Align succinate-semialdehyde dehydrogenase [NAD(P)+]; EC 1.2.1.16 (characterized)
to candidate 8501604 DvMF_2322 bifunctional acetaldehyde-CoA/alcohol dehydrogenase (RefSeq)
Query= CharProtDB::CH_007085 (453 letters) >FitnessBrowser__Miya:8501604 Length = 904 Score = 302 bits (773), Expect = 3e-86 Identities = 168/440 (38%), Positives = 247/440 (56%), Gaps = 7/440 (1%) Query: 3 NEVSIKELIEKAKVAQKKLEAYSQEQVDVLVKALGKVVYDNAEMFAKEAVEETEMGVYED 62 N +++ +++ + AQ+ ++Q+QVD + A A+ AV+ET MG+ ED Sbjct: 32 NSITVDDIVTRVNEAQRAFANFTQQQVDAIFHAAAAAATAQRIHLARMAVQETGMGILED 91 Query: 63 KVAKCHLKSGAIWNHIKDKKTVGIIKEEPERALVYVAKPKGVVAATTPITNPVVTPMCNA 122 KV K H S I+N KD KT G+I+++P VA P GV+A P TNP T + A Sbjct: 92 KVIKNHFASEYIYNKYKDDKTCGVIRDDPAYGYREVAAPIGVIAGIIPTTNPTSTTIFKA 151 Query: 123 MAAIKGRNTIIVAPHPKAKKVSAHTVELMNAELKKLGAPENIIQIVEAPSREAAKELMES 182 + A+K RN II APHP+A K + +++ GAP II VEAP+ + ++LM+ Sbjct: 152 LLALKTRNGIIFAPHPRAAKSTVEAARIVHEAAVAAGAPRGIIGWVEAPTPDLTRQLMQH 211 Query: 183 ADV--VIATGGAGRVKAAYSSGRPAYGVGPGNSQVIVDKGYDYNKAAQDIITGRKYDNGI 240 V ++ATGG G V AAYSSG+PA GVG GN+ V+VD + A II + +DNG+ Sbjct: 212 RGVALILATGGPGMVHAAYSSGKPAIGVGAGNTPVVVDASANVKMAVNSIILSKTFDNGM 271 Query: 241 ICSSEQSVIAPAEDYDKVIAAFVENGAFYVEDEETVEKFRSTLFKDGKINSKIIGKSVQI 300 IC+SEQ+VI D V A F G + +E E +F DG++N+ I+G+S Sbjct: 272 ICASEQAVIVEDAAADAVKAEFAARGCHFASPQE-AEALAGVVFTDGRLNAAIVGRSAAE 330 Query: 301 IADLAGVKVPEGTKVIVLKGKGAGEKDVLCKEKMCPVLVALKYDTFEEAVEIAMANYMYE 360 IA +AG+ VP TK+++ + D EK+ PVL + F AV++A Sbjct: 331 IAAMAGITVPPTTKILIAERDAIDPLDPFAHEKLSPVLGFYRAPDFAAAVDMAQRLVELG 390 Query: 361 GAGHTAGIHSD--NDENIRYAGTVLPISRLVVNQPAT--TAGGSFNNGFNPTTTLGCGSW 416 GAGHT+ ++++ N E I + VL R +VN P++ G +N P+ TLGCGSW Sbjct: 391 GAGHTSVLYTNEANRERIVHFQNVLTTGRTLVNMPSSQGAIGDVYNFELAPSLTLGCGSW 450 Query: 417 GRNSISENLTYEHLINVSRI 436 G NS+SEN+ +HL+NV + Sbjct: 451 GDNSVSENIGVKHLMNVKTV 470 Lambda K H 0.313 0.131 0.368 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: 882 Number of extensions: 51 Number of successful extensions: 4 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: 453 Length of database: 904 Length adjustment: 38 Effective length of query: 415 Effective length of database: 866 Effective search space: 359390 Effective search space used: 359390 Neighboring words threshold: 11 Window for multiple hits: 40 X1: 16 ( 7.2 bits) X2: 38 (14.6 bits) X3: 64 (24.7 bits) S1: 42 (21.9 bits) S2: 54 (25.4 bits)
This GapMind analysis is from Sep 17 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 the paper from 2019 on GapMind for amino acid biosynthesis, the paper from 2022 on GapMind for carbon sources, or view the source code.
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