Align succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) (characterized)
to candidate WP_022528925.1 L248_RS04605 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A0A0J9X1M8 (465 letters) >NCBI__GCF_000469325.1:WP_022528925.1 Length = 457 Score = 534 bits (1375), Expect = e-156 Identities = 257/452 (56%), Positives = 335/452 (74%), Gaps = 1/452 (0%) Query: 1 MAYQTIYPYTNEVLHTFDNMTDQGLADVLERAHLLYKKWRKEDHLEERKAQLHQVANILR 60 MAYQT+ PYTN+++ T+ TD L D L + H +Y WR++ R LH+VA +LR Sbjct: 1 MAYQTVDPYTNKLVKTYPAATDADLEDALAQGHRVYTDWRRQAPAA-RGPILHKVAQLLR 59 Query: 61 RDRDKYAEIMTKDMGKLFTEAQGEVDLCADIADYYADKADEFLMSTPLETDSGQAYYLKQ 120 + YA IMT+DMGKL EA+ EV+LCA IADY+AD + F+ PL + G+AYY++Q Sbjct: 60 EKKHDYAAIMTRDMGKLIGEAEAEVELCATIADYFADHGEAFMAPQPLTSSHGKAYYIRQ 119 Query: 121 STGVILAVEPWNFPYYQIMRVFAPNFIVGNPMVLKHASICPRSAQSFEELVLEAGAEAGS 180 +TGV++AVEPWNFP+YQ+MRVFAPNF+VGNPM+LKHAS P SA +FE++V EAGA G+ Sbjct: 120 ATGVLVAVEPWNFPFYQVMRVFAPNFMVGNPMILKHASNTPGSAAAFEDMVREAGAPEGA 179 Query: 181 ITNLFISYDQVSQVIADKRVVGVCLTGSERGGASIAEEAGKNLKKTTLELGGDDAFIILD 240 NLF+SYDQVSQ IAD RV GV LTGSERGGAS+A+EAGK LKK+++ELGG D FI L+ Sbjct: 180 FKNLFLSYDQVSQAIADPRVSGVALTGSERGGASVAQEAGKQLKKSSMELGGTDVFIALE 239 Query: 241 DADWDQLEKVLYFSRLYNAGQVCTSSKRFIVLDKDYDRFKELLTKVFKTAKWGDPMDPET 300 DADWD + + +RL N GQVCTSSKRFI+ YD F L FKT + GDPMDP T Sbjct: 240 DADWDAVYQAAPNARLRNVGQVCTSSKRFIIPASHYDEFVAQLAAAFKTYQPGDPMDPAT 299 Query: 301 TLAPLSSAQAKADVLDQIKLALDHGAELVYGGEAIDHPGHFVMPTIIAGLTKDNPIYYQE 360 TLAP++S +AK V QI A+ HGA + YG + ID PG F+ PTI+ + K NP++ QE Sbjct: 300 TLAPMNSERAKEKVQSQIDEAIAHGAHVAYGNQPIDLPGAFIQPTILTDIDKQNPLFSQE 359 Query: 361 IFGPVGEIYKVSSEEEAIEVANDSNYGLGGTIFSSNQEHAKAVAAKIETGMSFINSGWTS 420 IFGPV E++KV++++EAI +ANDS YGLG ++S + HA A+A +IETGM+ IN+ + + Sbjct: 360 IFGPVAEVFKVTNDDEAIALANDSRYGLGSVVYSQDPAHADAIARRIETGMTTINAPFIT 419 Query: 421 LPELPFGGIKHSGYGRELSELGFTSFVNEHLI 452 PELPFGG+K+SGYGRE+ E+GF +F NEH+I Sbjct: 420 SPELPFGGVKNSGYGREMDEIGFATFTNEHMI 451 Lambda K H 0.317 0.135 0.392 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: 580 Number of extensions: 23 Number of successful extensions: 2 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: 465 Length of database: 457 Length adjustment: 33 Effective length of query: 432 Effective length of database: 424 Effective search space: 183168 Effective search space used: 183168 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