Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_053545747.1 CDES_RS12085 aldehyde dehydrogenase
Query= BRENDA::Q65NN2 (516 letters) >NCBI__GCF_001277995.1:WP_053545747.1 Length = 506 Score = 204 bits (520), Expect = 5e-57 Identities = 161/503 (32%), Positives = 245/503 (48%), Gaps = 51/503 (10%) Query: 10 FTNFGIEENRKAFEKALETVNNEWLGQSYPLVIDGERYETENKIVSINPANKEEVVGTVS 69 + N G E + +EK E ++G + ++G+ E + + EV V+ Sbjct: 4 YANPGTEGSIVNYEKRYEN----YIGGKWVPPVEGQYLENISPVTG-------EVFCEVA 52 Query: 70 KATQDHAEKAIQAAAKAFETWRYTDPEERAAVLFRAVAKVRRKKHEFSALLVKEAGKPWN 129 + T+ E A+ AA A + W T ERA +L R ++ E + E GK Sbjct: 53 RGTKADIELALDAAHAAADAWGKTSVAERALMLHRIADRMEEHLEEIAVAETWENGKAVR 112 Query: 130 EA-DADTAEAIDFMEYYARQMIELAKGKPVNSREGERNQYVY---TPTGVTVVIPPWNFL 185 E AD AID Y+A + + + S + + N Y P GV I PWNF Sbjct: 113 ETLAADIPLAIDHFRYFAGAI----RAQEDRSSQIDHNTVAYHFNEPIGVVGQIIPWNFP 168 Query: 186 FAIMAGTTVAP-IVTGNTVVLKPASAAPVIAAKFVEVLEESGLPKGVVNFVPGSGAEVGD 244 +MA +AP + GN +V+KPA P + ++ + +P GVVN V G G E GD Sbjct: 169 I-LMATWKLAPALAAGNAIVMKPAEQTPASILYLMNIIGDL-IPDGVVNIVNGLGEEAGD 226 Query: 245 YLVDHPKTSIITFTGSREVGTRIFERAA--KVQPGQTHLKQVIAEMGGKDTVVVDEDCDI 302 L + I FTGS +VG +I RAA K+ P V E+GGK + ED Sbjct: 227 ALSSSDRIGKIAFTGSTQVG-KIINRAASDKIIP-------VTLELGGKSPSIFFEDV-- 276 Query: 303 ELAAQSIFT--SAFGFA------GQKCSAGSRAVVHEKVYDEVLKRVIEITESKKVGEPD 354 L+ F + GFA G+ C+ SRA+VHE + DE L+ ++ ++ K+G P Sbjct: 277 -LSKDDPFRKKAVEGFAMFALNQGEVCTCPSRALVHESIADEFLELGVQRVKNIKLGNPL 335 Query: 355 SADVYMGPVIDQASFNKIMDYIEIGKEEG-RLVSGGKGDD----SKGYFIEPTIFADLDP 409 + MG Q +KI Y++IG EEG ++GGK + GY+IEPT+F + Sbjct: 336 DTETMMGAQASQEQMDKISSYLKIGPEEGAETLTGGKINKVDGLDNGYYIEPTVFRGTND 395 Query: 410 KARLMQEEIFGPVVAFSKVSSFDEALEVANNTEYGLTGAVITKNRDHINRAKQEFHVGNL 469 R+ +EEIFGPV++ + S FDEA+ +AN+T YGL V +++++ + RA + G + Sbjct: 396 M-RIFREEIFGPVLSVATFSDFDEAIRIANDTNYGLGAGVWSRDQNTVYRAGRAIQAGRV 454 Query: 470 YFNRNCTGAIVGYHPFGGFKMSG 492 + N+ + FGG+K SG Sbjct: 455 WVNQYHN--YPAHSAFGGYKESG 475 Lambda K H 0.315 0.133 0.382 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: 613 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: 506 Length adjustment: 35 Effective length of query: 481 Effective length of database: 471 Effective search space: 226551 Effective search space used: 226551 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 24 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:
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