Align NAD(P)+ L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_101589837.1 BJEO58_RS12670 aldehyde dehydrogenase family protein
Query= metacyc::MONOMER-16244 (495 letters) >NCBI__GCF_900169175.1:WP_101589837.1 Length = 496 Score = 350 bits (897), Expect = e-101 Identities = 192/479 (40%), Positives = 275/479 (57%), Gaps = 6/479 (1%) Query: 16 TYEQPTGLFINNEFVQSKSKKTFGTVSPSTEEEITQVYEAFSEDIDDAVEAATAAFHSS- 74 T T L+I+ +V S T P+ E+ V EA ED++ A+ AA A+ Sbjct: 2 TTSDATTLYIDGSWVASSDGGTRTVTCPADGAEVGVVSEATPEDVERAIAAARRAYDDGV 61 Query: 75 WSTSDPQVRMKVLYKLADLIDEHADTLAHIEALDNGKSLMCSKGDVALTAAYFRSCAGWT 134 W+ R +L ++AD I D A EALD GK L+ ++GD+ A+ FR Sbjct: 62 WADRPASERGDLLLRVADGITARKDDFARAEALDTGKRLVEAEGDMDDIASAFRYFGKIA 121 Query: 135 DKIKGSVIETGDTH-FNYTRREPIGVCGQIIPWNFPLLMASWKLGPVLCTGCTTVLKTAE 193 D+ G +++ GD+ + EP+GVCG I PWNFPLL ASWK+ P L G + +LK AE Sbjct: 122 DQNPGRLVDAGDSSVISRVVYEPVGVCGMITPWNFPLLQASWKVAPALAAGNSFILKPAE 181 Query: 194 STPLSALYLASLIKEAGAPPGVVNVVSGFGPTAGAPISSHPKIKKVAFTGSTATGRHIMK 253 TP +++ L +++ AG P GV N+V G G T GAP+S+HP I V+FTG TGR I + Sbjct: 182 LTPHTSMLLMEVLEAAGLPAGVANLVLGAGGTVGAPLSTHPGIDLVSFTGGAVTGRKISE 241 Query: 254 AAAESNLKKVTLELGGKSPNIVFDDADVKSTIQHLVTGIFYNTGEVCCAGSRIYVQEGIY 313 +AA + +KKV LELGGK+PN+VF DAD ++ + + +T F ++G VC AG+R+ VQ+ I Sbjct: 242 SAA-ATVKKVALELGGKNPNVVFADADFEAAVDNALTAAFLDSGLVCSAGTRLIVQDTIA 300 Query: 314 DKIVSEFKNAAESLKIGDPFKEDTFMGAQTSQLQLDKILKYIDIGKKEGATVITGGERFG 373 ++ V E + AE + +G PF E G SQ DK+ Y+ G + GA + GG G Sbjct: 301 ERFVDELVSRAEGIVMGGPFDEKAETGPLISQEHRDKVTDYVTRGVEAGARLRVGGHWGG 360 Query: 374 NK---GYFIKPTIFGDVKEDHQIVRDEIFGPVVTITKFKTVEEVIALANDSEYGLAAGVH 430 + G+F PT+ D+ V +E FGPV+T+ F T E I AN +EYGLA V Sbjct: 361 EEHANGFFYAPTVLDQCTRDNPAVIEEGFGPVITVETFSTEAEAIQTANHTEYGLAGAVW 420 Query: 431 TTNLSTAISVSNKINSGTIWVNTYNDFHPMVPFGGYSQSGIGREMGEEALDNYTQVKAV 489 T++ A VS K+ GTIW+N Y+ + P +GG+ QSGIGRE+G + Y + K + Sbjct: 421 TSDAGVANRVSRKLRHGTIWINDYHPYLPQAEWGGFKQSGIGRELGPSGMGEYVEPKHI 479 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: 642 Number of extensions: 35 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: 496 Length adjustment: 34 Effective length of query: 461 Effective length of database: 462 Effective search space: 212982 Effective search space used: 212982 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