Align Methylmalonate-semialdehyde dehydrogenase [inositol] (EC 1.2.1.27) (characterized)
to candidate 15507 b1385 phenylacetaldehyde dehydrogenase (VIMSS)
Query= reanno::Koxy:BWI76_RS03070 (501 letters) >FitnessBrowser__Keio:15507 Length = 499 Score = 253 bits (646), Expect = 1e-71 Identities = 174/495 (35%), Positives = 256/495 (51%), Gaps = 30/495 (6%) Query: 5 GNFIGGKTVTSGSNKTMPVFDPATGKVVREVTLSTAQEVSDAIQVARDAFES--WSRTTP 62 G +I G+ + S K + +FDPATG+ + + +V +A+ A AF S W+ P Sbjct: 21 GLYIDGRPGPAQSEKRLAIFDPATGQEIASTADANEADVDNAVMSAWRAFVSRRWAGRLP 80 Query: 63 LRRARVMFNFKMLLEQHAEELAGIIVSEHGKVFSDAMGELTRGMEV------VEFACGIP 116 R R++ F L+EQH+EELA + E GK + ++R EV + + G+ Sbjct: 81 AERERILLRFADLVEQHSEELAQLETLEQGKSIA-----ISRAFEVGCTLNWMRYTAGLT 135 Query: 117 HLIKGE-----FSSDVGTGVDSYSLMQPLGVVAGITPFNFPAMVPMWMFPLALACGNSFV 171 I G+ G +++ +P+GVVAGI P+NFP M+ MW ALA G S V Sbjct: 136 TKIAGKTLDLSIPLPQGARYQAWTRKEPVGVVAGIVPWNFPLMIGMWKVMPALAAGCSIV 195 Query: 172 LKPPALAPTAAVRLAELLKEAGLPDGVFNVVHCSNE-DAEQLYRDPRIAAVSFVGSSGVA 230 +KP P +R+AEL EAG+PDGVFNVV S L P +A +SF GS+ Sbjct: 196 IKPSETTPLTMLRVAELASEAGIPDGVFNVVTGSGAVCGAALTSHPHVAKISFTGSTATG 255 Query: 231 EHIYKTASAYGKRVQAFGAAKNHAIVMPDADLDATVNAIMGGAFGSAGERCMALPVVVAV 290 + I +TA+ + RV KN AIV+ DAD + +M G+F + G+ C A + + Sbjct: 256 KGIARTAADHLTRVTLELGGKNPAIVLKDADPQWVIEGLMTGSFLNQGQVCAASSRIY-I 314 Query: 291 GDETADKLIARLKPLVESLKVGPGCMRGKEENEMGPVVSDTHQKKVLGYIDKGVSEGATL 350 D L++ + V+SL+VGPG ++ P+VS H KV ++D ++ A L Sbjct: 315 EAPLFDTLVSGFEQAVKSLQVGPGM---SPVAQINPLVSRAHCDKVCSFLDDAQAQQAEL 371 Query: 351 VVDGRKPQVPGFEEGYYVGGTLFDNVTPEMTIWREEIFGPVLGIVRVADYHSALELVNSH 410 + P EGYYV TL N ++ + REE+FGPV+ +VRVAD AL+L N Sbjct: 372 IRGSNGPA----GEGYYVAPTLVVNPDAKLRLTREEVFGPVVNLVRVADGEEALQLANDT 427 Query: 411 EFGNGSAVFTSNGHTAREFVHDVQAGMVGVNVPVPVPMAFHSFGGWKRSVFGALNVHGPD 470 E+G ++V+T N A E+ +QAG V VN + A FGG K+S G GPD Sbjct: 428 EYGLTASVWTQNLSQALEYSDRLQAGTVWVNSHTLID-ANLPFGGMKQS--GTGRDFGPD 484 Query: 471 GVRFYTRMKTATVRW 485 + + K+ VR+ Sbjct: 485 WLDGWCETKSVCVRY 499 Lambda K H 0.319 0.135 0.404 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: 636 Number of extensions: 30 Number of successful extensions: 7 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: 501 Length of database: 499 Length adjustment: 34 Effective length of query: 467 Effective length of database: 465 Effective search space: 217155 Effective search space used: 217155 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