Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_068168204.1 HTA01S_RS06375 betaine-aldehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_001592305.1:WP_068168204.1 Length = 485 Score = 296 bits (758), Expect = 1e-84 Identities = 184/475 (38%), Positives = 266/475 (56%), Gaps = 13/475 (2%) Query: 10 YIDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERAQPEWEALPAIERA 69 +I+GQ V G + + VNPAT + + + +D +A++AA W A+ A ER Sbjct: 9 FINGQTVNGGGQVF-ESVNPATGRAYAVVHEATQDDVNRAVEAAGAGFALWSAMSATERG 67 Query: 70 SWLRKISAGIRERASEISALIVEEGGK-IQQLAEVEVAFTADYIDYMAEWARRYEGEIIQ 128 LR+ + +RER E++AL V + GK IQ+ V+V AD I+Y A A G+ Sbjct: 68 RILRRAADILRERNHELAALEVRDCGKPIQEALVVDVMSGADCIEYFAGAAATLTGQ--- 124 Query: 129 SDRPGENILLF--KRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAI 186 P +N + K LGV GI WN+P + K APAL GN ++ KPSE TP A+ Sbjct: 125 -QYPLKNAFAYTRKEPLGVCVGIGAWNYPIQIACWKSAPALAAGNAMIFKPSELTPATAV 183 Query: 187 AFAKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNIT 246 A++ E G+P GVFN+V GRG VG LA +P VA VS+TGSV G+++M TAA + Sbjct: 184 KLAEVYLEAGVPPGVFNVVQGRG-AVGAMLAAHPDVAKVSVTGSVPTGKRVMETAAGTLK 242 Query: 247 KVCLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLG 306 +V +ELGGK+P +V DDADLE AV A + G+VC RV+VQ+GI +F+ RL Sbjct: 243 RVTMELGGKSPLLVFDDADLEQAVAAAMMGNFYTQGEVCTNCTRVFVQRGIAPRFLARLK 302 Query: 307 EAMQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGK--AVEGKG-Y 363 E ++ G+P + D +G LI+ A RV +A EGA + GG+ AVEG G Sbjct: 303 ERTLLLRVGDPTD-PDTEIGALISEAHTARVMDYIASGQAEGATLVCGGERVAVEGLGDQ 361 Query: 364 YYPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVA 423 + PT+ D R +M I+ EE FGPVL ++ FDT +AI+ AN S + L + ++T +L Sbjct: 362 FVAPTIFADCRDDMRIVREEIFGPVLSMLTFDTEAEAIARANQSRFSLAAGVFTTDLQRG 421 Query: 424 MKAIKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVYLQ 478 + ++ G +IN N ++ G +SGIG + L Y Q + VY++ Sbjct: 422 HRVAAQIRAGICWINNYNITPIEMPFGGVGESGIGSENSMAALDHYTQLKTVYVE 476 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: 525 Number of extensions: 27 Number of successful extensions: 5 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: 485 Length adjustment: 34 Effective length of query: 445 Effective length of database: 451 Effective search space: 200695 Effective search space used: 200695 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