Align aldehyde dehydrogenase (NAD+) (EC 1.2.1.3) (characterized)
to candidate WP_092992765.1 BLP65_RS03760 NAD-dependent succinate-semialdehyde dehydrogenase
Query= BRENDA::A6T8Z5 (462 letters) >NCBI__GCF_900102855.1:WP_092992765.1 Length = 454 Score = 439 bits (1128), Expect = e-127 Identities = 226/448 (50%), Positives = 297/448 (66%) Query: 11 SVNPTTGEVVSSLPWASEREVDAAITLAAAGYRQWRQTPLADRADALRRIGAALRARGEE 70 SVNP TG+ ++ + ++D+ + A W TP+ RA +RR+G LR + E+ Sbjct: 5 SVNPATGKRLAEFAYWDAEKLDSVLQQVADATPGWAATPVKGRALLIRRLGETLREQREQ 64 Query: 71 VAQMITLEMGKPIAQARGEVAKSANLCDWYAEHGPAMLATEATLVENNQAVIEYRPLGAI 130 +A +IT EMGK I +ARGE+ K A LCD+YAE GP LA E + ++++ Y+PLG + Sbjct: 65 LAAIITREMGKLIGEARGEIDKCAWLCDYYAESGPGFLADETLESDATRSLVAYQPLGTV 124 Query: 131 LAVMPWNFPVWQVMRGAVPILLAGNSYLLKHAPNVMGSARLLGEIFAAAGLPDGVFGWVN 190 LAVMPWNFP WQV R AVP LLAGN+ LLKHA NV A+ + +F AG P+GVF + Sbjct: 125 LAVMPWNFPFWQVFRFAVPGLLAGNTGLLKHASNVPQCAKSIENLFIEAGFPEGVFRSLM 184 Query: 191 ATNDGVSQIINDDRIAAVTVTGSVRAGKAIGAQAGAALKKCVLELGGSDPFIVLNDADLD 250 V +I D R+ AVT+TGS AG+ + A AGA LKK VLELGGSDPF+VL DADLD Sbjct: 185 IGASQVEGVIADLRVQAVTLTGSDSAGRKVAAAAGAHLKKSVLELGGSDPFVVLEDADLD 244 Query: 251 EAVKAAVTGRYQNSGQVCAASKRFILEAGIAEAFTRKFVDAVAALKMGDPRDEQNYVGPM 310 A +AAVT R+ N GQ C A+KRFIL +AE F +F V AL GDP EQ + PM Sbjct: 245 GAARAAVTSRFLNGGQSCIAAKRFILVDAVAENFLARFKAGVEALVPGDPMTEQATLPPM 304 Query: 311 ARFDLRDELHQQVTATLDEGATLLLGAEKIEGAGNYYAPTVLGNVTAGMTGFRQELFGPV 370 AR DLRD+LH+QV A++++GA + G +EG G +YA ++L V GM + +ELFGPV Sbjct: 305 ARTDLRDDLHRQVIASIEQGAEAVTGCRPLEGEGAFYAASILDRVEPGMPAYSEELFGPV 364 Query: 371 ATLTTARDADHALALANDSEFGLSATVYTTDEAQAQRFARELECGGVFLNGYCASDARVA 430 A + ARD AL +ANDS FGL +V++ D + + FAR LECG F+NG SD R+ Sbjct: 365 AIVLRARDEADALRIANDSPFGLGGSVWSADTQRGEAFARALECGCAFVNGMVKSDPRLP 424 Query: 431 FGGVKKSGFGRELSHFGLHEFCNAQTVW 458 FGG+K+SG+GRELSH G+ EF NA+T+W Sbjct: 425 FGGIKQSGYGRELSHHGIREFVNAKTIW 452 Lambda K H 0.319 0.133 0.392 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: 500 Number of extensions: 14 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: 462 Length of database: 454 Length adjustment: 33 Effective length of query: 429 Effective length of database: 421 Effective search space: 180609 Effective search space used: 180609 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: 51 (24.3 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