GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Paucidesulfovibrio gracilis DSM 16080

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate WP_234990588.1 B5D49_RS01275 L-threonine 3-dehydrogenase

Query= SwissProt::Q8U259
         (348 letters)



>NCBI__GCF_900167125.1:WP_234990588.1
          Length = 354

 Score =  288 bits (736), Expect = 2e-82
 Identities = 145/340 (42%), Positives = 216/340 (63%), Gaps = 3/340 (0%)

Query: 5   MVAIMKTKPEYGAELVEVDVPKPGPGEVLIKILATSICGTDLHIYEWNEWAQTRIRPPQI 64
           M A++K + + G  L E  VP+ G  +VL+++  T+ICGTD+HI+ W+EWA   I  P  
Sbjct: 11  MRALVKHEAKQGIRLQEAPVPEFGHNDVLVQVDKTAICGTDVHIFNWDEWAAATIPVPMT 70

Query: 65  MGHEVAGEVVEVGPGVEGIEVGDYVSVETHIVCGKCYACKRGQYHVCQNTKIFGVDTDGV 124
           +GHE +G VV VG  V G++ GD VS E H+ CG C  C+ G+ H+C+NT   GV+  G 
Sbjct: 71  VGHEFSGRVVAVGSEVRGLQPGDRVSAEGHVTCGHCRNCRAGKRHLCRNTVGIGVNRPGC 130

Query: 125 FAEYAVVPAQNVWKNPKNIPPEYATLQEPLGNAVDTVLAGPIAGKSVLITGAGPLGLLGI 184
           FA+Y  VPA NV+  P  +  E   + +PLGNAV T L+  + G+ VLITGAGP+G++ +
Sbjct: 131 FADYLSVPASNVFHLPDAVSDEMGAVLDPLGNAVHTALSFDLVGEDVLITGAGPIGMMAV 190

Query: 185 AVAKASGAYPVIVSEPSEFRRNLAKKVGADYVINPFEEDVVKEVMDITDGNGVDVFLEFS 244
           AVA+  GA  +++++ +++R +LA K+GA + +N   E++   +  +    G DV LE S
Sbjct: 191 AVARFVGARHIVITDVNDYRLDLAAKLGASHTVNVTRENLADTMAGLGMVEGFDVGLEMS 250

Query: 245 GAPKALEQGLQAVTPAGRVSLLGLFPGKVSIDFNNLIIFKALTVYGITGRHLWETWYTVS 304
           G P A  Q L  +   G V+LLG+ P   +ID+N  ++FK L + GI GR ++ETWY ++
Sbjct: 251 GNPSAFRQLLANMNHGGSVALLGILPESTAIDWNE-VVFKGLRLKGIYGREMFETWYKMA 309

Query: 305 RLLQSGKLNIDPIITHKYKGFDKYEEAFELMRAGKTGKVV 344
            ++QSG LNI P ITH+    D Y   F++MR+G +GKVV
Sbjct: 310 SMIQSG-LNIAPAITHRL-DVDDYANGFDVMRSGNSGKVV 347


Lambda     K      H
   0.318    0.138    0.417 

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: 316
Number of extensions: 8
Number of successful extensions: 3
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: 348
Length of database: 354
Length adjustment: 29
Effective length of query: 319
Effective length of database: 325
Effective search space:   103675
Effective search space used:   103675
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.3 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.7 bits)
S2: 49 (23.5 bits)

This GapMind analysis is from Apr 09 2024. The underlying query database was built on Sep 17 2021.

Links

Downloads

Related tools

About GapMind

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:

where "other" refers to the best ublast hit to a sequence that is not annotated as performing this step (and is not "ignored").

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