Align succinate-semialdehyde dehydrogenase (NAD+) (EC 1.2.1.24) (characterized)
to candidate WP_176342854.1 BZY95_RS11585 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-20455 (480 letters) >NCBI__GCF_002151265.1:WP_176342854.1 Length = 499 Score = 509 bits (1311), Expect = e-149 Identities = 255/477 (53%), Positives = 333/477 (69%) Query: 3 DSQLFKQHAYINGEWLSALGGETQSIFNPATGQLIGTVPMMGRQEARQAIAAANQALPAW 62 D +LF+QHAY+NG+W GG +++F+PATG++IG +P + + R+A+ +A+ A W Sbjct: 15 DPRLFRQHAYVNGKWTHGDGGREETVFDPATGEVIGYIPWLEAHQIREAVDSADAAFVHW 74 Query: 63 RALPAKERSARLRAWFELMLEHQEELARLMTIEQGKPLAEARNEILYAASFVEWFAEEGK 122 RAL A ER+ RL AW +L+ H+E+LA +MT+EQGKPL +AR E+ Y ASFV WFAEEGK Sbjct: 75 RALRADERAERLMAWHDLLQAHREDLAIIMTLEQGKPLPDARGEVEYGASFVRWFAEEGK 134 Query: 123 RVYGDVIPSPQADKRLLVIKQPVGVTAAITPWNFPSAMITRKAAPALAAGCTMVLKPAPQ 182 R +G+ IPS + L +K+PVG+ A ITPWNFP AMITRKAA ALAAGCT+V+KPA + Sbjct: 135 RTFGETIPSHIPNAALGTLKEPVGIAALITPWNFPLAMITRKAAAALAAGCTVVVKPAGE 194 Query: 183 TPFSALALAALAQRAGIPAGVFNVVTGSAQEIGGEFTGNPIVRKLTFTGSTHIGRLLMAQ 242 TPFSALALA LA+RAGIPAGVFNVV G E+ V+ L+FTGST +GRLL+ Q Sbjct: 195 TPFSALALAELAERAGIPAGVFNVVLGEPAEVSKILCAEERVKALSFTGSTRVGRLLLEQ 254 Query: 243 CAHDVKKMSLELGGNAPFIVFEDADLDKAAEGALIAKYRNNGQTCVCTNRIYVHDSVHDA 302 A VK++SLELGGNAPFIV D D +AA A+ AK++ GQ C+ NRI VH+S+HD Sbjct: 255 SAQTVKRVSLELGGNAPFIVGPDMDPKEAAFAAVAAKFQTAGQDCLAANRILVHESIHDE 314 Query: 303 FAGKLKKAVEGLRVGNGLEDGVTVGPLINDAAVQKVRSHIADAVGKGASILAGGKPHALG 362 F + + L VGNG+E V +GPLI+ AV K + + DA+ +GA+++AG + A G Sbjct: 315 FVEHFAERMAALTVGNGMESEVDLGPLIHRQAVDKAAAIVDDAISRGATLVAGDQTRAPG 374 Query: 363 GTFFEPTILANVPHDALVAHEETFGPLAPLFRFRDEAEVVGRANDTEYGLAAYFYTENLG 422 FF PT+L V V EE F P+A + +RD+ EV+ ANDTEYGLAAY YT ++ Sbjct: 375 ENFFMPTLLTGVTPQMKVWREENFAPVAGVTAYRDDDEVIEMANDTEYGLAAYVYTHDIR 434 Query: 423 RIFRVAEALEYGMVGINCGAISNEVAPFGGVKASGLGREGSKYGIEEYLEIKYLSLG 479 RI+++ ALEYGMV +N ++ PFGGVK SGLGREG GI+EYLE KY LG Sbjct: 435 RIWKLLRALEYGMVSVNSVKMTGPPVPFGGVKQSGLGREGGITGIDEYLETKYYCLG 491 Lambda K H 0.319 0.135 0.399 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: 673 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: 480 Length of database: 499 Length adjustment: 34 Effective length of query: 446 Effective length of database: 465 Effective search space: 207390 Effective search space used: 207390 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 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