Align NAD+-dependent L-lactaldehyde dehydrogenase (EC 1.2.1.22) (characterized)
to candidate WP_027721879.1 H589_RS0109990 aldehyde dehydrogenase
Query= metacyc::MONOMER-16246 (477 letters) >NCBI__GCF_000425265.1:WP_027721879.1 Length = 478 Score = 524 bits (1349), Expect = e-153 Identities = 264/474 (55%), Positives = 336/474 (70%), Gaps = 5/474 (1%) Query: 8 HRNYIDGAF--VESAAHLEVFNPANGALLSRVPAASAEEVERALAAARAAQKDWARKPAI 65 ++ YI+G F +S V NP +++ P + E AL AA AQK+WA K I Sbjct: 4 YQQYINGEFRNADSNEQFAVINPFTEKIIAMAPKGGKHDAELALEAASVAQKEWAAKSCI 63 Query: 66 ERAGHLRRIAAKIRADAGRIARTITLEQGKIASLAEVEVNFTADYLDYMAEWARRLEGEI 125 ERAG L+++A IR + +ART+ EQ KI LA+VE++ TA+Y DY A WAR+ EGE+ Sbjct: 64 ERAGFLKKMAEVIRENREMLARTLAEEQAKIFPLAQVEIDATAEYFDYYAGWARKYEGEV 123 Query: 126 IASDRPGENIFLFRKPLGVVAGILPWNFPFFLIARKMAPALLTGNTIVVKPSEETPNNCF 185 I SDR ENI L+R+P+GVV GI PWNFPFF++ARK+AP++LTG TIV+KPS ETPN F Sbjct: 124 IESDRTNENILLYRQPIGVVVGICPWNFPFFVMARKVAPSILTGCTIVLKPSSETPNTTF 183 Query: 186 EFARLVAETDLPRGVFNVVCGAGQ-VGGALSSHPGVDLISFTGSVETGARIMAAAAPNLT 244 EFA+LV+ LP GV N V G G +G AL V L++ TGSVETG RI+A+ A N+T Sbjct: 184 EFAKLVSSIGLPNGVLNFVSGGGSTLGDALVRSSQVGLVTLTGSVETGQRIIASTAENIT 243 Query: 245 KLNLELGGKAPAIVLADADLELAVKAIRDSRIINSGQVCNCAERVYVQRQVAEPFIERIA 304 K +LELGGKAP I+ AD D+++AVKA+ DSRII SGQVCNCAERVYV+ V + F++++ Sbjct: 244 KTSLELGGKAPVIICADCDMDMAVKAVVDSRIIFSGQVCNCAERVYVEAPVYDEFMDKVT 303 Query: 305 AAMAATRYGDPLAEPEVEMGPLINRLGLEKIDAKVRTALAQGATLVTGGAIAE--RPGHH 362 AMAA YGDP A+P M IN L KI+ V AL +GA ++ GG+ E G Sbjct: 304 RAMAAVAYGDPFADPAPNMSCQINSAQLTKIEGMVAKALEEGAEVLVGGSRCEDQPTGFF 363 Query: 363 YQPTVLTGCRADTRIMREEIFGPVLPIQIVDDLDEAIALANDCEYGLTSSVFTRDLNKAM 422 Y+PT+L C D I+R+EIFGPVLP+ V D DEA+ +ANDCE+GLTSS+FT +++K M Sbjct: 364 YKPTLLASCTQDMEIIRKEIFGPVLPVVKVTDFDEALNMANDCEFGLTSSIFTNNISKMM 423 Query: 423 HALRELDFGETYINREHFEAMQGFHAGVRKSGIGGADGKHGLYEYTHTHVVYLQ 476 A+ EL FGETY+NREHFEA+QGFHAG RKSGIGGADGKHGLYEY THV Y+Q Sbjct: 424 RAINELKFGETYVNREHFEAIQGFHAGWRKSGIGGADGKHGLYEYLQTHVAYIQ 477 Lambda K H 0.320 0.136 0.395 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: 561 Number of extensions: 18 Number of successful extensions: 3 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: 477 Length of database: 478 Length adjustment: 34 Effective length of query: 443 Effective length of database: 444 Effective search space: 196692 Effective search space used: 196692 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 51 (24.3 bits)
This GapMind analysis is from Apr 09 2024. 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