GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Pseudomonas stutzeri RCH2

Align L-threonine 3-dehydrogenase; TDH; L-threonine dehydrogenase; EC 1.1.1.103 (characterized)
to candidate GFF1391 Psest_1428 Threonine dehydrogenase and related Zn-dependent dehydrogenases

Query= SwissProt::Q8U259
         (348 letters)



>FitnessBrowser__psRCH2:GFF1391
          Length = 362

 Score =  172 bits (435), Expect = 2e-47
 Identities = 108/322 (33%), Positives = 167/322 (51%), Gaps = 15/322 (4%)

Query: 24  VPKPG---PGEVLIKILATSICGTDLHIYEWNE--------WAQTRIRPPQIMGHEVAGE 72
           VP PG   PG V I++    ICG+DLH Y               T I+   I+GHE  GE
Sbjct: 23  VPLPGAPQPGWVQIRVHWCGICGSDLHEYLAGPVFIPVDAPHPLTGIKGQCILGHEFCGE 82

Query: 73  VVEVGPGVEGIEVGDYVSVETHIVCGKCYACKRGQYHVCQNTKIFGVDTDGVFAEYAVVP 132
           +V +G GVEG   GD V+ +    CG+C  CK GQY++C+     G+  +G FAE+  VP
Sbjct: 83  IVAIGEGVEGYAPGDKVAADACQHCGQCRFCKTGQYNLCEQLAFTGLMNNGAFAEFVNVP 142

Query: 133 AQNVWKNPKNIPPEYATLQEPLGNAVDTV-LAGPIAGKSVLITGAGPLGLLGIAVAKASG 191
           A+ +++ P+  P E   L EPL   +  V  AG + G++V++ GAG +GL  I  AKA+G
Sbjct: 143 AELLYRLPEGFPLEAGALIEPLAVGMHAVKKAGSLLGETVVVVGAGTIGLCTIMCAKAAG 202

Query: 192 AYPVIVSEPSEFRRNLAKKVGADYVINPFEEDVVKEVMDITDGNGVDVFLEFSGAPKALE 251
           A  VI  E S  R+  A +VGA++VI+P E D + E+  +T G G  V  E  G     +
Sbjct: 203 AGQVIALEMSAARKAKALEVGANWVIDPSECDAIAEIKALTGGYGAGVSFECIGHKATAK 262

Query: 252 QGLQAVTPAGRVSLLGLFPGKVSIDFNNLIIFKALTVYGITGRHLWETWYTVSRLLQSGK 311
             +  +  AGR  ++G+F      +F  ++  +   +  +        +  V  L+  G+
Sbjct: 263 LAIDVIRKAGRCVMVGIFEEPSEFNFFEIVATEKQVIGSLA---YAGEFADVIALIDDGR 319

Query: 312 LNIDPIITHKYKGFDKYEEAFE 333
           +++ P+IT +    +  E+ FE
Sbjct: 320 IDVTPLITGRIGLDNILEQGFE 341


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: 332
Number of extensions: 19
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: 362
Length adjustment: 29
Effective length of query: 319
Effective length of database: 333
Effective search space:   106227
Effective search space used:   106227
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.

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