ + V Q Sbjct: 422 EALQCGIVGVNDGAPATPQAPFGGSKLSGLGAEGGKWGLEEYLQLRYVSFQ 472 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: 504 Number of extensions: 28 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: 475 Length adjustment: 33 Effective length of query: 446 Effective length of database: 442 Effective search space: 197132 Effective search space used: 197132 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: 51 (24.3 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