Align Alpha-ketoglutaric semialdehyde dehydrogenase 1; alphaKGSA dehydrogenase 1; 2,5-dioxovalerate dehydrogenase 1; 2-oxoglutarate semialdehyde dehydrogenase 1; KGSADH-I; Succinate-semialdehyde dehydrogenase [NAD(+)]; SSDH; EC 1.2.1.26; EC 1.2.1.24 (characterized)
to candidate WP_053938622.1 WG78_RS14820 aldehyde dehydrogenase
Query= SwissProt::Q1JUP4 (481 letters) >NCBI__GCF_001294205.1:WP_053938622.1 Length = 498 Score = 280 bits (716), Expect = 8e-80 Identities = 173/476 (36%), Positives = 260/476 (54%), Gaps = 13/476 (2%) Query: 12 LIDGEWVDAASGKTIDVVNPATGKPIGRVAHAGIADLDRALAAAQSGFEA--WRKVPAHE 69 LIDGE+ AASGKT D ++P GK + +VA G AD+D +A A+ FE+ W + + Sbjct: 24 LIDGEFTAAASGKTFDCISPIDGKLLTQVAWCGEADVDHTVAIARQRFESGVWSDLNPRQ 83 Query: 70 RAATMRKAAALVRERADAIAQLMTQEQGKPLTEAR-VEVLSAADIIEWFADEGRRVYGRI 128 R M + A L+R AD IA L T + GKP+ + V+V AA ++W+A+ + G + Sbjct: 84 RKEIMLRWAELIRVHADEIALLETLDAGKPIGDTTTVDVPGAAYTVQWYAEAIDKAGGEV 143 Query: 129 VPPRNLGAQQTVVKEPVGPVAAFTPWNFPVNQVVRKLSAALATGCSFLVKAPEETPASPA 188 P + V ++P+G VAA PWNFP+ K ALA G S ++K E++P S Sbjct: 144 APV-DYHLVGLVTRQPIGVVAAVVPWNFPILMAAWKFGPALAAGNSVILKPSEKSPLSAL 202 Query: 189 ALLRAFVDAGVPAGVIGLV--YGDPAEISSYLIPHPVIRKVTFTGSTPVGKQLASLAGL- 245 + + ++AG+P GV ++ +GD ++ L H + + FTGST VGKQL +G Sbjct: 203 RVAQLALEAGIPPGVFNVLPGFGDTGKL---LALHMDVDCLAFTGSTFVGKQLMQHSGQS 259 Query: 246 HMKRATMELGGHAPVIVAEDA-DVALAVKAAGGAKFRNAGQVCISPTRFLVHNSIRDEFT 304 ++KR +ELGG +P I+ D D+A A ++A GA F N G++C + +R LVH S++DEF Sbjct: 260 NLKRVWLELGGKSPNIIMPDCPDMARAARSAAGAIFYNMGEMCTAGSRLLVHRSVKDEFI 319 Query: 305 RALVKHAEGLKVGNGLEEGTTLGALANPRRLTAMASVIDNARKVGASIETGGERIGSEGN 364 +AL+ A K GN L+ T++GA+ + +L + S I+ + + GG + G Sbjct: 320 KALIAEAAAYKPGNPLDPATSMGAIVDHIQLERVMSYIETGKGEATLLLGGGRTLTETGG 379 Query: 365 FF-APTVIANVPLDADVFNNEPFGPVAAIRGFDKLEEAIAEANRLPFGLAGYAFTRSFAN 423 ++ PT+ +A V E FGPV ++ FD L+EAIA AN +GLA +T Sbjct: 380 YYIEPTIFDVASQEARVAAEEIFGPVLSVITFDTLDEAIALANASEYGLAAAIWTADLTT 439 Query: 424 VHLLTQRLEVGMLWIN-QPATPWPEMPFGGVKDSGYGSEGGPEALEPYLVTKSVTV 478 H +RL G +W+N PFGG K SG G + AL+ Y KS + Sbjct: 440 AHEAARRLRAGTVWVNCYDEGGDMNFPFGGFKQSGNGRDKSLHALDKYTELKSTLI 495 Lambda K H 0.318 0.134 0.393 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: 590 Number of extensions: 39 Number of successful extensions: 8 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: 481 Length of database: 498 Length adjustment: 34 Effective length of query: 447 Effective length of database: 464 Effective search space: 207408 Effective search space used: 207408 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