Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_073950325.1 RH94_RS25575 gamma-aminobutyraldehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_001906585.1:WP_073950325.1 Length = 511 Score = 466 bits (1199), Expect = e-136 Identities = 237/470 (50%), Positives = 309/470 (65%), Gaps = 7/470 (1%) Query: 7 INGELVSG-EGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAEWGQTTPKVRAE 65 I G L G G V +PATG+ + A + VDAAV AA AF W TP R++ Sbjct: 25 IAGRLTKGTSGRTHAVVDPATGEEVHTYELAGPDDVDAAVAAAREAFPGWAGATPGDRSD 84 Query: 66 CLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGLAAGE 125 L + A+V+ + + FA ES CGKPL ++P +D FFAGAAR L G +AGE Sbjct: 85 ALHRFAEVLADRAEDFARAESLQCGKPLKLTREFDVPGTIDNAAFFAGAARHLQGQSAGE 144 Query: 126 YLEGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTALKLA 185 Y HTS +RR+P+GVV SIAPWNYPL MAAWK+ PA+AAGN +VLKP+E+TPLT+L A Sbjct: 145 YSGDHTSYVRREPIGVVGSIAPWNYPLQMAAWKVLPAIAAGNTIVLKPAELTPLTSLLFA 204 Query: 186 ELAKDI-FPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIKRTH 244 + A + P GVINI+ G GK G+ L GHP V MVS TGS A G+ + +S+KR H Sbjct: 205 QAATEAGIPDGVINIVTGTGKEAGEHLVGHPDVAMVSFTGSTAVGKRVAEIATASVKRLH 264 Query: 245 MELGGKAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLGAAV 304 +ELGGKAP +VFDDAD+EA V G N GQDCTAA R Y Q+ +Y+ V + A + Sbjct: 265 LELGGKAPFVVFDDADLEAAVNGAVAGALINTGQDCTAATRAYVQRPLYEEFVARTAALM 324 Query: 305 ATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKG---NGYYYA 361 T++ G P T+LGPL S H +RV V+ A+A + +V+TGGE +G NG YY Sbjct: 325 ETVRLGDPFAPGTDLGPLISHVHRDRVAGFVDRARA--YARVVTGGEAPQGELKNGAYYR 382 Query: 362 PTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRAHRV 421 PTL+AGA QD IVQ E+FGPV+ V PFD++++ + AND+ YGLA+S W++DV RA+R Sbjct: 383 PTLIAGAAQDSEIVQSEIFGPVLVVLPFDSDDEGIRLANDTAYGLAASAWSRDVYRANRA 442 Query: 422 SARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVM 471 + ++ GC WVN H ++SEMPHGG K SG+GKDMS Y E+YT ++HVM Sbjct: 443 TREIKAGCVWVNDHIPIISEMPHGGSKQSGFGKDMSSYSFEEYTQIKHVM 492 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: 663 Number of extensions: 31 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: 511 Length adjustment: 34 Effective length of query: 440 Effective length of database: 477 Effective search space: 209880 Effective search space used: 209880 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