Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_007152862.1 MDG893_RS06100 2-hydroxymuconic semialdehyde dehydrogenase
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_000170835.1:WP_007152862.1 Length = 486 Score = 330 bits (846), Expect = 7e-95 Identities = 189/482 (39%), Positives = 271/482 (56%), Gaps = 14/482 (2%) Query: 24 FINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSSWSTSDPQVR 83 +IN ++V S S K F V+P+ + I++V+EA E++D AV+AA +A W + R Sbjct: 7 YINGQYVGSASGKLFDNVNPANGQVISKVHEAGREEVDAAVKAAKSALRGPWGKMTLEER 66 Query: 84 MKVLYKLADLIDEHADTLAHIEALDNGKSL-MCSKGDVALTAAYFRSCAGWTDKIKGSVI 142 +L+K+AD I+ + E LD GK + S D+ AA F+ A + Sbjct: 67 TGILHKVADGINARFEEFLEAECLDTGKPRSLASHIDIPRGAANFKVFADMIKNVPTESF 126 Query: 143 ET----GDTHFNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAESTPLS 198 E G NY R P GV G I PWN PLL+ +WK+GP L G T V+K +E TP + Sbjct: 127 EMPTPDGTGALNYAVRRPKGVIGVISPWNLPLLLMTWKVGPALACGNTVVVKPSEETPTT 186 Query: 199 ALYLASLIKEAGAPPGVVNVVSGFG-PTAGAPISSHPKIKKVAFTGSTATGRHIMKAAAE 257 L ++K+AG P GV NVV GFG +AGA ++ HP + FTG T TG IMKAAA+ Sbjct: 187 TALLGDVMKDAGVPDGVFNVVHGFGGDSAGAFLTEHPMVDGFTFTGETGTGEVIMKAAAK 246 Query: 258 SNLKKVTLELGGKSPNIVFDDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIYDKIV 317 ++ ++LELGGK+ +VF D D+ I+ + F N G+VC R+YV+ I+D+ V Sbjct: 247 G-IRDISLELGGKNAGLVFADCDMDKAIEGTMRSAFANCGQVCLGTERVYVERSIFDEFV 305 Query: 318 SEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGG------ER 371 K AAE +KIG P + MG S +K+L Y +GAT++TGG E Sbjct: 306 GRLKEAAEGIKIGPPDDIEADMGPLVSLKHREKVLSYYQKAVDDGATLVTGGGVPEMPEA 365 Query: 372 FGNKGYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVHT 431 G +++PTI+ + ED ++ DEIFGP V + F EE I LAN YGLA+ + + Sbjct: 366 LAG-GAWVQPTIWTGLPEDSAVITDEIFGPCVHLCPFDNEEEAIELANSLPYGLASAIWS 424 Query: 432 TNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAVRI 491 N++ A V+ +I +G IWVN++ PFGG QSGIGRE G +L+ YT++K + + Sbjct: 425 ENITRAHRVAGQIEAGIIWVNSWFLRDLRTPFGGSKQSGIGREGGVHSLEFYTEMKNICV 484 Query: 492 GL 493 L Sbjct: 485 KL 486 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: 641 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: 495 Length of database: 486 Length adjustment: 34 Effective length of query: 461 Effective length of database: 452 Effective search space: 208372 Effective search space used: 208372 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 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