Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_034274777.1 AMYHA_RS23925 gamma-aminobutyraldehyde dehydrogenase
Query= BRENDA::P77674 (474 letters) >NCBI__GCF_000504245.1:WP_034274777.1 Length = 479 Score = 472 bits (1214), Expect = e-137 Identities = 240/470 (51%), Positives = 304/470 (64%), Gaps = 5/470 (1%) Query: 4 KLLINGELV-SGEGEKQPVYNPATGDVLLEIAEASAEQVDAAVRAADAAFAE-WGQTTPK 61 K ING V + +G + +PATG V+ E +SA+ VD A RAA AF W TP Sbjct: 9 KNFINGAYVDAADGRTSEIVDPATGHVVAEAPLSSADDVDTAFRAAADAFENGWRDATPG 68 Query: 62 VRAECLLKLADVIEENGQVFAELESRNCGKPLHSAFNDEIPAIVDVFRFFAGAARCLNGL 121 R L K AD +E+ E NCGKP ++EI ++D RFFAGA+R L G Sbjct: 69 ERQIALNKFADAVEDRADELVAAEVANCGKPAQMTKDEEIFQVLDALRFFAGASRNLEGK 128 Query: 122 AAGEYLEGHTSMIRRDPLGVVASIAPWNYPLMMAAWKLAPALAAGNCVVLKPSEITPLTA 181 AAGEY+ GHTS +RR+P+G V I PWNYP+ MAAWK+ PALAAGN VVLKPS+ TP++ Sbjct: 129 AAGEYMAGHTSWVRREPIGPVGQITPWNYPMAMAAWKIGPALAAGNSVVLKPSDTTPMST 188 Query: 182 LKLAELAKDIFPAGVINILFGRGKTVGDPLTGHPKVRMVSLTGSIATGEHIISHTASSIK 241 L LAE+A + PAGV N++ G T G L HP R++SLTGS G+ I A +K Sbjct: 189 LLLAEIAAEFLPAGVFNVVTGDRDT-GRALVDHPTPRLISLTGSTRAGKEIAEAGAKDLK 247 Query: 242 RTHMELGGKAPVIVFDDADIEAVVEGVRTFGYYNAGQDCTAACRIYAQKGIYDTLVEKLG 301 R H+ELGGKAPV+VFDDADIEA EG+ GY+NAGQDCTAA R+ A GI+D L L Sbjct: 248 RLHLELGGKAPVVVFDDADIEAAAEGIAGAGYFNAGQDCTAATRVLAAPGIHDDLAAALA 307 Query: 302 AAVATLKSGAPDDESTELGPLSSLAHLERVGKAVEEAKATGHIKVITGGEKRKGNGYYYA 361 + PD+ + GPL++ L RV ++ +A H K++ GGE+ GY+YA Sbjct: 308 EQARKTVTAGPDNADADYGPLNNPNQLARVSGFID--RAPDHAKILAGGERVGDTGYFYA 365 Query: 362 PTLLAGALQDDAIVQKEVFGPVVSVTPFDNEEQVVNWANDSQYGLASSVWTKDVGRAHRV 421 PT++AG Q D + EVFGPVV+V FD+E+ VNWAN +YGLASSVWT+D RA RV Sbjct: 366 PTVVAGLRQGDELTTDEVFGPVVTVQRFDDEDTAVNWANSVEYGLASSVWTRDHARALRV 425 Query: 422 SARLQYGCTWVNTHFMLVSEMPHGGQKLSGYGKDMSLYGLEDYTVVRHVM 471 S RL +GC W+NTH L++EMPHGG K SGYGKD+S Y E+YT V+HVM Sbjct: 426 SRRLDFGCVWINTHIPLIAEMPHGGFKHSGYGKDLSAYSFEEYTRVKHVM 475 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: 619 Number of extensions: 27 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: 479 Length adjustment: 33 Effective length of query: 441 Effective length of database: 446 Effective search space: 196686 Effective search space used: 196686 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