Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_068107726.1 I601_RS07030 CoA-acylating methylmalonate-semialdehyde dehydrogenase
Query= reanno::pseudo5_N2C3_1:AO356_23175 (500 letters) >NCBI__GCF_001653335.1:WP_068107726.1 Length = 496 Score = 586 bits (1510), Expect = e-172 Identities = 287/491 (58%), Positives = 360/491 (73%), Gaps = 2/491 (0%) Query: 7 VGHYIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPAWSEQSSL 66 + H+IDGR + R S V+NPATG A V LA ++ AVASA AA W S Sbjct: 5 ISHWIDGRPSPGTSGRTSAVYNPATGQQSAEVDLAGADDLERAVASASAAAKQWRSASLS 64 Query: 67 RRSRVMFKFKELLDRHHDELAQIISREHGKVLSDAHGEVTRGIEIVEYACGAPNLLKTDF 126 R+ V+F F+E L + DELA I++ EHGKVL+DA GE+ RG+E VE+A G P+L+K F Sbjct: 65 TRAAVLFAFREQLHQRSDELAAIVTAEHGKVLADAAGEIARGLENVEFATGVPHLMKGGF 124 Query: 127 SDNIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERDPSASL 186 S+ G G+D +++RQ LGV AG+TPFNFP MVPLWM A+ GN FILKPSERDPSA++ Sbjct: 125 SEQAGTGVDVYSIRQALGVVAGITPFNFPAMVPLWMCANAIATGNAFILKPSERDPSAAV 184 Query: 187 LMARLLTEAGLPDGVFNVVQGDKVAVDALLQHPDIEAISFVGSTPIAEYIHQQGTAQGKR 246 +A L +AGLPDGVF V+ GDK AVD LL+HP++ AISFVGSTPIA YI++ GTAQGKR Sbjct: 185 FLAELWRDAGLPDGVFTVLHGDKEAVDGLLRHPEVAAISFVGSTPIARYIYETGTAQGKR 244 Query: 247 VQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDELIAKLLP 306 VQALGGAKNHM+V+PDAD+D AADA + AAYG+AGERCMAIS+ VAVGDV D L++ + Sbjct: 245 VQALGGAKNHMVVLPDADVDMAADAAVSAAYGAAGERCMAISVVVAVGDVADSLVSAVAD 304 Query: 307 RIDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFKVPGAEQGFF 366 R+ +L+IGNG G DMGPL++ EH+ KV G+I AG A GARL+VDGR VP +GFF Sbjct: 305 RLPRLRIGNGADDGVDMGPLISGEHRDKVAGYIAAGEAAGARLVVDGRRASVPA--EGFF 362 Query: 367 VGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCFTRDGGIAR 426 +G TL D VT +M++Y EIFGPVL +VRV + AVALINA+ + NG + FTRDGG AR Sbjct: 363 LGTTLLDDVTPDMTVYTDEIFGPVLSVVRVATYDEAVALINANPYANGTAIFTRDGGAAR 422 Query: 427 AFARSIKVGMVGINVPIPVPMAWHSFGGWKRSLFGDHHAYGEEGLRFYSRYKSVMQRWPD 486 F ++VGMVGINVPIPVP++++SFGGWK SLFGD H YG EG++F++R K V RWPD Sbjct: 423 EFQLDVEVGMVGINVPIPVPVSYYSFGGWKDSLFGDTHMYGPEGIKFFTRGKVVTSRWPD 482 Query: 487 SIAKGPEFSMP 497 + P Sbjct: 483 PATSQVDLGFP 493 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: 680 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: 500 Length of database: 496 Length adjustment: 34 Effective length of query: 466 Effective length of database: 462 Effective search space: 215292 Effective search space used: 215292 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