Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_068105462.1 I601_RS01380 aldehyde dehydrogenase family protein
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_001653335.1:WP_068105462.1 Length = 506 Score = 314 bits (805), Expect = 4e-90 Identities = 177/474 (37%), Positives = 263/474 (55%), Gaps = 17/474 (3%) Query: 13 SGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAF--AEWGQTTPKVRAECLLKL 70 + +G + ++ PA G ++ ++E + AAV AA +AF W T RA L +L Sbjct: 13 AADGATRDIHCPADGHHVVTVSEGGEQDAVAAVVAARSAFDNGPWPHTPAPERAALLHRL 72 Query: 71 ADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAAGEYLEGH 130 AD +E + A LES + GK + D + IV VFR FA A+ G + G Sbjct: 73 ADRLEADKDEVARLESLDTGKRFVESQID-VDDIVSVFRHFASLAQGEAGRVVDAGMPGV 131 Query: 131 TSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTALKLAELAKD 190 S + +P+GV I PWNYPL+ +WK+AP LAAGN +LKPSE+TP TA+ L D Sbjct: 132 VSRVVHEPIGVCTLITPWNYPLLQTSWKVAPCLAAGNTFILKPSELTPSTAIWLMGALSD 191 Query: 191 I-FPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIKRTHMELGG 249 P GV N++ G G VG LT P+V +VS TG + TG ++ A ++K+ +ELGG Sbjct: 192 AGLPDGVANLVLGAGDRVGPTLTEAPEVDLVSFTGGVVTGRRVMVAAAPTVKKVALELGG 251 Query: 250 KAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLGAAVATLKS 309 K P ++F DAD++A ++ T + ++GQ C+A R+ + ++D +V++L ++ Sbjct: 252 KNPNVIFADADLDAAIDNALTAVFLDSGQVCSAGARLVVEDTVHDQVVDELVRRAGRIRL 311 Query: 310 GAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKR-------KGNGYYYAP 362 G P D+ E GPL S AH ++V V A G + GG G+YY P Sbjct: 312 GGPFDDDAETGPLISAAHRDKVEAYVAAGIAEGATLRVGGGRPEGAGYAAGLAEGFYYLP 371 Query: 363 TLLAGALQDDAIVQKEVFGPVVSVTPFD------NEEQVVNWANDSQYGLASSVWTKDVG 416 T+L D + VQ+E FGPV++V F EE V+ AND+ YGLA +VWT D G Sbjct: 372 TILDDCSADMSCVQEESFGPVLTVERFTGEDADAREEAAVSIANDTVYGLAGAVWTSDAG 431 Query: 417 RAHRVSARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHV 470 RA RV++RL++G W+N + V++ GG K SG G+++ + GLE+Y +H+ Sbjct: 432 RAERVASRLRHGTIWINDYHPYVAQAEWGGYKQSGTGRELGIAGLEEYRETKHI 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: 609 Number of extensions: 25 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: 474 Length of database: 506 Length adjustment: 34 Effective length of query: 440 Effective length of database: 472 Effective search space: 207680 Effective search space used: 207680 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