Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_012276124.1 SHAL_RS05100 NADP-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000019185.1:WP_012276124.1 Length = 482 Score = 515 bits (1327), Expect = e-150 Identities = 254/476 (53%), Positives = 345/476 (72%), Gaps = 6/476 (1%) Query: 46 LLRGDSFVGGRWLPT--PATFPVYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEI 103 LLR ++ G+WL + DPA+ +G+V G E +AA+ AA A +W+ + Sbjct: 8 LLRQQCYIDGQWLEAINGEKVEIADPATHKVIGSVPVMGTTETKAAITAAEKALPAWRAL 67 Query: 104 SVKERSSLLRKWYDLMIQNKDELAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVY 163 + KER + L +W++L+++++D+LA ++T E GKPL EA+GE+ Y+A F+EWF+EEA+RVY Sbjct: 68 TAKERGAKLHRWFELLLEHQDDLALMMTTEQGKPLAEAKGEVAYAASFIEWFAEEAKRVY 127 Query: 164 GDIIYTSAKDKRGLVLKQPVGVASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPY 223 GD I DKR +V+KQ VGV + ITPWNFP+AMITRK ALAAGCT+VVKPA TP+ Sbjct: 128 GDTIPGHQGDKRLMVIKQSVGVTAAITPWNFPAAMITRKAAPALAAGCTMVVKPAPQTPF 187 Query: 224 SALALAQLANQAGIPPGVYNVIPCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHH 283 +ALALA+LA +AGIP GV++V+ A +G LC++P+V K+SFTGST G L+ Sbjct: 188 TALALAELAERAGIPAGVFSVV---TGDAIAIGNELCSNPVVRKLSFTGSTPVGIKLMQQ 244 Query: 284 AANSVKRVSMELGGLAPFIVFDSANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDS 343 A ++K++S+ELGG APFIVF+ A++D AV GAM +K+RNAGQTCVC+NR VQ ++D Sbjct: 245 CAPTLKKMSLELGGNAPFIVFNDADIDAAVEGAMIAKYRNAGQTCVCANRIYVQDRVYDE 304 Query: 344 FVTKFAEAMKKSLRVGNGFEEGTTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQS 403 F K A A+ K L+VG G E G T GPLIN AV KV++H++DA++KGAT+ GGK Sbjct: 305 FAEKLAAAVAK-LKVGVGTEAGVTTGPLINSDAVAKVQRHLDDALSKGATLFAGGKLASL 363 Query: 404 GGNFFEPTLLSNVTRDMLCITEETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDP 463 GGNFFEPT+L+NV + ML EETFGP+AP+ KF ++ + AN + GLA YFY +D Sbjct: 364 GGNFFEPTILTNVDKSMLVAKEETFGPLAPLFKFSDVDDVIEQANDTEFGLAAYFYGRDI 423 Query: 464 AQIWRVAEQLEVGMVGVNEGLISSVECPFGGVKQSGLGREGSKYGIDEYLEVKYVC 519 + +W+V+E LE GMVGVN GLIS+ PFGG+K SGLGREGSK+GI+EYLE+KY+C Sbjct: 424 SLVWKVSEALEYGMVGVNTGLISTEVAPFGGIKSSGLGREGSKFGIEEYLEMKYIC 479 Lambda K H 0.318 0.135 0.400 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: 25 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: 523 Length of database: 482 Length adjustment: 34 Effective length of query: 489 Effective length of database: 448 Effective search space: 219072 Effective search space used: 219072 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 (21.7 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