Align malonate-semialdehyde dehydrogenase (acetylating) (EC 1.2.1.18) (characterized)
to candidate 15507 b1385 phenylacetaldehyde dehydrogenase (VIMSS)
Query= reanno::pseudo5_N2C3_1:AO356_23175 (500 letters) >FitnessBrowser__Keio:15507 Length = 499 Score = 240 bits (612), Expect = 1e-67 Identities = 167/486 (34%), Positives = 253/486 (52%), Gaps = 16/486 (3%) Query: 8 GHYIDGRIQASDNARLSNVFNPATGAVQARVALAEPSTVDAAVASALAAFPA--WSEQSS 65 G YIDGR + + + +F+PATG A A A + VD AV SA AF + W+ + Sbjct: 21 GLYIDGRPGPAQSEKRLAIFDPATGQEIASTADANEADVDNAVMSAWRAFVSRRWAGRLP 80 Query: 66 LRRSRVMFKFKELLDRHHDELAQIISREHGKVLSDAHG-EVTRGIEIVEYACGAPNLL-- 122 R R++ +F +L+++H +ELAQ+ + E GK ++ + EV + + Y G + Sbjct: 81 AERERILLRFADLVEQHSEELAQLETLEQGKSIAISRAFEVGCTLNWMRYTAGLTTKIAG 140 Query: 123 KT-DFSDNI--GGGIDNWNLRQPLGVCAGVTPFNFPVMVPLWMIPLALVAGNCFILKPSE 179 KT D S + G W ++P+GV AG+ P+NFP+M+ +W + AL AG ++KPSE Sbjct: 141 KTLDLSIPLPQGARYQAWTRKEPVGVVAGIVPWNFPLMIGMWKVMPALAAGCSIVIKPSE 200 Query: 180 RDPSASLLMARLLTEAGLPDGVFNVVQGD-KVAVDALLQHPDIEAISFVGSTPIAEYIHQ 238 P L +A L +EAG+PDGVFNVV G V AL HP + ISF GST + I + Sbjct: 201 TTPLTMLRVAELASEAGIPDGVFNVVTGSGAVCGAALTSHPHVAKISFTGSTATGKGIAR 260 Query: 239 QGTAQGKRVQALGGAKNHMIVMPDADLDQAADALIGAAYGSAGERCMAISIAVAVGDVGD 298 RV G KN IV+ DAD + L+ ++ + G+ C A S + D Sbjct: 261 TAADHLTRVTLELGGKNPAIVLKDADPQWVIEGLMTGSFLNQGQVCAASSRIYIEAPLFD 320 Query: 299 ELIAKLLPRIDQLKIGNGQQPGTDMGPLVTAEHKAKVEGFIDAGVAEGARLIVDGRGFKV 358 L++ + L++G G P + PLV+ H KV F+D A+ A LI RG Sbjct: 321 TLVSGFEQAVKSLQVGPGMSPVAQINPLVSRAHCDKVCSFLDDAQAQQAELI---RGSNG 377 Query: 359 PGAEQGFFVGATLFDQVTAEMSIYQQEIFGPVLGIVRVPDFATAVALINAHEFGNGVSCF 418 P E G++V TL A++ + ++E+FGPV+ +VRV D A+ L N E+G S + Sbjct: 378 PAGE-GYYVAPTLVVNPDAKLRLTREEVFGPVVNLVRVADGEEALQLANDTEYGLTASVW 436 Query: 419 TRDGGIARAFARSIKVGMVGINVPIPVPMAWHSFGGWKRSLFGDHHAYGEEGLRFYSRYK 478 T++ A ++ ++ G V +N + A FGG K+S G +G + L + K Sbjct: 437 TQNLSQALEYSDRLQAGTVWVNSHTLID-ANLPFGGMKQS--GTGRDFGPDWLDGWCETK 493 Query: 479 SVMQRW 484 SV R+ Sbjct: 494 SVCVRY 499 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: 559 Number of extensions: 22 Number of successful extensions: 5 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: 499 Length adjustment: 34 Effective length of query: 466 Effective length of database: 465 Effective search space: 216690 Effective search space used: 216690 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 Apr 09 2024. 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