Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate Dsui_0437 Dsui_0437 succinate-semialdehyde dehydrogenase
Query= BRENDA::Q72IB9 (516 letters) >FitnessBrowser__PS:Dsui_0437 Length = 483 Score = 236 bits (602), Expect = 1e-66 Identities = 161/478 (33%), Positives = 233/478 (48%), Gaps = 22/478 (4%) Query: 41 YIGGEWVDTKERMVSLNPSAPSEVVGTTAKAGKAEAEAALEAAWKAFKTWKDWPQEDRSR 100 Y+ G+WV + NP++ +E+ + G AE AA+ AA A+ W+ ++R+ Sbjct: 14 YLNGQWVGGESDFPVHNPASGAELA-RVPRFGAAETRAAIAAADAAWPAWRSRTAKERTG 72 Query: 101 LLLKAAALMRRRKRELEATLVYEVGKNWVEASADVAEAIDFIEYYARAALRYRYPAVEVV 160 +L + LM + +L + E GK EA +VA A F+E++A A R E + Sbjct: 73 VLRRWFELMNQHADDLALLMTSEQGKPLAEARGEVAYAASFVEWFAEEAKR---AYGETI 129 Query: 161 PYPGEDNESFYV--PLGAGVVIAPWNFPVAIFTGMIMGPVAVGNTVIAKPAEDAVVVGAK 218 P D + P+G I PWNFP A+ T + +A G TV+ KPAE + Sbjct: 130 PAVAADKRMLVIKQPIGVCAAITPWNFPAAMITRKVAPALAAGCTVVVKPAEQTPLTALA 189 Query: 219 VFEIFHEAGFPPGVVNFLPGVGEEVGAYLVEHPRTRFINFTGSLEVGLKIYEAAGRLAPG 278 + E+ H AGFP GV N + G +G L +P R ++FTGS EVG + G+ AP Sbjct: 190 LAELAHRAGFPAGVFNVITGDPVAIGGELTSNPTVRKLSFTGSTEVGRLL---MGQCAPS 246 Query: 279 QTWFKRAYVETGGKDAIIVDETADFDLAAEGVVVSAYGFQGQKCSAASRLILTQGAYEPV 338 K+ +E GG IV + AD D A EG ++S Y GQ C A+RL++ G YE Sbjct: 247 ---IKKLSLELGGNAPFIVFDDADLDAAVEGAMISKYRNTGQTCVCANRLLVQDGIYEAF 303 Query: 339 LERVLKRAERLSVGP-AEENPDLGPVVSAEQERKVLSYIEIGKNEGQLVLGG----KRLE 393 R+ + L VG E GP++ A+ KV ++I G VL G +R Sbjct: 304 AARLAAKVATLKVGEGTEAGVTQGPLIDADALAKVEAHIADAVAHGARVLAGGRRHERYR 363 Query: 394 GEGYFIAPTVFTEVPPKARIAQEEIFGPVLSVIRVKDFAEALEVANDTPYGLTGGVYSRK 453 G F PTV +V P+ R+A+EE FGPV + R + EA+ +AN T +GL YSR Sbjct: 364 EGGAFFQPTVLADVTPQMRVAREETFGPVAPLFRFQTEEEAIALANATEFGLASYFYSRD 423 Query: 454 REHLEWARREFHVGNLYFNRKITGALVG-VQPFGGFKLSGTNAKTGALDYLRLFLEMK 510 + G + N TG + V PFGG K SG + G+ L +LE+K Sbjct: 424 IGRIFRVGEALEYGMVGVN---TGLISNEVAPFGGIKQSGL-GREGSKYGLEEYLEVK 477 Lambda K H 0.319 0.137 0.403 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: 582 Number of extensions: 32 Number of successful extensions: 6 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: 516 Length of database: 483 Length adjustment: 34 Effective length of query: 482 Effective length of database: 449 Effective search space: 216418 Effective search space used: 216418 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 (21.7 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