Align lactaldehyde dehydrogenase (EC 1.2.1.22); D-glyceraldehyde dehydrogenase (NADP+) (EC 1.2.1.89) (characterized)
to candidate WP_010529728.1 ON01_RS04100 betaine-aldehyde dehydrogenase
Query= BRENDA::P25553 (479 letters) >NCBI__GCF_000224785.1:WP_010529728.1 Length = 489 Score = 307 bits (786), Expect = 6e-88 Identities = 170/472 (36%), Positives = 267/472 (56%), Gaps = 7/472 (1%) Query: 11 IDGQFVTWRGDAWIDVVNPATEAVISRIPDGQAEDARKAIDAAERA--QPEWEALPAIER 68 IDG +VT DA D++NP + +++ + + D + AI AA +A Q +W PA ER Sbjct: 8 IDGSWVTSNSDAVRDIINPFNQKIVATVTESDESDTKAAITAARKAFDQGDWATTPAAER 67 Query: 69 ASWLRKISAGIRERASEISALIVEEGGKIQQLAEVEVAFTADYIDYMAEWARRYEGEIIQ 128 + KI+ I E++ L + GK + + ++ A Y AE A + GEII+ Sbjct: 68 GKIVHKIADLIERDREELAELESLDTGKTVEESLGDMDDIAGVFRYFAEMADKDGGEIIE 127 Query: 129 SDRPGENILLFKRALGVTTGILPWNFPFFLIARKMAPALLTGNTIVIKPSEFTPNNAIAF 188 S P + +GV I PWN+P + K+APAL GNT+V+KPSE TP +I Sbjct: 128 SPIPNSTSKVVHEPVGVCGQITPWNYPLLQASWKLAPALAAGNTLVMKPSEITPLTSIKV 187 Query: 189 AKIVDEIGLPRGVFNLVLGRGETVGQELAGNPKVAMVSMTGSVSAGEKIMATAAKNITKV 248 +++ E G+P GV NLVLG G++VG EL+ N V ++S TG + G+KIM A+ N+ + Sbjct: 188 FELMAEAGVPAGVVNLVLGPGDSVGAELSANDNVDLISFTGGIHTGKKIMQAASSNVKNL 247 Query: 249 CLELGGKAPAIVMDDADLELAVKAIVDSRVINSGQVCNCAERVYVQKGIYDQFVNRLGEA 308 LELGGK P IV DAD E AV +++ ++GQ+C+ R+ +++ I+D FV+ + + Sbjct: 248 ALELGGKNPNIVFADADFETAVDQAMNAVFFHAGQICSAGTRLIIEESIHDAFVSAIVDR 307 Query: 309 MQAVQFGNPAERNDIAMGPLINAAALERVEQKVARAVEEGARVAFGGKAVEG----KGYY 364 ++ ++ G+ + + MGPLI+ L +V V +EGA VA GG + G + Sbjct: 308 VKNIKLGSGFDES-TQMGPLISEDHLNKVVNYVENGKQEGATVAVGGSRPDDPELQNGLF 366 Query: 365 YPPTLLLDVRQEMSIMHEETFGPVLPVVAFDTLEDAISMANDSDYGLTSSIYTQNLNVAM 424 Y PT+L +M ++ +E FGPV+ V F T E+A+ +ANDS YGL+ ++T ++ A Sbjct: 367 YLPTILTGCTSDMRVVQDEGFGPVITVEKFTTEEEAVRLANDSIYGLSGGVFTNDIAKAE 426 Query: 425 KAIKGLKFGETYINRENFEAMQGFHAGWRKSGIGGADGKHGLHEYLQTQVVY 476 + + L+ G +IN N G+++SGIG GK GL EY +T+ ++ Sbjct: 427 RCVAKLRMGTVWINDVNLYFPHAPWGGYKQSGIGRELGKTGLEEYQETKHIF 478 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: 537 Number of extensions: 20 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: 489 Length adjustment: 34 Effective length of query: 445 Effective length of database: 455 Effective search space: 202475 Effective search space used: 202475 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