Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_067907935.1 AQZ52_RS07360 aldehyde dehydrogenase family protein
Query= BRENDA::C0P9J6 (505 letters) >NCBI__GCF_001519075.1:WP_067907935.1 Length = 474 Score = 322 bits (826), Expect = 1e-92 Identities = 190/490 (38%), Positives = 287/490 (58%), Gaps = 30/490 (6%) Query: 6 MVPLRQLFVDGEWRPPAQGRRLPVVNPTTEAHIGEIPAGTAEDVDAAVAAARAALKRNRG 65 M L +DGE A+ L V+NP E IG++PA AE++D AVAAAR A K Sbjct: 1 MTKLYPNLIDGELVTTAKA--LDVLNPANEQVIGQVPACGAEELDRAVAAARRAFKT--- 55 Query: 66 RDWARAPGAVRAKYLRAIAAKVIERKPELAKLEALDCGKPYDEAAWDMDDVAGCFEYFAD 125 W++ P R +RA+AA + EL +L + GKP+ +A ++ + GC Sbjct: 56 --WSKTPVDDRRAVIRAMAAAIDANFDELFRLLTAEQGKPHQQAQFE---IGGCSAMMNA 110 Query: 126 QA-----EALDKRQNSPVSLPMETFKCHLRREPIGVVGLITPWNYPLLMATWKIAPALAA 180 Q+ E +++ + +S RR P+GVVG I PWN+P+LMA KIAPA+ + Sbjct: 111 QSTLTLEETINEDSDERLS--------RTRRVPVGVVGGIVPWNFPVLMAVQKIAPAILS 162 Query: 181 GCTAVLKPSELASVTCLELADICKEVGLPSGVLNIVTGLGPDAGAPL-SAHPDVDKVAFT 239 GCT VLKPS +T L A++ K++ +P+GV+NI+TG DA P+ +AHPD+DK+ FT Sbjct: 163 GCTIVLKPSPFTPLTTLRFAELIKDI-VPAGVVNIITG--EDALGPMITAHPDIDKITFT 219 Query: 240 GSFETGKKIMASAAPMVKPVTLELGGKSPIVVFDDVDIDKAVEWTLFGCFWTNGQICSAT 299 GS TGKKIM A+ +K +TLELGG +V D D+ K E + F GQIC A Sbjct: 220 GSTATGKKIMEGASKDLKRITLELGGNDASIVLPDADVAKVAEQLFWSSFTNAGQICVAA 279 Query: 300 SRLLIHTKIAKKFNERMVAWAKNIKVSDPLEEGCRLGPVVSEGQYEKIKKFISNAKSQGA 359 R+ IH I + + + +AKN+KV D E+G +GP+ ++ Q++++ + I +AK+ G Sbjct: 280 KRIYIHEDIYDELSAAIAEYAKNVKVGDGSEQGTGVGPIQNKKQFDRVCELIEDAKTNGY 339 Query: 360 TILTGG-VRPAHLEKGFFIEPTIITDITTSMEIWREEVFGPVLCVKEFSTEDEAIELAND 418 L GG V P+ G+++ TI+ + I EE FGPV+ + +FS++DE I AN+ Sbjct: 340 KFLVGGDVDPS--GSGYYVPITILDNPPEDARIVAEEQFGPVMPLMKFSSDDEVIARANN 397 Query: 419 TQYGLAGAVISGDRERCQRLSEEIDAGCIWVNCSQPCFCQAPWGGNKRSGFGRELGEGGI 478 ++YGLAGAV + D ER +++E+++ G +W+N AP+GG+K+SGFG E G G+ Sbjct: 398 SEYGLAGAVWTKDTERGVKIAEQLETGTVWINEFLHLSPFAPFGGHKQSGFGAEYGIEGL 457 Query: 479 DNYLSVKQVT 488 + + +T Sbjct: 458 KEFTYSQVIT 467 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: 618 Number of extensions: 25 Number of successful extensions: 7 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: 474 Length adjustment: 34 Effective length of query: 471 Effective length of database: 440 Effective search space: 207240 Effective search space used: 207240 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