Align Glutarate-semialdehyde dehydrogenase; EC 1.2.1.- (characterized)
to candidate WP_086511804.1 BZY95_RS20815 NAD-dependent succinate-semialdehyde dehydrogenase
Query= SwissProt::Q9I6M5 (483 letters) >NCBI__GCF_002151265.1:WP_086511804.1 Length = 495 Score = 675 bits (1741), Expect = 0.0 Identities = 321/482 (66%), Positives = 399/482 (82%) Query: 2 QLKDAKLFRQQAYVDGAWVDADNGQTIKVNNPATGEIIGSVPKMGAAETRRAIEAADKAL 61 QL+D LFRQ AY+DG+WVDA + I+V +PA+ +GSVP++ A+ R AIE+AD+AL Sbjct: 14 QLQDPALFRQHAYIDGSWVDASDEAIIEVVDPASDTRLGSVPRLTQAQVREAIESADRAL 73 Query: 62 PAWRALTAKERANKLRRWFDLMIENQDDLARLMTIEQGKPLAEAKGEIAYAASFLEWFGE 121 P W+A TAKERA LRRW++L + +Q+DLAR++T+EQGKPLAEA+GEI Y ++F+EWF E Sbjct: 74 PQWKARTAKERAAILRRWYELCMAHQEDLARILTLEQGKPLAEARGEITYGSAFIEWFAE 133 Query: 122 EAKRIYGDTIPGHQPDKRIIVIKQPIGVTAAITPWNFPSAMITRKAGPALAAGCTMVLKP 181 EAKRIYGD IP H D+RI+V K+P+GV AAITPWNFP+AMITRKA A+AAGCT+V+KP Sbjct: 134 EAKRIYGDVIPAHAGDRRIVVTKEPVGVVAAITPWNFPNAMITRKAAAAMAAGCTVVVKP 193 Query: 182 ASQTPYSALALAELAERAGIPKGVFSVVTGSAGEVGGELTSNPIVRKLTFTGSTEIGRQL 241 AS TP+SALALAELAERAG+P+GV +VVTGSA VG ELT+NP+VRKL+FTGSTE+G+ L Sbjct: 194 ASSTPFSALALAELAERAGVPRGVLNVVTGSARTVGDELTANPLVRKLSFTGSTEVGKVL 253 Query: 242 MAECAQDIKKVSLELGGNAPFIVFDDADLDAAVEGALISKYRNNGQTCVCANRLYVQDGV 301 +A CAQ +KKVS+ELGGNAPFI+FDDADLD AV G + SK+RN GQTCVCANR++V + + Sbjct: 254 LAACAQTVKKVSMELGGNAPFIIFDDADLDQAVAGVMASKFRNTGQTCVCANRIFVHERI 313 Query: 302 YDAFVDKLKAAVAKLNIGNGLEAGVTTGPLIDAKAVAKVEEHIADAVSKGAKVVSGGKPH 361 Y F ++L AVA +GNGLE GVT GPLID AVAKVEEHIADA +GA V GG+ H Sbjct: 314 YADFAERLAQAVAAQRVGNGLEEGVTLGPLIDPAAVAKVEEHIADARERGASVYLGGQRH 373 Query: 362 ALGGTFFEPTILVDVPKNALVSKDETFGPLAPVFRFKDEAEVIAMSNDTEFGLASYFYAR 421 ALGG FFEPTIL DV +A + +ETFGP+AP+ RF DE EV+ ++NDT +GLASYFY R Sbjct: 374 ALGGNFFEPTILTDVSSDARLMNEETFGPVAPLLRFSDEQEVVRLANDTPYGLASYFYTR 433 Query: 422 DLARVFRVAEQLEYGMVGINTGLISNEVAPFGGIKASGLGREGSKYGIEDYLEIKYLCLG 481 D+ RV+RVAE LE G+VGIN G+IS+E+APFGG+K SG+GREGSKYGIEDY+EIKYLC+G Sbjct: 434 DVGRVWRVAEALECGIVGINEGIISSELAPFGGVKESGIGREGSKYGIEDYIEIKYLCMG 493 Query: 482 GI 483 G+ Sbjct: 494 GL 495 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: 686 Number of extensions: 10 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: 495 Length adjustment: 34 Effective length of query: 449 Effective length of database: 461 Effective search space: 206989 Effective search space used: 206989 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