Align NAD(P)-dependent succinate-semialdehyde dehydrogenase (EC 1.2.1.16) (characterized)
to candidate WP_089136075.1 CES79_RS01180 aldehyde dehydrogenase
Query= metacyc::MONOMER-15736 (480 letters) >NCBI__GCF_002217945.1:WP_089136075.1 Length = 485 Score = 327 bits (838), Expect = 6e-94 Identities = 176/477 (36%), Positives = 279/477 (58%), Gaps = 4/477 (0%) Query: 6 AQLFRQQAFIDGAWVDADNGQTIKVNNPATGEILGTVPKMGAAETRRAIEAADKALPAWR 65 ++L + +++G + D+ +G+ + V NP+TGE + TVP ET+ AI+ A +A W+ Sbjct: 2 SELKHYKMYVNGEFKDSKSGKLLTVINPSTGEKISTVPSATREETQEAIDDAYEAEKTWK 61 Query: 66 ALTAKERATKLRRWYELLIENQDDLGRLMTLEQGKPLAEAKGEIAYAASFIEWFAEEAKR 125 + A R L + ++ D L ++ EQGK + A EI ++A + ++ A A+ Sbjct: 62 FVPAATRGQYLHDVATEVRKDADHLIDMLQEEQGKIRSLATTEIMFSADYFDYMASAART 121 Query: 126 IYGDVIPGHQPDKRLIVIKQPIGVTAAITPWNFPAAMITRKAGPALAAGCTMVIKPASQT 185 G+++ ++ +++ KQPIGV A I PWNFP +I RK GPAL G T+V+KP+S T Sbjct: 122 YEGEILQSDNANENIMITKQPIGVAAGILPWNFPFFLIARKMGPALVTGNTIVMKPSSDT 181 Query: 186 PFSALALVELAHRAGIPKGVLSVVTGSAGDIGGELTSNPIVRKLSFTGSTEIGRQLMAEC 245 P AL ++ + GIPKGV++ VTG +G EL+ N + +S TGS G+ +MA Sbjct: 182 PNLALEFAKIVDKIGIPKGVVNFVTGPGSVVGDELSKNKKIGIISLTGSVGSGKHVMASA 241 Query: 246 AKDIKKVSLELGGNAPFIVFDDADLDKAVEGAIISKYRNNGQTCVCANRLYIQDSVYDAF 305 A + KVSLELGG AP IV DDAD+D AV+ I S+ NNGQ C R+Y+Q+ V D F Sbjct: 242 ATHMAKVSLELGGKAPAIVMDDADIDLAVQSIIDSRVDNNGQLCNNCERIYVQEGVADEF 301 Query: 306 AEKLKAAVAKLKIGNGL-EEGTTTGPLIDEKAVAKVQEHIADALKKGATLLAGGKSME-- 362 +KL A ++ +K+ N + ++ + GPLI++ A+ KV + A+K G + AGG ++ Sbjct: 302 IKKLSAKMSAIKVANPITDKDSGIGPLINQAALDKVSGMVDRAVKAGGKITAGGHKVQIE 361 Query: 363 -GNFFEPTILVNVPKDAAVAKEETFGPLAPLFRFKDEAEVIAMSNDTEFGLASYFYARDL 421 G ++EPT++ NV +D+ + ++E FGP+ P+ FK + I MSND++FGL S + +D+ Sbjct: 362 NGFYYEPTVITNVKQDSEIIQDEIFGPVLPVVTFKTLDDAIEMSNDSDFGLTSSIFTKDI 421 Query: 422 GRVFRVAEALEYGMVGVNTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCL 478 R A LE G +N G K SG+G + ++GI+++L + L Sbjct: 422 DNAQRAANELEDGETYINRFNFEAMNGSHSGWKESGIGGDDGRHGIDEFLNTHVIYL 478 Lambda K H 0.317 0.135 0.390 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: 22 Number of successful extensions: 5 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: 480 Length of database: 485 Length adjustment: 34 Effective length of query: 446 Effective length of database: 451 Effective search space: 201146 Effective search space used: 201146 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