Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_055436782.1 ASC41_RS11440 aldehyde dehydrogenase
Query= BRENDA::C6KEM4 (506 letters) >NCBI__GCF_001418085.1:WP_055436782.1 Length = 499 Score = 331 bits (848), Expect = 4e-95 Identities = 190/486 (39%), Positives = 278/486 (57%), Gaps = 19/486 (3%) Query: 11 GLFIGGAWREPCLGRRLPVVNPATEATIGDIPAGTAEDVEIAVAAARDAFSRDGGRQWSR 70 G FI G + EP G+ +P + I P EDVE+A+ AA A W Sbjct: 13 GNFINGKFVEPIGGQYFENTSPIDNSLIAKYPRSQKEDVEMALGAANAA-----KEAWGN 67 Query: 71 APGAVRANFLRAIAAKIKDRKSELALLETLDSGKPLDEASGDMDDVAACFEYYADLAEAL 130 RA L +A I+ E A++ET D+GKP+ E D+ +++ A + Sbjct: 68 TSATERATLLNKVADIIEANLEEFAIMETCDNGKPIRETLNA--DIPLAVDHWRYFAACI 125 Query: 131 DGKQRSPISLPMENFKSYVLKEPIGVVGLITPWNYPLLMATWKVAPALAAGCTTILKPSE 190 ++ S L +N S +KEP+GV+G I PWN+PLLM +WK+ PAL G +LKP+E Sbjct: 126 RSEEGSAAELD-QNTLSLNIKEPLGVIGQIIPWNFPLLMLSWKLPPALVTGNCVVLKPAE 184 Query: 191 LASVSCLELGAICMEIGLPPGVLNIITGLGPEAGAPLSSHSHVDKVAFTGSTETGKRIMT 250 + L E+ PPGV+NI+ G GPEAG PL+S S VDKVAFTG T TG+ IM Sbjct: 185 QTPSTATLLMEKIAEV-FPPGVINIVHGFGPEAGKPLASSSKVDKVAFTGETTTGQLIMQ 243 Query: 251 SAAQMVKPVSLELGGKSPLIVFDDIGD-----IDKAVEWTMFGIFANAGQVCSATSRLLL 305 A++ + PV++ELGGKSP + F+ + D +DKAVE + F N G+VC+A SR+L+ Sbjct: 244 YASKNLNPVTMELGGKSPNVFFNSVMDHDDAYLDKAVEGAVLFAF-NQGEVCTAPSRILV 302 Query: 306 HEKIAKKFLDRLVAWAKNIKVSDPLEEGCRLGSVISEGQYEKIKKFISTARSEGATILYG 365 E I F+ R+V I +P +G+ S+ QYEKI+ +I + EGA +L G Sbjct: 303 QEDIYDAFMKRVVERTNAIIQDNPYNANTMVGAQASKDQYEKIQSYIEIGKEEGAKVLAG 362 Query: 366 GGRPQ---HLRRGFFLEPTIITDVSTSMQIWQEEVFGPVICVKEFRTDSEAVELANDTHY 422 G + +L GF+++PTI+ + M+++QEE+FGPV+CV +F+ ++EA+E+ANDT Y Sbjct: 363 GSANKLEGNLANGFYIKPTIL-EGHNKMRVFQEEIFGPVVCVTKFKDEAEALEIANDTLY 421 Query: 423 GLAGAVISNDQERCERISKALHSGIIWINCSQPCFVQAPWGGNKRSGFGRELGEWGLDNY 482 GL V + D + +I +A+ +G +W+NC AP+GG K+SGFGRE L+ Y Sbjct: 422 GLGAGVWTRDAHQLYQIPRAIKAGRVWVNCYHAYPAHAPFGGYKKSGFGRENHVMMLNYY 481 Query: 483 LTVKQV 488 K + Sbjct: 482 RQTKNM 487 Lambda K H 0.318 0.136 0.418 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: 673 Number of extensions: 29 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: 506 Length of database: 499 Length adjustment: 34 Effective length of query: 472 Effective length of database: 465 Effective search space: 219480 Effective search space used: 219480 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 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