Align succinate-semialdehyde dehydrogenase (NADP+) (EC 1.2.1.79) (characterized)
to candidate WP_085124768.1 B9O00_RS21375 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P25526 (482 letters) >NCBI__GCF_900177295.1:WP_085124768.1 Length = 504 Score = 505 bits (1301), Expect = e-147 Identities = 253/477 (53%), Positives = 333/477 (69%) Query: 3 LNDSNLFRQQALINGEWLDANNGEAIDVTNPANGDKLGSVPKMGADETRAAIDAANRALP 62 L D LFR+ + I G W A + ++V +PA+G +G VP +GA AA+ AA A P Sbjct: 24 LADRRLFRELSYIGGRWTAAGDAGTLEVLDPADGCLVGRVPTLGAKAATAAVAAAQAAFP 83 Query: 63 AWRALTAKERATILRNWFNLMMEHQDDLARLMTLEQGKPLAEAKGEISYAASFIEWFAEE 122 AWR A+ERA +LR W L++ ++ DLA LM EQGKPLAEA+GEI YAA F+ W+AEE Sbjct: 84 AWRKRLARERAELLRAWHALIVANRRDLALLMVAEQGKPLAEAEGEIDYAAGFLAWYAEE 143 Query: 123 GKRIYGDTIPGHQADKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVLKPA 182 R+ +++P H V ++PIGV A +TPWNFP AMITRKA ALAAGC++V+ P+ Sbjct: 144 AVRVSAESLPSHLPGAETAVRREPIGVAALVTPWNFPTAMITRKAAAALAAGCSVVVHPS 203 Query: 183 SQTPFSALALAELAIRAGVPAGVFNVVTGSAGAVGNELTSNPLVRKLSFTGSTEIGRQLM 242 S+TPFSALALAELA RAG+PAGVFNVVTG A + ++ VR LSF GSTEIGR L Sbjct: 204 SETPFSALALAELADRAGLPAGVFNVVTGRAAEIVPAWCADTRVRALSFNGSTEIGRLLA 263 Query: 243 EQCAKDIKKVSLELGGNAPFIVFDDADLDKAVEGALASKFRNAGQTCVCANRLYVQDGVY 302 EQCA +K++ LELGG+APF+VF DADL++AVE L++KF +GQ C+ ANR+YV+ VY Sbjct: 264 EQCAPTVKQLILELGGHAPFVVFADADLERAVESCLSAKFATSGQDCLAANRIYVERPVY 323 Query: 303 DRFAEKLQQAVSKLHIGDGLDNGVTIGPLIDEKAVAKVEEHIADALEKGARVVCGGKAHE 362 F + + V L +G GL+ GV IGPLI E+A+AK+ E + DA +GAR++ GG H Sbjct: 324 QAFLARFLERVRDLKVGPGLEPGVEIGPLIHERALAKMAEQVEDATARGARLLLGGARHA 383 Query: 363 RGGNFFQPTILVDVPANAKVSKEETFGPLAPLFRFKDEADVIAQANDTEFGLAAYFYARD 422 GG FF+PT+L DVP A V EETFGP+A L F EA+V+A+AN TE+GL AY ++ D Sbjct: 384 LGGCFFEPTVLADVPDAALVFNEETFGPIAALAPFDSEAEVLAKANATEYGLIAYLHSGD 443 Query: 423 LSRVFRVGEALEYGIVGINTGIISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYMC 479 +R+ RV EALEYG+V +N ++ PFGG+K SGL REG + G+E + E+KY+C Sbjct: 444 RARIARVVEALEYGMVAVNRTKVTGAPVPFGGVKQSGLAREGGRAGLEAFTELKYVC 500 Lambda K H 0.318 0.135 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: 655 Number of extensions: 29 Number of successful extensions: 1 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: 482 Length of database: 504 Length adjustment: 34 Effective length of query: 448 Effective length of database: 470 Effective search space: 210560 Effective search space used: 210560 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 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