GapMind for Amino acid biosynthesis

 

Alignments for a candidate for thrC in Sphingomonas koreensis DSMZ 15582

Align Threonine synthase; TS; EC 4.2.3.1 (uncharacterized)
to candidate Ga0059261_1586 Ga0059261_1586 Threonine synthase

Query= curated2:Q58860
         (405 letters)



>FitnessBrowser__Korea:Ga0059261_1586
          Length = 475

 Score =  222 bits (566), Expect = 2e-62
 Identities = 127/376 (33%), Positives = 202/376 (53%), Gaps = 3/376 (0%)

Query: 5   CIKCGKTYDVDEIIYTCECGGLLEIIYDYEEIKDKVSEEKLRKREIGVWRYLEYLPVKDE 64
           C   G+ YD D +      G  L + YD + I+  VS   L  R   +WRY E LPV+  
Sbjct: 82  CSMTGERYDADTLHGLSRTGRPLLVRYDLDAIRAAVSPADLALRPADLWRYRELLPVRRT 141

Query: 65  SKIVSLCEGGTPLYRCNNLEKELGIKELYVKNEGANPTGSFKDRGMTVGVTRANELGVEV 124
             IVSL E  TP+   N +    G   L VK+E   PTGSFK RG+ + ++ A ELGV  
Sbjct: 142 ENIVSLGEIATPIVPLNKVAAGAGASTLLVKDESRLPTGSFKARGLVMAISMAKELGVTT 201

Query: 125 VGCASTGNTSASLAAYSARSGKKCIVLLPEGKVALGKLAQAMFYGAKVIQVKGNFDDALD 184
           +   + GN  A+ AAY+A++G + ++  P+    +  + +    GA+V +V G  DD   
Sbjct: 202 IAMPTNGNAGAAAAAYAAQAGIEAVIFCPDDTPEI-NVREIAAQGARVYRVNGLIDDCGK 260

Query: 185 MVKQLAKEKLIYLLNSI-NPFRLEGQKTIAFEICDQLNWQVPDRVIVPVGNAGNISAIWK 243
           +V    +    + L+++  P+R+EG+KT+  E+ +QL W++PD +  P G    +  +WK
Sbjct: 261 LVGAGKEANGWFDLSTLKEPYRIEGKKTMGLELAEQLGWELPDVIFYPTGGGTGLIGMWK 320

Query: 244 GFKEFEITGII-DELPKMTGIQADGAKPIVEAFRKRAKDIIPYKNPETIATAIRIGNPVN 302
            F+E E  G I  + P+M  +QA+G  P+V A++   +    +++  T+A  IR+   V 
Sbjct: 321 AFEELEALGWIGSKRPRMVAVQAEGCAPMVRAWQGGERHATRWEDAHTLAAGIRVPQAVG 380

Query: 303 APKALDAIYSSGGYAEAVTDEEIVEAQKLLARKEGIFVEPASASSIAGLKKLLEEGIIDR 362
               LDA+ +S G+A AV+D  I+EA    AR +G+ + P   +++A  +K L +G+I  
Sbjct: 381 DFLILDAVRASNGFAMAVSDSAILEAVDDAARLDGLLLCPEGGATLAAWRKALVDGLIAP 440

Query: 363 DERIVCITTGHGLKDP 378
           D+R V      GLK P
Sbjct: 441 DDRAVLFNCATGLKYP 456


Lambda     K      H
   0.317    0.137    0.395 

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: 461
Number of extensions: 22
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: 405
Length of database: 475
Length adjustment: 32
Effective length of query: 373
Effective length of database: 443
Effective search space:   165239
Effective search space used:   165239
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 (21.6 bits)
S2: 51 (24.3 bits)

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

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