Align lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_048192881.1 EJ01_RS10850 lactaldehyde dehydrogenase
Query= BRENDA::Q58806 (463 letters) >NCBI__GCF_000745485.1:WP_048192881.1 Length = 470 Score = 409 bits (1051), Expect = e-118 Identities = 216/471 (45%), Positives = 318/471 (67%), Gaps = 14/471 (2%) Query: 1 MFIDGKWINR-EDMDVINPYSLEVIKKIPALSREEAKEAIDTAEKYKEVMKNLPITKRYN 59 M I+GK +++ E +++ NP++ EVI +P + E+ + A+ A + K+ + +L + Sbjct: 3 MLINGKLMDKTEKIEIRNPFNNEVIDTVPQGNHEDVQNALIAANRAKKALNDLSSREISE 62 Query: 60 ILMNIAKQIKEKKEELAKILAIDAGKPIKQARVEVERSIGTFKLAAFYVKEHRDEVIPSD 119 L I +++ + + LAK++ ID GKPIK + EV RSI T L A K E IP D Sbjct: 63 NLYGIHEELSKNSKSLAKLITIDCGKPIKDSIEEVNRSIQTILLGAEESKRIYGETIPMD 122 Query: 120 ------DRLIFTRREPVGIVGAITPFNFPLNLSAHKIAPAIATGNVIVHHPSSKAPLVCI 173 + + FT R P+G+V AITPFN+PLNL+ HK+APAIA N ++ PS KAPL + Sbjct: 123 ACAGGENVIGFTMRLPLGVVAAITPFNYPLNLAIHKVAPAIAAKNSVILKPSMKAPLTAL 182 Query: 174 ELAKIIENALKKYNVPLGVYNLLTGAGEVVGDEIVVNEKVNMISFTGSSKVGELITKKAG 233 ++A+I++ + +P G N +TG G +GDEIV + VN ISFTGS ++GE I+K+AG Sbjct: 183 KMAEIMD-----FYLPDGALNAVTGHGRTIGDEIVTSPVVNKISFTGSVEIGEHISKQAG 237 Query: 234 FKKIALELGGVNPNIVLKDADLNKAVNALIKGSFIYAGQVCISVGMILVDESIADKFIEM 293 KK+ LELGG +P IVL+DAD+ KAV A ++GS++ AGQVCI V +++D+ IAD+FI+ Sbjct: 238 MKKLTLELGGNDPLIVLEDADIEKAVEAAVRGSYLNAGQVCIGVKRVILDDKIADEFIQK 297 Query: 294 FVNKAKVLNVGNPLDEKTDVGPLISVEHAEWVEKVVEKAIDEGGKLLLGGKRDKALFYPT 353 FVN K L G+P+D +TDVGPLI+ A VE V +A+++G +LL GGKR+ L+ PT Sbjct: 298 FVNNTKKLVTGDPMDPETDVGPLINKGAAIEVENRVNEAVNDGAELLCGGKREGTLYLPT 357 Query: 354 ILE-VDRDNILCKTETFAPVIPIIRTNE-EEMIDIANSTEYGLHSAIFTNDINKSLKFAE 411 IL+ VD + + ETF P+ PIIR N +E + +AN+T+YGL + IFTN+IN ++K + Sbjct: 358 ILDNVDSKMKIVQYETFGPISPIIRINGIDEAVKVANNTKYGLQAGIFTNNINNAMKAVK 417 Query: 412 NLEFGGVVINDSSLFRQDNMPFGGVKKSGLGREGVKYAMEEMSNIKTIIIS 462 +E GGV++N S +R DNMPFGG K SGLG+EG+KYA+E+M+ K ++I+ Sbjct: 418 EIESGGVIVNKPSTYRMDNMPFGGCKMSGLGKEGIKYAIEDMTKTKIVVIN 468 Lambda K H 0.317 0.137 0.381 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: 604 Number of extensions: 20 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: 463 Length of database: 470 Length adjustment: 33 Effective length of query: 430 Effective length of database: 437 Effective search space: 187910 Effective search space used: 187910 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: 51 (24.3 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