Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_012968462.1 KVAR_RS15340 succinylglutamate-semialdehyde dehydrogenase
Query= BRENDA::P76217 (492 letters) >NCBI__GCF_000025465.1:WP_012968462.1 Length = 492 Score = 784 bits (2025), Expect = 0.0 Identities = 380/486 (78%), Positives = 427/486 (87%) Query: 1 MTLWINGDWITGQGASRVKRNPVSGEVLWQGNDADAAQVEQACRAARAAFPRWARLSFAE 60 M+LWING+W G+G K++PV+ +V+WQG ADA QV +A AAR AFP WARL FA Sbjct: 1 MSLWINGEWRPGRGPGFSKQDPVNLKVVWQGEAADAGQVAEAVAAARQAFPAWARLPFAA 60 Query: 61 RHAVVERFAALLESNKAELTAIIARETGKPRWEAATEVTAMINKIAISIKAYHVRTGEQR 120 R A+VE+FAALLE++KAELTA+I ETGKPRWEAA EVTAMINK+AIS+KAYHVRTGEQ Sbjct: 61 RQAIVEKFAALLEASKAELTAMIGAETGKPRWEAAGEVTAMINKVAISVKAYHVRTGEQH 120 Query: 121 SEMPDGAASLRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNTIIFKPSELTPWSGEAV 180 S++PDGAA+LRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNT++FKPSELTP SGEAV Sbjct: 121 SDLPDGAATLRHRPHGVLAVFGPYNFPGHLPNGHIVPALLAGNTVVFKPSELTPCSGEAV 180 Query: 181 MRLWQQAGLPPGVLNLVQGGRETGQALSALEDLDGLLFTGSANTGYQLHRQLSGQPEKIL 240 ++LWQQAGLP GVLNLVQGGRETG+ALS D+DGLLFTGS+ TG+ LHRQL+GQP+KIL Sbjct: 181 VKLWQQAGLPAGVLNLVQGGRETGEALSGQADIDGLLFTGSSTTGFHLHRQLAGQPQKIL 240 Query: 241 ALEMGGNNPLIIDEVADIDAAVHLTIQSAFVTAGQRCTCARRLLLKSGAQGDAFLARLVA 300 ALEMGGNNPLI+D+ D+DAAVHLTIQSAF+TAGQRCTCARRLL++ G GDAFL+RLV Sbjct: 241 ALEMGGNNPLIVDDPRDVDAAVHLTIQSAFITAGQRCTCARRLLVRRGEAGDAFLSRLVT 300 Query: 301 VSQRLTPGNWDDEPQPFIGGLISEQAAQQVVTAWQQLEAMGGRPLLAPRLLQAGTSLLTP 360 VSQRL P WD EPQPF+GGLISE AAQ+V AW Q A G LL PRLLQAGTSLLTP Sbjct: 301 VSQRLIPAAWDAEPQPFLGGLISEPAAQKVHQAWLQRVAAGAVTLLEPRLLQAGTSLLTP 360 Query: 361 GIIEMTGVAGVPDEEVFGPLLRVWRYDTFDEAIRMANNTRFGLSCGLVSPEREKFDQLLL 420 GI++M+ VA V DEEVFGPLL VWRYDTF+EAI +AN TRFGLSCGL+SPEREKFD+LLL Sbjct: 361 GIVDMSDVANVEDEEVFGPLLGVWRYDTFEEAIALANATRFGLSCGLISPEREKFDRLLL 420 Query: 421 EARAGIVNWNKPLTGAASTAPFGGIGASGNHRPSAWYAADYCAWPMASLESDSLTLPATL 480 EARAGIVNWNKPLTGAASTAPFGG GASGNHRP AWYAADYCAWPMASLES +LTLPA+L Sbjct: 421 EARAGIVNWNKPLTGAASTAPFGGTGASGNHRPGAWYAADYCAWPMASLESPTLTLPASL 480 Query: 481 NPGLDF 486 NPGLDF Sbjct: 481 NPGLDF 486 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: 956 Number of extensions: 36 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: 492 Length adjustment: 34 Effective length of query: 458 Effective length of database: 458 Effective search space: 209764 Effective search space used: 209764 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 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