Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_110207793.1 DNK54_RS15005 aldehyde dehydrogenase
Query= BRENDA::Q72IB9 (516 letters) >NCBI__GCF_003194585.1:WP_110207793.1 Length = 501 Score = 252 bits (643), Expect = 3e-71 Identities = 165/488 (33%), Positives = 248/488 (50%), Gaps = 22/488 (4%) Query: 37 HYPLYIGGEWVDTKERMVSLNPSAPSEVVGTTAKAGKAEAEAALEAAWKAFKT--WKDWP 94 HY +I G W D + + +P A E+V T AK G AE +AA+ AA A W++ P Sbjct: 5 HYQNFINGAWTDNGQVLEVRSP-ATGELVATVAKGGAAEIDAAVAAAKAAHAAGVWRNTP 63 Query: 95 QEDRSRLLLKAAALMRRRKRELEATLVYEVGKNW-VEASADVAEAIDFIEYYARAALRYR 153 +R+ L+ A + R EL A E G V + V +I +++ A A Y Sbjct: 64 PAERAALINAVAGDLAGRLEELAALQSRENGATIRVTGALHVGLSIANMQFIAAQAAEYE 123 Query: 154 YPAV--EVVPYPGEDNESFYVPLGAGVVIAPWNFPVAIFTGMIMGPVAVGNTVIAKPAED 211 + E+ P P E PLG I PWN P+ + +A GNTV+ KP E Sbjct: 124 FEKAGPEIGPVPAEGILR-REPLGVVGAIVPWNIPLLTIVWKVTPALAAGNTVVLKPDEH 182 Query: 212 AVVVGAKVFEIFHEAGFPPGVVNFLPGVGEEVGAYLVEHPRTRFINFTGSLEVGLKIYEA 271 A ++ ++ + F AG P GV+N + G G + GA L +HP R I FTGS EVG I Sbjct: 183 APLLALELAKAFEAAGLPAGVLNVVVGEGHDAGARLSQHPDVRKIGFTGSTEVGKSI--- 239 Query: 272 AGRLAPGQTWFKRAYVETGGKDAIIVDETADFDLAAEGVVVSAYGFQGQKCSAASRLILT 331 L KR +E GGK I+ + AD D+A +G + + G+ C A +RL++ Sbjct: 240 ---LGASADNMKRVTLELGGKGPNILLDDADLDVAIDGAIYACMANNGEACEAGTRLLVP 296 Query: 332 QGAYEPVLERVLKRAERLSVG-PAEENPDLGPVVSAEQERKVLSYIEIGKNEG-QLVLGG 389 + ++ER++ R + +G P + D+GP+++A+Q +VL++I + +G ++ +GG Sbjct: 297 NSRKDEIVERLVARVGTMKIGNPLDPATDIGPLITADQRDRVLAHIAKAETQGAKVAIGG 356 Query: 390 KRLEGE----GYFIAPTVFTEVPPKARIAQEEIFGPVLSVIRVKDFAEALEVANDTPYGL 445 GE GYF+ PTV T+V P +A EE+FGPVLSV+ EA+ +ANDT YGL Sbjct: 357 SAPAGEEFANGYFVEPTVLTDVTPSMTVACEEVFGPVLSVLGYDTVDEAIAIANDTEYGL 416 Query: 446 TGGVYSRKREHLEWARREFHVGNLYFNRKITGALVGVQPFGGFKLSGTNAKTGALDYLRL 505 + GV+ + R+ G +Y N L PFGG+K SG + G + L Sbjct: 417 SAGVWGTDETRVLDVARQLEAGMIYVND--WHVLHPAYPFGGYKQSGL-GREGGPNALDA 473 Query: 506 FLEMKAVA 513 + E K ++ Sbjct: 474 YTEQKYIS 481 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: 643 Number of extensions: 31 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: 501 Length adjustment: 34 Effective length of query: 482 Effective length of database: 467 Effective search space: 225094 Effective search space used: 225094 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