Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_010443040.1 G7G_RS0118970 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000192475.1:WP_010443040.1 Length = 491 Score = 320 bits (821), Expect = 5e-92 Identities = 177/463 (38%), Positives = 271/463 (58%), Gaps = 4/463 (0%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 YI+G +V G+A V NPAT +I+ + D E R+ ID A A+ EW A ER Sbjct: 22 YINGAWV--EGEATFPVHNPATGDLIANVTDIDIEGTRQTIDVAYAAKKEWAAQTGKERG 79 Query: 70 SWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQS 129 + LRK + E A +++ ++ E GK A E+ + A +I++ AE A+R G++I Sbjct: 80 AILRKWFDLMVENADDLATILTAEMGKPWAEARGEILYGASFIEWFAEEAKRIYGDVIPG 139 Query: 130 DRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAFA 189 + + I++ K+ +GV I PWNFP +IARK+ PAL G T V +P+ TP +A+A A Sbjct: 140 HQRDKRIVVLKQPVGVVGSITPWNFPNAMIARKVGPALAVGCTFVARPATLTPLSALAMA 199 Query: 190 KIVDEIGLPRGVFNLVLGRGET-VGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKV 248 + + G+P GV N++ G + VG EL N KVA ++ TGS G+ +M AA I K+ Sbjct: 200 VLGERAGIPAGVLNVIPGTDSSGVGNELCTNDKVAKITFTGSTRVGQILMRQAAGTIKKM 259 Query: 249 CLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEA 308 LELGG AP IV DDAD++ AV + ++ N+GQ C CA R+YVQ G+YD+F +L E Sbjct: 260 SLELGGNAPFIVFDDADVDAAVDGAMIAKFRNNGQTCVCANRIYVQAGVYDEFAAKLAEK 319 Query: 309 MQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEGKGYYYPPT 368 + + GN + I GPLIN AA+ +VE+ ++ AV +GA V GGK + G ++ PT Sbjct: 320 TKDLNVGN-GFGDGITTGPLINDAAVAKVEEHISDAVSKGATVTMGGKRSDLGGTFFEPT 378 Query: 369 LLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAMKAIK 428 +L V ++M + +ETFGPV P+ F+ +D ++MANDS++GL S Y+++L + + Sbjct: 379 VLTGVTRDMVVAKDETFGPVAPLFKFEEEDDVVAMANDSEFGLASYFYSRDLARVWRVAE 438 Query: 429 GLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQ 471 L+ G +N G ++SG+G K+G ++L+ Sbjct: 439 ALESGMVGVNTGLISTEVAPFGGVKQSGLGREGSKYGTEDFLE 481 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: 563 Number of extensions: 23 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: 491 Length adjustment: 34 Effective length of query: 445 Effective length of database: 457 Effective search space: 203365 Effective search space used: 203365 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