Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_012536595.1 AFE_RS07230 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::B6ECN9 (505 letters) >NCBI__GCF_000021485.1:WP_012536595.1 Length = 475 Score = 281 bits (718), Expect = 5e-80 Identities = 166/475 (34%), Positives = 254/475 (53%), Gaps = 14/475 (2%) Query: 14 FIDGEWREPLKKNRLPIINPANEEIIGYIPAATEEDVDMAVKAARSALRRDDWGSTTGAQ 73 FIDG W + + R + +P N++++ + + D AV+AA A W TT Q Sbjct: 9 FIDGCWTD--LRARFVVQSPVNQQMLAEVSDCGPREADAAVQAATVAFAA--WRQTTVYQ 64 Query: 74 RAKYLRAIAAKVLEKKPELATLETIDNGKPWFEAASDIDDVVACFEYYADLAEALDSKKQ 133 RA L A + +LA L T + GKP ++ ++I VA +YA+ + + + Sbjct: 65 RALILSRWADLIQVHAEDLARLITWEMGKPIRQSRAEIKTAVALARWYAEECKRVTGES- 123 Query: 134 TEVKLHLDSFKTHVLREPLGVVGLITPWNYPLLMTTWKVAPALAAGCAAILKPSELASIT 193 + + + + P+G V ITPWN P+ M K+APALAAGC ILKP E ++ Sbjct: 124 --IPSQFPDKRLQIWKVPIGPVFAITPWNSPVSMVVRKIAPALAAGCTVILKPDEQTPLS 181 Query: 194 SLELGEICREVGLPPGALSILTGLGHEA-GSPLVSHPDVDKIAFTGSGPTGVKIMTAAAQ 252 +L+L E+ P G L +L L++ + K++FTGS G K+ + Sbjct: 182 ALKLAELWAAAEGPAGTLQVLPSADPAPLAERLMADSRIAKLSFTGSTAVGQKLYAQGSP 241 Query: 253 LVKPVTLELGGKSPIVVFDDIHNLDTAVEWTLFGCFWTNGQICSATSRLIIQETIAPQFL 312 +K ++LELGG +P+++F D ++D AV T+ F GQ C A +RL + E I P+F Sbjct: 242 TIKRLSLELGGHAPVLIFADA-DIDAAVAMTIHAKFRYAGQSCVAANRLYVDEAILPEFT 300 Query: 313 ARLLEWTKNIKISDPLEEDCKLGPVISRGQYEKILKFISTAKDEGATILYGGDRPEHLKK 372 AR LE ++K+ DP ED +GP++S +K + A GA +L GGD + Sbjct: 301 ARYLEAMGHLKVGDPFAEDTDIGPLVSEVAVQKFKAQLQDAMARGARLLCGGDA-----Q 355 Query: 373 GYYIQPTIITDVDTSMEIWKEEVFGPVLCVKTFKTEEEAIELANDTKFGLGAAILSKDLE 432 G + PT++ D+D I+ EE F P+L ++ F++E EA+ ANDT +GL A + ++DL Sbjct: 356 GLWCSPTLLADLDPQSRIFHEESFSPLLPIQGFRSEAEAVARANDTPYGLAAYLWTRDLG 415 Query: 433 RCERFTKAFQSGIVWINCSQPCFWQPPWGGKKRSGFGRELGEWSLENYLNIKQVT 487 R R +A Q GIV +N P Q P+GG K SG G E G+W LE YL ++ V+ Sbjct: 416 RAYRIAEALQCGIVGVNDGAPATPQAPFGGSKLSGLGAEGGKWGLEEYLQLRYVS 470 Lambda K H 0.318 0.136 0.421 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: 598 Number of extensions: 28 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: 505 Length of database: 475 Length adjustment: 34 Effective length of query: 471 Effective length of database: 441 Effective search space: 207711 Effective search space used: 207711 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 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