Align Aldehyde dehydrogenase family 2 member B4, mitochondrial; ALDH2a; EC 1.2.1.3 (characterized)
to candidate WP_068110307.1 I601_RS12775 gamma-aminobutyraldehyde dehydrogenase
Query= SwissProt::Q9SU63 (538 letters) >NCBI__GCF_001653335.1:WP_068110307.1 Length = 479 Score = 343 bits (879), Expect = 1e-98 Identities = 202/480 (42%), Positives = 280/480 (58%), Gaps = 12/480 (2%) Query: 59 QLLINGNFVDSASGKTFPTLDPRTGEVIAHVAEGDAEDINRAVKAARTAFDEGPWPKMSA 118 Q +ING VDSASG T+ +DP TGEV A AED++RA AA AF+ W + Sbjct: 7 QNVINGRLVDSASGATYDVIDPTTGEVYAQAPASGAEDVDRAYAAADAAFEGWGWGS-TP 65 Query: 119 YERSRVLLRFADLVEKHSEELASLETWDNGKPYQQSLTAEIPMFARLFRYYAGWADKIHG 178 +R+R LLR AD +E EE+ ++E D GKP ++ E+P + FR++AG A + G Sbjct: 66 QDRARALLRIADAIEDRVEEINAVECRDTGKPLGLTMAEEMPYASDHFRFFAGAARLLEG 125 Query: 179 LTIPADGNYQV-HTL---HEPIGVAGQIIPWNFPLLMFAWKVGPALACGNTIVLKTAEQT 234 + G Y HT EPIGV GQ+ PWN+PLLM WK+ PALA GNT+VLK ++ T Sbjct: 126 RSA---GEYMAEHTSWVRREPIGVVGQVTPWNYPLLMMIWKIAPALAAGNTVVLKPSDTT 182 Query: 235 PLTAFYAGKLFLEAGLPPGVLNIVSGFGATAGAALASHMDVDKLAFTGSTDTGKVILGLA 294 P ++ ++ E LPPGVLN+V G T G AL +H +A TGS G + G A Sbjct: 183 PASSTLLAQICQEF-LPPGVLNVVCGDRDT-GRALVAHPTPQMVAITGSVRAGMEVAGTA 240 Query: 295 ANSNLKPVTLELGGKSPFIVFEDADIDKAVELAHFALFFNQGQCCCAGSRTFVHEKVYDE 354 A +++K V LELGGK+P IVF+DADI KA E A FN GQ C A +R V V+DE Sbjct: 241 A-ADVKKVHLELGGKAPVIVFDDADIAKAAEGIAGAGLFNAGQDCTAATRVLVAPGVHDE 299 Query: 355 FVEKSKARALKRVVGDPFRKGIEQGPQIDLKQFEKVMKYIKSGIESNATLECGGDQIGDK 414 FV A G P +G+ GP + Q E V + + +A ++ GG + G Sbjct: 300 FVAALAEAARGMPTGRPDVEGVYYGPLNNAHQLEHVSGMVDR-LPDHARIDTGGTRQGSA 358 Query: 415 GYFIQPTVFSNVKDDMLIAQDEIFGPVQSILKFSDVDEVIKRANETKYGLAAGVFTKNLD 474 GYF +PTV S ++ D Q EIFGPV ++ +F+D E ++ AN+ +YGLA+ V+T + Sbjct: 359 GYFYEPTVLSGLRQDDEQVQTEIFGPVMTVQRFTDEAEALRWANDVQYGLASSVWTSDHA 418 Query: 475 TANRVSRALKAGTVWVNCFDVFDAAIPFGGYKMSGNGREKGIYSLNNYLQIKAVVTALNK 534 A RVSR L G VW+N F + +P GG+K SG G++ +Y L +Y +IK V++ + + Sbjct: 419 RAMRVSRRLDFGAVWINTHIPFVSEMPHGGFKHSGYGKDLSMYGLEDYTRIKHVMSYIGQ 478 Lambda K H 0.319 0.136 0.404 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: 641 Number of extensions: 28 Number of successful extensions: 6 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: 538 Length of database: 479 Length adjustment: 34 Effective length of query: 504 Effective length of database: 445 Effective search space: 224280 Effective search space used: 224280 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.4 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 41 (21.8 bits) S2: 52 (24.6 bits)
This GapMind analysis is from Apr 09 2024. 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