Align 2-aminomuconic semialdehyde dehydrogenase; Aldehyde dehydrogenase 12; Aldehyde dehydrogenase family 8 member A1; EC 1.2.1.32 (characterized)
to candidate WP_085634733.1 MGEO_RS00465 aldehyde dehydrogenase family protein
Query= SwissProt::Q9H2A2 (487 letters) >NCBI__GCF_002115805.1:WP_085634733.1 Length = 508 Score = 315 bits (806), Expect = 3e-90 Identities = 177/479 (36%), Positives = 277/479 (57%), Gaps = 11/479 (2%) Query: 12 NFIDGKFLPCSSYIDSYDPSTGEVYCRVPNSGKDEIEAAVKAAREAFPS--WSSRSPQER 69 + IDG ++ D PS G V G +E +AA+KAAR AF + WS S +ER Sbjct: 22 HLIDGAWVTGRETFDRVSPSHGTVVSTSSKGGPEETDAAIKAARRAFDAGIWSRISGRER 81 Query: 70 SRVLNQVADLLEQSLEEFAQAESKDQGKTLALARTMDIPRSVQNFRFFASSSLHHTSECT 129 + VL +VADL+E +++ A E+ + GK ++ ++ ++ + +R+ A+ L TS+ Sbjct: 82 AAVLLRVADLIEANVDRIALQETLESGKPISQSKG-EVAGAADLWRYAAA--LARTSQGD 138 Query: 130 QMDHLGC--MHYTVRAPVGVAGLISPWNLPLYLLTWKIAPAMAAGNTVIAKPSELTSVTA 187 + LG + V+ P+GV +I+PWN P ++L+ K+ A+AAG TV+ KPSE+T + Sbjct: 139 SHNTLGSDMLGVVVKDPIGVVSVITPWNFPFWILSQKLPFALAAGCTVVVKPSEMTPSST 198 Query: 188 WMLCKLLDKAGVPPGVVNIVFGTGPRVGEALVSHPEVPLISFTGSQPTAERITQLSAPHC 247 M+ +LL +AG+P GV NIV G G VG +HP+V +++FTGS + IT+ ++ Sbjct: 199 VMMGELLMQAGLPAGVCNIVLGYGDPVGSLKSTHPDVDMVTFTGSTAVGKLITKAASDTL 258 Query: 248 KKLSLELGGKNPAIIFEDANLDECIPATVRSSFANQGEICLCTSRIFVQKSIYSEFLKRF 307 KK++LELGGKNP +IF DA+L+ A + N G+ C +SRI V + I +F+ R Sbjct: 259 KKVALELGGKNPQVIFPDADLENAADAVTFGVYFNVGQCCNSSSRIIVHEDIAEDFVARV 318 Query: 308 VEATRKWKVGIPSDPLVSIGALISKAHLEKVRSYVKRALAEGAQIWCGEGVDKLSLPARN 367 V ++K K G P DP +GA+++ H ++ YV+ A+A GA++ G L Sbjct: 319 VALSKKVKFGDPLDPTTQVGAIVTPEHNARIDGYVQEAVAAGARLELGGAY----LDVEG 374 Query: 368 QAGYFMLPTVITDIKDESCCMTEEIFGPVTCVVPFDSEEEVIERANNVKYGLAATVWSSN 427 F PTVI+ + + EE+FGPV V+ F + ++ I N+ +YGL+A VWS + Sbjct: 375 LGDQFYQPTVISSVSADMAVAREEVFGPVLSVLTFRTLDDAIALTNDSEYGLSAGVWSES 434 Query: 428 VGRVHRVAKKLQSGLVWTNCWLIRELNLPFGGMKSSGIGREGAKDSYDFFTEIKTITVK 486 V A++ Q+G VWTN W+ L FGGMK SG GRE K ++ F E+K++ ++ Sbjct: 435 VHTCLEFARRAQAGTVWTNTWMDGYPELAFGGMKQSGTGREIGKYGFEEFLEVKSVVMR 493 Lambda K H 0.319 0.133 0.404 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: 541 Number of extensions: 19 Number of successful extensions: 4 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: 487 Length of database: 508 Length adjustment: 34 Effective length of query: 453 Effective length of database: 474 Effective search space: 214722 Effective search space used: 214722 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 (21.8 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