Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate WP_034273599.1 AMYHA_RS20335 aldehyde dehydrogenase family protein
Query= reanno::pseudo5_N2C3_1:AO356_23175 (500 letters) >NCBI__GCF_000504245.1:WP_034273599.1 Length = 496 Score = 250 bits (638), Expect = 9e-71 Identities = 161/478 (33%), Positives = 243/478 (50%), Gaps = 9/478 (1%) Query: 10 YIDGR-IQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFP--AWSEQSSL 66 +IDGR + + A V NPA A A V A+ VDAAVA+A AF W ++ Sbjct: 5 FIDGRWVDTTGTAPARVVLNPANAAELATVCEADEKDVDAAVAAARRAFDDSPWRATTAR 64 Query: 67 RRSRVMFKFKELLDRHHDELAQIISREHGKVLSDAHGEVTRGIEIVEYACGAPNLLKTDF 126 R ++ + LL R + LA+ S + GK +++ +V + Y + Sbjct: 65 ERGELLREIARLLQRDKEHLARTESLDTGKTMAEGRVDVDDVTSVFRYYANLADNEAGRV 124 Query: 127 SDNIGGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSERDPSASL 186 D + + + +P+GVC+ + P+N+P++ W + AL AGN ++KPSE P ++ Sbjct: 125 VDTGDASVISRVVHEPVGVCSLIAPWNYPLLQMSWKLAPALAAGNTVVMKPSEVTPLTTI 184 Query: 187 LMARLLTEAGLPDGVFNVVQGDKVAVDA-LLQHPDIEAISFVGSTPIAEYIHQQGTAQGK 245 + RL+ EAG+P GV N+V G V A ++ HPD++ +SF G + I K Sbjct: 185 ELMRLVEEAGVPAGVVNLVLGGGANVGAPMVSHPDVDLVSFTGGLETGKKIMAMAAEGVK 244 Query: 246 RVQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGDELIAKLL 305 RV G KN +V DAD D A D + AA+ +G+ C A S + D+ DE +A+L Sbjct: 245 RVALELGGKNPNVVFADADFDTAVDYALMAAFAHSGQVCSAGSRLIVESDIHDEFVAELA 304 Query: 306 PRIDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFKVPGAEQGF 365 R D +++G+G P T+ GPL +AEH+ KVE I+ EGARL+V G P G+ Sbjct: 305 RRADAIRLGDGLDPATECGPLSSAEHRDKVERHIEEAKTEGARLVVGGHRPTEPELADGY 364 Query: 366 FVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCFTRDGGIA 425 F+ T+F EM I Q E+FGPV+ + R A+ L N E+G + +T D A Sbjct: 365 FLRPTVFADCDREMRIVQDEVFGPVVTVERFDTEDEAIRLANDTEYGLAGAVWTSDASRA 424 Query: 426 RAFARSIKVGMVGINVPIP-VPMAWHSFGGWKRSLFGDHHAYGEEGLRFYSRYKSVMQ 482 + A +++ G V IN P +P A +GG+ +S G G GL Y K + Q Sbjct: 425 QRVAGALRHGTVWINDFHPYLPQA--EWGGFGKSGIG--RELGPSGLEEYRETKHIYQ 478 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: 538 Number of extensions: 22 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