Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_017549818.1 C792_RS0112615 aldehyde dehydrogenase family protein
Query= BRENDA::Q72IB9 (516 letters) >NCBI__GCF_000330705.1:WP_017549818.1 Length = 496 Score = 249 bits (636), Expect = 2e-70 Identities = 170/493 (34%), Positives = 249/493 (50%), Gaps = 20/493 (4%) Query: 28 RRVREEFGRHYPLYIGGEWVDTKE-RMVSLNPSAPSEVVGTTAKAGKAEAEAALEAAWKA 86 +RV E LYI G +V +M + A EV+ ++A +++ + A++AA KA Sbjct: 9 QRVNEFLDGEKGLYIDGGYVQAHGGKMFDVLNPATEEVIAQVSEADESDIDNAVQAARKA 68 Query: 87 FKT--WKDWPQEDRSRLLLKAAALMRRRKRELEATLVYEVGKNWVEA-SADVAEAIDFIE 143 F W +RSRL+ K A L+ + EL + GK + +A DV + Sbjct: 69 FDAGEWTKMEPAERSRLIYKFADLLEEHREELAQLEALDNGKAYQQALEDDVDGTVQHFR 128 Query: 144 YYARAALRYRYPAVEVVPYPGEDNESFYVPLGAGVV--IAPWNFPVAIFTGMIMGPVAVG 201 YYA A + V P D ++ V GVV I PWN+P+A+ + +A G Sbjct: 129 YYAGWATKISGKTPNVSP----DYVTYTVHEPVGVVGQIIPWNYPLAMAGWKLGAALAAG 184 Query: 202 NTVIAKPAEDAVVVGAKVFEIFHEAGFPPGVVNFLPGVGEEVGAYLVEHPRTRFINFTGS 261 T++ KPA + + ++F EAGFP GVVN +PG G G LV HP + FTGS Sbjct: 185 CTIVIKPASETPLSLLYAAKLFKEAGFPDGVVNVVPGAGSVAGNALVTHPGVDKVAFTGS 244 Query: 262 LEVGLKIYEAAGRLAPGQTWFKRAYVETGGKDAIIVDETADFDLAAEGVVVSAYGFQGQK 321 G I + A K +E GGK IV E AD D A +G+ GQ Sbjct: 245 TRTGGSIMKKAA------DDIKSVTLELGGKSPAIVLEDADLDTALDGIFDGTMYNTGQN 298 Query: 322 CSAASRLILTQGAYEPVLERVLKRAERLSVGPA-EENPDLGPVVSAEQERKVLSYIEIGK 380 CSA +R+ + + YE VL+ + +AE+ VGP +E D+GP+VS +Q VL YIE GK Sbjct: 299 CSATTRIYVHRNLYEKVLDALKDKAEKAVVGPGLDEATDMGPLVSEKQLDTVLGYIEKGK 358 Query: 381 NEG-QLVLGGKRLEGEGYFIAPTVFTEVPPKARIAQEEIFGPVLSVIRVKDFAEALEVAN 439 EG +L+ GG R +GYF+ PT+F +V IA+EEIFGPV+SV + E + AN Sbjct: 359 EEGARLITGGSRKGDKGYFVEPTIFADVEDDMTIAREEIFGPVMSVFVFDEVDEVISRAN 418 Query: 440 DTPYGLTGGVYSRKREHLEWARREFHVGNLYFNRKITGALVGVQPFGGFKLSGTNAKTGA 499 D+ YGL V++ + + + G ++ N G + PFGG+K SG + G Sbjct: 419 DSEYGLAASVWTENIKKGHYIAGKLESGTVWVND--FGLELETMPFGGYKKSGIGREMGG 476 Query: 500 LDYLRLFLEMKAV 512 + ++E+K+V Sbjct: 477 DYGISNYVEVKSV 489 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: 622 Number of extensions: 25 Number of successful extensions: 5 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: 496 Length adjustment: 34 Effective length of query: 482 Effective length of database: 462 Effective search space: 222684 Effective search space used: 222684 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 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