Align 2-aminomuconate 6-semialdehyde dehydrogenase (EC 1.2.1.32) (characterized)
to candidate WP_090219935.1 CV091_RS15630 NAD-dependent succinate-semialdehyde dehydrogenase
Query= metacyc::MONOMER-13361 (500 letters) >NCBI__GCF_002796795.1:WP_090219935.1 Length = 490 Score = 290 bits (741), Expect = 1e-82 Identities = 162/478 (33%), Positives = 259/478 (54%), Gaps = 10/478 (2%) Query: 23 YIDGNFVTSASSFANINPVNGKLISDVFEADAKQVNEAVVAAQNALKGPWGKLSVQDRAA 82 Y+ G F+++ ++F INP G +++ V + V A+ +A+ A K W + ++R+A Sbjct: 23 YVGGEFISTQNTFDVINPARGDVVAQVTDLTRADVAAAIASAETAQK-EWATWTGKERSA 81 Query: 83 LIHKIADGIQARFEEFVAAEVADTGRPVHQARTLDIPRAIANFRTFADLAKTSHTDLFEM 142 ++ + I E+ A+ G+P+ ++R +I + FA+ AK + + Sbjct: 82 VLRNWFNLIMENQEDLALILTAEMGKPLTESRG-EIAYGASFLEYFAEEAKRIYGETIPG 140 Query: 143 STSDGSGALNYTVRKPLGVIGVISPWNLPLLLFTWKVAPALACGNTVVAKPSEESPSSAT 202 D + +++P+GV I+PWN P + T K PALA G VA+P+E +P SAT Sbjct: 141 HQRDKRITV---IKQPIGVAASITPWNFPNAMITRKAGPALAAGCAFVARPAELTPLSAT 197 Query: 203 LLAEVMHDAGVPPGVFNLIHGFGKDSAGEFLTQHPGISALTFTGESKTGSTIMKAVADGV 262 LA + AG+P GVF+++ G+ ++P + +TFTG + G +++ A V Sbjct: 198 ALAVLAERAGLPSGVFSVVTTSDASETGKEFCENPTVRKITFTGSTAVGRILLQQAAGQV 257 Query: 263 KEVSFELGGKNAAVVFADADLDAAIEGVLRSSFTNSGQVCLCSERVYVHRSIFDEFVSGL 322 K+ S ELGG +VF DADLDAA+EG + F N+GQ C+C+ R+YV ++D F L Sbjct: 258 KKCSMELGGNAPFIVFDDADLDAAVEGAIMCKFRNNGQTCVCANRIYVQAGVYDAFAEKL 317 Query: 323 KVEAERLVVGYPDQDGVNMGPLISHGHRDKVLSYYRLAVDEGATVVTGGGVPKFNDERDQ 382 K + VG +DG GPLI+ +KV S+ A +G ++ GG N Sbjct: 318 KARVADMKVGDGFEDGTVFGPLINAKAMEKVKSHLTDATAKGGEIILGG-----NPSELG 372 Query: 383 GAYVQPTIWTGLSDKARCVTEEIFGPVCHISPFDDEDEVINRVNDSNYGLACAIWTTNLS 442 G + +PTI TG + TEE FGP+ + F+DEDEVI ND+ +GLA + +LS Sbjct: 373 GTFFEPTIVTGATTDMAFSTEETFGPLAPLFKFEDEDEVIALANDTIFGLASYFYAKDLS 432 Query: 443 RAHRVSRQIHVGLVWVNTWYLRDLRTPFGGVKLSGLGREGGRFSMDFYSDIANICIKI 500 R ++V+ + G+V VNT + PFGG+K SGLGREG ++ + ++ IC+ + Sbjct: 433 RVYKVAEALEYGIVGVNTGLISTEVAPFGGIKQSGLGREGSHHGIEEFLEMKYICMSV 490 Lambda K H 0.318 0.135 0.405 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: 559 Number of extensions: 20 Number of successful extensions: 3 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: 500 Length of database: 490 Length adjustment: 34 Effective length of query: 466 Effective length of database: 456 Effective search space: 212496 Effective search space used: 212496 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