Align aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate GFF5142 PS417_26340 betaine-aldehyde dehydrogenase
Query= BRENDA::Q83XU8 (485 letters) >FitnessBrowser__WCS417:GFF5142 Length = 490 Score = 338 bits (866), Expect = 3e-97 Identities = 187/463 (40%), Positives = 273/463 (58%), Gaps = 8/463 (1%) Query: 24 SPLNNAVIAKVHEAGRAEVDAAVAAAQAALKGAWGRMSLAQRVEVLYAVADGINRRFDDF 83 +P N V+A+V A + +V+ AV +A+ K W M+ +R +L D + R D+ Sbjct: 28 NPANGEVLAQVQRATKEDVERAVVSAEKGQK-IWAAMTAMERSRILRRAVDILRERNDEL 86 Query: 84 LAAEVEDTGKPMSLARHVDIPRGAANFKIFADVVKNVPTEFFEMPTPDGVGAINYAVRRP 143 A E DTGK S ++VDI GA + +A +V + E ++P D + Y R P Sbjct: 87 AALETLDTGKAFSETKYVDIVTGADVLEYYAGLVPAIEGE--QIPLRDT--SFVYTRREP 142 Query: 144 VGVVGVICPWNLPLLLMTWKVGPALACGNTVVVKPSEETPQTAALLGEVMNTAGVPPGVY 203 +GVV I WN P+ + WK PALA GN ++ KPSE T T L E+ AGVP GV+ Sbjct: 143 LGVVAGIGAWNYPIQIALWKSAPALAAGNAMIFKPSEVTSLTTLKLAEIYTEAGVPAGVF 202 Query: 204 NVVHGFGPNSTGEFLTSHPDVNAITFTGETGTGEAIMKAAADGA-RPVSLELGGKNAAIV 262 NV+ G G G +LT HP + ++FTG T TG+ +M +A+ + + V++ELGGK+ IV Sbjct: 203 NVLTGSG-REVGTWLTEHPRIEKVSFTGGTDTGKKVMASASSSSLKEVTMELGGKSPLIV 261 Query: 263 FADCDLDKAIEGTLRSCFANCGQVCLGTERVYVERPIFDRFVSRLKKGAEGMQLGRPEDL 322 F D DLD+A + + + F + GQVC RV+V + + F +++ + +++G P+D Sbjct: 262 FEDADLDRAADIAMMANFYSSGQVCTNGTRVFVPKHLQAAFEAKIVERVARIRVGNPQDD 321 Query: 323 ATGMGPLISQEHREKVLSYYKKAVEAGATVVTGGGVPEMPEALKGGAWVQPTIWTGLGDD 382 T GPL+S H E VL Y K E GA V+ GG E KG A+V PT++T D+ Sbjct: 322 NTNFGPLVSFAHMESVLGYIAKGKEEGARVLCGGDRLTDGEFAKG-AFVAPTVFTDCTDE 380 Query: 383 SVVAREEIFGPCALVMPFDSEEEVIRRANDNDYGLARRIWTTNLSRAHRVAGAIEVGIAW 442 + REEIFGP ++ +++EEEVIRRAND D+GLA + T +L+RAHRV +E GI W Sbjct: 381 MTIVREEIFGPVMSILTYETEEEVIRRANDTDFGLAAGLVTKDLNRAHRVIHQLEAGICW 440 Query: 443 VNSWFLRDLRTAFGGSKQSGIGREGGVHSLEFYTELKNVCIKL 485 +N+W D + GG KQSG+GRE G+ SL +T +K+V ++L Sbjct: 441 INAWGESDAKMPVGGYKQSGVGRENGISSLNNFTRIKSVQVEL 483 Lambda K H 0.318 0.135 0.406 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: 536 Number of extensions: 18 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: 485 Length of database: 490 Length adjustment: 34 Effective length of query: 451 Effective length of database: 456 Effective search space: 205656 Effective search space used: 205656 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 (21.7 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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