Align Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_176342854.1 BZY95_RS11585 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q9I6M5 (483 letters) >NCBI__GCF_002151265.1:WP_176342854.1 Length = 499 Score = 501 bits (1291), Expect = e-146 Identities = 246/481 (51%), Positives = 333/481 (69%) Query: 3 LKDAKLFRQQAYVDGAWVDADNGQTIKVNNPATGEIIGSVPKMGAAETRRAIEAADKALP 62 L D +LFRQ AYV+G W D G+ V +PATGE+IG +P + A + R A+++AD A Sbjct: 13 LDDPRLFRQHAYVNGKWTHGDGGREETVFDPATGEVIGYIPWLEAHQIREAVDSADAAFV 72 Query: 63 AWRALTAKERANKLRRWFDLMIENQDDLARLMTIEQGKPLAEAKGEIAYAASFLEWFGEE 122 WRAL A ERA +L W DL+ +++DLA +MT+EQGKPL +A+GE+ Y ASF+ WF EE Sbjct: 73 HWRALRADERAERLMAWHDLLQAHREDLAIIMTLEQGKPLPDARGEVEYGASFVRWFAEE 132 Query: 123 AKRIYGDTIPGHQPDKRIIVIKQPIGVTAAITPWNFPSAMITRKAGPALAAGCTMVLKPA 182 KR +G+TIP H P+ + +K+P+G+ A ITPWNFP AMITRKA ALAAGCT+V+KPA Sbjct: 133 GKRTFGETIPSHIPNAALGTLKEPVGIAALITPWNFPLAMITRKAAAALAAGCTVVVKPA 192 Query: 183 SQTPYSALALAELAERAGIPKGVFSVVTGSAGEVGGELTSNPIVRKLTFTGSTEIGRQLM 242 +TP+SALALAELAERAGIP GVF+VV G EV L + V+ L+FTGST +GR L+ Sbjct: 193 GETPFSALALAELAERAGIPAGVFNVVLGEPAEVSKILCAEERVKALSFTGSTRVGRLLL 252 Query: 243 AECAQDIKKVSLELGGNAPFIVFDDADLDAAVEGALISKYRNNGQTCVCANRLYVQDGVY 302 + AQ +K+VSLELGGNAPFIV D D A A+ +K++ GQ C+ ANR+ V + ++ Sbjct: 253 EQSAQTVKRVSLELGGNAPFIVGPDMDPKEAAFAAVAAKFQTAGQDCLAANRILVHESIH 312 Query: 303 DAFVDKLKAAVAKLNIGNGLEAGVTTGPLIDAKAVAKVEEHIADAVSKGAKVVSGGKPHA 362 D FV+ +A L +GNG+E+ V GPLI +AV K + DA+S+GA +V+G + A Sbjct: 313 DEFVEHFAERMAALTVGNGMESEVDLGPLIHRQAVDKAAAIVDDAISRGATLVAGDQTRA 372 Query: 363 LGGTFFEPTILVDVPKNALVSKDETFGPLAPVFRFKDEAEVIAMSNDTEFGLASYFYARD 422 G FF PT+L V V ++E F P+A V ++D+ EVI M+NDTE+GLA+Y Y D Sbjct: 373 PGENFFMPTLLTGVTPQMKVWREENFAPVAGVTAYRDDDEVIEMANDTEYGLAAYVYTHD 432 Query: 423 LARVFRVAEQLEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCLGG 482 + R++++ LEYGMV +N+ ++ PFGG+K SGLGREG GI++YLE KY CLG Sbjct: 433 IRRIWKLLRALEYGMVSVNSVKMTGPPVPFGGVKQSGLGREGGITGIDEYLETKYYCLGA 492 Query: 483 I 483 + Sbjct: 493 L 493 Lambda K H 0.317 0.135 0.391 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: 618 Number of extensions: 24 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: 483 Length of database: 499 Length adjustment: 34 Effective length of query: 449 Effective length of database: 465 Effective search space: 208785 Effective search space used: 208785 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