Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_041950131.1 VEIS_RS17310 aldehyde dehydrogenase family protein
Query= BRENDA::C0P9J6 (505 letters) >NCBI__GCF_000015565.1:WP_041950131.1 Length = 496 Score = 350 bits (897), Expect = e-101 Identities = 194/494 (39%), Positives = 290/494 (58%), Gaps = 11/494 (2%) Query: 11 QLFVDGEWRPPAQGRRLPVVNPTTEAHIGEIPAGTAEDVDAAVAAARAALKRNRGRDWAR 70 +L +DG+W A RRL +P + D A+ AAR A + W Sbjct: 13 RLLIDGQWCDAADARRLERRSPAHGQLVAVYAEAGVPDAQRAIGAARQAFDKG---PWPL 69 Query: 71 APGAVRAKYLRAIAAKVIERKPELAKLEALDCGKPYDEAAWDMDDVAGCFEYFADQAEAL 130 GA RA+ LR +A ++ R+ LA++E+L+ GKP ++ +++ A ++Y A A L Sbjct: 70 LKGAERARILRHVADGILARRHALARMESLENGKPLAQSLAEIEGAADLWQYAASLARNL 129 Query: 131 DKRQNSPVSLPMETFKCHLRREPIGVVGLITPWNYPLLMATWKIAPALAAGCTAVLKPSE 190 +S +L T LR EPIGVVG+ITPWN+P L+ + K+ ALAAGCTAV+KP+E Sbjct: 130 --HGDSYNTLGAATLALVLR-EPIGVVGIITPWNFPFLIVSQKLPFALAAGCTAVVKPAE 186 Query: 191 LASVTCLELADICKEVGLPSGVLNIVTGLGPDAGAPLSAHPDVDKVAFTGSFETGKKIMA 250 + S T + L +I E G+P+GV+NI+ G G G + +HPDVD ++FTGS GK+ +A Sbjct: 187 VTSGTTVMLGEILLEAGIPAGVVNILVGQGAVVGEAMVSHPDVDMLSFTGSTAVGKQAVA 246 Query: 251 SAAPMVKPVTLELGGKSPIVVFDDVDIDKAVEWTLFGCFWTNGQICSATSRLLIHTKIAK 310 +A +K V LELGGK+P +VF D D + AV+ ++G F+ GQ C++ SR+L+ +A Sbjct: 247 RSAATLKKVALELGGKNPQIVFADCDWEAAVDAAVYGIFFNAGQCCNSGSRILVQDAVAD 306 Query: 311 KFNERMVAWAKNIKVSDPLEEGCRLGPVVSEGQYEKIKKFISNAKSQGATILTGGVRPAH 370 KF E ++A ++ ++V DP +E ++G + +E Q I + A+ GAT+ GG R Sbjct: 307 KFAEAVIARSRQVRVGDPFDERTQVGAITTERQLHTILAHVEGARQAGATVALGGAR--- 363 Query: 371 LEK-GFFIEPTIITDITTSMEIWREEVFGPVLCVKEFSTEDEAIELANDTQYGLAGAVIS 429 L++ G ++EPT++T +T M I R+EVFGPVL + F T DEA++LAN T YGL+ AV S Sbjct: 364 LDRPGLYMEPTVLTGVTRDMAIARQEVFGPVLSMLRFGTLDEAVDLANSTLYGLSAAVWS 423 Query: 430 GDRERCQRLSEEIDAGCIWVNCSQPCFCQAPWGGNKRSGFGRELGEGGIDNYLSVKQVTE 489 D C + I+AG +WVN + P+GG + SG GRELG ++Y K V Sbjct: 424 QDINTCITAARRIEAGTVWVNTFLEGHAELPFGGYRESGIGRELGRFAAEDYTETKTVHL 483 Query: 490 YISDEPWGWYQSPS 503 ++ WY P+ Sbjct: 484 HLGART-DWYLPPA 496 Lambda K H 0.318 0.135 0.422 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: 600 Number of extensions: 22 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: 505 Length of database: 496 Length adjustment: 34 Effective length of query: 471 Effective length of database: 462 Effective search space: 217602 Effective search space used: 217602 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