Align Putative aldehyde dehydrogenase SSP0762; EC 1.2.1.3 (uncharacterized)
to candidate WP_008343682.1 BA79_RS18445 aldehyde dehydrogenase family protein
Query= curated2:Q49Z69 (475 letters) >NCBI__GCF_000691145.1:WP_008343682.1 Length = 475 Score = 592 bits (1527), Expect = e-174 Identities = 293/472 (62%), Positives = 360/472 (76%), Gaps = 1/472 (0%) Query: 1 MRNFTKQYINGEWVESTSGETLEVINPATEEVAGTIAKGNKEDVEKAVEAADNVYLEFRH 60 MRN K +INGEWV ST ET EVINPATEEV GTI+ G KED++KAV+AA + F Sbjct: 1 MRNQEKHFINGEWVASTGNETTEVINPATEEVIGTISLGTKEDLDKAVKAARAAFPSFSK 60 Query: 61 TSVKERQDLLDQIVQEYKNRKEDLIQAITDELGAPLSVAENVHYQMGLDHFEAARDALND 120 TS ER ++L+ IV+ Y+ RK++L++ +T ELGAPL V+E VHY+MG +HF A +AL Sbjct: 61 TSRNERVEMLENIVRGYEKRKDELVEVMTKELGAPLKVSEEVHYKMGYEHFSKAAEALKS 120 Query: 121 FQFEERRGDDLVVKEAIGVSGLITPWNFPTNQTSLKLAAAFAAGSPVVFKPSEETPFAAI 180 + F E RG ++KEAIGVSGLITPWNFPTNQTSLK+A A AAGSPVV KP+E TPFAA+ Sbjct: 121 YTFTEDRGGHTIIKEAIGVSGLITPWNFPTNQTSLKIAGAIAAGSPVVLKPAEITPFAAM 180 Query: 181 ILAEIFDKVGVPKGVFNLVNGDGQGVGNPLSEHPKVRMMSFTGSGPTGSSIMKKAAEDFK 240 ILAEI D+ GVPKGVFNLVNG G +G+ +S HP + +SFTGSG GS IM+ AA++ K Sbjct: 181 ILAEIIDEAGVPKGVFNLVNGTGDVIGDGISSHPDIDFVSFTGSGAVGSKIMENAADNVK 240 Query: 241 KVSLELGGKSPYIILDDADIDGAASAAANKVVFNTGQVCTAGTRTIVPASIKEDFLTAVK 300 KV+LELGGKSP I+LDDAD+D AA A + + NTGQVC+A TR ++P S+K+ F A+ Sbjct: 241 KVALELGGKSPLIVLDDADVDEAAETAIHHIAMNTGQVCSAATRVLIPESMKDKFEKALL 300 Query: 301 EKFSQVKVGNPREEGTQVGPIISKKQFDQVQAYIDKGIEEGAELLYGGPGKPEGLDKGYF 360 + VG+PRE+ GP++SKKQ+D VQ+YI+KGIEEGA LL GG GKP+G+DKGYF Sbjct: 301 NALPKFTVGDPREDHA-TGPLVSKKQWDTVQSYIEKGIEEGATLLAGGTGKPDGIDKGYF 359 Query: 361 ARPTIFNNVDNSMTIAQEEIFGPVMSVITYNDLDEAIKIANDTKYGLAGYVYGSDKDTLH 420 A+ TIF NV N MTIAQEEIFGPVMSVITY DLD A++IANDT YGLAGYV G D+ TL Sbjct: 360 AKHTIFTNVKNDMTIAQEEIFGPVMSVITYQDLDHALEIANDTVYGLAGYVVGQDEKTLK 419 Query: 421 KVARSIEAGTVEINEAGRKPDLPFGGYKQSGLGREWGDYGIEEFLEVKSIAG 472 VA I AG + IN A PFGG+KQSG+GREWGD+GIEE+LEVK++ G Sbjct: 420 YVAEHIRAGQITINNAETDYFAPFGGFKQSGIGREWGDFGIEEYLEVKAVMG 471 Lambda K H 0.313 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: 711 Number of extensions: 30 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: 475 Length of database: 475 Length adjustment: 33 Effective length of query: 442 Effective length of database: 442 Effective search space: 195364 Effective search space used: 195364 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 bits) S2: 51 (24.3 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