Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_017549192.1 C792_RS0109240 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P51650 (523 letters) >NCBI__GCF_000330705.1:WP_017549192.1 Length = 459 Score = 407 bits (1045), Expect = e-118 Identities = 205/451 (45%), Positives = 296/451 (65%), Gaps = 4/451 (0%) Query: 66 VYDPASGAKLGTVADCGVPEARAAVRAAYDAFSSWKEISVKERSSLLRKWYDLMIQNKDE 125 V +PA+G ++ ++ + A + A+ AF +K+ + +RS+LL +W L+ +NKDE Sbjct: 7 VMNPATGEEIRSIKKDSREDIEAKIETAHQAFKKYKKKNAHDRSALLSEWAKLIRENKDE 66 Query: 126 LAKIITAESGKPLKEAQGEILYSAFFLEWFSEEARRVYGDIIYTSAKDKRGLVLKQPVGV 185 +A++IT E+GKPL E+ GE+ Y+ ++++++EE +RVYG I D R +V KQP+GV Sbjct: 67 IAQLITKENGKPLAESLGEVEYACSYIDYYAEEGKRVYGRTIPPHEDDVRLVVTKQPIGV 126 Query: 186 ASIITPWNFPSAMITRKVGAALAAGCTVVVKPAEDTPYSALALAQLANQAGIPPGVYNVI 245 + ITPWNFP AM+ RK A+AAGCT +VKPA +TP SA+ LA AG GV + Sbjct: 127 VAAITPWNFPVAMMARKAAPAVAAGCTFLVKPARETPLSAMRFLDLAKDAGFEAGVIQYV 186 Query: 246 PCSRTKAKEVGEVLCTDPLVSKISFTGSTATGKILLHHAANSVKRVSMELGGLAPFIVFD 305 S K+ GEV V K++FTGSTA GK L+ AA++VK ++MELGG AP +V Sbjct: 187 NAS---GKDAGEVFSQSDKVMKLTFTGSTAVGKKLMEGAASTVKNITMELGGHAPLVVHK 243 Query: 306 SANVDQAVAGAMASKFRNAGQTCVCSNRFLVQRGIHDSFVTKFAEAMKKSLRVGNGFEEG 365 A+++ AV A+A+KFRN+GQTCVC+NRF V I D+F KF+E +KK L++GNG +EG Sbjct: 244 DADLETAVDHAIATKFRNSGQTCVCANRFYVHEDIADAFSEKFSEKVKK-LKMGNGMDEG 302 Query: 366 TTQGPLINEKAVEKVEKHVNDAVAKGATVVTGGKRHQSGGNFFEPTLLSNVTRDMLCITE 425 GP+IN+ +KV +H+NDA KG T+ GG + S G F EPT++++ T +M+ + E Sbjct: 303 VQVGPMINKDGYDKVMEHINDARQKGGTITAGGNGNNSEGYFIEPTVITDATDEMIIMNE 362 Query: 426 ETFGPVAPVIKFDKEEEAVAIANAADVGLAGYFYSQDPAQIWRVAEQLEVGMVGVNEGLI 485 ETFGPVAP+ F +EA+ AN + GLA YF+++ R+ E L G++G N G Sbjct: 363 ETFGPVAPIQTFSNLDEAIEKANDTEYGLAAYFFTESYRDGIRLQEGLNFGVLGWNNGKP 422 Query: 486 SSVECPFGGVKQSGLGREGSKYGIDEYLEVK 516 S+ PFGG+K+SG+GREG GI+ YLE K Sbjct: 423 SAAHIPFGGLKESGIGREGGLEGIEPYLETK 453 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: 565 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: 459 Length adjustment: 34 Effective length of query: 489 Effective length of database: 425 Effective search space: 207825 Effective search space used: 207825 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