Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_068166904.1 HTA01S_RS02155 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_001592305.1:WP_068166904.1 Length = 492 Score = 314 bits (805), Expect = 4e-90 Identities = 179/469 (38%), Positives = 271/469 (57%), Gaps = 9/469 (1%) Query: 6 LINGELVSGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTPKVRAE 65 LINGE V G + V +PATG L ++A + A+ AA+AA+A W T K R+ Sbjct: 22 LINGEWVKGSS-RFDVLDPATGQKLADVANLGPADAEKAIAAANAAWAGWKGKTAKERSI 80 Query: 66 CLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAAGE 125 L K D++ N + + GKPL A E+ +FA A+ +NG + Sbjct: 81 ILRKWYDLLMANQDDLGRIMTAEQGKPLAEA-KGEVTYGASFVEWFAEEAKRVNGETLPQ 139 Query: 126 YLEGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTALKLA 185 + M+ + P+GV A+I PWN+PL M K+APALAAG V++KP+E+TPLTAL A Sbjct: 140 FDNNRRLMVLKQPIGVCAAITPWNFPLAMITRKVAPALAAGCPVIIKPAELTPLTALAAA 199 Query: 186 ELA-KDIFPAGVINILFGRGKT---VGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIK 241 ELA + PAGV+N++ VG + VR +S TGS G +++ +A ++K Sbjct: 200 ELAIRAGIPAGVLNMITADASNSIAVGKVICASDVVRHISFTGSTEVGRILMAQSAPTVK 259 Query: 242 RTHMELGGKAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLG 301 + +ELGG AP IVF+DADI++ VEG Y NAGQ C + R+Y Q+G+YD V K Sbjct: 260 KMSLELGGNAPFIVFNDADIDSAVEGAFASKYRNAGQTCVCSNRLYVQEGVYDEFVAKFA 319 Query: 302 AAVATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKGNGYYYA 361 A V T K G ++ GPL A LE+V + V++AKA G +V+ GG + +G ++ Sbjct: 320 AKVKTAKVGNGFEDGVNQGPLIEEAALEKVQRHVDDAKAKGG-RVLVGGNRL--SGQFFE 376 Query: 362 PTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRAHRV 421 PT++A A D ++E FGP V F E++ V+ AN++++GLAS +++D+GR +RV Sbjct: 377 PTVVADATADMLCAKEETFGPFAPVFKFKTEQEAVDAANNTEFGLASYFYSRDIGRIYRV 436 Query: 422 SARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHV 470 + L+YG +N + +P GG K SG G++ S +G++DY ++++ Sbjct: 437 AEALEYGMVGINVGILATEHVPFGGVKQSGLGREGSHHGMDDYVEIKYL 485 Lambda K H 0.317 0.134 0.397 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: 564 Number of extensions: 25 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: 474 Length of database: 492 Length adjustment: 34 Effective length of query: 440 Effective length of database: 458 Effective search space: 201520 Effective search space used: 201520 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