Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate CA265_RS14635 CA265_RS14635 aldehyde dehydrogenase
Query= BRENDA::Q9K9B2 (515 letters) >lcl|FitnessBrowser__Pedo557:CA265_RS14635 CA265_RS14635 aldehyde dehydrogenase Length = 501 Score = 218 bits (555), Expect = 4e-61 Identities = 149/429 (34%), Positives = 222/429 (51%), Gaps = 25/429 (5%) Query: 76 EKAIQSADEAFQTWRNVNPEERANILVKAAAIIRRRKHEFSAWLVHEAGKPWKEA-DADT 134 E A+ +A EAF+TW + ER+ IL K A + +A + GK +E AD Sbjct: 54 ELAVDAAHEAFKTWSKTSSTERSIILNKIAQRMEDNLEYLAAVETIDNGKAVRETLAADL 113 Query: 135 AEAIDFLEYYARQMIELNRGKEILSRPGEQNRYFYTPMGVTVTISPWNFALAIMVGTAVA 194 +D Y+A +I G + + P+GV I PWNF L + + Sbjct: 114 PLGVDHFRYFAG-VIRAEEGSLSELDQNTVSLIVHEPIGVVAQIIPWNFPLLMGIWKLAP 172 Query: 195 PIVTGNTVVLKPASTTPVVAAKFVEVLEDAGLPKGVINYVPGSGAEVGDYLVDHPKTSLI 254 + GN VVLKPA +TPV +E++ D LP GV+N V G G+E+G LV +PK S Sbjct: 173 ALAAGNCVVLKPAESTPVSIMVLMELIGDL-LPPGVVNVVNGFGSELGRALVTNPKVSKA 231 Query: 255 TFTGSKDVGVRLYERAAVVRPGQNHLKRVIVEMGGKD------TVVVDRDADLDLAAESI 308 FTGS G V++ ++ V +E+GGK +V+ + DA LD A E Sbjct: 232 AFTGSTPTG------RLVMQYATENIIPVTLELGGKSPNIFFSSVMAEDDAFLDKAVEGA 285 Query: 309 LVSAFGFSGQKCSAGSRAVIHKDVYDEVLEKTVALAKNLTVGDPTNRDNYMGPVIDEKAF 368 ++ A G+ C+ SR +I +D+Y++ + K + K + +G P +R MG + F Sbjct: 286 VMFALN-QGEICTCPSRLLIQEDIYEKFIAKVIERTKAIKIGSPLDRTVMMGAQASKIQF 344 Query: 369 EKIMSYIEIGKKEG-RLMTGGE-----GDSSTGFFIQPTIIADLDPEAVIMQEEIFGPVV 422 EKI +YI++GK+EG ++TGGE G+ G++I+PTI + + I QEEIFGPV+ Sbjct: 345 EKIAAYIKLGKEEGAEVLTGGEINELPGELGGGYYIKPTIFKGHN-KMRIFQEEIFGPVL 403 Query: 423 AFSKANDFDHALEIANNTEYGLTGAVITRNRAHIEQAKREFHVGNLYFNRNCTGAIVGYH 482 A + + A+EIAN+T YGL V TR+ + Q R G ++ N+ A Sbjct: 404 AVTTFKTVEEAIEIANDTLYGLGAGVWTRDAHELYQVPRAIQAGRVWVNQ--YHAYPAGA 461 Query: 483 PFGGFKMSG 491 PFGG+K SG Sbjct: 462 PFGGYKQSG 470 Lambda K H 0.316 0.134 0.388 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: 592 Number of extensions: 36 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: 515 Length of database: 501 Length adjustment: 34 Effective length of query: 481 Effective length of database: 467 Effective search space: 224627 Effective search space used: 224627 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 (21.6 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 2021. 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 the paper from 2019 on GapMind for amino acid biosynthesis, the preprint on GapMind for carbon sources, or view the source code.
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