Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_012278669.1 SHAL_RS18645 succinylglutamate-semialdehyde dehydrogenase
Query= BRENDA::P76217 (492 letters) >NCBI__GCF_000019185.1:WP_012278669.1 Length = 486 Score = 585 bits (1507), Expect = e-171 Identities = 286/484 (59%), Positives = 363/484 (75%) Query: 1 MTLWINGDWITGQGASRVKRNPVSGEVLWQGNDADAAQVEQACRAARAAFPRWARLSFAE 60 MT +I G W+ G G NP + EV+W A QV QA AAR A W L F Sbjct: 1 MTQFIEGKWVAGLGHEVTSINPANQEVIWNSKTATPEQVSQAVDAARNAQFDWFMLGFEG 60 Query: 61 RHAVVERFAALLESNKAELTAIIARETGKPRWEAATEVTAMINKIAISIKAYHVRTGEQR 120 R A+VE + LE+NKAE+ +IA+ETGKP+WE ATE AMI KI +S+ AYH RTG Sbjct: 61 RLAIVEAYRDQLEANKAEMAEVIAQETGKPQWETATEAGAMIGKIGLSVAAYHKRTGTSE 120 Query: 121 SEMPDGAASLRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNTIIFKPSELTPWSGEAV 180 SE P G A LRH+PHGV+AVFGPYNFPGHLPNGHIVPALLAGNT++FKPSELTP E + Sbjct: 121 SETPAGRAVLRHKPHGVVAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSELTPKVAELM 180 Query: 181 MRLWQQAGLPPGVLNLVQGGRETGQALSALEDLDGLLFTGSANTGYQLHRQLSGQPEKIL 240 ++LW++AGLP GV+NLVQG ETG+AL+A +DGL FTGS+ TG+ LH+Q +G P KIL Sbjct: 181 LKLWEKAGLPAGVINLVQGEVETGKALAAHPQIDGLFFTGSSRTGHILHQQYAGDPGKIL 240 Query: 241 ALEMGGNNPLIIDEVADIDAAVHLTIQSAFVTAGQRCTCARRLLLKSGAQGDAFLARLVA 300 ALEMGGNNPLII +VAD AAVH IQSA+++AGQRCTCARRL ++ GA GDA L +LVA Sbjct: 241 ALEMGGNNPLIIKDVADTKAAVHDIIQSAYISAGQRCTCARRLYVEKGATGDALLEQLVA 300 Query: 301 VSQRLTPGNWDDEPQPFIGGLISEQAAQQVVTAWQQLEAMGGRPLLAPRLLQAGTSLLTP 360 +++ G W+ +PQPF+G +ISE AA+ +V A + L +G L+ ++AGT L++P Sbjct: 301 AIKQIKVGPWNAQPQPFMGSMISETAAKGMVEAQRNLLNLGANSLVELTHIEAGTGLVSP 360 Query: 361 GIIEMTGVAGVPDEEVFGPLLRVWRYDTFDEAIRMANNTRFGLSCGLVSPEREKFDQLLL 420 G+I++TGV +PDEE FGPLL+V RY FDEAI++AN TR+GLS G+++ RE +D L Sbjct: 361 GLIDVTGVIELPDEEYFGPLLQVVRYSDFDEAIKLANTTRYGLSAGILADSREDYDYFLA 420 Query: 421 EARAGIVNWNKPLTGAASTAPFGGIGASGNHRPSAWYAADYCAWPMASLESDSLTLPATL 480 RAGIVNWNK +TGA+ APFGG+GASGNHR SA+YAADYCA+P+AS+E+D+++LPATL Sbjct: 421 RIRAGIVNWNKQITGASGAAPFGGVGASGNHRASAFYAADYCAYPVASVEADAVSLPATL 480 Query: 481 NPGL 484 +PGL Sbjct: 481 SPGL 484 Lambda K H 0.318 0.134 0.412 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: 774 Number of extensions: 30 Number of successful extensions: 1 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: 492 Length of database: 486 Length adjustment: 34 Effective length of query: 458 Effective length of database: 452 Effective search space: 207016 Effective search space used: 207016 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 (21.7 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