Align Putative aldehyde dehydrogenase AldY; EC 1.2.1.3 (characterized)
to candidate WP_010531996.1 ON01_RS15505 aldehyde dehydrogenase family protein
Query= SwissProt::P94358 (485 letters) >NCBI__GCF_000224785.1:WP_010531996.1 Length = 485 Score = 444 bits (1143), Expect = e-129 Identities = 223/484 (46%), Positives = 312/484 (64%), Gaps = 1/484 (0%) Query: 2 SFETLNKSFINGKWTGGESGRTEDILNPYDQSVITTASLATGKQLEDAFDIAQKAQKEWA 61 + +LNK +I G W G S T NPY+ IT +AT + +++A+ AQ A EW Sbjct: 3 NINSLNKQYIAGTWRDGRSNNTLTDKNPYNGERITQFKMATTEDVDEAYKSAQDAMDEWN 62 Query: 62 KSTTEDRKAVLQKARGYLHENRDDIIMMIARETGGTIIKSTIELEQTIAILDEAMTYTGE 121 + ++ L+ A Y+ E+ +DI +I E GGT +K+ E+ ++ EA T+ Sbjct: 63 QINPYKQRDTLENAVTYIEEHEEDITDIIIDELGGTRLKAAFEIGLVKDMIKEAATFPLN 122 Query: 122 LGGVKEVPSDIEGKTNKIYRLPLGVISSISPFNFPMNLSMRSIAPAIALGNSVVHKPDIQ 181 G K +PS GK N++YR+P GV+ ISPFNFP LS++S+APAI GN VV K + Sbjct: 123 KEG-KILPSVENGKENRLYRMPAGVVGVISPFNFPFFLSIKSVAPAIGAGNGVVLKAHEE 181 Query: 182 TAISGGTIIAKAFEHAGLPAGVLNVMLTDVKEIGDGMLTNPIPRLISFTGSTAVGRHIGE 241 T I GGT+IAK FE AG+P G+ NV++TD+ EIGD + +PIPR+ISFTGST VG HIG+ Sbjct: 182 TPIMGGTLIAKIFEEAGVPKGLFNVVVTDINEIGDTFVEHPIPRIISFTGSTKVGSHIGQ 241 Query: 242 IAGRAFKRMALELGGNNPFAVLSDADVDRAVDAAIFGKFIHQGQICMIINRIIVHQDVYD 301 +A + FK+ LELGGN+ F +L DADVD AV+AA F +F HQGQICM NRIIVHQ +YD Sbjct: 242 LAVKHFKKPILELGGNSAFIILDDADVDYAVEAAAFSRFTHQGQICMSANRIIVHQSIYD 301 Query: 302 EFVEKFTARVKQLPYGDQTDPKTVVGPLINERQIEKALEIIEQAKTDGIELAVEGKRVGN 361 EF+ K+ ++ L GD DP TV+GP++NE E II++ G ++G GN Sbjct: 302 EFITKYKEKIASLKTGDPRDPDTVIGPVVNEGAAENLKAIIDKGIEQGATPILKGDISGN 361 Query: 362 VLTPYVFVGADNNSKIAQTELFAPIATIIKAGSDQEAIDMANDTEYGLSSAVFTSDLEKG 421 ++ P + ++ +AQ ELF P+ +++ +D+EAI +ANDTE+GLS AV TSD E+G Sbjct: 362 MVEPTILTDVTSDMAVAQEELFGPVVSVMTFETDEEAIKIANDTEFGLSGAVHTSDGERG 421 Query: 422 EKFALQIDSGMTHVNDQSVNDSPNIAFGGNKASGVGRFGNPWVVEEFTVTKWISIQKQYR 481 + A ++ +GM HVND ++ND P +AFGG K SG+GR W +EEFT KWIS+ Q R Sbjct: 422 VQLAKKVHTGMVHVNDITINDEPIVAFGGEKKSGMGRLNGDWSLEEFTTLKWISVHYQQR 481 Query: 482 KYPF 485 + P+ Sbjct: 482 EIPY 485 Lambda K H 0.316 0.134 0.380 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: 698 Number of extensions: 29 Number of successful extensions: 2 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: 485 Length of database: 485 Length adjustment: 34 Effective length of query: 451 Effective length of database: 451 Effective search space: 203401 Effective search space used: 203401 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 (21.6 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