GapMind for catabolism of small carbon sources

 

Alignments for a candidate for tdh in Acidovorax sp. GW101-3H11

Align L-threonine 3-dehydrogenase; TDH; EC 1.1.1.103 (uncharacterized)
to candidate Ac3H11_3163 S-(hydroxymethyl)glutathione dehydrogenase (EC 1.1.1.284)

Query= curated2:Q65JE7
         (346 letters)



>FitnessBrowser__acidovorax_3H11:Ac3H11_3163
          Length = 371

 Score =  124 bits (312), Expect = 3e-33
 Identities = 109/370 (29%), Positives = 169/370 (45%), Gaps = 52/370 (14%)

Query: 7   ALIKKPGEPGASFELVPIPKIDKHEVLIKVKAASICGTDVHIYNWDEWAKSRVKPPYVFG 66
           A+  K GEP    E+   P   K EVLI++    +C TD    + D+        P V G
Sbjct: 6   AVAFKAGEPLKIVEIDVAPP-KKGEVLIRITDTGVCHTDAFTLSGDD---PEGLFPVVLG 61

Query: 67  HEFSGEVVQVGENVTTVKEGEYVSAETHIVCGKCLPCLTGKEHVC---KKTLILGVDTDG 123
           HE +G VV+VGE VT+VK G++V       CG+CL C +GK ++C   + T   GV  DG
Sbjct: 62  HEGAGIVVEVGEGVTSVKPGDHVIPLYTAECGECLFCKSGKTNLCVSVRATQGKGVMPDG 121

Query: 124 ------------------CFAEYVKMPAANIWK-NPAGMPEDL----ASIQEPLGNAVHT 160
                              F+EY  +   ++ K NP   PE +      +   LG   +T
Sbjct: 122 TTRFSYNGQPIYHYMGCSTFSEYTVVAEVSLAKVNPQANPEQVCLLGCGVTTGLGAVKNT 181

Query: 161 VLTGMTAGVKVAVVGCGPIGLMAVAVAKASGAAQVIAIDKNEYRLDLALQMGATDIISVE 220
               +  G  VAV G G IGL  +  AK + A ++IA+D N  + DLA   GATD I+ +
Sbjct: 182 --AKVQEGDTVAVFGLGGIGLAVIQGAKLAKAGRIIAVDTNPSKFDLARTFGATDCINPK 239

Query: 221 KED-PLKNVSALTNGEGADLVCEMSGHPTAIRQSLKMAANGGRVHVL--------SLPEH 271
             D P++ V       G D   E  G+   +R +L+ A  G    V+         +   
Sbjct: 240 DFDKPIQQVIVEMTTWGVDHSFECIGNVNVMRAALECAHRGWGQSVIIGVAGAGQEISTR 299

Query: 272 PVCIDMTNDIVFKGLTVQGITGRKMFETWRQVSGLLQ---SGTIQIKPVITHRFPMEEFE 328
           P    +     + G    G+ GR       ++ G+++   +G IQ++P +TH   +++  
Sbjct: 300 P--FQLVTGRKWLGTAFGGVKGRS------ELPGMVEDAMAGKIQLEPFVTHTMGLKDIN 351

Query: 329 KGFELMRKGQ 338
           + F+LM +G+
Sbjct: 352 EAFDLMHEGK 361


Lambda     K      H
   0.318    0.136    0.410 

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: 341
Number of extensions: 14
Number of successful extensions: 5
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: 346
Length of database: 371
Length adjustment: 29
Effective length of query: 317
Effective length of database: 342
Effective search space:   108414
Effective search space used:   108414
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