Align Glutarate-semialdehyde dehydrogenase (EC 1.2.1.20) (characterized)
to candidate WP_074201782.1 BUQ81_RS07630 NAD-dependent succinate-semialdehyde dehydrogenase
Query= reanno::pseudo13_GW456_L13:PfGW456L13_495 (480 letters) >NCBI__GCF_900141795.1:WP_074201782.1 Length = 458 Score = 256 bits (654), Expect = 1e-72 Identities = 153/449 (34%), Positives = 241/449 (53%), Gaps = 6/449 (1%) Query: 32 NPATGEILGTVPKMGAAETRRAIEAADKALPAWRALTAKE-RATKLRRWYELIIENQDDL 90 NPAT E +P + A+ A A W T E R LR EL+ + +L Sbjct: 9 NPATEEENARIPVWDDDKLDTALRYAGYAQRDWAQQTPLETRCELLRNVAELLRVKKREL 68 Query: 91 ARLMTLEQGKPLAEAKGEIVYAASFIEWFAEEAKRIYGDVIPGHQPDKRLIVIKQPIGVT 150 A L T E GK + EA+ E+ A +++A++A + D + + + L+V QP+GV Sbjct: 69 AELATREMGKRIGEAEAEVEKCAWVCDFYADQAPAMLADEVVETEATRSLVVY-QPLGVI 127 Query: 151 AAITPWNFPAAMITRKAGPALAAGCTMVLKPASQTPFSAFALAELAQRAGIPAGVFSVVS 210 A+ PWNFP + R A PAL AG +VLK AS P A A+ L + AG P +F + Sbjct: 128 LAVMPWNFPYWQVFRAAAPALVAGNGVVLKHASNVPLCALAIEGLFKEAGFPEDLFQSLM 187 Query: 211 GSAGDIGSELTSNPIVRKLSFTGSTEIGRQLMSECAKDIKKVSLELGGNAPFIVFDDADL 270 ++ + + +P VR ++ TGS GR + S +++KK LELGG+ PF++ DADL Sbjct: 188 ITSAQVERAIC-HPDVRGVTLTGSEPAGRAVASIAGRELKKTVLELGGSDPFVILPDADL 246 Query: 271 DKAVEGAIISKYRNNGQTCVCANRLYIQDGVYDAFAEKLKVAVAKLKI-GNGLEAGTTTG 329 D+ V A+ +++ N GQ+C+ A R + ++D F + KVA+ + G+ ++ TT G Sbjct: 247 DEVVPMALKARFINMGQSCIAAKRFLVDKTMHDEFVARFKVAIEDYFVPGDPMDPATTLG 306 Query: 330 PLIDEKAVAKVQEHIADALSKGATVLAGGKPME--GNFFEPTILTNVPNNAAVAKEETFG 387 P+ + ++ + A GATV GG+ ++ G ++ PT+LTNV + +EE FG Sbjct: 307 PMARRDLMEELHNQVIRAQDYGATVETGGQTLDRPGAYYAPTLLTNVTTSNPAFQEELFG 366 Query: 388 PLAPLFRFKDEADVIAMSNDTEFGLASYFYARDLGRVFRVAEALEYGMVGVNTGLISNEV 447 P+A + + + + + ++N T FGL + D+ +A ++ G VN + S+ Sbjct: 367 PVATVTTYTEPSHALGLANATRFGLGGSVWTTDIATGEAIARGMQCGCAFVNDMVRSDPR 426 Query: 448 APFGGIKASGLGREGSKYGIEDYLEIKYL 476 PFGGIK SG GRE S YGI +++ IK L Sbjct: 427 LPFGGIKDSGYGRELSVYGIREFVNIKTL 455 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: 493 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: 458 Length adjustment: 33 Effective length of query: 447 Effective length of database: 425 Effective search space: 189975 Effective search space used: 189975 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: 51 (24.3 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