Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_053543863.1 CDES_RS00960 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= reanno::pseudo5_N2C3_1:AO356_23175 (500 letters) >NCBI__GCF_001277995.1:WP_053543863.1 Length = 504 Score = 566 bits (1458), Expect = e-166 Identities = 278/494 (56%), Positives = 351/494 (71%), Gaps = 3/494 (0%) Query: 1 MSDAPVVGHYIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPAW 60 MS+ ++ H+IDG S + + V+NPATG V V LA +DA +ASA A AW Sbjct: 1 MSEPQLITHWIDGAPAPSTSGNTAPVYNPATGQVTGNVVLANQEEIDATIASATKAAKAW 60 Query: 61 SEQSSLRRSRVMFKFKELLDRHHDELAQIISREHGKVLSDAHGEVTRGIEIVEYACGAPN 120 S +R V+F F+ELL+ +ELA II+ EHGKVLSDA GE+ RG E+VE A G P+ Sbjct: 61 GRLSIAKRQAVIFNFRELLNARKEELAAIITAEHGKVLSDALGEILRGQEVVELATGFPH 120 Query: 121 LLKTDFSDNIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSER 180 LLK FS+N+ G+D ++L+QPLGV ++PFNFP MVP+W P+A+ AGN ILKPSE+ Sbjct: 121 LLKGAFSENVSTGVDVYSLKQPLGVVGIISPFNFPAMVPMWFFPIAIAAGNAVILKPSEK 180 Query: 181 DPSASLLMARLLTEAGLPDGVFNVVQGDKVAVDALLQHPDIEAISFVGSTPIAEYIHQQG 240 DPSA+L MA+L EAGLPDGVFNV+QGDK+AVD LL P++ AISFVGSTPIA+YI++ Sbjct: 181 DPSAALWMAQLWKEAGLPDGVFNVLQGDKLAVDGLLNSPEVSAISFVGSTPIAQYIYETS 240 Query: 241 TAQGKRVQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDEL 300 GKRVQALGGAKNHM+V+PDADLD AD I + +G+AGERCMAIS+ +A+ + DEL Sbjct: 241 AKNGKRVQALGGAKNHMLVLPDADLDLVADQAINSGFGAAGERCMAISVVLAIDSIADEL 300 Query: 301 IAKLLPRIDQLKIGNG---QQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFK 357 I K+ RID L+IGNG Q DMGPL+T H+ KV G++D A+GAR++VDGR + Sbjct: 301 IEKIKERIDTLRIGNGAGDDQGEPDMGPLITDVHRDKVSGYVDIAEADGARIVVDGRNYA 360 Query: 358 VPGAEQGFFVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSC 417 V G E+GFF G TL D V Y +EIFGPVL +VRV F A+ LIN+ EFGNG + Sbjct: 361 VAGHEEGFFFGPTLIDDVPLTSRAYTEEIFGPVLSVVRVSSFDEAIELINSGEFGNGTAI 420 Query: 418 FTRDGGIARAFARSIKVGMVGINVPIPVPMAWHSFGGWKRSLFGDHHAYGEEGLRFYSRY 477 FT DGG AR F I+VGM+GINVPIPVP+A+HSFGGWK SLFGD AYG +G F++R Sbjct: 421 FTNDGGAARRFQNEIQVGMIGINVPIPVPVAYHSFGGWKNSLFGDAKAYGTQGFDFFTRE 480 Query: 478 KSVMQRWPDSIAKG 491 K++ RW D G Sbjct: 481 KAITSRWLDPATHG 494 Lambda K H 0.320 0.137 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: 703 Number of extensions: 18 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: 500 Length of database: 504 Length adjustment: 34 Effective length of query: 466 Effective length of database: 470 Effective search space: 219020 Effective search space used: 219020 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: 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