GapMind for catabolism of small carbon sources

 

Alignments for a candidate for etoh-dh-nad in Phaeobacter inhibens BS107

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate GFF3379 PGA1_c34320 L-threonine 3-dehydrogenase Tdh

Query= SwissProt::Q8U259
         (348 letters)



>FitnessBrowser__Phaeo:GFF3379
          Length = 342

 Score =  267 bits (683), Expect = 3e-76
 Identities = 142/341 (41%), Positives = 218/341 (63%), Gaps = 4/341 (1%)

Query: 5   MVAIMKTKPEYGAELVEVDVPKPGPGEVLIKILATSICGTDLHIYEWNEWAQTRIRPPQI 64
           M A+ K+ P  G  +V+  VP+ GP EVLIKI  T ICGTD+HI+ W+EWA   +  P I
Sbjct: 1   MKALEKSHPREGLWMVQAPVPEIGPDEVLIKIRTTGICGTDIHIWNWDEWASHTVPVPMI 60

Query: 65  MGHEVAGEVVEVGPGVEGIEVGDYVSVETHIVCGKCYACKRGQYHVCQNTKIFGVDTDGV 124
            GHE AGE+VE+G  V  + VG   S E H++       + G++H+   T+  GV+  G 
Sbjct: 61  TGHEFAGEIVEIGRNVTDLAVGQRCSGEGHLIQTDSRQSRAGKFHLDPGTRGIGVNEQGA 120

Query: 125 FAEYAVVPAQNVWKNPKNIPPEYATLQEPLGNAVDTVLAGPIAGKSVLITGAGPLGLLGI 184
           FA+Y  +PA NV   P++IP E   + +PLGNAV T L+  + G+ VLITGAGP+G++  
Sbjct: 121 FAQYLKLPAFNVVPLPEDIPDEIGAILDPLGNAVHTALSFDLLGEDVLITGAGPIGVMAA 180

Query: 185 AVAKASGAYPVIVSEPSEFRRNLAKK-VGADYVINPFEEDVVKEVMDITDGNGVDVFLEF 243
           AVA+ +GA  V++++ +  R  LA+  V A   +N  EED+   V ++    G DV LE 
Sbjct: 181 AVARHAGARHVVITDINPDRLALAEHVVPAVRAVNVAEEDLQDVVRELGLKQGFDVGLEM 240

Query: 244 SGAPKALEQGLQAVTPAGRVSLLGLFPGKVSIDFNNLIIFKALTVYGITGRHLWETWYTV 303
           SG+  AL+Q ++A+   G+++LLG+ PGK  +D++  I+FKA+T+ G+ GR ++ETWY +
Sbjct: 241 SGSQAALDQMVEALVMGGKIALLGIPPGKSPVDWSR-IVFKAITIKGVYGREMFETWYKM 299

Query: 304 SRLLQSGKLNIDPIITHKYKGFDKYEEAFELMRAGKTGKVV 344
             +LQ+G L++  +ITH++   + + E F  M++G++GKVV
Sbjct: 300 IAMLQNG-LDVSRVITHRF-DVEDFAEGFAAMKSGRSGKVV 338


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: 338
Number of extensions: 12
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: 348
Length of database: 342
Length adjustment: 29
Effective length of query: 319
Effective length of database: 313
Effective search space:    99847
Effective search space used:    99847
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 Sep 17 2021. The underlying query database was built on Sep 17 2021.

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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