Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate GFF3202 HP15_3144 NAD-dependent aldehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >FitnessBrowser__Marino:GFF3202 Length = 533 Score = 360 bits (925), Expect = e-104 Identities = 205/478 (42%), Positives = 292/478 (61%), Gaps = 17/478 (3%) Query: 24 FINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDPQVR 83 +I E+V + F ++P T I ++ + +EDID A++AA A +W + P R Sbjct: 49 YIGGEWVAPVKGQYFENITPVTGNVICEIPRSSAEDIDLALDAAHKAA-PAWGKTSPTER 107 Query: 84 MKVLYKLADLIDEHADTLAHIEALDNGKSLMCS-KGDVALTAAYFRSCAGWTDKIKGSVI 142 +L K+AD I+ + + LA E DNGK++ + D+ L A +FR AG +G + Sbjct: 108 SNILLKIADRIEANLEKLAVAETWDNGKAVRETLNADIPLAADHFRYFAGCLRAQEGHMG 167 Query: 143 ETGDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLSALYL 202 E Y EP+GV GQIIPWNFP+LMA+WKLGP L G TVLK AE TP S L L Sbjct: 168 EIDHNTVAYHFHEPLGVVGQIIPWNFPILMAAWKLGPCLAAGNCTVLKPAEQTPASILVL 227 Query: 203 ASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAESNLKK 262 +I + PPGV+N+V+G+G AG +++ +I K+AFTGST G HI+K AAE N+ Sbjct: 228 MEIIGDL-LPPGVLNIVNGYGIEAGQALATSKRIAKIAFTGSTPVGSHILKCAAE-NIIP 285 Query: 263 VTLELGGKSPNIVFDDADVKST--IQHLVTGI---FYNTGEVCCAGSRIYVQEGIYDKIV 317 T+ELGGKSPNI F D I V G+ F+N GEVC SR VQE ++++ + Sbjct: 286 STVELGGKSPNIYFSDVMKAEPEFIDKCVEGLVLAFFNQGEVCTCPSRALVQEDMFEEFM 345 Query: 318 SEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERFG---- 373 + +S+K G+P D +GAQ S+ Q DKI+ Y+ IGK+EGA V+TGG+R Sbjct: 346 QKVVQRTKSIKRGNPLDTDVQVGAQASKEQFDKIMSYLAIGKEEGAVVLTGGDREHLDEE 405 Query: 374 -NKGYFIKPTIF-GDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHT 431 N G++I+PT+F GD K ++ ++EIFGPVV +T FKT EE +A+AND+E+GL AGV T Sbjct: 406 FNNGFYIQPTLFKGDNKM--RVFQEEIFGPVVGVTTFKTEEEALAIANDTEFGLGAGVWT 463 Query: 432 TNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAV 489 + + A + I +G +W+N Y+ + FGGY +SG+GRE + AL++Y Q K + Sbjct: 464 RDTNLAYRMGRNIQAGRVWMNCYHAYPAHAAFGGYKKSGVGRETHKMALEHYQQTKCM 521 Lambda K H 0.316 0.133 0.389 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: 690 Number of extensions: 31 Number of successful extensions: 8 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: 495 Length of database: 533 Length adjustment: 35 Effective length of query: 460 Effective length of database: 498 Effective search space: 229080 Effective search space used: 229080 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 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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