Align aminobutyraldehyde dehydrogenase (EC 1.2.1.19) (characterized)
to candidate WP_108359063.1 B9Z44_RS11550 aldehyde dehydrogenase family protein
Query= BRENDA::Q93YB2 (503 letters) >NCBI__GCF_003063475.1:WP_108359063.1 Length = 477 Score = 326 bits (836), Expect = 1e-93 Identities = 199/484 (41%), Positives = 278/484 (57%), Gaps = 15/484 (3%) Query: 9 QLFINGDWKAPVLNKRIPVINPATQNIIGDIPAATKEDVDVAVAAAKTALTRNKGADWAT 68 ++FING + K + V++P +IP K DVD+AV AA AL + W Sbjct: 3 KMFINGQSVNALSGKVLDVLSPVDGQKFEEIPRGEKADVDLAVNAANKALD----SAWGK 58 Query: 69 ASGAVRARYLRAIAAKVTEKKPELAKLESIDCGKPLDEAAWDIDDVAGCFEYYADLAEKL 128 + R R L + KV E ELA LE+ D GKP+ A DI +A FE+Y A+K+ Sbjct: 59 MTALERGRLLMKLGEKVLEHHAELAALEARDTGKPMTTAKTDITVLARYFEFYGSGADKI 118 Query: 129 DARQKAPVSLP-MDTFKSHVLREPIGVVGLITPWNYPMLMATWKVAPALAAGCAAILKPS 187 + LP +D + +VLREP+GV I PWNYP M +APALA G A ++KP+ Sbjct: 119 HG-----LVLPFLDGYTVNVLREPLGVTAHIIPWNYPAQMLGRSIAPALAMGNAVVVKPA 173 Query: 188 ELASLTCLELGEICKEVGLPPGVLNILTGLGPEAGAPLATHPDVDKVAFTGSSATGSKIM 247 E A LT + + E+ ++VG P G +NI+TGLG EAGA L+ HP ++ ++FTGS+ G I Sbjct: 174 EDACLTPIRVAELARDVGFPDGAINIVTGLGEEAGAALSEHPGINFISFTGSNEVGVLIQ 233 Query: 248 TAAAQLVKPVSLELGGKSPLVVFEDVDLDKAAEWAIFGCFWTNGQICSATSRLILHESIA 307 AAA+ V LELGGKSP VVF D DLD+A G GQ C+A SRLI+ +SI Sbjct: 234 KAAAKNVIKCVLELGGKSPHVVFGDADLDRAVPIITRGIIANTGQTCTAGSRLIVQKSIY 293 Query: 308 TEFLNRIVKWIKNIKISDP-LEEGCRLGPVVSEGQYEKILKFVSNAKSEGATILTGG-SR 365 E + R+ K IK+ P ++ C GPVV+ Q +++ F+ A+ G ++ G Sbjct: 294 PEIMERLAKQFAQIKVGTPDMDLDC--GPVVNIAQRDRVAYFLKEAEKSGIEMVAQGVLS 351 Query: 366 PEHLKKGFFIEPTIITDVTTNMQIWREEVFGPVLCVKTFSTEEEAIDLANDTVYGLGAAV 425 P K+G+++ PT++ +V N + +EE+FGPVL +F TE E I LAN T +GL AAV Sbjct: 352 PGLPKEGYYVTPTLLGNVPANHRCAQEEIFGPVLAAMSFDTEAEGIALANGTDFGLMAAV 411 Query: 426 ISNDLERCERVTKAFKAGIVWVNC-SQPCFTQAPWGGVKRSGFGRELGEWGLDNYLSVKQ 484 + + R +RV+KA KAG V++N + P+GGVKRSG GRE G L+ + K Sbjct: 412 WTENGGRQQRVSKAIKAGQVYINAFGAGGGVELPFGGVKRSGHGREKGFLALEEVSTTKT 471 Query: 485 VTQY 488 V Y Sbjct: 472 VINY 475 Lambda K H 0.318 0.135 0.416 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: 575 Number of extensions: 19 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: 503 Length of database: 477 Length adjustment: 34 Effective length of query: 469 Effective length of database: 443 Effective search space: 207767 Effective search space used: 207767 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