Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_011811026.1 VEIS_RS16060 gamma-aminobutyraldehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_000015565.1:WP_011811026.1 Length = 477 Score = 584 bits (1505), Expect = e-171 Identities = 286/473 (60%), Positives = 348/473 (73%) Query: 1 MQHKLLINGELVSGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTP 60 M+ +L I+G+ + GE + + NP+TG+++ E+ EAS Q+ AV AA A+ W T+ Sbjct: 1 MRTELFIDGQFLQGEESAERILNPSTGELICEVREASPTQISRAVDAAHRAWPAWASTSA 60 Query: 61 KVRAECLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNG 120 K RA LLK+AD IE+N A+LE+ NCGKP +A DE+PAI DVFRFFAGA RC+ Sbjct: 61 KDRAAMLLKVADHIEQNAAGLAQLEALNCGKPYQAALADEMPAIADVFRFFAGAVRCMTA 120 Query: 121 LAAGEYLEGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLT 180 A EYL GHTSMIRRD LGVVASI+PWNYPLMMAAWK+ PA+A GN +VLKPSE TPLT Sbjct: 121 PVATEYLPGHTSMIRRDSLGVVASISPWNYPLMMAAWKICPAVATGNTIVLKPSEQTPLT 180 Query: 181 ALKLAELAKDIFPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSI 240 LKLAE IFP GVINI+ GRG++ G L P+VRM+S+TG ++TG+ ++ I Sbjct: 181 TLKLAEFIASIFPPGVINIVCGRGESAGATLIAQPQVRMISVTGDVSTGQKVMEAAVRGI 240 Query: 241 KRTHMELGGKAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKL 300 KRTH+ELGGKAPVIVFDDADI VV G+RTFGYYNAGQDCTAACR+YAQKGIYD LV L Sbjct: 241 KRTHLELGGKAPVIVFDDADIGEVVAGIRTFGYYNAGQDCTAACRVYAQKGIYDKLVADL 300 Query: 301 GAAVATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKGNGYYY 360 AAV+T++ G P D E+GP S RV VE A+ HIKV+ GG+ G++Y Sbjct: 301 AAAVSTIRIGEPGDVGVEMGPCISERQRSRVAAFVERAREEKHIKVVAGGKIADRRGFFY 360 Query: 361 APTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRAHR 420 PTLLA Q D IV+KEVFGPVVSVTPF + ++V+ ANDS YGLASSVW+ DVG+A R Sbjct: 361 QPTLLANCKQSDEIVRKEVFGPVVSVTPFSDLDEVIGLANDSDYGLASSVWSSDVGKAMR 420 Query: 421 VSARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVMVK 473 V+A L YG TW+NTHFMLV+EMPHGG K SGYGKD S++ LE+YT RHVMVK Sbjct: 421 VAAALHYGTTWINTHFMLVAEMPHGGMKKSGYGKDQSMFALEEYTCARHVMVK 473 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: 15 Number of successful extensions: 1 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: 477 Length adjustment: 33 Effective length of query: 441 Effective length of database: 444 Effective search space: 195804 Effective search space used: 195804 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: 51 (24.3 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