Align aminomuconate-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate SMc00094 SMc00094 betaine aldehyde dehydrogenase
Query= BRENDA::Q83XU8 (485 letters) >FitnessBrowser__Smeli:SMc00094 Length = 487 Score = 330 bits (847), Expect = 5e-95 Identities = 189/459 (41%), Positives = 262/459 (57%), Gaps = 9/459 (1%) Query: 25 PLNNAVIAKVHEAGRAEVDAAVAAAQAALKGAWGRMSLAQRVEVLYAVADGINRRFDDFL 84 P +IA++H A V+ A+AAA+ A + W MS R +L A+ + +R + Sbjct: 29 PATGEIIARLHAATPGIVEKAIAAAKRA-QPEWAAMSPTARGRILKRAAELMRQRNRELS 87 Query: 85 AAEVEDTGKPMSLARHVDIPRGAANFKIFADVVKNVPTEFFEMPTPDGVGAINYAVRRPV 144 E DTGKP+ D GA +F+ F V P P G G Y R P+ Sbjct: 88 ELETLDTGKPIQETIVADPTSGADSFEFFGGVA---PAALNGDYIPLG-GDFAYTKRVPL 143 Query: 145 GVVGVICPWNLPLLLMTWKVGPALACGNTVVVKPSEETPQTAALLGEVMNTAGVPPGVYN 204 GV I WN P + WK PAL GN +V KPSE TP A + E++ AG+P G++N Sbjct: 144 GVCVGIGAWNYPQQIACWKGAPALVAGNAMVFKPSENTPLGALKIAEILIEAGLPKGLFN 203 Query: 205 VVHGFGPNSTGEFLTSHPDVNAITFTGETGTGEAIMKAAADGARPVSLELGGKNAAIVFA 264 V+ G +TG L +HPDV ++ TG TG+ + AAA + V++ELGGK+ IVF Sbjct: 204 VIQG--DRATGPLLVNHPDVAKVSLTGSVPTGKKVAGAAAAELKHVTMELGGKSPLIVFD 261 Query: 265 DCDLDKAIEGTLRSCFANCGQVCLGTERVYVERPIFDRFVSRLKKGAEGMQLGRPEDLAT 324 D DL+ AI G + F + GQVC RV+V+R I + F++RLK+ E + +G P D AT Sbjct: 262 DADLESAIGGAMLGNFYSTGQVCSNGTRVFVQRKIKEPFLARLKERTEAIVIGDPLDEAT 321 Query: 325 GMGPLISQEHREKVLSYYKKAVEAGATVVTGGGVPEMPEALKGGAWVQPTIWTGLGDDSV 384 +GP++S R+KV SY K GA +VTGGG+P G ++QPT++ + D Sbjct: 322 QLGPMVSAAQRDKVFSYIGKGKAEGARLVTGGGIPN--NVSGEGTYIQPTVFADVTDGMT 379 Query: 385 VAREEIFGPCALVMPFDSEEEVIRRANDNDYGLARRIWTTNLSRAHRVAGAIEVGIAWVN 444 +AREEIFGP V+ FD E EVI RAN ++GL+ ++T +L+RAHRVA +E G W+N Sbjct: 380 IAREEIFGPVMCVLDFDDEVEVIARANATEFGLSAGVFTADLTRAHRVADRLEAGTLWIN 439 Query: 445 SWFLRDLRTAFGGSKQSGIGREGGVHSLEFYTELKNVCI 483 ++ L + FGGSKQSG GRE V +L YTELK V + Sbjct: 440 TYNLCPVEIPFGGSKQSGFGRENSVAALNHYTELKTVYV 478 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: 621 Number of extensions: 30 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: 487 Length adjustment: 34 Effective length of query: 451 Effective length of database: 453 Effective search space: 204303 Effective search space used: 204303 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