Align L-glutamate gamma-semialdehyde dehydrogenase (EC 1.2.1.88) (characterized)
to candidate WP_012607209.1 AFE_RS08085 aldehyde dehydrogenase
Query= BRENDA::Q72IB9 (516 letters) >NCBI__GCF_000021485.1:WP_012607209.1 Length = 506 Score = 204 bits (519), Expect = 6e-57 Identities = 160/479 (33%), Positives = 238/479 (49%), Gaps = 36/479 (7%) Query: 38 YPLYIGGEWV-DTKERMVSLNPSAPSEVVGTTAKAGKAEAEAALEAAWKAFKTWKDWPQE 96 Y +IGG+WV K + + + A++ + E AL+AA W Sbjct: 19 YDNFIGGKWVAPVKGQYFDVITPINGKSYTQAARSTAEDIELALDAAHAIADKWGKTSPA 78 Query: 97 DRSRLLLKAAALMRRRKRELEATLVYEVGKNWVEA-SADVAEAIDFIEYYARAALRYRYP 155 +R+ +LLK A + L + GK E +AD+ A+D Y+A +R + Sbjct: 79 ERANILLKVADRIEANLELLAYAETVDNGKPIRETLNADIPLAVDHFRYFA-GCVRAQEG 137 Query: 156 AVEVVPYPGEDNE---SFYVPLGAGVVIAPWNFPVAIFTGMIMGPVAVGNTVIAKPAEDA 212 + + ++N F+ PLG I PWNFP+ + + + + GN V+ KPAE Sbjct: 138 GISDI----DENTVAYHFHEPLGVVGQIIPWNFPILMASWKLAPALGAGNVVVLKPAEST 193 Query: 213 VVVGAKVFEIFHEAGFPPGVVNFLPGVGEEVGAYLVEHPRTRFINFTGSLEVGLKIYEAA 272 + + E+ + PPGV+N + G G E G L R I FTGS G I +AA Sbjct: 194 PISILILAELIADL-LPPGVLNIVNGYGREAGMPLATSKRIAKIAFTGSTTTGRVIAQAA 252 Query: 273 GR-LAPGQTWFKRAYVETGGKD-----AIIVDETADF-DLAAEGVVVSAYGFQGQKCSAA 325 L P A +E GGK A ++D+ F D A EG+V+ A+ QG+ C+ Sbjct: 253 ANSLIP-------ATLELGGKSPNIFFADVMDKDDSFLDKAIEGLVLFAFN-QGEVCTCP 304 Query: 326 SRLILTQGAYEPVLERVLKRAERLSVG-PAEENPDLGPVVSAEQERKVLSYIEIGKNEG- 383 SR ++ + Y+ +ER L R + + G P + N +G S EQ K+LSY+++GK EG Sbjct: 305 SRALIQESIYDKFMERCLDRIKAIKQGNPLDTNTMIGAQASKEQLTKILSYLDLGKQEGA 364 Query: 384 QLVLGGKR--LEGE---GYFIAPTVFTEVPPKARIAQEEIFGPVLSVIRVKDFAEALEVA 438 Q+++GG + ++G+ GY++ PT+F + K RI QEEIFGPVL+V KD AEAL +A Sbjct: 365 QVLIGGSQAIVDGDLDGGYYVQPTLF-KGHNKMRIFQEEIFGPVLAVTTFKDEAEALSIA 423 Query: 439 NDTPYGLTGGVYSRKREHLEWARREFHVGNLYFNRKITGALVGVQPFGGFKLSGTNAKT 497 NDT YGL GV+SR R G ++ N A FGG+K SG +T Sbjct: 424 NDTLYGLGAGVWSRNGNVAYRMGRAIKAGRVWIN--CYHAYPAHAAFGGYKESGIGRET 480 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: 576 Number of extensions: 35 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: 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 ( 7.4 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