GapMind for Amino acid biosynthesis

 

Alignments for a candidate for gatD in Shewanella oneidensis MR-1

Align Glutamyl-tRNA(Gln) amidotransferase subunit D; Glu-ADT subunit D; EC 6.3.5.- (uncharacterized)
to candidate 201565 SO2421 L-asparaginase I (NCBI ptt file)

Query= curated2:O59132
         (438 letters)



>FitnessBrowser__MR1:201565
          Length = 337

 Score =  154 bits (388), Expect = 5e-42
 Identities = 110/339 (32%), Positives = 175/339 (51%), Gaps = 21/339 (6%)

Query: 99  TGGTIASRIDYETGAVYPAFTAEELAKAVPEIFEIANIKPKLLFN-----IFSEDMKPKH 153
           TGGTI  +   + G    A    +  +++PE +      P+ + +     I S +M P  
Sbjct: 11  TGGTIGMQ-KTDNGFAPVAGFLTQCVQSMPEFYHAE--MPEFVIHEYCPLIDSSNMAPTD 67

Query: 154 WIKIAHEVAKSLNSGDSGVVVAHGTDTMGYTAAALSFMLRDLGKPVILVGAQRSSDRPSS 213
           W  IA ++  + +  D G V+ HGTDTM YTA+ALSFML+ L KPVI+ G+Q    +  S
Sbjct: 68  WQMIADDINANYDKYD-GFVILHGTDTMAYTASALSFMLQGLSKPVIVTGSQIPLAQLRS 126

Query: 214 DAAMNLICSVRMSTS-DVAEVMVVMHGETGDTYCLAHRGTKVRKMHTSRRDAFRSINDVP 272
           D   NL+ S+ ++ +  VAEV +  + +         RG +  K H    DAF S N   
Sbjct: 127 DGQTNLLNSLYIAANYPVAEVCLFFNNKL-------FRGNRSTKAHADGFDAFASPNFPL 179

Query: 273 IAKVWPNGKIEFLRDDYRRRSDSEVWVDDKLEEKVALVKVYPGISSEIIEFFIDKGYRGI 332
           + +     KI          S++ + V +   + V +V +YPGIS++I E  + +  + +
Sbjct: 180 LLEA--GIKINLRAGKIATPSNNPLEVANISPQPVGVVTLYPGISTQIFENILQQPVKAL 237

Query: 333 VIEGTGLGHTPNDI--IPSIQRATEEGIAVCMTSQCIYGRVNLNVYATGRRLLKAGVIPC 390
           ++   G+G+ P D+  + ++++A E GI +   +QC  G+VN+  YATG  L KAGVI  
Sbjct: 238 ILLTFGVGNAPQDVALLRTLKQADERGIVLVNLTQCFQGKVNMGGYATGNALAKAGVISG 297

Query: 391 EDMLPETAYVKLMWVLGHTQDLEEVRRMMLTNYAGEITP 429
            DM  E A  KL ++L       E++  ML N  GE++P
Sbjct: 298 ADMTIEAALAKLHYLLSKNLKPIEIKTAMLQNLVGELSP 336


Lambda     K      H
   0.320    0.138    0.403 

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: 333
Number of extensions: 13
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: 438
Length of database: 337
Length adjustment: 30
Effective length of query: 408
Effective length of database: 307
Effective search space:   125256
Effective search space used:   125256
Neighboring words threshold: 11
Window for multiple hits: 40
X1: 16 ( 7.4 bits)
X2: 38 (14.6 bits)
X3: 64 (24.7 bits)
S1: 41 (21.8 bits)
S2: 50 (23.9 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